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        <keyDates>
            <depositionDate>2020-03-09</depositionDate>
            <releaseDate>2020-04-09</releaseDate>
            <updateDate>2022-01-31</updateDate>
        </keyDates>
        <title>Cryo-EM structure of Lumazine Synthase</title>
        <correspondingAuthor private="true">
            <authorORCID>0000-0003-2096-8310</authorORCID>
            <firstName>David</firstName>
            <lastName>Bhella</lastName>
            <organization type="academic">MRC-University of Glasgow Centre for Virus Research</organization>
            <street>464 Bearsden Road</street>
            <townOrCity>Glasgow</townOrCity>
            <stateOrProvince>Glasgow</stateOrProvince>
            <country>United Kingdom</country>
            <postOrZipCode>G61 1QH</postOrZipCode>
        </correspondingAuthor>
        <principalInvestigator private="true">
            <authorORCID>0000-0003-2096-8310</authorORCID>
            <firstName>David</firstName>
            <lastName>Bhella</lastName>
            <organization type="academic">MRC-University of Glasgow Centre for Virus Research</organization>
            <street>464 Bearsden Road</street>
            <townOrCity>Glasgow</townOrCity>
            <stateOrProvince>Glasgow</stateOrProvince>
            <country>United Kingdom</country>
            <postOrZipCode>G61 1QH</postOrZipCode>
        </principalInvestigator>
        <authorsList>
            <author authorORCID="0000-0003-2096-8310">Bhella D</author>
            <author authorORCID="0000-0001-7808-605X">Streetley J</author>
            <author authorORCID="0000-0002-9658-4308">Clarke M</author>
            <author authorORCID="0000-0003-1813-7825">Cowton V</author>
            <author authorORCID="0000-0003-4600-2047">Patel A</author>
        </authorsList>
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        <entryDOI>10.6019/EMPIAR-10384</entryDOI>
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            <emdbEntry>EMD-10736</emdbEntry>
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                    <author authorORCID="0000-0003-2096-8310" order="1">Bhella D</author>
                    <title>Cryo-electron microscopy: an introduction to the technique, and considerations when working to establish a national facility</title>
                    <journal>Biophysical reviews</journal>
                    <journalAbbreviation>Biophys Rev</journalAbbreviation>
                    <country></country>
                    <issue>4</issue>
                    <volume>11</volume>
                    <firstPage>515</firstPage>
                    <lastPage>519</lastPage>
                    <year>2019</year>
                    <language>English</language>
                    <externalReferences type="doi">10.1007/s12551-019-00571-w</externalReferences>
                    <externalReferences type="pubmed">31359340</externalReferences>
                </journalCitation>
            </universalCitation>
        </citationList>
    </crossReferences>
    <imageSet>
        <name>Frame aligned multi-frame movies of Lumazine Synthase imaged on a CryoARM300 and DE64</name>
        <directory>/data</directory>
        <category>micrographs - multiframe</category>
        <headerFormat>MRC</headerFormat>
        <dataFormat>MRC</dataFormat>
        <numImagesOrTiltSeries>1198</numImagesOrTiltSeries>
        <framesPerImage>41</framesPerImage>
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            <frameRangeMin>1</frameRangeMin>
            <frameRangeMax>41</frameRangeMax>
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        <details>Lumazine Synthase was expressed in E.coli and purified by immobilised metal affinity chromatography. Particles were frozen on C-flat R1.2/1.3 grids. Imaging was performed at 200 kX magnification on a JEOL CryoARM 300 equipped with a Direct Electron DE64 detector. Energy filtered images were collected with a slit-width of 20eV using JADAS.  A single image was recorded per hole using electron counting with two times binning.</details>
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