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Crystal structure of the putative exported protein YPO2471 from yersinia pestis

Analyse Crystal structure of the putative exported protein YPO2471 from yersinia pestis in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7TEM
Type
protein
Length
809 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Putative exported protein YPO2471
UniProt
A0A5P8YGV9
Ligands
GLC, FRU, CL
Pockets
5 · best druggability 0.66

Structure

x-ray diffraction · 2 distinct chains · 52% helix, 17% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
APutative exported protein YPO2471protein40452% helix, 17% strandA0A5P8YGV9
BPutative exported protein YPO2471protein40551% helix, 17% strandA0A5P8YGV9

Ligands and binding sites

  • GLC · alpha-D-glucopyranose · sugar · 2 copies · chains A, B
  • FRU · beta-D-fructofuranose · sugar · 2 copies · chains A, B
  • CL · Chloride ion · ion · 2 copies · chains A, B
  • EDO · 1,2-ethanediol · additive · 6 copies · chains A, B
  • ACY · Acetic acid · additive · chains B
  • GOL · Glycerol · 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, 1 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
17060.660.7566FRU, EDO
22440.490.7428EDO, GOL
31990.470.7531empty
42050.470.7431ACY
5690.390.7915empty

Interfaces

1 interface between chains.

  • A–B · 513 Ų buried · 8 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 18 modified (engineered).

Compared structures

  • 7TEM · Crystal Structure of the Putative Exported Protein YPO2471 from Yersinia pestis · the same entry in another collection · chain A against A, TM-score 1.00

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