MolNFT v1 · #89016 · protein

Crystal structure of caspase 3, L168Y mutant

4DCO · Caspase-3 subunit P17: “Crystal structure of caspase 3, L168Y mutant”. X-ray diffraction, 1 ligand (ACE), 1 pocket (best druggability 0.66). MolNFT v1 #89016 on GenesisL1: 3D structure, binding sites and pockets in GL1X.

PDB: 4DCO
Type: protein
Length: 478 residues
Chains: 6
Method: x-ray diffraction
Collection: MolNFT v1 / PDB
Contract: 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner: 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule: Caspase-3 subunit P17; Caspase-3 subunit P12; Caspase inhibitor ac-devd-cho
EC: 3.4.22.56
UniProt: P42574
Ligands: ACE
Pockets: 1 · best druggability 0.66

Structure

x-ray diffraction · 4 distinct chains · 30% helix, 25% strand (DSSP).

Chain	Molecule	Type	Residues	Secondary structure	UniProt
A, D	Caspase-3 subunit P17 (EC 3.4.22.56)	protein	141	27% helix, 32% strand	P42574
B	Caspase-3 subunit P12 (EC 3.4.22.56)	protein	95	33% helix, 19% strand	P42574
C, F	Caspase inhibitor ac-devd-cho	protein	4	0% helix, 25% strand	—
E	Caspase-3 subunit P12 (EC 3.4.22.56)	protein	93	33% helix, 20% strand	P42574

Ligands and binding sites

ACE · Acetyl group · ligand · 2 copies · chains B, C, E, F

Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.

Pockets

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

Pocket	Volume (Å³)	Druggability	Buriedness	Lining residues	Inside
1	300	0.66	0.81	36	empty

Interfaces

10 interfaces between chains.

A–B · 2257 Å² buried · 35 hydrogen bonds · protein-protein
D–E · 2235 Å² buried · 33 hydrogen bonds · protein-protein
B–E · 1429 Å² buried · 19 hydrogen bonds · protein-protein
A–E · 443 Å² buried · 11 hydrogen bonds · protein-protein
B–C · 420 Å² buried · 9 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 2 covalent, 2 modified (covalent ligand, nonstandard).

Compared structures

4DCO · Crystal Structure of caspase 3, L168Y mutant · the same entry in another collection · chain F against F, TM-score 1.00
P42574 · AlphaFold monomer V2.0 prediction for caspase-3 (P42574) · a predicted model of the same protein · chain D against A, TM-score 0.99

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 4DCO · PDBe 4DCO · UniProt P42574

GL1X is a live explorer of the GenesisL1 blockchain. Turn on JavaScript for search, charts and interactive views.