登録情報 | データベース: PDB / ID: 6squ |
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タイトル | Crystal structure of human SHIP2 catalytic domain in complex with 1,2,4 Dimer |
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要素 | Phosphatidylinositol 3,4,5-trisphosphate 5-phosphatase 2 |
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キーワード | HYDROLASE |
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機能・相同性 | 機能・相同性情報
negative regulation of insulin-like growth factor receptor signaling pathway / inositol-polyphosphate 5-phosphatase activity / phosphatidylinositol-3,4,5-trisphosphate 5-phosphatase / phosphatidylinositol-3,4,5-trisphosphate 5-phosphatase activity / ruffle assembly / regulation of actin filament organization / phosphatidylinositol dephosphorylation / endochondral ossification / phosphatidylinositol biosynthetic process / Synthesis of IP3 and IP4 in the cytosol ...negative regulation of insulin-like growth factor receptor signaling pathway / inositol-polyphosphate 5-phosphatase activity / phosphatidylinositol-3,4,5-trisphosphate 5-phosphatase / phosphatidylinositol-3,4,5-trisphosphate 5-phosphatase activity / ruffle assembly / regulation of actin filament organization / phosphatidylinositol dephosphorylation / endochondral ossification / phosphatidylinositol biosynthetic process / Synthesis of IP3 and IP4 in the cytosol / Synthesis of PIPs at the plasma membrane / establishment of mitotic spindle orientation / immune system process / Interleukin receptor SHC signaling / regulation of immune response / ERK1 and ERK2 cascade / SH2 domain binding / actin filament organization / basal plasma membrane / post-embryonic development / filopodium / response to insulin / phosphatidylinositol 3-kinase/protein kinase B signal transduction / SH3 domain binding / glucose metabolic process / endocytosis / spindle pole / Signaling by CSF1 (M-CSF) in myeloid cells / lamellipodium / regulation of protein localization / actin binding / gene expression / cell adhesion / nuclear speck / negative regulation of cell population proliferation / negative regulation of gene expression / apoptotic process / Golgi apparatus / nucleus / cytosol類似検索 - 分子機能 SHIP1/2 second C2 domain / SHIP1/2 first C2 domain / Inositol polyphosphate-related phosphatase / Endonuclease/Exonuclease/phosphatase family 2 / Inositol polyphosphate phosphatase, catalytic domain homologues / SAM domain (Sterile alpha motif) / Endonuclease/exonuclease/phosphatase superfamily / SAM domain profile. / Sterile alpha motif. / Sterile alpha motif domain ...SHIP1/2 second C2 domain / SHIP1/2 first C2 domain / Inositol polyphosphate-related phosphatase / Endonuclease/Exonuclease/phosphatase family 2 / Inositol polyphosphate phosphatase, catalytic domain homologues / SAM domain (Sterile alpha motif) / Endonuclease/exonuclease/phosphatase superfamily / SAM domain profile. / Sterile alpha motif. / Sterile alpha motif domain / Sterile alpha motif/pointed domain superfamily / SH2 domain / Src homology 2 (SH2) domain profile. / Src homology 2 domains / SH2 domain / SH2 domain superfamily類似検索 - ドメイン・相同性 Chem-D7I / Phosphatidylinositol 3,4,5-trisphosphate 5-phosphatase 2類似検索 - 構成要素 |
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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: 2.27 Å |
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データ登録者 | Whitfield, H. / Brearley, C.A. / Hemmings, A.M. |
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引用 | ジャーナル: J.Med.Chem. / 年: 2021 タイトル: Allosteric Site on SHIP2 Identified Through Fluorescent Ligand Screening and Crystallography: A Potential New Target for Intervention. 著者: Whitfield, H. / Hemmings, A.M. / Mills, S.J. / Baker, K. / White, G. / Rushworth, S. / Riley, A.M. / Potter, B.V.L. / Brearley, C.A. |
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履歴 | 登録 | 2019年9月4日 | 登録サイト: PDBE / 処理サイト: PDBE |
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改定 1.0 | 2021年1月13日 | Provider: repository / タイプ: Initial release |
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改定 1.1 | 2021年7月28日 | Group: Database references / カテゴリ: citation / citation_author Item: _citation.country / _citation.journal_abbrev ..._citation.country / _citation.journal_abbrev / _citation.journal_id_ASTM / _citation.journal_id_CSD / _citation.journal_id_ISSN / _citation.journal_volume / _citation.page_first / _citation.page_last / _citation.pdbx_database_id_DOI / _citation.pdbx_database_id_PubMed / _citation.title / _citation.year |
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改定 1.2 | 2024年1月24日 | Group: Data collection / Database references / Refinement description カテゴリ: chem_comp_atom / chem_comp_bond ...chem_comp_atom / chem_comp_bond / database_2 / pdbx_initial_refinement_model Item: _database_2.pdbx_DOI / _database_2.pdbx_database_accession |
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