4D0S: Mtb InhA complex with Pyradizinone compound 14

Mtb InhA complex with Pyradizinone compound 14. Determined by X-ray diffraction at 1.64 Å resolution. Released 20 May 2015.

Method
X-ray diffraction
Resolution
1.64 Å
Organism
MYCOBACTERIUM TUBERCULOSIS
Chains
4
Atoms
8,580
Mol. weight
118.57 kDa
Ligands
NAD, 9G4, MG
Released
20 May 2015

Explore 4D0S in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

4D0S contains 50 α-helices and 36 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: 12 helices, 9 β-strands

ElementResiduesLengthSheet
β-strand9-1351
α-helix21-3111
β-strand35-4061
α-helix47-515
β-strand60-6231
α-helix68-8215
β-strand88-9361
α-helix108-1103
α-helix113-1208
α-helix121-1255
α-helix126-1349
α-helix135-1373
β-strand138-148111
β-strand15412
α-helix159-18022
β-strand185-19171
α-helix209-22517
α-helix236-24611
β-strand256-26051
α-helix264-2663
β-strand26713
Chain B: 12 helices, 9 β-strands
ElementResiduesLengthSheet
β-strand9-1354
α-helix21-3111
β-strand35-4064
α-helix44-518
β-strand60-6234
α-helix68-8215
β-strand88-9364
α-helix108-1103
α-helix113-1208
α-helix121-1255
α-helix126-1349
α-helix135-1373
β-strand138-148114
β-strand15413
α-helix159-18022
β-strand185-19174
α-helix214-22512
α-helix236-24611
β-strand256-26054
α-helix264-2663
β-strand26712
Chain C: 14 helices, 9 β-strands
ElementResiduesLengthSheet
β-strand9-1355
α-helix21-3111
α-helix341
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-strand15416
α-helix159-18022
β-strand185-19175
α-helix211-22515
α-helix236-24611
β-strand256-26055
α-helix264-2663
β-strand26717
Chain D: 12 helices, 9 β-strands
ElementResiduesLengthSheet
β-strand9-1358
α-helix21-3111
β-strand35-4068
α-helix44-518
β-strand60-6238
α-helix68-8215
β-strand88-9368
α-helix108-1103
α-helix113-1208
α-helix121-1255
α-helix126-1349
α-helix135-1373
β-strand138-148118
β-strand15417
α-helix159-18022
β-strand185-19178
α-helix209-22517
α-helix236-24611
β-strand256-26058
α-helix264-2663
β-strand26716

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Enoyl-[acyl-carrier-protein] reductase [NADH]A, B, C, Dprotein269MYCOBACTERIUM TUBERCULOSISP9WGR1 (AlphaFold model)
Sequence of entity 1 (A, B, C, D), FASTA
>4D0S_1 ENOYL-[ACYL-CARRIER-PROTEIN] REDUCTASE [NADH] (chains A, B, C, D)
MTGLLDGKRILVSGIITDSSIAFHIARVAQEQGAQLVLTGFDRLRLIQRITDRLPAKAPL
LELDVQNEEHLASLAGRVTEAIGAGNKLDGVVHSIGFMPQTGMGINPFFDAPYADVSKGI
HISAYSYASMAKALLPIMNPGGSIVGMDFDPSRAMPAYNWMTVAKSALESVNRFVAREAG
KYGVRSNLVAAGPIRTLAMSAIVGGALGEEAGAQIQLLEEGWDQRAPIGWNMKDATPVAK
TVCALLSDWLPATTGDIIYADGGAHTQLL

Ligands and cofactors

IDNameFormulaCopies
NADNicotinamide-adenine-dinucleotideC21 H27 N7 O14 P24
9G41-{4-[(acetylamino)methyl]phenyl}-4-(4-chlorophenoxy)-6-oxo-1,6-dihydropyridazi…C20 H17 Cl N4 O44
MGMagnesium ionMg2

Primary citation

Pyridazinones: A Novel Scaffold with Excellent Physicochemical Properties and Safety Profile for a Clinically Validated Target of Mycobacterium Tuberculosis. Lange, S. To be published.

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

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