Modelling the 2-kinase domain of 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase on adenylate kinase

被引:14
作者
Bertrand, L
Vertommen, D
Depiereux, E
Hue, L
Rider, MH
Feytmans, E
机构
[1] UNIV LOUVAIN,SCH MED,HORMONE & METAB RES UNIT,B-1200 BRUSSELS,BELGIUM
[2] INT INST CELLULAR & MOL PATHOL,B-1200 BRUSSELS,BELGIUM
[3] FAC UNIV NOTRE DAME PAIX,DEPT BIOL,B-5000 NAMUR,BELGIUM
关键词
D O I
10.1042/bj3210615
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
Simultaneous multiple alignment of available sequences of the bifunctional enzyme 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase revealed several segments of conserved residues in the 2-kinase domain. The sequence of the kinase domain was also compared with proteins of known three-dimensional structure. No similarity was found between the kinase domain of 6-phosphofructo-2-kinase and 6-phosphofructo-1-kinase. This questions the modelling of the 2-kinase domain on bacterial 6-phosphofructo-1-kinase that has previously been proposed [Bazan, Fletterick and Pilkis (1989) Proc. Natl. Acad. Sci. U.S.A. 86, 9642-9646]. However, sequence similarities were found between the 2-kinase domain and several nucleotide-binding proteins, the most similar being adenylate kinase. A structural model of the 2-kinase domain based on adenylate kinase is proposed. It accommodates all the results of site-directed mutagenesis studies carried out to date on residues in the 2-kinase domain. It also allows residues potentially involved in catalysis and/or substrate binding to be predicted.
引用
收藏
页码:615 / 621
页数:7
相关论文
共 52 条
[1]   MOLECULAR-CLONING, SEQUENCE-ANALYSIS, AND EXPRESSION OF A HUMAN-LIVER CDNA CODING FOR FRUCTOSE-6-P,2-KINASE-FRUCTOSE-2,6-BISPHOSPHATASE [J].
ALGAIER, J ;
UYEDA, K .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1988, 153 (01) :328-333
[2]  
ALTSCHUL SF, 1990, J MOL BIOL, V215, P403, DOI 10.1006/jmbi.1990.9999
[3]   EVOLUTION OF A BIFUNCTIONAL ENZYME - 6-PHOSPHOFRUCTO-2-KINASE FRUCTOSE-2,6-BISPHOSPHATASE [J].
BAZAN, JF ;
FLETTERICK, RJ ;
PILKIS, SJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (24) :9642-9646
[4]   SITE-DIRECTED MUTAGENESIS IDENTIFIES CATALYTIC RESIDUES IN THE ACTIVE-SITE OF ESCHERICHIA-COLI PHOSPHOFRUCTOKINASE [J].
BERGER, SA ;
EVANS, PR .
BIOCHEMISTRY, 1992, 31 (38) :9237-9242
[5]   ACTIVE-SITE MUTANTS ALTERING THE COOPERATIVITY OF ESCHERICHIA-COLI PHOSPHOFRUCTOKINASE [J].
BERGER, SA ;
EVANS, PR .
NATURE, 1990, 343 (6258) :575-576
[6]   Mutagenesis of charged residues in a conserved sequence in the 2-kinase domain of 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase [J].
Bertrand, L ;
Vertommen, D ;
Feytmans, E ;
DiPietro, A ;
Rider, MH ;
Hue, L .
BIOCHEMICAL JOURNAL, 1997, 321 :609-614
[7]   Site-directed mutagenesis of Lys-174, Asp-179 and Asp-191 in the 2-kinase domain of 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase [J].
Bertrand, L ;
Deprez, J ;
Vertommen, D ;
DiPietro, A ;
Hue, L ;
Rider, MH .
BIOCHEMICAL JOURNAL, 1997, 321 :623-627
[8]   CLONING AND SEQUENCING OF THE ADENYLATE KINASE GENE (ADK) OF ESCHERICHIA-COLI [J].
BRUNE, M ;
SCHUMANN, R ;
WITTINGHOFER, F .
NUCLEIC ACIDS RESEARCH, 1985, 13 (19) :7139-7151
[9]   MECHANISM OF ADENYLATE KINASE - THE ESSENTIAL LYSINE HELPS TO ORIENT THE PHOSPHATES AND THE ACTIVE-SITE RESIDUES TO PROPER CONFORMATIONS [J].
BYEON, IJL ;
SHI, ZT ;
TSAI, MD .
BIOCHEMISTRY, 1995, 34 (10) :3172-3182
[10]   ISOLATION AND CHARACTERIZATION OF THE GENE ENCODING THE MUSCLE-SPECIFIC ISOZYME OF HUMAN PHOSPHOGLYCERATE MUTASE [J].
CASTELLAESCOLA, J ;
OJCIUS, DM ;
LEBOULCH, P ;
JOULIN, V ;
BLOUQUIT, Y ;
GAREL, MC ;
VALENTIN, C ;
ROSA, R ;
CLIMENTROMEO, F ;
COHENSOLAL, M .
GENE, 1990, 91 (02) :225-232