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Wiskott–Aldrich syndrome protein

WAS
PBB Protein WAS image.jpg
Available structures
PDB Ortholog search: PDBe RCSB
Identifiers
Aliases WAS, SCNX, THC, THC1, WASPA, WASp, IMD2, Wiskott-Aldrich syndrome
External IDs OMIM: 300392 MGI: 105059 HomoloGene: 30970 GeneCards: WAS
Gene location (Human)
X chromosome (human)
Chr. X chromosome (human)
X chromosome (human)
Genomic location for WAS
Genomic location for WAS
Band Xp11.23 Start 48,676,596 bp
End 48,691,427 bp
RNA expression pattern
PBB GE WAS 205400 at fs.png

PBB GE WAS 38964 r at fs.png
More reference expression data
Orthologs
Species Human Mouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_000377

NM_009515

RefSeq (protein)

NP_000368
NP_000368.1

NP_033541

Location (UCSC) Chr X: 48.68 – 48.69 Mb Chr X: 8.08 – 8.09 Mb
PubMed search

1CEE, 1EJ5, 1T84, 2A3Z, 2K42, 2OT0

NM_000377

NM_009515

NP_000368
NP_000368.1

NP_033541

The Wiskott–Aldrich Syndrome protein (WASp) is a 502-amino acid protein expressed in cells of the hematopoietic system. In the inactive state, WASp exists in an autoinhibited conformation with sequences near its C-terminus binding to a region near its N-terminus. Its activation is dependent upon CDC42 and PIP2 acting to disrupt this interaction, causing the WASp protein to 'open'. This exposes a domain near the WASp C-terminus that binds to and activates the Arp2/3 complex. Activated Arp2/3 nucleates new F-actin.


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