Homo sapiens Protein: SRCAP | |||||||||||||||||||
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Summary | |||||||||||||||||||
InnateDB Protein | IDBP-26752.6 | ||||||||||||||||||
Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||||||||||||||||
Gene Symbol | SRCAP | ||||||||||||||||||
Protein Name | Snf2-related CREBBP activator protein | ||||||||||||||||||
Synonyms | DOMO1; EAF1; FLHS; SWR1; | ||||||||||||||||||
Species | Homo sapiens | ||||||||||||||||||
Ensembl Protein | ENSP00000262518 | ||||||||||||||||||
InnateDB Gene | IDBG-26746 (SRCAP) | ||||||||||||||||||
Protein Structure |
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UniProt Annotation | |||||||||||||||||||
Function | Catalytic component of the SRCAP complex which mediates the ATP-dependent exchange of histone H2AZ/H2B dimers for nucleosomal H2A/H2B, leading to transcriptional regulation of selected genes by chromatin remodeling. Acts as a coactivator for CREB-mediated transcription, steroid receptor-mediated transcription, and Notch-mediated transcription. {ECO:0000269PubMed:10347196, ECO:0000269PubMed:11522779, ECO:0000269PubMed:14500758, ECO:0000269PubMed:16024792, ECO:0000269PubMed:16634648, ECO:0000269PubMed:17617668}. | ||||||||||||||||||
Subcellular Localization | Nucleus {ECO:0000255PROSITE- ProRule:PRU00549, ECO:0000269PubMed:10702287}. | ||||||||||||||||||
Disease Associations | Floating-Harbor syndrome (FLHS) [MIM:136140]: A rare genetic disorder characterized by proportionate short stature, delayed bone age, delayed speech development, and typical facial features. The face is triangular with deep-set eyes, long eyelashes, bulbous nose, wide columella, short philtrum, and thin lips. {ECO:0000269PubMed:22265015}. Note=The disease is caused by mutations affecting the gene represented in this entry. | ||||||||||||||||||
Tissue Specificity | |||||||||||||||||||
Comments | |||||||||||||||||||
Interactions | |||||||||||||||||||
Number of Interactions |
This gene and/or its encoded proteins are associated with 28 experimentally validated interaction(s) in this database.
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Gene Ontology | |||||||||||||||||||
Molecular Function |
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Biological Process |
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Cellular Component |
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Protein Structure and Domains | |||||||||||||||||||
PDB ID | |||||||||||||||||||
InterPro |
IPR000330
SNF2-related IPR001650 Helicase, C-terminal IPR013999 HAS subgroup IPR014001 Helicase, superfamily 1/2, ATP-binding domain IPR014012 Helicase/SANT-associated, DNA binding IPR017956 AT hook, DNA-binding motif IPR020478 AT hook-like IPR027417 P-loop containing nucleoside triphosphate hydrolase |
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PFAM |
PF00176
PF00271 PF07529 PF02178 |
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PRINTS |
PR00929
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PIRSF | |||||||||||||||||||
SMART |
SM00490
SM00573 SM00487 SM00384 |
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TIGRFAMs | |||||||||||||||||||
Post-translational Modifications | |||||||||||||||||||
Modification | |||||||||||||||||||
Cross-References | |||||||||||||||||||
SwissProt | Q6ZRS2 | ||||||||||||||||||
PhosphoSite | PhosphoSite-Q6ZRS2 | ||||||||||||||||||
TrEMBL | G1UI29 | ||||||||||||||||||
UniProt Splice Variant | |||||||||||||||||||
Entrez Gene | 10847 | ||||||||||||||||||
UniGene | Hs.647334 | ||||||||||||||||||
RefSeq | NP_006653 | ||||||||||||||||||
HUGO | HGNC:16974 | ||||||||||||||||||
OMIM | 611421 | ||||||||||||||||||
CCDS | CCDS10689 | ||||||||||||||||||
HPRD | 18103 | ||||||||||||||||||
IMGT | |||||||||||||||||||
EMBL | AB002307 AB621816 AC093249 AC106886 AF143946 AK128030 BC159099 | ||||||||||||||||||
GenPept | AAD39760 AAI59100 BAA20768 BAC87237 BAK64152 | ||||||||||||||||||