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TargetLysyl oxidase homolog 3
LigandBDBM50232678
Substrate/Competitorn/a
Meas. Tech.ChEMBL_1901015 (CHEMBL4403237)
IC50 310±n/a nM
Citation Smithen, DALeung, LMHChallinor, MLawrence, RTang, HNiculescu-Duvaz, DPearce, SPMcleary, RLopes, FAljarah, MBrown, MJohnson, LThomson, GMarais, RSpringer, C 2-Aminomethylene-5-sulfonylthiazole Inhibitors of Lysyl Oxidase (LOX) and LOXL2 Show Significant Efficacy in Delaying Tumor Growth. J Med Chem63:2308-2324 (2020) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Lysyl oxidase homolog 3
Name:Lysyl oxidase homolog 3
Synonyms:1.4.3.- | 1.4.3.13 | LOXL | LOXL3 | LOXL3_HUMAN | Lysyl oxidase homolog 3 | Lysyl oxidase-like protein 3 | Synonyms=LOXL
Type:PROTEIN
Mol. Mass.:83173.13
Organism:Homo sapiens (Human)
Description:ChEMBL_117594
Residue:753
Sequence:
MRPVSVWQWSPWGLLLCLLCSSCLGSPSPSTGPEKKAGSQGLRFRLAGFPRKPYEGRVEI
QRAGEWGTICDDDFTLQAAHILCRELGFTEATGWTHSAKYGPGTGRIWLDNLSCSGTEQS
VTECASRGWGNSDCTHDEDAGVICKDQRLPGFSDSNVIEVEHHLQVEEVRIRPAVGWGRR
PLPVTEGLVEVRLPDGWSQVCDKGWSAHNSHVVCGMLGFPSEKRVNAAFYRLLAQRQQHS
FGLHGVACVGTEAHLSLCSLEFYRANDTARCPGGGPAVVSCVPGPVYAASSGQKKQQQSK
PQGEARVRLKGGAHPGEGRVEVLKASTWGTVCDRKWDLHAASVVCRELGFGSAREALSGA
RMGQGMGAIHLSEVRCSGQELSLWKCPHKNITAEDCSHSQDAGVRCNLPYTGAETRIRLS
GGRSQHEGRVEVQIGGPGPLRWGLICGDDWGTLEAMVACRQLGLGYANHGLQETWYWDSG
NITEVVMSGVRCTGTELSLDQCAHHGTHITCKRTGTRFTAGVICSETASDLLLHSALVQE
TAYIEDRPLHMLYCAAEENCLASSARSANWPYGHRRLLRFSSQIHNLGRADFRPKAGRHS
WVWHECHGHYHSMDIFTHYDILTPNGTKVAEGHKASFCLEDTECQEDVSKRYECANFGEQ
GITVGCWDLYRHDIDCQWIDITDVKPGNYILQVVINPNFEVAESDFTNNAMKCNCKYDGH
RIWVHNCHIGDAFSEEANRRFERYPGQTSNQII
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM50232678
n/a
NameBDBM50232678
Synonyms:CHEBI:27413 | CHEMBL1618272 | US10717734, Compound BAPN | US11098045, Compound BAPN
TypeSmall organic molecule
Emp. Form.C3H6N2
Mol. Mass.70.0931
SMILESNCCC#N
Structure
Search PDB for entries with ligand similarity:Similarity to this molecule at least: