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Open data
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Basic information
Entry | ![]() | |||||||||
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Title | Medusavirus Nucleosome Core Particle Native | |||||||||
![]() | Medusavirus medusae Nucleosome-like particle Native | |||||||||
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![]() | DNA Protein Complex / Nucleosome / Giant Virus / NCLDV / DNA BINDING PROTEIN | |||||||||
Biological species | ![]() ![]() | |||||||||
Method | single particle reconstruction / cryo EM / Resolution: 5.1 Å | |||||||||
![]() | Toner CM / Luger K | |||||||||
Funding support | ![]()
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![]() | ![]() Title: Characterization of Medusavirus encoded histones reveals nucleosome-like structures and a unique linker histone. Authors: Chelsea M Toner / Nicole M Hoitsma / Sashi Weerawarana / Karolin Luger / ![]() Abstract: The organization of DNA into nucleosomes is a ubiquitous and ancestral feature that was once thought to be exclusive to the eukaryotic domain of life. Intriguingly, several representatives of the ...The organization of DNA into nucleosomes is a ubiquitous and ancestral feature that was once thought to be exclusive to the eukaryotic domain of life. Intriguingly, several representatives of the Nucleocytoplasmic Large DNA Viruses (NCLDV) encode histone-like proteins that in Melbournevirus were shown to form nucleosome-like particles. Medusavirus medusae (MM), a distantly related giant virus, encodes all four core histone proteins and, unique amongst most giant viruses, a putative acidic protein with two domains resembling eukaryotic linker histone H1. Here, we report the structure of nucleosomes assembled with MM histones and highlight similarities and differences with eukaryotic and Melbournevirus nucleosomes. Our structure provides insight into how variations in histone tail and loop lengths are accommodated within the context of the nucleosome. We show that MM-histones assemble into tri-nucleosome arrays, and that the putative linker histone H1 does not function in chromatin compaction. These findings expand our limited understanding of chromatin organization by virus-encoded histones. | |||||||||
History |
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Structure visualization
Supplemental images |
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Downloads & links
-EMDB archive
Map data | ![]() | 59.7 MB | ![]() | |
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Header (meta data) | ![]() ![]() | 19.6 KB 19.6 KB | Display Display | ![]() |
Images | ![]() | 101.2 KB | ||
Filedesc metadata | ![]() | 5.5 KB | ||
Others | ![]() ![]() | 59.4 MB 59.4 MB | ||
Archive directory | ![]() ![]() | HTTPS FTP |
-Related structure data
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Links
EMDB pages | ![]() ![]() |
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Map
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Annotation | Medusavirus medusae Nucleosome-like particle Native | ||||||||||||||||||||||||||||||||||||
Projections & slices | Image control
Images are generated by Spider. | ||||||||||||||||||||||||||||||||||||
Voxel size | X=Y=Z: 1.017 Å | ||||||||||||||||||||||||||||||||||||
Density |
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Symmetry | Space group: 1 | ||||||||||||||||||||||||||||||||||||
Details | EMDB XML:
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-Supplemental data
-Half map: Medusavirus medusae Nucleosome-like particle Native half map A
File | emd_45981_half_map_1.map | ||||||||||||
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Annotation | Medusavirus medusae Nucleosome-like particle Native half map A | ||||||||||||
Projections & Slices |
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Density Histograms |
-Half map: Medusavirus medusae Nucleosome-like particle Native half map B
File | emd_45981_half_map_2.map | ||||||||||||
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Annotation | Medusavirus medusae Nucleosome-like particle Native half map B | ||||||||||||
Projections & Slices |
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Density Histograms |
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Sample components
-Entire : Medusavirus Nucleosome Core Particle
Entire | Name: Medusavirus Nucleosome Core Particle |
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Components |
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-Supramolecule #1: Medusavirus Nucleosome Core Particle
Supramolecule | Name: Medusavirus Nucleosome Core Particle / type: complex / ID: 1 / Parent: 0 / Macromolecule list: all |
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-Supramolecule #2: Histone Complex
Supramolecule | Name: Histone Complex / type: complex / ID: 2 / Parent: 1 / Macromolecule list: #1-#4 |
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Source (natural) | Organism: ![]() |
-Supramolecule #3: WIDOM 601 DNA
Supramolecule | Name: WIDOM 601 DNA / type: complex / ID: 3 / Parent: 1 / Macromolecule list: #5-#6 |
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Source (natural) | Organism: synthetic construct (others) |
-Macromolecule #1: Histone H3
Macromolecule | Name: Histone H3 / type: protein_or_peptide / ID: 1 / Enantiomer: LEVO |
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Source (natural) | Organism: ![]() |
Recombinant expression | Organism: ![]() ![]() |
Sequence | String: MHHHHHHGKP IPNPLLGLDS TENLYFQGID PFTMPKERAI KKSKSAVKKV AEKKAAIKSK AKKAATGVKK PHRFRPGTTA KRLSKKEQKL SSTKTTVRRA PFGRIVRTIA SLSSADSMRF SANAVDLLQQ GIELYMLDLM KNAALAAKQA KRMTLMGKDI DLIQTANHEM ...String: MHHHHHHGKP IPNPLLGLDS TENLYFQGID PFTMPKERAI KKSKSAVKKV AEKKAAIKSK AKKAATGVKK PHRFRPGTTA KRLSKKEQKL SSTKTTVRRA PFGRIVRTIA SLSSADSMRF SANAVDLLQQ GIELYMLDLM KNAALAAKQA KRMTLMGKDI DLIQTANHEM IDEAHAAKLA NTSSAGFARR RVTKKE |
-Macromolecule #2: Histone H4
Macromolecule | Name: Histone H4 / type: protein_or_peptide / ID: 2 / Enantiomer: LEVO |
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Source (natural) | Organism: ![]() |
Recombinant expression | Organism: ![]() ![]() |
Sequence | String: MHHHHHHGKP IPNPLLGLDS TENLYFQGID PFTMPKKIAA RRSSKHIKNL GEEIGNSAVR KTVLRTGVVF RLDKTVRPKF HKVMLSKLYE AVNIAKLAAK HSGRSTIQPK DVRLGLKLAS IKLLA |
-Macromolecule #3: Histone H2A
Macromolecule | Name: Histone H2A / type: protein_or_peptide / ID: 3 / Enantiomer: LEVO |
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Source (natural) | Organism: ![]() |
Recombinant expression | Organism: ![]() ![]() |
Sequence | String: MHHHHHHGKP IPNPLLGLDS TENLYFQGID PFTMEIDSHV QPAEVLAAAS ESMQLEEQTQ LPASAAGEAL EELQTEGKKT SPAKKRTSSG KNVKRANERA GLKLPPGRIQ KIIKANQTTD VGRSSPTASV FLTAVIEDIV KEIIKGADKK SEERGRIRIS PQDILKYLTE ...String: MHHHHHHGKP IPNPLLGLDS TENLYFQGID PFTMEIDSHV QPAEVLAAAS ESMQLEEQTQ LPASAAGEAL EELQTEGKKT SPAKKRTSSG KNVKRANERA GLKLPPGRIQ KIIKANQTTD VGRSSPTASV FLTAVIEDIV KEIIKGADKK SEERGRIRIS PQDILKYLTE NGEAYMHILG DAFVSHGGVG QVAEMAAAAA NTGIKKRKRA ASTAEGAPKK KIAKKAAAKK ATGAKKVVKK KSGSTKSKTT GKSVTKKASS RKVASA |
-Macromolecule #4: Histone H2B
Macromolecule | Name: Histone H2B / type: protein_or_peptide / ID: 4 / Enantiomer: LEVO |
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Source (natural) | Organism: ![]() |
Recombinant expression | Organism: ![]() ![]() |
Sequence | String: MHHHHHHGKP IPNPLLGLDS TENLYFQGID PFTMSQIDEH VTEMTEFEAE HESTYSEHSD EEEQELGARV PSRKQKGKAA AKKVKKAVAK KSGEERRRKK NYDSFATFIA KLVGPNGKGR KPGFSAKGME VLESIVKSLA TEMTIVANEL AKHQGRQTLG AGDFRTALAV ...String: MHHHHHHGKP IPNPLLGLDS TENLYFQGID PFTMSQIDEH VTEMTEFEAE HESTYSEHSD EEEQELGARV PSRKQKGKAA AKKVKKAVAK KSGEERRRKK NYDSFATFIA KLVGPNGKGR KPGFSAKGME VLESIVKSLA TEMTIVANEL AKHQGRQTLG AGDFRTALAV RGSLIAREPA TVKALTEMGE KAVLKYQSSL GRPAKTAPKK KKATKKASA |
-Macromolecule #5: WIDOM 601 DNA (207 MER) strand 1
Macromolecule | Name: WIDOM 601 DNA (207 MER) strand 1 / type: dna / ID: 5 / Details: 5' - 3', double stranded / Classification: DNA |
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Source (natural) | Organism: synthetic construct (others) |
Sequence | String: ATCGGACCCT ATCGCGAGCC AGGCCTGAGA ATCCGGTGCC GAGGCCGCTC AATTGGTCGT AGACAGCTCT AGCACCGCTT AAACGCACGT ACGCGCTGTC CCCCGCGTTT TAACCGCCAA GGGGATTACT CCCTAGTCTC CAGGCACGTG TCAGATATAT ACATCCAGGC ...String: ATCGGACCCT ATCGCGAGCC AGGCCTGAGA ATCCGGTGCC GAGGCCGCTC AATTGGTCGT AGACAGCTCT AGCACCGCTT AAACGCACGT ACGCGCTGTC CCCCGCGTTT TAACCGCCAA GGGGATTACT CCCTAGTCTC CAGGCACGTG TCAGATATAT ACATCCAGGC CTTGTGTCGC GAAATTCATA TTAATTAATA CTAGAT |
-Macromolecule #6: WIDOM 601 DNA (207 MER) Strand 2
Macromolecule | Name: WIDOM 601 DNA (207 MER) Strand 2 / type: dna / ID: 6 / Classification: DNA |
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Source (natural) | Organism: synthetic construct (others) |
Sequence | String: ATCTAGTATT AATTAATATG AATTTCGCGA CACAAGGCCT GGATGTATAT ATCTGACACG TGCCTGGAG ACTAGGGAGT AATCCCCTTG GCGGTTAAAA CGCGGGGGAC AGCGCGTACG T GCGTTTAA GCGGTGCTAG AGCTGTCTAC GACCAATTGA GCGGCCTCGG ...String: ATCTAGTATT AATTAATATG AATTTCGCGA CACAAGGCCT GGATGTATAT ATCTGACACG TGCCTGGAG ACTAGGGAGT AATCCCCTTG GCGGTTAAAA CGCGGGGGAC AGCGCGTACG T GCGTTTAA GCGGTGCTAG AGCTGTCTAC GACCAATTGA GCGGCCTCGG CACCGGATTC TC AGGCCTG GCTCGCGATA GGGTCCGAT |
-Experimental details
-Structure determination
Method | cryo EM |
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![]() | single particle reconstruction |
Aggregation state | particle |
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Sample preparation
Concentration | 0.8 mg/mL | ||||||||||||
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Buffer | pH: 7.5 Component:
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Vitrification | Cryogen name: ETHANE / Chamber humidity: 100 % / Chamber temperature: 277 K |
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Electron microscopy
Microscope | FEI TITAN KRIOS |
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Image recording | Film or detector model: FEI FALCON IV (4k x 4k) / Average electron dose: 46.0 e/Å2 |
Electron beam | Acceleration voltage: 300 kV / Electron source: ![]() |
Electron optics | Illumination mode: FLOOD BEAM / Imaging mode: BRIGHT FIELD / Nominal defocus max: 2.0 µm / Nominal defocus min: 0.4 µm |
Experimental equipment | ![]() Model: Titan Krios / Image courtesy: FEI Company |
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Image processing
Startup model | Type of model: INSILICO MODEL |
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Final reconstruction | Resolution.type: BY AUTHOR / Resolution: 5.1 Å / Resolution method: FSC 0.143 CUT-OFF / Number images used: 72768 |
Initial angle assignment | Type: MAXIMUM LIKELIHOOD |
Final angle assignment | Type: MAXIMUM LIKELIHOOD |