Target
Histone-lysine N-methyltransferase KMT5C
Ligand
BDBM223980
Substrate
n/a
Meas. Tech.
Scintillation Proximity Assay (SPA)
pH
8±0
Temperature
298.15±0 K
IC50
1.2e+3±n/a nM
Citation
 Bromberg, KDMitchell, TRUpadhyay, AKJakob, CGJhala, MAComess, KMLasko, LMLi, CTuzon, CTDai, YLi, FEram, MSNuber, ASoni, NBManaves, VAlgire, MASweis, RFTorrent, MSchotta, GSun, CMichaelides, MRShoemaker, ARArrowsmith, CHBrown, PJSanthakumar, VMartin, ARice, JCChiang, GGVedadi, MBarsyte-Lovejoy, DPappano, WN The SUV4-20 inhibitor A-196 verifies a role for epigenetics in genomic integrity. Nat Chem Biol 13:317-324 (2017) [PubMed]  Article 
Target
Name:
Histone-lysine N-methyltransferase KMT5C
Synonyms:
Histone-lysine N-methyltransferase SUV420H2 | KMT5C | KMT5C_HUMAN | Lysine N-methyltransferase 5C | Protein lysine methyltransferase SUV4-20H2 (SUV4-20H2) | SUV420H2 | Su(var)4-20 homolog 2 | Suppressor of variegation 4-20 homolog 2 | Suv4-20h2
Type:
Enzyme
Mol. Mass.:
52147.69
Organism:
Homo sapiens (Human)
Description:
Q86Y97
Residue:
462
Sequence:
MGPDRVTARELCENDDLATSLVLDPYLGFRTHKMNVSPVPPLRRQQHLRSALETFLRQRDLEAAYRALTLGGWTARYFQSRGPRQEAALKTHVYRYLRAFLPESGFTILPCTRYSMETNGAKIVSTRAWKKNEKLELLVGCIAELREADEGLLRAGENDFSIMYSTRKRSAQLWLGPAAFINHDCKPNCKFVPADGNAACVKVLRDIEPGDEVTCFYGEGFFGEKNEHCECHTCERKGEGAFRTRPREPALPPRPLDKYQLRETKRRLQQGLDSGSRQGLLGPRACVHPSPLRRDPFCAACQPLRLPACSARPDTSPLWLQWLPQPQPRVRPRKRRRPRPRRAPVLSTHHAARVSLHRWGGCGPHCRLRGEALVALGQPPHARWAPQQDWHWARRYGLPYVVRVDLRRLAPAPPATPAPAGTPGPILIPKQALAFAPFSPPKRLRLVVSHGSIDLDVGGEEL
  
Inhibitor
Name:
BDBM223980
Synonyms:
6,7-Dichloro-N-cyclopentylquinolin-4-amine (2)
Type:
Small organic molecule
Emp. Form.:
C14H14Cl2N2
Mol. Mass.:
281.18
SMILES:
Clc1cc2nccc(NC3CCCC3)c2cc1Cl
Structure:
Search PDB for entries with ligand similarity: