Log page index: User:ProteinBoxBot/PBB_Log_Index
Protein Status Quick Log - Date: 18:22, 9 November 2007 (UTC)[edit]
Proteins without matches (20)[edit]
Proteins with a High Potential Match (5)[edit]
Created (8)[edit]
Manual Inspection (Page not found) (17)[edit]
Protein Status Grid - Date: 18:22, 9 November 2007 (UTC)[edit]
Vebose Log - Date: 18:22, 9 November 2007 (UTC)[edit]
- INFO: Beginning work on ACADM... {November 9, 2007 2:10:10 AM PST}
- UPLOAD: Added new Image to wiki: File:PBB Protein ACADM image.jpg {November 9, 2007 2:10:54 AM PST}
- AMBIGUITY: Did not locate an acceptable page to update. {November 9, 2007 2:11:08 AM PST}
<!-- The PBB_Controls template provides controls for Protein Box Bot, please see Template:PBB_Controls for details. -->
{{PBB_Controls
| update_page = yes
| require_manual_inspection = no
| update_protein_box = yes
| update_summary = yes
| update_citations = yes
}}
<!-- The GNF_Protein_box is automatically maintained by Protein Box Bot. See Template:PBB_Controls to Stop updates. -->
{{GNF_Protein_box
| image = PBB_Protein_ACADM_image.jpg
| image_source = [[Protein_Data_Bank|PDB]] rendering based on 1egc.
| PDB = {{PDB2|1egc}}, {{PDB2|1egd}}, {{PDB2|1ege}}, {{PDB2|1t9g}}, {{PDB2|2a1t}}
| Name = Acyl-Coenzyme A dehydrogenase, C-4 to C-12 straight chain
| HGNCid = 89
| Symbol = ACADM
| AltSymbols =; ACAD1; MCAD; MCADH
| OMIM = 607008
| ECnumber =
| Homologene = 3
| MGIid =
| Function = {{GNF_GO|id=GO:0003995 |text = acyl-CoA dehydrogenase activity}} {{GNF_GO|id=GO:0050660 |text = FAD binding}}
| Component = {{GNF_GO|id=GO:0005739 |text = mitochondrion}} {{GNF_GO|id=GO:0005759 |text = mitochondrial matrix}}
| Process = {{GNF_GO|id=GO:0006118 |text = electron transport}} {{GNF_GO|id=GO:0006629 |text = lipid metabolic process}} {{GNF_GO|id=GO:0006631 |text = fatty acid metabolic process}} {{GNF_GO|id=GO:0006635 |text = fatty acid beta-oxidation}} {{GNF_GO|id=GO:0008152 |text = metabolic process}}
| Orthologs = {{GNF_Ortholog_box
| Hs_EntrezGene = 34
| Hs_Ensembl = ENSG00000117054
| Hs_RefseqProtein = NP_000007
| Hs_RefseqmRNA = NM_000016
| Hs_GenLoc_db =
| Hs_GenLoc_chr = 1
| Hs_GenLoc_start = 75962624
| Hs_GenLoc_end = 76001952
| Hs_Uniprot = P11310
| Mm_EntrezGene =
| Mm_Ensembl =
| Mm_RefseqmRNA =
| Mm_RefseqProtein =
| Mm_GenLoc_db =
| Mm_GenLoc_chr =
| Mm_GenLoc_start =
| Mm_GenLoc_end =
| Mm_Uniprot =
}}
}}
'''Acyl-Coenzyme A dehydrogenase, C-4 to C-12 straight chain''', also known as '''ACADM''', is a human [[gene]].
<!-- The PBB_Summary template is automatically maintained by Protein Box Bot. See Template:PBB_Controls to Stop updates. -->
{{PBB_Summary
| section_title =
| summary_text = This gene encodes the medium-chain specific (C4 to C12 straight chain) acyl-Coenzyme A dehydrogenase. The homotetramer enzyme catalyzes the initial step of the mitochondrial fatty acid beta-oxidation pathway. Clinical phenotypes are associated with ACADM hereditary deficiency.<ref>{{cite web | title = Entrez Gene: ACADM acyl-Coenzyme A dehydrogenase, C-4 to C-12 straight chain| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=34| accessdate = }}</ref>
}}
==References==
{{reflist}}
==Further reading==
{{refbegin | 2}}
{{PBB_Further_reading
| citations =
*{{cite journal | author=Tanaka K, Yokota I, Coates PM, ''et al.'' |title=Mutations in the medium chain acyl-CoA dehydrogenase (MCAD) gene. |journal=Hum. Mutat. |volume=1 |issue= 4 |pages= 271-9 |year= 1993 |pmid= 1363805 |doi= 10.1002/humu.1380010402 }}
}}
{{refend}}
{{protein-stub}}
- INFO: Beginning work on ACTA2... {November 9, 2007 2:11:08 AM PST}
- UPLOAD: Added new Image to wiki:
{November 9, 2007 2:11:58 AM PST}
- AMBIGUITY: Did not locate an acceptable page to update. {November 9, 2007 2:12:15 AM PST}
<!-- The PBB_Controls template provides controls for Protein Box Bot, please see Template:PBB_Controls for details. -->
{{PBB_Controls
| update_page = yes
| require_manual_inspection = no
| update_protein_box = yes
| update_summary = yes
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<!-- The GNF_Protein_box is automatically maintained by Protein Box Bot. See Template:PBB_Controls to Stop updates. -->
{{GNF_Protein_box
| image = PBB_Protein_ACTA2_image.jpg
| image_source = [[Protein_Data_Bank|PDB]] rendering based on 1atn.
| PDB = {{PDB2|1atn}}, {{PDB2|1c0f}}, {{PDB2|1c0g}}, {{PDB2|1d4x}}, {{PDB2|1dej}}, {{PDB2|1eqy}}, {{PDB2|1esv}}, {{PDB2|1h1v}}, {{PDB2|1hlu}}, {{PDB2|1ijj}}, {{PDB2|1j6z}}, {{PDB2|1kxp}}, {{PDB2|1lcu}}, {{PDB2|1lot}}, {{PDB2|1m8q}}, {{PDB2|1ma9}}, {{PDB2|1mdu}}, {{PDB2|1mvw}}, {{PDB2|1nlv}}, {{PDB2|1nm1}}, {{PDB2|1nmd}}, {{PDB2|1nwk}}, {{PDB2|1o18}}, {{PDB2|1o19}}, {{PDB2|1o1a}}, {{PDB2|1o1b}}, {{PDB2|1o1c}}, {{PDB2|1o1d}}, {{PDB2|1o1e}}, {{PDB2|1o1f}}, {{PDB2|1o1g}}, {{PDB2|1p8z}}, {{PDB2|1qz5}}, {{PDB2|1qz6}}, {{PDB2|1rdw}}, {{PDB2|1rfq}}, {{PDB2|1rgi}}, {{PDB2|1s22}}, {{PDB2|1sqk}}, {{PDB2|1t44}}, {{PDB2|1wua}}, {{PDB2|1y64}}, {{PDB2|1yxq}}, {{PDB2|2a3z}}, {{PDB2|2a40}}, {{PDB2|2a41}}, {{PDB2|2a42}}, {{PDB2|2a5x}}, {{PDB2|2asm}}, {{PDB2|2aso}}, {{PDB2|2asp}}, {{PDB2|2btf}}, {{PDB2|2d1k}}, {{PDB2|2ff3}}, {{PDB2|2ff6}}, {{PDB2|2fxu}}, {{PDB2|2gwj}}, {{PDB2|2gwk}}, {{PDB2|2hf3}}, {{PDB2|2hf4}}, {{PDB2|2hmp}}, {{PDB2|2oan}}, {{PDB2|2q1n}}, {{PDB2|2q31}}, {{PDB2|2q36}}
| Name = Actin, alpha 2, smooth muscle, aorta
| HGNCid = 130
| Symbol = ACTA2
| AltSymbols =; ACTSA
| OMIM = 102620
| ECnumber =
| Homologene = 48026
| MGIid = 87909
| GeneAtlas_image1 = PBB_GE_ACTA2_200974_at_tn.png
| Function = {{GNF_GO|id=GO:0000166 |text = nucleotide binding}} {{GNF_GO|id=GO:0005198 |text = structural molecule activity}} {{GNF_GO|id=GO:0005515 |text = protein binding}} {{GNF_GO|id=GO:0005524 |text = ATP binding}}
| Component = {{GNF_GO|id=GO:0005856 |text = cytoskeleton}}
| Process =
| Orthologs = {{GNF_Ortholog_box
| Hs_EntrezGene = 59
| Hs_Ensembl = ENSG00000107796
| Hs_RefseqProtein = NP_001604
| Hs_RefseqmRNA = NM_001613
| Hs_GenLoc_db =
| Hs_GenLoc_chr = 10
| Hs_GenLoc_start = 90684811
| Hs_GenLoc_end = 90741084
| Hs_Uniprot = P62736
| Mm_EntrezGene = 11475
| Mm_Ensembl = ENSMUSG00000035783
| Mm_RefseqmRNA = NM_007392
| Mm_RefseqProtein = NP_031418
| Mm_GenLoc_db =
| Mm_GenLoc_chr = 19
| Mm_GenLoc_start = 34307088
| Mm_GenLoc_end = 34321333
| Mm_Uniprot = Q3U122
}}
}}
'''Actin, alpha 2, smooth muscle, aorta''', also known as '''ACTA2''', is a human [[gene]].
<!-- The PBB_Summary template is automatically maintained by Protein Box Bot. See Template:PBB_Controls to Stop updates. -->
{{PBB_Summary
| section_title =
| summary_text = Actin alpha 2, the human aortic smooth muscle actin gene, is one of six different actin isoforms which have been identified. Actins are highly conserved proteins that are involved in cell motility, structure and integrity. Alpha actins are a major constituent of the contractile apparatus.<ref>{{cite web | title = Entrez Gene: ACTA2 actin, alpha 2, smooth muscle, aorta| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=59| accessdate = }}</ref>
}}
==References==
{{reflist}}
==Further reading==
{{refbegin | 2}}
{{PBB_Further_reading
| citations =
*{{cite journal | author=Snásel J, Pichová I |title=The cleavage of host cell proteins by HIV-1 protease. |journal=Folia Biol. (Praha) |volume=42 |issue= 5 |pages= 227-30 |year= 1997 |pmid= 8997639 |doi= }}
}}
{{refend}}
{{protein-stub}}
- INFO: Beginning work on ERVWE1... {November 9, 2007 10:12:36 AM PST}
- AMBIGUITY: Did not locate an acceptable page to update. {November 9, 2007 10:13:05 AM PST}
<!-- The PBB_Controls template provides controls for Protein Box Bot, please see Template:PBB_Controls for details. -->
{{PBB_Controls
| update_page = yes
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| update_protein_box = yes
| update_summary = yes
| update_citations = yes
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<!-- The GNF_Protein_box is automatically maintained by Protein Box Bot. See Template:PBB_Controls to Stop updates. -->
{{GNF_Protein_box
| image =
| image_source =
| PDB =
| Name = Endogenous retroviral family W, env(C7), member 1 (syncytin)
| HGNCid = 13525
| Symbol = ERVWE1
| AltSymbols =; Env-W; HERV-7q; HERV-W; HERV-W-ENV; HERVW; env
| OMIM = 604659
| ECnumber =
| Homologene =
| MGIid =
| Function = {{GNF_GO|id=GO:0005198 |text = structural molecule activity}}
| Component = {{GNF_GO|id=GO:0016020 |text = membrane}} {{GNF_GO|id=GO:0016021 |text = integral to membrane}} {{GNF_GO|id=GO:0019028 |text = viral capsid}} {{GNF_GO|id=GO:0019031 |text = viral envelope}}
| Process = {{GNF_GO|id=GO:0006313 |text = transposition, DNA-mediated}} {{GNF_GO|id=GO:0006949 |text = syncytium formation}} {{GNF_GO|id=GO:0009653 |text = anatomical structure morphogenesis}}
| Orthologs = {{GNF_Ortholog_box
| Hs_EntrezGene = 30816
| Hs_Ensembl = ENSG00000197604
| Hs_RefseqProtein = NP_055405
| Hs_RefseqmRNA = NM_014590
| Hs_GenLoc_db =
| Hs_GenLoc_chr = 7
| Hs_GenLoc_start = 91936015
| Hs_GenLoc_end = 91937631
| Hs_Uniprot = Q9UQF0
| Mm_EntrezGene =
| Mm_Ensembl =
| Mm_RefseqmRNA =
| Mm_RefseqProtein =
| Mm_GenLoc_db =
| Mm_GenLoc_chr =
| Mm_GenLoc_start =
| Mm_GenLoc_end =
| Mm_Uniprot =
}}
}}
'''Endogenous retroviral family W, env(C7), member 1 (syncytin)''', also known as '''ERVWE1''', is a human [[gene]].
<!-- The PBB_Summary template is automatically maintained by Protein Box Bot. See Template:PBB_Controls to Stop updates. -->
{{PBB_Summary
| section_title =
| summary_text = Many different human endogenous retrovirus (HERV) families are expressed in normal placental tissue at high levels, suggesting that HERVs are functionally important in reproduction. This gene is part of an HERV provirus on chromosome 7 that has inactivating mutations in the gag and pol genes. This gene is the envelope glycoprotein gene which appears to have been selectively preserved. The product of this gene, syncytin, is expressed in the placental syncytiotrophoblast and is involved in fusion of the cytotrophoblast cells to form the syncytial layer of the placenta. The protein has the characteristics of a typical retroviral envelope protein, including a furin cleavage site that separates the surface (SU) and transmembrane (TM) proteins which form a heterodimer.<ref>{{cite web | title = Entrez Gene: ERVWE1 endogenous retroviral family W, env(C7), member 1 (syncytin)| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=30816| accessdate = }}</ref>
}}
==References==
{{reflist}}
==Further reading==
{{refbegin | 2}}
{{PBB_Further_reading
| citations =
*{{cite journal | author=Muir A, Lever A, Moffett A |title=Expression and functions of human endogenous retroviruses in the placenta: an update. |journal=Placenta |volume=25 Suppl A |issue= |pages= S16-25 |year= 2004 |pmid= 15033302 |doi= 10.1016/j.placenta.2004.01.012 }}
}}
{{refend}}
{{protein-stub}}
- INFO: Beginning work on FBXW7... {November 9, 2007 10:13:45 AM PST}
- UPLOAD: Added new Image to wiki: File:PBB Protein FBXW7 image.jpg {November 9, 2007 10:14:22 AM PST}
- AMBIGUITY: Did not locate an acceptable page to update. {November 9, 2007 10:14:47 AM PST}
<!-- The PBB_Controls template provides controls for Protein Box Bot, please see Template:PBB_Controls for details. -->
{{PBB_Controls
| update_page = yes
| require_manual_inspection = no
| update_protein_box = yes
| update_summary = yes
| update_citations = yes
}}
<!-- The GNF_Protein_box is automatically maintained by Protein Box Bot. See Template:PBB_Controls to Stop updates. -->
{{GNF_Protein_box
| image = PBB_Protein_FBXW7_image.jpg
| image_source = [[Protein_Data_Bank|PDB]] rendering based on 2ovp.
| PDB = {{PDB2|2ovp}}, {{PDB2|2ovq}}, {{PDB2|2ovr}}
| Name = F-box and WD repeat domain containing 7
| HGNCid = 16712
| Symbol = FBXW7
| AltSymbols =; AGO; CDC4; DKFZp686F23254; FBW7; FBX30; FBXW6; SEL-10; SEL10
| OMIM = 606278
| ECnumber =
| Homologene = 69520
| MGIid = 1354695
| GeneAtlas_image1 = PBB_GE_FBXW7_218751_s_at_tn.png
| Function = {{GNF_GO|id=GO:0003700 |text = transcription factor activity}} {{GNF_GO|id=GO:0005515 |text = protein binding}}
| Component = {{GNF_GO|id=GO:0005634 |text = nucleus}} {{GNF_GO|id=GO:0005783 |text = endoplasmic reticulum}} {{GNF_GO|id=GO:0005794 |text = Golgi apparatus}}
| Process = {{GNF_GO|id=GO:0007219 |text = Notch signaling pathway}} {{GNF_GO|id=GO:0016567 |text = protein ubiquitination}}
| Orthologs = {{GNF_Ortholog_box
| Hs_EntrezGene = 55294
| Hs_Ensembl = ENSG00000109670
| Hs_RefseqProtein = NP_001013433
| Hs_RefseqmRNA = NM_001013415
| Hs_GenLoc_db =
| Hs_GenLoc_chr = 4
| Hs_GenLoc_start = 153461860
| Hs_GenLoc_end = 153675622
| Hs_Uniprot = Q969H0
| Mm_EntrezGene = 50754
| Mm_Ensembl = ENSMUSG00000028086
| Mm_RefseqmRNA = NM_080428
| Mm_RefseqProtein = NP_536353
| Mm_GenLoc_db =
| Mm_GenLoc_chr = 3
| Mm_GenLoc_start = 85038138
| Mm_GenLoc_end = 85063572
| Mm_Uniprot = Q8VBV4
}}
}}
'''F-box and WD repeat domain containing 7''', also known as '''FBXW7''', is a human [[gene]].
<!-- The PBB_Summary template is automatically maintained by Protein Box Bot. See Template:PBB_Controls to Stop updates. -->
{{PBB_Summary
| section_title =
| summary_text = This gene encodes a member of the F-box protein family which is characterized by an approximately 40 amino acid motif, the F-box. The F-box proteins constitute one of the four subunits of ubiquitin protein ligase complex called SCFs (SKP1-cullin-F-box), which function in phosphorylation-dependent ubiquitination. The F-box proteins are divided into 3 classes: Fbws containing WD-40 domains, Fbls containing leucine-rich repeats, and Fbxs containing either different protein-protein interaction modules or no recognizable motifs. The protein encoded by this gene was previously referred to as FBX30, and belongs to the Fbws class; in addition to an F-box, this protein contains 7 tandem WD40 repeats. This protein binds directly to cyclin E and probably targets cyclin E for ubiquitin-mediated degradation. Mutations in this gene are detected in ovarian and breast cancer cell lines, implicating the gene's potential role in the pathogenesis of human cancers. Three transcript variants encoding three different isoforms have been found for this gene.<ref>{{cite web | title = Entrez Gene: FBXW7 F-box and WD repeat domain containing 7| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=55294| accessdate = }}</ref>
}}
==References==
{{reflist}}
{{refbegin | 2}}
{{PBB_Further_reading
| citations =
}}
{{refend}}
{{protein-stub}}
- INFO: Beginning work on GTF2H2... {November 9, 2007 9:54:57 AM PST}
- UPLOAD: Added new Image to wiki: File:PBB Protein GTF2H2 image.jpg {November 9, 2007 9:55:11 AM PST}
- AMBIGUITY: Did not locate an acceptable page to update. {November 9, 2007 9:55:30 AM PST}
<!-- The PBB_Controls template provides controls for Protein Box Bot, please see Template:PBB_Controls for details. -->
{{PBB_Controls
| update_page = yes
| require_manual_inspection = no
| update_protein_box = yes
| update_summary = yes
| update_citations = yes
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<!-- The GNF_Protein_box is automatically maintained by Protein Box Bot. See Template:PBB_Controls to Stop updates. -->
{{GNF_Protein_box
| image = PBB_Protein_GTF2H2_image.jpg
| image_source = [[Protein_Data_Bank|PDB]] rendering based on 1z60.
| PDB = {{PDB2|1z60}}
| Name = General transcription factor IIH, polypeptide 2, 44kDa
| HGNCid = 4656
| Symbol = GTF2H2
| AltSymbols =; BTF2; TFIIH; BTF2P44; MGC102806; T-BTF2P44
| OMIM = 601748
| ECnumber =
| Homologene = 1159
| MGIid = 1345669
| Function = {{GNF_GO|id=GO:0003700 |text = transcription factor activity}} {{GNF_GO|id=GO:0003702 |text = RNA polymerase II transcription factor activity}} {{GNF_GO|id=GO:0008135 |text = translation factor activity, nucleic acid binding}} {{GNF_GO|id=GO:0008270 |text = zinc ion binding}} {{GNF_GO|id=GO:0046872 |text = metal ion binding}}
| Component = {{GNF_GO|id=GO:0005634 |text = nucleus}} {{GNF_GO|id=GO:0005675 |text = holo TFIIH complex}}
| Process = {{GNF_GO|id=GO:0006281 |text = DNA repair}} {{GNF_GO|id=GO:0006352 |text = transcription initiation}} {{GNF_GO|id=GO:0006355 |text = regulation of transcription, DNA-dependent}} {{GNF_GO|id=GO:0009411 |text = response to UV}}
| Orthologs = {{GNF_Ortholog_box
| Hs_EntrezGene = 2966
| Hs_Ensembl =
| Hs_RefseqProtein = NP_001506
| Hs_RefseqmRNA = NM_001515
| Hs_GenLoc_db =
| Hs_GenLoc_chr =
| Hs_GenLoc_start =
| Hs_GenLoc_end =
| Hs_Uniprot =
| Mm_EntrezGene = 23894
| Mm_Ensembl = ENSMUSG00000021639
| Mm_RefseqmRNA = NM_022011
| Mm_RefseqProtein = NP_071294
| Mm_GenLoc_db =
| Mm_GenLoc_chr = 13
| Mm_GenLoc_start = 101568837
| Mm_GenLoc_end = 101592836
| Mm_Uniprot = Q7TPV0
}}
}}
'''General transcription factor IIH, polypeptide 2, 44kDa''', also known as '''GTF2H2''', is a human [[gene]].
<!-- The PBB_Summary template is automatically maintained by Protein Box Bot. See Template:PBB_Controls to Stop updates. -->
{{PBB_Summary
| section_title =
| summary_text = This gene is part of a 500 kb inverted duplication on chromosome 5q13. This duplicated region contains at least four genes and repetitive elements which make it prone to rearrangements and deletions. The repetitiveness and complexity of the sequence have also caused difficulty in determining the organization of this genomic region. This gene is within the telomeric copy of the duplication. Deletion of this gene sometimes accompanies deletion of the neighboring SMN1 gene in spinal muscular atrophy (SMA) patients but it is unclear if deletion of this gene contributes to the SMA phenotype. This gene encodes the 44 kDa subunit of RNA polymerase II transcription initiation factor IIH which is involved in basal transcription and nucleotide excision repair. Transcript variants for this gene have been described, but their full length nature has not been determined. A second copy of this gene within the centromeric copy of the duplication has been described in the literature. It is reported to be different by either two or four base pairs; however, no sequence data is currently available for the centromeric copy of the gene.<ref>{{cite web | title = Entrez Gene: GTF2H2 general transcription factor IIH, polypeptide 2, 44kDa| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=2966| accessdate = }}</ref>
}}
==References==
{{reflist}}
==Further reading==
{{refbegin | 2}}
{{PBB_Further_reading
| citations =
*{{cite journal | author=Svejstrup JQ, Vichi P, Egly JM |title=The multiple roles of transcription/repair factor TFIIH. |journal=Trends Biochem. Sci. |volume=21 |issue= 9 |pages= 346-50 |year= 1996 |pmid= 8870499 |doi= }}
*{{cite journal | author=Jeang KT |title=Tat, Tat-associated kinase, and transcription. |journal=J. Biomed. Sci. |volume=5 |issue= 1 |pages= 24-7 |year= 1998 |pmid= 9570510 |doi= }}
*{{cite journal | author=Yankulov K, Bentley D |title=Transcriptional control: Tat cofactors and transcriptional elongation. |journal=Curr. Biol. |volume=8 |issue= 13 |pages= R447-9 |year= 1998 |pmid= 9651670 |doi= }}
}}
{{refend}}
{{protein-stub}}
- INFO: Beginning work on HLA-DMA... {November 9, 2007 9:56:25 AM PST}
- UPLOAD: Added new Image to wiki: File:PBB Protein HLA-DMA image.jpg {November 9, 2007 9:56:58 AM PST}
- AMBIGUITY: Did not locate an acceptable page to update. {November 9, 2007 9:57:15 AM PST}
<!-- The PBB_Controls template provides controls for Protein Box Bot, please see Template:PBB_Controls for details. -->
{{PBB_Controls
| update_page = yes
| require_manual_inspection = no
| update_protein_box = yes
| update_summary = yes
| update_citations = yes
}}
<!-- The GNF_Protein_box is automatically maintained by Protein Box Bot. See Template:PBB_Controls to Stop updates. -->
{{GNF_Protein_box
| image = PBB_Protein_HLA-DMA_image.jpg
| image_source = [[Protein_Data_Bank|PDB]] rendering based on 1hdm.
| PDB = {{PDB2|1hdm}}, {{PDB2|2bc4}}
| Name = Major histocompatibility complex, class II, DM alpha
| HGNCid = 4934
| Symbol = HLA-DMA
| AltSymbols =; D6S222E; DMA; HLADM; RING6
| OMIM = 142855
| ECnumber =
| Homologene = 4464
| MGIid = 95921
| GeneAtlas_image1 = PBB_GE_HLA-DMA_217478_s_at_tn.png
| Function = {{GNF_GO|id=GO:0005515 |text = protein binding}} {{GNF_GO|id=GO:0032395 |text = MHC class II receptor activity}}
| Component = {{GNF_GO|id=GO:0005575 |text = cellular_component}} {{GNF_GO|id=GO:0005622 |text = intracellular}} {{GNF_GO|id=GO:0005765 |text = lysosomal membrane}} {{GNF_GO|id=GO:0005771 |text = multivesicular body}} {{GNF_GO|id=GO:0010008 |text = endosome membrane}} {{GNF_GO|id=GO:0016020 |text = membrane}} {{GNF_GO|id=GO:0016021 |text = integral to membrane}} {{GNF_GO|id=GO:0042613 |text = MHC class II protein complex}}
| Process = {{GNF_GO|id=GO:0002504 |text = antigen processing and presentation of peptide or polysaccharide antigen via MHC class II}} {{GNF_GO|id=GO:0006461 |text = protein complex assembly}} {{GNF_GO|id=GO:0006955 |text = immune response}} {{GNF_GO|id=GO:0008150 |text = biological_process}} {{GNF_GO|id=GO:0015031 |text = protein transport}} {{GNF_GO|id=GO:0016064 |text = immunoglobulin mediated immune response}} {{GNF_GO|id=GO:0019886 |text = antigen processing and presentation of exogenous peptide antigen via MHC class II}} {{GNF_GO|id=GO:0045059 |text = positive thymic T cell selection}} {{GNF_GO|id=GO:0045582 |text = positive regulation of T cell differentiation}} {{GNF_GO|id=GO:0050778 |text = positive regulation of immune response}} {{GNF_GO|id=GO:0051085 |text = chaperone cofactor-dependent protein folding}}
| Orthologs = {{GNF_Ortholog_box
| Hs_EntrezGene = 3108
| Hs_Ensembl = ENSG00000204257
| Hs_RefseqProtein = NP_006111
| Hs_RefseqmRNA = NM_006120
| Hs_GenLoc_db =
| Hs_GenLoc_chr = 6
| Hs_GenLoc_start = 33024367
| Hs_GenLoc_end = 33028877
| Hs_Uniprot = P28067
| Mm_EntrezGene = 14998
| Mm_Ensembl = ENSMUSG00000037649
| Mm_RefseqmRNA = NM_010386
| Mm_RefseqProtein = NP_034516
| Mm_GenLoc_db =
| Mm_GenLoc_chr = 17
| Mm_GenLoc_start = 33746125
| Mm_GenLoc_end = 33748991
| Mm_Uniprot = Q31096
}}
}}
'''Major histocompatibility complex, class II, DM alpha''', also known as '''HLA-DMA''', is a human [[gene]].
<!-- The PBB_Summary template is automatically maintained by Protein Box Bot. See Template:PBB_Controls to Stop updates. -->
{{PBB_Summary
| section_title =
| summary_text = HLA-DMA belongs to the HLA class II alpha chain paralogues. This class II molecule is a heterodimer consisting of an alpha (DMA) and a beta chain (DMB), both anchored in the membrane. It is located in intracellular vesicles. DM plays a central role in the peptide loading of MHC class II molecules by helping to release the CLIP molecule from the peptide binding site. Class II molecules are expressed in antigen presenting cells (APC: B lymphocytes, dendritic cells, macrophages). The alpha chain is approximately 33-35 kDa and its gene contains 5 exons. Exon one encodes the leader peptide, exons 2 and 3 encode the two extracellular domains, exon 4 encodes the transmembrane domain and the cytoplasmic tail.<ref>{{cite web | title = Entrez Gene: HLA-DMA major histocompatibility complex, class II, DM alpha| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=3108| accessdate = }}</ref>
}}
==References==
{{reflist}}
==Further reading==
{{refbegin | 2}}
{{PBB_Further_reading
| citations =
*{{cite journal | author=Vogt AB, Kropshofer H |title=HLA-DM - an endosomal and lysosomal chaperone for the immune system. |journal=Trends Biochem. Sci. |volume=24 |issue= 4 |pages= 150-4 |year= 1999 |pmid= 10322421 |doi= }}
*{{cite journal | author=Kropshofer H, Hämmerling GJ, Vogt AB |title=The impact of the non-classical MHC proteins HLA-DM and HLA-DO on loading of MHC class II molecules. |journal=Immunol. Rev. |volume=172 |issue= |pages= 267-78 |year= 2000 |pmid= 10631952 |doi= }}
}}
{{refend}}
{{protein-stub}}
- INFO: Beginning work on HSP90AB1... {November 9, 2007 9:57:15 AM PST}
- UPLOAD: Added new Image to wiki: File:PBB Protein HSP90AB1 image.jpg {November 9, 2007 9:57:34 AM PST}
- CREATE: Found no pages, creating new page. {November 9, 2007 9:57:56 AM PST}
- CREATED: Created new protein page: HSP90AB1 {November 9, 2007 9:58:03 AM PST}
- INFO: Beginning work on ICAM2... {November 9, 2007 9:58:03 AM PST}
- UPLOAD: Added new Image to wiki: File:PBB Protein ICAM2 image.jpg {November 9, 2007 9:58:57 AM PST}
- CREATE: Found no pages, creating new page. {November 9, 2007 9:59:07 AM PST}
- CREATED: Created new protein page: ICAM2 {November 9, 2007 9:59:14 AM PST}
- INFO: Beginning work on IDUA... {November 9, 2007 9:59:14 AM PST}
- AMBIGUITY: Did not locate an acceptable page to update. {November 9, 2007 10:00:05 AM PST}
<!-- The PBB_Controls template provides controls for Protein Box Bot, please see Template:PBB_Controls for details. -->
{{PBB_Controls
| update_page = yes
| require_manual_inspection = no
| update_protein_box = yes
| update_summary = yes
| update_citations = yes
}}
<!-- The GNF_Protein_box is automatically maintained by Protein Box Bot. See Template:PBB_Controls to Stop updates. -->
{{GNF_Protein_box
| image =
| image_source =
| PDB =
| Name = Iduronidase, alpha-L-
| HGNCid = 5391
| Symbol = IDUA
| AltSymbols =; IDA; MPS1
| OMIM = 252800
| ECnumber =
| Homologene = 170
| MGIid = 96418
| GeneAtlas_image1 = PBB_GE_IDUA_205059_s_at_tn.png
| GeneAtlas_image2 = PBB_GE_IDUA_205057_s_at_tn.png
| Function = {{GNF_GO|id=GO:0003940 |text = L-iduronidase activity}} {{GNF_GO|id=GO:0004553 |text = hydrolase activity, hydrolyzing O-glycosyl compounds}} {{GNF_GO|id=GO:0043169 |text = cation binding}}
| Component = {{GNF_GO|id=GO:0005764 |text = lysosome}}
| Process = {{GNF_GO|id=GO:0005975 |text = carbohydrate metabolic process}} {{GNF_GO|id=GO:0005984 |text = disaccharide metabolic process}} {{GNF_GO|id=GO:0008152 |text = metabolic process}} {{GNF_GO|id=GO:0030203 |text = glycosaminoglycan metabolic process}}
| Orthologs = {{GNF_Ortholog_box
| Hs_EntrezGene = 3425
| Hs_Ensembl = ENSG00000127415
| Hs_RefseqProtein = NP_000194
| Hs_RefseqmRNA = NM_000203
| Hs_GenLoc_db =
| Hs_GenLoc_chr = 4
| Hs_GenLoc_start = 970785
| Hs_GenLoc_end = 988316
| Hs_Uniprot = P35475
| Mm_EntrezGene = 15932
| Mm_Ensembl = ENSMUSG00000033540
| Mm_RefseqmRNA = NM_008325
| Mm_RefseqProtein = NP_032351
| Mm_GenLoc_db =
| Mm_GenLoc_chr = 5
| Mm_GenLoc_start = 108909613
| Mm_GenLoc_end = 108924856
| Mm_Uniprot = Q3TDU4
}}
}}
'''Iduronidase, alpha-L-''', also known as '''IDUA''', is a human [[gene]].
<!-- The PBB_Summary template is automatically maintained by Protein Box Bot. See Template:PBB_Controls to Stop updates. -->
{{PBB_Summary
| section_title =
| summary_text = This gene encodes an enzyme that hydrolyzes the teminal alpha-L-iduronic acid residues of two glycosaminoglycans, dermatan sulfate and heparan sulfate. This hydrolysis is required for the lysosomal degradation of these glycosaminoglycans. Mutations in this gene that result in enzymatic deficiency lead to the autosomal recessive disease Mucopolysaccharidosis Type I (MPS I).<ref>{{cite web | title = Entrez Gene: IDUA iduronidase, alpha-L-| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=3425| accessdate = }}</ref>
}}
==References==
{{reflist}}
==Further reading==
{{refbegin | 2}}
{{PBB_Further_reading
| citations =
*{{cite journal | author=Neufeld EF |title=Lysosomal storage diseases. |journal=Annu. Rev. Biochem. |volume=60 |issue= |pages= 257-80 |year= 1991 |pmid= 1883197 |doi= 10.1146/annurev.bi.60.070191.001353 }}
*{{cite journal | author=Scott HS, Bunge S, Gal A, ''et al.'' |title=Molecular genetics of mucopolysaccharidosis type I: diagnostic, clinical, and biological implications. |journal=Hum. Mutat. |volume=6 |issue= 4 |pages= 288-302 |year= 1996 |pmid= 8680403 |doi= 10.1002/humu.1380060403 }}
}}
{{refend}}
{{protein-stub}}
- INFO: Beginning work on LIFR... {November 9, 2007 10:00:05 AM PST}
- AMBIGUITY: Did not locate an acceptable page to update. {November 9, 2007 10:00:55 AM PST}
<!-- The PBB_Controls template provides controls for Protein Box Bot, please see Template:PBB_Controls for details. -->
{{PBB_Controls
| update_page = yes
| require_manual_inspection = no
| update_protein_box = yes
| update_summary = yes
| update_citations = yes
}}
<!-- The GNF_Protein_box is automatically maintained by Protein Box Bot. See Template:PBB_Controls to Stop updates. -->
{{GNF_Protein_box
| image =
| image_source =
| PDB =
| Name = Leukemia inhibitory factor receptor alpha
| HGNCid = 6597
| Symbol = LIFR
| AltSymbols =; CD118; SJS2; STWS; SWS
| OMIM = 151443
| ECnumber =
| Homologene = 1735
| MGIid = 96788
| GeneAtlas_image1 = PBB_GE_LIFR_205876_at_tn.png
| Function = {{GNF_GO|id=GO:0004872 |text = receptor activity}} {{GNF_GO|id=GO:0004923 |text = leukemia inhibitory factor receptor activity}} {{GNF_GO|id=GO:0005515 |text = protein binding}}
| Component = {{GNF_GO|id=GO:0005887 |text = integral to plasma membrane}} {{GNF_GO|id=GO:0016020 |text = membrane}}
| Process = {{GNF_GO|id=GO:0007166 |text = cell surface receptor linked signal transduction}} {{GNF_GO|id=GO:0008284 |text = positive regulation of cell proliferation}}
| Orthologs = {{GNF_Ortholog_box
| Hs_EntrezGene = 3977
| Hs_Ensembl = ENSG00000113594
| Hs_RefseqProtein = NP_002301
| Hs_RefseqmRNA = NM_002310
| Hs_GenLoc_db =
| Hs_GenLoc_chr = 5
| Hs_GenLoc_start = 38510823
| Hs_GenLoc_end = 38631253
| Hs_Uniprot = P42702
| Mm_EntrezGene = 16880
| Mm_Ensembl = ENSMUSG00000054263
| Mm_RefseqmRNA = NM_013584
| Mm_RefseqProtein = NP_038612
| Mm_GenLoc_db =
| Mm_GenLoc_chr = 15
| Mm_GenLoc_start = 7101575
| Mm_GenLoc_end = 7138433
| Mm_Uniprot = O35672
}}
}}
'''Leukemia inhibitory factor receptor alpha''', also known as '''LIFR''', is a human [[gene]].
<!-- The PBB_Summary template is automatically maintained by Protein Box Bot. See Template:PBB_Controls to Stop updates. -->
{{PBB_Summary
| section_title =
| summary_text = The leukemia inhibitory factor is a polyfunctional cytokine that affects the differentiation, survival, and proliferation of a wide variety of cells in the adult and the embryo. LIF action appears to be mediated through a high-affinity receptor complex composed of a low-affinity LIF binding chain (LIF receptor) and a high-affinity converter subunit, gp130. Both LIFR and gp130 are members of a family of cytokine receptors that includes components of the receptors for the majority of hematopoietic cytokines and for cytokines that affect other systems, including the ciliary neurotrophic factor, growth hormone and prolactin.<ref>{{cite web | title = Entrez Gene: LIFR leukemia inhibitory factor receptor alpha| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=3977| accessdate = }}</ref>
}}
==References==
{{reflist}}
==Further reading==
{{refbegin | 2}}
{{PBB_Further_reading
| citations =
*{{cite journal | author=Tomida M |title=Structural and functional studies on the leukemia inhibitory factor receptor (LIF-R): gene and soluble form of LIF-R, and cytoplasmic domain of LIF-R required for differentiation and growth arrest of myeloid leukemic cells. |journal=Leuk. Lymphoma |volume=37 |issue= 5-6 |pages= 517-25 |year= 2003 |pmid= 11042511 |doi= }}
*{{cite journal | author=Lass A, Weiser W, Munafo A, Loumaye E |title=Leukemia inhibitory factor in human reproduction. |journal=Fertil. Steril. |volume=76 |issue= 6 |pages= 1091-6 |year= 2002 |pmid= 11730732 |doi= }}
}}
{{refend}}
{{protein-stub}}
- INFO: Beginning work on MAP2K7... {November 9, 2007 10:07:41 AM PST}
- AMBIGUITY: Did not locate an acceptable page to update. {November 9, 2007 10:08:01 AM PST}
<!-- The PBB_Controls template provides controls for Protein Box Bot, please see Template:PBB_Controls for details. -->
{{PBB_Controls
| update_page = yes
| require_manual_inspection = no
| update_protein_box = yes
| update_summary = yes
| update_citations = yes
}}
<!-- The GNF_Protein_box is automatically maintained by Protein Box Bot. See Template:PBB_Controls to Stop updates. -->
{{GNF_Protein_box
| image =
| image_source =
| PDB =
| Name = Mitogen-activated protein kinase kinase 7
| HGNCid = 6847
| Symbol = MAP2K7
| AltSymbols =; Jnkk2; MAPKK7; MKK7; PRKMK7
| OMIM = 603014
| ECnumber =
| Homologene = 56548
| MGIid = 1346871
| Function = {{GNF_GO|id=GO:0000166 |text = nucleotide binding}} {{GNF_GO|id=GO:0000287 |text = magnesium ion binding}} {{GNF_GO|id=GO:0004674 |text = protein serine/threonine kinase activity}} {{GNF_GO|id=GO:0004708 |text = MAP kinase kinase activity}} {{GNF_GO|id=GO:0004713 |text = protein-tyrosine kinase activity}} {{GNF_GO|id=GO:0005515 |text = protein binding}} {{GNF_GO|id=GO:0005524 |text = ATP binding}} {{GNF_GO|id=GO:0016740 |text = transferase activity}} {{GNF_GO|id=GO:0019901 |text = protein kinase binding}}
| Component = {{GNF_GO|id=GO:0005634 |text = nucleus}} {{GNF_GO|id=GO:0005737 |text = cytoplasm}}
| Process = {{GNF_GO|id=GO:0006468 |text = protein amino acid phosphorylation}} {{GNF_GO|id=GO:0006950 |text = response to stress}} {{GNF_GO|id=GO:0007165 |text = signal transduction}} {{GNF_GO|id=GO:0051403 |text = stress-activated MAPK cascade}}
| Orthologs = {{GNF_Ortholog_box
| Hs_EntrezGene = 5609
| Hs_Ensembl =
| Hs_RefseqProtein = NP_660186
| Hs_RefseqmRNA = NM_145185
| Hs_GenLoc_db =
| Hs_GenLoc_chr =
| Hs_GenLoc_start =
| Hs_GenLoc_end =
| Hs_Uniprot =
| Mm_EntrezGene = 26400
| Mm_Ensembl = ENSMUSG00000002948
| Mm_RefseqmRNA = NM_001042557
| Mm_RefseqProtein = NP_001036022
| Mm_GenLoc_db =
| Mm_GenLoc_chr = 8
| Mm_GenLoc_start = 4238828
| Mm_GenLoc_end = 4251420
| Mm_Uniprot = Q8CE90
}}
}}
'''Mitogen-activated protein kinase kinase 7''', also known as '''MAP2K7''', is a human [[gene]].
<!-- The PBB_Summary template is automatically maintained by Protein Box Bot. See Template:PBB_Controls to Stop updates. -->
{{PBB_Summary
| section_title =
| summary_text = The protein encoded by this gene is a dual specificity protein kinase that belongs to the MAP kinase kinase family. This kinase specifically activates MAPK8/JNK1 and MAPK9/JNK2, and this kinase itself is phosphorylated and activated by MAP kinase kinase kinases including MAP3K1/MEKK1, MAP3K2/MEKK2,MAP3K3/MEKK5, and MAP4K2/GCK. This kinase is involved in the signal transduction mediating the cell responses to proinflammatory cytokines, and environmental stresses. Multiple alternatively spliced transcript variants encoding distinct isoforms have been found, but only one transcript variant has been supported and defined.<ref>{{cite web | title = Entrez Gene: MAP2K7 mitogen-activated protein kinase kinase 7| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=5609| accessdate = }}</ref>
}}
==References==
{{reflist}}
{{refbegin | 2}}
{{PBB_Further_reading
| citations =
}}
{{refend}}
{{protein-stub}}
- INFO: Beginning work on MCAM... {November 9, 2007 10:00:55 AM PST}
- AMBIGUITY: Did not locate an acceptable page to update. {November 9, 2007 10:02:23 AM PST}
<!-- The PBB_Controls template provides controls for Protein Box Bot, please see Template:PBB_Controls for details. -->
{{PBB_Controls
| update_page = yes
| require_manual_inspection = no
| update_protein_box = yes
| update_summary = yes
| update_citations = yes
}}
<!-- The GNF_Protein_box is automatically maintained by Protein Box Bot. See Template:PBB_Controls to Stop updates. -->
{{GNF_Protein_box
| image =
| image_source =
| PDB =
| Name = Melanoma cell adhesion molecule
| HGNCid = 6934
| Symbol = MCAM
| AltSymbols =; CD146; MUC18
| OMIM = 155735
| ECnumber =
| Homologene = 4742
| MGIid = 1933966
| GeneAtlas_image1 = PBB_GE_MCAM_211340_s_at_tn.png
| GeneAtlas_image2 = PBB_GE_MCAM_209086_x_at_tn.png
| GeneAtlas_image3 = PBB_GE_MCAM_209087_x_at_tn.png
| Function = {{GNF_GO|id=GO:0005515 |text = protein binding}}
| Component = {{GNF_GO|id=GO:0005886 |text = plasma membrane}} {{GNF_GO|id=GO:0005887 |text = integral to plasma membrane}}
| Process = {{GNF_GO|id=GO:0007155 |text = cell adhesion}} {{GNF_GO|id=GO:0009653 |text = anatomical structure morphogenesis}}
| Orthologs = {{GNF_Ortholog_box
| Hs_EntrezGene = 4162
| Hs_Ensembl = ENSG00000076706
| Hs_RefseqProtein = NP_006491
| Hs_RefseqmRNA = NM_006500
| Hs_GenLoc_db =
| Hs_GenLoc_chr = 11
| Hs_GenLoc_start = 118684444
| Hs_GenLoc_end = 118693050
| Hs_Uniprot = P43121
| Mm_EntrezGene = 84004
| Mm_Ensembl = ENSMUSG00000032135
| Mm_RefseqmRNA = NM_023061
| Mm_RefseqProtein = NP_075548
| Mm_GenLoc_db =
| Mm_GenLoc_chr = 9
| Mm_GenLoc_start = 43885666
| Mm_GenLoc_end = 43893719
| Mm_Uniprot = Q8R2Y2
}}
}}
'''Melanoma cell adhesion molecule''', also known as '''MCAM''', is a human [[gene]].
<!-- The PBB_Summary template is automatically maintained by Protein Box Bot. See Template:PBB_Controls to Stop updates. -->
{{PBB_Summary
| section_title =
| summary_text =
}}
==Further reading==
{{refbegin | 2}}
{{PBB_Further_reading
| citations =
*{{cite journal | author=Johnson JP, Rothbächer U, Sers C |title=The progression associated antigen MUC18: a unique member of the immunoglobulin supergene family. |journal=Melanoma Res. |volume=3 |issue= 5 |pages= 337-40 |year= 1994 |pmid= 8292890 |doi= }}
*{{cite journal | author=Shih IM |title=The role of CD146 (Mel-CAM) in biology and pathology. |journal=J. Pathol. |volume=189 |issue= 1 |pages= 4-11 |year= 2000 |pmid= 10451481 |doi= 10.1002/(SICI)1096-9896(199909)189:1<4::AID-PATH332>3.0.CO;2-P }}
*{{cite journal | author=McGary EC, Lev DC, Bar-Eli M |title=Cellular adhesion pathways and metastatic potential of human melanoma. |journal=Cancer Biol. Ther. |volume=1 |issue= 5 |pages= 459-65 |year= 2003 |pmid= 12496470 |doi= }}
}}
{{refend}}
{{protein-stub}}
- INFO: Beginning work on NCF4... {November 9, 2007 10:02:47 AM PST}
- UPLOAD: Added new Image to wiki: File:PBB Protein NCF4 image.jpg {November 9, 2007 10:03:40 AM PST}
- AMBIGUITY: Did not locate an acceptable page to update. {November 9, 2007 10:03:56 AM PST}
<!-- The PBB_Controls template provides controls for Protein Box Bot, please see Template:PBB_Controls for details. -->
{{PBB_Controls
| update_page = yes
| require_manual_inspection = no
| update_protein_box = yes
| update_summary = yes
| update_citations = yes
}}
<!-- The GNF_Protein_box is automatically maintained by Protein Box Bot. See Template:PBB_Controls to Stop updates. -->
{{GNF_Protein_box
| image = PBB_Protein_NCF4_image.jpg
| image_source = [[Protein_Data_Bank|PDB]] rendering based on 1h6h.
| PDB = {{PDB2|1h6h}}, {{PDB2|1oey}}, {{PDB2|1w6x}}, {{PDB2|1w70}}, {{PDB2|1z9q}}, {{PDB2|2dyb}}
| Name = Neutrophil cytosolic factor 4, 40kDa
| HGNCid = 7662
| Symbol = NCF4
| AltSymbols =; MGC3810; NCF; P40PHOX; SH3PXD4
| OMIM = 601488
| ECnumber =
| Homologene = 525
| MGIid = 109186
| GeneAtlas_image1 = PBB_GE_NCF4_207677_s_at_tn.png
| GeneAtlas_image2 = PBB_GE_NCF4_205147_x_at_tn.png
| Function = {{GNF_GO|id=GO:0035091 |text = phosphoinositide binding}} {{GNF_GO|id=GO:0046983 |text = protein dimerization activity}}
| Component = {{GNF_GO|id=GO:0005829 |text = cytosol}} {{GNF_GO|id=GO:0016020 |text = membrane}} {{GNF_GO|id=GO:0043020 |text = NADPH oxidase complex}}
| Process = {{GNF_GO|id=GO:0006118 |text = electron transport}} {{GNF_GO|id=GO:0006955 |text = immune response}} {{GNF_GO|id=GO:0007154 |text = cell communication}}
| Orthologs = {{GNF_Ortholog_box
| Hs_EntrezGene = 4689
| Hs_Ensembl = ENSG00000100365
| Hs_RefseqProtein = NP_000622
| Hs_RefseqmRNA = NM_000631
| Hs_GenLoc_db =
| Hs_GenLoc_chr = 22
| Hs_GenLoc_start = 35586976
| Hs_GenLoc_end = 35604003
| Hs_Uniprot = Q15080
| Mm_EntrezGene = 17972
| Mm_Ensembl = ENSMUSG00000071715
| Mm_RefseqmRNA = NM_008677
| Mm_RefseqProtein = NP_032703
| Mm_GenLoc_db =
| Mm_GenLoc_chr = 15
| Mm_GenLoc_start = 78072089
| Mm_GenLoc_end = 78089829
| Mm_Uniprot = Q3TBC6
}}
}}
'''Neutrophil cytosolic factor 4, 40kDa''', also known as '''NCF4''', is a human [[gene]].
<!-- The PBB_Summary template is automatically maintained by Protein Box Bot. See Template:PBB_Controls to Stop updates. -->
{{PBB_Summary
| section_title =
| summary_text = The protein encoded by this gene is a cytosolic regulatory component of the superoxide-producing phagocyte NADPH-oxidase, a multicomponent enzyme system important for host defense. This protein is preferentially expressed in cells of myeloid lineage. It interacts primarily with neutrophil cytosolic factor 2 (NCF2/p67-phox) to form a complex with neutrophil cytosolic factor 1 (NCF1/p47-phox), which further interacts with the small G protein RAC1 and translocates to the membrane upon cell stimulation. This complex then activates flavocytochrome b, the membrane-integrated catalytic core of the enzyme system. The PX domain of this protein can bind phospholipid products of the PI(3) kinase, which suggests its role in PI(3) kinase-mediated signaling events. The phosphorylation of this protein was found to negatively regulate the enzyme activity. Alternatively spliced transcript variants encoding distinct isoforms have been observed.<ref>{{cite web | title = Entrez Gene: NCF4 neutrophil cytosolic factor 4, 40kDa| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=4689| accessdate = }}</ref>
}}
==References==
{{reflist}}
==Further reading==
{{refbegin | 2}}
{{PBB_Further_reading
| citations =
*{{cite journal | author=Matute JD, Arias AA, Dinauer MC, Patiño PJ |title=p40phox: the last NADPH oxidase subunit. |journal=Blood Cells Mol. Dis. |volume=35 |issue= 2 |pages= 291-302 |year= 2006 |pmid= 16102984 |doi= 10.1016/j.bcmd.2005.06.010 }}
}}
{{refend}}
{{protein-stub}}
- INFO: Beginning work on ND3... {November 9, 2007 10:02:23 AM PST}
- CREATE: Found no pages, creating new page. {November 9, 2007 10:02:39 AM PST}
- CREATED: Created new protein page: ND3 {November 9, 2007 10:02:47 AM PST}
- INFO: Beginning work on NOTCH2... {November 9, 2007 10:03:56 AM PST}
- UPLOAD: Added new Image to wiki: File:PBB Protein NOTCH2 image.jpg {November 9, 2007 10:05:26 AM PST}
- CREATE: Found no pages, creating new page. {November 9, 2007 10:05:38 AM PST}
- CREATED: Created new protein page: NOTCH2 {November 9, 2007 10:05:45 AM PST}
- INFO: Beginning work on PAX5... {November 9, 2007 10:06:40 AM PST}
- UPLOAD: Added new Image to wiki: {November 9, 2007 10:07:30 AM PST}
- AMBIGUITY: Did not locate an acceptable page to update. {November 9, 2007 10:07:41 AM PST}
<!-- The PBB_Controls template provides controls for Protein Box Bot, please see Template:PBB_Controls for details. -->
{{PBB_Controls
| update_page = yes
| require_manual_inspection = no
| update_protein_box = yes
| update_summary = yes
| update_citations = yes
}}
<!-- The GNF_Protein_box is automatically maintained by Protein Box Bot. See Template:PBB_Controls to Stop updates. -->
{{GNF_Protein_box
| image = PBB_Protein_PAX5_image.jpg
| image_source = [[Protein_Data_Bank|PDB]] rendering based on 1k78.
| PDB = {{PDB2|1k78}}, {{PDB2|1mdm}}
| Name = Paired box gene 5 (B-cell lineage specific activator)
| HGNCid = 8619
| Symbol = PAX5
| AltSymbols =; BSAP
| OMIM = 167414
| ECnumber =
| Homologene = 56419
| MGIid = 97489
| GeneAtlas_image1 = PBB_GE_PAX5_206802_at_tn.png
| GeneAtlas_image2 = PBB_GE_PAX5_221969_at_tn.png
| Function = {{GNF_GO|id=GO:0003677 |text = DNA binding}} {{GNF_GO|id=GO:0003700 |text = transcription factor activity}} {{GNF_GO|id=GO:0005515 |text = protein binding}}
| Component = {{GNF_GO|id=GO:0005634 |text = nucleus}}
| Process = {{GNF_GO|id=GO:0006350 |text = transcription}} {{GNF_GO|id=GO:0006355 |text = regulation of transcription, DNA-dependent}} {{GNF_GO|id=GO:0006366 |text = transcription from RNA polymerase II promoter}} {{GNF_GO|id=GO:0006959 |text = humoral immune response}} {{GNF_GO|id=GO:0007275 |text = multicellular organismal development}} {{GNF_GO|id=GO:0007283 |text = spermatogenesis}} {{GNF_GO|id=GO:0007399 |text = nervous system development}} {{GNF_GO|id=GO:0009887 |text = organ morphogenesis}} {{GNF_GO|id=GO:0030154 |text = cell differentiation}}
| Orthologs = {{GNF_Ortholog_box
| Hs_EntrezGene = 5079
| Hs_Ensembl = ENSG00000196092
| Hs_RefseqProtein = NP_057953
| Hs_RefseqmRNA = NM_016734
| Hs_GenLoc_db =
| Hs_GenLoc_chr = 9
| Hs_GenLoc_start = 36823272
| Hs_GenLoc_end = 37024476
| Hs_Uniprot = Q02548
| Mm_EntrezGene = 18507
| Mm_Ensembl = ENSMUSG00000014030
| Mm_RefseqmRNA = NM_008782
| Mm_RefseqProtein = NP_032808
| Mm_GenLoc_db =
| Mm_GenLoc_chr = 4
| Mm_GenLoc_start = 44552606
| Mm_GenLoc_end = 44731762
| Mm_Uniprot = Q02650
}}
}}
'''Paired box gene 5 (B-cell lineage specific activator)''', also known as '''PAX5''', is a human [[gene]].
<!-- The PBB_Summary template is automatically maintained by Protein Box Bot. See Template:PBB_Controls to Stop updates. -->
{{PBB_Summary
| section_title =
| summary_text = The PAX5 gene is a member of the paired box (PAX) family of transcription factors. The central feature of this gene family is a novel, highly conserved DNA-binding motif, known as the paired box. The PAX proteins are important regulators in early development, and alterations in the expression of their genes are thought to contribute to neoplastic transformation. The PAX5 gene encodes the B-cell lineage specific activator protein (BSAP) that is expressed at early, but not late stages of B-cell differentiation. Its expression has also been detected in developing CNS and testis, therefore, PAX5 gene product may not only play an important role in B-cell differentiation, but also in neural development and spermatogenesis. The PAX5 gene is located in chromosome 9p13 region, which is involved in t(9;14)(p13;q32) translocations recurring in small lymphocytic lymphomas of the plasmacytoid subtype, and in derived large-cell lymphomas. This translocation brings the potent E-mu enhancer of the IgH gene into close proximity of the PAX5 promoters, suggesting that the deregulation of PAX5 gene transcription contributes to the pathogenesis of these lymphomas. A transcript variant arising as a consequence of alternative promoter usage, and containing a different coding exon 1(B), has been described, however, its full-length nature is not known.<ref>{{cite web | title = Entrez Gene: PAX5 paired box gene 5 (B-cell lineage specific activator)| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=5079| accessdate = }}</ref>
}}
==References==
{{reflist}}
==Further reading==
{{refbegin | 2}}
{{PBB_Further_reading
| citations =
*{{cite journal | author=Hagman J, Wheat W, Fitzsimmons D, ''et al.'' |title=Pax-5/BSAP: regulator of specific gene expression and differentiation in B lymphocytes. |journal=Curr. Top. Microbiol. Immunol. |volume=245 |issue= 1 |pages= 169-94 |year= 1999 |pmid= 10533313 |doi= }}
*{{cite journal | author=Calame KL, Lin KI, Tunyaplin C |title=Regulatory mechanisms that determine the development and function of plasma cells. |journal=Annu. Rev. Immunol. |volume=21 |issue= |pages= 205-30 |year= 2003 |pmid= 12524387 |doi= 10.1146/annurev.immunol.21.120601.141138 }}
*{{cite journal | author=Carotta S, Holmes ML, Pridans C, Nutt SL |title=Pax5 maintains cellular identity by repressing gene expression throughout B cell differentiation. |journal=Cell Cycle |volume=5 |issue= 21 |pages= 2452-6 |year= 2007 |pmid= 17102626 |doi= }}
}}
{{refend}}
{{protein-stub}}
- INFO: Beginning work on PRDX1... {November 9, 2007 10:05:45 AM PST}
- UPLOAD: Added new Image to wiki: File:PBB Protein PRDX1 image.jpg {November 9, 2007 10:06:19 AM PST}
- AMBIGUITY: Did not locate an acceptable page to update. {November 9, 2007 10:06:40 AM PST}
<!-- The PBB_Controls template provides controls for Protein Box Bot, please see Template:PBB_Controls for details. -->
{{PBB_Controls
| update_page = yes
| require_manual_inspection = no
| update_protein_box = yes
| update_summary = yes
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<!-- The GNF_Protein_box is automatically maintained by Protein Box Bot. See Template:PBB_Controls to Stop updates. -->
{{GNF_Protein_box
| image = PBB_Protein_PRDX1_image.jpg
| image_source = [[Protein_Data_Bank|PDB]] rendering based on 1qq2.
| PDB = {{PDB2|1qq2}}
| Name = Peroxiredoxin 1
| HGNCid = 9352
| Symbol = PRDX1
| AltSymbols =; MSP23; NKEFA; PAG; PAGA; PAGB; TDPX2
| OMIM = 176763
| ECnumber =
| Homologene = 21685
| MGIid = 99523
| GeneAtlas_image1 = PBB_GE_PRDX1_208680_at_tn.png
| Function = {{GNF_GO|id=GO:0016491 |text = oxidoreductase activity}} {{GNF_GO|id=GO:0051920 |text = peroxiredoxin activity}}
| Component =
| Process = {{GNF_GO|id=GO:0001501 |text = skeletal development}} {{GNF_GO|id=GO:0008283 |text = cell proliferation}}
| Orthologs = {{GNF_Ortholog_box
| Hs_EntrezGene = 5052
| Hs_Ensembl = ENSG00000117450
| Hs_RefseqProtein = NP_002565
| Hs_RefseqmRNA = NM_002574
| Hs_GenLoc_db =
| Hs_GenLoc_chr = 1
| Hs_GenLoc_start = 45749295
| Hs_GenLoc_end = 45760215
| Hs_Uniprot = Q06830
| Mm_EntrezGene = 18477
| Mm_Ensembl = ENSMUSG00000028691
| Mm_RefseqmRNA = NM_011034
| Mm_RefseqProtein = NP_035164
| Mm_GenLoc_db =
| Mm_GenLoc_chr = 4
| Mm_GenLoc_start = 116183531
| Mm_GenLoc_end = 116197932
| Mm_Uniprot = Q3U9J9
}}
}}
'''Peroxiredoxin 1''', also known as '''PRDX1''', is a human [[gene]].
<!-- The PBB_Summary template is automatically maintained by Protein Box Bot. See Template:PBB_Controls to Stop updates. -->
{{PBB_Summary
| section_title =
| summary_text = This gene encodes a member of the peroxiredoxin family of antioxidant enzymes, which reduce hydrogen peroxide and alkyl hydroperoxides. The encoded protein may play an antioxidant protective role in cells, and may contribute to the antiviral activity of CD8(+) T-cells. This protein may have a proliferative effect and play a role in cancer development or progression. Three transcript variants encoding the same protein have been identified for this gene.<ref>{{cite web | title = Entrez Gene: PRDX1 peroxiredoxin 1| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=5052| accessdate = }}</ref>
}}
==References==
{{reflist}}
==Further reading==
{{refbegin | 2}}
{{PBB_Further_reading
| citations =
*{{cite journal | author=Wood ZA, Schröder E, Robin Harris J, Poole LB |title=Structure, mechanism and regulation of peroxiredoxins. |journal=Trends Biochem. Sci. |volume=28 |issue= 1 |pages= 32-40 |year= 2003 |pmid= 12517450 |doi= }}
}}
{{refend}}
{{protein-stub}}
- INFO: Beginning work on PRKAG2... {November 9, 2007 10:13:05 AM PST}
- AMBIGUITY: Did not locate an acceptable page to update. {November 9, 2007 10:13:45 AM PST}
<!-- The PBB_Controls template provides controls for Protein Box Bot, please see Template:PBB_Controls for details. -->
{{PBB_Controls
| update_page = yes
| require_manual_inspection = no
| update_protein_box = yes
| update_summary = yes
| update_citations = yes
}}
<!-- The GNF_Protein_box is automatically maintained by Protein Box Bot. See Template:PBB_Controls to Stop updates. -->
{{GNF_Protein_box
| image =
| image_source =
| PDB =
| Name = Protein kinase, AMP-activated, gamma 2 non-catalytic subunit
| HGNCid = 9386
| Symbol = PRKAG2
| AltSymbols =; AAKG; AAKG2; CMH6; H91620p; WPWS
| OMIM = 602743
| ECnumber =
| Homologene = 81846
| MGIid = 1336153
| GeneAtlas_image1 = PBB_GE_PRKAG2_218292_s_at_tn.png
| Function = {{GNF_GO|id=GO:0003674 |text = molecular_function}}
| Component = {{GNF_GO|id=GO:0005575 |text = cellular_component}}
| Process = {{GNF_GO|id=GO:0006633 |text = fatty acid biosynthetic process}} {{GNF_GO|id=GO:0006695 |text = cholesterol biosynthetic process}}
| Orthologs = {{GNF_Ortholog_box
| Hs_EntrezGene = 51422
| Hs_Ensembl = ENSG00000106617
| Hs_RefseqProtein = NP_001035723
| Hs_RefseqmRNA = NM_001040633
| Hs_GenLoc_db =
| Hs_GenLoc_chr = 7
| Hs_GenLoc_start = 150884960
| Hs_GenLoc_end = 151204728
| Hs_Uniprot = Q9UGJ0
| Mm_EntrezGene = 108099
| Mm_Ensembl = ENSMUSG00000028944
| Mm_RefseqmRNA = NM_145401
| Mm_RefseqProtein = NP_663376
| Mm_GenLoc_db =
| Mm_GenLoc_chr = 5
| Mm_GenLoc_start = 24372813
| Mm_GenLoc_end = 24610495
| Mm_Uniprot = Q3TMN8
}}
}}
'''Protein kinase, AMP-activated, gamma 2 non-catalytic subunit''', also known as '''PRKAG2''', is a human [[gene]].
<!-- The PBB_Summary template is automatically maintained by Protein Box Bot. See Template:PBB_Controls to Stop updates. -->
{{PBB_Summary
| section_title =
| summary_text = AMP-activated protein kinase (AMPK) is a heterotrimeric protein composed of a catalytic alpha subunit, a noncatalytic beta subunit, and a noncatalytic regulatory gamma subunit. Various forms of each of these subunits exist, encoded by different genes. AMPK is an important energy-sensing enzyme that monitors cellular energy status and functions by inactivating key enzymes involved in regulating de novo biosynthesis of fatty acid and cholesterol. This gene is a member of the AMPK gamma subunit family and encodes a protein with four cystathionine beta-synthase domains. Mutations in this gene have been associated with ventricular pre-excitation (Wolff-Parkinson-White syndrome), progressive conduction system disease and cardiac hypertrophy. Alternate transcriptional splice variants, encoding different isoforms, have been characterized.<ref>{{cite web | title = Entrez Gene: PRKAG2 protein kinase, AMP-activated, gamma 2 non-catalytic subunit| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=51422| accessdate = }}</ref>
}}
==References==
{{reflist}}
==Further reading==
{{refbegin | 2}}
{{PBB_Further_reading
| citations =
*{{cite journal | author=Gollob MH, Green MS, Tang AS, Roberts R |title=PRKAG2 cardiac syndrome: familial ventricular preexcitation, conduction system disease, and cardiac hypertrophy. |journal=Curr. Opin. Cardiol. |volume=17 |issue= 3 |pages= 229-34 |year= 2002 |pmid= 12015471 |doi= }}
*{{cite journal | author=Gollob MH |title=Glycogen storage disease as a unifying mechanism of disease in the PRKAG2 cardiac syndrome. |journal=Biochem. Soc. Trans. |volume=31 |issue= Pt 1 |pages= 228-31 |year= 2003 |pmid= 12546691 |doi= 10.1042/ }}
}}
{{refend}}
{{protein-stub}}
- INFO: Beginning work on PTGER4... {November 9, 2007 10:08:01 AM PST}
- CREATE: Found no pages, creating new page. {November 9, 2007 10:08:19 AM PST}
- CREATED: Created new protein page: PTGER4 {November 9, 2007 10:08:26 AM PST}
- INFO: Beginning work on PURA... {November 9, 2007 10:08:26 AM PST}
- CREATE: Found no pages, creating new page. {November 9, 2007 10:09:23 AM PST}
- CREATED: Created new protein page: PURA {November 9, 2007 10:09:30 AM PST}
- INFO: Beginning work on PYGM... {November 9, 2007 10:09:30 AM PST}
- UPLOAD: Added new Image to wiki: File:PBB Protein PYGM image.jpg {November 9, 2007 10:10:03 AM PST}
- AMBIGUITY: Did not locate an acceptable page to update. {November 9, 2007 10:10:11 AM PST}
<!-- The PBB_Controls template provides controls for Protein Box Bot, please see Template:PBB_Controls for details. -->
{{PBB_Controls
| update_page = yes
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<!-- The GNF_Protein_box is automatically maintained by Protein Box Bot. See Template:PBB_Controls to Stop updates. -->
{{GNF_Protein_box
| image = PBB_Protein_PYGM_image.jpg
| image_source = [[Protein_Data_Bank|PDB]] rendering based on 1a8i.
| PDB = {{PDB2|1a8i}}, {{PDB2|1abb}}, {{PDB2|1axr}}, {{PDB2|1b4d}}, {{PDB2|1bx3}}, {{PDB2|1c50}}, {{PDB2|1c8k}}, {{PDB2|1c8l}}, {{PDB2|1e1y}}, {{PDB2|1fs4}}, {{PDB2|1ftq}}, {{PDB2|1ftw}}, {{PDB2|1fty}}, {{PDB2|1fu4}}, {{PDB2|1fu7}}, {{PDB2|1fu8}}, {{PDB2|1gfz}}, {{PDB2|1gg8}}, {{PDB2|1ggn}}, {{PDB2|1gpa}}, {{PDB2|1gpb}}, {{PDB2|1gpy}}, {{PDB2|1h5u}}, {{PDB2|1hlf}}, {{PDB2|1k06}}, {{PDB2|1k08}}, {{PDB2|1kti}}, {{PDB2|1lwn}}, {{PDB2|1lwo}}, {{PDB2|1noi}}, {{PDB2|1noj}}, {{PDB2|1nok}}, {{PDB2|1p29}}, {{PDB2|1p2b}}, {{PDB2|1p2d}}, {{PDB2|1p2g}}, {{PDB2|1p4g}}, {{PDB2|1p4h}}, {{PDB2|1p4j}}, {{PDB2|1pyg}}, {{PDB2|1uzu}}, {{PDB2|1wut}}, {{PDB2|1wuy}}, {{PDB2|1wv0}}, {{PDB2|1wv1}}, {{PDB2|1ww2}}, {{PDB2|1ww3}}, {{PDB2|1xc7}}, {{PDB2|1xkx}}, {{PDB2|1xl0}}, {{PDB2|1xl1}}, {{PDB2|1z62}}, {{PDB2|1z6p}}, {{PDB2|1z6q}}, {{PDB2|1z8d}}, {{PDB2|2amv}}, {{PDB2|2f3p}}, {{PDB2|2f3q}}, {{PDB2|2f3s}}, {{PDB2|2f3u}}, {{PDB2|2fet}}, {{PDB2|2ff5}}, {{PDB2|2ffr}}, {{PDB2|2g9q}}, {{PDB2|2g9r}}, {{PDB2|2g9u}}, {{PDB2|2g9v}}, {{PDB2|2gj4}}, {{PDB2|2gm9}}, {{PDB2|2gpa}}, {{PDB2|2gpb}}, {{PDB2|2gpn}}, {{PDB2|2ieg}}, {{PDB2|2iei}}, {{PDB2|2pri}}, {{PDB2|2prj}}, {{PDB2|2skc}}, {{PDB2|2skd}}, {{PDB2|2ske}}, {{PDB2|3amv}}, {{PDB2|3gpb}}, {{PDB2|4gpb}}, {{PDB2|5gpb}}, {{PDB2|6gpb}}, {{PDB2|7gpb}}, {{PDB2|8gpb}}, {{PDB2|9gpb}}
| Name = Phosphorylase, glycogen; muscle (McArdle syndrome, glycogen storage disease type V)
| HGNCid = 9726
| Symbol = PYGM
| AltSymbols =;
| OMIM = 608455
| ECnumber =
| Homologene = 2145
| MGIid = 97830
| GeneAtlas_image1 = PBB_GE_PYGM_205577_at_tn.png
| Function = {{GNF_GO|id=GO:0000166 |text = nucleotide binding}} {{GNF_GO|id=GO:0008184 |text = glycogen phosphorylase activity}} {{GNF_GO|id=GO:0016757 |text = transferase activity, transferring glycosyl groups}} {{GNF_GO|id=GO:0030170 |text = pyridoxal phosphate binding}}
| Component =
| Process = {{GNF_GO|id=GO:0005975 |text = carbohydrate metabolic process}} {{GNF_GO|id=GO:0005980 |text = glycogen catabolic process}}
| Orthologs = {{GNF_Ortholog_box
| Hs_EntrezGene = 5837
| Hs_Ensembl = ENSG00000068976
| Hs_RefseqProtein = NP_005600
| Hs_RefseqmRNA = NM_005609
| Hs_GenLoc_db =
| Hs_GenLoc_chr = 11
| Hs_GenLoc_start = 64270437
| Hs_GenLoc_end = 64284763
| Hs_Uniprot = P11217
| Mm_EntrezGene = 19309
| Mm_Ensembl = ENSMUSG00000032648
| Mm_RefseqmRNA = NM_011224
| Mm_RefseqProtein = NP_035354
| Mm_GenLoc_db =
| Mm_GenLoc_chr = 19
| Mm_GenLoc_start = 6384429
| Mm_GenLoc_end = 6398459
| Mm_Uniprot = Q9CTZ0
}}
}}
'''Phosphorylase, glycogen; muscle (McArdle syndrome, glycogen storage disease type V)''', also known as '''PYGM''', is a human [[gene]].
<!-- The PBB_Summary template is automatically maintained by Protein Box Bot. See Template:PBB_Controls to Stop updates. -->
{{PBB_Summary
| section_title =
| summary_text = Glycogen phosphorylase (EC 2.4.1.1) catalyzes and regulates the breakdown of glycogen to glucose-1-phosphate.[supplied by OMIM]<ref>{{cite web | title = Entrez Gene: PYGM phosphorylase, glycogen; muscle (McArdle syndrome, glycogen storage disease type V)| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=5837| accessdate = }}</ref>
}}
==References==
{{reflist}}
{{refbegin | 2}}
{{PBB_Further_reading
| citations =
}}
{{refend}}
{{protein-stub}}
- INFO: Beginning work on RAD17... {November 9, 2007 10:10:12 AM PST}
- CREATE: Found no pages, creating new page. {November 9, 2007 10:11:34 AM PST}
- CREATED: Created new protein page: RAD17 {November 9, 2007 10:11:41 AM PST}
- INFO: Beginning work on RAP1GAP... {November 9, 2007 10:11:41 AM PST}
- UPLOAD: Added new Image to wiki: File:PBB Protein RAP1GAP image.jpg {November 9, 2007 10:12:15 AM PST}
- CREATE: Found no pages, creating new page. {November 9, 2007 10:12:29 AM PST}
- CREATED: Created new protein page: RAP1GAP {November 9, 2007 10:12:36 AM PST}
- INFO: Beginning work on RHOC... {November 9, 2007 2:12:15 AM PST}
- UPLOAD: Added new Image to wiki: File:PBB Protein RHOC image.jpg {November 9, 2007 9:54:33 AM PST}
- AMBIGUITY: Did not locate an acceptable page to update. {November 9, 2007 9:54:57 AM PST}
<!-- The PBB_Controls template provides controls for Protein Box Bot, please see Template:PBB_Controls for details. -->
{{PBB_Controls
| update_page = yes
| require_manual_inspection = no
| update_protein_box = yes
| update_summary = yes
| update_citations = yes
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<!-- The GNF_Protein_box is automatically maintained by Protein Box Bot. See Template:PBB_Controls to Stop updates. -->
{{GNF_Protein_box
| image = PBB_Protein_RHOC_image.jpg
| image_source = [[Protein_Data_Bank|PDB]] rendering based on 1a2b.
| PDB = {{PDB2|1a2b}}, {{PDB2|1cc0}}, {{PDB2|1cxz}}, {{PDB2|1dpf}}, {{PDB2|1ftn}}, {{PDB2|1kmq}}, {{PDB2|1lb1}}, {{PDB2|1ow3}}, {{PDB2|1s1c}}, {{PDB2|1tx4}}, {{PDB2|1x86}}, {{PDB2|1xcg}}, {{PDB2|1z2c}}, {{PDB2|2gcn}}, {{PDB2|2gco}}, {{PDB2|2gcp}}
| Name = Ras homolog gene family, member C
| HGNCid = 669
| Symbol = RHOC
| AltSymbols =; ARH9; ARHC; H9; MGC1448; MGC61427; RHOH9
| OMIM = 165380
| ECnumber =
| Homologene = 56380
| MGIid = 106028
| GeneAtlas_image1 = PBB_GE_RHOC_200885_at_tn.png
| Function = {{GNF_GO|id=GO:0000166 |text = nucleotide binding}} {{GNF_GO|id=GO:0003924 |text = GTPase activity}} {{GNF_GO|id=GO:0004871 |text = signal transducer activity}} {{GNF_GO|id=GO:0005525 |text = GTP binding}}
| Component = {{GNF_GO|id=GO:0005622 |text = intracellular}} {{GNF_GO|id=GO:0016020 |text = membrane}}
| Process = {{GNF_GO|id=GO:0007264 |text = small GTPase mediated signal transduction}} {{GNF_GO|id=GO:0043123 |text = positive regulation of I-kappaB kinase/NF-kappaB cascade}}
| Orthologs = {{GNF_Ortholog_box
| Hs_EntrezGene = 389
| Hs_Ensembl = ENSG00000155366
| Hs_RefseqProtein = NP_001036143
| Hs_RefseqmRNA = NM_001042678
| Hs_GenLoc_db =
| Hs_GenLoc_chr = 1
| Hs_GenLoc_start = 113045251
| Hs_GenLoc_end = 113051579
| Hs_Uniprot = P08134
| Mm_EntrezGene = 11853
| Mm_Ensembl = ENSMUSG00000002233
| Mm_RefseqmRNA = NM_007484
| Mm_RefseqProtein = NP_031510
| Mm_GenLoc_db =
| Mm_GenLoc_chr = 3
| Mm_GenLoc_start = 104917090
| Mm_GenLoc_end = 104922515
| Mm_Uniprot = Q62159
}}
}}
'''Ras homolog gene family, member C''', also known as '''RHOC''', is a human [[gene]].
<!-- The PBB_Summary template is automatically maintained by Protein Box Bot. See Template:PBB_Controls to Stop updates. -->
{{PBB_Summary
| section_title =
| summary_text = This gene encodes a member of the Rho family of small GTPases, which cycle between inactive GDP-bound and active GTP-bound states and function as molecular switches in signal transduction cascades. Rho proteins promote reorganization of the actin cytoskeleton and regulate cell shape, attachment, and motility. The protein encoded by this gene is prenylated at its C-terminus, and localizes to the cytoplasm and plasma membrane. It is thought to be important in cell locomotion. Overexpression of this gene is associated with tumor cell proliferation and metastasis. Multiple alternatively spliced variants, encoding the same protein, have been identified.<ref>{{cite web | title = Entrez Gene: RHOC ras homolog gene family, member C| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=389| accessdate = }}</ref>
}}
==References==
{{reflist}}
==Further reading==
{{refbegin | 2}}
{{PBB_Further_reading
| citations =
*{{cite journal | author=Wennerberg K, Der CJ |title=Rho-family GTPases: it's not only Rac and Rho (and I like it). |journal=J. Cell. Sci. |volume=117 |issue= Pt 8 |pages= 1301-12 |year= 2004 |pmid= 15020670 |doi= 10.1242/jcs.01118 }}
*{{cite journal | author=Wheeler AP, Ridley AJ |title=Why three Rho proteins? RhoA, RhoB, RhoC, and cell motility. |journal=Exp. Cell Res. |volume=301 |issue= 1 |pages= 43-9 |year= 2004 |pmid= 15501444 |doi= 10.1016/j.yexcr.2004.08.012 }}
}}
{{refend}}
{{protein-stub}}
- INFO: Beginning work on SERPIND1... {November 9, 2007 9:55:30 AM PST}
- UPLOAD: Added new Image to wiki: File:PBB Protein SERPIND1 image.jpg {November 9, 2007 9:56:02 AM PST}
- AMBIGUITY: Did not locate an acceptable page to update. {November 9, 2007 9:56:25 AM PST}
<!-- The PBB_Controls template provides controls for Protein Box Bot, please see Template:PBB_Controls for details. -->
{{PBB_Controls
| update_page = yes
| require_manual_inspection = no
| update_protein_box = yes
| update_summary = yes
| update_citations = yes
}}
<!-- The GNF_Protein_box is automatically maintained by Protein Box Bot. See Template:PBB_Controls to Stop updates. -->
{{GNF_Protein_box
| image = PBB_Protein_SERPIND1_image.jpg
| image_source = [[Protein_Data_Bank|PDB]] rendering based on 1jmj.
| PDB = {{PDB2|1jmj}}, {{PDB2|1jmo}}
| Name = Serpin peptidase inhibitor, clade D (heparin cofactor), member 1
| HGNCid = 4838
| Symbol = SERPIND1
| AltSymbols =; D22S673; HC2; HCF2; HCII; HLS2; LS2
| OMIM = 142360
| ECnumber =
| Homologene = 36018
| MGIid = 96051
| GeneAtlas_image1 = PBB_GE_SERPIND1_205576_at_tn.png
| Function = {{GNF_GO|id=GO:0004867 |text = serine-type endopeptidase inhibitor activity}} {{GNF_GO|id=GO:0008201 |text = heparin binding}}
| Component = {{GNF_GO|id=GO:0005576 |text = extracellular region}}
| Process = {{GNF_GO|id=GO:0006935 |text = chemotaxis}} {{GNF_GO|id=GO:0007596 |text = blood coagulation}}
| Orthologs = {{GNF_Ortholog_box
| Hs_EntrezGene = 3053
| Hs_Ensembl = ENSG00000099937
| Hs_RefseqProtein = NP_000176
| Hs_RefseqmRNA = NM_000185
| Hs_GenLoc_db =
| Hs_GenLoc_chr = 22
| Hs_GenLoc_start = 19458383
| Hs_GenLoc_end = 19472008
| Hs_Uniprot = P05546
| Mm_EntrezGene = 15160
| Mm_Ensembl = ENSMUSG00000022766
| Mm_RefseqmRNA = NM_008223
| Mm_RefseqProtein = NP_032249
| Mm_GenLoc_db =
| Mm_GenLoc_chr = 16
| Mm_GenLoc_start = 17244978
| Mm_GenLoc_end = 17257137
| Mm_Uniprot = Q5FW62
}}
}}
'''Serpin peptidase inhibitor, clade D (heparin cofactor), member 1''', also known as '''SERPIND1''', is a human [[gene]].
<!-- The PBB_Summary template is automatically maintained by Protein Box Bot. See Template:PBB_Controls to Stop updates. -->
{{PBB_Summary
| section_title =
| summary_text = The product encoded by this gene is a serine proteinase inhibitor which rapidly inhibits thrombin in the presence of dermatan sulfate or heparin. The gene contains five exons and four introns. This protein shares homology with antithrombin III and other members of the alpha 1-antitrypsin superfamily. Mutations in this gene are associated with heparin cofactor II deficiency.<ref>{{cite web | title = Entrez Gene: SERPIND1 serpin peptidase inhibitor, clade D (heparin cofactor), member 1| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=3053| accessdate = }}</ref>
}}
==References==
{{reflist}}
==Further reading==
{{refbegin | 2}}
{{PBB_Further_reading
| citations =
*{{cite journal | author=Uszyński M |title=Tissue anticoagulants in the human placenta: preliminary study with a heparin-like anticoagulant and review of the literature. |journal=Gynecol. Obstet. Invest. |volume=32 |issue= 3 |pages= 129-33 |year= 1992 |pmid= 1836773 |doi= }}
*{{cite journal | author=Pizzo SV |title=Serpin receptor 1: a hepatic receptor that mediates the clearance of antithrombin III-proteinase complexes. |journal=Am. J. Med. |volume=87 |issue= 3B |pages= 10S-14S |year= 1989 |pmid= 2552799 |doi= }}
}}
{{refend}}
{{protein-stub}}
end log.
