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Humicola insolens cutinase in complex with mono-ethylphosphate

Analyse Humicola insolens cutinase in complex with mono-ethylphosphate in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4OYL
Type
protein
Length
573 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Cutinase
Pockets
4 · best druggability 0.57

Structure

x-ray diffraction · 1 distinct chain · 44% helix, 15% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, CCutinaseprotein19144% helix, 15% strand—

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12230.570.7933empty
22070.560.7927empty
31810.510.7818empty
41850.440.7431empty

Interfaces

3 interfaces between chains.

  • B–C · 366 Ų buried · 10 hydrogen bonds · protein-protein
  • A–B · 245 Ų buried · 4 hydrogen bonds · protein-protein
  • A–C · 220 Ų buried · 2 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 6 disulfide, 6 modified (disulfide, nonstandard).

Compared structures

  • 4OYL · Humicola insolens cutinase in complex with mono-ethylphosphate · the same entry in another collection · chain A against A, TM-score 1.00

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