登録情報 | データベース: PDB / ID: 4ewh |
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タイトル | Co-crystal structure of ACK1 with inhibitor |
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要素 | Activated CDC42 kinase 1 |
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キーワード | TRANSFERASE/TRANSFERASE INHIBITOR / Drug Design / Enzyme Inhibitors / TRANSFERASE-TRANSFERASE INHIBITOR complex |
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機能・相同性 | 機能・相同性情報
regulation of clathrin-dependent endocytosis / regulation of keratinocyte differentiation / Grb2-EGFR complex / GTPase inhibitor activity / cytoophidium / WW domain binding / clathrin-coated vesicle / epidermal growth factor receptor binding / small GTPase-mediated signal transduction / negative regulation of epidermal growth factor receptor signaling pathway ...regulation of clathrin-dependent endocytosis / regulation of keratinocyte differentiation / Grb2-EGFR complex / GTPase inhibitor activity / cytoophidium / WW domain binding / clathrin-coated vesicle / epidermal growth factor receptor binding / small GTPase-mediated signal transduction / negative regulation of epidermal growth factor receptor signaling pathway / clathrin-coated pit / protein serine/threonine/tyrosine kinase activity / adherens junction / non-specific protein-tyrosine kinase / non-membrane spanning protein tyrosine kinase activity / cytoplasmic vesicle membrane / endocytosis / positive regulation of peptidyl-tyrosine phosphorylation / protein tyrosine kinase activity / cell surface receptor signaling pathway / non-specific serine/threonine protein kinase / endosome / phosphorylation / intracellular membrane-bounded organelle / protein serine kinase activity / protein serine/threonine kinase activity / ubiquitin protein ligase binding / perinuclear region of cytoplasm / ATP binding / identical protein binding / membrane / nucleus / metal ion binding / plasma membrane / cytoplasm / cytosol類似検索 - 分子機能 Activated CDC42 kinase 1 / Cdc42 binding domain-like superfamily / : / Cdc42 binding domain-like / Mig-6 domain / GTPase binding / EGFR receptor inhibitor Mig-6 / Variant SH3 domain / Src homology 3 domains / SH3-like domain superfamily ...Activated CDC42 kinase 1 / Cdc42 binding domain-like superfamily / : / Cdc42 binding domain-like / Mig-6 domain / GTPase binding / EGFR receptor inhibitor Mig-6 / Variant SH3 domain / Src homology 3 domains / SH3-like domain superfamily / Src homology 3 (SH3) domain profile. / SH3 domain / Tyrosine-protein kinase, catalytic domain / Tyrosine kinase, catalytic domain / Tyrosine protein kinases specific active-site signature. / Tyrosine-protein kinase, active site / Protein tyrosine and serine/threonine kinase / Serine-threonine/tyrosine-protein kinase, catalytic domain / Transferase(Phosphotransferase) domain 1 / Transferase(Phosphotransferase); domain 1 / Phosphorylase Kinase; domain 1 / Phosphorylase Kinase; domain 1 / Protein kinase, ATP binding site / Protein kinases ATP-binding region signature. / Protein kinase domain profile. / Protein kinase domain / Protein kinase-like domain superfamily / 2-Layer Sandwich / Orthogonal Bundle / Mainly Alpha / Alpha Beta類似検索 - ドメイン・相同性 |
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生物種 | Homo sapiens (ヒト) |
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手法 | X線回折 / シンクロトロン / 分子置換 / 解像度: 2.5 Å |
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データ登録者 | Liu, J. / Walker, N. / Wang, Z. |
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引用 | ジャーナル: Bioorg.Med.Chem.Lett. / 年: 2012 タイトル: Synthesis and optimization of substituted furo[2,3-d]-pyrimidin-4-amines and 7H-pyrrolo[2,3-d]pyrimidin-4-amines as ACK1 inhibitors. 著者: Jiao, X. / Kopecky, D.J. / Liu, J. / Liu, J. / Jaen, J.C. / Cardozo, M.G. / Sharma, R. / Walker, N. / Wesche, H. / Li, S. / Farrelly, E. / Xiao, S.H. / Wang, Z. / Kayser, F. |
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履歴 | 登録 | 2012年4月27日 | 登録サイト: RCSB / 処理サイト: RCSB |
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改定 1.0 | 2012年9月19日 | Provider: repository / タイプ: Initial release |
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改定 1.1 | 2012年10月31日 | Group: Database references |
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