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TargetSodium- and chloride-dependent glycine transporter 2
LigandBDBM50056486
Substrate/Competitorn/a
Meas. Tech.ChEMBL_1935501 (CHEMBL4481260)
IC50 9000±n/a nM
Citation Mostyn, SNRawling, TMohammadi, SShimmon, SFrangos, ZJSarker, SYousuf, AVetter, IRyan, RMChristie, MJVandenberg, RJ Development of an N-Acyl Amino Acid That Selectively Inhibits the Glycine Transporter 2 To Produce Analgesia in a Rat Model of Chronic Pain. J Med Chem62:2466-2484 (2019) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Sodium- and chloride-dependent glycine transporter 2
Name:Sodium- and chloride-dependent glycine transporter 2
Synonyms:GLYT2 | Glycine transporter 2 | NET1 | SC6A5_HUMAN | SLC6A5 | Sodium- and chloride-dependent glycine transporter 2
Type:Enzyme Catalytic Domain
Mol. Mass.:87438.56
Organism:Homo sapiens (Human)
Description:Glycine-2-transporter 0 HUMAN::Q9Y345
Residue:797
Sequence:
MDCSAPKEMNKLPANSPEAAAAQGHPDGPCAPRTSPEQELPAAAAPPPPRVPRSASTGAQ
TFQSADARACEAERPGVGSCKLSSPRAQAASAALRDLREAQGAQASPPPGSSGPGNALHC
KIPFLRGPEGDANVSVGKGTLERNNTPVVGWVNMSQSTVVLATDGITSVLPGSVATVATQ
EDEQGDENKARGNWSSKLDFILSMVGYAVGLGNVWRFPYLAFQNGGGAFLIPYLMMLALA
GLPIFFLEVSLGQFASQGPVSVWKAIPALQGCGIAMLIISVLIAIYYNVIICYTLFYLFA
SFVSVLPWGSCNNPWNTPECKDKTKLLLDSCVISDHPKIQIKNSTFCMTAYPNVTMVNFT
SQANKTFVSGSEEYFKYFVLKISAGIEYPGEIRWPLALCLFLAWVIVYASLAKGIKTSGK
VVYFTATFPYVVLVILLIRGVTLPGAGAGIWYFITPKWEKLTDATVWKDAATQIFFSLSA
AWGGLITLSSYNKFHNNCYRDTLIVTCTNSATSIFAGFVIFSVIGFMANERKVNIENVAD
QGPGIAFVVYPEALTRLPLSPFWAIIFFLMLLTLGLDTMFATIETIVTSISDEFPKYLRT
HKPVFTLGCCICFFIMGFPMITQGGIYMFQLVDTYAASYALVIIAIFELVGISYVYGLQR
FCEDIEMMIGFQPNIFWKVCWAFVTPTILTFILCFSFYQWEPMTYGSYRYPNWSMVLGWL
MLACSVIWIPIMFVIKMHLAPGRFIERLKLVCSPQPDWGPFLAQHRGERYKNMIDPLGTS
SLGLKLPVKDLELGTQC
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  Blast E-value cutoff:
BDBM50056486
n/a
NameBDBM50056486
Synonyms:((5Z,8Z)-Icosa-5,8,11,14-tetraenoylamino)-acetic acid | ((5Z,8Z,11Z,14Z)-Icosa-5,8,11,14-tetraenoylamino)-acetic acid | Arachidonoyl glycine | CHEMBL161343
TypeSmall organic molecule
Emp. Form.C22H35NO3
Mol. Mass.361.5182
SMILESCCCCC\C=C/C\C=C/C\C=C/C\C=C/CCCC(=O)NCC(O)=O
Structure
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