Research workbench
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).
| Chain | Molecule | Type | Residues | Secondary structure | UniProt |
|---|---|---|---|---|---|
| A | Procaspase-3 (EC 3.4.22.56) | protein | 194 | 36% helix, 26% strand | P42574 |
| B | Procaspase-3 (EC 3.4.22.56) | protein | 205 | 35% helix, 24% strand | P42574 |
Pockets
3 pockets found on a 1 Å grid, 1 with a druggability of 0.5 or more.
| Volume (ų) | Druggability | Buriedness | Lining residues | Inside | |
|---|---|---|---|---|---|
| 1 | 301 | 0.59 | 0.78 | 37 | empty |
| 2 | 134 | 0.40 | 0.74 | 21 | empty |
| 3 | 101 | 0.37 | 0.75 | 21 | empty |
Interfaces
1 interface between chains.
- A–B · 1212 Ų buried · 26 hydrogen bonds · protein-protein
Compared structures
Analyse
- Open in the research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides and crosslinks on the 3D structure
- Every structure of UniProt P42574
- Elsewhere: RCSB PDB 4JQY · PDBe 4JQY · UniProt P42574
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