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5KZQ

Metabotropic Glutamate Receptor in complex with antagonist (1~{S},2~{R},3~{S},4~{S},5~{R},6~{R})-2-azanyl-3-[[3,4-bis(fluoranyl)phenyl]sulfanylmethyl]-4-oxidanyl-bicyclo[3.1.0]hexane-2,6-dicarboxylic acid

5KZQ の概要
エントリーDOI10.2210/pdb5kzq/pdb
関連するPDBエントリー5KZN
分子名称Metabotropic glutamate receptor 2, (1~{S},2~{R},3~{S},4~{S},5~{R},6~{R})-2-azanyl-3-[[3,4-bis(fluoranyl)phenyl]sulfanylmethyl]-4-oxidanyl-bicyclo[3.1.0]hexane-2,6-dicarboxylic acid, 2-acetamido-2-deoxy-beta-D-glucopyranose, ... (4 entities in total)
機能のキーワードmglur2, antagonist, antidepressent, signaling protein
由来する生物種Homo sapiens (Human)
タンパク質・核酸の鎖数1
化学式量合計63891.11
構造登録者
主引用文献Chappell, M.D.,Li, R.,Smith, S.C.,Dressman, B.A.,Tromiczak, E.G.,Tripp, A.E.,Blanco, M.J.,Vetman, T.,Quimby, S.J.,Matt, J.,Britton, T.C.,Fivush, A.M.,Schkeryantz, J.M.,Mayhugh, D.,Erickson, J.A.,Bures, M.G.,Jaramillo, C.,Carpintero, M.,Diego, J.E.,Barberis, M.,Garcia-Cerrada, S.,Soriano, J.F.,Antonysamy, S.,Atwell, S.,MacEwan, I.,Condon, B.,Sougias, C.,Wang, J.,Zhang, A.,Conners, K.,Groshong, C.,Wasserman, S.R.,Koss, J.W.,Witkin, J.M.,Li, X.,Overshiner, C.,Wafford, K.A.,Seidel, W.,Wang, X.S.,Heinz, B.A.,Swanson, S.,Catlow, J.T.,Bedwell, D.W.,Monn, J.A.,Mitch, C.H.,Ornstein, P.L.
Discovery of (1S,2R,3S,4S,5R,6R)-2-Amino-3-[(3,4-difluorophenyl)sulfanylmethyl]-4-hydroxy-bicyclo[3.1.0]hexane-2,6-dicarboxylic Acid Hydrochloride (LY3020371HCl): A Potent, Metabotropic Glutamate 2/3 Receptor Antagonist with Antidepressant-Like Activity.
J. Med. Chem., 59:10974-10993, 2016
Cited by
PubMed Abstract: As part of our ongoing efforts to identify novel ligands for the metabotropic glutamate 2 and 3 (mGlu) receptors, we have incorporated substitution at the C3 and C4 positions of the (1S,2R,5R,6R)-2-amino-bicyclo[3.1.0]hexane-2,6-dicarboxylic acid scaffold to generate mGlu antagonists. Exploration of this structure-activity relationship (SAR) led to the identification of (1S,2R,3S,4S,5R,6R)-2-amino-3-[(3,4-difluorophenyl)sulfanylmethyl]-4-hydroxy-bicyclo[3.1.0]hexane-2,6-dicarboxylic acid hydrochloride (LY3020371·HCl, 19f), a potent, selective, and maximally efficacious mGlu antagonist. Further characterization of compound 19f binding to the human metabotropic 2 glutamate (hmGlu) site was established by cocrystallization of this molecule with the amino terminal domain (ATD) of the hmGlu receptor protein. The resulting cocrystal structure revealed the specific ligand-protein interactions, which likely explain the high affinity of 19f for this site and support its functional mGlu antagonist pharmacology. Further characterization of 19f in vivo demonstrated an antidepressant-like signature in the mouse forced-swim test (mFST) assay when brain levels of this compound exceeded the cellular mGlu IC value.
PubMed: 28002967
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2.8 Å)
構造検証レポート
Validation report summary of 5kzq
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件を2024-11-13に公開中

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