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- PDB-8bur: Structure of DDB1 bound to DS50-engaged CDK12-cyclin K -

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基本情報

登録情報
データベース: PDB / ID: 8bur
タイトルStructure of DDB1 bound to DS50-engaged CDK12-cyclin K
要素
  • Cyclin-K
  • Cyclin-dependent kinase 12
  • DNA damage-binding protein 1
キーワードLIGASE / kinase / cyclin / ubiquitin / degrader
機能・相同性
機能・相同性情報


cyclin K-CDK12 complex / cyclin K-CDK13 complex / nuclear cyclin-dependent protein kinase holoenzyme complex / regulation of MAP kinase activity / cyclin/CDK positive transcription elongation factor complex / host-mediated suppression of viral genome replication / negative regulation of intracellular estrogen receptor signaling pathway / positive regulation by virus of viral protein levels in host cell / negative regulation of stem cell differentiation / spindle assembly involved in female meiosis ...cyclin K-CDK12 complex / cyclin K-CDK13 complex / nuclear cyclin-dependent protein kinase holoenzyme complex / regulation of MAP kinase activity / cyclin/CDK positive transcription elongation factor complex / host-mediated suppression of viral genome replication / negative regulation of intracellular estrogen receptor signaling pathway / positive regulation by virus of viral protein levels in host cell / negative regulation of stem cell differentiation / spindle assembly involved in female meiosis / regulation of cyclin-dependent protein serine/threonine kinase activity / epigenetic programming in the zygotic pronuclei / cyclin-dependent protein serine/threonine kinase activator activity / UV-damage excision repair / [RNA-polymerase]-subunit kinase / positive regulation of DNA-templated transcription, elongation / biological process involved in interaction with symbiont / regulation of mitotic cell cycle phase transition / WD40-repeat domain binding / Cul4A-RING E3 ubiquitin ligase complex / Cul4-RING E3 ubiquitin ligase complex / Cul4B-RING E3 ubiquitin ligase complex / ubiquitin ligase complex scaffold activity / negative regulation of reproductive process / negative regulation of developmental process / cullin family protein binding / viral release from host cell / RNA polymerase II transcribes snRNA genes / HIV elongation arrest and recovery / Pausing and recovery of HIV elongation / cellular response to estrogen stimulus / regulation of signal transduction / ectopic germ cell programmed cell death / cyclin-dependent kinase / cyclin-dependent protein serine/threonine kinase activity / positive regulation of viral genome replication / Formation of HIV elongation complex in the absence of HIV Tat / proteasomal protein catabolic process / RNA Polymerase II Transcription Elongation / negative regulation of MAPK cascade / Formation of RNA Pol II elongation complex / RNA Polymerase II Pre-transcription Events / positive regulation of gluconeogenesis / RNA polymerase II CTD heptapeptide repeat kinase activity / RNA splicing / cyclin binding / SMAD2/SMAD3:SMAD4 heterotrimer regulates transcription / Recognition of DNA damage by PCNA-containing replication complex / DNA Damage Recognition in GG-NER / nucleotide-excision repair / TP53 Regulates Transcription of DNA Repair Genes / Dual Incision in GG-NER / Transcription-Coupled Nucleotide Excision Repair (TC-NER) / positive regulation of transcription elongation by RNA polymerase II / Formation of TC-NER Pre-Incision Complex / Formation of Incision Complex in GG-NER / regulation of circadian rhythm / Dual incision in TC-NER / Gap-filling DNA repair synthesis and ligation in TC-NER / Wnt signaling pathway / mRNA processing / positive regulation of protein catabolic process / cellular response to UV / rhythmic process / site of double-strand break / Neddylation / ubiquitin-dependent protein catabolic process / protein-macromolecule adaptor activity / damaged DNA binding / proteasome-mediated ubiquitin-dependent protein catabolic process / transcription by RNA polymerase II / chromosome, telomeric region / protein ubiquitination / protein kinase activity / nuclear speck / cell division / protein serine kinase activity / DNA repair / apoptotic process / DNA damage response / protein kinase binding / negative regulation of apoptotic process / protein-containing complex binding / nucleolus / positive regulation of transcription by RNA polymerase II / protein-containing complex / extracellular space / DNA binding / extracellular exosome / nucleoplasm / ATP binding / nucleus / cytoplasm
類似検索 - 分子機能
Cyclin-T2-like, C-terminal domain / DNA polymerase; domain 1 - #910 / Cyclin/Cyclin-like subunit Ssn8 / Cyclin, C-terminal domain / Cyclin_C / RSE1/DDB1/CPSF1 second beta-propeller / Cleavage/polyadenylation specificity factor, A subunit, C-terminal / Cleavage/polyadenylation specificity factor, A subunit, N-terminal / : / CPSF A subunit region ...Cyclin-T2-like, C-terminal domain / DNA polymerase; domain 1 - #910 / Cyclin/Cyclin-like subunit Ssn8 / Cyclin, C-terminal domain / Cyclin_C / RSE1/DDB1/CPSF1 second beta-propeller / Cleavage/polyadenylation specificity factor, A subunit, C-terminal / Cleavage/polyadenylation specificity factor, A subunit, N-terminal / : / CPSF A subunit region / RSE1/DDB1/CPSF1 first beta-propeller / Cyclin, N-terminal / Cyclin, N-terminal domain / Cyclin-like / domain present in cyclins, TFIIB and Retinoblastoma / Cyclin-like superfamily / : / YVTN repeat-like/Quinoprotein amine dehydrogenase / 7 Propeller / Methylamine Dehydrogenase; Chain H / DNA polymerase; domain 1 / Phosphorylase Kinase; domain 1 / Phosphorylase Kinase; domain 1 / Transferase(Phosphotransferase) domain 1 / Transferase(Phosphotransferase); domain 1 / Serine/threonine-protein kinase, active site / Serine/Threonine protein kinases active-site signature. / WD40-repeat-containing domain superfamily / Protein kinase domain / Serine/Threonine protein kinases, catalytic domain / WD40/YVTN repeat-like-containing domain superfamily / 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 Beta / Mainly Alpha / Alpha Beta
類似検索 - ドメイン・相同性
Chem-RQU / Cyclin-K / DNA damage-binding protein 1 / Cyclin-dependent kinase 12
類似検索 - 構成要素
生物種Homo sapiens (ヒト)
手法X線回折 / シンクロトロン / 分子置換 / 解像度: 3.64 Å
データ登録者Kozicka, Z. / Kempf, G. / Focht, V. / Thoma, N.H.
資金援助European Union, スイス, 7件
組織認可番号
European Research Council (ERC)666068European Union
Swiss National Science Foundation31003A_179541 スイス
Swiss National Science Foundation310030_301206 スイス
Swiss Cancer League4980-02-2020 スイス
Swiss National Science FoundationCRSII5_186230 スイス
Marie Sklodowska-Curie Actions, FragNET ITN765445European Union
Other private スイス
引用ジャーナル: Nat.Chem.Biol. / : 2024
タイトル: Design principles for cyclin K molecular glue degraders.
著者: Kozicka, Z. / Suchyta, D.J. / Focht, V. / Kempf, G. / Petzold, G. / Jentzsch, M. / Zou, C. / Di Genua, C. / Donovan, K.A. / Coomar, S. / Cigler, M. / Mayor-Ruiz, C. / Schmid-Burgk, J.L. / ...著者: Kozicka, Z. / Suchyta, D.J. / Focht, V. / Kempf, G. / Petzold, G. / Jentzsch, M. / Zou, C. / Di Genua, C. / Donovan, K.A. / Coomar, S. / Cigler, M. / Mayor-Ruiz, C. / Schmid-Burgk, J.L. / Haussinger, D. / Winter, G.E. / Fischer, E.S. / Slabicki, M. / Gillingham, D. / Ebert, B.L. / Thoma, N.H.
履歴
登録2022年11月30日登録サイト: PDBE / 処理サイト: PDBE
改定 1.02023年9月13日Provider: repository / タイプ: Initial release
改定 1.12024年3月27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_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
改定 1.22024年10月9日Group: Structure summary
カテゴリ: pdbx_entry_details / pdbx_modification_feature
Item: _pdbx_entry_details.has_protein_modification

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構造の表示

構造ビューア分子:
MolmilJmol/JSmol

ダウンロードとリンク

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集合体

登録構造単位
D: DNA damage-binding protein 1
E: Cyclin-dependent kinase 12
F: Cyclin-K
A: DNA damage-binding protein 1
B: Cyclin-dependent kinase 12
C: Cyclin-K
G: DNA damage-binding protein 1
H: Cyclin-dependent kinase 12
I: Cyclin-K
ヘテロ分子


分子量 (理論値)分子数
合計 (水以外)500,51536
ポリマ-496,5589
非ポリマー3,95727
00
1
D: DNA damage-binding protein 1
E: Cyclin-dependent kinase 12
F: Cyclin-K
ヘテロ分子


分子量 (理論値)分子数
合計 (水以外)166,74211
ポリマ-165,5193
非ポリマー1,2238
0
タイプ名称対称操作
identity operation1_555x,y,z1
2
A: DNA damage-binding protein 1
B: Cyclin-dependent kinase 12
C: Cyclin-K
ヘテロ分子


分子量 (理論値)分子数
合計 (水以外)167,03114
ポリマ-165,5193
非ポリマー1,51111
0
タイプ名称対称操作
identity operation1_555x,y,z1
3
G: DNA damage-binding protein 1
H: Cyclin-dependent kinase 12
I: Cyclin-K
ヘテロ分子


分子量 (理論値)分子数
合計 (水以外)166,74211
ポリマ-165,5193
非ポリマー1,2238
0
タイプ名称対称操作
identity operation1_555x,y,z1
単位格子
Length a, b, c (Å)250.266, 250.266, 217.643
Angle α, β, γ (deg.)90.000, 90.000, 120.000
Int Tables number152
Space group name H-MP3121
Space group name HallP312"
Symmetry operation#1: x,y,z
#2: -y,x-y,z+1/3
#3: -x+y,-x,z+2/3
#4: x-y,-y,-z+2/3
#5: -x,-x+y,-z+1/3
#6: y,x,-z
非結晶学的対称性 (NCS)NCSドメイン:
IDEns-ID詳細
d_1ens_1(chain "A" and (resid 1 through 393 or resid 709 through 1140))
d_2ens_1(chain "D" and (resid 1 through 393 or resid 709 through 1140))
d_3ens_1(chain "G" and (resid 1 through 393 or resid 709 through 1140))
d_1ens_2(chain "B" and resid 715 through 1039)
d_2ens_2(chain "E" and resid 715 through 1039)
d_3ens_2(chain "H" and resid 715 through 1039)
d_1ens_3chain "C"
d_2ens_3chain "F"
d_3ens_3chain "I"

NCSドメイン領域:
Dom-IDComponent-IDEns-IDBeg label comp-IDEnd label comp-IDLabel asym-IDLabel seq-ID
d_11ens_1METGLYE1 - 393
d_12ens_1LYSHISE396 - 827
d_21ens_1METGLYA1 - 393
d_22ens_1LYSHISA395 - 826
d_31ens_1METGLYI1 - 393
d_32ens_1LYSHISI395 - 826
d_11ens_2THRCYSF1 - 325
d_21ens_2THRCYSB1 - 325
d_31ens_2THRCYSJ1 - 325
d_11ens_3THRHISH1 - 248
d_21ens_3THRHISD1 - 248
d_31ens_3THRHISL1 - 248

NCSアンサンブル:
ID
ens_1
ens_2
ens_3

NCS oper:
IDCodeMatrixベクター
1given(-0.473378900922, 0.505277517258, -0.721531043487), (-0.510960117135, 0.509717549664, 0.692176117951), (0.717518065877, 0.696335156457, 0.016887125963)-179.063880818, -30.5305707552, 37.8470451082
2given(-0.503189922858, -0.499102316937, 0.705476277959), (0.553650421585, 0.440624858074, 0.706626453741), (-0.663529285121, 0.746154549457, 0.0546102198425)-127.596667669, 83.623880856, -104.451181386
3given(-0.512266388454, 0.494826991888, -0.70194686078), (-0.51643988825, 0.475564533793, 0.712129353434), (0.686201857389, 0.727313290335, 0.0119326701906)-181.296781855, -28.0760945057, 32.5720126034
4given(-0.468446100279, -0.524962889057, 0.710613971328), (0.543058322248, 0.46334481501, 0.700285114108), (-0.696882995754, 0.713950661823, 0.0680333940977)-122.440366765, 80.7973910212, -105.70220367
5given(-0.559777007111, 0.474588038463, -0.679276008746), (-0.51203216144, 0.446415069033, 0.733850565027), (0.651515746518, 0.75860383593, -0.00688855214462)-185.36281672, -25.1013006425, 25.4820000941
6given(-0.445287357922, -0.525365820093, 0.725058565878), (0.520866044845, 0.506670966374, 0.687010258411), (-0.728297832073, 0.683575370323, 0.0480310408565)-118.911162916, 74.7803023239, -109.119448351

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要素

#1: タンパク質 DNA damage-binding protein 1 / DDB p127 subunit / DNA damage-binding protein a / DDBa / Damage-specific DNA-binding protein 1 / ...DDB p127 subunit / DNA damage-binding protein a / DDBa / Damage-specific DNA-binding protein 1 / HBV X-associated protein 1 / XAP-1 / UV-damaged DNA-binding factor / UV-damaged DNA-binding protein 1 / UV-DDB 1 / XPE-binding factor / XPE-BF / Xeroderma pigmentosum group E-complementing protein / XPCe


分子量: 93675.438 Da / 分子数: 3 / 由来タイプ: 組換発現 / 由来: (組換発現) Homo sapiens (ヒト) / 遺伝子: DDB1, XAP1 / 発現宿主: Trichoplusia ni (イラクサキンウワバ) / 参照: UniProt: Q16531
#2: タンパク質 Cyclin-dependent kinase 12 / Cdc2-related kinase / arginine/serine-rich / CrkRS / Cell division cycle 2-related protein kinase 7 ...Cdc2-related kinase / arginine/serine-rich / CrkRS / Cell division cycle 2-related protein kinase 7 / CDC2-related protein kinase 7 / Cell division protein kinase 12 / hCDK12


分子量: 40143.328 Da / 分子数: 3 / 由来タイプ: 組換発現 / 由来: (組換発現) Homo sapiens (ヒト) / 遺伝子: CDK12, CRK7, CRKRS, KIAA0904 / 発現宿主: Trichoplusia ni (イラクサキンウワバ)
参照: UniProt: Q9NYV4, cyclin-dependent kinase, [RNA-polymerase]-subunit kinase
#3: タンパク質 Cyclin-K


分子量: 31700.471 Da / 分子数: 3 / 由来タイプ: 組換発現 / 由来: (組換発現) Homo sapiens (ヒト) / 遺伝子: CCNK, CPR4 / 発現宿主: Trichoplusia ni (イラクサキンウワバ) / 参照: UniProt: O75909
#4: 化合物...
ChemComp-SO4 / SULFATE ION / 硫酸ジアニオン


分子量: 96.063 Da / 分子数: 24 / 由来タイプ: 合成 / : SO4
#5: 化合物 ChemComp-RQU / ~{N}-[2-(2-methoxyphenyl)ethyl]-2-[[9-propan-2-yl-6-[(4-pyridin-2-ylphenyl)methylamino]purin-2-yl]amino]ethanamide


分子量: 550.654 Da / 分子数: 3 / 由来タイプ: 合成 / : C31H34N8O2 / タイプ: SUBJECT OF INVESTIGATION
研究の焦点であるリガンドがあるかY
Has protein modificationY

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実験情報

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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: 3.93 Å3/Da / 溶媒含有率: 68.68 %
結晶化温度: 293 K / 手法: 蒸気拡散法, シッティングドロップ法 / 詳細: 1.42 M ammonium sulphate, 0.07 M HEPES, pH 7.0

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データ収集

回折平均測定温度: 100 K / Serial crystal experiment: N
放射光源由来: シンクロトロン / サイト: SLS / ビームライン: X10SA / 波長: 1 Å
検出器タイプ: DECTRIS EIGER2 X 16M / 検出器: PIXEL / 日付: 2021年3月19日
放射プロトコル: SINGLE WAVELENGTH / 単色(M)・ラウエ(L): M / 散乱光タイプ: x-ray
放射波長波長: 1 Å / 相対比: 1
反射解像度: 3.64→216.737 Å / Num. obs: 79836 / % possible obs: 96.1 % / 冗長度: 21.4 % / CC1/2: 0.993 / Net I/σ(I): 7.9
反射 シェル解像度: 3.643→3.812 Å / Num. unique obs: 3990 / CC1/2: 0.273

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解析

ソフトウェア
名称バージョン分類
PHENIX1.20.1_4487精密化
XDSデータ削減
Cootモデル構築
STARANISOデータスケーリング
autoPROCdata processing
PHASER位相決定
精密化構造決定の手法: 分子置換 / 解像度: 3.64→97.25 Å / SU ML: 0.4417 / 交差検証法: FREE R-VALUE / σ(F): 1.34 / 位相誤差: 23.2112
立体化学のターゲット値: GeoStd + Monomer Library + CDL v1.2
Rfactor反射数%反射
Rfree0.2337 3981 4.99 %
Rwork0.1894 75796 -
obs0.1916 79777 90.68 %
溶媒の処理減衰半径: 0.9 Å / VDWプローブ半径: 1.11 Å / 溶媒モデル: FLAT BULK SOLVENT MODEL
原子変位パラメータBiso mean: 144.55 Å2
精密化ステップサイクル: LAST / 解像度: 3.64→97.25 Å
タンパク質核酸リガンド溶媒全体
原子数33652 0 243 0 33895
拘束条件
Refine-IDタイプDev ideal
X-RAY DIFFRACTIONf_bond_d0.005834721
X-RAY DIFFRACTIONf_angle_d0.928846957
X-RAY DIFFRACTIONf_chiral_restr0.05465167
X-RAY DIFFRACTIONf_plane_restr0.00655995
X-RAY DIFFRACTIONf_dihedral_angle_d12.191113106
Refine LS restraints NCS
Ens-IDDom-IDAuth asym-IDRefine-IDタイプRms dev position (Å)
ens_1d_2EX-RAY DIFFRACTIONTorsion NCS1.08842578136
ens_1d_3EX-RAY DIFFRACTIONTorsion NCS0.905314902863
ens_2d_2FX-RAY DIFFRACTIONTorsion NCS1.05654097605
ens_2d_3FX-RAY DIFFRACTIONTorsion NCS1.05039917175
ens_3d_2HX-RAY DIFFRACTIONTorsion NCS0.735324108286
ens_3d_3HX-RAY DIFFRACTIONTorsion NCS0.652086811846
LS精密化 シェル
解像度 (Å)Rfactor RfreeNum. reflection RfreeRfactor RworkNum. reflection RworkRefine-ID% reflection obs (%)
3.64-3.690.424380.3145246X-RAY DIFFRACTION8.16
3.69-3.730.3626470.3112818X-RAY DIFFRACTION28.11
3.73-3.780.3618900.30761527X-RAY DIFFRACTION52.16
3.78-3.840.34191220.29262232X-RAY DIFFRACTION75.81
3.84-3.890.29861500.2942592X-RAY DIFFRACTION87.55
3.89-3.950.35531460.3012786X-RAY DIFFRACTION93.91
3.95-4.010.3091520.27312827X-RAY DIFFRACTION95.82
4.01-4.080.30221370.24752882X-RAY DIFFRACTION97.32
4.08-4.150.28461630.23972960X-RAY DIFFRACTION99.24
4.15-4.220.25311480.22322949X-RAY DIFFRACTION99.84
4.22-4.30.24631450.2072970X-RAY DIFFRACTION100
4.3-4.390.23551380.20222973X-RAY DIFFRACTION99.97
4.39-4.490.26191770.18992971X-RAY DIFFRACTION100
4.49-4.590.21371550.17732949X-RAY DIFFRACTION100
4.59-4.710.21671520.17362982X-RAY DIFFRACTION100
4.71-4.830.22141710.16962966X-RAY DIFFRACTION100
4.83-4.970.1851600.16772960X-RAY DIFFRACTION100
4.97-5.130.24181760.17642955X-RAY DIFFRACTION99.97
5.14-5.320.22331120.17853038X-RAY DIFFRACTION100
5.32-5.530.23231340.18313018X-RAY DIFFRACTION100
5.53-5.780.25411490.18482990X-RAY DIFFRACTION100
5.78-6.090.22731560.19362985X-RAY DIFFRACTION100
6.09-6.470.27361770.20022991X-RAY DIFFRACTION100
6.47-6.970.26541630.19672995X-RAY DIFFRACTION100
6.97-7.670.23421780.17913005X-RAY DIFFRACTION100
7.67-8.780.20511670.16073024X-RAY DIFFRACTION100
8.78-11.060.16251680.12253057X-RAY DIFFRACTION99.88
11.06-97.250.19151400.17893148X-RAY DIFFRACTION98.56
精密化 TLS

手法: refined / Refine-ID: X-RAY DIFFRACTION

IDL112)L122)L132)L222)L232)L332)S11 (Å °)S12 (Å °)S13 (Å °)S21 (Å °)S22 (Å °)S23 (Å °)S31 (Å °)S32 (Å °)S33 (Å °)T112)T122)T132)T222)T232)T332)Origin x (Å)Origin y (Å)Origin z (Å)
11.434142661141.10384061071-0.04188492022550.640702939656-0.1937434586071.1736969856-0.0766064250086-0.310733523606-0.07050608685390.270377466590.0370884272346-0.1952730389640.3551905584020.4210333339538.90276988048E-61.372668997350.275571008354-0.31389941691.19971787034-0.07974499759241.34327180533-57.3361883757-7.4903643058427.989592801
20.237832163702-0.206781718375-1.451430764180.1385743602580.1516094728730.519358184422-0.00718240512309-0.598448651333-0.1380023706180.6035671998610.376856427336-0.388255418788-0.03326067227520.3188276213376.14551985032E-61.431074753370.0704128519012-0.3096505778621.22829854787-0.1843728968821.24490646436-72.846551161810.190413563139.9725232306
31.73925177415-0.295666473977-0.863121611251.79813042344-1.205613503561.449145382880.1131163409890.0388885702896-0.01714160994010.0653990978090.0315480531453-0.00702328060628-0.0562861966279-0.16688089215-2.27218533895E-51.170228736960.0525780207673-0.0397284880940.882932867315-0.08187738331830.953343294044-88.955999048216.012310784824.8946723846
41.49699340694-0.414227208252-0.4163202999220.353750682663-0.2814983610860.6929745941190.1929257787510.109846516740.3013707090480.0765028853391-0.030964764653-0.293695482721-0.2335524493290.301879833854-1.99291399794E-51.19852045937-0.0619539327144-0.1316148202411.00749272114-0.2092087332371.24280766772-63.464597631829.571237740821.393733985
50.3308093389890.6295094034870.554683900634-0.0176499712712-0.1030825155931.213990176240.2071843540170.02452833936510.09805082099430.2395934790220.1465755185840.246130393826-0.2228106607220.159378985414-1.166694524E-51.32315858293-0.0263567488455-0.05981538748731.27024023858-0.1372731696721.25723360175-61.863751086331.6858207254-14.7761836319
60.5357232864040.2707190795470.2904328300992.14009021033-1.637843007581.048310070980.05430753802090.0604888051277-0.250997642248-0.1140386180830.02492159924580.547737159748-0.09188715526780.1225486298928.49838554898E-51.364626504570.01011044605550.0472782553671.21442788692-0.1906958034641.29510980401-57.072743080520.0528718703-12.0925890911
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371.741437341060.287530039311-0.3110655340721.99427482049-0.8586890418710.331958824301-0.210341677301-0.5673896887580.1292709725180.9416610795870.123125762011-0.303772335279-0.525863606568-0.10232371987-9.52849511286E-51.725584187750.324894454667-0.05676008990441.00333550986-0.03988580195730.982826915035-148.87088603433.050745437218.1261823392
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精密化 TLSグループ

Refine-ID: X-RAY DIFFRACTION

IDRefine TLS-IDSelection detailsAuth asym-IDLabel asym-IDAuth seq-IDLabel seq-ID
11chain 'D' and (resid 1 through 307 )DA1 - 3071 - 307
22chain 'D' and (resid 308 through 716 )DA308 - 716308 - 402
33chain 'D' and (resid 717 through 819 )DA717 - 819403 - 505
44chain 'D' and (resid 820 through 1140 )DA820 - 1140506 - 826
55chain 'E' and (resid 715 through 794 )EB715 - 7941 - 80
66chain 'E' and (resid 795 through 890 )EB795 - 89081 - 176
77chain 'E' and (resid 891 through 1040 )EB891 - 1040177 - 326
88chain 'F' and (resid 20 through 42 )FD20 - 421 - 23
99chain 'F' and (resid 43 through 63 )FD43 - 6324 - 44
1010chain 'F' and (resid 64 through 150 )FD64 - 15045 - 131
1111chain 'F' and (resid 151 through 218 )FD151 - 218132 - 199
1212chain 'F' and (resid 219 through 243 )FD219 - 243200 - 224
1313chain 'F' and (resid 244 through 267 )FD244 - 267225 - 248
1414chain 'A' and (resid 1 through 358 )AE1 - 3581 - 358
1515chain 'A' and (resid 359 through 761 )AE359 - 761359 - 448
1616chain 'A' and (resid 762 through 856 )AE762 - 856449 - 543
1717chain 'A' and (resid 857 through 1140 )AE857 - 1140544 - 827
1818chain 'B' and (resid 715 through 768 )BF715 - 7681 - 54
1919chain 'B' and (resid 769 through 788 )BF769 - 78855 - 74
2020chain 'B' and (resid 789 through 814 )BF789 - 81475 - 100
2121chain 'B' and (resid 815 through 880 )BF815 - 880101 - 166
2222chain 'B' and (resid 881 through 901 )BF881 - 901167 - 187
2323chain 'B' and (resid 902 through 931 )BF902 - 931188 - 217
2424chain 'B' and (resid 932 through 980 )BF932 - 980218 - 266
2525chain 'B' and (resid 981 through 1026 )BF981 - 1026267 - 312
2626chain 'B' and (resid 1027 through 1044 )BF1027 - 1044313 - 330
2727chain 'C' and (resid 20 through 42 )CH20 - 421 - 23
2828chain 'C' and (resid 43 through 106 )CH43 - 10624 - 87
2929chain 'C' and (resid 107 through 150 )CH107 - 15088 - 131
3030chain 'C' and (resid 151 through 218 )CH151 - 218132 - 199
3131chain 'C' and (resid 219 through 243 )CH219 - 243200 - 224
3232chain 'C' and (resid 244 through 267 )CH244 - 267225 - 248
3333chain 'G' and (resid 1 through 294 )GI1 - 2941 - 294
3434chain 'G' and (resid 295 through 743 )GI295 - 743295 - 429
3535chain 'G' and (resid 744 through 795 )GI744 - 795430 - 481
3636chain 'G' and (resid 796 through 856 )GI796 - 856482 - 542
3737chain 'G' and (resid 857 through 1140 )GI857 - 1140543 - 826
3838chain 'H' and (resid 715 through 768 )HJ715 - 7681 - 54
3939chain 'H' and (resid 769 through 819 )HJ769 - 81955 - 105
4040chain 'H' and (resid 820 through 901 )HJ820 - 901106 - 187
4141chain 'H' and (resid 902 through 1039 )HJ902 - 1039188 - 325
4242chain 'I' and (resid 20 through 42 )IL20 - 421 - 23
4343chain 'I' and (resid 43 through 63 )IL43 - 6324 - 44
4444chain 'I' and (resid 64 through 150 )IL64 - 15045 - 131
4545chain 'I' and (resid 151 through 217 )IL151 - 217132 - 198
4646chain 'I' and (resid 218 through 243 )IL218 - 243199 - 224
4747chain 'I' and (resid 244 through 267 )IL244 - 267225 - 248

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万見について

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お知らせ

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2022年2月9日: EMDBエントリの付随情報ファイルのフォーマットが新しくなりました

EMDBエントリの付随情報ファイルのフォーマットが新しくなりました

  • EMDBのヘッダファイルのバージョン3が、公式のフォーマットとなりました。
  • これまでは公式だったバージョン1.9は、アーカイブから削除されます。

関連情報:EMDBヘッダ

外部リンク:wwPDBはEMDBデータモデルのバージョン3へ移行します

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2020年8月12日: 新型コロナ情報

新型コロナ情報

URL: https://pdbj.org/emnavi/covid19.php

新ページ: EM Navigatorに新型コロナウイルスの特設ページを開設しました。

関連情報:Covid-19情報 / 2020年3月5日: 新型コロナウイルスの構造データ

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2020年3月5日: 新型コロナウイルスの構造データ

新型コロナウイルスの構造データ

関連情報:万見生物種 / 2020年8月12日: 新型コロナ情報

外部リンク:COVID-19特集ページ - PDBj / 今月の分子2020年2月:コロナウイルスプロテーアーゼ

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2019年1月31日: EMDBのIDの桁数の変更

EMDBのIDの桁数の変更

  • EMDBエントリに付与されているアクセスコード(EMDB-ID)は4桁の数字(例、EMD-1234)でしたが、間もなく枯渇します。これまでの4桁のID番号は4桁のまま変更されませんが、4桁の数字を使い切った後に発行されるIDは5桁以上の数字(例、EMD-12345)になります。5桁のIDは2019年の春頃から発行される見通しです。
  • EM Navigator/万見では、接頭語「EMD-」は省略されています。

関連情報:Q: 「EMD」とは何ですか? / 万見/EM NavigatorにおけるID/アクセスコードの表記

外部リンク:EMDB Accession Codes are Changing Soon! / PDBjへお問い合わせ

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2017年7月12日: PDB大規模アップデート

PDB大規模アップデート

  • 新バージョンのPDBx/mmCIF辞書形式に基づくデータがリリースされました。
  • 今回の更新はバージョン番号が4から5になる大規模なもので、全エントリデータの書き換えが行われる「Remediation」というアップデートに該当します。
  • このバージョンアップで、電子顕微鏡の実験手法に関する多くの項目の書式が改定されました(例:em_softwareなど)。
  • EM NavigatorとYorodumiでも、この改定に基づいた表示内容になります。

外部リンク:wwPDB Remediation / OneDepデータ基準に準拠した、より強化された内容のモデル構造ファイルが、PDBアーカイブで公開されました。

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万見 (Yorodumi)

幾万の構造データを、幾万の視点から

  • 万見(Yorodumi)は、EMDB/PDB/SASBDBなどの構造データを閲覧するためのページです。
  • EM Navigatorの詳細ページの後継、Omokage検索のフロントエンドも兼ねています。

関連情報:EMDB / PDB / SASBDB / 3つのデータバンクの比較 / 万見検索 / 2016年8月31日: 新しいEM Navigatorと万見 / 万見文献 / Jmol/JSmol / 機能・相同性情報 / 新しいEM Navigatorと万見の変更点

他の情報も見る