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New antiparallel dimer of aureochrome 1A lov domain mutants from phaeodactylum tricornutum

Analyse New antiparallel dimer of aureochrome 1A lov domain mutants from phaeodactylum… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6T74
Type
protein
Length
281 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
PTAUREO1A LOV2 domain
UniProt
A0A140UHJ0
Ligands
FMN, NA
Pockets
5 · best druggability 0.69

Structure

x-ray diffraction · 2 distinct chains · 40% helix, 28% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
APTAUREO1A LOV2 domainprotein14040% helix, 28% strandA0A140UHJ0
BPTAUREO1A LOV2 domainprotein14139% helix, 28% strandA0A140UHJ0

Ligands and binding sites

  • FMN · Flavin mononucleotide · ligand · 2 copies · chains A, B
  • NA · Sodium ion · metal · 2 copies · chains A, B
  • 1PE · Pentaethylene glycol · additive · 3 copies · chains A, B
  • GOL · Glycerol · additive · 2 copies · chains A, B
  • MLI · Malonate ion · additive · chains 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, 2 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11730.690.8822FMN
21710.680.8724FMN
3670.380.7816GOL
4830.370.7616empty
5570.310.7612empty

Interfaces

1 interface between chains.

  • A–B · 931 Ų buried · 2 hydrogen bonds · protein-protein

Compared structures

  • 6T74 · New antiparallel dimer of aureochrome 1a LOV domain mutants from Phaeodactylum tricornutum · the same entry in another collection · chain A against A, TM-score 1.00

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