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Structural basis of multidrug transport by the acrb multidrug efflux pump

Analyse Structural basis of multidrug transport by the acrb multidrug efflux pump in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1T9Y
Type
protein
Length
1,016 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Acriflavine resistance protein B
UniProt
P31224
Ligands
MC2
Pockets
8 · best druggability 0.86

Structure

x-ray diffraction · 1 distinct chain · 47% helix, 15% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AAcriflavine resistance protein Bprotein101647% helix, 15% strandP31224

Ligands and binding sites

  • MC2 · N2-(L-phenylalanyl)-N1-(naphthalenyl)-L-arigninamide · ligand · 2 copies · chains A

Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.

Pockets

8 pockets found on a 1 Å grid, 5 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
19450.860.87112empty
23680.650.7951empty
31650.630.8532empty
43000.590.7736empty
51120.510.8232empty

Compared structures

  • 1T9Y · Structural Basis of Multidrug Transport by the AcrB Multidrug Efflux Pump · the same entry in another collection · chain A against A, TM-score 1.00
  • P31224 · AlphaFold monomer V2.0 prediction for multidrug efflux pump subunit acrb (P31224) · a predicted model of the same protein · chain A against A, TM-score 0.95

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