2GYO: 3-oxoacyl-[acyl-carrier-protein] synthase 3

Methanethiol-Cys 112 Inhibition Complex of E. Coli Ketoacyl Synthase III (FabH) and Coenzyme A. Determined by X-ray diffraction at 2.0 Å resolution. Released 5 Jun 2007.

Method
X-ray diffraction
Resolution
2.0 Å
Organism
Escherichia coli
Chains
2
Atoms
5,027
Mol. weight
68.1 kDa
Ligands
MEE, COA
Released
5 Jun 2007

Explore 2GYO in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

2GYO contains 33 α-helices and 38 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, 19 β-strands

ElementResiduesLengthSheet
β-strand2-11101
β-strand15-1842
α-helix19-257
α-helix30-378
β-strand41-4442
α-helix51-6616
α-helix70-723
β-strand75-7951
β-strand85-8733
α-helix90-989
β-strand10214
β-strand105-10951
α-helix111-1133
α-helix114-12815
β-strand133-14081
α-helix151-1544
β-strand15715
β-strand160-169101
β-strand174-18186
α-helix183-1886
β-strand189-19027
β-strand191-19228
β-strand206-20727
α-helix209-23022
α-helix235-2373
β-strand240-24346
α-helix248-25710
α-helix262-2643
β-strand26516
α-helix269-2724
β-strand27415
α-helix276-2783
α-helix279-28911
β-strand298-30586
β-strand309-31686
Chain B: 17 helices, 19 β-strands
ElementResiduesLengthSheet
β-strand2-11101
β-strand15-1849
α-helix19-257
α-helix30-367
β-strand41-4449
α-helix51-6616
α-helix70-723
β-strand75-7951
β-strand85-8738
α-helix90-978
β-strand10216
β-strand105-10951
α-helix111-1133
α-helix114-12714
β-strand133-14081
α-helix151-1544
β-strand157110
β-strand160-169101
β-strand174-18184
α-helix183-1886
β-strand189-190211
β-strand191-19223
α-helix193-1942
β-strand206-207211
α-helix209-23022
α-helix235-2373
β-strand240-24344
α-helix248-25811
α-helix262-2643
β-strand26514
α-helix269-2724
β-strand274110
α-helix276-2783
α-helix279-28911
β-strand298-30584
β-strand309-31684

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
3-oxoacyl-[acyl-carrier-protein] synthase 3A, Bprotein317Escherichia coliP0A6R0 (AlphaFold model)
Sequence of entity 1 (A, B), FASTA
>2GYO_1 3-oxoacyl-[acyl-carrier-protein] synthase 3 (chains A, B)
MYTKIIGTGSYLPEQVRTNADLEKMVDTSDEWIVTRTGIRERHIAAPNETVSTMGFEAAT
RAIEMAGIEKDQIGLIVVATTSATHAFPSAACQIQSMLGIKGCPAFDVAAACAGFTYALS
VADQYVKSGAVKYALVVGSDVLARTCDPTDRGTIIIFGDGAGAAVLAASEEPGIISTHLH
ADGSYGELLTLPNADRVNPENSIHLTMAGNEVFKVAVTELAHIVDETLAANNLDRSQLDW
LVPHQANLRIISATAKKLGMSMDNVVVTLDRHGNTSAASVPCALDEAVRDGRIKPGQLVL
LEAFGGGFTWGSALVRF

Ligands and cofactors

IDNameFormulaCopies
MEEMethanethiolC H4 S1
COACoenzyme aC21 H36 N7 O16 P3 S1

Water and common crystallization additives (SO4) are not listed.

Primary citation

Alkyl-CoA Disulfides as Inhibitors and Mechanistic Probes for FabH Enzymes. Alhamadsheh, M.M., Musayev, F., Komissarov, A.A. et al. Chem Biol (2007) 14:513-524. DOI 10.1016/j.chembiol.2007.03.013 · PubMed

Other PDB entries of the same protein (UniProt P0A6R0 (AlphaFold model), which also has an AlphaFold model), best resolution first:

Browse structure collections

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