Structural Basis for Par-4 Recognition by the SPRY Domain- and SOCS Box-Containing Proteins SPSB1, SPSB2, and SPSB4

被引:59
作者
Filippakopoulos, Panagis [2 ]
Low, Andrew [1 ]
Sharpe, Timothy D. [2 ]
Uppenberg, Jonas [2 ]
Yao, Shenggen [1 ]
Kuang, Zhihe [1 ]
Savitsky, Pavel [2 ]
Lewis, Rowena S. [1 ]
Nicholson, Sandra E. [1 ]
Norton, Raymond S. [1 ]
Bullock, Alex N. [2 ]
机构
[1] Walter & Eliza Hall Inst Med Res, Parkville, Vic 3052, Australia
[2] Univ Oxford, Struct Genom Consortium, Oxford OX3 7DQ, England
基金
英国医学研究理事会; 英国惠康基金;
关键词
X-ray crystallography; NMR; ITC; protein structure; protein-peptide interaction; CHEMICAL-SHIFTS; H-1; C-13; APOPTOSIS; GENE;
D O I
10.1016/j.jmb.2010.06.017
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The mammalian SPRY domain- and SOCS box-containing proteins, SPSB1 to SPSB4, belong to the SOCS box family of E3 ubiquitin ligases. Substrate recognition sites for the SPRY domain are identified only for human Par-4 (ELNNNL) and for the Drosophila orthologue GUSTAVUS binding to the DEAD-box RNA helicase VASA (DINNNN). To further investigate this consensus motif, we determined the crystal structures of SPSB1, SPSB2, and SPSB4, as well as their binding modes and affinities for both Par-4 and VASA. Mutation of each of the three Asn residues in Par-4 abrogated binding to all three SPSB proteins, while changing EL to DI enhanced binding. By comparison to SPSB1 and SPSB4, the more divergent protein SPSB2 showed only weak binding to Par-4 and was hypersensitive to DI substitution. Par-4((59-77)) binding perturbed NMR resonances from a number of SPSB2 residues flanking the ELNNN binding site, including loop D, which binds the EL/DI sequence. Although interactions with the consensus peptide motif were conserved in all structures, flanking sites in SPSB2 were identified as sites of structural change. These structural changes limit high-affinity interactions for SPSB2 to aspartate-containing sequences, whereas SPSB1 and SPSB4 bind strongly to both Par-4 and VASA peptides. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:389 / 402
页数:14
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