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Human procaspase-3, crystal form 2

Analyse Human procaspase-3, crystal form 2 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4JQZ
Type
protein
Length
379 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 0.63

Structure

x-ray diffraction · 2 distinct chains · 35% helix, 23% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AProcaspase-3 (EC 3.4.22.56)protein19734% helix, 24% strandP42574
BProcaspase-3 (EC 3.4.22.56)protein18237% helix, 22% strandP42574

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
14550.630.7761empty
2940.470.8118empty
3890.320.7322empty

Interfaces

1 interface between chains.

  • A–B · 1137 Ų buried · 21 hydrogen bonds · protein-protein

Compared structures

  • 4JQZ · Human procaspase-3, crystal form 2 · 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 B against A, TM-score 0.95

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