Target
Protein-L-isoaspartate(D-aspartate) O-methyltransferase
Ligand
BDBM50368311
Substrate
n/a
Meas. Tech.
ChEMBL_161419 (CHEMBL766687)
Ki
1680000±n/a nM
Citation
 Barton, DHGéro, SDLawrence, FRobert-Gero, MQuiclet-Sire, BSamadi, M Total synthesis of uracil analogues of sinefungin. J Med Chem 35:63-7 (1992) [PubMed]  Article 
Target
Name:
Protein-L-isoaspartate(D-aspartate) O-methyltransferase
Synonyms:
PCMT1 | PIMT_HUMAN | Protein-beta-aspartate methyltransferase
Type:
PROTEIN
Mol. Mass.:
24639.13
Organism:
Homo sapiens (Human)
Description:
ChEMBL_161420
Residue:
227
Sequence:
MAWKSGGASHSELIHNLRKNGIIKTDKVFEVMLATDRSHYAKCNPYMDSPQSIGFQATISAPHMHAYALELLFDQLHEGAKALDVGSGSGILTACFARMVGCTGKVIGIDHIKELVDDSVNNVRKDDPTLLSSGRVQLVVGDGRMGYAEEAPYDAIHVGAAAPVVPQALIDQLKPGGRLILPVGPAGGNQMLEQYDKLQDGSIKMKPLMGVIYVPLTDKEKQWSRWK
  
Inhibitor
Name:
BDBM50368311
Synonyms:
CHEMBL609345
Type:
Small organic molecule
Emp. Form.:
C14H22N4O7
Mol. Mass.:
358.3471
SMILES:
NC(CC[C@H](N)C(O)=O)C[C@H]1OC([C@H](O)[C@@H]1O)n1ccc(=O)[nH]c1=O |r|
Structure:
Search PDB for entries with ligand similarity: