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Atomic structure of the buried catalytic pocket of escherichia COLI chorismate mutase

Analyse Atomic structure of the buried catalytic pocket of escherichia COLI chorismate… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1ECM
Type
protein
Length
186 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Endo-oxabicyclic transition state analogue
UniProt
P07022
Ligands
TSA
Pockets
2 · best druggability 0.75

Structure

x-ray diffraction · 2 distinct chains · 87% helix, 0% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AEndo-oxabicyclic transition state analogueprotein9186% helix, 0% strandP07022
BEndo-oxabicyclic transition state analogueprotein9587% helix, 0% strandP07022

Ligands and binding sites

  • TSA · 8-hydroxy-2-oxa-bicyclo[3.3.1]non-6-ene-3,5-dicarboxylic acid · ligand · 2 copies · 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
1840.750.9717TSA
2780.720.9617TSA

Interfaces

1 interface between chains.

  • A–B · 2580 Ų buried · 25 hydrogen bonds · protein-protein

Compared structures

  • 1ECM · Atomic structure of the buried catalytic pocket of escherichia COLI chorismate mutase · the same entry in another collection · chain A against A, TM-score 1.00

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