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The crystal structure of pesticin from yersinia pestis

Analyse The crystal structure of pesticin 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
4EPF
Type
protein
Length
668 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Pesticin
UniProt
Q57159
Pockets
6 · best druggability 0.46

Structure

x-ray diffraction · 2 distinct chains · 42% helix, 18% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
APesticinprotein33342% helix, 18% strandQ57159
BPesticinprotein33541% helix, 18% strandQ57159

Pockets

6 pockets found on a 1 Å grid, 0 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12190.460.7326empty
21080.410.7620empty
31520.400.7321empty
4720.380.7713empty
5780.350.7520empty

Interfaces

1 interface between chains.

  • A–B · 812 Ų buried · 1 hydrogen bond · protein-protein

Modifications

Observed in the structure: 12 modified (engineered).

Compared structures

  • 4EPF · The crystal structure of pesticin from Yersinia pestis · the same entry in another collection · chain A against A, TM-score 1.00

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