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MolNFT v1 · #118124 · protein

Saccharomyces cerevisiae CYP51 (lanosterol 14-alpha demethylase) G464S mutant complexed with itraconazole

5ESK: “Saccharomyces cerevisiae CYP51 (lanosterol 14-alpha demethylase) G464S mutant complexed with itraconazole”. X-ray diffraction, 2 ligands (1YN, HEM), 4 pockets (best druggability 0.87). MolNFT v1 #118124 on GenesisL1: 3D structure…

PDB
5ESK
Type
protein
Length
527 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Lanosterol 14-alpha demethylase
UniProt
A6ZSR0
Ligands
1YN, HEM
Pockets
4 · best druggability 0.87

Structure

x-ray diffraction · 1 distinct chain · 53% helix, 10% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ALanosterol 14-alpha demethylaseprotein52753% helix, 10% strandA6ZSR0

Ligands and binding sites

  • 1YN · 2-[(2R)-butan-2-yl]-4-{4-[4-(4-{[(2R,4S)-2-(2,4-dichlorophenyl)-2-(1H-1,2,4-triazol-1-ylmethyl)-1,3-dioxolan-4-yl]methoxy}phenyl)piperazin-1-yl]phenyl}-2,4-dihydro-3H-1,2,4-triazol-3-one · ligand · chains A
  • HEM · Protoporphyrin IX containing Fe · ligand · chains A

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
18920.870.89821YN, HEM
21850.570.8137empty
32290.570.7833empty
41540.480.7724empty

Compared structures

  • 5ESK · Saccharomyces cerevisiae CYP51 (Lanosterol 14-alpha demethylase) G464S mutant complexed… · the same entry in another collection · chain A against A, TM-score 1.00

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