Structure of astacin with a transition-state analogue inhibitor

被引:140
作者
Grams, F
Dive, V
Yiotakis, A
Yiallouros, I
Vassiliou, S
Zwilling, R
Bode, W
Stocker, W
机构
[1] UNIV HEIDELBERG,INST ZOOL,D-69120 HEIDELBERG,GERMANY
[2] MAX PLANCK INST BIOCHEM,ABT STRUKTURFORSCH,D-82152 PLANEGG,GERMANY
[3] CENS,CEA,DEPT INGN& ETUD PROT,F-91191 GIF SUR YVETTE,FRANCE
[4] UNIV ATHENS,DEPT ORGAN CHEM,ZOGRATU 15771,ATHENS,GREECE
来源
NATURE STRUCTURAL BIOLOGY | 1996年 / 3卷 / 08期
关键词
D O I
10.1038/nsb0896-671
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 structure of the zinc peptidase astacin in complex with a phosphinic peptide suggests that a special role is played by the side chain of a zinc-bound tyrosine, which is shifted to form bond to the phosphinyl group-a mimic of the carboxyanion of the transition state.
引用
收藏
页码:671 / 675
页数:5
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