<emd xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" emdb_id="EMD-1003" 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>2002-06-26</deposition>
         <header_release>2002-08-22</header_release>
         <map_release>2002-08-22</map_release>
         <update>2012-10-17</update>
      </key_dates>
      <title>Solution structure of the E. coli 70S ribosome at 11.5 A resolution.</title>
      <authors_list>
         <author>Gabashvili IS</author>
      </authors_list>
      <keywords>
         </keywords>
   </admin>
   <crossreferences>
      <citation_list>
         <primary_citation>
            <journal_citation published="true">
               <author order="1">Gabashvili IS</author>
               <author order="2">Agrawal RK</author>
               <author order="3">Spahn CM</author>
               <author order="4">Grassucci RA</author>
               <author order="5">Svergun DI</author>
               <author order="6">Frank J</author>
               <author order="7">Penczek P</author>
               <title>Solution structure of the E. coli 70S ribosome at 11.5 A resolution.</title>
               <journal>CELL(CAMBRIDGE,MASS.)</journal>
               <volume>100</volume>
               <first_page>537</first_page>
               <last_page>549</last_page>
               <year>2000</year>
               <external_references type="PUBMED">10721991</external_references>
               <external_references type="DOI">doi:10.1016/S0092-8674(00)80690-X</external_references>
            </journal_citation>
         </primary_citation>
      </citation_list>
      <pdb_list>
         <pdb_reference>
            <pdb_id>1eg0</pdb_id>
            <relationship>
               <in_frame>FULLOVERLAP</in_frame>
            </relationship>
         </pdb_reference>
      </pdb_list>
   </crossreferences>
   <sample>
      <name>FMet-tRNAMet 70S Ribosome from E.coli</name>
      <supramolecule_list>
         <sample_supramolecule supramolecule_id="1000">
            <name>FMet-tRNAMet 70S Ribosome from E.coli</name>
            <details>preparation and buffer conditions are as described in
      Malhotra et al., J. Mol. Biol. (1998) 280, 103-116</details>
            <number_unique_components>3</number_unique_components>
            <molecular_weight>
               <theoretical units="MDa">2.5</theoretical>
            </molecular_weight>
         </sample_supramolecule>
         <complex_supramolecule supramolecule_id="1">
            <name>70S ribosome Escherichia coli</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>fMet-tRNA</name>
            <natural_source database="NCBI">
               <organism ncbi="562">Escherichia coli</organism>
            </natural_source>
            <classification>OTHER</classification>
            <structure>DOUBLE HELIX</structure>
            <synthetic_flag>false</synthetic_flag>
         </rna>
         <rna macromolecule_id="2">
            <name>MF-mRNA</name>
            <natural_source database="NCBI">
               <organism ncbi="562">Escherichia coli</organism>
            </natural_source>
            <details>46 nucleotides</details>
            <classification>OTHER</classification>
            <structure>SINGLE STRANDED</structure>
            <synthetic_flag>false</synthetic_flag>
         </rna>
      </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">0.09</concentration>
               <buffer>
                  <ph>7.6</ph>
                  <details>20 mM Hepes, 6 mM Mg(CH3COO)2 150 mM NH4Cl, 4 mM
          beta-Mercaptoethanol, 0.5 mM Spermine, 2 mM Spermidine.</details>
               </buffer>
               <vitrification>
                  <cryogen_name>ETHANE</cryogen_name>
                  <instrument>HOMEMADE PLUNGER</instrument>
                  <details>Vitrification instrument: 2 side blotting plunger</details>
                  <method>Blot and plunge</method>
               </vitrification>
            </single_particle_preparation>
         </specimen_preparation_list>
         <microscopy_list>
            <single_particle_microscopy microscopy_id="1">
               <microscope>FEI/PHILIPS CM200FEG/ST</microscope>
               <illumination_mode>FLOOD BEAM</illumination_mode>
               <imaging_mode>BRIGHT FIELD</imaging_mode>
               <electron_source>FIELD EMISSION GUN</electron_source>
               <acceleration_voltage units="kV">200</acceleration_voltage>
               <nominal_cs units="mm">2.0</nominal_cs>
               <nominal_defocus_min units="&#181;m">2.17</nominal_defocus_min>
               <nominal_defocus_max units="&#181;m">4.34</nominal_defocus_max>
               <nominal_magnification>50000.0</nominal_magnification>
               <calibrated_magnification>51200.0</calibrated_magnification>
               <specimen_holder_model>GATAN LIQUID NITROGEN</specimen_holder_model>
               <temperature>
                  <temperature_average units="K">93</temperature_average>
               </temperature>
               <details>25 % of data from Philips EM420 with LaB6 at 100kV</details>
               <date>1997-10-04</date>
               <image_recording_list>
                  <image_recording>
                     <film_or_detector_model category="FILM">KODAK SO-163 FILM</film_or_detector_model>
                     <digitization_details>
                        <scanner>PERKIN ELMER</scanner>
                        <sampling_interval units="&#181;m">15</sampling_interval>
                     </digitization_details>
                     <number_real_images>239</number_real_images>
                     <average_electron_dose_per_image units="e/&#8491;^2">10</average_electron_dose_per_image>
                     <bits_per_pixel>12.</bits_per_pixel>
                  </image_recording>
               </image_recording_list>
               <specimen_holder>Cryo Transfer</specimen_holder>
               <tilt_angle_min>0</tilt_angle_min>
               <tilt_angle_max>0</tilt_angle_max>
            </single_particle_microscopy>
         </microscopy_list>
         <singleparticle_processing image_processing_id="1">
            <ctf_correction>
               <details>Wiener filtration of defocus group volumes</details>
            </ctf_correction>
            <final_reconstruction>
               <applied_symmetry>
                  <point_group>C1</point_group>
               </applied_symmetry>
               <algorithm>OTHER</algorithm>
               <resolution res_type="BY AUTHOR" units="&#8491;">11.5</resolution>
               <resolution_method>FSC 0.5 CUT-OFF</resolution_method>
               <software_list>
                  <software>
                     <name>SPIDER/WEB</name>
                  </software>
               </software_list>
               <number_images_used>73523</number_images_used>
            </final_reconstruction>
         </singleparticle_processing>
      </structure_determination>
   </structure_determination_list>
   <map format="CCP4" size_kbytes="7631">
      <file>emd_1003.map.gz</file>
      <symmetry>
         <space_group>1</space_group>
      </symmetry>
      <data_type>IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES)</data_type>
      <dimensions>
         <col>125</col>
         <row>125</row>
         <sec>125</sec>
      </dimensions>
      <origin>
         <col>-62</col>
         <row>-62</row>
         <sec>-62</sec>
      </origin>
      <spacing>
         <x>125</x>
         <y>125</y>
         <z>125</z>
      </spacing>
      <cell>
         <a units="&#8491;">366.25</a>
         <b units="&#8491;">366.25</b>
         <c units="&#8491;">366.25</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>-141.974999999999994</minimum>
         <maximum>339.987000000000023</maximum>
         <average>1.85585</average>
         <std>38.046700000000001</std>
      </statistics>
      <pixel_spacing>
         <x units="&#8491;">2.93</x>
         <y units="&#8491;">2.93</y>
         <z units="&#8491;">2.93</z>
      </pixel_spacing>
      <contour_list>
         <contour primary="true">
            <level>82.799999999999997</level>
         </contour>
      </contour_list>
      <annotation_details>E. coli 70S Ribosome</annotation_details>
      <details>::::EMDATABANK.org::::EMD-1003::::</details>
   </map>
   <interpretation>
      <modelling_list>
         <modelling>
            <refinement_protocol>RIGID BODY FIT</refinement_protocol>
            <software_list>
               <software>
                  <name>O</name>
               </software>
            </software_list>
            <details>manual fitting using O Mol_Id: 1; Molecule: S4 Ribosomal Protein; Chain: A; Other_Details: Modeled By Analogous Protein Of B. Stearothermophilus Taken From Pdb Entry 1C06 Mol_Id: 2; Molecule: S5 Ribosomal Protein; Chain: B; Other_Details: Modeled By Analogous Protein Of B. Stearothermophilus Taken From Pdb Entry 1Pkp Mol_Id: 3; Molecule: S6 Ribosomal Protein; Chain: C; Other_Details: Modeled By Analogous Protein Of T. Thermophilus Taken From Pdb Entry 1Ris Mol_Id: 4; Molecule: S7 Ribosomal Protein; Chain: D; Other_Details: Modeled By Analogous Protein Of T. Thermophilus Taken From Pdb Entry 1Rss Mol_Id: 5; Molecule: S8 Ribosomal Protein; Chain: E; Other_Details: Modeled By Analogous Protein Of T. Thermophilus Taken From Pdb Entry 1An7 Mol_Id: 6; Molecule: S15 Ribosomal Protein; Chain: F; Other_Details: Modeled By Analogous Protein Of B. Stearothermophilus Taken From Pdb Entry 1A32 Mol_Id: 7; Molecule: S17 Ribosomal Protein; Chain: G; Other_Details: Modeled By Analogous Protein Of B. Stearothermophilus Taken From Pdb Entries 1Rip and 1Qd7 Mol_Id: 8; Molecule: S20 Ribosomal Protein; Chain: H; Other_Details: Modeled By Analogous Protein Of T. Thermophilus Taken From Pdb Entry 1Qd7 Mol_Id: 9; Molecule: Ribosomal Protein L1; Chain: N; Other_Details: Modeled By Analogous Protein Of T. Thermophilus Taken From Pdb Entry 1Ad2 Mol_Id: 10; Molecule: Ribosomal Protein L6; Chain: J; Mutation: Yes; Other_Details: Modeled By Analogous Protein Of T. Stearothermophilus Taken From Pdb Entry 1Rl6 Mol_Id: 11; Molecule: Ribosomal Protein L11; Chain: K; Other_Details: Modeled By Analogous Protein Of T. Maritima Taken From Pdb Entry 1Mms Mol_Id: 12; Molecule: Fragment Of 16S Rrna Helix 23; Chain: I; Fragment: Residues 673-713; Other_Details: Modeled As Analogous Fragment Of T. Thermophilus Taken From Pdb Entry 1Qd7 Mol_Id: 13; Molecule: Fragment Of 23S Rrna; Chain: L; Fragment: Residues 1051-1108; Other_Details: T. Maritima RNA Sequence and Model Taken From Pdb Entry 1Mms Mol_Id: 14; Molecule: Helix 95 Of 23S Rrna; Chain: M; Other_Details: E. Coli RNA Sequence and Model Taken From Pdb Entry 480D Mol_Id: 15; Molecule: Formyl-Methionyl-tRNA; Chain: O; Synonym: Fmet-tRNA; Other_Details: E. Coli Fmet-tRNA Sequence and Model Taken From Pdb Entry 2Fmt</details>
         </modelling>
      </modelling_list>
   </interpretation>
</emd>