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TargetS-adenosylmethionine synthase
LigandBDBM102425
Substrate/Competitorn/a
Meas. Tech.Inhibition Assay
IC50 2.1e+3±n/a nM
Citation Zhang, WSviripa, VChen, XShi, JYu, THamza, AWard, NDKril, LMVander Kooi, CWZhan, CGEvers, BMWatt, DSLiu, C Fluorinated N,N-dialkylaminostilbenes repress colon cancer by targeting methionine S-adenosyltransferase 2A. ACS Chem Biol8:796-803 (2013) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
S-adenosylmethionine synthase
Name:S-adenosylmethionine synthase
Synonyms:Chain A, S-adenosylmethionine Synthetase | MAT2A | METK_ECOSM | metK
Type:n/a
Mol. Mass.:41940.55
Organism:Escherichia coli
Description:B1LDF1
Residue:384
Sequence:
MAKHLFTSESVSEGHPDKIADQISDAVLDAILEQDPKARVACETYVKTGMVLVGGEITTS
AWVDIEEITRNTVREIGYVHSDMGFDANSCAVLSAIGKQSPDINQGVDRADPLEQGAGDQ
GLMFGYATNETDVLMPAPITYAHRLVQRQAEVRKNGTLPWLRPDAKSQVTFQYDDGKIVG
IDAVVLSTQHSEEIDQKSLQEAVMEEIIKPILPAEWLTSATKFFINPTGRFVIGGPMGDC
GLTGRKIIVDTYGGMARHGGGAFSGKDPSKVDRSAAYAARYVAKNIVAAGLADRCEIQVS
YAIGVAEPTSIMVETFGTEKVPSEQLTLLVREFFDLRPYGLIQMLDLLHPIYKETAAYGH
FGREHFPWEKTDKAQLLRDAAGLK
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  Blast E-value cutoff:
BDBM102425
n/a
NameBDBM102425
Synonyms:FIDAS-5 | Fluorinated N,N-Dialkylaminostilbenes 5
TypeSmall organic molecule
Emp. Form.C15H13ClFN
Mol. Mass.261.722
SMILESCNc1ccc(\C=C\c2c(F)cccc2Cl)cc1
Structure
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