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Crystal structure of enterococcus faecalis ahpc

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

PDB
5Y63
Type
protein
Length
832 residues
Chains
5
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Alkyl hydroperoxide reductase, C subunit
UniProt
H7C7A0
Pockets
6 · best druggability 0.67

Structure

x-ray diffraction · 3 distinct chains · 33% helix, 28% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, C, DAlkyl hydroperoxide reductase, C subunitprotein16734% helix, 28% strandH7C7A0
BAlkyl hydroperoxide reductase, C subunitprotein16633% helix, 27% strandH7C7A0
EAlkyl hydroperoxide reductase, C subunitprotein16533% helix, 27% strandH7C7A0

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1770.670.9329empty
22930.570.7741empty
33290.570.7642empty
41400.430.7520empty
5690.300.7421empty

Interfaces

5 interfaces between chains.

  • A–B · 1321 Ų buried · 21 hydrogen bonds · protein-protein
  • C–D · 1249 Ų buried · 18 hydrogen bonds · protein-protein
  • B–C · 667 Ų buried · 7 hydrogen bonds · protein-protein
  • D–E · 665 Ų buried · 3 hydrogen bonds · protein-protein
  • C–E · 51 Ų buried · 0 hydrogen bonds · protein-protein

Compared structures

  • 5Y63 · Crystal structure of Enterococcus faecalis AhpC · the same entry in another collection · chain A against A, TM-score 1.00

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