4D46: E. coli FabI

Crystal structure of E. coli FabI in complex with NAD and 5-bromo-2-(4-chloro-2-hydroxyphenoxy)benzonitrile. Determined by X-ray diffraction at 2.0 Å resolution. Released 4 Mar 2015.

Method
X-ray diffraction
Resolution
2.0 Å
Organism
ESCHERICHIA COLI
Chains
2
Atoms
3,996
Mol. weight
59.9 kDa
Ligands
NAD, J47
Released
4 Mar 2015

Explore 4D46 in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

4D46 contains 34 α-helices and 14 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: 16 helices, 7 β-strands

ElementResiduesLengthSheet
β-strand8-1141
α-helix20-3011
β-strand34-3961
α-helix42-5413
β-strand60-6231
α-helix68-7912
β-strand85-9061
α-helix97-1004
α-helix104-1074
α-helix110-1178
α-helix118-1225
α-helix123-1319
α-helix132-1343
β-strand135-145111
α-helix147-1493
α-helix158-17720
α-helix178-1803
β-strand182-18981
α-helix190-1912
α-helix222-23211
α-helix235-2373
β-strand244-24741
α-helix251-2533
Chain B: 18 helices, 7 β-strands
ElementResiduesLengthSheet
β-strand8-1142
α-helix20-3011
β-strand34-3962
α-helix42-443
α-helix45-5410
β-strand60-6232
α-helix68-7912
β-strand85-9062
α-helix97-1004
α-helix104-1074
α-helix110-1178
α-helix118-1225
α-helix123-1319
α-helix132-1343
β-strand135-145112
α-helix147-1493
α-helix158-17720
α-helix178-1803
β-strand182-18982
α-helix190-1912
α-helix195-1973
α-helix222-23211
α-helix235-2373
β-strand244-24742
α-helix251-2533

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Enoyl-[acyl-carrier-protein] reductase [NADH]A, Bprotein270ESCHERICHIA COLIP0AEK4 (AlphaFold model)
Sequence of entity 1 (A, B), FASTA
>4D46_1 ENOYL-[ACYL-CARRIER-PROTEIN] REDUCTASE [NADH] (chains A, B)
MGFLSGKRILVTGVASKLSIAYGIAQAMHREGAELAFTYQNDKLKGRVEEFAAQLGSDIV
LQCDVAEDASIDTMFAELGKVWPKFDGFVHSIGFAPGDQLDGDYVNAVTREGFKIAHDIS
SYSFVAMAKACRSMLNPGSALLTLSYLGAERAIPNYNVMGLAKASLEANVRYMANAMGPE
GVRVNAISAGPIRTLAASGIKDFRKMLAHCEAVTPIRRTVTIEDVGNSAAFLCSDLSAGI
SGEVVHVDGGFSIAAMNELELKLEHHHHHH

Ligands and cofactors

IDNameFormulaCopies
NADNicotinamide-adenine-dinucleotideC21 H27 N7 O14 P22
J475-bromo-2-(4-chloro-2-hydroxyphenoxy)benzonitrileC13 H7 Br Cl N O22

Primary citation

An Ordered Water Channel in Staphylococcus Aureus Fabi: Unraveling the Mechanism of Substrate Recognition and Reduction. Schiebel, J., Chang, A., Merget, B. et al. Biochemistry (2015) 54:1943. DOI 10.1021/BI5014358 · PubMed

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

Browse structure collections

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