PROSTAGLANDIN-H SYNTHASE

被引:25
作者
GARAVITO, RM
PICOT, D
LOLL, PJ
机构
[1] Department of Biochemistry and Molecular Biology, University of Chicago, Chicago, IL 60637
基金
美国国家卫生研究院;
关键词
D O I
10.1016/S0959-440X(94)90215-1
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 prostaglandin H synthase structure reveals that the enzyme has a fold similar to those of other heme peroxidases, but differing in that a second active site has evolved within this fold which catalyzes the cyclooxygenase reaction. The protein has also acquired two additional domains: a membrane-binding motif that lacks transmembrane segments, mediating attachment to the membrane via helices that lie parallel to the membrane, and an epidermal growth factor-like module found just before the membrane-binding motif. The epidermal growth factor-like module is located in the dimer interface.
引用
收藏
页码:529 / 535
页数:7
相关论文
共 50 条
[21]   THYROPEROXIDASE, AN AUTO-ANTIGEN WITH A MOSAIC STRUCTURE MADE OF NUCLEAR AND MITOCHONDRIAL GENE MODULES [J].
LIBERT, F ;
RUEL, J ;
LUDGATE, M ;
SWILLENS, S ;
ALEXANDER, N ;
VASSART, G ;
DINSART, C .
EMBO JOURNAL, 1987, 6 (13) :4193-4196
[22]  
MAGNUSSON RP, 1990, PEROXIDASES CHEM BIO, P199
[23]  
Marnet L. J., 1991, PEROXIDASES CHEM BIO, V1, P293
[24]  
MEADE EA, 1993, J BIOL CHEM, V268, P6610
[25]  
MERLIE JP, 1988, J BIOL CHEM, V263, P3550
[26]   SELECTIVITY OF NONSTEROIDAL ANTIINFLAMMATORY DRUGS AS INHIBITORS OF CONSTITUTIVE AND INDUCIBLE CYCLOOXYGENASE [J].
MITCHELL, JA ;
AKARASEREENONT, P ;
THIEMERMANN, C ;
FLOWER, RJ ;
VANE, JR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (24) :11693-11697
[27]  
Morita Y, 1991, BIOCH MOL PHYSL ASPE, P81
[28]   STRUCTURE AND FUNCTION OF THE ESCHERICHIA-COLI RIBONUCLEOTIDE REDUCTASE PROTEIN R2 [J].
NORDLUND, P ;
EKLUND, H .
JOURNAL OF MOLECULAR BIOLOGY, 1993, 232 (01) :123-164
[29]  
OTTO JC, 1993, J BIOL CHEM, V268, P18234
[30]   PROTEIN-RADICAL ENZYMES [J].
PEDERSEN, JZ ;
FINAZZIAGRO, A .
FEBS LETTERS, 1993, 325 (1-2) :53-58