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5ZXN

Crystal structure of CurA from Vibrio vulnificus

Summary for 5ZXN
Entry DOI10.2210/pdb5zxn/pdb
DescriptorNADP-dependent oxidoreductase, 2-(N-MORPHOLINO)-ETHANESULFONIC ACID, 1,2-ETHANEDIOL, ... (4 entities in total)
Functional Keywordsreductase, oxidoreductase
Biological sourceVIBRIO VULNIFICUS MO6-24/O
Total number of polymer chains2
Total formula weight76093.24
Authors
Kim, M.-K.,Bae, D.-W.,Cha, S.-S. (deposition date: 2018-05-21, release date: 2019-04-03, Last modification date: 2024-10-30)
Primary citationPark, S.B.,Bae, D.W.,Clavio, N.A.B.,Zhao, L.,Jeong, C.S.,Choi, B.M.,Macalino, S.J.Y.,Cha, H.J.,Park, J.B.,Lee, J.H.,Nam, S.J.,Choi, S.,Kim, M.K.,Cha, S.S.
Structural and Biochemical Characterization of the Curcumin-Reducing Activity of CurA from Vibrio vulnificus.
J. Agric. Food Chem., 66:10608-10616, 2018
Cited by
PubMed Abstract: Curcumin is a yellow-colored ingredient in dietary spice turmeric ( Curcuma longa Linn). This nontoxic polyphenol has antitumor, anti-inflammatory, apoptotic, and antioxidant activities. The ingested curcumin is reduced to multihydrated forms with more potent therapeutic potentials by the curcumin reductase (CurA) from commensal Escherichia coli. In this study, we demonstrated that Vibrio vulnificus CurA ( VvCurA) with 87% sequence similarity to the E. coli CurA exhibits the curcumin-reducing activity through spectrophotometric detection of NADPH oxidation and high performance liquid chromatographic analysis of curcumin consumption and product generation. Afterward, we determined the crystal structures of VvCurA and the VvCurA/NADPH complex, and made the in silico model of the VvCurA/NADPH/curcumin ternary complex through induced fit docking. Based on structural information, active site residues that play critical roles in catalysis have been identified and characterized by mutational and kinetic studies, leading us to propose the reaction mechanism of CurA.
PubMed: 30251539
DOI: 10.1021/acs.jafc.8b03647
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.855 Å)
Structure validation

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