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Automated refinement of diffraction data obtained from an endothiapepsin crystal treated with fragment 242

Analyse Automated refinement of diffraction data obtained from an endothiapepsin… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5P5H
Type
protein
Length
330 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v2 / PDB Bank
Contract
0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
Owner
0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
Resolution
1.09
Source
Cryphonectria parasitica
Molecule
endothiapepsin
EC
3.4.23.22
UniProt
P11838
Pockets
1 · best druggability 0.58

Structure

x-ray diffraction · resolution 1.09 · 1 distinct chain · 11% helix, 45% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
Aendothiapepsin (EC 3.4.23.22)protein33011% helix, 45% strandP11838

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
13030.580.7635empty

Modifications

Observed in the structure: 1 disulfide (disulfide).

Compared structures

  • 5P5H · Automated refinement of diffraction data obtained from an endothiapepsin crystal treated… · the same entry in another collection · chain A against A, TM-score 1.00
  • P11838 · AlphaFold monomer V2.0 prediction for endothiapepsin (P11838) · a predicted model of the same protein · chain A against A, TM-score 1.00

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