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Crystal structure of ABC transporter substrate-binding protein from sinorhizobium meliloti

Analyse Crystal structure of ABC transporter substrate-binding protein from… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4WED
Type
protein
Length
483 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
ABC transporter, periplasmic solute-binding protein
UniProt
Q92YH7
Ligands
NA
Pockets
5 · best druggability 0.64

Structure

x-ray diffraction · 1 distinct chain · 27% helix, 23% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AABC transporter, periplasmic solute-binding proteinprotein48327% helix, 23% strandQ92YH7

Ligands and binding sites

  • NA · Sodium ion · metal · chains A
  • FMT · Formic acid · additive · chains A
  • GOL · Glycerol · additive · chains A

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
13960.640.7846empty
21490.630.8625empty
33110.610.7848NA, FMT, GOL
42970.550.7638empty
52220.550.7830empty

Modifications

Observed in the structure: 8 modified (engineered).

Compared structures

  • 4WED · Crystal structure of ABC transporter substrate-binding protein from Sinorhizobium meliloti · the same entry in another collection · chain A against A, TM-score 1.00

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