Homo sapiens Protein: SMARCD1
Summary
InnateDB Protein IDBP-29962.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol SMARCD1
Protein Name SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 1
Synonyms BAF60A; CRACD1; Rsc6p;
Species Homo sapiens
Ensembl Protein ENSP00000370924
InnateDB Gene IDBG-32344 (SMARCD1)
Protein Structure
UniProt Annotation
Function Involved in chromatin remodeling. Belongs to the neural progenitors-specific chromatin remodeling complex (npBAF complex) and the neuron-specific chromatin remodeling complex (nBAF complex). During neural development a switch from a stem/progenitor to a post-mitotic chromatin remodeling mechanism occurs as neurons exit the cell cycle and become committed to their adult state. The transition from proliferating neural stem/progenitor cells to post-mitotic neurons requires a switch in subunit composition of the npBAF and nBAF complexes. As neural progenitors exit mitosis and differentiate into neurons, npBAF complexes which contain ACTL6A/BAF53A and PHF10/BAF45A, are exchanged for homologous alternative ACTL6B/BAF53B and DPF1/BAF45B or DPF3/BAF45C subunits in neuron-specific complexes (nBAF). The npBAF complex is essential for the self-renewal/proliferative capacity of the multipotent neural stem cells. The nBAF complex along with CREST plays a role regulating the activity of genes essential for dendrite growth (By similarity). Has a strong influence on the Vitamin D-mediated transcriptional activity from an enhancer Vitamin D receptor element (VDRE). May be a link between mammalian SWI-SNF-like chromatin remodeling complexes and the vitamin D receptor (VDR) heterodimer. Mediates critical interactions between nuclear receptors and the BRG1/SMARCA4 chromatin-remodeling complex for transactivation. Also involved in vitamin D-coupled transcription regulation via its association with the WINAC complex, a chromatin-remodeling complex recruited by vitamin D receptor (VDR), which is required for the ligand- bound VDR-mediated transrepression of the CYP27B1 gene. {ECO:0000250, ECO:0000269PubMed:12837248, ECO:0000269PubMed:12917342, ECO:0000269PubMed:14698202, ECO:0000269PubMed:8804307}.
Subcellular Localization Nucleus {ECO:0000269PubMed:8804307, ECO:0000305}.
Disease Associations
Tissue Specificity Expressed in all tissues tested, including brain, heart, kidney, liver, lung, muscle, pancreas and placenta. {ECO:0000269PubMed:8804307}.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 100 experimentally validated interaction(s) in this database.
They are also associated with 11 interaction(s) predicted by orthology.
Experimentally validated
Total 100 [view]
Protein-Protein 100 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 11 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0003713 transcription coactivator activity
GO:0005515 protein binding
GO:0032947 protein complex scaffold
Biological Process
GO:0006337 nucleosome disassembly
GO:0006338 chromatin remodeling
GO:0006357 regulation of transcription from RNA polymerase II promoter
GO:0007399 nervous system development
GO:0048096 chromatin-mediated maintenance of transcription
Cellular Component
GO:0016514 SWI/SNF complex
GO:0071564 npBAF complex
GO:0071565 nBAF complex
Protein Structure and Domains
PDB ID
InterPro IPR003121 SWIB/MDM2 domain
IPR019835 SWIB domain
PFAM PF02201
PRINTS
PIRSF
SMART SM00151
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q96GM5
PhosphoSite PhosphoSite-Q96GM5
TrEMBL F8VW95
UniProt Splice Variant
Entrez Gene 6602
UniGene Hs.79335
RefSeq NP_620710
HUGO HGNC:11106
OMIM 601735
CCDS CCDS8798
HPRD 03438
IMGT
EMBL AC025154 AF109733 BC009368 CH471111 U66617
GenPept AAC50695 AAD23390 AAH09368 EAW58122 EAW58124