<?xml version="1.0" encoding="UTF-8"?>
<emdEntry accessCode="2042" version="1.9.6">
    <admin>
        <lastUpdate>2013-04-17</lastUpdate>
    </admin>
    <deposition>
        <status prior="HOLD1">OBS</status>
        <depositionDate>2012-02-07</depositionDate>
        <depositionSite>PDBe</depositionSite>
        <processingSite>PDBe</processingSite>
        <headerReleaseDate>2012-02-15</headerReleaseDate>
        <mapReleaseDate>2013-02-27</mapReleaseDate>
        <obsoletedDate>2013-04-17</obsoletedDate>
        <details>Author withdrawal of the entry.</details>
        <title>Yersinia enterocolitica Injectisome in situ</title>
        <authors>Kudryashev M, Amstutz M, Castano-Diez D, Bleck CKE, Kowal J, Cornelis GR, Stahlberg H</authors>
        <keywords>Type III secretion, needle complex</keywords>
        <primaryReference published="false">
            <journalArticle>
                <authors>Kudryashev M, Amstutz M, Castano-Diez D, Bleck CKE, Kowal J, Cornelis GR, Stahlberg H</authors>
                <articleTitle>In situ structure of the Yersinia enterocolitica injectisome</articleTitle>
                <journal>To Be Published</journal>
                <volume/>
                <firstPage/>
                <lastPage/>
                <year/>
            </journalArticle>
        </primaryReference>
    </deposition>
    <map>
        <file format="CCP4" sizeKb="8193" type="map">emd_2042.map.gz</file>
        <dataType>Image stored as Reals</dataType>
        <dimensions>
            <numColumns>128</numColumns>
            <numRows>128</numRows>
            <numSections>128</numSections>
        </dimensions>
        <origin>
            <originCol>0</originCol>
            <originRow>0</originRow>
            <originSec>0</originSec>
        </origin>
        <limit>
            <limitCol>127</limitCol>
            <limitRow>127</limitRow>
            <limitSec>127</limitSec>
        </limit>
        <spacing>
            <spacingCol>128</spacingCol>
            <spacingRow>128</spacingRow>
            <spacingSec>128</spacingSec>
        </spacing>
        <cell>
            <cellA units="A">94.72</cellA>
            <cellB units="A">94.72</cellB>
            <cellC units="A">94.72</cellC>
            <cellAlpha units="degrees">90.0</cellAlpha>
            <cellBeta units="degrees">90.0</cellBeta>
            <cellGamma units="degrees">90.0</cellGamma>
        </cell>
        <axisOrder>
            <axisOrderFast>X</axisOrderFast>
            <axisOrderMedium>Y</axisOrderMedium>
            <axisOrderSlow>Z</axisOrderSlow>
        </axisOrder>
        <statistics>
            <minimum>-4.04227829</minimum>
            <maximum>5.45056105</maximum>
            <average>-0.00742681</average>
            <std>1.00132513</std>
        </statistics>
        <spaceGroupNumber>1</spaceGroupNumber>
        <details>::::EMDATABANK.org::::EMD-2042::::</details>
        <pixelSpacing>
            <pixelX units="A">0.74</pixelX>
            <pixelY units="A">0.74</pixelY>
            <pixelZ units="A">0.74</pixelZ>
        </pixelSpacing>
        <annotationDetails>Structure of Yersinia enterocolitica injectisome in situ, wild type</annotationDetails>
    </map>
    <supplement>
        <maskSet/>
        <sliceSet/>
        <figureSet/>
        <fscSet/>
    </supplement>
    <sample>
        <numComponents>1</numComponents>
        <name>Entire Injectisome/type III secretion system of Yersinia enterocolitica</name>
        <details>Individual injectisomes were extracted from tomograms of intact bacterial cells</details>
        <sampleComponentList>
            <sampleComponent componentID="1">
                <entry>cellular-component</entry>
                <sciName>Entire Injectisome/type III secretion system of Yersinia enterocolitica</sciName>
                <cellular-component>
                    <recombinantExpFlag>false</recombinantExpFlag>
                    <sciSpeciesName ncbiTaxId="630">Yersinia enterocolitica</sciSpeciesName>
                    <externalReferences/>
                    <natSource/>
                    <engSource/>
                </cellular-component>
            </sampleComponent>
        </sampleComponentList>
    </sample>
    <experiment>
        <vitrification>
            <method>Blot for 2 seconds before plunging</method>
            <cryogenName>ETHANE</cryogenName>
            <humidity>90</humidity>
            <instrument>FEI VITROBOT MARK IV</instrument>
        </vitrification>
        <imaging>
            <electronSource>FIELD EMISSION GUN</electronSource>
            <electronDose units="e/A**2">20</electronDose>
            <energyFilter>Gatan post column Image Filter</energyFilter>
            <imagingMode>BRIGHT FIELD</imagingMode>
            <nominalDefocusMin units="nm">-2000</nominalDefocusMin>
            <nominalDefocusMax units="nm">-15000</nominalDefocusMax>
            <illuminationMode>FLOOD BEAM</illuminationMode>
            <detector>GATAN ULTRASCAN 1000 (2k x 2k)</detector>
            <nominalCs units="mm">2.8</nominalCs>
            <tiltAngleMin units="degrees">-60</tiltAngleMin>
            <tiltAngleMax units="degrees">60</tiltAngleMax>
            <temperature units="Kelvin">100</temperature>
            <microscope>FEI TITAN KRIOS</microscope>
            <date>01-JAN-2010</date>
            <specimenHolderModel>OTHER</specimenHolderModel>
            <acceleratingVoltage units="kV">300</acceleratingVoltage>
            <nominalMagnification>19500</nominalMagnification>
            <energyWindow units="eV">0-20</energyWindow>
        </imaging>
        <imageAcquisition/>
        <fitting/>
        <specimenPreparation>
            <staining>non-stained</staining>
            <specimenSupportDetails>Quantifoil holey carbon grid with 3.5/1 spacing</specimenSupportDetails>
            <buffer>
                <details>PBS</details>
            </buffer>
        </specimenPreparation>
    </experiment>
    <processing>
        <method>subtomogramAveraging</method>
        <reconstruction>
            <algorithm>6d-search with missing wedge compensation</algorithm>
            <software>AV3,Dynamo</software>
            <ctfCorrection>Focal pair tomography</ctfCorrection>
            <resolutionByAuthor>37</resolutionByAuthor>
            <resolutionMethod>1-bit information threshold</resolutionMethod>
        </reconstruction>
        <subtomogramAveraging>
            <details>We used focal pair tomography in a combination with the standard sub-tomogram processing routines in AV3 (Forster et al, PNAS 2005) and Dynamo (Castano-Diez et al, 2012, www.dynamo-em.org). Average number of tilts used in the 3D reconstructions: 61. Average tomographic tilt angle increment: 2.</details>
        </subtomogramAveraging>
    </processing>
</emdEntry>
