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L122K mutant of FMN-binding protein from desulfovibrio vulgaris (miyazaki F)

Analyse L122K mutant of FMN-binding protein from desulfovibrio vulgaris (miyazaki F) in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3A20
Type
protein
Length
244 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
FMN-binding protein
UniProt
Q46604
Ligands
FMN
Pockets
4 · best druggability 0.60

Structure

x-ray diffraction · 1 distinct chain · 18% helix, 47% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, BFMN-binding proteinprotein12218% helix, 47% strandQ46604

Ligands and binding sites

  • FMN · Flavin mononucleotide · ligand · 2 copies · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12470.600.8028FMN
22150.590.8024FMN
3920.450.8018empty
4550.310.7618empty

Interfaces

1 interface between chains.

  • A–B · 1158 Ų buried · 17 hydrogen bonds · protein-protein

Compared structures

  • 3A20 · L122K mutant of FMN-binding protein from Desulfovibrio vulgaris (Miyazaki F) · the same entry in another collection · chain A against A, TM-score 1.00
  • Q46604 · AlphaFold monomer V2.0 prediction for FMN-binding protein (Q46604) · a predicted model of the same protein · chain B against A, TM-score 1.00

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