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High pressure cryocooling of capillary sample cryoprotection and diffraction phasing at long wavelengths

Analyse High pressure cryocooling of capillary sample cryoprotection and diffraction… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2OQU
Type
protein
Length
240 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Elastase-1
EC
3.4.21.36
UniProt
P00772
Ligands
CA, SO4, XE
Pockets
2 · best druggability 0.57

Structure

x-ray diffraction · 1 distinct chain · 11% helix, 39% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AElastase-1 (EC 3.4.21.36)protein24011% helix, 39% strandP00772

Ligands and binding sites

  • CA · Calcium ion · metal · chains A
  • SO4 · Sulfate ion · ion · chains A
  • XE · Xenon · ion · 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
1530.570.9016empty
2590.310.7617XE

Modifications

Observed in the structure: 4 disulfide (disulfide).

Compared structures

  • 2OQU · High Pressure Cryocooling of Capillary Sample Cryoprotection and Diffraction Phasing at… · the same entry in another collection · chain A against A, TM-score 1.00
  • P00772 · AlphaFold monomer V2.0 prediction for chymotrypsin-like elastase family member 1 (P00772) · a predicted model of the same protein · chain A against A, TM-score 1.00

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