PROTEIN TARGETS FOR STRUCTURE-BASED DRUG DESIGN

被引:32
作者
WALKINSHAW, MD
机构
[1] Sandoz Pharma AG, Basel
关键词
D O I
10.1002/med.2610120403
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
The aim of this review is to discuss those proteins for which the known 3D structure may be relevant to drug design. The majority of available information to date is from protein x-ray crystallography, though a growing number of studies are based on molecular modeling and NMR spectroscopy. The review concentrates on major progress reported in the literature from 1985 through the first half of 1991. Protein structures and related drug design studies have been loosely classified here into a number of major therapeutic areas: immunology, inflammation, cardiovascular disorders, cancer, viral and bacterial infection. Table I [GRAPHICS] lists those proteins discussed in this review for which 3D structural information is available.
引用
收藏
页码:317 / 372
页数:56
相关论文
共 209 条
[131]   CRYSTALLOGRAPHIC STUDY OF A BETA-LACTAM INHIBITOR COMPLEX WITH ELASTASE AT 1.84-A RESOLUTION [J].
NAVIA, MA ;
SPRINGER, JP ;
LIN, TY ;
WILLIAMS, HR ;
FIRESTONE, RA ;
PISANO, JM ;
DOHERTY, JB ;
FINKE, PE ;
HOOGSTEEN, K .
NATURE, 1987, 327 (6117) :79-82
[132]   ROLES OF G-PROTEIN SUBUNITS IN TRANSMEMBRANE SIGNALING [J].
NEER, EJ ;
CLAPHAM, DE .
NATURE, 1988, 333 (6169) :129-134
[133]   THE ADAPTABILITY OF THE ACTIVE-SITE OF TRYPANOSOMAL TRIOSEPHOSPHATE ISOMERASE AS OBSERVED IN THE CRYSTAL-STRUCTURES OF 3 DIFFERENT COMPLEXES [J].
NOBLE, MEM ;
WIERENGA, RK ;
LAMBEIR, AM ;
OPPERDOES, FR ;
THUNNISSEN, AMWH ;
KALK, KH ;
GROENDIJK, H ;
HOL, WGJ .
PROTEINS-STRUCTURE FUNCTION AND GENETICS, 1991, 10 (01) :50-69
[134]   REFINED CRYSTAL-STRUCTURE OF BETA-LACTAMASE FROM CITROBACTER-FREUNDII INDICATES A MECHANISM FOR BETA-LACTAM HYDROLYSIS [J].
OEFNER, C ;
DARCY, A ;
DALY, JJ ;
GUBERNATOR, K ;
CHARNAS, RL ;
HEINZE, I ;
HUBSCHWERLEN, C ;
WINKLER, FK .
NATURE, 1990, 343 (6255) :284-288
[135]   CRYSTAL-STRUCTURE OF HUMAN DIHYDROFOLATE-REDUCTASE COMPLEXED WITH FOLATE [J].
OEFNER, C ;
DARCY, A ;
WINKLER, FK .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1988, 174 (02) :377-385
[136]   STRUCTURE OF AN ANTIBODY ANTIGEN COMPLEX - CRYSTAL-STRUCTURE OF THE HYHEL-10 FAB-LYSOZYME COMPLEX [J].
PADLAN, EA ;
SILVERTON, EW ;
SHERIFF, S ;
COHEN, GH ;
SMITHGILL, SJ ;
DAVIES, DR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (15) :5938-5942
[137]   STRUCTURE OF THE GUANINE-NUCLEOTIDE-BINDING DOMAIN OF THE HA-RAS ONCOGENE PRODUCT P21 IN THE TRIPHOSPHATE CONFORMATION [J].
PAI, EF ;
KABSCH, W ;
KRENGEL, U ;
HOLMES, KC ;
JOHN, J ;
WITTINGHOFER, A .
NATURE, 1989, 341 (6239) :209-214
[138]   REFINED CRYSTAL-STRUCTURE OF THE TRIPHOSPHATE CONFORMATION OF H-RAS P21 AT 1.35 A RESOLUTION - IMPLICATIONS FOR THE MECHANISM OF GTP HYDROLYSIS [J].
PAI, EF ;
KRENGEL, U ;
PETSKO, GA ;
GOODY, RS ;
KABSCH, W ;
WITTINGHOFER, A .
EMBO JOURNAL, 1990, 9 (08) :2351-2359
[139]   THE STRUCTURE OF BETA-LACTOGLOBULIN AND ITS SIMILARITY TO PLASMA RETINOL-BINDING PROTEIN [J].
PAPIZ, MZ ;
SAWYER, L ;
ELIOPOULOS, EE ;
NORTH, ACT ;
FINDLAY, JBC ;
SIVAPRASADARAO, R ;
JONES, TA ;
NEWCOMER, ME ;
KRAULIS, PJ .
NATURE, 1986, 324 (6095) :383-385
[140]  
Parry D A, 1988, J Mol Recognit, V1, P107, DOI 10.1002/jmr.300010302