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TargetLecithin retinol acyltransferase
LigandBDBM19
Substrate/Competitorn/a
Meas. Tech.ChEMBL_96915 (CHEMBL707894)
IC50 14900±n/a nM
Citation Ryu, DHTan, CHRando, RR Synthesis of (+),(-)-neamine and their positional isomers as potential antibiotics. Bioorg Med Chem Lett13:901-3 (2003) [PubMed]
More Info.:Get all data from this article,  Assay Method
 
Lecithin retinol acyltransferase
Name:Lecithin retinol acyltransferase
Synonyms:LRAT | LRAT_HUMAN | Lecithin retinol acyltransferase | Phosphatidylcholine--retinol O-acyltransferase | Phosphatidylcholine-retinol O-acyltransferase
Type:PROTEIN
Mol. Mass.:25705.63
Organism:Homo sapiens (Human)
Description:ChEMBL_96915
Residue:230
Sequence:
MKNPMLEVVSLLLEKLLLISNFTLFSSGAAGEDKGRNSFYETSSFHRGDVLEVPRTHLTH
YGIYLGDNRVAHMMPDILLALTDDMGRTQKVVSNKRLILGVIVKVASIRVDTVEDFAYGA
NILVNHLDESLQKKALLNEEVARRAEKLLGFTPYSLLWNNCEHFVTYCRYGTPISPQSDK
FCETVKIIIRDQRSVLASAVLGLASIVCTGLVSYTTLPAIFIPFFLWMAG
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM19
n/a
NameBDBM19
Synonyms:(2S,3S,4R,5R,6R)-5-amino-2-(aminomethyl)-6-{[(2R,3S,4R,5S)-5-{[(1R,2R,3S,5R,6S)-3,5-diamino-2-{[(2R,3R,4R,5S,6R)-3-amino-6-(aminomethyl)-4,5-dihydroxyoxan-2-yl]oxy}-6-hydroxycyclohexyl]oxy}-4-hydroxy-2-(hydroxymethyl)oxolan-3-yl]oxy}oxane-3,4-diol | KDR Kinase Inhibitor, 3 | Neomycin | Neomycin B
TypeSmall organic molecule
Emp. Form.C23H46N6O13
Mol. Mass.614.6437
SMILESNC[C@@H]1O[C@H](O[C@@H]2[C@@H](CO)O[C@@H](O[C@@H]3[C@@H](O)[C@H](N)C[C@H](N)[C@H]3O[C@H]3O[C@H](CN)[C@@H](O)[C@H](O)[C@H]3N)[C@@H]2O)[C@H](N)[C@@H](O)[C@@H]1O |r|
Structure
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