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Crystal structure of a conserved protein of unknown function from enterococcus faecalis V583

Analyse Crystal structure of a conserved protein of unknown function from enterococcus… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3CLQ
Type
protein
Length
1,681 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Uncharacterized protein
UniProt
Q82ZN9
Pockets
12 · best druggability 0.73

Structure

x-ray diffraction · 3 distinct chains · 44% helix, 20% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AUncharacterized proteinprotein42044% helix, 20% strandQ82ZN9
B, CUncharacterized proteinprotein42143% helix, 21% strandQ82ZN9
DUncharacterized proteinprotein41945% helix, 21% strandQ82ZN9

Ligands and binding sites

  • PEG · Di(hydroxyethyl)ether · additive · 4 copies · chains B, A, C, D

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1590.730.9819empty
2570.710.9828empty
3570.710.9824empty
44200.640.7859empty
54160.590.7536empty

Interfaces

4 interfaces between chains.

  • C–D · 1380 Ų buried · 10 hydrogen bonds · protein-protein
  • A–B · 1374 Ų buried · 11 hydrogen bonds · protein-protein
  • A–C · 554 Ų buried · 9 hydrogen bonds · protein-protein
  • B–C · 25 Ų buried · 0 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 80 modified (engineered).

Compared structures

  • 3CLQ · Crystal structure of a conserved protein of unknown function from Enterococcus faecalis… · the same entry in another collection · chain A against A, TM-score 1.00

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