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Crystal structure of a FAD-binding protein (MLL6688) from mesorhizobium loti at 1.95 a resolution

Analyse Crystal structure of a FAD-binding protein (MLL6688) from mesorhizobium loti at… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
2HQ9
Type
protein
Length
273 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
MLL6688 protein
UniProt
Q988L5
Ligands
FAD, CL
Pockets
1 · best druggability 0.77

Structure

x-ray diffraction · 2 distinct chains · 27% helix, 48% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AMLL6688 proteinprotein13529% helix, 50% strandQ988L5
BMLL6688 proteinprotein13826% helix, 47% strandQ988L5

Ligands and binding sites

  • FAD · Flavin-adenine dinucleotide · ligand · 2 copies · chains A, B
  • CL · Chloride ion · ion · chains A
  • EDO · 1,2-ethanediol · additive · chains A, B

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

Pockets

1 pocket found on a 1 Å grid, 1 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
18040.770.8175FAD, EDO

Interfaces

1 interface between chains.

  • A–B · 1361 Ų buried · 16 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 6 modified (engineered).

Compared structures

  • 2HQ9 · Crystal structure of a fad-binding protein (mll6688) from mesorhizobium loti at 1.95 A… · the same entry in another collection · chain A against A, TM-score 1.00

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