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Description for Protein SMARCD2

SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily d, member 2
5 total interacting proteins;
Icon Book Platelet Evidence (proteome studies/others : 0/0)
(Not detected in platelets)
Summary:
The protein encoded by this gene is a member of the SWI/SNF family of proteins, whose members display helicase and ATPase activities and which are thought to regulate transcription of certain genes by altering the chromatin structure around those genes. The encoded protein is part of the large ATP-dependent chromatin remodeling complex SNF/SWI and has sequence similarity to the yeast Swp73 protein. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq] (PubMed Links)
Domains and Motifs:
None Available
Gene Ontology:
Gene Ontology Annotations
KEGG - Enzyme ID(s):
None Available
KEGG - Orthology:
K11650
KEGG - Pathway(s):
None Available
Nomenclature / Alternative Names:
Mammalian chromatin remodeling complex, BRG1 associated factor 60B; SWI/SNF related, matrix associated actin dependent regulator of chromatin, subfamily D, member 2; BRG1 associated factor B, 60KD; BAF60B; Chromatin remodeling complex BAF60B subunit; SWP73; SWI/SNF-related matrix-associated actin-dependent regulator of chromatin d2 isoform 2; SWI/SNF-related matrix-associated actin-dependent regulator of chromatin d2 isoform 1
Approved Symbol:
SMARCD2
(De-) Phosphorylations:
Total (de-) phosphorylation sites: 6
Human (de-) phosphorylation sites: 6; No platelet phosphorylation sites
Phosphorylation Targets:
Total phosphorylation targets: 0
Human phosphorylation targets: 0;Predicted platelet targets: 0
Protein Characteristics:
Isoform-specific Information
Icon DrugsAssociated Drugs (DrugBank Accession):

None Available

Associated Genetic Diseases:

None Available
Predicted Transmembrane Domains:
  • Isoform 2 : 0
  • Isoform 1 : 0
    • Additional Identifiers:

    HPRD: 03439 Entrez Gene ID: 6603 OMIM ID: 601736 Swissprot Accession: Q92925; B4DV56;