5CFZ: E. coli FabI in apo form

Crystal structure of E. coli FabI in apo form. Determined by X-ray diffraction at 1.97 Å resolution. Released 9 Dec 2015.

Method
X-ray diffraction
Resolution
1.97 Å
Organism
Escherichia coli (strain K12)
Chains
2
Atoms
3,879
Mol. weight
65.38 kDa
Released
9 Dec 2015

Explore 5CFZ in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

5CFZ contains 35 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: 17 helices, 7 β-strands

ElementResiduesLengthSheet
β-strand8-1141
α-helix20-3011
β-strand34-3961
α-helix45-5410
β-strand60-6231
α-helix68-8114
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-helix203-21311
α-helix222-23312
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-helix97-993
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-helix205-2139
α-helix222-23312
α-helix235-2373
β-strand244-24742
α-helix251-2533

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Enoyl-[acyl-carrier-protein] reductase [NADH] FabIA, Bprotein305Escherichia coli (strain K12)P0AEK4 (AlphaFold model)
Sequence of entity 1 (A, B), FASTA
>5CFZ_1 Enoyl-[acyl-carrier-protein] reductase [NADH] FabI (chains A, B)
MHHHHHHSSGLVPRGSGMKETAAAKFERQHMDSPDLGTDDDDKMGFLSGKRILVTGVASK
LSIAYGIAQAMHREGAELAFTYQNDKLKGRVEEFAAQLGSDIVLQCDVAEDASIDTMFAE
LGKVWPKFDGFVHSIGFAPGDQLDGDYVNAVTREGFKIAHDISSYSFVAMAKACRSMLNP
GSALLTLSYLGAERAIPNYNVMGLAKASLEANVRYMANAMGPEGVRVNAISAGPIRTLAA
SGIKDFRKMLAHCEAVTPIRRTVTIEDVGNSAAFLCSDLSAGISGEVVHVDGGFSIAAMN
ELELK

Primary citation

Crystallographic insights into the structure-activity relationships of diazaborine enoyl-ACP reductase inhibitors. Jordan, C.A., Sandoval, B.A., Serobyan, M.V. et al. Acta Crystallogr F Struct Biol Commun (2015) 71:1521-1530. DOI 10.1107/S2053230X15022098 · 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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