Wiskott–Aldrich syndrome protein
WAS |
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Identifiers |
Aliases |
WAS, SCNX, THC, THC1, WASPA, WASp, IMD2, Wiskott-Aldrich syndrome |
External IDs |
OMIM: 300392 MGI: 105059 HomoloGene: 30970 GeneCards: WAS |
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Gene location (Mouse) |
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Chr. |
X chromosome (mouse) |
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Band |
X A1.1|X 3.65 cM |
Start |
8,081,453 bp |
End |
8,090,498 bp |
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Orthologs |
Species |
Human |
Mouse |
Entrez |
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Ensembl |
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UniProt |
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RefSeq (mRNA) |
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RefSeq (protein) |
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Location (UCSC) |
Chr X: 48.68 – 48.69 Mb |
Chr X: 8.08 – 8.09 Mb |
PubMed search |
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1CEE, 1EJ5, 1T84, 2A3Z, 2K42, 2OT0
7454
22376
ENSG00000015285
ENSMUSG00000031165
P42768
P70315
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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