<?xml version="1.0" encoding="UTF-8"?>
<emd xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="https://github.com/emdb-empiar/emdb-schemas/blob/master/v3/v3_0_1_7/emdb.xsd" emdb_id="EMD-10451" version="3.0.1.7">
    <admin>
        <current_status>
            <date>2020-02-12</date>
            <code>REL</code>
            <processing_site>PDBe</processing_site>
        </current_status>
        <sites>
            <deposition>PDBe</deposition>
            <last_processing>PDBe</last_processing>
        </sites>
        <key_dates>
            <deposition>2019-11-04</deposition>
            <header_release>2019-12-11</header_release>
            <map_release>2019-12-11</map_release>
            <update>2020-02-12</update>
        </key_dates>
        <grant_support>
            <grant_reference>
                <funding_body>Seneca Foundation</funding_body>
                <country>Spain</country>
            </grant_reference>
        </grant_support>
        <title>ER microsome released with the code in (Martinez-Sanchez et al., Nature Methods)</title>
        <authors_list>
            <author>Martinez-Sanchez A</author>
            <author>Lucic V</author>
            <author>Pfeffer S</author>
            <author>Forster F</author>
        </authors_list>
    </admin>
    <crossreferences>
        <citation_list>
            <primary_citation>
                <journal_citation published="true">
                    <author order="1">Martinez-Sanchez A</author>
                    <author order="2">Kochovski Z</author>
                    <author order="3">Laugks U</author>
                    <author order="4">Meyer Zum Alten Borgloh J</author>
                    <author order="5">Chakraborty S</author>
                    <author order="6">Pfeffer S</author>
                    <author order="7">Baumeister W</author>
                    <author order="8">Lucic V</author>
                    <title>Template-free detection and classification of membrane-bound complexes in cryo-electron tomograms.</title>
                    <journal_abbreviation>Nat.Methods</journal_abbreviation>
                    <country>US</country>
                    <volume>17</volume>
                    <first_page>209</first_page>
                    <last_page>216</last_page>
                    <year>2020</year>
                    <external_references type="PUBMED">31907446</external_references>
                    <external_references type="DOI">doi:10.1038/s41592-019-0675-5</external_references>
                    <external_references type="ISSN">1548-7105</external_references>
                </journal_citation>
            </primary_citation>
            <secondary_citation>
                <journal_citation published="true">
                    <author order="9">Pfeffer S</author>
                    <author order="10">Forster F</author>
                    <title>Structure of the native Sec61 protein-conducting channel</title>
                    <journal_abbreviation>Nature Communications</journal_abbreviation>
                    <country>UK</country>
                    <volume>6</volume>
                    <year>2015</year>
                    <external_references type="ISSN">2041-1723</external_references>
                </journal_citation>
            </secondary_citation>
        </citation_list>
        <emdb_list>
            <emdb_reference>
                <emdb_id>EMD-3072</emdb_id>
                <relationship>
                    <other>other EM volume</other>
                </relationship>
                <details>Same sample (original publication)</details>
            </emdb_reference>
            <emdb_reference>
                <emdb_id>EMD-0074</emdb_id>
                <relationship>
                    <other>other EM volume</other>
                </relationship>
                <details>Averged density obtained from this sample</details>
            </emdb_reference>
            <emdb_reference>
                <emdb_id>EMD-0084</emdb_id>
                <relationship>
                    <other>other EM volume</other>
                </relationship>
                <details>Averged density obtained from this sample</details>
            </emdb_reference>
            <emdb_reference>
                <emdb_id>EMD-0075</emdb_id>
                <relationship>
                    <other>other EM volume</other>
                </relationship>
                <details>Averged density obtained from this sample</details>
            </emdb_reference>
            <emdb_reference>
                <emdb_id>EMD-0085</emdb_id>
                <relationship>
                    <other>other EM volume</other>
                </relationship>
                <details>Averged density obtained from this sample</details>
            </emdb_reference>
            <emdb_reference>
                <emdb_id>EMD-0086</emdb_id>
                <relationship>
                    <other>other EM volume</other>
                </relationship>
                <details>Averged density obtained from this sample</details>
            </emdb_reference>
            <emdb_reference>
                <emdb_id>EMD-10449</emdb_id>
                <relationship>
                    <other>other EM volume</other>
                </relationship>
                <details>Same sample and same publication</details>
            </emdb_reference>
            <emdb_reference>
                <emdb_id>EMD-10450</emdb_id>
                <relationship>
                    <other>other EM volume</other>
                </relationship>
                <details>Same sample and same publication</details>
            </emdb_reference>
            <emdb_reference>
                <emdb_id>EMD-10451</emdb_id>
                <relationship>
                    <other>associated EM volume</other>
                </relationship>
            </emdb_reference>
            <emdb_reference>
                <emdb_id>EMD-0087</emdb_id>
                <relationship>
                    <other>other EM volume</other>
                </relationship>
                <details>Averaged density obtained from this sample</details>
            </emdb_reference>
        </emdb_list>
    </crossreferences>
    <sample>
        <name>Representative tomogram of a canine pancreatic rough Endoplasmic Reticulum vesicle.</name>
        <supramolecule_list>
            <organelle_or_cellular_component_supramolecule supramolecule_id="1">
                <name>Representative tomogram of a canine pancreatic rough Endoplasmic Reticulum vesicle.</name>
                <parent>0</parent>
                <natural_source database="NCBI">
                    <organism ncbi="9615">Canis lupus familiaris</organism>
                    <tissue>pancreas</tissue>
                </natural_source>
            </organelle_or_cellular_component_supramolecule>
        </supramolecule_list>
    </sample>
    <structure_determination_list>
        <structure_determination structure_determination_id="1">
            <method>tomography</method>
            <aggregation_state>particle</aggregation_state>
            <specimen_preparation_list>
                <tomography_preparation preparation_id="1">
                    <concentration units="mg/mL">2.00</concentration>
                    <buffer>
                        <ph>7.6</ph>
                        <component>
                            <concentration units="mM">20.0</concentration>
                            <name>Hepes</name>
                        </component>
                        <component>
                            <concentration units="mM">50.0</concentration>
                            <formula>KCl</formula>
                        </component>
                        <component>
                            <concentration units="mM">2.0</concentration>
                            <formula>MgCl2</formula>
                        </component>
                    </buffer>
                    <vitrification>
                        <cryogen_name>ETHANE-PROPANE</cryogen_name>
                        <chamber_humidity units="percentage">70</chamber_humidity>
                        <instrument>FEI VITROBOT MARK IV</instrument>
                        <details>Blot 3 seconds before plunging.. </details>
                    </vitrification>
                    <fiducial_markers_list>
                        <fiducial_marker>
                            <manufacturer>Aurion, Wageningen, The Netherlands</manufacturer>
                            <diameter units="nanometer">10</diameter>
                        </fiducial_marker>
                    </fiducial_markers_list>
                    <sectioning>
                        <other_sectioning>NO SECTIONING</other_sectioning>
                    </sectioning>
                </tomography_preparation>
            </specimen_preparation_list>
            <microscopy_list>
                <tomography_microscopy microscopy_id="1">
                    <microscope>FEI TITAN KRIOS</microscope>
                    <illumination_mode>OTHER</illumination_mode>
                    <imaging_mode>OTHER</imaging_mode>
                    <electron_source>FIELD EMISSION GUN</electron_source>
                    <acceleration_voltage units="kV">300</acceleration_voltage>
                    <c2_aperture_diameter units="µm">70.0</c2_aperture_diameter>
                    <nominal_cs units="mm">2.7</nominal_cs>
                    <nominal_defocus_min units="µm">3.0</nominal_defocus_min>
                    <nominal_defocus_max units="µm">4.0</nominal_defocus_max>
                    <nominal_magnification>42000.0</nominal_magnification>
                    <cooling_holder_cryogen>NITROGEN</cooling_holder_cryogen>
                    <alignment_procedure>
                        <basic/>
                    </alignment_procedure>
                    <image_recording_list>
                        <image_recording image_recording_id="1">
                            <film_or_detector_model>GATAN K2 SUMMIT (4k x 4k)</film_or_detector_model>
                            <detector_mode>COUNTING</detector_mode>
                            <average_electron_dose_per_image units="e/Å^2">1.5</average_electron_dose_per_image>
                        </image_recording>
                    </image_recording_list>
                </tomography_microscopy>
            </microscopy_list>
            <tomography_processing image_processing_id="1">
                <image_recording_id>1</image_recording_id>
                <details>Reconstruction of a single microsome after two binning steps (from 2.62A/pixel to 10.48A/pixel)</details>
                <final_reconstruction>
                    <software_list>
                        <software>
                            <name>PyTom</name>
                        </software>
                    </software_list>
                    <number_images_used>61</number_images_used>
                </final_reconstruction>
                <ctf_correction>
                    <software_list>
                        <software>
                            <name>PyTom</name>
                        </software>
                    </software_list>
                </ctf_correction>
            </tomography_processing>
        </structure_determination>
    </structure_determination_list>
    <map format="CCP4" size_kbytes="5512">
        <file>emd_10451.map.gz</file>
        <symmetry>
            <space_group>1</space_group>
        </symmetry>
        <data_type>IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES)</data_type>
        <dimensions>
            <col>166</col>
            <row>166</row>
            <sec>50</sec>
        </dimensions>
        <origin>
            <col>0</col>
            <row>0</row>
            <sec>0</sec>
        </origin>
        <spacing>
            <x>166</x>
            <y>166</y>
            <z>50</z>
        </spacing>
        <cell>
            <a units="Å">1739.6799</a>
            <b units="Å">1739.6799</b>
            <c units="Å">524.0</c>
            <alpha units="deg">90.0</alpha>
            <beta units="deg">90.0</beta>
            <gamma units="deg">90.0</gamma>
        </cell>
        <axis_order>
            <fast>X</fast>
            <medium>Y</medium>
            <slow>Z</slow>
        </axis_order>
        <statistics>
            <minimum>-1.323595</minimum>
            <maximum>0.82137954</maximum>
            <average>0.0010220177</average>
            <std>0.097294405</std>
        </statistics>
        <pixel_spacing>
            <x units="Å">10.48</x>
            <y units="Å">10.48</y>
            <z units="Å">10.48</z>
        </pixel_spacing>
        <contour_list>
            <contour primary="true">
                <source>AUTHOR</source>
            </contour>
        </contour_list>
        <label>::::EMDATABANK.org::::EMD-10451::::</label>
        <annotation_details>ER microsome used in the code released in (Martinez-Sanchez et al., Nature Methods)</annotation_details>
    </map>
</emd>
