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MolNFT v1 · #118466 · protein

Crystal structure of mycobacterial fatty acid O-methyltransferase in complex with sah and 3-hydroxy-decanoate.

5F2N: “Crystal structure of mycobacterial fatty acid O-methyltransferase in complex with sah and 3-hydroxy-decanoate.”. X-ray diffraction, 2 ligands (SAH, 5UF), 9 pockets (best druggability 0.80). MolNFT v1 #118466 on GenesisL1: 3D…

PDB
5F2N
Type
protein
Length
713 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Fatty acid O-methyltransferase
UniProt
B2HHT4
Ligands
SAH, 5UF
Pockets
9 · best druggability 0.80

Structure

x-ray diffraction · 2 distinct chains · 43% helix, 18% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AFatty acid O-methyltransferaseprotein35743% helix, 18% strandB2HHT4
BFatty acid O-methyltransferaseprotein35644% helix, 18% strandB2HHT4

Ligands and binding sites

  • SAH · S-adenosyl-L-homocysteine · ligand · 2 copies · chains A, B
  • 5UF · (3~{S})-3-oxidanyldecanoic acid · ligand · 2 copies · chains A, B

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
11920.800.9433empty
24480.790.8773SAH, 5UF
35590.780.8476SAH, 5UF
41010.420.7723empty
5900.420.7822empty

Interfaces

1 interface between chains.

  • A–B · 1084 Ų buried · 10 hydrogen bonds · protein-protein

Compared structures

  • 5F2N · Crystal structure of mycobacterial fatty acid O-methyltransferase in complex with SAH and… · the same entry in another collection · chain A against A, TM-score 1.00

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