+Open data
-Basic information
Entry | Database: EMDB / ID: EMD-42392 | ||||||||||||
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Title | Cryo-EM Structure of the Helicobacter pylori cagYdAP PR | ||||||||||||
Map data | |||||||||||||
Sample |
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Keywords | T4SS / protein translocation / MEMBRANE PROTEIN | ||||||||||||
Biological species | Helicobacter pylori 26695 (bacteria) | ||||||||||||
Method | single particle reconstruction / cryo EM / Resolution: 6.6 Å | ||||||||||||
Authors | Roberts JR | ||||||||||||
Funding support | United States, 3 items
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Citation | Journal: Life Science Alliance / Year: 2024 Title: Subdomains of the H. pylori Cag T4SS outer membrane core complex exhibit structural independence Authors: Roberts JR / Tran SC / Frick-Cheng AF / Bryant KN / Okoye CD / Cover TL / Ohi MD | ||||||||||||
History |
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-Structure visualization
Supplemental images |
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-Downloads & links
-EMDB archive
Map data | emd_42392.map.gz | 978.8 MB | EMDB map data format | |
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Header (meta data) | emd-42392-v30.xml emd-42392.xml | 16.5 KB 16.5 KB | Display Display | EMDB header |
FSC (resolution estimation) | emd_42392_fsc.xml | 21.6 KB | Display | FSC data file |
Images | emd_42392.png | 69.1 KB | ||
Filedesc metadata | emd-42392.cif.gz | 5.6 KB | ||
Others | emd_42392_half_map_1.map.gz emd_42392_half_map_2.map.gz | 964.5 MB 964.5 MB | ||
Archive directory | http://ftp.pdbj.org/pub/emdb/structures/EMD-42392 ftp://ftp.pdbj.org/pub/emdb/structures/EMD-42392 | HTTPS FTP |
-Links
EMDB pages | EMDB (EBI/PDBe) / EMDataResource |
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-Map
File | Download / File: emd_42392.map.gz / Format: CCP4 / Size: 1 GB / Type: IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES) | ||||||||||||||||||||
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Voxel size | X=Y=Z: 1.08 Å | ||||||||||||||||||||
Density |
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Symmetry | Space group: 1 | ||||||||||||||||||||
Details | EMDB XML:
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-Supplemental data
-Half map: #2
File | emd_42392_half_map_1.map | ||||||||||||
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Projections & Slices |
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Density Histograms |
-Half map: #1
File | emd_42392_half_map_2.map | ||||||||||||
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Projections & Slices |
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Density Histograms |
-Sample components
-Entire : Helicobacter pylori CagYdAP PR
Entire | Name: Helicobacter pylori CagYdAP PR |
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Components |
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-Supramolecule #1: Helicobacter pylori CagYdAP PR
Supramolecule | Name: Helicobacter pylori CagYdAP PR / type: complex / ID: 1 / Parent: 0 / Macromolecule list: all |
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Source (natural) | Organism: Helicobacter pylori 26695 (bacteria) / Strain: 26695 / Location in cell: membrane |
-Macromolecule #1: Cag pathogenicity island protein (Cag8)
Macromolecule | Name: Cag pathogenicity island protein (Cag8) / type: protein_or_peptide / ID: 1 / Enantiomer: LEVO |
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Source (natural) | Organism: Helicobacter pylori 26695 (bacteria) |
Sequence | String: MGQAFFKKIV GCFCLGYLF L SSAIEAAA LD IKNFNRG RVK VVNKKI AYLG DEKPI TIWTS LDNV TVIQLE KDE TISYITT GF NKGWSIVP N SNHIFIQPK SVKSNLMFEK EAVNFALMT R DYQEFLKT KK LIVDAPD PKE LEEQKK ALEK EKEAK ...String: MGQAFFKKIV GCFCLGYLF L SSAIEAAA LD IKNFNRG RVK VVNKKI AYLG DEKPI TIWTS LDNV TVIQLE KDE TISYITT GF NKGWSIVP N SNHIFIQPK SVKSNLMFEK EAVNFALMT R DYQEFLKT KK LIVDAPD PKE LEEQKK ALEK EKEAK EQAQK AQKD KREKRK EER AKNRANL EN LTNAMSNP Q NLSNNKNLS EFIKQQRENE LDQMERLED M QEQAQANA LK QIEELNK KQA EETIKQ RAKD KINIK TDKPQ KSPE DNSIEL SPS DSAWRTN LV VRTNKALY Q FILRIAQKD NFASAYLTVK LEYPQRHEV S SVIEELKK RE EAKRQKE LIK QENLNT TAYI NRVMM ASNEQ IINK EKIREE KQK IILDQAK AL ETQYVHNA L KRNPVPRNY NYYQAPEKRS KHIMPSEIF D DGTFTYFG FK NITLQPA IFV VQPDGK LSMT DAAID PNMTN SGLR WYRVNE IAE KFKLIKD KA LVTVINKG Y GKNPLTKNY NIKNYGELER VIKKLPEVR D K |
-Macromolecule #2: Cag pathogenicity island protein (Cag7)
Macromolecule | Name: Cag pathogenicity island protein (Cag7) / type: protein_or_peptide / ID: 2 / Enantiomer: LEVO |
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Source (natural) | Organism: Helicobacter pylori 26695 (bacteria) |
Sequence | String: MNEENDKLET SKKAQQDSPQ DLSNEEATEA NHFENLLKES KESSDHHLDN PTETQTHFDG DKSEETQTQM DSEGNETSES SNGSLADKLF KKARKLVDNK KPFTQQKNLD EETQELNEED DQENNEYQEE TQTDLIDDET SKKTQQHSPQ DLSNEEATEA NHFENLLKES ...String: MNEENDKLET SKKAQQDSPQ DLSNEEATEA NHFENLLKES KESSDHHLDN PTETQTHFDG DKSEETQTQM DSEGNETSES SNGSLADKLF KKARKLVDNK KPFTQQKNLD EETQELNEED DQENNEYQEE TQTDLIDDET SKKTQQHSPQ DLSNEEATEA NHFENLLKES KESSDHHLDN PTETQTNFDG DKSEETQTQM DSEGNETSES SNGSLADKLF KKARKLVDNK KPFTQQKNLD EETQELNEED DQENNEYQEE TQTDLIDDET SKKTQQHSPQ DLSNEEATEA NHFENLLKES KESSDHHLDN PTETQTNFDG DKSEEITDDS NDQEIIKGSK KKYIIGGIVV AVLIVIILFS RSIFHYFMPL EDKSSRFSKD RNLYVNDEIQ IRQEYNRLLK ERNEKGNMID KNLFFNDDPN RTLYNYLNIA EIEDKNPLRA FYECISNGGN YEECLKLIKD KKLQDQMKKT LEAYNDCIKN AKTEEERIKC LDLIKDENLK KSLLNQQKVQ VALDCLKNAK TDEERNECLK LINDPEIREK FRKELELQKE LQEYKDCIKN AKTEAEKNKC LKGLSKEAIE RLKQQALDCL KNAKTDEERN ECLKNIPQDL QKELLADMSV KAYKDCVSKA RNEKEKQECE KLLTPEARKK LEQQVLDCLK NAKTDEERKK CLKDLPKDLQ SDILAKESLK AYKDCVSQAK TEAEKKECEK LLTPEAKKLL EEEAKESVKA YLDCVSQAKT EAEKKECEKL LTPEAKKKLE EAKKSVKAYL DCVSRARNEK EKKECEKLLT PEAKKLLEQQ ALDCLKNAKT DKERKKCLKD LPKDLQKKVL AKESVKAYLD CVSQAKTEAE KKECEKLLTP EARKLLEEAK KSVKAYLDCV SQAKTEAEKK ECEKLLTPEA RKLLEEXAKE SVKAYLDCVS QAKNEAEKKE CEKLLTLESK KKLEEAKKSV KAYLDCVSQA KTEAEKKECE KLLTPEAKKL LEQQALDCLK NAKTEADKKR CVKDLPKDLQ KKVLAKESLK AYKDCVSKAR NEKEKKECEK LLTPEAKKLL EEAKKSVKAY LDCVSQAKTE AEKKECEKLL TPEARKLLEE AKESVKAYKD CVSKARNEKE KKECEKLLTP EAKKLLEQQV LDCLKNAKTE ADKKRCVKDL PKDLQKKVLA KESVKAYLDC VSRARNEKEK KECEKLLTPE AKKLLEEAKE SLKAYKDCLS QARNEEERRA CEKLLTPEAR KLLEQEVKKS IKAYLDCVSR ARNEKEKKEC EKLLTPEARK FLAKQVLNCL EKAGNEEERK ACLKNLPKDL QENILAKESL KAYKDCLSQA RNEEERRACE KLLTPEARKL LEQEVKKSVK AYLDCVSRAR NEKEKKECEK LLTPEARKFL AKELQQKDKA IKDCLKNADP NDRAAIMKCL DGLSDEEKLK YLQEAREKAV ADCLAMAKTD EEKRKCQNLY SDLIQEIQNK RTQNKQNQLS KTERLHQASE CLDNLDDPTD QEAIEQCLEG LSDSERALIL GIKRQADEVD LIYSDLRNRK TFDNMAAKGY PLLPMDFKNG GDIATINATN VDADKIASDN PIYASIEPDI AKQYETEKTI KDKNLEAKLA KALGGNKKDD DKEKSKKSTA EAKAENNKID KDVAETAKNI SEIALKNKKE KSGEFVDENG NPIDDKKKAE KQDETSPVKQ AFIGKSDPTF VLAQYTPIEI TLTSKVDATL TGIVSGVVAK DVWNMNGTMI LLDKGTKVYG NYQSVKGGTP IMTRLMIVFT KAITPDGVII PLANAQAAGM LGEAGVDGYV NNMNIPPSFY KNEGDSIKIL TMDDIDFSGV YDVKITNKSV VDEIIKQSTK TLSREHEEIT TSPKGGN |
-Experimental details
-Structure determination
Method | cryo EM |
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Processing | single particle reconstruction |
Aggregation state | particle |
-Sample preparation
Concentration | 0.4 mg/mL |
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Buffer | pH: 7 |
Vitrification | Cryogen name: NITROGEN |
-Electron microscopy
Microscope | TFS KRIOS |
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Electron beam | Acceleration voltage: 300 kV / Electron source: FIELD EMISSION GUN |
Electron optics | Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELDBright-field microscopy / Nominal defocus max: 2.5 µm / Nominal defocus min: 1.0 µm |
Specialist optics | Energy filter - Name: GIF Bioquantum / Energy filter - Slit width: 20 eV |
Image recording | Film or detector model: GATAN K3 (6k x 4k) / Average electron dose: 60.0 e/Å2 |
Experimental equipment | Model: Titan Krios / Image courtesy: FEI Company |