GL1X · GenesisL1 explorer

MolNFT v1 · #119202 · protein

Humanised monomeric rada in complex with fhaa tetrapeptide

5FOX · DNA repair and recombination protein rada: “Humanised monomeric rada in complex with fhaa tetrapeptide”. X-ray diffraction, 3 ligands (ACE, NH2, PO4), 2 pockets (best druggability 0.42). MolNFT v1 #119202 on GenesisL1: 3D structure…

PDB
5FOX
Type
protein
Length
226 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
DNA repair and recombination protein rada; Fhaa peptide
EC
3.6.4.-
UniProt
O74036
Ligands
ACE, NH2, PO4
Pockets
2 · best druggability 0.42

Structure

x-ray diffraction · 2 distinct chains · 36% helix, 27% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ADNA repair and recombination protein rada (EC 3.6.4.-)protein22237% helix, 26% strandO74036
CFhaa peptideprotein40% helix, 50% strand—

Ligands and binding sites

  • ACE · Acetyl group · ligand · chains A, C
  • NH2 · Amino group · ion · chains A, C
  • PO4 · Phosphate ion · ion · chains A
  • GOL · Glycerol · additive · chains A

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

Pockets

2 pockets found on a 1 Å grid, 0 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1890.420.7917empty
2710.320.7521PO4

Interfaces

1 interface between chains.

  • A–C · 315 Ų buried · 4 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 1 covalent (covalent ligand).

Compared structures

  • 5FOX · Humanised monomeric rada in complex with fhaa tetrapeptide · the same entry in another collection · chain A against A, TM-score 1.00
  • O74036 · AlphaFold monomer V2.0 prediction for DNA repair and recombination protein rada (O74036) · a predicted model of the same protein · chain A against A, TM-score 0.97

Analyse

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