WIPF1

Revision as of 15:55, 6 September 2012 by WikiBot (talk | contribs) (Robot: Automated text replacement (-{{reflist}} +{{reflist|2}}, -<references /> +{{reflist|2}}, -{{WikiDoc Cardiology Network Infobox}} +))
(diff) ← Older revision | Latest revision (diff) | Newer revision → (diff)
Jump to navigation Jump to search


WAS/WASL interacting protein family, member 1
File:PBB Protein WIPF1 image.jpg
PDB rendering based on 2a41.
Available structures
PDB Ortholog search: Template:Homologene2PDBe PDBe, Template:Homologene2uniprot RCSB
Identifiers
Symbols WIPF1 ; MGC111041; PRPL-2; WASPIP; WIP
External IDs Template:OMIM5 Template:MGI HomoloGene86891
RNA expression pattern
File:PBB GE WIPF1 202664 at tn.png
File:PBB GE WIPF1 202663 at tn.png
File:PBB GE WIPF1 202665 s at tn.png
More reference expression data
Orthologs
Template:GNF Ortholog box
Species Human Mouse
Entrez n/a n/a
Ensembl n/a n/a
UniProt n/a n/a
RefSeq (mRNA) n/a n/a
RefSeq (protein) n/a n/a
Location (UCSC) n/a n/a
PubMed search n/a n/a

WAS/WASL interacting protein family, member 1, also known as WIPF1, is a human gene.[1]

This gene encodes a protein that plays an important role in the organization of the actin cytoskeleton. The encoded protein binds to a region of Wiskott-Aldrich syndrome protein that is frequently mutated in Wiskott-Aldrich syndrome, an X-linked recessive disorder. Impairment of the interaction between these two proteins may contribute to the disease. Two transcript variants encoding the same protein have been identified for this gene.[1]

References

  1. 1.0 1.1 "Entrez Gene: WIPF1 WAS/WASL interacting protein family, member 1".

Further reading

  • Ramesh N, Antón IM, Martínez-Quiles N, Geha RS (1999). "Waltzing with WASP". Trends Cell Biol. 9 (1): 15–9. PMID 10087612.
  • Ramesh N, Antón IM, Hartwig JH, Geha RS (1998). "WIP, a protein associated with wiskott-aldrich syndrome protein, induces actin polymerization and redistribution in lymphoid cells". Proc. Natl. Acad. Sci. U.S.A. 94 (26): 14671–6. PMID 9405671.
  • Antón IM, Lu W, Mayer BJ; et al. (1998). "The Wiskott-Aldrich syndrome protein-interacting protein (WIP) binds to the adaptor protein Nck". J. Biol. Chem. 273 (33): 20992–5. PMID 9694849.
  • Stewart DM, Tian L, Nelson DL (1999). "Mutations that cause the Wiskott-Aldrich syndrome impair the interaction of Wiskott-Aldrich syndrome protein (WASP) with WASP interacting protein". J. Immunol. 162 (8): 5019–24. PMID 10202051.
  • Vaduva G, Martinez-Quiles N, Anton IM; et al. (1999). "The human WASP-interacting protein, WIP, activates the cell polarity pathway in yeast". J. Biol. Chem. 274 (24): 17103–8. PMID 10358064.
  • Moreau V, Frischknecht F, Reckmann I; et al. (2000). "A complex of N-WASP and WIP integrates signalling cascades that lead to actin polymerization". Nat. Cell Biol. 2 (7): 441–8. doi:10.1038/35017080. PMID 10878810.
  • Vetterkind S, Miki H, Takenawa T; et al. (2002). "The rat homologue of Wiskott-Aldrich syndrome protein (WASP)-interacting protein (WIP) associates with actin filaments, recruits N-WASP from the nucleus, and mediates mobilization of actin from stress fibers in favor of filopodia formation". J. Biol. Chem. 277 (1): 87–95. doi:10.1074/jbc.M104555200. PMID 11687573.
  • Antón IM, de la Fuente MA, Sims TN; et al. (2002). "WIP deficiency reveals a differential role for WIP and the actin cytoskeleton in T and B cell activation". Immunity. 16 (2): 193–204. PMID 11869681.
  • Scott MP, Zappacosta F, Kim EY; et al. (2002). "Identification of novel SH3 domain ligands for the Src family kinase Hck. Wiskott-Aldrich syndrome protein (WASP), WASP-interacting protein (WIP), and ELMO1". J. Biol. Chem. 277 (31): 28238–46. doi:10.1074/jbc.M202783200. PMID 12029088.
  • Benesch S, Lommel S, Steffen A; et al. (2002). "Phosphatidylinositol 4,5-biphosphate (PIP2)-induced vesicle movement depends on N-WASP and involves Nck, WIP, and Grb2". J. Biol. Chem. 277 (40): 37771–6. doi:10.1074/jbc.M204145200. PMID 12147689.
  • Zettl M, Way M (2003). "The WH1 and EVH1 domains of WASP and Ena/VASP family members bind distinct sequence motifs". Curr. Biol. 12 (18): 1617–22. PMID 12372256.
  • Volkman BF, Prehoda KE, Scott JA; et al. (2002). "Structure of the N-WASP EVH1 domain-WIP complex: insight into the molecular basis of Wiskott-Aldrich Syndrome". Cell. 111 (4): 565–76. PMID 12437929.
  • Strausberg RL, Feingold EA, Grouse LH; et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. doi:10.1073/pnas.242603899. PMID 12477932.
  • Sasahara Y, Rachid R, Byrne MJ; et al. (2003). "Mechanism of recruitment of WASP to the immunological synapse and of its activation following TCR ligation". Mol. Cell. 10 (6): 1269–81. PMID 12504004.
  • Luthi JN, Gandhi MJ, Drachman JG (2003). "X-linked thrombocytopenia caused by a mutation in the Wiskott-Aldrich syndrome (WAS) gene that disrupts interaction with the WAS protein (WASP)-interacting protein (WIP)". Exp. Hematol. 31 (2): 150–8. PMID 12591280.
  • Kinley AW, Weed SA, Weaver AM; et al. (2003). "Cortactin interacts with WIP in regulating Arp2/3 activation and membrane protrusion". Curr. Biol. 13 (5): 384–93. PMID 12620186.
  • Ota T, Suzuki Y, Nishikawa T; et al. (2004). "Complete sequencing and characterization of 21,243 full-length human cDNAs". Nat. Genet. 36 (1): 40–5. doi:10.1038/ng1285. PMID 14702039.
  • Kim MK, Kim ES, Kim DS; et al. (2004). "Two novel mutations of Wiskott-Aldrich syndrome: the molecular prediction of interaction between the mutated WASP L101P with WASP-interacting protein by molecular modeling". Biochim. Biophys. Acta. 1690 (2): 134–40. doi:10.1016/j.bbadis.2004.06.007. PMID 15469902.
  • Gerhard DS, Wagner L, Feingold EA; et al. (2004). "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)". Genome Res. 14 (10B): 2121–7. doi:10.1101/gr.2596504. PMID 15489334.

Template:WikiDoc Sources