Wiskott-Aldrich syndrome protein
From Proteopedia
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Mutations in WASP can cause Wiskott-Aldrich syndrome which is a rare inherited disease characterized by immune disregulation<ref>PMID:18043243</ref>. | Mutations in WASP can cause Wiskott-Aldrich syndrome which is a rare inherited disease characterized by immune disregulation<ref>PMID:18043243</ref>. | ||
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- | </StructureSection> | ||
== 3D Structures of Wiskott-Aldrich syndrome protein == | == 3D Structures of Wiskott-Aldrich syndrome protein == | ||
- | + | [[Wiskott-Aldrich syndrome protein 3D structures]] | |
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- | *WASP; Domains - CRIB 242-310; WH2 430-458 | ||
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- | **[[1ej5]] – hWASP CRIB domain + 461-492 autoinhibited – human - NMR<br /> | ||
- | **[[1t84]] – hWASP CRIB domain + 461-492 autoinhibited + wiskostatin - NMR<br /> | ||
- | **[[1cee]] – hWASP CRIB domain + CDC42 - NMR<br /> | ||
- | **[[2a3z]] – hWASP WH2 domain + α-actin + DNAse I + ATP<br /> | ||
- | **[[2ot0]] – hWASP C terminal + fructose-bisphosphate aldolase<br /> | ||
- | **[[2k42]] – hWASP CRIB domain + ESPFU - NMR<br /> | ||
- | **[[3p8c]] – hWASP + SRA1 + NAP 1 + BRICK1 + ABL interactor <br /> | ||
- | **[[4n78]] – hWASP + SRA1 + NAP 1 + BRICK1 + WIRS + ABL interactor <br /> | ||
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- | *Neural WASP | ||
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- | **[[1mke]], [[2ifs]] – hWASP EVH1 domain 26-147/rWIP 461-485 - NMR<br /> | ||
- | **[[2ff3]] – hWASP WH2-2 domain + α-actin + gelsolin domain 1<br /> | ||
- | **[[2vcp]] – hWASP WH2-1,2,C domain 392-484 + α-actin<br /> | ||
- | **[[2lnh]] – hWASP CRIB + ESPFU + insulin receptor tyrosine kinase substrate - NMR<br /> | ||
- | **[[3m3n]] – mWASP tandem W domain 397-444 + α-actin - mouse<br /> | ||
- | **[[6uhc]] – mWASP in ARP2/3 complex – Cryo EM<br /> | ||
- | }} | ||
== References == | == References == | ||
<references/> | <references/> | ||
+ | </StructureSection> | ||
[[Category:Topic Page]] | [[Category:Topic Page]] |
Revision as of 08:01, 4 April 2024
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