POSSIBILITY FOR THE EXISTENCE OF A GENERAL CONFORMATIONAL MOTIF IN THE ACTIVE-SITES OF ENZYMES WHICH ARE INVOLVED IN NUCLEIC-ACIDS METABOLISM

被引:19
作者
KRAYEVSKY, AA [1 ]
WATANABE, KA [1 ]
机构
[1] SLOAN KETTERING INST CANC RES,NEW YORK,NY 10021
来源
NUCLEOSIDES & NUCLEOTIDES | 1993年 / 12卷 / 06期
基金
美国国家卫生研究院;
关键词
D O I
10.1080/07328319308019019
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
Many different modified nucleosides and nucleotides with conformationally restricted partly flattened sugar residues are analyzed as substrates or inhibitors of several groups of enzymes of nucleic acid metabolism. A detailed examination of the sugar moiety of large group of modified nucleosides showed that there is a striking conformational similarity, i.e., they are flattened. We propose herein a hypothesis which can represent a general conformational elements in the structure of the active sites of several different groups of enzymes. This proposal envisions that during the enzymatic process natural substrates should reflect these flattened conformations. This hypothesis allows computation of conformational analyses of the enzyme actives centers as well as the design of new actively metabolized modified nucleosides.
引用
收藏
页码:649 / 670
页数:22
相关论文
共 83 条
[31]  
GURSKAYA GV, 1990, DOKL AKAD NAUK SSSR, V12, P101
[32]   STRUCTURAL STUDIES OF THE ANTI-HIV AGENT 2',3'-DIDEHYDRO-2',3'-DIDEOXYTHYMIDINE (D4T) [J].
HARTE, WE ;
STARRETT, JE ;
MARTIN, JC ;
MANSURI, MM .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1991, 175 (01) :298-304
[33]  
HAYASHI M, 1986, J ANTIBIOT, V34, P675
[34]   ADENALLENE AND CYTALLENE - ACYCLIC NUCLEOSIDE ANALOGS THAT INHIBIT REPLICATION AND CYTOPATHIC EFFECT OF HUMAN IMMUNODEFICIENCY VIRUS INVITRO [J].
HAYASHI, S ;
PHADTARE, S ;
ZEMLICKA, J ;
MATSUKURA, M ;
MITSUYA, H ;
BRODER, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (16) :6127-6131
[35]  
HERDEWIJN PAM, 1991, MED CHEM RES, V1, P9
[36]   CELLULAR PHARMACOLOGY OF 2',3'-DIDEOXY-2',3'-DIDEHYDROTHYMIDINE, A NUCLEOSIDE ANALOG ACTIVE AGAINST HUMAN IMMUNODEFICIENCY VIRUS [J].
HO, HT ;
HITCHCOCK, MJM .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1989, 33 (06) :844-849
[37]  
IERDASZUK B, 1992, MOL PHARMACOL, V43, P197
[38]   4',5'-UNSATURATED 5'-HALOGENATED NUCLEOSIDES - MECHANISM-BASED AND COMPETITIVE INHIBITORS OF S-ADENOSYL-L-HOMOCYSTEINE HYDROLASE [J].
JARVI, ET ;
MCCARTHY, JR ;
MEHDI, S ;
MATTHEWS, DP ;
EDWARDS, ML ;
PRAKASH, NJ ;
BOWLIN, TL ;
SUNKARA, PS ;
BEY, P .
JOURNAL OF MEDICINAL CHEMISTRY, 1991, 34 (02) :647-656
[39]  
KANG GJ, 1989, J BIOL CHEM, V264, P713
[40]   SYNTHESIS OF NUCLEOSIDES AND RELATED-COMPOUNDS .21. SYNTHESIS OF 9-(T-2,C-3-DIHYDROXYMETHYL-R-1-CYCLOPROPYL)-9H-ADENINE (A LOWER METHYLENE HOMOLOG OF CARBOCYCLIC OXETANOCIN) AND RELATED-COMPOUNDS [J].
KATAGIRI, N ;
SATO, H ;
KANEKO, C .
CHEMICAL & PHARMACEUTICAL BULLETIN, 1990, 38 (11) :3184-3186