Structure of EVH1, a novel proline-rich ligand-binding module involved in cytoskeletal dynamics and neural function

被引:96
作者
Fedorov, AA
Fedorov, E
Gertler, F
Almo, SC
机构
[1] Yeshiva Univ Albert Einstein Coll Med, Dept Biochem, Bronx, NY 10461 USA
[2] MIT, Dept Biol, Cambridge, MA 02142 USA
[3] MIT, Ctr Canc Res, Cambridge, MA 02142 USA
基金
美国国家卫生研究院;
关键词
D O I
10.1038/10717
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 Ena-VASP homology (EVH1) domain is a protein interaction module found in several proteins that are involved in transducing migratory and morphological signals into cytoskeletal reorganization. EVH1 specifically recognizes proline-rich sequences in its binding partners and directs the localization and formation of multicomponent assemblies involved in actin-based motile processes and neural development. The structure of the complex between an EVH1 domain and the target peptide sequence EFPPPPT identifies the interactions responsible for recognition and distinguishes it from other proline-rich binding modules, including SH3 and WW domains. Surprisingly, the EVH1 domain has structural similarity to pleckstrin homology (PH), phosphotyrosine-binding (PTB) and ran-binding (RanBD) domains.
引用
收藏
页码:661 / 665
页数:5
相关论文
共 37 条
[1]   Mutations in Drosophila enabled and rescue by human vasodilator-stimulated phosphoprotein (VASP) indicate important functional roles for Ena/VASP homology domain 1 (EVH1) and EVH2 domains [J].
Ahern-Djamali, SM ;
Conner, AR ;
Bachmann, C ;
Kastenmeier, AS ;
Reddy, SK ;
Beckerle, MC ;
Walter, U ;
Hoffmann, FM .
MOLECULAR BIOLOGY OF THE CELL, 1998, 9 (08) :2157-2171
[2]   PROLINE-RICH SEQUENCES THAT BIND TO SRC HOMOLOGY-3 DOMAINS WITH INDIVIDUAL SPECIFICITIES [J].
ALEXANDROPOULOS, K ;
CHENG, GH ;
BALTIMORE, D .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (08) :3110-3114
[3]   The vasodilator-stimulated phosphoprotein (VASP) is involved in cGMP- and cAMP-mediated inhibition of agonist-induced platelet aggregation, but is dispensable for smooth muscle function [J].
Aszódi, A ;
Pfeifer, A ;
Ahmad, M ;
Glauner, M ;
Zhou, XH ;
Ny, L ;
Andersson, KE ;
Kehrel, B ;
Offermanns, S ;
Fässler, R .
EMBO JOURNAL, 1999, 18 (01) :37-48
[4]   THE CCP4 SUITE - PROGRAMS FOR PROTEIN CRYSTALLOGRAPHY [J].
BAILEY, S .
ACTA CRYSTALLOGRAPHICA SECTION D-BIOLOGICAL CRYSTALLOGRAPHY, 1994, 50 :760-763
[5]  
BRUNGER AT, 1993, XPLOR VERSION 3 1 MA
[6]   EVH1/WH1 domains of VASP and WASP proteins belong to a large family including Ran-binding domains of the RanBP1 family [J].
Callebaut, I ;
Cossart, P ;
Dehoux, P .
FEBS LETTERS, 1998, 441 (02) :181-185
[7]   Formin binding proteins bear WWP/WW domains that bind proline-rich peptides and functionally resemble SH3 domains [J].
Chan, DC ;
Bedford, MT ;
Leder, P .
EMBO JOURNAL, 1996, 15 (05) :1045-1054
[8]   THE WW DOMAIN OF YES-ASSOCIATED PROTEIN BINDS A PROLINE-RICH LIGAND THAT DIFFERS FROM THE CONSENSUS ESTABLISHED FOR SRC HOMOLOGY 3-BINDING MODULES [J].
CHEN, HI ;
SUDOL, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (17) :7819-7823
[9]   Structure of the IRS-1 PTB domain bound to the juxtamembrane region of the insulin receptor [J].
Eck, MJ ;
DhePaganon, S ;
Trub, T ;
Nolte, RT ;
Shoelson, SE .
CELL, 1996, 85 (05) :695-705
[10]   The WW domain of neural protein FE65 interacts with proline-rich motifs in Mena, the mammalian homolog of Drosophila enabled [J].
Ermekova, KS ;
Zambrano, N ;
Linn, H ;
Minopoli, G ;
Gertler, F ;
Russo, T ;
Sudol, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (52) :32869-32877