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4MQP

Mycobaterium tuberculosis transaminase BioA complexed with 2-hydrazinylbenzo[d]thiazole

Summary for 4MQP
Entry DOI10.2210/pdb4mqp/pdb
Related4MQN 4MQO 4MQQ 4MQR
DescriptorAdenosylmethionine-8-amino-7-oxononanoate aminotransferase, (4-{[(E)-1,3-benzothiazol-2-yldiazenyl]methyl}-5-hydroxy-6-methylpyridin-3-yl)methyl dihydrogen phosphate, 1,2-ETHANEDIOL, ... (5 entities in total)
Functional Keywordsplp, transaminase, transferase
Biological sourceMycobacterium tuberculosis
Cellular locationCytoplasm (By similarity): P0A4X6
Total number of polymer chains2
Total formula weight98154.05
Authors
Finzel, B.C.,Dai, R. (deposition date: 2013-09-16, release date: 2014-03-05, Last modification date: 2023-09-20)
Primary citationDai, R.,Wilson, D.J.,Geders, T.W.,Aldrich, C.C.,Finzel, B.C.
Inhibition of Mycobacterium tuberculosis Transaminase BioA by Aryl Hydrazines and Hydrazides.
Chembiochem, 15:575-586, 2014
Cited by
PubMed Abstract: 7,8-Diaminopelargonic acid synthase (BioA) of Mycobacterium tuberculosis is a recently validated target for therapeutic intervention in the treatment of tuberculosis (TB). Using biophysical fragment screening and structural characterization of compounds, we have identified a potent aryl hydrazine inhibitor of BioA that reversibly modifies the pyridoxal-5'-phosphate (PLP) cofactor, forming a stable quinonoid. Analogous hydrazides also form covalent adducts that can be observed crystallographically but are incapable of inactivating the enzyme. In the X-ray crystal structures, small molecules induce unexpected conformational remodeling in the substrate binding site. We compared these conformational changes to those induced upon binding of the substrate (7-keto-8-aminopelargonic acid), and characterized the inhibition kinetics and the X-ray crystal structures of BioA with the hydrazine compound and analogues to unveil the mechanism of this reversible covalent modification.
PubMed: 24482078
DOI: 10.1002/cbic.201300748
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.83 Å)
Structure validation

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数据于2025-06-25公开中

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