Crystal structure of YHI9, the yeast member of the phenazine biosynthesis PhzF enzyme superfamily

被引:10
作者
Liger, D
Quevillon-Cheruel, S
Sorel, I
Bremang, M
Blondeau, K
Aboulfath, I
Janin, J
van Tilbeurgh, H
Leulliot, N
机构
[1] Univ Paris 11, UMR 8619, Inst Biochim & Biophys Mol & Cellulaire, CNRS, F-91405 Orsay, France
[2] CNRS, UPR 9063, Lab Enzymol & Biochim Struct, Gif Sur Yvette, France
[3] Univ Paris 11, CNRS, UMR 8621, Inst Genet & Microbiol, Orsay, France
关键词
PhzF family; gene duplication and fusion; domain swapping;
D O I
10.1002/prot.20548
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
In the Pseudomonas bacterial genomes, the PhzF proteins are involved in the production of phenazine derivative antibiotic and antifungal compounds. The PhzF superfamily however also encompasses proteins in all genomes from bacteria to eukaryotes, for which no function has been assigned. We have determined the three dimensional crystal structure at 2.05 angstrom resolution of YHI9, the yeast member of the PhzF family. YHI9 has a fold similar to bacterial diaminopimelate epimerase, revealing a bimodular structure with an internal symmetry. Residue conservation identifies a putative active site at the interface between the two domains. Evolution of this protein by gene duplication, gene fusion and domain swapping from an ancestral gene containing the "hot dog" fold, identifies the protein as a "kinked double hot dog" fold.
引用
收藏
页码:778 / 786
页数:9
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