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MolNFT v1 · #14348 · protein

Crystal structure of salicylic acid carboxyl methyltransferase (samt)

1M6E · S-adenosyl-L-METHIONNINE:SALICYLIC acid carboxyl…: “Crystal structure of salicylic acid carboxyl methyltransferase (samt)”. X-ray diffraction, 3 ligands (SAH, SAL, LU), 1 pocket (best druggability 0.83). MolNFT v1 #14348 on…

PDB
1M6E
Type
protein
Length
359 residues
Chains
1
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
S-adenosyl-L-METHIONNINE:SALICYLIC acid carboxyl methyltransferase
UniProt
Q9SPV4
Ligands
SAH, SAL, LU
Pockets
1 · best druggability 0.83

Structure

x-ray diffraction · 1 distinct chain · 34% helix, 16% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
XS-adenosyl-L-METHIONNINE:SALICYLIC acid carboxyl methyltransferaseprotein35934% helix, 16% strandQ9SPV4

Ligands and binding sites

  • SAH · S-adenosyl-L-homocysteine · ligand · chains X
  • SAL · 2-hydroxybenzoic acid · ligand · chains X
  • LU · Lutetium (III) ion · metal · chains X

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

Pockets

1 pocket found on a 1 Å grid, 1 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12470.830.9546SAH, SAL

Compared structures

  • 1M6E · Crystal structure of salicylic acid carboxyl methyltransferase (samt) · the same entry in another collection · chain X against X, TM-score 1.00
  • Q9SPV4 · AlphaFold monomer V2.0 prediction for salicylate carboxymethyltransferase (Q9SPV4) · a predicted model of the same protein · chain X against A, TM-score 0.96

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