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Crystal structure of a trap periplasmic solute binding protein from desulfovibrio vulgaris (DEVAL_0042, target efi-510114) bound to copurified (R)-pantoic acid

Analyse Crystal structure of a trap periplasmic solute 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
4XEQ
Type
protein
Length
1,211 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Trap dicarboxylate transporter, dctp subunit
UniProt
E3ILJ0
Ligands
PAF
Pockets
11 · best druggability 0.81

Structure

x-ray diffraction · 3 distinct chains · 52% helix, 20% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ATrap dicarboxylate transporter, dctp subunitprotein30352% helix, 18% strandE3ILJ0
BTrap dicarboxylate transporter, dctp subunitprotein30453% helix, 20% strandE3ILJ0
C, DTrap dicarboxylate transporter, dctp subunitprotein30251% helix, 20% strandE3ILJ0

Ligands and binding sites

  • PAF · Pantoate · ligand · 4 copies · chains A, B, C, D

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

Pockets

11 pockets found on a 1 Å grid, 6 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
110410.810.8293empty
2560.720.9821PAF
3630.720.9721PAF
4530.710.9820PAF
53940.620.7741empty

Interfaces

4 interfaces between chains.

  • C–D · 571 Ų buried · 9 hydrogen bonds · protein-protein
  • A–C · 453 Ų buried · 8 hydrogen bonds · protein-protein
  • A–B · 365 Ų buried · 2 hydrogen bonds · protein-protein
  • B–C · 126 Ų buried · 3 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 32 modified (engineered).

Compared structures

  • 4XEQ · CRYSTAL STRUCTURE OF A TRAP PERIPLASMIC SOLUTE BINDING PROTEIN FROM DESULFOVIBRIO… · the same entry in another collection · chain A against A, TM-score 1.00

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