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Crystal structure of C115A mutant L-methionine gamma-lyase from citrobacter freundii modified by allicine

Analyse Crystal structure of C115A mutant L-methionine gamma-lyase from citrobacter… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4MKK
Type
protein
Length
388 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Methionine gamma-lyase
EC
4.4.1.11
UniProt
Q84AR1
Ligands
NA, K, CL
Pockets
2 · best druggability 0.55

Structure

x-ray diffraction · 1 distinct chain · 43% helix, 15% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AMethionine gamma-lyase (EC 4.4.1.11)protein38843% helix, 15% strandQ84AR1

Ligands and binding sites

  • NA · Sodium ion · metal · 5 copies · chains A
  • K · Potassium ion · metal · chains A
  • CL · Chloride ion · ion · chains A
  • PGE · Triethylene glycol · additive · 2 copies · chains A

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12120.550.7835K
2690.320.7517empty

Modifications

Observed in the structure: 3 modified (nonstandard, cofactor).

Compared structures

  • 4MKK · Crystal structure of C115A mutant L-methionine gamma-lyase from Citrobacter freundii… · the same entry in another collection · chain A against A, TM-score 1.00

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