<emd xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" emdb_id="EMD-1072" 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>2004-03-14</deposition>
         <header_release>2004-03-14</header_release>
         <map_release>2004-04-28</map_release>
         <update>2012-10-31</update>
      </key_dates>
      <title>Three-dimensional structures of translating ribosomes by Cryo-EM.</title>
      <authors_list>
         <author>Gilbert RJC</author>
         <author>Fucini P</author>
         <author>Connell S</author>
         <author>Fuller SD</author>
         <author>Nierhaus KH</author>
         <author>Robinson CV</author>
         <author>Dobson CM</author>
         <author>Stuart DI</author>
      </authors_list>
      <keywords>
         </keywords>
   </admin>
   <crossreferences>
      <citation_list>
         <primary_citation>
            <journal_citation published="true">
               <author order="1">Gilbert RJ</author>
               <author order="2">Fucini P</author>
               <author order="3">Connell S</author>
               <author order="4">Fuller SD</author>
               <author order="5">Nierhaus KH</author>
               <author order="6">Robinson CV</author>
               <author order="7">Dobson CM</author>
               <author order="8">Stuart DI</author>
               <title>Three-dimensional structures of translating ribosomes by Cryo-EM.</title>
               <journal>MOLECULAR CELL</journal>
               <volume>14</volume>
               <first_page>57</first_page>
               <last_page>66</last_page>
               <year>2004</year>
               <external_references type="PUBMED">15068803</external_references>
               <external_references type="DOI">doi:10.1016/S1097-2765(04)00163-7</external_references>
            </journal_citation>
         </primary_citation>
      </citation_list>
   </crossreferences>
   <sample>
      <name>E. coli ribosome translating GFP</name>
      <supramolecule_list>
         <sample_supramolecule supramolecule_id="1000">
            <name>E. coli ribosome translating GFP</name>
            <details>The sample was monodisperse.</details>
            <oligomeric_state>30S subunit and 50S subunit, 2 tRNA molecules and 1
      nascent protein</oligomeric_state>
            <number_unique_components>5</number_unique_components>
         </sample_supramolecule>
         <complex_supramolecule supramolecule_id="1">
            <name synonym="30S">E. coli 30S subunit</name>
            <recombinant_exp_flag>false</recombinant_exp_flag>
            <natural_source database="NCBI">
               <organism ncbi="562">Escherichia coli</organism>
            </natural_source>
            <recombinant_expression database="NCBI">
               </recombinant_expression>
            <ribosome-details>ribosome-prokaryote: SSU 30S</ribosome-details>
         </complex_supramolecule>
         <complex_supramolecule supramolecule_id="2">
            <name synonym="50S">E. coli 50S subunit</name>
            <recombinant_exp_flag>false</recombinant_exp_flag>
            <natural_source database="NCBI">
               <organism ncbi="562">Escherichia coli</organism>
            </natural_source>
            <recombinant_expression database="NCBI">
               </recombinant_expression>
            <ribosome-details>ribosome-prokaryote: LSU 50S</ribosome-details>
         </complex_supramolecule>
      </supramolecule_list>
      <macromolecule_list>
         <rna macromolecule_id="1">
            <name>P site tRNA</name>
            <natural_source database="NCBI">
               <organism ncbi="562">Escherichia coli</organism>
            </natural_source>
            <details>partial occupancy</details>
            <classification>OTHER</classification>
            <structure>SINGLE STRANDED</structure>
            <synthetic_flag>false</synthetic_flag>
         </rna>
         <rna macromolecule_id="2">
            <name>E site tRNA</name>
            <natural_source database="NCBI">
               <organism ncbi="562">Escherichia coli</organism>
            </natural_source>
            <details>partial occupancy lower than P site</details>
            <classification>OTHER</classification>
            <structure>SINGLE STRANDED</structure>
            <synthetic_flag>false</synthetic_flag>
         </rna>
         <protein_or_peptide macromolecule_id="3">
            <name synonym="GFP">Green fluorescent protein</name>
            <natural_source database="NCBI">
               <organism ncbi="6100">Aequorea victoria</organism>
            </natural_source>
            <number_of_copies>1</number_of_copies>
            <oligomeric_state>Monomer</oligomeric_state>
            <recombinant_exp_flag>true</recombinant_exp_flag>
            <recombinant_expression database="NCBI">
               <recombinant_organism>In vitro transcription.translation system</recombinant_organism>
               <recombinant_plasmid>pIVEX2.3</recombinant_plasmid>
            </recombinant_expression>
            <sequence>
               </sequence>
         </protein_or_peptide>
      </macromolecule_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">5.0</concentration>
               <buffer>
                  <details>20 mM HEPES, 150 mM ammonium acetate, 6 mM
          magnesium       acetate, 2 mM spermidine, 0.05 mM spermine and
          4 mM       2-mercaptoethanol. Concentration of ribosomes
          expressed to       A260 units.</details>
               </buffer>
               <grid>
                  <details>300 mesh copper grid with holey carbon film</details>
               </grid>
               <vitrification>
                  <cryogen_name>ETHANE</cryogen_name>
                  <chamber_temperature units="K">100</chamber_temperature>
                  <instrument>HOMEMADE PLUNGER</instrument>
                  <details>Vitrification instrument: Standard unmodified guillotine plunger</details>
               </vitrification>
            </single_particle_preparation>
         </specimen_preparation_list>
         <microscopy_list>
            <single_particle_microscopy microscopy_id="1">
               <microscope>FEI/PHILIPS CM200FEG</microscope>
               <illumination_mode>OTHER</illumination_mode>
               <imaging_mode>OTHER</imaging_mode>
               <electron_source>FIELD EMISSION GUN</electron_source>
               <acceleration_voltage units="kV">200</acceleration_voltage>
               <nominal_cs units="mm">2</nominal_cs>
               <nominal_defocus_min units="&#181;m">1.805</nominal_defocus_min>
               <nominal_defocus_max units="&#181;m">5.96</nominal_defocus_max>
               <nominal_magnification>50000.0</nominal_magnification>
               <specimen_holder_model>GATAN LIQUID NITROGEN</specimen_holder_model>
               <temperature>
                  <temperature_average units="K">100</temperature_average>
               </temperature>
               <date>2000-05-02</date>
               <image_recording_list>
                  <image_recording>
                     <film_or_detector_model category="FILM">KODAK SO-163 FILM</film_or_detector_model>
                     <digitization_details>
                        <scanner>OTHER</scanner>
                        <sampling_interval units="&#181;m">8.322</sampling_interval>
                     </digitization_details>
                     <number_real_images>10</number_real_images>
                     <details>Scanner model:UMAX PowerLook 3000</details>
                     <od_range>5.0</od_range>
                     <bits_per_pixel>8.</bits_per_pixel>
                  </image_recording>
               </image_recording_list>
               <specimen_holder>Eucentric</specimen_holder>
            </single_particle_microscopy>
         </microscopy_list>
         <singleparticle_processing image_processing_id="1">
            <ctf_correction>
               <details>Each negative dataset</details>
            </ctf_correction>
            <final_reconstruction>
               <applied_symmetry>
                  <point_group>C1</point_group>
               </applied_symmetry>
               <algorithm>OTHER</algorithm>
               <resolution res_type="BY AUTHOR" units="&#8491;">16.0</resolution>
               <resolution_method>FSC 0.5 CUT-OFF</resolution_method>
               <software_list>
                  <software>
                     <name>SPIDER, IMAGIC, GAP, CNS, XPLOR</name>
                  </software>
               </software_list>
               <details>Final maps were calculated from 2276 images         from
        a total of       4500 from 10 individual         datasets,
        with scaling       in reciprocal space to
        crystallographic       ribosome       structures and
        correction for       map       anisotropy       by
        B-factor       weighting       of       amplitudes       in
        XPLOR       with       respect to a       similarly-treated
        control       inactive       ribosome. Selection       of
        particles for inclusion       in       the       final
        maps was by correlation       coefficient with       respect
        to the alignment model, designed to       maximise       nascent
        chain occupancy in the selected images.</details>
               <number_images_used>2276</number_images_used>
            </final_reconstruction>
            <final_angle_assignment>
               <details>SPIDER euler</details>
            </final_angle_assignment>
         </singleparticle_processing>
      </structure_determination>
   </structure_determination_list>
   <map format="CCP4" size_kbytes="8193">
      <file>emd_1072.map.gz</file>
      <symmetry>
         <space_group>1</space_group>
      </symmetry>
      <data_type>IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES)</data_type>
      <dimensions>
         <col>128</col>
         <row>128</row>
         <sec>128</sec>
      </dimensions>
      <origin>
         <col>0</col>
         <row>0</row>
         <sec>0</sec>
      </origin>
      <spacing>
         <x>128</x>
         <y>128</y>
         <z>128</z>
      </spacing>
      <cell>
         <a units="&#8491;">426.24</a>
         <b units="&#8491;">426.24</b>
         <c units="&#8491;">426.24</c>
         <alpha units="deg">90</alpha>
         <beta units="deg">90</beta>
         <gamma units="deg">90</gamma>
      </cell>
      <axis_order>
         <fast>Z</fast>
         <medium>X</medium>
         <slow>Y</slow>
      </axis_order>
      <statistics>
         <minimum>-1.96596</minimum>
         <maximum>3.05542</maximum>
         <average>0.00000000025867</average>
         <std>0.422637</std>
      </statistics>
      <pixel_spacing>
         <x units="&#8491;">3.33</x>
         <y units="&#8491;">3.33</y>
         <z units="&#8491;">3.33</z>
      </pixel_spacing>
      <contour_list>
         <contour primary="true">
            <level>1.06</level>
         </contour>
      </contour_list>
      <annotation_details>3D reconstruction of E. coli ribosome stalled
      in       translation of Green Fluorescent Protein</annotation_details>
      <details>::::EMDATABANK.org::::EMD-1072::::</details>
   </map>
   <interpretation>
      <modelling_list>
         <modelling>
            <refinement_protocol>RIGID BODY FIT</refinement_protocol>
            <software_list>
               <software>
                  <name>GAP</name>
               </software>
            </software_list>
            <details>Protocol: Rigid body</details>
            <target_criteria>R-factor and correlation coefficient</target_criteria>
            <refinement_space>REAL</refinement_space>
         </modelling>
      </modelling_list>
   </interpretation>
</emd>