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データを開く
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基本情報
| 登録情報 | データベース: PDB / ID: 1jst | ||||||
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| タイトル | PHOSPHORYLATED CYCLIN-DEPENDENT KINASE-2 BOUND TO CYCLIN A | ||||||
要素 |
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キーワード | COMPLEX (PROTEIN KINASE/CYCLIN) / COMPLEX (PROTEIN KINASE-CYCLIN) / CYCLIN / CDK / PHOSPHORYLATION / COMPLEX (PROTEIN KINASE-CYCLIN) complex | ||||||
| 機能・相同性 | 機能・相同性情報: / cyclin A2-CDK1 complex / cell cycle G1/S phase transition / cellular response to luteinizing hormone stimulus / Transcription of E2F targets under negative control by p107 (RBL1) and p130 (RBL2) in complex with HDAC1 / cellular response to leptin stimulus / male pronucleus / female pronucleus / cellular response to cocaine / response to glucagon ...: / cyclin A2-CDK1 complex / cell cycle G1/S phase transition / cellular response to luteinizing hormone stimulus / Transcription of E2F targets under negative control by p107 (RBL1) and p130 (RBL2) in complex with HDAC1 / cellular response to leptin stimulus / male pronucleus / female pronucleus / cellular response to cocaine / response to glucagon / positive regulation of DNA biosynthetic process / cyclin-dependent protein serine/threonine kinase regulator activity / cellular response to insulin-like growth factor stimulus / cyclin A1-CDK2 complex / cyclin E2-CDK2 complex / cyclin E1-CDK2 complex / cyclin A2-CDK2 complex / positive regulation of DNA-templated DNA replication initiation / G2 Phase / Y chromosome / cyclin-dependent protein kinase activity / Phosphorylation of proteins involved in G1/S transition by active Cyclin E:Cdk2 complexes / positive regulation of heterochromatin formation / p53-Dependent G1 DNA Damage Response / X chromosome / PTK6 Regulates Cell Cycle / regulation of anaphase-promoting complex-dependent catabolic process / Defective binding of RB1 mutants to E2F1,(E2F2, E2F3) / centriole replication / Regulation of APC/C activators between G1/S and early anaphase / microtubule organizing center / regulation of DNA replication / telomere maintenance in response to DNA damage / centrosome duplication / G0 and Early G1 / cochlea development / Telomere Extension By Telomerase / animal organ regeneration / Activation of the pre-replicative complex / cyclin-dependent kinase / cyclin-dependent protein serine/threonine kinase activity / TP53 Regulates Transcription of Genes Involved in G1 Cell Cycle Arrest / Regulation of MITF-M-dependent genes involved in cell cycle and proliferation / Cajal body / Activation of ATR in response to replication stress / Cyclin E associated events during G1/S transition / Cyclin A/B1/B2 associated events during G2/M transition / Cyclin A:Cdk2-associated events at S phase entry / cyclin-dependent protein kinase holoenzyme complex / condensed chromosome / regulation of G2/M transition of mitotic cell cycle / cellular response to platelet-derived growth factor stimulus / mitotic G1 DNA damage checkpoint signaling / cellular response to nitric oxide / post-translational protein modification / cyclin binding / regulation of mitotic cell cycle / positive regulation of DNA replication / meiotic cell cycle / male germ cell nucleus / Cdc20:Phospho-APC/C mediated degradation of Cyclin A / cellular response to estradiol stimulus / G1/S transition of mitotic cell cycle / peptidyl-serine phosphorylation / DNA Damage/Telomere Stress Induced Senescence / potassium ion transport / CDK-mediated phosphorylation and removal of Cdc6 / Meiotic recombination / SCF(Skp2)-mediated degradation of p27/p21 / G2/M transition of mitotic cell cycle / Transcriptional regulation of granulopoiesis / Orc1 removal from chromatin / positive regulation of fibroblast proliferation / Cyclin D associated events in G1 / cellular senescence / Regulation of TP53 Degradation / nuclear envelope / Factors involved in megakaryocyte development and platelet production / Processing of DNA double-strand break ends / regulation of gene expression / Senescence-Associated Secretory Phenotype (SASP) / transcription regulator complex / cellular response to hypoxia / Regulation of TP53 Activity through Phosphorylation / Ras protein signal transduction / chromosome, telomeric region / DNA replication / protein phosphorylation / endosome / Ub-specific processing proteases / chromatin remodeling / protein domain specific binding / cell division / protein serine kinase activity / DNA repair / protein serine/threonine kinase activity / positive regulation of cell population proliferation / DNA-templated transcription / centrosome / protein kinase binding 類似検索 - 分子機能 | ||||||
| 生物種 | Homo sapiens (ヒト) | ||||||
| 手法 | X線回折 / シンクロトロン / 解像度: 2.6 Å | ||||||
データ登録者 | Russo, A.A. / Jeffrey, P.D. / Pavletich, N.P. | ||||||
引用 | ジャーナル: Nat.Struct.Biol. / 年: 1996タイトル: Structural basis of cyclin-dependent kinase activation by phosphorylation. 著者: Russo, A.A. / Jeffrey, P.D. / Pavletich, N.P. | ||||||
| 履歴 |
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構造の表示
| 構造ビューア | 分子: Molmil Jmol/JSmol |
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ダウンロードとリンク
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ダウンロード
| PDBx/mmCIF形式 | 1jst.cif.gz | 233.4 KB | 表示 | PDBx/mmCIF形式 |
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| PDB形式 | pdb1jst.ent.gz | 187.7 KB | 表示 | PDB形式 |
| PDBx/mmJSON形式 | 1jst.json.gz | ツリー表示 | PDBx/mmJSON形式 | |
| その他 | その他のダウンロード |
-検証レポート
| 文書・要旨 | 1jst_validation.pdf.gz | 544 KB | 表示 | wwPDB検証レポート |
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| 文書・詳細版 | 1jst_full_validation.pdf.gz | 591.1 KB | 表示 | |
| XML形式データ | 1jst_validation.xml.gz | 29.4 KB | 表示 | |
| CIF形式データ | 1jst_validation.cif.gz | 43.4 KB | 表示 | |
| アーカイブディレクトリ | https://data.pdbj.org/pub/pdb/validation_reports/js/1jst ftp://data.pdbj.org/pub/pdb/validation_reports/js/1jst | HTTPS FTP |
-関連構造データ
| 類似構造データ |
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リンク
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集合体
| 登録構造単位 | ![]()
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| 単位格子 |
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要素
| #1: タンパク質 | 分子量: 34056.469 Da / 分子数: 2 / 由来タイプ: 組換発現 / 詳細: PHOSPHORYLATED / 由来: (組換発現) Homo sapiens (ヒト)解説: CYCLIN A-BOUND FORM PHOSPHORYLATED ON THR 160 IN VITRO USING A CDK-ACTIVATING KINASE CONSISTING OF THE CYCLINH-CDK7 COMPLEX; 細胞株: SF9 / プラスミド: PET3A 発現宿主: ![]() 株 (発現宿主): SF9 参照: UniProt: P24941, 転移酵素; リンを含む基を移すもの; キナーゼ(アルコールにつなげるもの) #2: タンパク質 | 分子量: 29624.297 Da / 分子数: 2 / Fragment: RESIDUES 173-432 / 由来タイプ: 組換発現 / 由来: (組換発現) Homo sapiens (ヒト)解説: THE FRAGMENT USED IN THE CRYSTALLIZATION (RESIDUES 173-432) WAS PRODUCED BY THE CLEAVAGE OF FULL-LENGTH CYCLIN A BY SUBTILISIN 細胞株: SF9 / プラスミド: PET3A / 発現宿主: ![]() #3: 化合物 | #4: 化合物 | #5: 水 | ChemComp-HOH / | Has protein modification | Y | |
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-実験情報
-実験
| 実験 | 手法: X線回折 |
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試料調製
| 結晶 | マシュー密度: 3.03 Å3/Da / 溶媒含有率: 59.41 % | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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| 結晶化 | *PLUS 温度: 4 ℃ / pH: 7 / 手法: 蒸気拡散法, ハンギングドロップ法 / 詳細: Jeffrey, P.D., (1995) Nature, 376, 313. | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| 溶液の組成 | *PLUS
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-データ収集
| 放射光源 | 由来: シンクロトロン / サイト: CHESS / ビームライン: A1 / 波長: 0.92 |
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| 検出器 | 検出器: CCD / 日付: 1995年12月22日 |
| 放射 | 単色(M)・ラウエ(L): M / 散乱光タイプ: x-ray |
| 放射波長 | 波長: 0.92 Å / 相対比: 1 |
| 反射 | % possible obs: 98.9 % / 冗長度: 6 % / Rmerge(I) obs: 0.066 |
| 反射 | *PLUS 最高解像度: 2.6 Å / 最低解像度: 20 Å / Num. obs: 48448 / Num. measured all: 290942 |
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解析
| ソフトウェア |
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| 精密化 | 解像度: 2.6→7 Å / σ(F): 2 /
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| 精密化ステップ | サイクル: LAST / 解像度: 2.6→7 Å
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| 拘束条件 |
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| ソフトウェア | *PLUS 名称: TNT / 分類: refinement | ||||||||||||||||||||||||||||||||||||||||
| 精密化 | *PLUS Rfactor obs: 0.2 / Rfactor Rwork: 0.2 | ||||||||||||||||||||||||||||||||||||||||
| 溶媒の処理 | *PLUS | ||||||||||||||||||||||||||||||||||||||||
| 原子変位パラメータ | *PLUS |
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万見について




Homo sapiens (ヒト)
X線回折
引用

















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