+Open data
-Basic information
Entry | Database: EMDB / ID: EMD-11836 | |||||||||||||||
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Title | Cryo-EM density map corresponding to BcsRQAB subcomplex | |||||||||||||||
Map data | ||||||||||||||||
Sample |
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Function / homology | Function and homology information bacterial cellulose biosynthetic process / negative regulation of cell division / cytoplasmic side of plasma membrane / cell division / ATP hydrolysis activity / ATP binding / cytosol Similarity search - Function | |||||||||||||||
Biological species | Escherichia coli (E. coli) | |||||||||||||||
Method | single particle reconstruction / cryo EM / Resolution: 4.5 Å | |||||||||||||||
Authors | Zouhir S | |||||||||||||||
Funding support | France, 4 items
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Citation | Journal: Sci Adv / Year: 2021 Title: Architecture and regulation of an enterobacterial cellulose secretion system. Authors: Wiem Abidi / Samira Zouhir / Meryem Caleechurn / Stéphane Roche / Petya Violinova Krasteva / Abstract: Many free-living and pathogenic enterobacteria secrete biofilm-promoting cellulose using a multicomponent, envelope-embedded Bcs secretion system under the control of intracellular second messenger c- ...Many free-living and pathogenic enterobacteria secrete biofilm-promoting cellulose using a multicomponent, envelope-embedded Bcs secretion system under the control of intracellular second messenger c-di-GMP. The molecular understanding of system assembly and cellulose secretion has been largely limited to the crystallographic studies of a distantly homologous BcsAB synthase tandem and a low-resolution reconstruction of an assembled macrocomplex that encompasses most of the inner membrane and cytosolic subunits and features an atypical layered architecture. Here, we present cryo-EM structures of the assembled Bcs macrocomplex, as well as multiple crystallographic snapshots of regulatory Bcs subcomplexes. The structural and functional data uncover the mechanism of asymmetric secretion system assembly and periplasmic crown polymerization and reveal unexpected subunit stoichiometry, multisite c-di-GMP recognition, and ATP-dependent regulation. | |||||||||||||||
History |
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-Structure visualization
Movie |
Movie viewer |
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Structure viewer | EM map: SurfViewMolmilJmol/JSmol |
Supplemental images |
-Downloads & links
-EMDB archive
Map data | emd_11836.map.gz | 239.2 MB | EMDB map data format | |
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Header (meta data) | emd-11836-v30.xml emd-11836.xml | 29.2 KB 29.2 KB | Display Display | EMDB header |
Images | emd_11836.png | 45.4 KB | ||
Others | emd_11836_additional_1.map.gz emd_11836_additional_2.map.gz emd_11836_additional_3.map.gz emd_11836_additional_4.map.gz | 126.5 MB 131.2 MB 131.4 MB 11.2 MB | ||
Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-11836 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-11836 | HTTPS FTP |
-Validation report
Summary document | emd_11836_validation.pdf.gz | 245.7 KB | Display | EMDB validaton report |
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Full document | emd_11836_full_validation.pdf.gz | 244.9 KB | Display | |
Data in XML | emd_11836_validation.xml.gz | 7.1 KB | Display | |
Arichive directory | https://ftp.pdbj.org/pub/emdb/validation_reports/EMD-11836 ftp://ftp.pdbj.org/pub/emdb/validation_reports/EMD-11836 | HTTPS FTP |
-Related structure data
Related structure data | 6yarC 6yayC 6yb3C 6yb5C 6ybbC 6ybuC 6yg8C C: citing same article (ref.) |
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Similar structure data |
-Links
EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
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-Map
File | Download / File: emd_11836.map.gz / Format: CCP4 / Size: 262.9 MB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Voxel size | X=Y=Z: 1.05248 Å | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Density |
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Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Details | EMDB XML:
CCP4 map header:
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-Supplemental data
-Additional map: #1
File | emd_11836_additional_1.map | ||||||||||||
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Projections & Slices |
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Density Histograms |
-Additional map: #3
File | emd_11836_additional_2.map | ||||||||||||
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Projections & Slices |
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Density Histograms |
-Additional map: #4
File | emd_11836_additional_3.map | ||||||||||||
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Projections & Slices |
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Density Histograms |
-Additional map: #2
File | emd_11836_additional_4.map | ||||||||||||
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Projections & Slices |
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Density Histograms |
-Sample components
-Entire : Cryo-EM density map corresponding to BcsR2Q2AB subcomplex obtaine...
Entire | Name: Cryo-EM density map corresponding to BcsR2Q2AB subcomplex obtained after local refinement within the assembled Bcs macrocomplex(BcsRQABEF-BcsMacrocomplex.mrc). |
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Components |
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-Supramolecule #1: Cryo-EM density map corresponding to BcsR2Q2AB subcomplex obtaine...
Supramolecule | Name: Cryo-EM density map corresponding to BcsR2Q2AB subcomplex obtained after local refinement within the assembled Bcs macrocomplex(BcsRQABEF-BcsMacrocomplex.mrc). type: complex / ID: 1 / Parent: 0 / Macromolecule list: all Details: Bcs macrocomplex was purified using recombinant co-expression of constructs pRSFDuet1-Bcs(Strep)E-F-G and pCDFDuet1-Bcs(His)R-Q-A(HA-FLAG)-B and affinity pull-down using an anti-FLAG M2 ...Details: Bcs macrocomplex was purified using recombinant co-expression of constructs pRSFDuet1-Bcs(Strep)E-F-G and pCDFDuet1-Bcs(His)R-Q-A(HA-FLAG)-B and affinity pull-down using an anti-FLAG M2 resin (Sigma). The proposed stoichiometry for the resultant assembly is BcsR2-Q2-E2-F2-A-B(5-6). Densities corresponding to a BcsR2Q2AB subcomplex were improved after particle subtraction and local refinement in cryoSPARC V2. BcsE and BcsF partake in the assembled Bcs macrocomplex, BcsG does not co-purify stably with the macrocomplex. |
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Source (natural) | Organism: Escherichia coli (E. coli) / Strain: 1094 / Location in cell: Inner membrane |
Recombinant expression | Organism: Escherichia coli BL21(DE3) (bacteria) Recombinant plasmid: pRSFDuet1-Bcs(Strep)EFG and pCDFDuet1-Bcs(His)RQA(HA-FLAG)B |
Molecular weight | Theoretical: 257 KDa |
-Macromolecule #1: Bacterial cellulose synthase regulator protein BcsB
Macromolecule | Name: Bacterial cellulose synthase regulator protein BcsB / type: protein_or_peptide / ID: 1 Details: Genome-encoded BcsB harbors a signal sequence to be addressed to the periplam where according to the ServerP4.1 server prediction would result in a mature form starting with the residue #26 ...Details: Genome-encoded BcsB harbors a signal sequence to be addressed to the periplam where according to the ServerP4.1 server prediction would result in a mature form starting with the residue #26 TPATQ BcsB sequence was cloned in a pCDFDuet1 vector along Bcs(His)R, BcsQ and BcsA(HA-FLAG). 1 copy in locally refined BcsR2Q2AB map, up to 6 copies in the assembled Bcs macrocomplex. Enantiomer: LEVO |
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Source (natural) | Organism: Escherichia coli (E. coli) / Strain: 1094 |
Recombinant expression | Organism: Escherichia coli BL21(DE3) (bacteria) |
Sequence | String: TPATQPLINA EPAVAAQTEQ NPQVGQVMPG VQGAD APVV AQNGPSRDVK LTFAQIAPPP GSMVLRGINP NGSIEFGMRS DEVVTKAMLN LEYTPS PSL LPVQSQLKVY LNDELMGVLP VTKEQLGKKT LAQMPINPLF ITDFNRVRLE FVGHYQD VC ENPASTTLWL ...String: TPATQPLINA EPAVAAQTEQ NPQVGQVMPG VQGAD APVV AQNGPSRDVK LTFAQIAPPP GSMVLRGINP NGSIEFGMRS DEVVTKAMLN LEYTPS PSL LPVQSQLKVY LNDELMGVLP VTKEQLGKKT LAQMPINPLF ITDFNRVRLE FVGHYQD VC ENPASTTLWL DVGRSSGLDL TYQTLNVKND LSHFPVPFFD PRDNRTNTLP MVFAGAPD V GLQQASAIVA SWFGSRSGWR GQNFPVLYNQ LPDRNAIVFA TNDKRPDFLR DHPAVKAPV IEMINHPQNP YVKLLVVFGR DDKDLLQAAK GIAQGNILFR GESVVVNEVK PLLPRKPYDA PNWVRTDRP VTFGELKTYE EQLQSSGLEP AAINVSLNLP PDLYLMRSTG IDMDINYRYT M PPVKDSSR MDISLNNQFL QSFNLSSKQE ANRLLLRIPV LQGLLDGKTD VSIPALKLGA TN QLRFDFE YMNPMPGGSV DNCITFQPVQ NHVVIGDDST IDFSKYYHFI PMPDLRAFAN AGF PFSRMA DLSQTITVMP KAPNEAQMET LLNTVGFIGA QTGFPAINLT VTDDGSTIQG KDAD IMIIG GIPDKLKDDK QIDLLVQATE SWVKTPMRQT PFPGIVPDES DRAAETRSTL TSSGA MAAV IGFQSPYNDQ RSVIALLADS PRGYEMLNDA VNDSGKRATM FGSVAVIRES GINSLR VGD VYYVGHLPWF ERLWYALANH PILLAVLAAI SVILLAWVLW RLLRIISRRR LNPDNE |
-Macromolecule #2: Bacterial cellulose synthase protein BcsA
Macromolecule | Name: Bacterial cellulose synthase protein BcsA / type: protein_or_peptide / ID: 2 Details: BcsA sequence was cloned in pCDFDuet1 vector along with Bcs(His)R, BcsQ and BcsB. BcsA harbours a C-terminus HA-Flag Tag. 1 copy in both the locally refined BcsR2Q2AB complex and the assembled Bcs macrocomplex. Enantiomer: LEVO |
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Source (natural) | Organism: Escherichia coli (E. coli) / Strain: 1094 |
Recombinant expression | Organism: Escherichia coli BL21(DE3) (bacteria) |
Sequence | String: MSILTRWLLI PPVNARLIGR YRDYRRHGAS AFSATLGCFW MILAWIFIPL EHPRWQRIRA EHKNLYPHIN ASRPRPLDPV RYLIQTCWLL IGASRKETPK PRRRAFSGLQ NIRGRYHQWM NELPERVSHK TQHLDEKKEL GHLSAGARRL ILGIIVTFSL ILALICVTQP ...String: MSILTRWLLI PPVNARLIGR YRDYRRHGAS AFSATLGCFW MILAWIFIPL EHPRWQRIRA EHKNLYPHIN ASRPRPLDPV RYLIQTCWLL IGASRKETPK PRRRAFSGLQ NIRGRYHQWM NELPERVSHK TQHLDEKKEL GHLSAGARRL ILGIIVTFSL ILALICVTQP FNPLAQFIFL MLLWGVALIV RRMPGRFSAL MLIVLSLTVS CRYIWWRYTS TLNWDDPVSL VCGLILLFAE TYAWIVLVLG YFQVVWPLNR QPVPLPKDMS LWPSVDIFVP TYNEDLNVVK NTIYASLGID WPKDKLNIWI LDDGGREEFR QFAQNVGVKY IARTTHEHAK AGNINNALKY AKGEFVSIFD CDHVPTRSFL QMTMGWFLKE KQLAMMQTPH HFFSPDPFER NLGRFRKTPN EGTLFYGLVQ DGNDMWDATF FCGSCAVIRR KPLDEIGGIA VETVTEDAHT SLRLHRRGYT SAYMRIPQAA GLATESLSAH IGQRIRWARG MVQIFRLDNP LTGKGLKFAQ RLCYVNAMFH FLSGIPRLIF LTAPLAFLLL HAYIIYAPAL MIALFVLPHM IHASLTNSKI QGKYRHSFWS EIYETVLAWY IAPPTLVALI NPHKGKFNVT AKGGLVEEEY VDWVISRPYI FLVLLNLVGV AVGIWRYFYG PPTEMLTVVV SMVWVFYNLI VLGGAVAVSV ESKQVRRSHR VEMTMPAAIA REDGHLFSCT VQDFSDGGLG IKINGQAQIL EGQKVNLLLK RGQQEYVFPT QVARVMGNEV GLKLMPLTTQ QHIDFVQCTF ARADTWALWQ DSYPEDKPLE SLLDILKLGF RGYRHLAEFA PSSVKGIFRV LTSLVSWVVS FIPRRPERSE TAQPSDQALA QQGSARSSGR TGLEFEEFYP YDVPDYAADY KDDDDKRS |
-Macromolecule #3: Bacterial cellulose synthase regulator protein BcsR
Macromolecule | Name: Bacterial cellulose synthase regulator protein BcsR / type: protein_or_peptide / ID: 3 Details: BcsR sequence was cloned in pCDFDuet1 vector along with BcsQ, BcsA(HA-FLAG) and BcsB. BcsR harbours a N-terminal octahistidine tag (N-His8). Likely two copies in the assembled secretion ...Details: BcsR sequence was cloned in pCDFDuet1 vector along with BcsQ, BcsA(HA-FLAG) and BcsB. BcsR harbours a N-terminal octahistidine tag (N-His8). Likely two copies in the assembled secretion complexes, however the local resolution does not allow backbone tracing. High-resolution structures solved by X-ray crystallography. Enantiomer: LEVO |
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Source (natural) | Organism: Escherichia coli (E. coli) / Strain: 1094 |
Recombinant expression | Organism: Escherichia coli BL21(DE3) (bacteria) |
Sequence | String: MGSSHHHHHH HHAAGSMNNN EPDTLPDPAI GYIFQNDIVA LKQAFSLPDI DYADISQREQ LAAALKRWPL LAEFAQQK |
-Macromolecule #4: Bacterial cellulose synthase regulator protein BcsQ
Macromolecule | Name: Bacterial cellulose synthase regulator protein BcsQ / type: protein_or_peptide / ID: 4 Details: BcsQ sequence was cloned in pCDFDuet1 vector along with Bcs(His)R, BcsA(HA-FLAG) and BcsB Enantiomer: LEVO |
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Source (natural) | Organism: Escherichia coli (E. coli) / Strain: 1094 |
Recombinant expression | Organism: Escherichia coli BL21(DE3) (bacteria) |
Sequence | String: MAVLGLQGVR GGVGTTTITA ALAWSLQMLG ENVLVVDACP DNLLRLSFNV DFTHRQGWAR AMLDGQDWRD AGLRYTSQLD LLPFGQLSIE EQENPQHWQT RLSDICSGLQ QLKASGRYQW ILIDLPRDAS QITHQLLSLC DHSLAIVNVD ANCHIRLHQQ ALPDGAHILI ...String: MAVLGLQGVR GGVGTTTITA ALAWSLQMLG ENVLVVDACP DNLLRLSFNV DFTHRQGWAR AMLDGQDWRD AGLRYTSQLD LLPFGQLSIE EQENPQHWQT RLSDICSGLQ QLKASGRYQW ILIDLPRDAS QITHQLLSLC DHSLAIVNVD ANCHIRLHQQ ALPDGAHILI NNFRIGSQVQ DDIYQLWLQS QRRLLPMLIH RDEAMAECLA AKQPVGEYRS DALAAEEILT LANWCLLNYS GLKTPVGSKS |
-Experimental details
-Structure determination
Method | cryo EM |
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Processing | single particle reconstruction |
Aggregation state | particle |
-Sample preparation
Concentration | 0.8 mg/mL | ||||||||||||||
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Buffer | pH: 8 Component:
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Grid | Model: Quantifoil R1.2/1.3 / Material: GOLD / Pretreatment - Type: GLOW DISCHARGE / Details: Elmo Glow Discharge system | ||||||||||||||
Vitrification | Cryogen name: ETHANE / Chamber humidity: 100 % / Chamber temperature: 277 K / Instrument: FEI VITROBOT MARK IV |
-Electron microscopy
Microscope | FEI TITAN KRIOS |
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Specialist optics | Energy filter - Name: GIF Quantum LS |
Image recording | Film or detector model: GATAN K2 SUMMIT (4k x 4k) / Detector mode: COUNTING / Average electron dose: 1.2 e/Å2 |
Electron beam | Acceleration voltage: 300 kV / Electron source: FIELD EMISSION GUN |
Electron optics | C2 aperture diameter: 100.0 µm / Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Cs: 2.7 mm / Nominal defocus max: 2.75 µm / Nominal defocus min: 0.75 µm / Nominal magnification: 130000 |
Experimental equipment | Model: Titan Krios / Image courtesy: FEI Company |