1LX6: Enoyl-[acyl-carrier-protein] reductase [NADH]

Crystal Structure of E. Coli Enoyl Reductase-NAD+ with a Bound Benzamide Inhibitor. Determined by X-ray diffraction at 2.4 Å resolution. Released 4 Sept 2002.

Method
X-ray diffraction
Resolution
2.4 Å
Organism
Escherichia coli
Chains
2
Atoms
3,989
Mol. weight
57.87 kDa
Ligands
ZAM, NAD
Released
4 Sept 2002

Explore 1LX6 in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

1LX6 contains 35 α-helices and 18 β-strands across 2 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, 9 β-strands

ElementResiduesLengthSheet
β-strand8-1141
α-helix20-3011
β-strand34-3961
α-helix42-443
α-helix45-5410
β-strand60-6231
α-helix68-8114
β-strand8512
β-strand88-9031
α-helix97-1004
α-helix104-1074
α-helix110-1178
α-helix118-1225
α-helix123-1319
β-strand13512
α-helix1361
β-strand139-14571
α-helix147-1493
α-helix159-17719
α-helix178-1803
β-strand182-18981
α-helix190-1912
α-helix207-2137
α-helix222-23211
α-helix235-2373
β-strand244-24741
Chain B: 18 helices, 9 β-strands
ElementResiduesLengthSheet
β-strand8-1143
α-helix20-3011
β-strand34-3963
α-helix42-5413
β-strand60-6233
α-helix68-7912
β-strand8514
β-strand88-9033
α-helix97-1004
α-helix104-1074
α-helix110-1178
α-helix118-1225
α-helix123-1319
α-helix132-1343
β-strand13514
α-helix1361
β-strand139-14573
α-helix147-1493
α-helix158-17720
α-helix178-1803
β-strand182-18983
α-helix190-1912
α-helix207-2137
α-helix222-23211
α-helix235-2373
β-strand244-24743
α-helix251-2533

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Enoyl-[acyl-carrier-protein] reductase [NADH]A, Bprotein262Escherichia coliP0AEK4 (AlphaFold model)
Sequence of entity 1 (A, B), FASTA
>1LX6_1 Enoyl-[acyl-carrier-protein] reductase [NADH] (chains A, B)
MGFLSGKRILVTGVASKLSIAYGIAQAMHREGAELAFTYQNDKLKGRVEEFAAQLGSDIV
LQCDVAEDASIDTMFAELGKVWPKFDGFVHSIGFAPGDQLDGDYVNAVTREGFKIAHDIS
SYSFVAMAKACRSMLNPGSALLTLSYLGAERAIPNYNVMGLAKASLEANVRYMANAMGPE
GVRVNAISAGPIRTLAASGIKDFRKMLAHCEAVTPIRRTVTIEDVGNSAAFLCSDLSAGI
SGEVVHVDGGFSIAAMNELELK

Ligands and cofactors

IDNameFormulaCopies
ZAM3-[(acetyl-methyl-amino)-methyl]-4-amino-N-methyl-N-(1-methyl-1H-indol-2-ylmeth…C22 H26 N4 O22
NADNicotinamide-adenine-dinucleotideC21 H27 N7 O14 P22

Primary citation

Discovery of aminopyridine-based inhibitors of bacterial enoyl-ACP reductase (FabI). Miller, W.H., Seefeld, M.A., Newlander, K.A. et al. J Med Chem (2002) 45:3246-3256. DOI 10.1021/jm020050+ · PubMed

Other PDB entries of the same protein (UniProt P0AEK4 (AlphaFold model), which also has an AlphaFold model), best resolution first:

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