Evolutionary families of peptidase inhibitors

被引:449
作者
Rawlings, ND [1 ]
Tolle, DP [1 ]
Barrett, AJ [1 ]
机构
[1] Wellcome Trust Sanger Inst, Hinxton CB10 1SA, Cambs, England
关键词
clan; compound inhibitor; domain repeat; MEROPS database; peptidase inhibitor; protease inhibitor;
D O I
10.1042/BJ20031825
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 proteins that inhibit peptidases are of great importance in medicine and biotechnology, but there has never been a comprehensive system of classification for them. Some of the terminology currently in use is potentially confusing. In the hope of facilitating the exchange, storage and retrieval of information about this important group of proteins, we now describe a system wherein the inhibitor units of the peptidase inhibitors are assigned to 48 families on the basis of similarities detectable at the level of amino acid sequence. Then, on the basis of three-dimensional structures, 31 of the families are assigned to 26 clans. A simple system of nomenclature is introduced for reference to each clan, family and inhibitor. We briefly discuss the specificities and mechanisms of the interactions of the inhibitors in the various families with their target enzymes. The system of families and clans of inhibitors described has been implemented in the MEROPS peptidase database (http://merops.sanger.ac.uk/), and this will provide a mechanism for updating it as new information becomes available.
引用
收藏
页码:705 / 716
页数:12
相关论文
共 109 条
[91]   Inhibition of distant caspase homologues by natural caspase inhibitors [J].
Snipas, SJ ;
Stennicke, HR ;
Riedl, S ;
Potempa, J ;
Travis, J ;
Barrett, AJ ;
Salvesen, GS .
BIOCHEMICAL JOURNAL, 2001, 357 (02) :575-580
[92]  
SOTTRUPJENSEN L, 1989, J BIOL CHEM, V264, P15781
[93]  
SOTTRUPJENSEN L, 1989, J BIOL CHEM, V264, P11539
[94]  
St Charles R, 2000, PROTEIN SCI, V9, P265
[95]   Reprieval from execution: the molecular basis of caspase inhibition [J].
Stennicke, HR ;
Ryan, CA ;
Salvesen, GS .
TRENDS IN BIOCHEMICAL SCIENCES, 2002, 27 (02) :94-101
[96]   Equistatin, a protease inhibitor from the sea anemone Actinia equina, is composed of three structural and functional domains [J].
Strukelj, B ;
Lenarcic, B ;
Gruden, K ;
Pungercar, J ;
Rogelj, B ;
Turk, V ;
Bosch, D ;
Jongsma, MA .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2000, 269 (03) :732-736
[97]   An endogenous target protease, SAM-P26, of Streptomyces protease inhibitor (SSI):: Primary structure, enzymatic characterization, and its interaction with SSI [J].
Taguchi, S ;
Yamada, S ;
Kojima, S ;
Momose, H .
JOURNAL OF BIOCHEMISTRY, 1998, 124 (04) :804-810
[98]   THE REACTIVE SITE OF MARINOSTATIN, A PROTEINASE-INHIBITOR FROM MARINE ALTEROMONAS SP B-10-31 [J].
TAKANO, R ;
IMADA, C ;
KAMEI, K ;
HARA, S .
JOURNAL OF BIOCHEMISTRY, 1991, 110 (06) :856-858
[99]   Bitter gourd proteinase inhibitors:: potential growth inhibitors of Helicoverpa armigera and Spodoptera litura [J].
Telang, M ;
Srinivasan, A ;
Patankar, A ;
Harsulkar, A ;
Joshi, V ;
Damle, A ;
Deshpande, V ;
Sainani, M ;
Ranjekar, P ;
Gupta, G ;
Birah, A ;
Rani, S ;
Kachole, M ;
Giri, A ;
Gupta, V .
PHYTOCHEMISTRY, 2003, 63 (06) :643-652
[100]   CLUSTAL-W - IMPROVING THE SENSITIVITY OF PROGRESSIVE MULTIPLE SEQUENCE ALIGNMENT THROUGH SEQUENCE WEIGHTING, POSITION-SPECIFIC GAP PENALTIES AND WEIGHT MATRIX CHOICE [J].
THOMPSON, JD ;
HIGGINS, DG ;
GIBSON, TJ .
NUCLEIC ACIDS RESEARCH, 1994, 22 (22) :4673-4680