4EZW: Substrate binding domain of E.coli DnaK

Crystal structure of the substrate binding domain of E.coli DnaK in complex with the designer peptide NRLLLTG. Determined by X-ray diffraction at 1.8 Å resolution. Released 17 Apr 2013.

Method
X-ray diffraction
Resolution
1.8 Å
Organism
Escherichia coli
Chains
8
Atoms
7,447
Mol. weight
99.3 kDa
Released
17 Apr 2013

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

Secondary structure: helices and β-sheets

4EZW contains 32 α-helices and 52 β-strands across 8 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: 7 helices, 12 β-strands

ElementResiduesLengthSheet
β-strand392-39541
β-strand399-40352
β-strand407-41262
β-strand416-41721
β-strand420-42673
β-strand427-42824
β-strand435-44282
β-strand44712
α-helix448-4503
β-strand452-46092
α-helix462-4643
β-strand472-47873
β-strand484-49073
β-strand496-50163
α-helix509-52113
α-helix523-55230
α-helix559-57719
α-helix581-59313
α-helix596-6005
Chain B: 8 helices, 12 β-strands
ElementResiduesLengthSheet
β-strand392-39545
β-strand399-40356
β-strand407-41266
β-strand416-41725
β-strand420-42677
β-strand427-42828
β-strand435-44286
β-strand44716
α-helix448-4503
β-strand452-46096
α-helix462-4643
β-strand472-47877
β-strand484-49077
β-strand496-50167
α-helix509-52113
α-helix523-55331
α-helix554-5563
α-helix559-57618
α-helix581-59313
α-helix596-6027
Chain C: 8 helices, 12 β-strands
ElementResiduesLengthSheet
β-strand392-39431
β-strand399-40359
β-strand407-41269
β-strand41711
β-strand420-426710
β-strand427-428211
β-strand436-44279
β-strand44719
α-helix448-4503
β-strand452-45989
α-helix462-4643
β-strand472-478710
β-strand484-490710
β-strand496-501610
α-helix509-52113
α-helix523-55331
α-helix554-5563
α-helix559-57618
α-helix581-59414
α-helix596-6027
Chain D: 9 helices, 12 β-strands
ElementResiduesLengthSheet
β-strand392-39435
β-strand399-403512
β-strand407-412612
α-helix4161
β-strand41715
β-strand420-426713
β-strand427-428214
β-strand435-442812
β-strand447112
α-helix448-4503
β-strand452-460912
α-helix462-4632
β-strand472-478713
β-strand484-490713
β-strand496-501613
α-helix509-52113
α-helix523-55331
α-helix554-5563
α-helix559-57719
α-helix581-59313
α-helix596-6038
Chains E, F, G and H: 0 helices, 1 β-strand
ElementResiduesLengthSheet
β-strand4-524

Molecules and chains

MoleculeChainsTypeLengthOrganismUniProt
Chaperone protein DnaKA, B, C, Dprotein219Escherichia coliP0A6Y8 (AlphaFold model)
synthetic peptide NRLLLTGE, F, G, Hprotein7
Sequence of entity 1 (A, B, C, D), FASTA
>4EZW_1 Chaperone protein DnaK (chains A, B, C, D)
VLLLDVTPLSLGIETMGGVMTTLIAKNTTIPTKHSQVFSTAEDNQSAVTIHVLQGERKRA
ADNKSLGQFNLDGINPAPRGMPQIEVTFDIDADGILHVSAKDKNSGKEQKITIKASSGLN
EDEIQKMVRDAEANAEADRKFEELVQTRNQGDHLLHSTRKQVEEAGDKLPADDKTAIESA
LTALETALKGEDKAAIEAKMQELAQVSQKLMEIAQQQHA
Sequence of entity 2 (E, F, G, H), FASTA
>4EZW_2 synthetic peptide NRLLLTG (chains E, F, G, H)
NRLLLTG

Primary citation

Structural Studies on the Forward and Reverse Binding Modes of Peptides to the Chaperone DnaK. Zahn, M., Berthold, N., Kieslich, B. et al. J Mol Biol (2013) 425:2463-2479. DOI 10.1016/j.jmb.2013.03.041 · PubMed

Other PDB entries of the same protein (UniProt P0A6Y8 (AlphaFold model), which also has an AlphaFold model), best resolution first:

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