Structure of PDB 3bft Chain A Binding Site BS01
Receptor Information
>3bft Chain A (length=259) Species:
10116
(Rattus norvegicus) [
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NKTVVVTTILESPYVMMKKNHEMLEGNERYEGYCVDLAAEIAKHCGFKYK
LTIVGDGKYGARDADTKIWNGMVGELVYGKADIAIAPLTITLVREEVIDF
SKPFMSLGISIMIKKGTPIESAEDLSKQTEIAYGTLDSGSTKEFFRRSKI
AVFDKMWTYMRSAEPSVFVRTTAEGVARVRKSKGKYAYLLESTMNEYIEQ
RKPCDTMKVGGNLDSKGYGIATPKGSSLGNAVNLAVLKLNEQGLLDKLKN
KWWYDKGEC
Ligand information
Ligand ID
S2P
InChI
InChI=1S/C5H7N3O3S/c6-2(5(10)11)1-3-4(9)8-12-7-3/h2H,1,6H2,(H,8,9)(H,10,11)/t2-/m0/s1
InChIKey
SEVVPWOEIHLQGH-REOHCLBHSA-N
SMILES
Software
SMILES
CACTVS 3.341
N[C@@H](Cc1nsnc1O)C(O)=O
ACDLabs 10.04
O=C(O)C(N)Cc1nsnc1O
OpenEye OEToolkits 1.5.0
C(c1c(nsn1)O)[C@@H](C(=O)O)N
CACTVS 3.341
N[CH](Cc1nsnc1O)C(O)=O
OpenEye OEToolkits 1.5.0
C(c1c(nsn1)O)C(C(=O)O)N
Formula
C5 H7 N3 O3 S
Name
(2S)-2-amino-3-(4-hydroxy-1,2,5-thiadiazol-3-yl)propanoic acid
ChEMBL
CHEMBL429594
DrugBank
ZINC
PDB chain
3bft Chain A Residue 1009 [
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Receptor-Ligand Complex Structure
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PDB
3bft
Structures of the ligand-binding core of iGluR2 in complex with the agonists (R)- and (S)-2-amino-3-(4-hydroxy-1,2,5-thiadiazol-3-yl)propionic acid explain their unusual equipotency.
Resolution
2.27 Å
Binding residue
(original residue number in PDB)
Y61 T91 R96 G141 S142 T143 E193 M196
Binding residue
(residue number reindexed from 1)
Y59 T89 R94 G139 S140 T141 E191 M194
Annotation score
1
Binding affinity
MOAD
: Ki=323nM
PDBbind-CN
: -logKd/Ki=6.49,Ki=323nM
Enzymatic activity
Enzyme Commision number
?
Gene Ontology
Molecular Function
GO:0015276
ligand-gated monoatomic ion channel activity
Cellular Component
GO:0016020
membrane
View graph for
Molecular Function
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Cellular Component
External links
PDB
RCSB:3bft
,
PDBe:3bft
,
PDBj:3bft
PDBsum
3bft
PubMed
18269227
UniProt
P19491
|GRIA2_RAT Glutamate receptor 2 (Gene Name=Gria2)
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