<emd xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" emdb_id="EMD-1058" version="3.0.1.1" xsi:schemaLocation="https://github.com/emdb-empiar/emdb-schemas/blob/master/v3/v3_0_1_1/emdb_relaxed.xsd">
   <admin>
      <current_status>
         <code>REL</code>
         <processing_site>PDBe</processing_site>
      </current_status>
      <sites>
         <deposition>PDBe</deposition>
         <last_processing>PDBe</last_processing>
      </sites>
      <key_dates>
         <deposition>2003-10-08</deposition>
         <header_release>2003-10-08</header_release>
         <map_release>2003-11-25</map_release>
         <update>2011-05-26</update>
      </key_dates>
      <title>The structure of echovirus type 12 bound to a two-domain fragment of its cellular attachment protein decay-accelerating factor (CD 55).</title>
      <authors_list>
         <author>Bhella D</author>
         <author>Goodfellow IG</author>
         <author>Roversi P</author>
         <author>Pettigrew D</author>
         <author>Chaudhry Y</author>
         <author>Evans DJ</author>
         <author>Lea SM</author>
      </authors_list>
      <keywords>
         </keywords>
   </admin>
   <crossreferences>
      <citation_list>
         <primary_citation>
            <journal_citation published="true">
               <author order="1">Bhella D</author>
               <author order="2">Goodfellow IG</author>
               <author order="3">Roversi P</author>
               <author order="4">Pettigrew D</author>
               <author order="5">Chaudhry Y</author>
               <author order="6">Evans DJ</author>
               <author order="7">Lea SM</author>
               <title>The structure of echovirus type 12 bound to a two-domain fragment of its cellular attachment protein decay-accelerating factor (CD 55).</title>
               <journal>J.BIOL.CHEM.</journal>
               <volume>279</volume>
               <first_page>8325</first_page>
               <last_page>8332</last_page>
               <year>2004</year>
               <external_references type="PUBMED">14634014</external_references>
               <external_references type="DOI">doi:10.1074/jbc.M311334200</external_references>
            </journal_citation>
         </primary_citation>
      </citation_list>
      <pdb_list>
         <pdb_reference>
            <pdb_id>1upn</pdb_id>
            <relationship>
               <in_frame>FULLOVERLAP</in_frame>
            </relationship>
         </pdb_reference>
      </pdb_list>
   </crossreferences>
   <sample>
      <name>Echovirus type 12</name>
      <supramolecule_list>
         <sample_supramolecule supramolecule_id="1000">
            <name>Echovirus type 12</name>
            <number_unique_components>1</number_unique_components>
         </sample_supramolecule>
         <virus_supramolecule supramolecule_id="1">
            <name synonym="EV12">Human echovirus 12</name>
            <sci_species_name ncbi="35293">Human echovirus 12</sci_species_name>
            <natural_host database="NCBI">
               <organism ncbi="9606">Homo sapiens</organism>
               <synonym_organism>VERTEBRATES</synonym_organism>
            </natural_host>
            <host_system database="NCBI">
               </host_system>
            <virus_type>VIRION</virus_type>
            <virus_isolate>SEROTYPE</virus_isolate>
            <virus_enveloped>false</virus_enveloped>
            <virus_empty>false</virus_empty>
            <syn_species_name>EV12</syn_species_name>
         </virus_supramolecule>
      </supramolecule_list>
   </sample>
   <structure_determination_list>
      <structure_determination structure_determination_id="1">
         <method>singleParticle</method>
         <aggregation_state>particle</aggregation_state>
         <specimen_preparation_list>
            <single_particle_preparation preparation_id="1">
               <concentration units="mg/mL">0.2</concentration>
               <buffer>
                  <ph>7.4</ph>
                  <details>PBS A</details>
               </buffer>
               <staining>
                  <type>NEGATIVE</type>
                  <details>Absorb protein to grid, float on 20% ammonium molybdate
        pH       7.4 for 10 seconds blot and plunge</details>
               </staining>
               <grid>
                  <details>400 mesh Quantifoils</details>
               </grid>
               <vitrification>
                  <cryogen_name>ETHANE</cryogen_name>
                  <method>blot for 2 seconds, wait for 2 seconds, plunge</method>
               </vitrification>
            </single_particle_preparation>
         </specimen_preparation_list>
         <microscopy_list>
            <single_particle_microscopy microscopy_id="1">
               <microscope>JEOL 1200EXII</microscope>
               <illumination_mode>FLOOD BEAM</illumination_mode>
               <imaging_mode>BRIGHT FIELD</imaging_mode>
               <electron_source>LAB6</electron_source>
               <acceleration_voltage units="kV">120</acceleration_voltage>
               <nominal_cs units="mm">3.4</nominal_cs>
               <nominal_defocus_min units="&#181;m">0.3</nominal_defocus_min>
               <nominal_defocus_max units="&#181;m">2.0</nominal_defocus_max>
               <nominal_magnification>30000.0</nominal_magnification>
               <calibrated_magnification>29200.0</calibrated_magnification>
               <specimen_holder_model>OTHER</specimen_holder_model>
               <alignment_procedure>
                  <legacy>
                     <astigmatism>objective lens corrected at 200k x</astigmatism>
                  </legacy>
               </alignment_procedure>
               <details>MICROSCOPE JEOL 1200 EX with OXFORD INSTRUMENTS
        CRYO-TRANSFER STAGE</details>
               <image_recording_list>
                  <image_recording>
                     <film_or_detector_model category="CCD">KODAK SO-163 FILM</film_or_detector_model>
                     <digitization_details>
                        <sampling_interval units="&#181;m">3.42</sampling_interval>
                     </digitization_details>
                     <number_real_images>28</number_real_images>
                     <details>Scanned with a Dunvegan HiScan</details>
                     <bits_per_pixel>16.</bits_per_pixel>
                  </image_recording>
               </image_recording_list>
               <specimen_holder>side entry</specimen_holder>
            </single_particle_microscopy>
         </microscopy_list>
         <singleparticle_processing image_processing_id="1">
            <ctf_correction>
               <details>merge of focal pair images of single particles</details>
            </ctf_correction>
            <final_reconstruction>
               <applied_symmetry>
                  <point_group>I</point_group>
               </applied_symmetry>
               <algorithm>OTHER</algorithm>
               <resolution res_type="BY AUTHOR" units="&#8491;">18.0</resolution>
               <resolution_method>FSC 0.5 CUT-OFF</resolution_method>
               <software_list>
                  <software>
                     <name>EM3DR2, PFT2, CTFMIX</name>
                  </software>
               </software_list>
               <details>Particles were aligned using a model based       strategy
        starting with a  model derived from the       crystallographic
        co-ordinates of EV-1, filtered to 16       Angstroms resolution.
        The       program  is called PFT (Polar       Fourier
        Transform).       The       reconstructions were calculated
        using the EM3DR2       program which is       based on the
        standard       method of       calculating icosahedral
        reconstructions as       described       by Crowther,'Fourier-Bessel'.</details>
               <number_images_used>617</number_images_used>
            </final_reconstruction>
         </singleparticle_processing>
      </structure_determination>
   </structure_determination_list>
   <map format="CCP4" size_kbytes="20937">
      <file>emd_1058.map.gz</file>
      <symmetry>
         <space_group>1</space_group>
      </symmetry>
      <data_type>IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES)</data_type>
      <dimensions>
         <col>175</col>
         <row>175</row>
         <sec>175</sec>
      </dimensions>
      <origin>
         <col>-87</col>
         <row>-87</row>
         <sec>-87</sec>
      </origin>
      <spacing>
         <x>175</x>
         <y>175</y>
         <z>175</z>
      </spacing>
      <cell>
         <a units="&#8491;">598.5</a>
         <b units="&#8491;">598.5</b>
         <c units="&#8491;">598.5</c>
         <alpha units="deg">90</alpha>
         <beta units="deg">90</beta>
         <gamma units="deg">90</gamma>
      </cell>
      <axis_order>
         <fast>X</fast>
         <medium>Y</medium>
         <slow>Z</slow>
      </axis_order>
      <statistics>
         <minimum>0.0</minimum>
         <maximum>255.0</maximum>
         <average>72.036100000000005</average>
         <std>25.678999999999998</std>
      </statistics>
      <pixel_spacing>
         <x units="&#8491;">3.42</x>
         <y units="&#8491;">3.42</y>
         <z units="&#8491;">3.42</z>
      </pixel_spacing>
      <contour_list>
         <contour primary="true">
            <level>149.0</level>
         </contour>
      </contour_list>
      <annotation_details>Reconstruction of Echovirus type 12 from
      cryo-negative stain image data</annotation_details>
      <details>::::EMDATABANK.org::::EMD-1058::::</details>
   </map>
   <interpretation>
      <modelling_list>
         <modelling>
            <details>3D crystal structure fitting details lodged with PDB 1UPN</details>
         </modelling>
      </modelling_list>
   </interpretation>
</emd>