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Human mitochondrial branched chain aminotransferase isozyme: Structural role of the CXXC center in catalysis

Islam, Mohammad Mainul; Conway, Myra; Islam, Mohammad M.; Yennawar, Neela H.; Conway, Myra E.; Wallin, Reidar; Hutson, Susan M.

Authors

Mohammad Mainul Islam

Myra Conway

Mohammad M. Islam

Neela H. Yennawar

Myra Conway Myra.Conway@uwe.ac.uk
Occasional Associate Lecturer - CHSS - DAS

Reidar Wallin

Susan M. Hutson



Abstract

Mammalian branched chain aminotransferases (BCATs) have a unique CXXC center. Kinetic and structural studies of three CXXC center mutants (C315A, C318A, and C315A/C318A) of human mitochondrial (hBCATm) isozyme and the oxidized hBCATm enzyme (hBCATm-Ox) have been used to elucidate the role of this center in hBCATm catalysis. X-ray crystallography revealed that the CXXC motif, through its network of hydrogen bonds, plays a crucial role in orienting the substrate optimally for catalysis. In all structures, there were changes in the structure of the β-turn preceding the CXXC motif when compared with wild type protein. The N-terminal loop between residues 15 and 32 is flexible in the oxidized and mutant enzymes, the disorder greater in the oxidized protein. Disordering of the N-terminal loop disrupts the integrity of the side chain binding pocket, particularly for the branched chain side chain, less so for the dicarboxylate substrate side chain. The kinetic studies of the mutant and oxidized enzymes support the structural analysis. The kinetic results showed that the predominant effect of oxidation was on the second half-reaction rather than the first half-reaction. The oxidized enzyme was completely inactive, whereas the mutants showed limited activity. Model building of the second half-reaction substrate α-ketoisocaproate in the pyridoxamine 5′-phosphate-hBCATm structure suggests that disruption of the CXXC center results in altered substrate orientation and deprotonation of the amino group of pyridoxamine 5′-phosphate, which inhibits catalysis. © 2006 by The American Society for Biochemistry and Molecular Biology, Inc.

Citation

Conway, M., Islam, M. M., Yennawar, N. H., Islam, M. M., Conway, M. E., Wallin, R., & Hutson, S. M. (2006). Human mitochondrial branched chain aminotransferase isozyme: Structural role of the CXXC center in catalysis. Journal of Biological Chemistry, 281(51), 39660-39671. https://doi.org/10.1074/jbc.M607552200

Journal Article Type Article
Publication Date Dec 22, 2006
Journal Journal of Biological Chemistry
Print ISSN 0021-9258
Electronic ISSN 1083-351X
Publisher American Society for Biochemistry and Molecular Biology
Peer Reviewed Not Peer Reviewed
Volume 281
Issue 51
Pages 39660-39671
DOI https://doi.org/10.1074/jbc.M607552200
Keywords aminotransferase, CXCC center
Public URL https://uwe-repository.worktribe.com/output/1034935
Publisher URL http://dx.doi.org/10.1074/jbc.M607552200