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Crystal structure of the cusba heavy-metal efflux complex from escherichia COLI, R mutant

Analyse Crystal structure of the cusba heavy-metal efflux complex from escherichia… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4DOP
Type
protein
Length
1,677 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Cation efflux system protein cusb; Cation efflux system protein cusa
UniProt
P77239, P38054
Pockets
20 · best druggability 0.85

Structure

x-ray diffraction · 3 distinct chains · 39% helix, 26% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
BCation efflux system protein cusbprotein32216% helix, 38% strandP77239
CCation efflux system protein cusbprotein32420% helix, 41% strandP77239
ACation efflux system protein cusaprotein103151% helix, 18% strandP38054

Pockets

20 pockets found on a 1 Å grid, 11 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
13320.850.9546empty
211520.820.8394empty
39210.820.8382empty
41610.800.9632empty
5690.720.9721empty

Interfaces

3 interfaces between chains.

  • B–A · 2203 Ų buried · 33 hydrogen bonds · protein-protein
  • B–C · 1793 Ų buried · 26 hydrogen bonds · protein-protein
  • C–A · 1704 Ų buried · 17 hydrogen bonds · protein-protein

Compared structures

  • 4DOP · Crystal structure of the CusBA heavy-metal efflux complex from Escherichia coli, R mutant · the same entry in another collection · chain B against B, TM-score 1.00
  • P77239 · AlphaFold monomer V2.0 prediction for cation efflux system protein cusb (P77239) · a predicted model of the same protein · chain C against A, TM-score 0.99
  • P38054 · AlphaFold monomer V2.0 prediction for cation efflux system protein cusa (P38054) · a predicted model of the same protein · chain A against A, TM-score 0.99

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