Title of article :
The ScPex13p SH3 Domain Exposes Two Distinct Binding Sites for Pex5p and Pex14p
Author/Authors :
José R. Pires Manso، نويسنده , , Xinji Hong، نويسنده , , Christoph Brockmann، نويسنده , , Rudolf Volkmer-Engert، نويسنده , , Ruben Abagyan and Jens Schneider-Mergener، نويسنده , , Ronald Kühne and Hartmut Oschkinat، نويسنده , , Ralf Erdmann، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2003
Pages :
9
From page :
1427
To page :
1435
Abstract :
Pex13p is an essential component of the peroxisomal protein import machinery and interacts via its C-terminal SH3 domain with the type II SH3-ligand Pex14p and the non-PXXP protein Pex5p. We report the solution structure of the SH3 domain of Pex13p from Saccharomyces cerevisiae and the identification of a novel-binding pocket, which binds a non-PXXP-peptide representing the binding site of Pex5p. Chemical shift assays revealed the binding sites for Pex5p and Pex14p ligand peptides to be distinct and spatially separated. Competition assays demonstrated that the two ligand peptides can bind simultaneously to the SH3 domain.
Keywords :
PEX13 , SH3 domain , PEX5 , peroxin , peroxisome
Journal title :
Journal of Molecular Biology
Serial Year :
2003
Journal title :
Journal of Molecular Biology
Record number :
1242460
Link To Document :
بازگشت