3PJD: ENR G93A mutant-NAD+-Triclosan complex

Structure of ENR G93A mutant-NAD+-Triclosan complex. Determined by X-ray diffraction at 2.5 Å resolution. Released 20 Apr 2011.

Method
X-ray diffraction
Resolution
2.5 Å
Organism
Escherichia coli
Chains
2
Atoms
4,028
Mol. weight
59.86 kDa
Ligands
TCL, NAD
Released
20 Apr 2011

Explore 3PJD in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

3PJD contains 36 α-helices and 16 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: 18 helices, 7 β-strands

ElementResiduesLengthSheet
β-strand7-1151
α-helix20-3011
β-strand33-3971
α-helix42-5413
β-strand60-6231
α-helix68-8114
β-strand85-9061
α-helix97-993
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-helix197-1993
α-helix204-2085
α-helix210-2134
α-helix222-23312
α-helix235-2373
β-strand244-24741
α-helix251-2533
Chain B: 18 helices, 9 β-strands
ElementResiduesLengthSheet
β-strand8-1142
α-helix20-3011
α-helix331
β-strand34-3962
α-helix42-5413
β-strand60-6232
α-helix68-7811
β-strand8513
β-strand88-9032
α-helix97-1004
α-helix104-1074
α-helix110-1178
α-helix118-1225
α-helix123-1319
α-helix132-1343
β-strand13513
α-helix1361
β-strand139-14572
α-helix147-1493
α-helix158-17720
β-strand182-18982
α-helix196-1994
α-helix204-21310
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
>3PJD_1 Enoyl-[acyl-carrier-protein] reductase [NADH] (chains A, B)
MGFLSGKRILVTGVASKLSIAYGIAQAMHREGAELAFTYQNDKLKGRVEEFAAQLGSDIV
LQCDVAEDASIDTMFAELGKVWPKFDGFVHSIAFAPGDQLDGDYVNAVTREGFKIAHDIS
SYSFVAMAKACRSMLNPGSALLTLSYLGAERAIPNYNVMGLAKASLEANVRYMANAMGPE
GVRVNAISAGPIRTLAASGIKDFRKMLAHCEAVTPIRRTVTIEDVGNSAAFLCSDLSAGI
SGEVVHVDGGFSIAAMNELELKLEHHHHHH

Ligands and cofactors

IDNameFormulaCopies
TCLTriclosanC12 H7 Cl3 O22
NADNicotinamide-adenine-dinucleotideC21 H27 N7 O14 P22

Primary citation

Structural basis of triclosan resistance. Jiten Singh, N., Shin, D.G., Lee, H.M. et al. J Struct Biol (2011) 174:173-179. DOI 10.1016/j.jsb.2010.11.008 · 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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