PDB ID: 5OIT
Hetero Atom Contents
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Code | Name | Style | Show | Link | |
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9WH | 5-[(5-azanyl-3-methyl-pyrazol-1-yl)methyl]-~{N}-[1-[(2-chloranyl-6-fluoranyl-phenyl)methyl]pyrazol-3-yl]-1,3,4-thiadiazol-2-amine | PoSSuM | |||
NAD | Nicotinamide-adenine-dinucleotide | PoSSuM |
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Download interaction data: 5OIT
Structure summary
Code : | 5OIT PDBj RCSB PDB PDBe | ||||||||||||
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Header : | OXIDOREDUCTASE | ||||||||||||
Title : | InhA (T2A mutant) complexed with 5-((5-Amino-3-methyl-1H-pyrazol-1-yl)methyl)-N-(1-(2-chloro-6-fluorobenzyl)-1H-pyrazol-3-yl)-1,3,4-thiadiazol-2-amine | ||||||||||||
Release Data : | 2018-02-14 | ||||||||||||
Compound : |
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Authors : | Convery, M.A. | ||||||||||||
Keywords : | Inhibitor, complex, fragment based drug discovery, tuberculosis, OXIDOREDUCTASE | ||||||||||||
Exp. method : | X-RAY DIFFRACTION ( 2.58 Å ) | ||||||||||||
Citation : |
Screening of a Novel Fragment Library with Functional Complexity against Mycobacterium tuberculosis InhA.
Prati, F.,Zuccotto, F.,Fletcher, D.
et al.
PubMed: 29399991 |
Reaction
Chain : | B, D, F, H | |||||||||||||||||||||||||||||||||||||||
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UniProt : | P9WGR1 (INHA_MYCTU) | |||||||||||||||||||||||||||||||||||||||
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