Bazan J F, Fletterick R J, Pilkis S J
Department of Biochemistry and Biophysics, University of California, San Francisco 94143.
Proc Natl Acad Sci U S A. 1989 Dec;86(24):9642-6. doi: 10.1073/pnas.86.24.9642.
The bifunctional rat liver enzyme 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase (ATP:D-fructose-6-phosphate 2-phosphotransferase/D-fructose-2,6-bisphosphate 2-phosphohydrolase, EC 2.7.1.105/EC 3.1.3.46) is constructed of two independent catalytic domains. We present evidence that the kinase and bisphosphatase halves of the bifunctional enzyme are, respectively, structurally similar to the glycolytic enzymes 6-phosphofructo-1-kinase and phosphoglycerate mutase. Computer-assisted modeling of the C-terminal bisphosphatase domain reveals a hydrophobic core and active site residue constellation equivalent to the yeast mutase structure; structural differences map to length-variable, surface-located loops. Sequence patterns derived from the structural alignment of mutases and the bisphosphatase further detect a significant similarity to a family of acid phosphatases. The N-terminal kinase domain, in turn, is predicted to form a nucleotide-binding fold that is analogous to a segment of 6-phosphofructo-1-kinase, suggesting that these unrelated enzymes bind fructose 6-phosphate and ATP substrates in a similar geometry. This analysis indicates that the bifunctional enzyme is the likely product of gene fusion of kinase and mutase/phosphatase catalytic units.
双功能大鼠肝脏酶6-磷酸果糖-2-激酶/果糖-2,6-二磷酸酶(ATP:D-果糖-6-磷酸2-磷酸转移酶/D-果糖-2,6-二磷酸2-磷酸水解酶,EC 2.7.1.105/EC 3.1.3.46)由两个独立的催化结构域组成。我们提供的证据表明,双功能酶的激酶和双磷酸酶部分在结构上分别类似于糖酵解酶6-磷酸果糖-1-激酶和磷酸甘油酸变位酶。对C端双磷酸酶结构域的计算机辅助建模揭示了一个疏水核心和与酵母变位酶结构相当的活性位点残基组合;结构差异映射到长度可变的表面环。从变位酶和双磷酸酶的结构比对中得出的序列模式进一步检测到与酸性磷酸酶家族有显著相似性。反过来,N端激酶结构域预计会形成一个与6-磷酸果糖-1-激酶的一段类似的核苷酸结合折叠,这表明这些不相关的酶以相似的几何形状结合果糖6-磷酸和ATP底物。该分析表明,双功能酶可能是激酶和变位酶/磷酸酶催化单元基因融合的产物。