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Crystal structure of chorismate mutase from helicobacter pylori in complex with prephenate

Analyse Crystal structure of chorismate mutase from helicobacter pylori in complex with… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6AL9
Type
protein
Length
181 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Chorismate mutase
UniProt
O25064
Ligands
PRE, PYR, PHB
Pockets
2 · best druggability 0.74

Structure

x-ray diffraction · 2 distinct chains · 77% helix, 0% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AChorismate mutaseprotein9077% helix, 0% strandO25064
BChorismate mutaseprotein9178% helix, 0% strandO25064

Ligands and binding sites

  • PRE · Prephenic acid · ligand · chains A, B
  • PYR · Pyruvic acid · ligand · chains A, B
  • PHB · P-hydroxybenzoic acid · ligand · chains A, 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, 2 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11510.740.9222PRE
21420.730.9221PYR, PHB

Interfaces

1 interface between chains.

  • A–B · 2490 Ų buried · 41 hydrogen bonds · protein-protein

Compared structures

  • 6AL9 · Crystal structure of chorismate mutase from Helicobacter pylori in complex with prephenate · the same entry in another collection · chain A against A, TM-score 1.00

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