2XMF


Conserved Protein Domain Family
SH3_MyoIe_If_like

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cd11827: SH3_MyoIe_If_like 
Click on image for an interactive view with Cn3D
Src homology 3 domain of Myosins Ie, If, and similar proteins
Myosins Ie (MyoIe) and If (MyoIf) are nonmuscle, unconventional, long tailed, class I myosins containing an N-terminal motor domain and a myosin tail with TH1, TH2, and SH3 domains. MyoIe interacts with the endocytic proteins, dynamin and synaptojanin-1, through its SH3 domain; it may play a role in clathrin-dependent endocytosis. In the kidney, MyoIe is critical for podocyte function and normal glomerular filtration. Mutations in MyoIe is associated with focal segmental glomerulosclerosis, a disease characterized by massive proteinuria and progression to end-stage kidney disease. MyoIf is predominantly expressed in the immune system; it plays a role in immune cell motility and innate immunity. Mutations in MyoIf may be associated with the loss of hearing. The MyoIf gene has also been found to be fused to the MLL (Mixed lineage leukemia) gene in infant acute myeloid leukemias (AML). 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: 212761
Aligned: 17 rows
Threshold Bit Score: 108.271
Created: 31-May-2011
Updated: 2-Oct-2020
Structure
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Program:
Drawing:
Aligned Rows:
 
peptide ligand
Conserved site includes 9 residues -Click on image for an interactive view with Cn3D
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              # #  #   #                 ##            # ##   
2XMF_A          7 QCKALYAYDAQDTDELSFNANDIIDIIKEDPSGWWTGRLRGKQGLFPNNYVTK 59   house mouse
XP_002124785 1153 KCKAIYSYDAQDTDEISFTEGDIIEILKEDASGWWSGRIGNREGLFPGNYVEK 1205 Ciona intestinalis
P70248       1046 RCRALYQYIGQDVDELSFNVNEVIEILIEDSSGWWKGRLHGQEGLFPGNYVEK 1098 house mouse
NP_990585    1046 RCQALYQYIGQDVDELSFNVGDVIDILLEDISGWWKGRLHGREGLFPGNYVQK 1098 chicken
NP_001086041 1043 RCKAIYQYLGQDVDELSFNVNDVIDIILEDPSGWWKGRLHGKEGLFPGNYVQK 1095 African clawed frog
NP_001118234 1065 KCRTIYPYDAGDTDELSFGEGETIEIILEDASGWWRGKLRGREGLFPANYIEK 1117 purple urchin
XP_002153960  929 MAKTLYTYDPQEADELKFVEGDIIEIIKEDPSGWWTGRLRGKEGLFPSNYVEK 981  green hydra
ADV40230      123 QCKAIYAYEAQDTDELTFNVDDIITVIKQDPSGWWLGKIKGKEGLFPSNYVEI 175  Latrodectus hesperus
XP_002414115  973 TCRAIYGYEPQDTDELAVTEGDVIEILKEDASGWWLGRLKGKEGLFPANYVER 1025 black-legged tick
XP_003390292  549 QCKAIYDYDANDTDELTFKEGDTIELVKKDPSGWWTGKIGRKEGLFPSNYVEE 601  Amphimedon queenslandica

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