| Literature DB >> 30231198 |
Ting Yao1, Yiyou Huang2, Meng Zhang1, Yujuan Chen1, Hairun Pei1, Jianyou Shi2,3, Huanchen Wang4, Yousheng Wang1, Hengming Ke2.
Abstract
The cAMP signaling system plays important roles in the physiological processes of pathogen yeast Candida albicans, but its functional mechanism has not been well illustrated. Here, we report the enzymatic characterization and crystal structures of C. albicans phosphodiesterase 2 (caPDE2) in the unliganded and 3-isobutyl-1-methylxanthine-complexed forms. caPDE2 is a monomer in liquid and crystal states and specifically hydrolyzes cAMP with a KM of 35 nM. It does not effectively hydrolyze cGMP as shown by the 1.32 × 105-fold specificity of cAMP/cGMP. The crystal structure of caPDE2 shows significant differences from those of human PDEs. First, the N-terminal fragment of caPDE2 (residues 1-201) tightly associates with the catalytic domain to form a rigid molecular entity, implying its stable molecular conformation for C. albicans to resist environmental stresses. Second, the M-loop, a critical fragment for binding of the substrate and inhibitors to human PDEs, is not a part of the caPDE2 active site. This feature of caPDE2 may provide a structural basis for the design of selective inhibitors for the treatment of yeast infection.Entities:
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Year: 2018 PMID: 30231198 PMCID: PMC9364965 DOI: 10.1021/acs.biochem.8b00707
Source DB: PubMed Journal: Biochemistry ISSN: 0006-2960 Impact factor: 3.321