[English] 日本語
![](img/lk-miru.gif)
- EMDB-12559: Substrate receptor scaffolding module of yeast Chelator-GID SR4 E... -
+
Open data
-
Basic information
Entry | Database: EMDB / ID: EMD-12559 | |||||||||
---|---|---|---|---|---|---|---|---|---|---|
Title | Substrate receptor scaffolding module of yeast Chelator-GID SR4 E3 ubiquitin ligase bound to Fbp1 substrate | |||||||||
![]() | ||||||||||
![]() |
| |||||||||
Function / homology | ![]() protein catabolic process in the vacuole / GID complex / Regulation of pyruvate metabolism / ascospore formation / traversing start control point of mitotic cell cycle / fructose-bisphosphatase / fructose 1,6-bisphosphate 1-phosphatase activity / vacuole / negative regulation of gluconeogenesis / Neutrophil degranulation ...protein catabolic process in the vacuole / GID complex / Regulation of pyruvate metabolism / ascospore formation / traversing start control point of mitotic cell cycle / fructose-bisphosphatase / fructose 1,6-bisphosphate 1-phosphatase activity / vacuole / negative regulation of gluconeogenesis / Neutrophil degranulation / ubiquitin protein ligase activity / proteasome-mediated ubiquitin-dependent protein catabolic process / carbohydrate metabolic process / nucleus / metal ion binding / cytoplasm Similarity search - Function | |||||||||
Biological species | ![]() ![]() ![]() ![]() | |||||||||
Method | single particle reconstruction / cryo EM / Resolution: 3.5 Å | |||||||||
![]() | Sherpa D / Chrustowicz J / Prabu JR / Schulman BA | |||||||||
Funding support | ![]()
| |||||||||
![]() | ![]() Title: GID E3 ligase supramolecular chelate assembly configures multipronged ubiquitin targeting of an oligomeric metabolic enzyme. Authors: Dawafuti Sherpa / Jakub Chrustowicz / Shuai Qiao / Christine R Langlois / Laura A Hehl / Karthik Varma Gottemukkala / Fynn M Hansen / Ozge Karayel / Susanne von Gronau / J Rajan Prabu / ...Authors: Dawafuti Sherpa / Jakub Chrustowicz / Shuai Qiao / Christine R Langlois / Laura A Hehl / Karthik Varma Gottemukkala / Fynn M Hansen / Ozge Karayel / Susanne von Gronau / J Rajan Prabu / Matthias Mann / Arno F Alpi / Brenda A Schulman / ![]() Abstract: How are E3 ubiquitin ligases configured to match substrate quaternary structures? Here, by studying the yeast GID complex (mutation of which causes deficiency in glucose-induced degradation of ...How are E3 ubiquitin ligases configured to match substrate quaternary structures? Here, by studying the yeast GID complex (mutation of which causes deficiency in glucose-induced degradation of gluconeogenic enzymes), we discover supramolecular chelate assembly as an E3 ligase strategy for targeting an oligomeric substrate. Cryoelectron microscopy (cryo-EM) structures show that, to bind the tetrameric substrate fructose-1,6-bisphosphatase (Fbp1), two minimally functional GID E3s assemble into the 20-protein Chelator-GID, which resembles an organometallic supramolecular chelate. The Chelator-GID assembly avidly binds multiple Fbp1 degrons so that multiple Fbp1 protomers are simultaneously ubiquitylated at lysines near the allosteric and substrate binding sites. Importantly, key structural and biochemical features, including capacity for supramolecular assembly, are preserved in the human ortholog, the CTLH E3. Based on our integrative structural, biochemical, and cell biological data, we propose that higher-order E3 ligase assembly generally enables multipronged targeting, capable of simultaneously incapacitating multiple protomers and functionalities of oligomeric substrates. #1: ![]() Title: GID E3 ligase supramolecular chelate assembly configures multipronged ubiquitin targeting of an oligomeric metabolic enzyme Authors: Sherpa D / Chrustowicz J / Qiao S / Langlois CR / Hehl LA / Gottemukkala KV / Hansen FM / Karayel O / Prabu JR / Mann M / Alpi AF / Schulman BA | |||||||||
History |
|
-
Structure visualization
Movie |
![]() |
---|---|
Structure viewer | EM map: ![]() ![]() ![]() |
Supplemental images |
-
Downloads & links
-EMDB archive
Map data | ![]() | 4.4 MB | ![]() | |
---|---|---|---|---|
Header (meta data) | ![]() ![]() | 25.6 KB 25.6 KB | Display Display | ![]() |
FSC (resolution estimation) | ![]() | 10.2 KB | Display | ![]() |
Images | ![]() | 147 KB | ||
Masks | ![]() | 91.1 MB | ![]() | |
Others | ![]() ![]() | 71.3 MB 71.2 MB | ||
Archive directory | ![]() ![]() | HTTPS FTP |
-Related structure data
Related structure data | ![]() 7ns3MC ![]() 7ns4C ![]() 7ns5C ![]() 7nsbC ![]() 7nscC C: citing same article ( M: atomic model generated by this map |
---|---|
Similar structure data |
-
Links
EMDB pages | ![]() ![]() |
---|---|
Related items in Molecule of the Month |
-
Map
File | ![]() | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Voxel size | X=Y=Z: 1.58 Å | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Density |
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Details | EMDB XML:
CCP4 map header:
|
-Supplemental data
-Mask #1
File | ![]() | ||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Projections & Slices |
| ||||||||||||
Density Histograms |
-Half map: #2
File | emd_12559_half_map_1.map | ||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Projections & Slices |
| ||||||||||||
Density Histograms |
-Half map: #1
File | emd_12559_half_map_2.map | ||||||||||||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Projections & Slices |
| ||||||||||||
Density Histograms |
-
Sample components
-Entire : Substrate receptor scaffolding module of yeast Chelator-GID SR4 c...
Entire | Name: Substrate receptor scaffolding module of yeast Chelator-GID SR4 comprising Gid1, Gid4, Gid5, Gid8 and Gid9 bound to Fbp1 |
---|---|
Components |
|
-Supramolecule #1: Substrate receptor scaffolding module of yeast Chelator-GID SR4 c...
Supramolecule | Name: Substrate receptor scaffolding module of yeast Chelator-GID SR4 comprising Gid1, Gid4, Gid5, Gid8 and Gid9 bound to Fbp1 type: complex / ID: 1 / Parent: 0 / Macromolecule list: all Details: Generated by focused refinement of Chelator-GID SR4 + Fbp1 map |
---|---|
Source (natural) | Organism: ![]() ![]() |
Recombinant expression | Organism: ![]() |
Molecular weight | Theoretical: 310 KDa |
-Macromolecule #1: Vacuolar import and degradation protein 28
Macromolecule | Name: Vacuolar import and degradation protein 28 / type: protein_or_peptide / ID: 1 / Number of copies: 1 / Enantiomer: LEVO |
---|---|
Source (natural) | Organism: ![]() ![]() Strain: ATCC 204508 / S288c |
Molecular weight | Theoretical: 105.609133 KDa |
Recombinant expression | Organism: ![]() |
Sequence | String: MTVAYSLENL KKISNSLVGD QLAKVDYFLA PKCQIFQCLL SIEQSDGVEL KNAKLDLLYT LLHLEPQQRD IVGTYYFDIV SAIYKSMSL ASSFTKNNSS TNYKYIKLLN LCAGVYPNCG FPDLQYLQNG FIQLVNHKFL RSKCKIDEVV TIIELLKLFL L VDEKNCSD ...String: MTVAYSLENL KKISNSLVGD QLAKVDYFLA PKCQIFQCLL SIEQSDGVEL KNAKLDLLYT LLHLEPQQRD IVGTYYFDIV SAIYKSMSL ASSFTKNNSS TNYKYIKLLN LCAGVYPNCG FPDLQYLQNG FIQLVNHKFL RSKCKIDEVV TIIELLKLFL L VDEKNCSD FNKSKFMEEE REVTETSHYQ DFKMAESLEH IIVKISSKYL DQISLKYIVR LKVSRPASPS SVKNDPFDNK GV DCTRAIP KKINISNMYD SSLLSLALLL YLRYHYMIPG DRKLRNDATF KMFVLGLLKS NDVNIRCVAL KFLLQPYFTE DKK WEDTRT LEKILPYLVK SFNYDPLPWW FDPFDMLDSL IVLYNEITPM NNPVLTTLAH TNVIFCILSR FAQCLSLPQH NEAT LKTTT KFIKICASFA ASDEKYRLLL LNDTLLLNHL EYGLESHITL IQDFISLKDE IKETTTESHS MCLPPIYDHD FVAAW LLLL KSFSRSVSAL RTTLKRNKIA QLLLQILSKT YTLTKECYFA GQDFMKPEIM IMGITLGSIC NFVVEFSNLQ SFMLRN GII DIIEKMLTDP LFNSKKAWDD NEDERRIALQ GIPVHEVKAN SLWVLRHLMY NCQNEEKFQL LAKIPMNLIL DFINDPC WA VQAQCFQLLR NLTCNSRKIV NILLEKFKDV EYKIDPQTGN KISIGSTYLF EFLAKKMRLL NPLDTQQKKA MEGILYII V NLAAVNENKK QLVIEQDEIL NIMSEILVET TTDSSSNGND SNLKLACLWV LNNLLWNSSV SHYTQYAIEN GLEPGHSPS DSENPQSTVT IGYNESVAGG YSRGKYYDEP DGDDSSSNAN DDEDDDNDEG DDEGDEFVRT PAAKGSTSNV QVTRATVERC RKLVEVGLY DLVRKNITDE SLSVREKART LLYHMDLLLK VK |
-Macromolecule #2: Glucose-induced degradation protein 8
Macromolecule | Name: Glucose-induced degradation protein 8 / type: protein_or_peptide / ID: 2 / Number of copies: 1 / Enantiomer: LEVO |
---|---|
Source (natural) | Organism: ![]() ![]() Strain: ATCC 204508 / S288c |
Molecular weight | Theoretical: 55.803309 KDa |
Recombinant expression | Organism: ![]() |
Sequence | String: MTISTLSNET TKSGSCSGQG KNGGKDFTYG KKCFTKEEWK EQVAKYSAMG ELYANKTIHY PLKIQPNSSG GSQDEGFATI QTTPIEPTL PRLLLNYFVS MAYEDSSIRM AKELGFIRNN KDIAVFNDLY KIKERFHIKH LIKLGRINEA MEEINSIFGL E VLEETFNA ...String: MTISTLSNET TKSGSCSGQG KNGGKDFTYG KKCFTKEEWK EQVAKYSAMG ELYANKTIHY PLKIQPNSSG GSQDEGFATI QTTPIEPTL PRLLLNYFVS MAYEDSSIRM AKELGFIRNN KDIAVFNDLY KIKERFHIKH LIKLGRINEA MEEINSIFGL E VLEETFNA TGSYTGRTDR QQQQQQQQFD IDGDLHFKLL LLNLIEMIRS HHQQENITKD SNDFILNLIQ YSQNKLAIKA SS SVKKMQE LELAMTLLLF PLSDSADSGS IKLPKSLQNL YSISLRSKIA DLVNEKLLKF IHPRIQFEIS NNNSKFPDLL NSD KKIITQ NFTVYNNNLV NGSNGTKITH ISSDQPINEK MSSNEVTAAA NSVWLNQRDG NVGTGSAATT FHNLENKNYW NQTS ELLSS SNGKEKGLEF NNYYSSEFPY EPRLTQIMKL WCWCENQLHH NQIGVPRVEN SDENLYFQSG WSHPQFEKGG GSGGG SGGS AWSHPQFEK |
-Macromolecule #3: BJ4_G0018240.mRNA.1.CDS.1
Macromolecule | Name: BJ4_G0018240.mRNA.1.CDS.1 / type: protein_or_peptide / ID: 3 / Number of copies: 1 / Enantiomer: LEVO |
---|---|
Source (natural) | Organism: ![]() ![]() |
Molecular weight | Theoretical: 108.28768 KDa |
Recombinant expression | Organism: ![]() |
Sequence | String: MSEYMDDVDR EFINCLFPSY LLQQPVAYDL WILYLQHRKL FHKLKNTNLI NADENPTGVG MGRTKLTALT RKEIWSKLMN LGVLGTISF EAVNDDYLIQ VYKYFYPDVN DFTLRFGVKD SNKNSVRVMK ASSDMRKNAQ ELLEPVLSER EMALNSNTSL E NDRNDDDD ...String: MSEYMDDVDR EFINCLFPSY LLQQPVAYDL WILYLQHRKL FHKLKNTNLI NADENPTGVG MGRTKLTALT RKEIWSKLMN LGVLGTISF EAVNDDYLIQ VYKYFYPDVN DFTLRFGVKD SNKNSVRVMK ASSDMRKNAQ ELLEPVLSER EMALNSNTSL E NDRNDDDD DDDDDDDDDD DDDDDDDESD LESLEGEVDT DTDDNNEGDG SDNHEEGGEE GSRGADADVS SAQQRAERVA DP WIYQRSR SAINIETESR NLWDTSDKNS GLQYYPPDQS PSSSFSSPRV SSGNDKNDNE ATNVLSNSGS KKKNSMIPDI YKI LGYFLP SRWQAQPNNS LQLSQDGITH LQPNPDYHSY MTYERSSASS ASTRNRLRTS FENSGKVDFA VTWANKSLPD NKLT IFYYE IKVLSVTSTE SAENSNIVIG YKLVENELME ATTKKSVSRS SVAGSSSSLG GSNNMSSNRV PSTSFTMEGT QRRDY IYEG GVSAMSLNVD GSINKCQKYG FDLNVFGYCG FDGLITNSTE QSKEYAKPFG RDDVIGCGIN FIDGSIFFTK NGIHLG NAF TDLNDLEFVP YVALRPGNSI KTNFGLNEDF VFDIIGYQDK WKSLAYEHIC RGRQMDVSIE EFDSDESEED ETENGPE EN KSTNVNEDLM DIDQEDGAAG NKDTKKLNDE KDNNLKFLLG EDNRFIDGKL VRPDVNNINN LSVDDGSLPN TLNVMIND Y LIHEGLVDVA KGFLKDLQKD AVNVNGQHSE SKDVIRHNER QIMKEERMVK IRQELRYLIN KGQISKCINY IDNEIPDLL KNNLELVFEL KLANYLVMIK KSSSKDDDEI ENLILKGQEL SNEFIYDTKI PQSLRDRFSG QLSNVSALLA YSNPLVEAPK EISGYLSDE YLQERLFQVS NNTILTFLHK DSECALENVI SNTRAMLSTL LEYNAFGSTN SSDPRYYKAI NFDEDVLNL |
-Macromolecule #4: Protein FYV10
Macromolecule | Name: Protein FYV10 / type: protein_or_peptide / ID: 4 / Number of copies: 1 / Enantiomer: LEVO |
---|---|
Source (natural) | Organism: ![]() ![]() |
Molecular weight | Theoretical: 59.975102 KDa |
Recombinant expression | Organism: ![]() |
Sequence | String: MAEKSIFNEP DVDFHLKLNQ QLFHIPYELL SKRIKHTQAV INKETKSLHE HTAALNQIFE HNDVEHDELA LAKITEMIRK VDHIERFLN TQIKSYCQIL NRIKKRLEFF HELKDIKSQN SGTSHNGNNE GTRTKLIQWY QSYTNILIGD YLTRNNPIKY N SETKDHWN ...String: MAEKSIFNEP DVDFHLKLNQ QLFHIPYELL SKRIKHTQAV INKETKSLHE HTAALNQIFE HNDVEHDELA LAKITEMIRK VDHIERFLN TQIKSYCQIL NRIKKRLEFF HELKDIKSQN SGTSHNGNNE GTRTKLIQWY QSYTNILIGD YLTRNNPIKY N SETKDHWN SGVVFLKQSQ LDDLIDYDVL LEANRISTSL LHERNLLPLI SWINENKKTL TKKSSILEFQ ARLQEYIELL KV DNYTDAI VCFQRFLLPF VKSNFTDLKL ASGLLIFIKY CNDQKPTSST SSGFDTEEIK SQSLPMKKDR IFQHFFHKSL PRI TSKPAV NTTDYDKSSL INLQSGDFER YLNLLDDQRW SVLNDLFLSD FYSMYGISQN DPLLIYLSLG ISSLKTRDCL HPSD DENGN QETETATTAE KEVEDLQLFT LHSLKRKNCP VCSETFKPIT QALPFAHHIQ SQLFENPILL PNGNVYDSKK LKKLA KTLK KQNLISLNPG QIMDPVDMKI FCESDSIKMY PT |
-Macromolecule #5: Vacuolar import and degradation protein 24
Macromolecule | Name: Vacuolar import and degradation protein 24 / type: protein_or_peptide / ID: 5 / Number of copies: 1 / Enantiomer: LEVO |
---|---|
Source (natural) | Organism: ![]() ![]() |
Molecular weight | Theoretical: 41.291934 KDa |
Recombinant expression | Organism: ![]() ![]() |
Sequence | String: MINNPKVDSV AEKPKAVTSK QSEQAASPEP TPAPPVSRNQ YPITFNLTST APFHLHDRHR YLQEQDLYKC ASRDSLSSLQ QLAHTPNGS TRKKYIVEDQ SPYSSENPVI VTSSYNHTVC TNYLRPRMQF TGYQISGYKR YQVTVNLKTV DLPKKDCTSL S PHLSGFLS ...String: MINNPKVDSV AEKPKAVTSK QSEQAASPEP TPAPPVSRNQ YPITFNLTST APFHLHDRHR YLQEQDLYKC ASRDSLSSLQ QLAHTPNGS TRKKYIVEDQ SPYSSENPVI VTSSYNHTVC TNYLRPRMQF TGYQISGYKR YQVTVNLKTV DLPKKDCTSL S PHLSGFLS IRGLTNQHPE ISTYFEAYAV NHKELGFLSS SWKDEPVLNE FKATDQTDLE HWINFPSFRQ LFLMSQKNGL NS TDDNGTT NAAKKLPPQQ LPTTPSADAG NISRIFSQEK QFDNYLNERF IFMKWKEKFL VPDALLMEGV DGASYDGFYY IVH DQVTGN IQGFYYHQDA EKFQQLELVP SLKNKVESSD CSFEFA |
-Macromolecule #6: Fructose-bisphosphatase
Macromolecule | Name: Fructose-bisphosphatase / type: protein_or_peptide / ID: 6 / Number of copies: 1 / Enantiomer: LEVO / EC number: fructose-bisphosphatase |
---|---|
Source (natural) | Organism: ![]() ![]() |
Molecular weight | Theoretical: 38.303473 KDa |
Recombinant expression | Organism: ![]() ![]() |
Sequence | String: MPTLVNGPRR DSTEGFDTDI ITLPRFIIEH QKQFKNATGD FTLVLNALQF AFKFVSHTIR RAELVNLVGL AGASNFTGDQ QKKLDVLGD EIFINAMRAS GIIKVLVSEE QEDLIVFPTN TGSYAVCCDP IDGSSNLDAG VSVGTIASIF RLLPDSSGTI N DVLRCGKE ...String: MPTLVNGPRR DSTEGFDTDI ITLPRFIIEH QKQFKNATGD FTLVLNALQF AFKFVSHTIR RAELVNLVGL AGASNFTGDQ QKKLDVLGD EIFINAMRAS GIIKVLVSEE QEDLIVFPTN TGSYAVCCDP IDGSSNLDAG VSVGTIASIF RLLPDSSGTI N DVLRCGKE MVAACYAMYG SSTHLVLTLG DGVDGFTLDT NLGEFILTHP NLRIPPQKAI YSINEGNTLY WNETIRTFIE KV KQPQADN NNKPFSARYV GSMVADVHRT FLYGGLFAYP CDKKSPNGKL RLLYEAFPMA FLMEQAGGKA VNDRGERILD LVP SHIHDK SSIWLGSSGE IDKFLDHIGK SQ |
-Experimental details
-Structure determination
Method | cryo EM |
---|---|
![]() | single particle reconstruction |
Aggregation state | particle |
-
Sample preparation
Buffer | pH: 7.5 |
---|---|
Vitrification | Cryogen name: ETHANE |
-
Electron microscopy
Microscope | FEI TITAN KRIOS |
---|---|
Image recording | Film or detector model: GATAN K3 BIOQUANTUM (6k x 4k) / Average electron dose: 79.2 e/Å2 |
Electron beam | Acceleration voltage: 300 kV / Electron source: ![]() |
Electron optics | Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD |
Experimental equipment | ![]() Model: Titan Krios / Image courtesy: FEI Company |