Peptidase inhibitors in the MEROPS database

被引:62
作者
Rawlings, Neil D. [1 ]
机构
[1] Wellcome Trust Sanger Inst, Hinxton CB10 1SA, Cambs, England
基金
英国惠康基金;
关键词
Peptidase; Protease; Proteinase; Inhibitor; Reactive site;
D O I
10.1016/j.biochi.2010.04.013
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 MEROPS website (http://merops.sanger.ac.uk) includes information on peptidase inhibitors as well as on peptidases and their substrates. Displays have been put in place to link peptidases and inhibitors together. The classification of protein peptidase inhibitors is continually being revised, and currently inhibitors are grouped into 67 families based on comparisons of protein sequences. These families can be further grouped into 38 clans based on comparisons of tertiary structure. Small molecule inhibitors are important reagents for peptidase characterization and, with the increasing importance of peptidases as drug targets, they are also important to the pharmaceutical industry. Small molecule inhibitors are now included in MEROPS and over 160 summaries have been written. (C) 2010 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:1463 / 1483
页数:21
相关论文
共 2 条
  • [1] A novel viper venom metalloproteinase, alborhagin, is an agonist at the platelet collagen receptor GPVI
    Andrews, RK
    Gardiner, EE
    Asazuma, N
    Berlanga, O
    Tulasne, D
    Nieswandt, B
    Smith, AI
    Berndt, MC
    Watson, SP
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (30) : 28092 - 28097
  • [2] S17092-1, a highly potent, specific and cell permeant inhibitor of human proline endopeptidase
    Barelli, H
    Petit, A
    Hirsch, E
    Wilk, S
    De Nanteuil, G
    Morain, P
    Checler, F
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1999, 257 (03) : 657 - 661