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R2-like ligand-binding oxidase V72L mutant with aerobically reconstituted MN/FE cofactor

Analyse R2-like ligand-binding oxidase V72L mutant with aerobically reconstituted MN/FE… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6F6H
Type
protein
Length
557 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Ribonucleotide reductase small subunit
EC
1.17.4.1
UniProt
Q5KW80
Ligands
PLM, MN, MN3, FE
Pockets
5 · best druggability 0.84

Structure

x-ray diffraction · 2 distinct chains · 79% helix, 0% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ARibonucleotide reductase small subunit (EC 1.17.4.1)protein28578% helix, 0% strandQ5KW80
BRibonucleotide reductase small subunit (EC 1.17.4.1)protein27281% helix, 0% strandQ5KW80

Ligands and binding sites

  • PLM · Palmitic acid · ligand · 2 copies · chains A, B
  • MN · Manganese (II) ion · metal · 2 copies · chains A, B
  • MN3 · Manganese (III) ion · metal · 2 copies · chains A, B
  • FE · Fe (III) ion · metal · 2 copies · chains A, B

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

Pockets

5 pockets found on a 1 Å grid, 4 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12220.840.9640PLM
22350.770.9039PLM
31140.740.9526empty
41320.510.8023empty
51410.490.7823empty

Interfaces

1 interface between chains.

  • A–B · 2717 Ų buried · 49 hydrogen bonds · protein-protein

Compared structures

  • 6F6H · R2-like ligand-binding oxidase V72L mutant with aerobically reconstituted Mn/Fe cofactor · the same entry in another collection · chain A against A, TM-score 1.00

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