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MolNFT v1 · #51850 · protein

Formyl-CoA transferase with aspartyl-formyl anhydide intermediate

2VJM · Formyl-coenzyme a transferase: “Formyl-CoA transferase with aspartyl-formyl anhydide intermediate”. X-ray diffraction, 2 ligands (COA, NA), 13 pockets (best druggability 0.75). MolNFT v1 #51850 on GenesisL1: 3D structure, binding…

PDB
2VJM
Type
protein
Length
854 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Formyl-coenzyme a transferase
EC
2.8.3.16
UniProt
O06644
Ligands
COA, NA
Pockets
13 · best druggability 0.75

Structure

x-ray diffraction · 2 distinct chains · 38% helix, 13% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AFormyl-coenzyme a transferase (EC 2.8.3.16)protein42738% helix, 13% strandO06644
BFormyl-coenzyme a transferase (EC 2.8.3.16)protein42738% helix, 13% strandO06644

Ligands and binding sites

  • COA · Coenzyme A · ligand · 2 copies · chains A, B
  • NA · Sodium ion · metal · chains A
  • EPE · 4-(2-hydroxyethyl)-1-piperazine ethanesulfonic acid · additive · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
1860.750.9838empty
24380.720.8253COA
33410.700.8340COA
42270.620.8232empty
52080.610.8238empty

Interfaces

1 interface between chains.

  • A–B · 6226 Ų buried · 76 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 1 covalent, 1 modified (covalent ligand, nonstandard).

Compared structures

  • 2VJM · Formyl-CoA transferase with aspartyl-formyl anhydide intermediate · the same entry in another collection · chain A against A, TM-score 1.00
  • O06644 · AlphaFold monomer V2.0 prediction for formyl-COA:OXALATE CoA- transferase (O06644) · a predicted model of the same protein · chain A against A, TM-score 1.00

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