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データを開く
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基本情報
登録情報 | ![]() | |||||||||
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タイトル | Cryo-EM structure of Phi dynein tail | |||||||||
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![]() | human / motor protein / complex | |||||||||
機能・相同性 | ![]() intracellular transport of viral protein in host cell / secretory vesicle / deoxyribonuclease inhibitor activity / negative regulation of DNA strand resection involved in replication fork processing / transport along microtubule / intraciliary retrograde transport / visual behavior / dynein light chain binding / dynein heavy chain binding / motile cilium assembly ...intracellular transport of viral protein in host cell / secretory vesicle / deoxyribonuclease inhibitor activity / negative regulation of DNA strand resection involved in replication fork processing / transport along microtubule / intraciliary retrograde transport / visual behavior / dynein light chain binding / dynein heavy chain binding / motile cilium assembly / Activation of BIM and translocation to mitochondria / negative regulation of phosphorylation / ciliary tip / Intraflagellar transport / positive regulation of intracellular transport / regulation of metaphase plate congression / establishment of spindle localization / positive regulation of spindle assembly / regulation of G protein-coupled receptor signaling pathway / microtubule-dependent intracellular transport of viral material towards nucleus / dynein complex / COPI-independent Golgi-to-ER retrograde traffic / retrograde axonal transport / minus-end-directed microtubule motor activity / P-body assembly / microtubule motor activity / dynein light intermediate chain binding / cytoplasmic dynein complex / centrosome localization / dynein intermediate chain binding / nuclear migration / microtubule-based movement / Macroautophagy / establishment of mitotic spindle orientation / enzyme inhibitor activity / tertiary granule membrane / ficolin-1-rich granule membrane / cytoplasmic microtubule / COPI-mediated anterograde transport / Amplification of signal from unattached kinetochores via a MAD2 inhibitory signal / cytoplasmic microtubule organization / axon cytoplasm / Mitotic Prometaphase / substantia nigra development / EML4 and NUDC in mitotic spindle formation / Loss of Nlp from mitotic centrosomes / Loss of proteins required for interphase microtubule organization from the centrosome / stress granule assembly / Recruitment of mitotic centrosome proteins and complexes / MHC class II antigen presentation / Recruitment of NuMA to mitotic centrosomes / regulation of mitotic spindle organization / Anchoring of the basal body to the plasma membrane / Resolution of Sister Chromatid Cohesion / HSP90 chaperone cycle for steroid hormone receptors (SHR) in the presence of ligand / AURKA Activation by TPX2 / mitotic spindle organization / filopodium / RHO GTPases Activate Formins / cellular response to nerve growth factor stimulus / kinetochore / negative regulation of neurogenesis / spindle / microtubule cytoskeleton organization / HCMV Early Events / Aggrephagy / mitotic spindle / Separation of Sister Chromatids / azurophil granule lumen / Regulation of PLK1 Activity at G2/M Transition / late endosome / nervous system development / host cell / site of double-strand break / positive regulation of cold-induced thermogenesis / cell cortex / secretory granule lumen / vesicle / microtubule / ficolin-1-rich granule lumen / cytoskeleton / cilium / symbiont entry into host cell / cell division / apoptotic process / centrosome / DNA damage response / Neutrophil degranulation / Golgi apparatus / ATP hydrolysis activity / mitochondrion / RNA binding / extracellular exosome / extracellular region / ATP binding / identical protein binding / nucleus / membrane / plasma membrane / cytosol 類似検索 - 分子機能 | |||||||||
生物種 | ![]() | |||||||||
手法 | 単粒子再構成法 / クライオ電子顕微鏡法 / 解像度: 4.4 Å | |||||||||
![]() | Nguyen KHV / Kendrick AA / Leschziner AE | |||||||||
資金援助 | ![]()
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![]() | ![]() タイトル: Cryo-EM structure of Pre-Chi dynein bound to Lis1 著者: Nguyen KHV / Kendrick AA / Leschziner AE | |||||||||
履歴 |
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構造の表示
添付画像 |
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ダウンロードとリンク
-EMDBアーカイブ
マップデータ | ![]() | 259.3 MB | ![]() | |
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ヘッダ (付随情報) | ![]() ![]() | 27.7 KB 27.7 KB | 表示 表示 | ![]() |
FSC (解像度算出) | ![]() ![]() | 13.9 KB 13.9 KB | 表示 表示 | ![]() |
画像 | ![]() | 56.4 KB | ||
Filedesc metadata | ![]() | 9.9 KB | ||
その他 | ![]() ![]() | 254.6 MB 254.6 MB | ||
アーカイブディレクトリ | ![]() ![]() | HTTPS FTP |
-検証レポート
文書・要旨 | ![]() | 1.2 MB | 表示 | ![]() |
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文書・詳細版 | ![]() | 1.2 MB | 表示 | |
XML形式データ | ![]() | 16.4 KB | 表示 | |
CIF形式データ | ![]() | 19.5 KB | 表示 | |
アーカイブディレクトリ | ![]() ![]() | HTTPS FTP |
-関連構造データ
関連構造データ | ![]() 9e28MC ![]() 9dzyC ![]() 9e0kC ![]() 9e0tC ![]() 9e0uC ![]() 9e0wC ![]() 9e0xC ![]() 9e0yC ![]() 9e22C ![]() 9e23C C: 同じ文献を引用 ( M: このマップから作成された原子モデル |
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類似構造データ | 類似検索 - 機能・相同性 ![]() |
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リンク
EMDBのページ | ![]() ![]() |
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「今月の分子」の関連する項目 |
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マップ
ファイル | ![]() | ||||||||||||||||||||||||||||||||||||
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投影像・断面図 | 画像のコントロール
画像は Spider により作成 | ||||||||||||||||||||||||||||||||||||
ボクセルのサイズ | X=Y=Z: 0.935 Å | ||||||||||||||||||||||||||||||||||||
密度 |
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対称性 | 空間群: 1 | ||||||||||||||||||||||||||||||||||||
詳細 | EMDB XML:
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-添付データ
-ハーフマップ: #2
ファイル | emd_47443_half_map_1.map | ||||||||||||
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投影像・断面図 |
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密度ヒストグラム |
-ハーフマップ: #1
ファイル | emd_47443_half_map_2.map | ||||||||||||
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投影像・断面図 |
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密度ヒストグラム |
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試料の構成要素
-全体 : Human Cytoplasmic dynein-1
全体 | 名称: Human Cytoplasmic dynein-1 |
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要素 |
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-超分子 #1: Human Cytoplasmic dynein-1
超分子 | 名称: Human Cytoplasmic dynein-1 / タイプ: complex / ID: 1 / 親要素: 0 / 含まれる分子: #4, #3, #5-#6, #2, #1 |
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由来(天然) | 生物種: ![]() |
-分子 #1: Cytoplasmic dynein 1 heavy chain 1
分子 | 名称: Cytoplasmic dynein 1 heavy chain 1 / タイプ: protein_or_peptide / ID: 1 / コピー数: 4 / 光学異性体: LEVO |
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由来(天然) | 生物種: ![]() |
分子量 | 理論値: 554.12625 KDa |
組換発現 | 生物種: ![]() ![]() |
配列 | 文字列: GDYDIPTTEN LYFQGDKDCE MKRTTLDSPL GKLELSGCEQ GLHRIIFLGK GTSAADAVEV PAPAAVLGGP EPLMQATAWL NAYFHQPEA IEEFPVPALH HPVFQQESFT RQVLWKLLKV VKFGEVISYS HLAALAGNPA ATAAVKTALS GNPVPILIPC H RVVQGDLD ...文字列: GDYDIPTTEN LYFQGDKDCE MKRTTLDSPL GKLELSGCEQ GLHRIIFLGK GTSAADAVEV PAPAAVLGGP EPLMQATAWL NAYFHQPEA IEEFPVPALH HPVFQQESFT RQVLWKLLKV VKFGEVISYS HLAALAGNPA ATAAVKTALS GNPVPILIPC H RVVQGDLD VGGYEGGLAV KEWLLAHEGH RLGKPGLGGS SEPGGGGGED GSAGLEVSAV QNVADVSVLQ KHLRKLVPLL LE DGGEAPA ALEAALEEKS ALEQMRKFLS DPQVHTVLVE RSTLKEDVGD EGEEEKEFIS YNINIDIHYG VKSNSLAFIK RTP VIDADK PVSSQLRVLT LSEDSPYETL HSFISNAVAP FFKSYIRESG KADRDGDKMA PSVEKKIAEL EMGLLHLQQN IEIP EISLP IHPMITNVAK QCYERGEKPK VTDFGDKVED PTFLNQLQSG VNRWIREIQK VTKLDRDPAS GTALQEISFW LNLER ALYR IQEKRESPEV LLTLDILKHG KRFHATVSFD TDTGLKQALE TVNDYNPLMK DFPLNDLLSA TELDKIRQAL VAIFTH LRK IRNTKYPIQR ALRLVEAISR DLSSQLLKVL GTRKLMHVAY EEFEKVMVAC FEVFQTWDDE YEKLQVLLRD IVKRKRE EN LKMVWRINPA HRKLQARLDQ MRKFRRQHEQ LRAVIVRVLR PQVTAVAQQN QGEVPEPQDM KVAEVLFDAA DANAIEEV N LAYENVKEVD GLDVSKEGTE AWEAAMKRYD ERIDRVETRI TARLRDQLGT AKNANEMFRI FSRFNALFVR PHIRGAIRE YQTQLIQRVK DDIESLHDKF KVQYPQSQAC KMSHVRDLPP VSGSIIWAKQ IDRQLTAYMK RVEDVLGKGW ENHVEGQKLK QDGDSFRMK LNTQEIFDDW ARKVQQRNLG VSGRIFTIES TRVRGRTGNV LKLKVNFLPE IITLSKEVRN LKWLGFRVPL A IVNKAHQA NQLYPFAISL IESVRTYERT CEKVEERNTI SLLVAGLKKE VQALIAEGIA LVWESYKLDP YVQRLAETVF NF QEKVDDL LIIEEKIDLE VRSLETCMYD HKTFSEILNR VQKAVDDLNL HSYSNLPIWV NKLDMEIERI LGVRLQAGLR AWT QVLLGQ AEDKAEVDMD TDAPQVSHKP GGEPKIKNVV HELRITNQVI YLNPPIEECR YKLYQEMFAW KMVVLSLPRI QSQR YQVGV HYELTEEEKF YRNALTRMPD GPVALEESYS AVMGIVSEVE QYVKVWLQYQ CLWDMQAENI YNRLGEDLNK WQALL VQIR KARGTFDNAE TKKEFGPVVI DYGKVQSKVN LKYDSWHKEV LSKFGQMLGS NMTEFHSQIS KSRQELEQHS VDTAST SDA VTFITYVQSL KRKIKQFEKQ VELYRNGQRL LEKQRFQFPP SWLYIDNIEG EWGAFNDIMR RKDSAIQQQV ANLQMKI VQ EDRAVESRTT DLLTDWEKTK PVTGNLRPEE ALQALTIYEG KFGRLKDDRE KCAKAKEALE LTDTGLLSGS EERVQVAL E ELQDLKGVWS ELSKVWEQID QMKEQPWVSV QPRKLRQNLD ALLNQLKSFP ARLRQYASYE FVQRLLKGYM KINMLVIEL KSEALKDRHW KQLMKRLHVN WVVSELTLGQ IWDVDLQKNE AIVKDVLLVA QGEMALEEFL KQIREVWNTY ELDLVNYQNK CRLIRGWDD LFNKVKEHIN SVSAMKLSPY YKVFEEDALS WEDKLNRIMA LFDVWIDVQR RWVYLEGIFT GSADIKHLLP V ETQRFQSI STEFLALMKK VSKSPLVMDV LNIQGVQRSL ERLADLLGKI QKALGEYLER ERSSFPRFYF VGDEDLLEII GN SKNVAKL QKHFKKMFAG VSSIILNEDN SVVLGISSRE GEEVMFKTPV SITEHPKINE WLTLVEKEMR VTLAKLLAES VTE VEIFGK ATSIDPNTYI TWIDKYQAQL VVLSAQIAWS ENVETALSSM GGGGDAAPLH SVLSNVEVTL NVLADSVLME QPPL RRRKL EHLITELVHQ RDVTRSLIKS KIDNAKSFEW LSQMRFYFDP KQTDVLQQLS IQMANAKFNY GFEYLGVQDK LVQTP LTDR CYLTMTQALE ARLGGSPFGP AGTGKTESVK ALGHQLGRFV LVFNCDETFD FQAMGRIFVG LCQVGAWGCF DEFNRL EER MLSAVSQQVQ CIQEALREHS NPNYDKTSAP ITCELLNKQV KVSPDMAIFI TMNPGYAGRS NLPDNLKKLF RSLAMTK PD RQLIAQVMLY SQGFRTAEVL ANKIVPFFKL CDEQLSSQSH YDFGLRALKS VLVSAGNVKR ERIQKIKREK EERGEAVD E GEIAENLPEQ EILIQSVCET MVPKLVAEDI PLLFSLLSDV FPGVQYHRGE MTALREELKK VCQEMYLTYG DGEEVGGMW VEKVLQLYQI TQINHGLMMV GPSGSGKSMA WRVLLKALER LEGVEGVAHI IDPKAISKDH LYGTLDPNTR EWTDGLFTHV LRKIIDSVR GELQKRQWIV FDGDVDPEWV ENLNSVLDDN KLLTLPNGER LSLPPNVRIM FEVQDLKYAT LATVSRCGMV W FSEDVLST DMIFNNFLAR LRSIPLDEGE DEAQRRRKGK EDEGEEAASP MLQIQRDAAT IMQPYFTSNG LVTKALEHAF QL EHIMDLT RLRCLGSLFS MLHQACRNVA QYNANHPDFP MQIEQLERYI QRYLVYAILW SLSGDSRLKM RAELGEYIRR ITT VPLPTA PNIPIIDYEV SISGEWSPWQ AKVPQIEVET HKVAAPDVVV PTLDTVRHEA LLYTWLAEHK PLVLCGPPGS GKTM TLFSA LRALPDMEVV GLNFSSATTP ELLLKTFDHY CEYRRTPNGV VLAPVQLGKW LVLFCDEINL PDMDKYGTQR VISFI RQMV EHGGFYRTSD QTWVKLERIQ FVGACNPPTD PGRKPLSHRF LRHVPVVYVD YPGPASLTQI YGTFNRAMLR LIPSLR TYA EPLTAAMVEF YTMSQERFTQ DTQPHYIYSP REMTRWVRGI FEALRPLETL PVEGLIRIWA HEALRLFQDR LVEDEER RW TDENIDTVAL KHFPNIDREK AMSRPILYSN WLSKDYIPVD QEELRDYVKA RLKVFYEEEL DVPLVLFNEV LDHVLRID R IFRQPQGHLL LIGVSGAGKT TLSRFVAWMN GLSVYQIKVH RKYTGEDFDE DLRTVLRRSG CKNEKIAFIM DESNVLDSG FLERMNTLLA NGEVPGLFEG DEYATLMTQC KEGAQKEGLM LDSHEELYKW FTSQVIRNLH VVFTMNPSSE GLKDRAATSP ALFNRCVLN WFGDWSTEAL YQVGKEFTSK MDLEKPNYIV PDYMPVVYDK LPQPPSHREA IVNSCVFVHQ TLHQANARLA K RGGRTMAI TPRHYLDFIN HYANLFHEKR SELEEQQMHL NVGLRKIKET VDQVEELRRD LRIKSQELEV KNAAANDKLK KM VKDQQEA EKKKVMSQEI QEQLHKQQEV IADKQMSVKE DLDKVEPAVI EAQNAVKSIK KQHLVEVRSM ANPPAAVKLA LES ICLLLG ESTTDWKQIR SIIMRENFIP TIVNFSAEEI SDAIREKMKK NYMSNPSYNY EIVNRASLAC GPMVKWAIAQ LNYA DMLKR VEPLRNELQK LEDDAKDNQQ KANEVEQMIR DLEASIARYK EEYAVLISEA QAIKADLAAV EAKVNRSTAL LKSLS AERE RWEKTSETFK NQMSTIAGDC LLSAAFIAYA GYFDQQMRQN LFTTWSHHLQ QANIQFRTDI ARTEYLSNAD ERLRWQ ASS LPADDLCTEN AIMLKRFNRY PLIIDPSGQA TEFIMNEYKD RKITRTSFLD DAFRKNLESA LRFGNPLLVQ DVESYDP VL NPVLNREVRR TGGRVLITLG DQDIDLSPSF VIFLSTRDPT VEFPPDLCSR VTFVNFTVTR SSLQSQCLNE VLKAERPD V DEKRSDLLKL QGEFQLRLRQ LEKSLLQALN EVKGRILDDD TIITTLENLK REAAEVTRKV EETDIVMQEV ETVSQQYLP LSTACSSIYF TMESLKQIHF LYQYSLQFFL DIYHNVLYEN PNLKGVTDHT QRLSIITKDL FQVAFNRVAR GMLHQDHITF AMLLARIKL KGTVGEPTYD AEFQHFLRGN EIVLSAGSTP RIQGLTVEQA EAVVRLSCLP AFKDLIAKVQ ADEQFGIWLD S SSPEQTVP YLWSEETPAT PIGQAIHRLL LIQAFRPDRL LAMAHMFVST NLGESFMSIM EQPLDLTHIV GTEVKPNTPV LM CSVPGYD ASGHVEDLAA EQNTQITSIA IGSAEGFNQA DKAINTAVKS GRWVMLKNVH LAPGWLMQLE KKLHSLQPHA CFR LFLTME INPKVPVNLL RAGRIFVFEP PPGVKANMLR TFSSIPVSRI CKSPNERARL YFLLAWFHAI IQERLRYAPL GWSK KYEFG ESDLRSACDT VDTWLDDTAK GRQNISPDKI PWSALKTLMA QSIYGGRVDN EFDQRLLNTF LERLFTTRSF DSEFK LACK VDGHKDIQMP DGIRREEFVQ WVELLPDTQT PSWLGLPNNA ERVLLTTQGV DMISKMLKMQ MLEDEDDLAY AETEKK TRT DSTSDGRPAW MRTLHTTASN WLHLIPQTLS HLKRTVENIK DPLFRFFERE VKMGAKLLQD VRQDLADVVQ VCEGKKK QT NYLRTLINEL VKGILPRSWS HYTVPAGMTV IQWVSDFSER IKQLQNISLA AASGGAKELK NIHVCLGGLF VPEAYITA T RQYVAQANSW SLEELCLEVN VTTSQGATLD ACSFGVTGLK LQGATCNNNK LSLSNAISTA LPLTQLRWVK QTNTEKKAS VVTLPVYLNF TRADLIFTVD FEIATKEDPR SFYERGVAVL CTE UniProtKB: Cytoplasmic dynein 1 heavy chain 1 |
-分子 #2: Cytoplasmic dynein 1 light intermediate chain 2
分子 | 名称: Cytoplasmic dynein 1 light intermediate chain 2 / タイプ: protein_or_peptide / ID: 2 / コピー数: 2 / 光学異性体: LEVO |
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由来(天然) | 生物種: ![]() |
分子量 | 理論値: 54.173156 KDa |
組換発現 | 生物種: ![]() ![]() |
配列 | 文字列: MAPVGVEKKL LLGPNGPAVA AAGDLTSEEE EGQSLWSSIL SEVSTRARSK LPSGKNILVF GEDGSGKTTL MTKLQGAEHG KKGRGLEYL YLSVHDEDRD DHTRCNVWIL DGDLYHKGLL KFAVSAESLP ETLVIFVADM SRPWTVMESL QKWASVLREH I DKMKIPPE ...文字列: MAPVGVEKKL LLGPNGPAVA AAGDLTSEEE EGQSLWSSIL SEVSTRARSK LPSGKNILVF GEDGSGKTTL MTKLQGAEHG KKGRGLEYL YLSVHDEDRD DHTRCNVWIL DGDLYHKGLL KFAVSAESLP ETLVIFVADM SRPWTVMESL QKWASVLREH I DKMKIPPE KMRELERKFV KDFQDYMEPE EGCQGSPQRR GPLTSGSDEE NVALPLGDNV LTHNLGIPVL VVCTKCDAVS VL EKEHDYR DEHLDFIQSH LRRFCLQYGA ALIYTSVKEE KNLDLLYKYI VHKTYGFHFT TPALVVEKDA VFIPAGWDNE KKI AILHEN FTTVKPEDAY EDFIVKPPVR KLVHDKELAA EDEQVFLMKQ QSLLAKQPAT PTRASESPAR GPSGSPRTQG RGGP ASVPS SSPGTSVKKP DPNIKNNAAS EGVLASFFNS LLSKKTGSPG SPGAGGVQST AKKSGQKTVL SNVQEELDRM TRKPD SMVT NSSTENEA UniProtKB: Cytoplasmic dynein 1 light intermediate chain 2 |
-分子 #3: Isoform 2C of Cytoplasmic dynein 1 intermediate chain 2
分子 | 名称: Isoform 2C of Cytoplasmic dynein 1 intermediate chain 2 タイプ: protein_or_peptide / ID: 3 / コピー数: 4 / 光学異性体: LEVO |
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由来(天然) | 生物種: ![]() |
分子量 | 理論値: 68.442141 KDa |
組換発現 | 生物種: ![]() ![]() |
配列 | 文字列: MSDKSELKAE LERKKQRLAQ IREEKKRKEE ERKKKETDQK KEAVAPVQEE SDLEKKRREA EALLQSMGLT PESPIVPPPM SPSSKSVST PSEAGSQDSG DGAVGSRRGP IKLGMAKITQ VDFPPREIVT YTKETQTPVM AQPKEDEEED DDVVAPKPPI E PEEEKTLK ...文字列: MSDKSELKAE LERKKQRLAQ IREEKKRKEE ERKKKETDQK KEAVAPVQEE SDLEKKRREA EALLQSMGLT PESPIVPPPM SPSSKSVST PSEAGSQDSG DGAVGSRRGP IKLGMAKITQ VDFPPREIVT YTKETQTPVM AQPKEDEEED DDVVAPKPPI E PEEEKTLK KDEENDSKAP PHELTEEEKQ QILHSEEFLS FFDHSTRIVE RALSEQINIF FDYSGRDLED KEGEIQAGAK LS LNRQFFD ERWSKHRVVS CLDWSSQYPE LLVASYNNNE DAPHEPDGVA LVWNMKYKKT TPEYVFHCQS AVMSATFAKF HPN LVVGGT YSGQIVLWDN RSNKRTPVQR TPLSAAAHTH PVYCVNVVGT QNAHNLISIS TDGKICSWSL DMLSHPQDSM ELVH KQSKA VAVTSMSFPV GDVNNFVVGS EEGSVYTACR HGSKAGISEM FEGHQGPITG IHCHAAVGAV DFSHLFVTSS FDWTV KLWS TKNNKPLYSF EDNAGYVYDV MWSPTHPALF ACVDGMGRLD LWNLNNDTEV PTASISVEGN PALNRVRWTH SGREIA VGD SEGQIVIYDV GEQIAVPRND EWARFGRTLA EINANRADAE EEAATRIPA UniProtKB: Cytoplasmic dynein 1 intermediate chain 2 |
-分子 #4: Dynein light chain roadblock-type 1
分子 | 名称: Dynein light chain roadblock-type 1 / タイプ: protein_or_peptide / ID: 4 / コピー数: 2 / 光学異性体: LEVO |
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由来(天然) | 生物種: ![]() |
分子量 | 理論値: 10.934576 KDa |
組換発現 | 生物種: ![]() ![]() |
配列 | 文字列: MAEVEETLKR LQSQKGVQGI IVVNTEGIPI KSTMDNPTTT QYASLMHSFI LKARSTVRDI DPQNDLTFLR IRSKKNEIMV APDKDYFLI VIQNPTE UniProtKB: Dynein light chain roadblock-type 1 |
-分子 #5: Dynein light chain 1, cytoplasmic
分子 | 名称: Dynein light chain 1, cytoplasmic / タイプ: protein_or_peptide / ID: 5 / コピー数: 2 / 光学異性体: LEVO |
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由来(天然) | 生物種: ![]() |
分子量 | 理論値: 10.381899 KDa |
組換発現 | 生物種: ![]() ![]() |
配列 | 文字列: MCDRKAVIKN ADMSEEMQQD SVECATQALE KYNIEKDIAA HIKKEFDKKY NPTWHCIVGR NFGSYVTHET KHFIYFYLGQ VAILLFKSG UniProtKB: Dynein light chain 1, cytoplasmic |
-分子 #6: Dynein light chain Tctex-type 1
分子 | 名称: Dynein light chain Tctex-type 1 / タイプ: protein_or_peptide / ID: 6 / コピー数: 2 / 光学異性体: LEVO |
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由来(天然) | 生物種: ![]() |
分子量 | 理論値: 12.461996 KDa |
組換発現 | 生物種: ![]() ![]() |
配列 | 文字列: MEDYQAAEET AFVVDEVSNI VKEAIESAIG GNAYQHSKVN QWTTNVVEQT LSQLTKLGKP FKYIVTCVIM QKNGAGLHTA SSCFWDSST DGSCTVRWEN KTMYCIVSAF GLSI UniProtKB: Dynein light chain Tctex-type 1 |
-実験情報
-構造解析
手法 | クライオ電子顕微鏡法 |
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![]() | 単粒子再構成法 |
試料の集合状態 | particle |
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試料調製
緩衝液 | pH: 7.4 |
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凍結 | 凍結剤: ETHANE-PROPANE / 装置: HOMEMADE PLUNGER |
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電子顕微鏡法
顕微鏡 | TFS KRIOS |
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撮影 | フィルム・検出器のモデル: FEI FALCON IV (4k x 4k) 平均電子線量: 55.0 e/Å2 |
電子線 | 加速電圧: 300 kV / 電子線源: ![]() |
電子光学系 | 照射モード: FLOOD BEAM / 撮影モード: BRIGHT FIELD / 最大 デフォーカス(公称値): 3.25 µm / 最小 デフォーカス(公称値): 0.61 µm |
実験機器 | ![]() モデル: Titan Krios / 画像提供: FEI Company |