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TargetAmine oxidase [flavin-containing] B
LigandBDBM50113851
Substrate/Competitorn/a
Meas. Tech.ChEMBL_1434488 (CHEMBL3388874)
IC50 1050±n/a nM
Citation Vianello, PBotrugno, OACappa, ACiossani, GDessanti, PMai, AMattevi, AMeroni, GMinucci, SThaler, FTortorici, MTrifiró, PValente, SVilla, MVarasi, MMercurio, C Synthesis, biological activity and mechanistic insights of 1-substituted cyclopropylamine derivatives: a novel class of irreversible inhibitors of histone demethylase KDM1A. Eur J Med Chem86:352-63 (2014) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Amine oxidase [flavin-containing] B
Name:Amine oxidase [flavin-containing] B
Synonyms:AOFB_HUMAN | MAO-B | MAOB | Monoamine oxidase type B | Monoamine oxidase type B (MAO B) | Monoamine oxidase type B (MAO B) | Monoamine oxidase type B (MAOB)
Type:Protein
Mol. Mass.:58768.76
Organism:Homo sapiens (Human)
Description:P27338
Residue:520
Sequence:
MSNKCDVVVVGGGISGMAAAKLLHDSGLNVVVLEARDRVGGRTYTLRNQKVKYVDLGGSY
VGPTQNRILRLAKELGLETYKVNEVERLIHHVKGKSYPFRGPFPPVWNPITYLDHNNFWR
TMDDMGREIPSDAPWKAPLAEEWDNMTMKELLDKLCWTESAKQLATLFVNLCVTAETHEV
SALWFLWYVKQCGGTTRIISTTNGGQERKFVGGSGQVSERIMDLLGDRVKLERPVIYIDQ
TRENVLVETLNHEMYEAKYVISAIPPTLGMKIHFNPPLPMMRNQMITRVPLGSVIKCIVY
YKEPFWRKKDYCGTMIIDGEEAPVAYTLDDTKPEGNYAAIMGFILAHKARKLARLTKEER
LKKLCELYAKVLGSLEALEPVHYEEKNWCEEQYSGGCYTTYFPPGILTQYGRVLRQPVDR
IYFAGTETATHWSGYMEGAVEAGERAAREILHAMGKIPEDEIWQSEPESVDVPAQPITTT
FLERHLPSVPGLLRLIGLTTIFSATALGFLAHKRGLLVRV
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM50113851
n/a
NameBDBM50113851
Synonyms:(+/-)-Tranylcypromine | 2-PCPA | 2-Phenyl-cyclopropylamine | 2-phenylcyclopropanamine | CHEMBL313833 | TRANYLCYPROMINE | Tranylcypromine,(+) | Tranylcypromine,(-) | US8609708, 6 Tranyl- cypromine | US8609708, 6 Tranylcypromine
TypeSmall organic molecule
Emp. Form.C9H11N
Mol. Mass.133.1903
SMILESNC1CC1c1ccccc1
Structure
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