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Crystal structure of putative triphosphoribosyl-dephospho-CoA synthase from archaeoglobus fulgidus

Analyse Crystal structure of putative triphosphoribosyl-dephospho-CoA synthase from… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3H9P
Type
protein
Length
665 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Putative triphosphoribosyl-dephospho-CoA synthase
UniProt
O28441
Ligands
CL
Pockets
7 · best druggability 0.79

Structure

x-ray diffraction · 3 distinct chains · 76% helix, 0% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
APutative triphosphoribosyl-dephospho-CoA synthaseprotein22675% helix, 0% strandO28441
BPutative triphosphoribosyl-dephospho-CoA synthaseprotein22177% helix, 0% strandO28441
CPutative triphosphoribosyl-dephospho-CoA synthaseprotein21877% helix, 0% strandO28441

Ligands and binding sites

  • CL · Chloride ion · ion · chains A
  • GOL · Glycerol · additive · chains A
  • PG4 · Tetraethylene glycol · additive · chains B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
111670.790.8072empty
23920.610.7639empty
32390.530.7630empty
41510.450.7521empty
51740.440.7428empty

Interfaces

2 interfaces between chains.

  • A–B · 985 Ų buried · 16 hydrogen bonds · protein-protein
  • A–C · 223 Ų buried · 3 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 15 modified (engineered).

Compared structures

  • 3H9P · Crystal structure of putative triphosphoribosyl-dephospho-coA synthase from Archaeoglobus… · the same entry in another collection · chain A against A, TM-score 1.00

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