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X-ray diffraction analysis of the CsStefin-1

Analyse X-ray diffraction analysis of the CsStefin-1 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5ZC1
Type
protein
Length
596 residues
Chains
6
Method
x-ray diffraction
Collection
MolNFT v2 / PDB Bank
Contract
0xd58B01f6C18086e5202cdC5D7Ad3E41790360102
Owner
0xF4e1AA6f26B7DA48EeAD9B24a97927303eeA07b8
Resolution
2.30271
Source
Clonorchis sinensis
Molecule
Cystatin-1
UniProt
A6YID9
Pockets
4 · best druggability 0.75

Structure

x-ray diffraction · resolution 2.30271 · 3 distinct chains · 21% helix, 37% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BCystatin-1protein10121% helix, 40% strandA6YID9
CCystatin-1protein10019% helix, 37% strandA6YID9
D, E, FCystatin-1protein9822% helix, 36% strandA6YID9

Pockets

4 pockets found on a 1 Å grid, 2 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
17490.750.8079empty
21570.660.8723empty
3950.330.7321empty
4540.280.7417empty

Interfaces

11 interfaces between chains.

  • A–E · 355 Ų buried · 4 hydrogen bonds · protein-protein
  • B–C · 340 Ų buried · 3 hydrogen bonds · protein-protein
  • A–F · 337 Ų buried · 2 hydrogen bonds · protein-protein
  • B–E · 334 Ų buried · 1 hydrogen bond · protein-protein
  • B–F · 310 Ų buried · 5 hydrogen bonds · protein-protein

Compared structures

  • 5ZC1 · X-ray diffraction analysis of the csstefin-1 · the same entry in another collection · chain A against A, TM-score 1.00

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