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Crystal structure of E. COLI oppa complexed with the tripeptide kge

Analyse Crystal structure of E. COLI oppa complexed with the tripeptide kge in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3TCG
Type
protein
Length
4,160 residues
Chains
16
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Periplasmic oligopeptide-binding protein; Kge peptide
UniProt
P23843
Pockets
20 · best druggability 0.83

Structure

x-ray diffraction · 2 distinct chains · 36% helix, 22% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, D, E, F, G, HPeriplasmic oligopeptide-binding proteinprotein51736% helix, 22% strandP23843
I, J, K, L, M, N, O, PKge peptideprotein30% helix, 33% strand—

Pockets

20 pockets found on a 1 Å grid, 20 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
19190.830.8480empty
211800.810.82106empty
3940.760.9831empty
41420.720.9136empty
51630.700.8940empty

Interfaces

19 interfaces between chains.

  • B–G · 851 Ų buried · 17 hydrogen bonds · protein-protein
  • B–D · 848 Ų buried · 12 hydrogen bonds · protein-protein
  • E–H · 837 Ų buried · 16 hydrogen bonds · protein-protein
  • A–E · 828 Ų buried · 14 hydrogen bonds · protein-protein
  • G–O · 428 Ų buried · 10 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 8 disulfide (disulfide).

Compared structures

  • 3TCG · Crystal structure of E. coli OppA complexed with the tripeptide KGE · the same entry in another collection · chain P against P, TM-score 1.00

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