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Crystal structure of mannitol operon repressor (mtlr) from vibrio parahaemolyticus rimd 2210633

Analyse Crystal structure of mannitol operon repressor (mtlr) from vibrio… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3BRJ
Type
protein
Length
667 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Mannitol operon repressor
UniProt
Q87SQ4
Pockets
2 · best druggability 0.42

Structure

x-ray diffraction · 4 distinct chains · 69% helix, 0% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AMannitol operon repressorprotein16768% helix, 0% strandQ87SQ4
BMannitol operon repressorprotein16970% helix, 0% strandQ87SQ4
CMannitol operon repressorprotein16367% helix, 0% strandQ87SQ4
DMannitol operon repressorprotein16870% helix, 0% strandQ87SQ4

Ligands and binding sites

  • EDO · 1,2-ethanediol · additive · 4 copies · chains A, B, C, D
  • GOL · Glycerol · additive · chains B

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

Pockets

2 pockets found on a 1 Å grid, 0 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11090.420.7732empty
2570.300.7515empty

Interfaces

4 interfaces between chains.

  • A–B · 811 Ų buried · 2 hydrogen bonds · protein-protein
  • C–D · 796 Ų buried · 3 hydrogen bonds · protein-protein
  • A–D · 471 Ų buried · 6 hydrogen bonds · protein-protein
  • B–C · 468 Ų buried · 7 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 8 modified (engineered).

Compared structures

  • 3BRJ · Crystal structure of mannitol operon repressor (MtlR) from Vibrio parahaemolyticus RIMD… · the same entry in another collection · chain B against B, TM-score 1.00

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