Homo sapiens Protein: SMARCC2
Summary
InnateDB Protein IDBP-40154.5
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol SMARCC2
Protein Name SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily c, member 2
Synonyms BAF170; CRACC2; Rsc8;
Species Homo sapiens
Ensembl Protein ENSP00000267064
InnateDB Gene IDBG-40152 (SMARCC2)
Protein Structure
UniProt Annotation
Function Involved in transcriptional activation and repression of select genes by chromatin remodeling (alteration of DNA-nucleosome topology). Can stimulate the ATPase activity of the catalytic subunit of these complexes. May be required for CoREST dependent repression of neuronal specific gene promoters in non-neuronal cells. 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. 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). {ECO:0000250}.
Subcellular Localization Nucleus.
Disease Associations
Tissue Specificity Ubiquitously expressed.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 127 experimentally validated interaction(s) in this database.
They are also associated with 13 interaction(s) predicted by orthology.
Experimentally validated
Total 127 [view]
Protein-Protein 125 [view]
Protein-DNA 2 [view]
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 13 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0000978 RNA polymerase II core promoter proximal region sequence-specific DNA binding
GO:0000980 RNA polymerase II distal enhancer sequence-specific DNA binding
GO:0003677 DNA binding
GO:0003682 chromatin binding
GO:0003713 transcription coactivator activity
GO:0005515 protein binding
GO:0031492 nucleosomal DNA binding
Biological Process
GO:0000122 negative regulation of transcription from RNA polymerase II promoter
GO:0006337 nucleosome disassembly
GO:0006338 chromatin remodeling
GO:0006351 transcription, DNA-templated
GO:0006357 regulation of transcription from RNA polymerase II promoter
GO:0007399 nervous system development
GO:0021882 regulation of transcription from RNA polymerase II promoter involved in forebrain neuron fate commitment
GO:0043044 ATP-dependent chromatin remodeling
GO:0045892 negative regulation of transcription, DNA-templated
GO:0045893 positive regulation of transcription, DNA-templated
Cellular Component
GO:0000790 nuclear chromatin
GO:0005634 nucleus
GO:0016514 SWI/SNF complex
GO:0017053 transcriptional repressor complex
GO:0043234 protein complex
GO:0071564 npBAF complex
GO:0071565 nBAF complex
Protein Structure and Domains
PDB ID
InterPro IPR000953 Chromo domain/shadow
IPR001005 SANT/Myb domain
IPR001357 BRCT domain
IPR007526 SWIRM domain
IPR009057 Homeodomain-like
IPR016197 Chromo domain-like
IPR017877 Myb-like domain
PFAM PF00249
PF00533
PF12738
PF04433
PRINTS
PIRSF
SMART SM00298
SM00717
SM00292
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q8TAQ2
PhosphoSite PhosphoSite-Q8TAQ2
TrEMBL F8VZW6
UniProt Splice Variant
Entrez Gene 6601
UniGene Hs.733233
RefSeq NP_003066
HUGO HGNC:11105
OMIM 601734
CCDS CCDS8907
HPRD 03437
IMGT
EMBL AB209006 AC073896 BC009067 BC013045 BC026222 BT009924 CH471054 U66616
GenPept AAC50694 AAH09067 AAH13045 AAH26222 AAP88926 BAD92243 EAW96906 EAW96907