共 25 条
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;
D O I:
暂无
中图分类号:
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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