METHIONINE ADENOSYLTRANSFERASE - STRUCTURE AND FUNCTION

被引:116
作者
KOTB, M
GELLER, AM
机构
[1] VET AFFAIRS MED CTR, MEMPHIS, TN 38104 USA
[2] UNIV TENNESSEE CTR HLTH SCI, DEPT MICROBIOL & IMMUNOL, MEMPHIS, TN 38163 USA
[3] UNIV TENNESSEE CTR HLTH SCI, DEPT BIOCHEM, MEMPHIS, TN 38163 USA
关键词
D O I
10.1016/0163-7258(93)90042-C
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Methionine adenosyltransferase (MAT), a key enzyme in metabolism, catalyzes the synthesis of one of the most important and pivotal biological molecules, S-adenosylmethionine. In every organism studied thus far, MAT exists in multiple forms; most are encoded by related, but distinct genes. Molecular and immunological studies revealed the presence of considerable conservation in the structure of MAT from different species; however, the various MAT isozymes differ in their physical and kinetic properties in ways that allow them to be regulated differently. Recent studies suggest that human MAT is composed of nonidentical subunits that can assume multiple states of aggregation, each with different kinetic characteristics. The tissue distribution of MAT isozymes and the ability of cells within the same tissue to switch between the different forms of MAT suggest that this mode of regulation is important for cellular function and differentiation. Therefore, understanding the regulation and structure-function relationship of this fascinating enzyme should help us clarify its role in biology and may provide us with tools to effectively manipulate its activity in clinical situations such as cancer, autoimmunity and organ transplantation.
引用
收藏
页码:125 / 143
页数:19
相关论文
共 100 条
[91]   SAM2 ENCODES THE 2ND-METHIONINE S-ADENOSYL TRANSFERASE IN SACCHAROMYCES-CEREVISIAE - PHYSIOLOGY AND REGULATION OF BOTH ENZYMES [J].
THOMAS, D ;
ROTHSTEIN, R ;
ROSENBERG, N ;
SURDINKERJAN, Y .
MOLECULAR AND CELLULAR BIOLOGY, 1988, 8 (12) :5132-5139
[92]   THE SYNTHESIS OF THE 2 S-ADENOSYL-METHIONINE SYNTHETASES IS DIFFERENTLY REGULATED IN SACCHAROMYCES-CEREVISIAE [J].
THOMAS, D ;
SURDINKERJAN, Y .
MOLECULAR & GENERAL GENETICS, 1991, 226 (1-2) :224-232
[93]  
THOMAS D, 1987, J BIOL CHEM, V262, P16704
[94]   S-ADENOSYLMETHIONINE SYNTHETASE ISOENZYME PATTERNS FROM RAT HEPATOMA INDUCED BY N-2-FLUORENYLACETAMIDE [J].
TSUKADA, K ;
OKADA, G .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1980, 94 (04) :1078-1082
[95]   APPROACHES TO ISOZYME-SPECIFIC INHIBITORS .16. A NOVEL METHYL-C5' COVALENT ADDUCT OF L-ETHIONINE AND BETA,GAMMA-IMIDO-ATP AS A POTENT MULTISUBSTRATE INHIBITOR OF RAT METHIONINE ADENOSYLTRANSFERASES [J].
VRUDHULA, VM ;
KAPPLER, F ;
AFSHAR, C ;
GINELL, SL ;
LESSINGER, L ;
HAMPTON, A .
JOURNAL OF MEDICINAL CHEMISTRY, 1989, 32 (04) :885-890
[96]   THE ROLE OF SAME IN THE TREATMENT OF LIVER-DISEASE - INTRODUCTION [J].
WILLIAMS, R ;
LIEBER, CS .
DRUGS, 1990, 40 :1-2
[97]  
XUE GP, 1989, BIOCHEM INT, V18, P525
[98]   EFFECT OF DL-ALPHA-DIFLUOROMETHYLORNITHINE ON METHIONINE CYCLE INTERMEDIATES IN TRYPANOSOMA-BRUCEI-BRUCEI [J].
YARLETT, N ;
BACCHI, CJ .
MOLECULAR AND BIOCHEMICAL PARASITOLOGY, 1988, 27 (01) :1-10
[99]   PROTEIN METHYLASES IN TRYPANOSOMA-BRUCEI-BRUCEI - ACTIVITIES AND RESPONSE TO DL-ALPHA-DIFLUOROMETHYLORNITHINE [J].
YARLETT, N ;
QUAMINA, A ;
BACCHI, CJ .
JOURNAL OF GENERAL MICROBIOLOGY, 1991, 137 :717-724
[100]  
YARLETT N, 1993, IN PRESS BIOPHYS BIO