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            <depositionDate>2025-04-04</depositionDate>
            <releaseDate>2025-05-14</releaseDate>
            <updateDate>2025-05-14</updateDate>
        </keyDates>
        <title>Single-particle cryo-EM of Staphylococcus aureus ribosomes inhibited by fusidic acid and fusidic acid cyclopentane</title>
        <correspondingAuthor private="true">
            <authorORCID>0000-0002-4302-6855</authorORCID>
            <firstName>Adrián</firstName>
            <lastName>González-López</lastName>
            <organization type="academic">Department of Cell and Molecular Biology (ICM), Uppsala University</organization>
            <street>Box 596</street>
            <townOrCity>Uppsala</townOrCity>
            <stateOrProvince>Uppland</stateOrProvince>
            <country>Sweden</country>
            <postOrZipCode>75124</postOrZipCode>
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            <firstName>Maria</firstName>
            <lastName>Selmer</lastName>
            <organization type="academic">Department of Cell and Molecular Biology (ICM), Uppsala University</organization>
            <street>Box 596</street>
            <townOrCity>Uppsala</townOrCity>
            <stateOrProvince>Uppland</stateOrProvince>
            <country>Sweden</country>
            <postOrZipCode>75124</postOrZipCode>
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            <author authorORCID="0000-0002-4302-6855">González-López A</author>
            <author authorORCID="0000-0001-7683-6419">Larsson DSD</author>
            <author authorORCID="0000-0001-9079-2774">Selmer M</author>
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                <fundingBody>Swedish Research Council</fundingBody>
                <code>2017-03827</code>
                <country>Sweden</country>
            </grantReference>
            <grantReference>
                <fundingBody>Swedish Research Council</fundingBody>
                <code>2022-04511</code>
                <country>Sweden</country>
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        <entryDOI>10.6019/EMPIAR-12723</entryDOI>
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        <scale>molecule</scale>
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    <crossReferences>
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            <emdbEntry>EMD-17365</emdbEntry>
            <emdbEntry>EMD-17363</emdbEntry>
            <emdbEntry>EMD-17364</emdbEntry>
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                    <author authorORCID="0000-0002-4302-6855" order="1">González-López A</author>
                    <author order="2">Larsson DSD</author>
                    <author order="3">Koripella RK</author>
                    <author order="4">Cain BN</author>
                    <author order="5">Chavez MG</author>
                    <author order="6">Hergenrother PJ</author>
                    <author order="7">Sanyal S</author>
                    <author authorORCID="0000-0001-9079-2774" order="8">Selmer M</author>
                    <title>Structures of the Staphylococcus aureus ribosome inhibited by fusidic acid and fusidic acid cyclopentane</title>
                    <journal>Scientific reports</journal>
                    <journalAbbreviation>Sci Rep</journalAbbreviation>
                    <country></country>
                    <issue>1</issue>
                    <volume>14</volume>
                    <year>2024</year>
                    <language>English</language>
                    <externalReferences type="doi">10.1038/s41598-024-64868-x</externalReferences>
                    <externalReferences type="pubmed">38902339</externalReferences>
                </journalCitation>
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        <name>Unaligned multi-frame micrographs of FA-CP inhibited ribosomes</name>
        <directory>/data/FA-CP_Krios_dataset/raw_movies</directory>
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        <headerFormat>EER</headerFormat>
        <dataFormat>EER</dataFormat>
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        <voxelType>UNSIGNED BYTE</voxelType>
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            <imageHeight>4096</imageHeight>
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        <details>Data (raw movies) were collected at SciLifeLab in Umeå, Sweden in a Titan Krios G2 operated at 300 kV and equipped with a Falcon-4i direct electron detector and Selectris energy filter using 10 eV slit. The data were acquired at 165,000 x nominal magnification with a calibrated pixel size of 0.728 Å. A 50 µm C2 aperture was inserted and the TEM was operated in nanoprobe mode at spot size 6 and 520 nm beam size. The EER formatted movies were collected in 684 raw frames with a total dose of 27.77 e-/Å2 (12.45 e-/pixel/s) over 2.23 s with a set defocus between -0.7 to -1.3 µm.
The movies are not gain-corrected, use the file provided within the main folder.</details>
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        <directory>/data/FA_Krios_dataset/raw_movies</directory>
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            <imageHeight>4092</imageHeight>
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        <details>Data (raw movies) were collected at SciLifeLab in Solna, Sweden on a Titan Krios G2 operated at 300 kV and equipped with a K3 BioQuantum direct electron detector and energy filter using 20 eV slit. The data were acquired at 105,000 x nominal magnification with a calibrated pixel size of 0.824 Å. A 50 µm C2 aperture was inserted and the TEM was operated in nanoprobe mode at spot size 6 and 670 nm beam size. The movies were collected in 30 frames over 1.3 s with a total dose of 30.83 e-/Å2 (16.1 e-/pixel/s) with a set defocus between -0.5 to -1.5 µm.
The movies are gain-corrected.</details>
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    <imageSet>
        <name>EMD-17364 particles (FA-CP CHI)</name>
        <directory>/data/FA-CP_Krios_dataset/particles_EMD-17364_PDB-8P2G</directory>
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        <framesPerImage>1</framesPerImage>
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    <imageSet>
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        <directory>/data/FA-CP_Krios_dataset/particles_EMD-17363_PDB-8P2F</directory>
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        <headerFormat>MRC</headerFormat>
        <dataFormat>MRC</dataFormat>
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    <imageSet>
        <name>EMD-17365 particles (FA CHI)</name>
        <directory>/data/FA_Krios_dataset/particles_EMD-17365_PDB-8P2H</directory>
        <category>picked particles - single frame - processed</category>
        <headerFormat>MRC</headerFormat>
        <dataFormat>MRC</dataFormat>
        <numImagesOrTiltSeries>178679</numImagesOrTiltSeries>
        <framesPerImage>1</framesPerImage>
        <voxelType>UNSIGNED BYTE</voxelType>
        <dimensions>
            <imageWidth>600</imageWidth>
            <pixelWidth>0.824</pixelWidth>
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            <pixelHeight>0.824</pixelHeight>
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    <imageSet>
        <name>Unaligned multi-frame micrographs of FA-CP inhibited ribosomes screening Glacios data</name>
        <directory>/data/FA-CP_Glacios_screening_data/raw_movies</directory>
        <category>micrographs - multiframe</category>
        <headerFormat>TIFF</headerFormat>
        <dataFormat>TIFF</dataFormat>
        <numImagesOrTiltSeries>6052</numImagesOrTiltSeries>
        <framesPerImage>31</framesPerImage>
        <voxelType>SIGNED 16 BIT INTEGER</voxelType>
        <dimensions>
            <imageWidth>4096</imageWidth>
            <pixelWidth>0.952</pixelWidth>
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            <pixelHeight>0.952</pixelHeight>
        </dimensions>
        <details>Raw movies from the FA-CP inhibited ribosomes screening in a Glacios microscope operated at 200 kV with a magnification of 150,000x with a pixel size of 0.952 Å/pix. The movies were collected in 31 frames over 28.74 s with a total dose of 29.8 e-/Å2 (0.94 e-/pixel/s) with a set defocus between -0.5 to -1.5 µm.
The movies are gain corrected.</details>
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    <imageSet>
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        <directory>/data/FA_Glacios_screening_data/raw_movies</directory>
        <category>micrographs - multiframe</category>
        <headerFormat>TIFF</headerFormat>
        <dataFormat>TIFF</dataFormat>
        <numImagesOrTiltSeries>1460</numImagesOrTiltSeries>
        <framesPerImage>30</framesPerImage>
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        <dimensions>
            <imageWidth>4096</imageWidth>
            <pixelWidth>0.952</pixelWidth>
            <imageHeight>4096</imageHeight>
            <pixelHeight>0.952</pixelHeight>
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        <details>Raw movies from the FA inhibited ribosomes screening in a Glacios microscope operated at 200 kV with a magnification of 150,000x with a pixel size of 0.952 Å/pix. The movies were collected in 30 frames over 27.79 s with a total dose of 30 e-/Å2 (1.00 e-/pixel/s) with a set defocus between -0.5 to -1.5 µm.
The movies are gain corrected.</details>
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