GL1X · GenesisL1 explorer

MolNFT v1 · #121995 · protein

Crystal structure of caspase-3 deve peptide complex

5IC4 · Caspase-3 subunit P17: “Crystal structure of caspase-3 deve peptide complex”. X-ray diffraction, 3 pockets (best druggability 0.65). MolNFT v1 #121995 on GenesisL1: 3D structure, binding sites and pockets in GL1X.

PDB
5IC4
Type
protein
Length
938 residues
Chains
12
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Caspase-3 subunit P17; Caspase-3 subunit P12; Deve peptide
EC
3.4.22.56
UniProt
P42574
Pockets
3 · best druggability 0.65

Structure

x-ray diffraction · 5 distinct chains · 29% helix, 27% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, C, ECaspase-3 subunit P17 (EC 3.4.22.56)protein13929% helix, 32% strandP42574
B, HCaspase-3 subunit P12 (EC 3.4.22.56)protein9234% helix, 21% strandP42574
D, FCaspase-3 subunit P12 (EC 3.4.22.56)protein9134% helix, 20% strandP42574
GCaspase-3 subunit P17 (EC 3.4.22.56)protein13924% helix, 31% strandP42574
I, J, K, LDeve peptideprotein40% helix, 50% strand—

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12790.650.8136empty
22800.630.8038empty
31690.420.7421empty

Interfaces

21 interfaces between chains.

  • C–D · 2151 Ų buried · 32 hydrogen bonds · protein-protein
  • A–B · 2143 Ų buried · 30 hydrogen bonds · protein-protein
  • E–F · 2112 Ų buried · 32 hydrogen bonds · protein-protein
  • G–H · 2079 Ų buried · 31 hydrogen bonds · protein-protein
  • F–H · 1431 Ų buried · 19 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 4 modified (nonstandard).

Compared structures

  • 5IC4 · Crystal structure of caspase-3 DEVE peptide complex · the same entry in another collection · chain L against L, TM-score 1.00

Analyse

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