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Human procaspase-3, crystal form 1

Analyse Human procaspase-3, crystal form 1 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4JQY
Type
protein
Length
399 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Procaspase-3
EC
3.4.22.56
UniProt
P42574
Pockets
3 · best druggability 0.59

Structure

x-ray diffraction · 2 distinct chains · 35% helix, 25% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AProcaspase-3 (EC 3.4.22.56)protein19436% helix, 26% strandP42574
BProcaspase-3 (EC 3.4.22.56)protein20535% helix, 24% strandP42574

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
13010.590.7837empty
21340.400.7421empty
31010.370.7521empty

Interfaces

1 interface between chains.

  • A–B · 1212 Ų buried · 26 hydrogen bonds · protein-protein

Compared structures

  • 4JQY · Human procaspase-3, crystal form 1 · the same entry in another collection · chain A against A, TM-score 1.00
  • P42574 · AlphaFold monomer V2.0 prediction for caspase-3 (P42574) · a predicted model of the same protein · chain A against A, TM-score 0.93

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