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Covalent complex of orotidine monophosphate decarboxylase D70A mutant from M. thermoautotrophicus with 6-cyano-ump

Analyse Covalent complex of orotidine monophosphate decarboxylase D70A mutant from M.… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2ZZ3
Type
protein
Length
430 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Orotidine 5'-phosphate decarboxylase
EC
4.1.1.23
UniProt
O26232
Ligands
6CN
Pockets
1 · best druggability 0.83

Structure

x-ray diffraction · 1 distinct chain · 52% helix, 19% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BOrotidine 5'-phosphate decarboxylase (EC 4.1.1.23)protein21552% helix, 19% strandO26232

Ligands and binding sites

  • 6CN · 6-cyanouridine 5'-phosphate · ligand · 2 copies · chains A, B
  • GOL · Glycerol · additive · 4 copies · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12230.830.96736CN

Interfaces

1 interface between chains.

  • A–B · 1714 Ų buried · 14 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 2 covalent (covalent ligand).

Compared structures

  • 2ZZ3 · Covalent complex of orotidine monophosphate decarboxylase D70A mutant from M.… · the same entry in another collection · chain A against A, TM-score 1.00

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