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Open data
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Basic information
| Entry | ![]() | ||||||||||||
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| Title | Structure of M. tuberculosis type-I FAS in the apo state | ||||||||||||
Map data | Main sharpened map | ||||||||||||
Sample |
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Keywords | Fatty acid synthase / BIOSYNTHETIC PROTEIN | ||||||||||||
| Function / homology | Function and homology informationfatty acid synthase complex / beta-ketoacyl-[acyl-carrier-protein] synthase I / enoyl-[acyl-carrier-protein] reductase (NADH) activity / fatty acid synthase activity / fatty acid biosynthetic process / hydrolase activity Similarity search - Function | ||||||||||||
| Biological species | ![]() | ||||||||||||
| Method | single particle reconstruction / cryo EM / Resolution: 2.83 Å | ||||||||||||
Authors | Mazhab-Jafari MT / Samani EK | ||||||||||||
| Funding support | Canada, 3 items
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Citation | Journal: To Be PublishedTitle: Structural basis of product recognition by Mycobacterium Tuberculosis fatty acid synthase Authors: Samani EK / Mazhab-Jafari MT | ||||||||||||
| History |
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Structure visualization
| Supplemental images |
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Downloads & links
-EMDB archive
| Map data | emd_71792.map.gz | 204.1 MB | EMDB map data format | |
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| Header (meta data) | emd-71792-v30.xml emd-71792.xml | 20.7 KB 20.7 KB | Display Display | EMDB header |
| Images | emd_71792.png | 95.6 KB | ||
| Filedesc metadata | emd-71792.cif.gz | 7.9 KB | ||
| Others | emd_71792_half_map_1.map.gz emd_71792_half_map_2.map.gz | 226.4 MB 226.4 MB | ||
| Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-71792 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-71792 | HTTPS FTP |
-Validation report
| Summary document | emd_71792_validation.pdf.gz | 1.1 MB | Display | EMDB validaton report |
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| Full document | emd_71792_full_validation.pdf.gz | 1.1 MB | Display | |
| Data in XML | emd_71792_validation.xml.gz | 15.9 KB | Display | |
| Data in CIF | emd_71792_validation.cif.gz | 19 KB | Display | |
| Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-71792 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-71792 | HTTPS FTP |
-Related structure data
| Related structure data | ![]() 9pqxMC ![]() 9pqyC ![]() 9pqzC M: atomic model generated by this map C: citing same article ( |
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| Similar structure data | Similarity search - Function & homology F&H Search |
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Links
| EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
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| Related items in Molecule of the Month |
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Map
| File | Download / File: emd_71792.map.gz / Format: CCP4 / Size: 244.1 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||
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| Annotation | Main sharpened map | ||||||||||||||||||||||||||||||||||||
| Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||
| Voxel size | X=Y=Z: 0.93 Å | ||||||||||||||||||||||||||||||||||||
| Density |
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| Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||
| Details | EMDB XML:
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-Supplemental data
-Half map: half map A
| File | emd_71792_half_map_1.map | ||||||||||||
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| Annotation | half map A | ||||||||||||
| Projections & Slices |
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| Density Histograms |
-Half map: half map B
| File | emd_71792_half_map_2.map | ||||||||||||
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| Annotation | half map B | ||||||||||||
| Projections & Slices |
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| Density Histograms |
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Sample components
-Entire : Fatty acid synthase
| Entire | Name: Fatty acid synthase |
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| Components |
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-Supramolecule #1: Fatty acid synthase
| Supramolecule | Name: Fatty acid synthase / type: complex / ID: 1 / Parent: 0 / Macromolecule list: #1 |
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| Source (natural) | Organism: ![]() |
| Molecular weight | Theoretical: 1.8 MDa |
-Macromolecule #1: 3-oxoacyl-ACP synthase
| Macromolecule | Name: 3-oxoacyl-ACP synthase / type: protein_or_peptide / ID: 1 / Number of copies: 6 / Enantiomer: LEVO / EC number: beta-ketoacyl-[acyl-carrier-protein] synthase I |
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| Source (natural) | Organism: ![]() |
| Molecular weight | Theoretical: 326.601562 KDa |
| Recombinant expression | Organism: ![]() |
| Sequence | String: MTIHEHDRVS ADRGGDSPHT THALVDRLMA GEPYAVAFGG QGSAWLETLE ELVSATGIET ELATLVGEAE LLLDPVTDEL IVVRPIGFE PLQWVRALAA EDPVPSDKHL TSAAVSVPGV LLTQIAATRA LARQGMDLVA TPPVAMAGHS QGVLAVEALK A GGARDVEL ...String: MTIHEHDRVS ADRGGDSPHT THALVDRLMA GEPYAVAFGG QGSAWLETLE ELVSATGIET ELATLVGEAE LLLDPVTDEL IVVRPIGFE PLQWVRALAA EDPVPSDKHL TSAAVSVPGV LLTQIAATRA LARQGMDLVA TPPVAMAGHS QGVLAVEALK A GGARDVEL FALAQLIGAA GTLVARRRGI SVLGDRPPMV SVTNADPERI GRLLDEFAQD VRTVLPPVLS IRNGRRAVVI TG TPEQLSR FELYCRQISE KEEADRKNKV RGGDVFSPVF EPVQVEVGFH TPRLSDGIDI VAGWAEKAGL DVALARELAD AIL IRKVDW VDEITRVHAA GARWILDLGP GDILTRLTAP VIRGLGIGIV PAATRGGQRN LFTVGATPEV ARAWSSYAPT VVRL PDGRV KLSTKFTRLT GRSPILLAGM TPTTVDAKIV AAAANAGHWA ELAGGGQVTE EIFGNRIEQM AGLLEPGRTY QFNAL FLDP YLWKLQVGGK RLVQKARQSG AAIDGVVISA GIPDLDEAVE LIDELGDIGI SHVVFKPGTI EQIRSVIRIA TEVPTK PVI MHVEGGRAGG HHSWEDLDDL LLATYSELRS RANITVCVGG GIGTPRRAAE YLSGRWAQAY GFPLMPIDGI LVGTAAM AT KESTTSPSVK RMLVDTQGTD QWISAGKAQG GMASSRSQLG ADIHEIDNSA SRCGRLLDEV AGDAEAVAER RDEIIAAM A KTAKPYFGDV ADMTYLQWLR RYVELAIGEG NSTADTASVG SPWLADTWRD RFEQMLQRAE ARLHPQDFGP IQTLFTDAG LLDNPQQAIA ALLARYPDAE TVQLHPADVP FFVTLCKTLG KPVNFVPVID QDVRRWWRSD SLWQAHDARY DADAVCIIPG TASVAGITR MDEPVGELLD RFEQAAIDEV LGAGVEPKDV ASRRLGRADV AGPLAVVLDA PDVRWAGRTV TNPVHRIADP A EWQVHDGP ENPRATHSST GARLQTHGDD VALSVPVSGT WVDIRFTLPA NTVDGGTPVI ATEDATSAMR TVLAIAAGVD SP EFLPAVA NGTATLTVDW HPERVADHTG VTATFGEPLA PSLTNVPDAL VGPCWPAVFA AIGSAVTDTG EPVVEGLLSL VHL DHAARV VGQLPTVPAQ LTVTATAANA TDTDMGRVVP VSVVVTGADG AVIATLEERF AILGRTGSAE LADPARAGGA VSAN ATDTP RRRRRDVTIT APVDMRPFAV VSGDHNPIHT DRAAALLAGL ESPIVHGMWL SAAAQHAVTA TDGQARPPAR LVGWT ARFL GMVRPGDEVD FRVERVGIDQ GAEIVDVAAR VGSDLVMSAS ARLAAPKTVY AFPGQGIQHK GMGMEVRARS KAARKV WDT ADKFTRDTLG FSVLHVVRDN PTSIIASGVH YHHPDGVLYL TQFTQVAMAT VAAAQVAEMR EQGAFVEGAI ACGHSVG EY TALACVTGIY QLEALLEMVF HRGSKMHDIV PRDELGRSNY RLAAIRPSQI DLDDADVPAF VAGIAESTGE FLEIVNFN L RGSQYAIAGT VRGLEALEAE VERRRELTGG RRSFILVPGI DVPFHSRVLR VGVAEFRRSL DRVMPRDADP DLIIGRYIP NLVPRLFTLD RDFIQEIRDL VPAEPLDEIL ADYDTWLRER PREMARTVFI ELLAWQFASP VRWIETQDLL FIEEAAGGLG VERFVEIGV KSSPTVAGLA TNTLKLPEYA HSTVEVLNAE RDAAVLFATD TDPEPEPEED EPVAESPAPD VVSEAAPVAP A ASSAGPRP DDLVFDAADA TLALIALSAK MRIDQIEELD SIESITDGAS SRRNQLLVDL GSELNLGAID GAAESDLAGL RS QVTKLAR TYKPYGPVLS DAINDQLRTV LGPSGKRPGA IAERVKKTWE LGEGWAKHVT VEVALGTREG SSVRGGAMGH LHE GALADA ASVDKVIDAA VASVAARQGV SVALPSAGSG GGATIDAAAL SEFTDQITGR EGVLASAARL VLGQLGLDDP VNAL PAAPD SELIDLVTAE LGADWPRLVA PVFDPKKAVV FDDRWASARE DLVKLWLTDE GDIDADWPRL AERFEGAGHV VATQA TWWQ GKSLAAGRQI HASLYGRIAA GAENPEPGRY GGEVAVVTGA SKGSIAASVV ARLLDGGATV IATTSKLDEE RLAFYR TLY RDHARYGAAL WLVAANMASY SDVDALVEWI GTEQTESLGP QSIHIKDAQT PTLLFPFAAP RVVGDLSEAG SRAEMEM KV LLWAVQRLIG GLSTIGAERD IASRLHVVLP GSPNRGMFGG DGAYGEAKSA LDAVVSRWHA ESSWAARVSL AHALIGWT R GTGLMGHNDA IVAAVEEAGV TTYSTDEMAA LLLDLCDAES KVAAARSPIK ADLTGGLAEA NLDMAELAAK AREQMSAAA AVDEDAEAPG AIAALPSPPR GFTPAPPPQW DDLDVDPADL VVIVGGAEIG PYGSSRTRFE MEVENELSAA GVLELAWTTG LIRWEDDPQ PGWYDTESGE MVDESELVQR YHDAVVQRVG IREFVDDGAI DPDHASPLLV SVFLEKDFAF VVSSEADARA F VEFDPEHT VIRPVPDSTD WQVIRKAGTE IRVPRKTKLS RVVGGQIPTG FDPTVWGISA DMAGSIDRLA VWNMVATVDA FL SSGFSPA EVMRYVHPSL VANTQGTGMG GGTSMQTMYH GNLLGRNKPN DIFQEVLPNI IAAHVVQSYV GSYGAMIHPV AAC ATAAVS VEEGVDKIRL GKAQLVVAGG LDDLTLEGII GFGDMAATAD TSMMCGRGIH DSKFSRPNDR RRLGFVEAQG GGTI LLARG DLALRMGLPV LAVVAFAQSF GDGVHTSIPA PGLGALGAGR GGKDSPLARA LAKLGVAADD VAVISKHDTS TLAND PNET ELHERLADAL GRSEGAPLFV VSQKSLTGHA KGGAAVFQMM GLCQILRDGV IPPNRSLDCV DDELAGSAHF VWVRDT LRL GGKFPLKAGM LTSLGFGHVS GLVALVHPQA FIASLDPAQR ADYQRRADAR LLAGQRRLAS AIAGGAPMYQ RPGDRRF DH HAPERPQEAS MLLNPAARLG DGEAYIG UniProtKB: 3-oxoacyl-ACP synthase |
-Macromolecule #2: FLAVIN MONONUCLEOTIDE
| Macromolecule | Name: FLAVIN MONONUCLEOTIDE / type: ligand / ID: 2 / Number of copies: 6 / Formula: FMN |
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| Molecular weight | Theoretical: 456.344 Da |
| Chemical component information | ![]() ChemComp-FMN: |
-Experimental details
-Structure determination
| Method | cryo EM |
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Processing | single particle reconstruction |
| Aggregation state | particle |
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Sample preparation
| Concentration | 2 mg/mL |
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| Buffer | pH: 7.4 |
| Grid | Model: Homemade / Material: COPPER/RHODIUM / Mesh: 400 / Support film - Material: GOLD / Support film - topology: HOLEY / Support film - Film thickness: 30 / Pretreatment - Type: GLOW DISCHARGE / Pretreatment - Time: 25 sec. / Pretreatment - Atmosphere: AIR |
| Vitrification | Cryogen name: ETHANE / Chamber humidity: 100 % / Chamber temperature: 277 K / Instrument: FEI VITROBOT MARK IV |
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Electron microscopy
| Microscope | TFS KRIOS |
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| Image recording | Film or detector model: FEI FALCON IV (4k x 4k) / Average electron dose: 40.0 e/Å2 |
| Electron beam | Acceleration voltage: 300 kV / Electron source: FIELD EMISSION GUN |
| Electron optics | Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Nominal defocus max: 2.5 µm / Nominal defocus min: 0.6 µm |
| Experimental equipment | ![]() Model: Titan Krios / Image courtesy: FEI Company |
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About Yorodumi




Keywords
Authors
Canada, 3 items
Citation







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Y (Row.)
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Processing
FIELD EMISSION GUN

