+データを開く
-基本情報
登録情報 | データベース: PDB / ID: 1cwk | ||||||
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タイトル | HUMAN CYCLOPHILIN A COMPLEXED WITH 1-(6,7-DIHYDRO)MEBMT 2-VAL 3-D-(2-S-METHYL)SARCOSINE CYCLOSPORIN | ||||||
要素 |
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キーワード | ISOMERASE/IMMUNOSUPPRESSANT / ISOMERASE-IMMUNOSUPPRESSANT COMPLEX / CYCLOPHILIN-CYCLOSPORIN COMPLEX / CYCLOSPORIN D / IMMUNOSUPPRESSANT / CYCLOPHILIN | ||||||
機能・相同性 | 機能・相同性情報 negative regulation of protein K48-linked ubiquitination / regulation of apoptotic signaling pathway / cell adhesion molecule production / negative regulation of viral life cycle / lipid droplet organization / heparan sulfate binding / regulation of viral genome replication / virion binding / leukocyte chemotaxis / endothelial cell activation ...negative regulation of protein K48-linked ubiquitination / regulation of apoptotic signaling pathway / cell adhesion molecule production / negative regulation of viral life cycle / lipid droplet organization / heparan sulfate binding / regulation of viral genome replication / virion binding / leukocyte chemotaxis / endothelial cell activation / negative regulation of stress-activated MAPK cascade / Basigin interactions / cyclosporin A binding / Minus-strand DNA synthesis / Plus-strand DNA synthesis / Uncoating of the HIV Virion / Early Phase of HIV Life Cycle / Integration of provirus / APOBEC3G mediated resistance to HIV-1 infection / viral release from host cell / protein peptidyl-prolyl isomerization / Calcineurin activates NFAT / Binding and entry of HIV virion / positive regulation of viral genome replication / negative regulation of oxidative stress-induced intrinsic apoptotic signaling pathway / : / neutrophil chemotaxis / activation of protein kinase B activity / Gene and protein expression by JAK-STAT signaling after Interleukin-12 stimulation / negative regulation of protein phosphorylation / peptidylprolyl isomerase / positive regulation of protein secretion / peptidyl-prolyl cis-trans isomerase activity / negative regulation of protein kinase activity / Assembly Of The HIV Virion / Budding and maturation of HIV virion / neuron differentiation / platelet activation / platelet aggregation / SARS-CoV-1 activates/modulates innate immune responses / unfolded protein binding / integrin binding / protein folding / Platelet degranulation / positive regulation of NF-kappaB transcription factor activity / cellular response to oxidative stress / secretory granule lumen / vesicle / ficolin-1-rich granule lumen / positive regulation of MAPK cascade / positive regulation of protein phosphorylation / intracellular membrane-bounded organelle / focal adhesion / Neutrophil degranulation / apoptotic process / protein-containing complex / RNA binding / extracellular space / extracellular exosome / extracellular region / membrane / nucleus / cytosol / cytoplasm 類似検索 - 分子機能 | ||||||
生物種 | HOMO SAPIENS (ヒト) TOLYPOCLADIUM INFLATUM (菌類) | ||||||
手法 | X線回折 / PROTEIN STRUCTURE KNOWN IN THIS CELL / 解像度: 1.8 Å | ||||||
データ登録者 | Mikol, V. / Kallen, J. / Taylor, P. / Walkinshaw, M.D. | ||||||
引用 | ジャーナル: J.Mol.Biol. / 年: 1998 タイトル: X-Ray Structures and Analysis of 11 Cyclosporin Derivatives Complexed with Cyclophilin A. 著者: Kallen, J. / Mikol, V. / Taylor, P. / Walkinshaw, M.D. | ||||||
履歴 |
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-構造の表示
構造ビューア | 分子: MolmilJmol/JSmol |
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-ダウンロードとリンク
-ダウンロード
PDBx/mmCIF形式 | 1cwk.cif.gz | 48 KB | 表示 | PDBx/mmCIF形式 |
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PDB形式 | pdb1cwk.ent.gz | 36.3 KB | 表示 | PDB形式 |
PDBx/mmJSON形式 | 1cwk.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 | 1cwk_validation.pdf.gz | 380.3 KB | 表示 | wwPDB検証レポート |
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文書・詳細版 | 1cwk_full_validation.pdf.gz | 381.6 KB | 表示 | |
XML形式データ | 1cwk_validation.xml.gz | 5.8 KB | 表示 | |
CIF形式データ | 1cwk_validation.cif.gz | 8.7 KB | 表示 | |
アーカイブディレクトリ | https://data.pdbj.org/pub/pdb/validation_reports/cw/1cwk ftp://data.pdbj.org/pub/pdb/validation_reports/cw/1cwk | HTTPS FTP |
-関連構造データ
-リンク
-集合体
登録構造単位 |
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1 |
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単位格子 |
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-要素
#1: タンパク質 | 分子量: 18036.504 Da / 分子数: 1 / 由来タイプ: 組換発現 / 由来: (組換発現) HOMO SAPIENS (ヒト) / 遺伝子: CYCLOPHILIN / 遺伝子 (発現宿主): CYCLOPHILIN / 発現宿主: ESCHERICHIA COLI (大腸菌) 参照: UniProt: P05092, UniProt: P62937*PLUS, peptidylprolyl isomerase |
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#2: タンパク質・ペプチド | タイプ: Cyclic peptide / クラス: 免疫抑制剤 / 分子量: 1282.759 Da / 分子数: 1 / Mutation: YES / 由来タイプ: 合成 詳細: (2-S-METHYL) SARCOSINE AT POSITION 7,(6,7-DIHYDRO)4-[(E)-BUTENYL]-4, N-DIMETHYL-THREONINE AT POSITION 5, CYCLOSPORIN IS A CYCLIC UNDECAPEPTIDE. CYCLIZATION IS ACHIEVED BY LINKING THE N- AND ...詳細: (2-S-METHYL) SARCOSINE AT POSITION 7,(6,7-DIHYDRO)4-[(E)-BUTENYL]-4, N-DIMETHYL-THREONINE AT POSITION 5, CYCLOSPORIN IS A CYCLIC UNDECAPEPTIDE. CYCLIZATION IS ACHIEVED BY LINKING THE N- AND THE C- TERMINI. CYCLOSPORIN D IS A NATURAL ANALOG OF CYCLOSPORIN A, OBTAINED IN DIFFERENT NUTRIENT BROTH AND DIFFERS FROM CYCLOSPORIN IN RESIDUE 6 (ABA6VAL). THE CYCLOSPORIN D MOLECULE WAS MODIFIED AT POSITIONS 5 AND 7 TO BE (6,7-DIHYDRO)4-[(E)-BUTENYL]-4,N-DIMETHYL-THREONINE AND (2-S-METHYL)-SARCOSINE, RESPECTIVELY. 由来: (合成) TOLYPOCLADIUM INFLATUM (菌類) / 参照: NOR: NOR00036, CYCLOSPORIN D, 5,7 mutation |
#3: 水 | ChemComp-HOH / |
構成要素の詳細 | CYCLOSPORI |
-実験情報
-実験
実験 | 手法: X線回折 / 使用した結晶の数: 1 |
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-試料調製
結晶 | マシュー密度: 2.19 Å3/Da / 溶媒含有率: 41 % | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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結晶化 | pH: 8 / 詳細: PH 8.0 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
結晶 | *PLUS | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
結晶化 | *PLUS 温度: 295 K / 手法: 蒸気拡散法, ハンギングドロップ法 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
溶液の組成 | *PLUS
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-データ収集
回折 | 平均測定温度: 293 K |
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放射光源 | 由来: 回転陽極 / タイプ: ENRAF-NONIUS FR571 / 波長: 1.5418 |
検出器 | タイプ: ENRAF-NONIUS / 検出器: AREA DETECTOR / 日付: 1993年6月1日 |
放射 | モノクロメーター: GRAPHITE(002) / 単色(M)・ラウエ(L): M / 散乱光タイプ: x-ray |
放射波長 | 波長: 1.5418 Å / 相対比: 1 |
反射 | 最高解像度: 1.8 Å / Num. obs: 14288 / % possible obs: 92.3 % / Observed criterion σ(I): 2 / 冗長度: 3.2 % / Rsym value: 0.058 |
反射 | *PLUS Num. measured all: 45753 / Rmerge(I) obs: 0.058 |
-解析
ソフトウェア |
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精密化 | 構造決定の手法: PROTEIN STRUCTURE KNOWN IN THIS CELL 開始モデル: PDB ENTRY 1CWF 解像度: 1.8→8 Å / Data cutoff high absF: 30000 / Data cutoff low absF: 0.1 / σ(F): 2 /
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原子変位パラメータ | Biso mean: 18.87 Å2 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
精密化ステップ | サイクル: LAST / 解像度: 1.8→8 Å
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拘束条件 |
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Xplor file |
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