Structural biology of the purine biosynthetic pathway

被引:0
|
作者
Y. Zhang
M. Morar
S. E. Ealick
机构
[1] Cornell University,Department of Chemistry and Chemical Biology, Baker Laboratory
来源
Cellular and Molecular Life Sciences | 2008年 / 65卷
关键词
Purine biosynthesis; protein evolution; ATP-grasp superfamily; PurM superfamily; amidotransferases;
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学科分类号
摘要
Purine biosynthesis requires ten enzymatic transformations to generate inosine monophosphate. PurF, PurD, PurL, PurM, PurC, and PurB are common to all pathways, while PurN or PurT, PurK/PurE-I or PurE-II, PurH or PurP, and PurJ or PurO catalyze the same steps in different organisms. X-ray crystal structures are available for all 15 purine biosynthetic enzymes, including 7 ATP-dependent enzymes, 2 amidotransferases and 2 tetrahydrofolate-dependent enzymes. Here we summarize the structures of the purine biosynthetic enzymes, discuss similarities and differences, and present arguments for pathway evolution. Four of the ATP-dependent enzymes belong to the ATP-grasp superfamily and 2 to the PurM superfamily. The amidotransferases are unrelated, with one utilizing an N-terminal nucleophileglutaminase and the other utilizing a triad glutaminase. Likewise the tetrahydrofolate-dependent enzymes are unrelated. Ancestral proteins may have included a broad specificity enzyme instead of PurD, PurT, PurK, PurC, and PurP, and a separate enzyme instead of PurM and PurL.
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页码:3699 / 3724
页数:25
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