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4H7H

Crystal structure of haloalkane dehalogenase LinB T135A mutant from Sphingobium sp. MI1205

Summary for 4H7H
Entry DOI10.2210/pdb4h7h/pdb
Related4H77 4H7D 4H7E 4H7F 4H7I 4H7J 4H7K
DescriptorHaloalkane dehalogenase, CHLORIDE ION, CALCIUM ION, ... (4 entities in total)
Functional Keywordsalpha/beta hydrolase fold, hydrolase
Biological sourceSphingobium
Total number of polymer chains1
Total formula weight34142.09
Authors
Okai, M.,Ohtsuka, J.,Imai, L.F.,Mase, T.,Moriuchi, R.,Tsuda, M.,Nagata, K.,Nagata, Y.,Tanokura, M. (deposition date: 2012-09-20, release date: 2013-06-05, Last modification date: 2023-11-08)
Primary citationOkai, M.,Ohtsuka, J.,Imai, L.F.,Mase, T.,Moriuchi, R.,Tsuda, M.,Nagata, K.,Nagata, Y.,Tanokura, M.
Crystal Structure and Site-Directed Mutagenesis Analyses of Haloalkane Dehalogenase LinB from Sphingobium sp. Strain MI1205.
J.Bacteriol., 195:2642-2651, 2013
Cited by
PubMed Abstract: The enzymes LinB(UT) and LinB(MI) (LinB from Sphingobium japonicum UT26 and Sphingobium sp. MI1205, respectively) catalyze the hydrolytic dechlorination of β-hexachlorocyclohexane (β-HCH) and yield different products, 2,3,4,5,6-pentachlorocyclohexanol (PCHL) and 2,3,5,6-tetrachlorocyclohexane-1,4-diol (TCDL), respectively, despite their 98% identity in amino acid sequence. To reveal the structural basis of their different enzymatic properties, we performed site-directed mutagenesis and X-ray crystallographic studies of LinB(MI) and its seven point mutants. The mutation analysis revealed that the seven amino acid residues uniquely found in LinB(MI) were categorized into three groups based on the efficiency of the first-step (from β-HCH to PCHL) and second-step (from PCHL to TCDL) conversions. Crystal structure analyses of wild-type LinB(MI) and its seven point mutants indicated how each mutated residue contributed to the first- and second-step conversions by LinB(MI). The dynamics simulation analyses of wild-type LinB(MI) and LinB(UT) revealed that the entrance of the substrate access tunnel of LinB(UT) was more flexible than that of LinB(MI), which could lead to the different efficiencies of dehalogenation activity between these dehalogenases.
PubMed: 23564170
DOI: 10.1128/JB.02020-12
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.1 Å)
Structure validation

226707

數據於2024-10-30公開中

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