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Crystal structure of wild type marr (apo form) from E.COLI

Analyse Crystal structure of wild type marr (apo form) from E.COLI in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3VOE
Type
protein
Length
271 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Multiple antibiotic resistance protein marr
UniProt
P27245
Pockets
2 · best druggability 0.75

Structure

x-ray diffraction · 2 distinct chains · 66% helix, 8% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AMultiple antibiotic resistance protein marrprotein13665% helix, 8% strandP27245
BMultiple antibiotic resistance protein marrprotein13567% helix, 8% strandP27245

Pockets

2 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
19410.750.7868empty
22240.610.8125empty

Interfaces

1 interface between chains.

  • A–B · 1996 Ų buried · 12 hydrogen bonds · protein-protein

Compared structures

  • 3VOE · Crystal Structure of wild type MarR (apo form) from E.coli · the same entry in another collection · chain A against A, TM-score 1.00
  • P27245 · AlphaFold monomer V2.0 prediction for multiple antibiotic resistance protein marr (P27245) · a predicted model of the same protein · chain B against A, TM-score 0.84

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