4OHU: Mycobacterium tuberculosis InhA

Crystal structure of Mycobacterium tuberculosis InhA in complex with inhibitor PT92. Determined by X-ray diffraction at 1.6 Å resolution. Released 30 Apr 2014.

Method
X-ray diffraction
Resolution
1.6 Å
Organism
Mycobacterium tuberculosis
Chains
4
Atoms
8,461
Mol. weight
126.96 kDa
Ligands
NAD, 2TK
Released
30 Apr 2014

Explore 4OHU in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

4OHU contains 63 α-helices and 42 β-strands across 4 chains. Residue ranges use author residue numbering, as in the PDB file, from PDBe. To see them in 3D, choose the Cartoon representation with Secondary structure coloring: helices, sheets and coils get different colors.

Chain A: 17 helices, 11 β-strands

ElementResiduesLengthSheet
β-strand9-1351
α-helix21-3111
α-helix341
β-strand35-4061
α-helix44-518
β-strand60-6231
α-helix68-8215
β-strand88-9361
α-helix100-1023
β-strand10412
α-helix108-1103
α-helix113-1208
α-helix121-1255
α-helix126-1349
α-helix135-1373
β-strand138-148111
β-strand15413
β-strand15712
α-helix159-18022
β-strand185-19171
α-helix1971
α-helix198-2036
α-helix204-2063
α-helix211-22515
α-helix236-24611
β-strand256-26051
α-helix264-2663
β-strand26714
Chain B: 14 helices, 9 β-strands
ElementResiduesLengthSheet
β-strand9-1355
α-helix21-3111
β-strand35-4065
α-helix44-518
β-strand60-6235
α-helix68-8215
β-strand88-9365
α-helix100-1023
α-helix108-1103
α-helix113-1208
α-helix121-1255
α-helix126-1349
α-helix135-1373
β-strand138-148115
β-strand15414
α-helix159-18022
β-strand185-19175
α-helix200-2034
α-helix210-22516
α-helix236-24611
β-strand256-26055
α-helix264-2663
β-strand26713
Chain C: 16 helices, 11 β-strands
ElementResiduesLengthSheet
β-strand9-1356
α-helix21-3111
β-strand35-4066
α-helix44-518
β-strand60-6236
α-helix68-8215
β-strand88-9366
α-helix100-1023
β-strand10417
α-helix108-1103
α-helix113-1208
α-helix121-1255
α-helix126-1349
α-helix135-1373
β-strand138-148116
β-strand15418
β-strand15717
α-helix159-18022
β-strand185-19176
α-helix1971
α-helix198-2047
α-helix205-2073
α-helix216-22510
α-helix236-24611
β-strand256-26056
α-helix264-2663
β-strand26719
Chain D: 16 helices, 11 β-strands
ElementResiduesLengthSheet
β-strand9-13510
α-helix21-3111
β-strand35-40610
α-helix44-518
β-strand60-62310
α-helix68-8215
β-strand88-93610
α-helix100-1023
β-strand104111
α-helix108-1103
α-helix113-1208
α-helix121-1255
α-helix126-1349
α-helix135-1373
β-strand138-1481110
β-strand15419
β-strand157111
α-helix159-18022
β-strand185-191710
α-helix1971
α-helix198-2047
α-helix205-2062
α-helix222-2254
α-helix236-24611
β-strand256-260510
α-helix264-2663
β-strand26718

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Enoyl-[acyl-carrier-protein] reductase [NADH]A, B, C, Dprotein289Mycobacterium tuberculosisP9WGR1 (AlphaFold model)
Sequence of entity 1 (A, B, C, D), FASTA
>4OHU_1 Enoyl-[acyl-carrier-protein] reductase [NADH] (chains A, B, C, D)
MGSSHHHHHHSSGLVPRGSHMTGLLDGKRILVSGIITDSSIAFHIARVAQEQGAQLVLTG
FDRLRLIQRITDRLPAKAPLLELDVQNEEHLASLAGRVTEAIGAGNKLDGVVHSIGFMPQ
TGMGINPFFDAPYADVSKGIHISAYSYASMAKALLPIMNPGGSIVGMDFDPSRAMPAYNW
MTVAKSALESVNRFVAREAGKYGVRSNLVAAGPIRTLAMSAIVGGALGEEAGAQIQLLEE
GWDQRAPIGWNMKDATPVAKTVCALLSDWLPATTGDIIYADGGAHTQLL

Ligands and cofactors

IDNameFormulaCopies
NADNicotinamide-adenine-dinucleotideC21 H27 N7 O14 P24
2TK2-(2-bromophenoxy)-5-hexylphenolC18 H21 Br O24

Primary citation

A Structural and Energetic Model for the Slow-Onset Inhibition of the Mycobacterium tuberculosis Enoyl-ACP Reductase InhA. Li, H.J., Lai, C.T., Pan, P. et al. ACS Chem Biol (2014) 9:986-993. DOI 10.1021/cb400896g · PubMed

Other PDB entries of the same protein (UniProt P9WGR1 (AlphaFold model), which also has an AlphaFold model), best resolution first:

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