Solution structure of the PX domain, a target of the SH3 domain

被引:145
作者
Hiroaki, H
Ago, T
Ito, T
Sumimoto, H
Kohda, D
机构
[1] Biomol Engn Res Inst, Dept Biol Struct, Osaka 5650874, Japan
[2] Kyushu Univ, Grad Sch Med Sci, Dept Mol & Struct Biol, Higashi Ku, Fukuoka 8120082, Japan
[3] Kanazawa Univ, Canc Res Inst, Kanazawa, Ishikawa 9200934, Japan
关键词
D O I
10.1038/88591
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 phox homology (PX) domain is a novel protein module containing a conserved proline-rich motif, We have shown that the PX domain isolated from the human p47(phox) protein, a soluble subunit of phagocyte NADPH oxidase, binds specifically to the C-terminal SH3 domain derived from the same protein. The solution structure of p47 PX has an alpha + beta structure with a novel folding moth topology and reveals that the proline-rich motif is presented on the molecular surface for easy recognition by the SH3 domain. The proline-rich moth of p47 PX in the free state adopts a distorted left-handed polyproline type II helix conformation.
引用
收藏
页码:526 / 530
页数:5
相关论文
共 26 条
  • [1] Structural basis of presequence recognition by the mitochondrial protein import receptor Tom20
    Abe, Y
    Shodai, T
    Muto, T
    Mihara, K
    Torii, H
    Nishikawa, S
    Endo, T
    Kohda, D
    [J]. CELL, 2000, 100 (05) : 551 - 560
  • [2] Mechanism for phosphorylation-induced activation of the phagocyte NADPH oxidase protein p47 phox - Triple replacement of serines 303, 304, and 328 with aspartates disrupts the SH3 domain-mediated intramolecular interaction in p47 phox, thereby activating the oxidase
    Ago, T
    Nunoi, H
    Ito, T
    Sumimoto, H
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (47) : 33644 - 33653
  • [3] THE PROGRAM XEASY FOR COMPUTER-SUPPORTED NMR SPECTRAL-ANALYSIS OF BIOLOGICAL MACROMOLECULES
    BARTELS, C
    XIA, TH
    BILLETER, M
    GUNTERT, P
    WUTHRICH, K
    [J]. JOURNAL OF BIOMOLECULAR NMR, 1995, 6 (01) : 1 - 10
  • [4] DELAINE M, 1995, PHYS WORLD, V8, P6
  • [5] Assembly of the phagocyte NADPH oxidase: Molecular interaction of oxidase proteins
    DeLeo, FR
    Quinn, MT
    [J]. JOURNAL OF LEUKOCYTE BIOLOGY, 1996, 60 (06) : 677 - 691
  • [6] 2 BINDING ORIENTATIONS FOR PEPTIDES TO THE SRC SH3 DOMAIN - DEVELOPMENT OF A GENERAL-MODEL FOR SH3-LIGAND INTERACTIONS
    FENG, SB
    CHEN, JK
    YU, HT
    SIMON, JA
    SCHREIBER, SL
    [J]. SCIENCE, 1994, 266 (5188) : 1241 - 1247
  • [7] Structure of the p53 tumor suppressor bound to the ankyrin and SH3 domains of 53BP2
    Gorina, S
    Pavletich, NP
    [J]. SCIENCE, 1996, 274 (5289) : 1001 - 1005
  • [8] Torsion angle dynamics for NMR structure calculation with the new program DYANA
    Guntert, P
    Mumenthaler, C
    Wuthrich, K
    [J]. JOURNAL OF MOLECULAR BIOLOGY, 1997, 273 (01) : 283 - 298
  • [9] PROTEIN-STRUCTURE COMPARISON BY ALIGNMENT OF DISTANCE MATRICES
    HOLM, L
    SANDER, C
    [J]. JOURNAL OF MOLECULAR BIOLOGY, 1993, 233 (01) : 123 - 138
  • [10] The importance of being proline: the interaction of proline-rich motifs in signaling proteins with their cognate domains
    Kay, BK
    Williamson, MP
    Sudol, P
    [J]. FASEB JOURNAL, 2000, 14 (02) : 231 - 241