Lindqvist Y, Schneider G, Ermler U, Sundström M
Department of Molecular Biology, Swedish University of Agricultural Sciences, Uppsala Biomedical Center.
EMBO J. 1992 Jul;11(7):2373-9. doi: 10.1002/j.1460-2075.1992.tb05301.x.
The crystal structure of Saccharomyces cerevisiae transketolase, a thiamine diphosphate dependent enzyme, has been determined to 2.5 A resolution. The enzyme is a dimer with the active sites located at the interface between the two identical subunits. The cofactor, vitamin B1 derived thiamine diphosphate, is bound at the interface between the two subunits. The enzyme subunit is built up of three domains of the alpha/beta type. The diphosphate moiety of thiamine diphosphate is bound to the enzyme at the carboxyl end of the parallel beta-sheet of the N-terminal domain and interacts with the protein through a Ca2+ ion. The thiazolium ring interacts with residues from both subunits, whereas the pyrimidine ring is buried in a hydrophobic pocket of the enzyme, formed by the loops at the carboxyl end of the beta-sheet in the middle domain in the second subunit. The structure analysis identifies amino acids critical for cofactor binding and provides mechanistic insights into thiamine catalysis.
已测定出酿酒酵母转酮醇酶(一种依赖硫胺二磷酸的酶)的晶体结构,分辨率达到2.5埃。该酶为二聚体,活性位点位于两个相同亚基之间的界面处。辅因子,即维生素B1衍生的硫胺二磷酸,结合在两个亚基之间的界面处。酶亚基由三个α/β型结构域组成。硫胺二磷酸的二磷酸部分在N端结构域平行β折叠的羧基末端与酶结合,并通过一个Ca2+离子与蛋白质相互作用。噻唑环与两个亚基的残基相互作用,而嘧啶环则埋在酶的一个疏水口袋中,该口袋由第二个亚基中间结构域β折叠羧基末端的环形成。结构分析确定了对辅因子结合至关重要的氨基酸,并为硫胺催化提供了机制上的见解。