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6KXR

Crystal structure of wild type Alp1U from the biosynthesis of kinamycins

Summary for 6KXR
Entry DOI10.2210/pdb6kxr/pdb
Related6KXH 6kxp
DescriptorPutative hydrolase, D-MALATE (3 entities in total)
Functional Keywordshydrolyse epoxide, cis-vicinal diol, hydrolase
Biological sourceStreptomyces ambofaciens (strain ATCC 23877 / 3486 / DSM 40053 / JCM 4204 / NBRC 12836 / NRRL B-2516)
Total number of polymer chains4
Total formula weight148337.74
Authors
Zhang, L.,Yingli, Z.,De, B.C.,Zhang, C. (deposition date: 2019-09-12, release date: 2020-09-16, Last modification date: 2024-03-27)
Primary citationZhang, L.,De, B.C.,Zhang, W.,Mandi, A.,Fang, Z.,Yang, C.,Zhu, Y.,Kurtan, T.,Zhang, C.
Mutation of an atypical oxirane oxyanion hole improves regioselectivity of the alpha / beta-fold epoxide hydrolase Alp1U.
J.Biol.Chem., 295:16987-16997, 2020
Cited by
PubMed Abstract: Epoxide hydrolases (EHs) have been characterized and engineered as biocatalysts that convert epoxides to valuable chiral vicinal diol precursors of drugs and bioactive compounds. Nonetheless, the regioselectivity control of the epoxide ring opening by EHs remains challenging. Alp1U is an α/β-fold EH that exhibits poor regioselectivity in the epoxide hydrolysis of fluostatin C (compound 1) and produces a pair of stereoisomers. Herein, we established the absolute configuration of the two stereoisomeric products and determined the crystal structure of Alp1U. A Trp-186/Trp-187/Tyr-247 oxirane oxygen hole was identified in Alp1U that replaced the canonical Tyr/Tyr pair in α/β-EHs. Mutation of residues in the atypical oxirane oxygen hole of Alp1U improved the regioselectivity for epoxide hydrolysis on 1. The single site Y247F mutation led to highly regioselective (98%) attack at C-3 of 1, whereas the double mutation W187F/Y247F resulted in regioselective (94%) nucleophilic attack at C-2. Furthermore, single-crystal X-ray structures of the two regioselective Alp1U variants in complex with 1 were determined. These findings allowed insights into the reaction details of Alp1U and provided a new approach for engineering regioselective epoxide hydrolases.
PubMed: 33004437
DOI: 10.1074/jbc.RA120.015563
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.45073679781 Å)
Structure validation

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數據於2024-11-06公開中

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