Homo sapiens Protein: CHD1 | |||||||||||||||||||||||
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Summary | |||||||||||||||||||||||
InnateDB Protein | IDBP-35194.6 | ||||||||||||||||||||||
Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||||||||||||||||||||
Gene Symbol | CHD1 | ||||||||||||||||||||||
Protein Name | chromodomain helicase DNA binding protein 1 | ||||||||||||||||||||||
Synonyms | |||||||||||||||||||||||
Species | Homo sapiens | ||||||||||||||||||||||
Ensembl Protein | ENSP00000284049 | ||||||||||||||||||||||
InnateDB Gene | IDBG-35192 (CHD1) | ||||||||||||||||||||||
Protein Structure |
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UniProt Annotation | |||||||||||||||||||||||
Function | ATP-dependent chromatin-remodeling factor which functions as substrate recognition component of the transcription regulatory histone acetylation (HAT) complex SAGA. Regulates polymerase II transcription. Also required for efficient transcription by RNA polymerase I, and more specifically the polymerase I transcription termination step. Regulates negatively DNA replication. Not only involved in transcription-related chromatin-remodeling, but also required to maintain a specific chromatin configuration across the genome. Is also associated with histone deacetylase (HDAC) activity (By similarity). Required for the bridging of SNF2, the FACT complex, the PAF complex as well as the U2 snRNP complex to H3K4me3. Functions to modulate the efficiency of pre-mRNA splicing in part through physical bridging of spliceosomal components to H3K4me3. Required for maintaining open chromatin and pluripotency in embryonic stem cells. {ECO:0000250, ECO:0000269PubMed:18042460}. | ||||||||||||||||||||||
Subcellular Localization | Nucleus. Cytoplasm {ECO:0000250}. Note=Is released into the cytoplasm when cells enter mitosis and is reincorporated into chromatin during telophase-cytokinesis. {ECO:0000250}. | ||||||||||||||||||||||
Disease Associations | |||||||||||||||||||||||
Tissue Specificity | |||||||||||||||||||||||
Comments | |||||||||||||||||||||||
Interactions | |||||||||||||||||||||||
Number of Interactions |
This gene and/or its encoded proteins are associated with 58 experimentally validated interaction(s) in this database.
They are also associated with 1 interaction(s) predicted by orthology.
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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 IPR000953 Chromo domain/shadow IPR001650 Helicase, C-terminal IPR009057 Homeodomain-like IPR014001 Helicase, superfamily 1/2, ATP-binding domain IPR016197 Chromo domain-like IPR023780 Chromo domain IPR027417 P-loop containing nucleoside triphosphate hydrolase |
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PFAM |
PF00176
PF00271 PF00385 |
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PRINTS | |||||||||||||||||||||||
PIRSF | |||||||||||||||||||||||
SMART |
SM00298
SM00490 SM00487 |
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TIGRFAMs | |||||||||||||||||||||||
Post-translational Modifications | |||||||||||||||||||||||
Modification | |||||||||||||||||||||||
Cross-References | |||||||||||||||||||||||
SwissProt | O14646 | ||||||||||||||||||||||
PhosphoSite | PhosphoSite-O14646 | ||||||||||||||||||||||
TrEMBL | |||||||||||||||||||||||
UniProt Splice Variant | |||||||||||||||||||||||
Entrez Gene | 1105 | ||||||||||||||||||||||
UniGene | Hs.718669 | ||||||||||||||||||||||
RefSeq | NP_001261 | ||||||||||||||||||||||
HUGO | HGNC:1915 | ||||||||||||||||||||||
OMIM | 602118 | ||||||||||||||||||||||
CCDS | CCDS34204 | ||||||||||||||||||||||
HPRD | 03668 | ||||||||||||||||||||||
IMGT | |||||||||||||||||||||||
EMBL | AC022121 AF006513 BC117134 | ||||||||||||||||||||||
GenPept | AAB87381 AAI17135 | ||||||||||||||||||||||