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Crystal structure of the enterococcus faecalis gluconate specific eiia phosphotransferase system component

Analyse Crystal structure of the enterococcus faecalis gluconate specific eiia… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3IPR
Type
protein
Length
836 residues
Chains
6
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Pts system, iia component
UniProt
Q82ZC8
Ligands
CA
Pockets
3 · best druggability 0.49

Structure

x-ray diffraction · 3 distinct chains · 51% helix, 19% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
APts system, iia componentprotein13750% helix, 19% strandQ82ZC8
B, D, E, FPts system, iia componentprotein14053% helix, 19% strandQ82ZC8
CPts system, iia componentprotein13950% helix, 19% strandQ82ZC8

Ligands and binding sites

  • CA · Calcium ion · metal · 10 copies · chains A, B, C, D, E, F

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12620.490.7434empty
21300.370.7322empty
31260.360.7323empty

Interfaces

8 interfaces between chains.

  • E–F · 1884 Ų buried · 19 hydrogen bonds · protein-protein
  • C–D · 1882 Ų buried · 20 hydrogen bonds · protein-protein
  • A–B · 1860 Ų buried · 18 hydrogen bonds · protein-protein
  • A–F · 498 Ų buried · 9 hydrogen bonds · protein-protein
  • B–E · 157 Ų buried · 0 hydrogen bonds · protein-protein

Compared structures

  • 3IPR · Crystal structure of the Enterococcus faecalis gluconate specific EIIA phosphotransferase… · the same entry in another collection · chain A against A, TM-score 1.00

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