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TargetHistone-lysine N-methyltransferase SMYD3
LigandBDBM378459
Substrate/Competitorn/a
Meas. Tech.ChEMBL_1576461 (CHEMBL3803389)
Ki 4.7±n/a nM
Citation Mitchell, LHBoriack-Sjodin, PASmith, SThomenius, MRioux, NMunchhof, MMills, JEKlaus, CTotman, JRiera, TVRaimondi, AJacques, SLWest, KFoley, MWaters, NJKuntz, KWWigle, TJScott, MPCopeland, RASmith, JJChesworth, R Novel Oxindole Sulfonamides and Sulfamides: EPZ031686, the First Orally Bioavailable Small Molecule SMYD3 Inhibitor. ACS Med Chem Lett7:134-8 (2016) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Histone-lysine N-methyltransferase SMYD3
Name:Histone-lysine N-methyltransferase SMYD3
Synonyms:SET and MYND domain-containing protein 3 | SMYD3 | SMYD3_HUMAN | ZMYND1 | ZNFN3A1 | Zinc finger MYND domain-containing protein 1
Type:Enzyme
Mol. Mass.:49101.22
Organism:Homo sapiens (Human)
Description:Q9H7B4-2
Residue:428
Sequence:
MEPLKVEKFATAKRGNGLRAVTPLRPGELLFRSDPLAYTVCKGSRGVVCDRCLLGKEKLM
RCSQCRVAKYCSAKCQKKAWPDHKRECKCLKSCKPRYPPDSVRLLGRVVFKLMDGAPSES
EKLYSFYDLESNINKLTEDKKEGLRQLVMTFQHFMREEIQDASQLPPAFDLFEAFAKVIC
NSFTICNAEMQEVGVGLYPSISLLNHSCDPNCSIVFNGPHLLLRAVRDIEVGEELTICYL
DMLMTSEERRKQLRDQYCFECDCFRCQTQDKDADMLTGDEQVWKEVQESLKKIEELKAHW
KWEQVLAMCQAIISSNSERLPDINIYQLKVLDCAMDACINLGLLEEALFYGTRTMEPYRI
FFPGSHPVRGVQVMKVGKLQLHQGMFPQAMKNLRLAFDIMRVTHGREHSLIEDLILLLEE
CDANIRAS
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM378459
n/a
NameBDBM378459
Synonyms:N-((1R,3r,5S)-8-((4-(benzylamino)piperidin-1-yl)sulfonyl)-8-azabicyclo[3.2.1]octan-3-yl)-6-chloro-2-oxoindoline-5-carboxamide | US10266526, Compound 592
TypeSmall organic molecule
Emp. Form.C28H34ClN5O4S
Mol. Mass.572.119
SMILESClc1cc2NC(=O)Cc2cc1C(=O)N[C@@H]1C[C@@H]2CC[C@H](C1)N2S(=O)(=O)N1CCC(CC1)NCc1ccccc1 |r,TLB:22:21:15.14.20:18.17|
Structure
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