2PE5: Lac Repressor

Crystal Structure of the Lac Repressor bound to ONPG in repressed state. Determined by X-ray diffraction at 3.5 Å resolution. Released 18 Mar 2008.

Method
X-ray diffraction
Resolution
3.5 Å
Organisms
synthetic construct, Escherichia coli
Chains
6
Atoms
8,527
Mol. weight
125.53 kDa
Ligands
145
Released
18 Mar 2008

Explore 2PE5 in 3D Show helices and sheets RCSB PDB PDBe

Secondary structure: helices and β-sheets

2PE5 contains 43 α-helices and 50 β-strands across 3 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: 15 helices, 16 β-strands

ElementResiduesLengthSheet
α-helix6-138
α-helix17-259
α-helix32-343
α-helix35-4410
α-helix51-577
β-strand63-6971
α-helix74-9017
β-strand93-9971
α-helix104-11512
β-strand122-12541
α-helix130-13910
β-strand145-14731
β-strand158-16141
α-helix163-17614
β-strand182-18652
α-helix192-20615
β-strand214-21742
α-helix222-23312
β-strand241-24442
α-helix247-26014
β-strand26413
β-strand26813
β-strand269-27132
β-strand27414
α-helix277-2815
α-helix285-2862
β-strand28712
β-strand288-29034
α-helix293-30917
β-strand316-31941
β-strand322-32434
Chain B: 14 helices, 17 β-strands
ElementResiduesLengthSheet
α-helix6-138
α-helix17-248
α-helix33-4210
α-helix51-577
β-strand62-6875
α-helix74-8916
β-strand92-9875
α-helix104-11613
β-strand121-12555
α-helix130-13910
β-strand145-14735
β-strand158-16145
α-helix163-17715
β-strand182-18656
α-helix192-20615
β-strand215-21736
α-helix222-23514
β-strand241-24446
α-helix247-25913
β-strand26417
β-strand26817
β-strand269-27136
β-strand27418
α-helix277-2815
α-helix285-2862
β-strand28716
β-strand288-28929
β-strand29018
α-helix293-30917
β-strand316-31945
β-strand323-32429
Chain C: 14 helices, 17 β-strands
ElementResiduesLengthSheet
α-helix10-145
α-helix17-237
α-helix36-449
α-helix51-566
β-strand63-69710
α-helix74-9017
β-strand93-99710
α-helix104-11613
β-strand121-125510
α-helix130-13910
β-strand145-147310
β-strand158-161410
α-helix163-17715
β-strand182-186511
α-helix192-20615
β-strand215-217311
α-helix222-23413
β-strand241-244411
α-helix247-25913
β-strand264112
β-strand268112
β-strand269-271311
β-strand274113
α-helix278-2814
α-helix285-2862
β-strand287111
β-strand288-289214
β-strand290113
α-helix293-30917
β-strand316-319410
β-strand323-324214

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
DNA (5'-d(*dap*dap*dtp*dtp*dgp*dtp*dgp*dap*dgp*dcp*dgp*dcp*dtp*dcp*dap*dcp*dap*dap*dtp*dt)-3')D, E, FDNA20synthetic construct
Lactose operon repressorA, B, Cprotein330Escherichia coliP03023 (AlphaFold model)
Sequence of entity 1 (D, E, F), FASTA
>2PE5_1 DNA (5'-D(*DAP*DAP*DTP*DTP*DGP*DTP*DGP*DAP*DGP*DCP*DGP*DCP*DTP*DCP*DAP*DCP*DAP*DAP*DTP*DT)-3') (chains D, E, F)
AATTGTGAGCGCTCACAATT
Sequence of entity 2 (A, B, C), FASTA
>2PE5_2 Lactose operon repressor (chains A, B, C)
KPVTLYDVAEYAGVSYQTVSRVVNQASHVSAKTREKVEAAMAELNYIPNRVAQQLAGKQL
LLIGVATSSLALHAPSQIVAAIKSRADQLGASVVVSMVERSGVEACKAAVHNLLAQRVSG
LIINYPLDDQDAIAVEAACTNVPALFLDVSDQTPINSIIFSHEDGTRLGVEHLVALGHQQ
IALLAGPLSSVSARLRLAGWHKYLTRNQIQPIAEREGDWSAMSGFQQTMQMLNEGIVPTA
MLVANDQMALGAMRAITESGLRVGADISVVGYDDTEDSSCYIPPLTTIKQDFRLLGQTSV
DRLLQLSQGQAVKGNQLLPVSLVKRKTTLA

Ligands and cofactors

IDNameFormulaCopies
1452-nitrophenyl beta-D-galactopyranosideC12 H15 N O83

Primary citation

Structural analysis of lac repressor bound to allosteric effectors. Daber, R., Stayrook, S., Rosenberg, A. et al. J Mol Biol (2007) 370:609-619. DOI 10.1016/j.jmb.2007.04.028 · PubMed

Other PDB entries of the same protein (UniProt P03023 (AlphaFold model), which also has an AlphaFold model), best resolution first:

Browse structure collections

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