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.
Explore 1LX6 in 3D Show helices and sheets RCSB PDB PDBe
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.
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 8-11 | 4 | 1 |
| α-helix | 20-30 | 11 | |
| β-strand | 34-39 | 6 | 1 |
| α-helix | 42-44 | 3 | |
| α-helix | 45-54 | 10 | |
| β-strand | 60-62 | 3 | 1 |
| α-helix | 68-81 | 14 | |
| β-strand | 85 | 1 | 2 |
| β-strand | 88-90 | 3 | 1 |
| α-helix | 97-100 | 4 | |
| α-helix | 104-107 | 4 | |
| α-helix | 110-117 | 8 | |
| α-helix | 118-122 | 5 | |
| α-helix | 123-131 | 9 | |
| β-strand | 135 | 1 | 2 |
| α-helix | 136 | 1 | |
| β-strand | 139-145 | 7 | 1 |
| α-helix | 147-149 | 3 | |
| α-helix | 159-177 | 19 | |
| α-helix | 178-180 | 3 | |
| β-strand | 182-189 | 8 | 1 |
| α-helix | 190-191 | 2 | |
| α-helix | 207-213 | 7 | |
| α-helix | 222-232 | 11 | |
| α-helix | 235-237 | 3 | |
| β-strand | 244-247 | 4 | 1 |
| Element | Residues | Length | Sheet |
|---|---|---|---|
| β-strand | 8-11 | 4 | 3 |
| α-helix | 20-30 | 11 | |
| β-strand | 34-39 | 6 | 3 |
| α-helix | 42-54 | 13 | |
| β-strand | 60-62 | 3 | 3 |
| α-helix | 68-79 | 12 | |
| β-strand | 85 | 1 | 4 |
| β-strand | 88-90 | 3 | 3 |
| α-helix | 97-100 | 4 | |
| α-helix | 104-107 | 4 | |
| α-helix | 110-117 | 8 | |
| α-helix | 118-122 | 5 | |
| α-helix | 123-131 | 9 | |
| α-helix | 132-134 | 3 | |
| β-strand | 135 | 1 | 4 |
| α-helix | 136 | 1 | |
| β-strand | 139-145 | 7 | 3 |
| α-helix | 147-149 | 3 | |
| α-helix | 158-177 | 20 | |
| α-helix | 178-180 | 3 | |
| β-strand | 182-189 | 8 | 3 |
| α-helix | 190-191 | 2 | |
| α-helix | 207-213 | 7 | |
| α-helix | 222-232 | 11 | |
| α-helix | 235-237 | 3 | |
| β-strand | 244-247 | 4 | 3 |
| α-helix | 251-253 | 3 |
| Molecule | Chains | Type | Length | Organism | UniProt |
|---|---|---|---|---|---|
| Enoyl-[acyl-carrier-protein] reductase [NADH] | A, B | protein | 262 | Escherichia coli | P0AEK4 (AlphaFold model) |
>1LX6_1 Enoyl-[acyl-carrier-protein] reductase [NADH] (chains A, B) MGFLSGKRILVTGVASKLSIAYGIAQAMHREGAELAFTYQNDKLKGRVEEFAAQLGSDIV LQCDVAEDASIDTMFAELGKVWPKFDGFVHSIGFAPGDQLDGDYVNAVTREGFKIAHDIS SYSFVAMAKACRSMLNPGSALLTLSYLGAERAIPNYNVMGLAKASLEANVRYMANAMGPE GVRVNAISAGPIRTLAASGIKDFRKMLAHCEAVTPIRRTVTIEDVGNSAAFLCSDLSAGI SGEVVHVDGGFSIAAMNELELK
| ID | Name | Formula | Copies |
|---|---|---|---|
| ZAM | 3-[(acetyl-methyl-amino)-methyl]-4-amino-N-methyl-N-(1-methyl-1H-indol-2-ylmeth… | C22 H26 N4 O2 | 2 |
| NAD | Nicotinamide-adenine-dinucleotide | C21 H27 N7 O14 P2 | 2 |
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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