GL1X · GenesisL1 explorer

MolNFT v1 · #3060 · protein

Hydrogenase maturating endopeptidase hybd from E. COLI

1CFZ · Hydrogenase 2 maturation protease: “Hydrogenase maturating endopeptidase hybd from E. COLI”. X-ray diffraction, 1 ligand (CD), 2 pockets (best druggability 0.56). MolNFT v1 #3060 on GenesisL1: 3D structure, binding sites and pockets…

PDB
1CFZ
Type
protein
Length
972 residues
Chains
6
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Hydrogenase 2 maturation protease
EC
3.4.-.-
UniProt
P37182
Ligands
CD
Pockets
2 · best druggability 0.56

Structure

x-ray diffraction · 1 distinct chain · 40% helix, 23% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, D, E, FHydrogenase 2 maturation protease (EC 3.4.-.-)protein16240% helix, 23% strandP37182

Ligands and binding sites

  • CD · Cadmium ion · metal · 6 copies · chains A, B, C, D, E, F

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
14260.560.7365empty
2500.280.7414empty

Interfaces

6 interfaces between chains.

  • A–E · 505 Ų buried · 12 hydrogen bonds · protein-protein
  • A–F · 405 Ų buried · 5 hydrogen bonds · protein-protein
  • A–B · 396 Ų buried · 6 hydrogen bonds · protein-protein
  • C–D · 391 Ų buried · 5 hydrogen bonds · protein-protein
  • C–E · 390 Ų buried · 3 hydrogen bonds · protein-protein

Compared structures

  • 1CFZ · Hydrogenase maturating endopeptidase hybd from E. COLI · the same entry in another collection · chain C against C, TM-score 1.00
  • P37182 · AlphaFold monomer V2.0 prediction for hydrogenase 2 maturation protease (P37182) · a predicted model of the same protein · chain A against A, TM-score 1.00

Analyse

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