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MolNFT v1 · #181984 · protein

Crystal structure of staphylococcus aureus cystathionine gamma lyase, holoenzyme with bound NL1

7MCT · Bifunctional cystathionine gamma-LYASE/HOMOCYSTEINE…: “Crystal structure of staphylococcus aureus cystathionine gamma lyase, holoenzyme with bound NL1”. X-ray diffraction, 3 ligands (LB6, PLP, NA), 3 pockets (best druggability…

PDB
7MCT
Type
protein
Length
380 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Bifunctional cystathionine gamma-LYASE/HOMOCYSTEINE desulfhydrase
EC
4.4.1.1, 4.4.1.8, 2.5.1.48
UniProt
X5E0F1
Ligands
LB6, PLP, NA
Pockets
3 · best druggability 0.55

Structure

x-ray diffraction · 1 distinct chain · 40% helix, 17% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
HBifunctional cystathionine gamma-LYASE/HOMOCYSTEINE desulfhydrase (EC 4.4.1.1, 4.4.1.8, 2.5.1.48)protein38040% helix, 17% strandX5E0F1

Ligands and binding sites

  • LB6 · N-[(6-bromo-1H-indol-1-yl)acetyl]glycine · ligand · 5 copies · chains H
  • PLP · Pyridoxal-5'-phosphate · ligand · chains H
  • NA · Sodium ion · metal · 2 copies · chains H
  • GOL · Glycerol · additive · 5 copies · chains H

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12330.550.7728LB6
21140.400.7518LB6
3510.280.7517empty

Modifications

Observed in the structure: 1 cofactor, 1 modified (pyridoxal phosphate Schiff base, cofactor).

Compared structures

  • 7MCT · Crystal structure of Staphylococcus aureus Cystathionine gamma lyase, Holoenzyme with… · the same entry in another collection · chain H against H, TM-score 1.00

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