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        <keyDates>
            <depositionDate>2026-03-18</depositionDate>
            <releaseDate>2026-04-08</releaseDate>
            <updateDate>2026-04-08</updateDate>
        </keyDates>
        <title>Cryo-EM micrographs of phosphorylated AP2 bound to the endocytic regulator NECAP</title>
        <correspondingAuthor private="true">
            <authorORCID>0000-0003-1136-6000</authorORCID>
            <firstName>Richard</firstName>
            <middleName>Wayne</middleName>
            <lastName>Baker</lastName>
            <organization type="academic">University of North Carolina at Chapel Hill</organization>
            <street>3049E Genetic Medicine Bldg</street>
            <townOrCity>Chapel Hill</townOrCity>
            <stateOrProvince>NC</stateOrProvince>
            <country>United States</country>
            <postOrZipCode>27599</postOrZipCode>
        </correspondingAuthor>
        <principalInvestigator private="true">
            <authorORCID>0000-0003-1136-6000</authorORCID>
            <firstName>Gunther</firstName>
            <lastName>Hollopeter</lastName>
            <organization type="academic">Cornell University</organization>
            <townOrCity>Ithaca</townOrCity>
            <stateOrProvince>NY</stateOrProvince>
            <country>United States</country>
            <postOrZipCode>14853</postOrZipCode>
        </principalInvestigator>
        <authorsList>
            <author authorORCID="0000-0001-5513-088X">Partlow EA</author>
            <author authorORCID="0000-0003-1136-6000">Baker RW</author>
            <author authorORCID="0000-0002-7732-7023">Leschziner AE</author>
            <author authorORCID="0000-0002-6409-0530">Hollopeter G</author>
        </authorsList>
        <grantSupport>
            <grantReference>
                <fundingBody>National Institutes of Health/National Institute of General Medical Sciences (NIH/NIGMS)</fundingBody>
                <code>R01 GM127548</code>
                <country>United States</country>
            </grantReference>
            <grantReference>
                <fundingBody>National Institutes of Health/National Institute of General Medical Sciences (NIH/NIGMS)</fundingBody>
                <code>R01 GM127548-01A1</code>
                <country>United States</country>
            </grantReference>
            <grantReference>
                <fundingBody>Damon Runyon Cancer Research Foundation</fundingBody>
                <code>DRG-#2285-17/</code>
                <country>United States</country>
            </grantReference>
            <grantReference>
                <fundingBody>National Institutes of Health (NIH)</fundingBody>
                <code>S10 OD018516</code>
                <country>United States</country>
            </grantReference>
        </grantSupport>
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        <entryDOI>10.6019/EMPIAR-13389</entryDOI>
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        <scale>molecule</scale>
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    <crossReferences>
        <relatedEMDBEntries>
            <emdbEntry>EMD-20215</emdbEntry>
            <emdbEntry>EMD-20220</emdbEntry>
        </relatedEMDBEntries>
        <citationList>
            <universalCitation>
                <journalCitation published="true" preprint="false">
                    <author authorORCID="0000-0001-5513-088X" order="1">Partlow EA</author>
                    <author authorORCID="0000-0003-1136-6000" order="2">Baker RW</author>
                    <author authorORCID="0000-0002-7732-7023" order="3">Leschziner AE</author>
                    <author authorORCID="0000-0002-6409-0530" order="4">Hollopeter G</author>
                    <title>A structural mechanism for phosphorylation-dependent inactivation of the AP2 complex</title>
                    <journal>eLife</journal>
                    <journalAbbreviation>Elife</journalAbbreviation>
                    <country></country>
                    <volume>8</volume>
                    <year>2019</year>
                    <language>English</language>
                    <externalReferences type="doi">10.7554/elife.50003</externalReferences>
                    <externalReferences type="pubmed">31464684</externalReferences>
                    <details>Raw, unaligned movies of phosphorylated AP2 in three distinct states. 
Phosphorylated AP2
Phosphorylated AP2 bound to NECAP
Phosphorylated AP2 bound to NECAP and DNA</details>
                </journalCitation>
            </universalCitation>
        </citationList>
    </crossReferences>
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        <name>Raw, unaligned cryo-EM micrographs of phosphorylated AP-2</name>
        <directory>/data/pAP2</directory>
        <category>micrographs - multiframe</category>
        <headerFormat>TIFF</headerFormat>
        <dataFormat>TIFF</dataFormat>
        <numImagesOrTiltSeries>542</numImagesOrTiltSeries>
        <framesPerImage>60</framesPerImage>
        <voxelType>UNSIGNED BYTE</voxelType>
        <dimensions>
            <imageWidth>7676</imageWidth>
            <pixelWidth>0.58</pixelWidth>
            <imageHeight>7420</imageHeight>
            <pixelHeight>0.58</pixelHeight>
        </dimensions>
        <details>Raw, unaligned cryo-EM movies of phosphorylated AP-2 (pAP2). Movies were collected on a Talos Arctica cryoTEM with a Gatan K2 camera operating in super-resolution mode.

200 keV Talos Arctica cryoTEM
Images were collected at 36,000x, yielding a final pixel size of 1.16 Å for counting mode and 0.58 Å for super resolution mode
exposure rate of ~6 e-/pixel/s with 200 ms frames and a total exposure of ~50 e-/Å2
Cs - 2.7 mm
Ac - 0.1</details>
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        <name>Raw, unaligned cryo-EM micrographs of phosphorylated AP-2 bound to NECAP</name>
        <directory>/data/pAP2+NECAP</directory>
        <category>micrographs - multiframe</category>
        <headerFormat>TIFF</headerFormat>
        <dataFormat>TIFF</dataFormat>
        <numImagesOrTiltSeries>2860</numImagesOrTiltSeries>
        <framesPerImage>60</framesPerImage>
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        <dimensions>
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            <pixelWidth>0.58</pixelWidth>
            <imageHeight>7420</imageHeight>
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        <details>Raw, unaligned cryo-EM movies of phosphorylated AP-2 (pAP2) bound to the endocytic regulator NECAP. Movies were collected on a Talos Arctica cryoTEM with a Gatan K2 camera operating in super-resolution mode.

200 keV Talos Arctica cryoTEM
Images were collected at 36,000x, yielding a final pixel size of 1.16 Å for counting mode and 0.58 Å for super resolution mode
exposure rate of ~6 e-/pixel/s with 200 ms frames and a total exposure of ~50 e-/Å2
Cs - 2.7 mm
Ac - 0.1</details>
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    <imageSet>
        <name>Raw, unaligned cryo-EM micrographs of phosphorylated AP-2 bound to NECAP in the presence of DNA</name>
        <directory>/data/pAP2+NECAP+DNA</directory>
        <category>micrographs - multiframe</category>
        <headerFormat>TIFF</headerFormat>
        <dataFormat>TIFF</dataFormat>
        <numImagesOrTiltSeries>2314</numImagesOrTiltSeries>
        <framesPerImage>60</framesPerImage>
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            <imageWidth>3838</imageWidth>
            <pixelWidth>1.16</pixelWidth>
            <imageHeight>3710</imageHeight>
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        </dimensions>
        <details>Raw, unaligned cryo-EM movies of phosphorylated AP-2 (pAP2) bound to the endocytic regulator NECAP in the presence of DNA. Movies were collected on a Talos Arctica cryoTEM with a Gatan K2 camera operating in counting mode.

200 keV Talos Arctica cryoTEM
Images were collected at 36,000x, yielding a final pixel size of 1.16 Å for counting mode and 0.58 Å for super resolution mode
exposure rate of ~6 e-/pixel/s with 200 ms frames and a total exposure of ~50 e-/Å2
Cs - 2.7 mm
Ac - 0.1</details>
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