UniProt:Q92925 SMARCD2

chain
  • chain:1-531
checksum 8C92168AE7782814
comment
  • FUNCTION Involved in transcriptional activation and repression of select genes by chromatin remodeling (alteration of DNA-nucleosome topology). Component of SWI/SNF chromatin remodeling complexes that carry out key enzymatic activities, changing chromatin structure by altering DNA-histone contacts within a nucleosome in an ATP-dependent manner (PubMed:22952240, PubMed:26601204). Critical regulator of myeloid differentiation, controlling granulocytopoiesis and the expression of genes involved in neutrophil granule formation (PubMed:28369036).SUBUNIT Component of the multiprotein chromatin-remodeling complexes SWI/SNF: SWI/SNF-A (BAF), SWI/SNF-B (PBAF) and related complexes. The canonical complex contains a catalytic subunit (either SMARCA4/BRG1/BAF190A or SMARCA2/BRM/BAF190B), and at least SMARCE1, ACTL6A/BAF53, SMARCC1/BAF155, SMARCC2/BAF170, and SMARCB1/SNF5/BAF47. Other subunits specific to each of the complexes may also be present permitting several possible combinations developmentally and tissue specific (PubMed:22952240). Component of the BAF complex, which includes at least actin (ACTB), ARID1A/BAF250A, ARID1B/BAF250B, SMARCA2/BRM, SMARCA4/BRG1, ACTL6A/BAF53, ACTL6B/BAF53B, SMARCE1/BAF57, SMARCC1/BAF155, SMARCC2/BAF170, SMARCB1/SNF5/INI1, and one or more SMARCD1/BAF60A, SMARCD2/BAF60B, or SMARCD3/BAF60C (PubMed:18765789). In muscle cells, the BAF complex also contains DPF3. Component of the SWI/SNF-B (PBAF) chromatin remodeling complex, at least composed of SMARCA4/BRG1, SMARCB1/BAF47/SNF5, ACTL6A/BAF53A or ACTL6B/BAF53B, SMARCE1/BAF57, SMARCD1/BAF60A, SMARCD2/BAF60B, perhaps SMARCD3/BAF60C, SMARCC1/BAF155, SMARCC2/BAF170, PBRM1/BAF180, ARID2/BAF200 and actin (ACTB) (PubMed:22952240, PubMed:26601204). Interacts with UNKL (PubMed:20148946). Interacts with CEBPE (PubMed:28369036).INTERACTION Isoform 2 is expressed in the pancreas.PTM Ubiquitinated through a signaling process involving RAC1 and the RING finger protein UNKL.DISEASE The disease is caused by variants affecting the gene represented in this entry.MISCELLANEOUS Produced by aberrant splicing sites.SIMILARITY Belongs to the SMARCD family.SEQUENCE CAUTION Truncated N-terminus.SEQUENCE CAUTION Truncated N-terminus.
created [InstanceEdit:217385] Schmidt, EE, 2008-03-27 06:23:53
crossReference
databaseName UniProt
dbId 248691
description
  • recommendedName: SWI/SNF-related matrix-associated actin-dependent regulator of chromatin subfamily D member 2 alternativeName: 60 kDa BRG-1/Brm-associated factor subunit B alternativeName: BRG1-associated factor 60B shortName: BAF60B
displayName UniProt:Q92925 SMARCD2
geneName
  • SMARCD2
  • BAF60B
  • PRO2451
identifier Q92925
isSequenceChanged false
keyword
  • Alternative splicing
  • Chromatin regulator
  • Isopeptide bond
  • Methylation
  • Nucleus
  • Phosphoprotein
  • Proteomics identification
  • Reference proteome
  • Transcription
  • Transcription regulation
  • Ubl conjugation
modified [InstanceEdit:9926675] Weiser, Joel, 2024-11-03
moleculeType Protein
name
  • SMARCD2
otherIdentifier
  • 11717063_s_at
  • 11742080_a_at
  • 11747710_a_at
  • 16847644
  • 201827_PM_at
  • 201827_at
  • 34694_at
  • 34695_at
  • 3766414
  • 3766416
  • 3766417
  • 3766418
  • 3766419
  • 3766420
  • 3766421
  • 3766422
  • 3766423
  • 3766424
  • 3766425
  • 3766426
  • 3766427
  • 3766428
  • 3766429
  • 3766430
  • 3766431
  • 3766432
  • 3766433
  • 3766434
  • 3766435
  • 3766436
  • 3766437
  • 3766438
  • 3766439
  • 3766440
  • 3766441
  • 3766442
  • 3766443
  • 3766444
  • 3766445
  • 3766446
  • 455_at
  • 6603
  • 8017460
  • GE87462
  • GO:0000776
  • GO:0000785
  • GO:0003677
  • GO:0003712
  • GO:0003713
  • GO:0005515
  • GO:0005634
  • GO:0005654
  • GO:0006325
  • GO:0006337
  • GO:0006338
  • GO:0006355
  • GO:0006357
  • GO:0016363
  • GO:0016514
  • GO:0016586
  • GO:0030071
  • GO:0031492
  • GO:0032991
  • GO:0035060
  • GO:0043226
  • GO:0045582
  • GO:0045597
  • GO:0045663
  • GO:0045893
  • GO:0070316
  • GO:0140092
  • GO:2000045
  • GO:2000781
  • GO:2000819
  • HMNXSV003012771
  • ILMN_1692684
  • PH_hs_0013265
  • TC17001787.hg
  • U66618_at
  • g6642761_3p_at
physicalEntity
referenceDatabase [ReferenceDatabase:2] UniProt
referenceGene
referenceTranscript
schemaClass ReferenceGeneProduct
secondaryIdentifier
  • SMRD2_HUMAN
  • A5PLL5
  • A6NNQ7
  • B4DV56
  • B4E1R6
  • Q7L2I6
  • Q9UHZ1
sequenceLength 531
species [Species:48887] Homo sapiens
stId uniprot:Q92925
url http://purl.uniprot.org/uniprot/Q92925

Referrals

(referenceEntity)
(interactor)
Cite Us!