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Crystal structure of geranyltransferase from helicobacter pylori 26695

Analyse Crystal structure of geranyltransferase from helicobacter pylori 26695 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3LLW
Type
protein
Length
1,151 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Geranyltranstransferase (ispa)
UniProt
O25583
Ligands
SO4
Pockets
9 · best druggability 0.76

Structure

x-ray diffraction · 4 distinct chains · 74% helix, 1% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AGeranyltranstransferase (ispa)protein28874% helix, 1% strandO25583
BGeranyltranstransferase (ispa)protein28874% helix, 1% strandO25583
CGeranyltranstransferase (ispa)protein28675% helix, 1% strandO25583
DGeranyltranstransferase (ispa)protein28974% helix, 1% strandO25583

Ligands and binding sites

  • SO4 · Sulfate ion · ion · 9 copies · chains A, B, C, D

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

Pockets

9 pockets found on a 1 Å grid, 4 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
111630.760.79105SO4
25900.720.8061SO4
35990.700.7960SO4
44470.660.7849SO4
51210.440.7723empty

Interfaces

5 interfaces between chains.

  • A–B · 2383 Ų buried · 17 hydrogen bonds · protein-protein
  • C–D · 2369 Ų buried · 16 hydrogen bonds · protein-protein
  • B–D · 391 Ų buried · 4 hydrogen bonds · protein-protein
  • A–C · 224 Ų buried · 3 hydrogen bonds · protein-protein
  • A–D · 186 Ų buried · 1 hydrogen bond · protein-protein

Compared structures

  • 3LLW · Crystal structure of geranyltransferase from helicobacter pylori 26695 · the same entry in another collection · chain C against C, TM-score 1.00

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