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MolNFT v1 · #20015 · protein

Ribonucleotide reductase R1 protein mutant Y730F with a reduced active site from escherichia COLI

1R1R: “Ribonucleotide reductase R1 protein mutant Y730F with a reduced active site from escherichia COLI”. X-ray diffraction, 20 pockets (best druggability 0.74). MolNFT v1 #20015 on GenesisL1: 3D structure, binding sites and pockets in…

PDB
1R1R
Type
protein
Length
2,253 residues
Chains
7
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Ribonucleotide reductase R1 protein; Ribonucleotide reductase R2 protein
EC
1.17.4.1
UniProt
P00452, P69924
Pockets
20 · best druggability 0.74

Structure

x-ray diffraction · 3 distinct chains · 46% helix, 13% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, CRibonucleotide reductase R1 protein (EC 1.17.4.1)protein73447% helix, 13% strandP00452
D, E, FRibonucleotide reductase R2 proteinprotein1625% helix, 13% strandP69924
PRibonucleotide reductase R2 proteinprotein30% helix, 0% strandP69924

Pockets

20 pockets found on a 1 Å grid, 8 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
19630.740.7896empty
29730.740.7788empty
37830.730.7990empty
42040.720.8932empty
51410.560.8219empty

Interfaces

7 interfaces between chains.

  • A–B · 1238 Ų buried · 12 hydrogen bonds · protein-protein
  • A–D · 882 Ų buried · 8 hydrogen bonds · protein-protein
  • C–F · 880 Ų buried · 8 hydrogen bonds · protein-protein
  • B–E · 874 Ų buried · 8 hydrogen bonds · protein-protein
  • A–P · 226 Ų buried · 4 hydrogen bonds · protein-protein

Compared structures

  • 1R1R · Ribonucleotide reductase R1 protein mutant Y730F with a reduced active site from… · the same entry in another collection · chain P against P, TM-score 1.00
  • P00452 · AlphaFold monomer V2.0 prediction for ribonucleoside-diphosphate reductase 1 subunit… · a predicted model of the same protein · chain A against A, TM-score 0.99

Analyse

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