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Protein Page:
WIP (human)
p Phosphorylation
a Acetylation
m Methylation
m1 Mono-methylation
m2 Di-methylation
m3 Tri-methylation
u Ubiquitination
s Sumoylation
n Neddylation
g O-GlcNAc
h Palmitoylation
ad Adenylylation
sn S-Nitrosylation
ca Caspase cleavage

Overview
WIP a cytoskeleton-associated protein that interacts with the Wiskott-Aldrich syndrome protein (WASP) in resting cells. Plays an important role in the organization of the actin cytoskeleton. Phosphorylation by PKC-theta following T cell receptor signaling disengages it from WASP, releasing WASP from WIP inhibition. Binds to a region of WASP that is frequently mutated in Wiskott-Aldrich syndrome. Note: This description may include information from UniProtKB.
Protein type: Actin binding protein; Motility/polarity/chemotaxis
Cellular Component: cytoplasmic membrane-bound vesicle; actin filament; actin cytoskeleton
Molecular Function: protein binding; actin binding; profilin binding
Biological Process: positive regulation of protein export from nucleus; actin filament-based movement; actin polymerization and/or depolymerization; protein complex assembly
Reference #:  O43516 (UniProtKB)
Alt. Names/Synonyms: MGC111041; Protein PRPL-2; PRPL-2; WAS/WASL interacting protein family, member 1; WAS/WASL-interacting protein family member 1; WASP-interacting protein; WASPIP; WIP; WIPF1; Wiskott-Aldrich syndrome protein interacting protein; Wiskott-Aldrich syndrome protein-interacting protein
Gene Symbols: WIPF1
Molecular weight: 51,258 Da
Basal Isoelectric point: 11.47  Predict pI for various phosphorylation states
Select Structure to View Below

WIP

Protein Structure Not Found.


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Sites Implicated In
molecular association, regulation: S488‑p

Modification Sites and Domains Show Modification Legend
Click here to view phosphorylation modifications only

Modification Sites in Parent Protein, Orthologs, and Isoforms Show Modification Legend
 

Show Multiple Sequence Alignment


 SS 

SS: The number of records in which this modification site was determined using site-specific methods. SS methods include amino acid sequencing, site-directed mutagenesis, modification site-specific antibodies, specific MS strategies, etc.


 MS 

MS: The number of records in which this modification site was assigned using ONLY proteomic discovery-mode mass spectrometry.


       human

 
0 9 R33-m2 NKTEQAGrNALLSDI
0 1 S91-p GGGGGGGsFGGGGPP
0 5 R134-m1 PLLPPGGrSTSAKPF
0 3 S142-p STSAKPFsPPSGPGr
0 1 R149-m2 sPPSGPGrFPVPsPG
0 5 S154-p PGrFPVPsPGHRSGP
0 1 R211-m2 PPVPGGPrQPsPGPT
0 1 S214-p PGGPrQPsPGPTPPP
0 1 R226-m1 PPPFPGNrGTALGGG
0 2 S234-p GTALGGGsIRQSPLS
0 4 S276-p PPVGNRPsIHREAVP
0 21 S340-p RLPQRNLsLSSstPP
0 1 S342 PQRNLsLSSstPPLP
0 1 S344-p RNLsLSSstPPLPsP
0 19 T345-p NLsLSSstPPLPsPG
0 22 S350-p SstPPLPsPGRSGPL
0 7 T398-p TSRALPAtPQLPSRS
3 0 S488-p RNESRSGsNRRERGA
  mouse

 
R33-m2 NKTEQAGrNALLSDI
N92 GGGGSGGNFGGGGPP
R135-m1 PILPPGGrATSAKPF
S143-p ATSAKPFsPPSGPGR
R150 sPPSGPGRFPAPSPG
S155 PGRFPAPSPGHRSGP
R212 PAGLGAPRPPFPGNR
- gap
R219 RPPFPGNRGAAFGAG
S227 GAAFGAGSARQNPSG
S268-p PPVGNRPsMHREAVP
S330-p RLPQRNLsLtSSAPP
T332-p PQRNLsLtSSAPPLP
S334 RNLsLtSSAPPLPsP
A335 NLsLtSSAPPLPsPG
S340-p SSAPPLPsPGRSGPL
T388-p TARALPAtPQLPSRS
S478 RNESRSGSNRRERGA
  rat

 
R33 NKTEQAGRNALLSDI
N87 GSSGGGGNFGGGGPP
R130 PILPPGGRATSAKPF
S138 ATSAKPFSSPSGPGR
R145 SSPSGPGRFPAPSPG
S150 PGRFPAPSPGHRSGP
R207 PAGLGAPRPPFPGNR
- gap
R214 RPPFPGNRGAAFGAG
S222 GAAFGAGSVRQNLSS
S263 PPVGNRPSMHREAVP
S324-p RLPQRNLsLTSPTPP
T326 PQRNLsLTSPTPPLP
P328 RNLsLTSPTPPLPSP
T329 NLsLTSPTPPLPSPG
S334 SPTPPLPSPGRSGPL
T382 TARALPATPQLPSRS
S472 RSESRSGSNRRERGA
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