Stiers Kyle M, Muenks Andrew G, Beamer Lesa J
University of Missouri, Columbia, MO, United States.
University of Missouri, Columbia, MO, United States.
Adv Protein Chem Struct Biol. 2017;109:265-304. doi: 10.1016/bs.apcsb.2017.04.005. Epub 2017 May 17.
Enzymes in the α-d-phosphohexomutases superfamily catalyze the reversible conversion of phosphosugars, such as glucose 1-phosphate and glucose 6-phosphate. These reactions are fundamental to primary metabolism across the kingdoms of life and are required for a myriad of cellular processes, ranging from exopolysaccharide production to protein glycosylation. The subject of extensive mechanistic characterization during the latter half of the 20th century, these enzymes have recently benefitted from biophysical characterization, including X-ray crystallography, NMR, and hydrogen-deuterium exchange studies. This work has provided new insights into the unique catalytic mechanism of the superfamily, shed light on the molecular determinants of ligand recognition, and revealed the evolutionary conservation of conformational flexibility. Novel associations with inherited metabolic disease and the pathogenesis of bacterial infections have emerged, spurring renewed interest in the long-appreciated functional roles of these enzymes.
α -d-磷酸己糖变位酶超家族中的酶催化磷酸糖(如1-磷酸葡萄糖和6-磷酸葡萄糖)的可逆转化。这些反应是生命各王国初级代谢的基础,也是从胞外多糖产生到蛋白质糖基化等无数细胞过程所必需的。在20世纪后半叶,这些酶是广泛的机制表征的对象,最近它们受益于生物物理表征,包括X射线晶体学、核磁共振和氢-氘交换研究。这项工作为超家族独特的催化机制提供了新的见解,阐明了配体识别的分子决定因素,并揭示了构象灵活性的进化保守性。与遗传性代谢疾病和细菌感染发病机制的新关联已经出现,激发了人们对这些酶长期以来备受重视的功能作用的新兴趣。