Conserved Protein Domain Family
SH3_ARHGAP32_33

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cd11835: SH3_ARHGAP32_33 
Src homology 3 domain of Rho GTPase-activating proteins 32 and 33, and similar proteins
Members of this family contain N-terminal PX and Src Homology 3 (SH3) domains, a central Rho GAP domain, and C-terminal extensions. RhoGAPs (or ARHGAPs) bind to Rho proteins and enhance the hydrolysis rates of bound GTP. ARHGAP32 is also called RICS, PX-RICS, p250GAP, or p200RhoGAP. It is a Rho GTPase-activating protein for Cdc42 and Rac1, and is implicated in the regulation of postsynaptic signaling and neurite outgrowth. PX-RICS, a variant of RICS that contain PX and SH3 domains, is the main isoform expressed during neural development. It is involved in neural functions including axon and dendrite extension, postnatal remodeling, and fine-tuning of neural circuits during early brain development. ARHGAP33, also called sorting nexin 26 or TCGAP (Tc10/CDC42 GTPase-activating protein), is widely expressed in the brain where it is involved in regulating the outgrowth of axons and dendrites and is regulated by the protein tyrosine kinase Fyn. It is translocated to the plasma membrane in adipocytes in response to insulin and may be involved in the regulation of insulin-stimulated glucose transport. SH3 domains are protein interaction domains that bind to proline-rich ligands with moderate affinity and selectivity, preferentially to PxxP motifs. They play versatile and diverse roles in the cell including the regulation of enzymes, changing the subcellular localization of signaling pathway components, and mediating the formation of multiprotein complex assemblies.
Statistics
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PSSM-Id: 212769
Aligned: 13 rows
Threshold Bit Score: 101.757
Created: 31-May-2011
Updated: 2-Oct-2020
Structure
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Aligned Rows:
 
peptide ligand
Feature 1:peptide ligand binding site [polypeptide binding site]
Evidence:
  • Comment:based on the binding of peptide ligands to the SH3 domains of other superfamily members
  • Comment:SH3 domains typically bind proline-rich ligands, preferentially to PxxP motifs.
  • Citation:PMID 7664083
  • Citation:PMID 7735837
  • Comment:flanking hinge and loops (RT and n-Src) confer sequence specificity for ligand residues outside the core binding motif

Sequence Alignment
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Format: Row Display: Color Bits: Type Selection:
Feature 1              # #  #   #                    ##                  # ## 
O14559        190 AAHVIKRYTAQAPDELSFEVGDIVSVIDMPPTEDRSWWRGKRG------FQVGFFPSECV 243  human
Q6GPD0        266 AAHVIKRYNAQAPDELSFEVGDIVSVIDMPPKELTTWWRGKHG------FQVGFFPSECV 319  African clawed frog
XP_002414431   56 AAYVTRSYQAQAPDEISFQVGDMVSVIDMPPADESTWWRGKRG------FEVGFFPSECV 109  black-legged tick
XP_001623506  164 AAHVIKRYHAQAADEISLEVGDIISIIDMPPVDESIWWRGKRG------FEVGFFPSQCV 217  starlet sea anemone
Q9VIS1        299 AAYGVRRYQAQAPDEINIEVGDMISVIDMPSPAESIWWRGKKShlqkslYEVGFFPQSCV 358  fruit fly
EFW39897      660 VGMVIAPYEGQEEDELSLQAGEVISIVDMPSTQESPWWRGFKGa----sEMVGFFPRDCV 715  Capsaspora owczarzaki ATCC 30864
EFW47286      429 LGVVIINYTAQQSDELSLAVGEMVSIIDMPSPEESPWWRGNKG------FASGFFPSQCV 482  Capsaspora owczarzaki ATCC 30864
XP_698214     229 AAHVIKRYTAQASDEISIEVGDILSVIDMPPKEDTTWWRGKHG------FQVGFFPSECV 282  zebrafish
XP_003224994  190 AAHVVKRYTAQASDELSFEVGDIISVIDMPPKEDRSWWRGKHG------FQVGFFPSECV 243  green anole
NP_001090769  186 AAHVIKRYTAQAPDELSFEVGDIVSVIDMPPREDTSWWRGKHS------FQVGFFPSECV 239  western clawed frog
XP_002597127  153 AAHVIKRYAAQASDEISLEVGDIVSVIDMPPTHETLWWRGKKG------FEVGFFPSQCV 206  Florida lancelet
AAH51236       81 AAHVIKRYTARAPDELTLEVGDIVSVIDMPPKVLSTWWRGKHG------FQVGLFPGHCV 134  human
EFX84422      173 AAYAVRRYAAVASDEISFEVGDMISVIDMPPPEESMWWRGKRG------FDVGFFPSECV 226  common water flea

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