<emd emdb_id="EMD-1098" version="3.0.1.1" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" 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>2004-08-23</deposition>
            <header_release>2004-10-06</header_release>
            <map_release>2004-10-06</map_release>
            <update>2012-10-24</update>
        </key_dates>
        <title>Three-dimensional structure of a bacterial oxalate transporter.</title>
        <authors_list>
            <author>Hirai T</author>
            <author>Heymann JAW</author>
            <author>Shi D</author>
            <author>Sarker R</author>
            <author>Maloney PC</author>
            <author>Subramaniam S</author>
        </authors_list>
        <keywords />
    </admin>
    <crossreferences>
        <citation_list>
            <primary_citation>
                <journal_citation published="true">
                    <author order="1">Hirai T</author>
                    <author order="2">Heymann JA</author>
                    <author order="3">Shi D</author>
                    <author order="4">Sarker R</author>
                    <author order="5">Maloney PC</author>
                    <author order="6">Subramaniam S</author>
                    <title>Three-dimensional structure of a bacterial oxalate transporter.</title>
                    <journal>NAT.STRUCT.BIOL.</journal>
                    <volume>9</volume>
                    <first_page>597</first_page>
                    <last_page>600</last_page>
                    <year>2002</year>
                    <external_references type="PUBMED">12118242</external_references>
                    <external_references type="DOI">doi:10.1038/nsb821</external_references>
                </journal_citation>
            </primary_citation>
        </citation_list>
    </crossreferences>
    <sample>
        <name>Oxalate Transporter</name>
        <supramolecule_list>
            <sample_supramolecule supramolecule_id="1000">
                <name>Oxalate Transporter</name>
                <number_unique_components>1</number_unique_components>
            </sample_supramolecule>
        </supramolecule_list>
        <macromolecule_list>
            <protein_or_peptide macromolecule_id="1">
                <name synonym="OxlT">oxalate transporter</name>
                <natural_source database="NCBI">
                    <organism ncbi="847">Oxalobacter formigenes</organism>
                    <cellular_location>cell membrane</cellular_location>
                </natural_source>
                <molecular_weight>
                    <experimental units="MDa">0.044</experimental>
                </molecular_weight>
                <details>Oxalate(-ooc-coo-) is believed to be bound in the central cavity of OxlT in this crystal form. Endogenous E.coli lipids and added synthetic lipids
 are expected to be present in this two
 dimensional crystal. No detectable
 density for lipid or oxalate is observed at current resolution.</details>
                <recombinant_exp_flag>true</recombinant_exp_flag>
                <recombinant_expression database="NCBI">
                    <recombinant_organism ncbi="562">Escherichia coli</recombinant_organism>
                    <recombinant_plasmid>pBluescript II SKplus and pMS421</recombinant_plasmid>
                </recombinant_expression>
                <sequence />
            </protein_or_peptide>
        </macromolecule_list>
    </sample>
    <structure_determination_list>
        <structure_determination structure_determination_id="1">
            <method>electronCrystallography</method>
            <aggregation_state>twoDArray</aggregation_state>
            <specimen_preparation_list>
                <crystallography_preparation preparation_id="1">
                    <grid>
                        <details>400 mesh Cu grid</details>
                    </grid>
                    <vitrification>
                        <cryogen_name>NITROGEN</cryogen_name>
                        <chamber_temperature units="K">77</chamber_temperature>
                        <instrument>HOMEMADE PLUNGER</instrument>
                        <details>Vitrification instrument: MRC plunger</details>
                    </vitrification>
                    <crystal_formation />
                </crystallography_preparation>
            </specimen_preparation_list>
            <microscopy_list>
                <crystallography_microscopy microscopy_id="1">
                    <microscope>FEI TECNAI F30</microscope>
                    <illumination_mode>SPOT SCAN</illumination_mode>
                    <imaging_mode>BRIGHT FIELD</imaging_mode>
                    <electron_source>FIELD EMISSION GUN</electron_source>
                    <acceleration_voltage units="kV">300</acceleration_voltage>
                    <nominal_cs units="mm">2.2</nominal_cs>
                    <nominal_defocus_min units="&#181;m">0.1</nominal_defocus_min>
                    <nominal_defocus_max units="&#181;m">2.0</nominal_defocus_max>
                    <nominal_magnification>59000.0</nominal_magnification>
                    <calibrated_magnification>57000.0</calibrated_magnification>
                    <specimen_holder_model>GATAN LIQUID NITROGEN</specimen_holder_model>
                    <temperature>
                        <temperature_min units="K">90</temperature_min>
                        <temperature_max units="K">95</temperature_max>
                    </temperature>
                    <alignment_procedure>
                        <legacy>
                            <astigmatism>astigmatism was corrected at 200,000 times magnification</astigmatism>
                        </legacy>
                    </alignment_procedure>
                    <details>Tecnai12, 120KV with tungsten filament was also used at
        early stage.   Floodbeam was also used for some images as
        illumination mode.</details>
                    <image_recording_list>
                        <image_recording>
                            <film_or_detector_model category="FILM">KODAK SO-163 FILM</film_or_detector_model>
                            <digitization_details>
                                <scanner>ZEISS SCAI</scanner>
                                <sampling_interval units="&#181;m">7</sampling_interval>
                            </digitization_details>
                            <number_real_images>47</number_real_images>
                            <average_electron_dose_per_image units="e/&#8491;^2">10</average_electron_dose_per_image>
                            <details>The best images were selected by optical diffraction.</details>
                            <od_range>0.5</od_range>
                            <bits_per_pixel>10.</bits_per_pixel>
                        </image_recording>
                    </image_recording_list>
                    <specimen_holder>side entry</specimen_holder>
                    <tilt_angle_min>0</tilt_angle_min>
                    <tilt_angle_max>45</tilt_angle_max>
                    <tilt_series>
                        <axis1>
                            <min_angle units="deg">0</min_angle>
                            <max_angle units="deg">45</max_angle>
                        </axis1>
                    </tilt_series>
                </crystallography_microscopy>
            </microscopy_list>
            <crystallography_processing image_processing_id="1">
                <details>Specimens were either embedded in 3.5% trehalose or
 prepared as frozen-hydrated specimens.</details>
                <final_reconstruction>
                    <resolution res_type="BY AUTHOR" units="&#8491;">6.5</resolution>
                    <resolution_method>OTHER</resolution_method>
                    <software_list>
                        <software>
                            <name>MRC</name>
                        </software>
                    </software_list>
                    <details>Amplitudes were scaled with respect to reference
        amplitudes       from the helix model.</details>
                </final_reconstruction>
                <crystal_parameters>
                    <unit_cell>
                        <a units="&#8491;">100.3</a>
                        <b units="&#8491;">79</b>
                        <c units="&#8491;">100</c>
                        <gamma units="deg">90</gamma>
                        <alpha units="deg">90</alpha>
                        <beta units="deg">90</beta>
                    </unit_cell>
                    <plane_group>P 2 21 21</plane_group>
                </crystal_parameters>
                <ctf_correction>
                    <details>ctfsearch or ttrefine on each image</details>
                </ctf_correction>
            </crystallography_processing>
        </structure_determination>
    </structure_determination_list>
    <map format="CCP4" size_kbytes="3430">
        <file>emd_1098.map.gz</file>
        <symmetry>
            <space_group>18</space_group>
        </symmetry>
        <data_type>IMAGE STORED AS FLOATING POINT NUMBER (4 BYTES)</data_type>
        <dimensions>
            <col>86</col>
            <row>65</row>
            <sec>157</sec>
        </dimensions>
        <origin>
            <col>81</col>
            <row>14</row>
            <sec>-78</sec>
        </origin>
        <spacing>
            <x>150</x>
            <y>182</y>
            <z>182</z>
        </spacing>
        <cell>
            <a units="&#8491;">100.30002</a>
            <b units="&#8491;">79.00005</b>
            <c units="&#8491;">100.000084</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>-162.380218509999992</minimum>
            <maximum>256.0</maximum>
            <average>5.49867582</average>
            <std>48.494132999999998</std>
        </statistics>
        <pixel_spacing>
            <x units="&#8491;">0.551099</x>
            <y units="&#8491;">0.526667</y>
            <z units="&#8491;">0.549451</z>
        </pixel_spacing>
        <contour_list>
            <contour primary="true">
                <level>54.0</level>
                <source>AUTHOR</source>
            </contour>
        </contour_list>
        <annotation_details>This is an image of the bacterial oxalate
 transporter(OxlT)in the oxalate-bound, "closed" state. OxlT is a representative member of the Major Facilitator Superfamily (MFS).</annotation_details>
        <details>::::EMDATABANK.org::::EMD-1098::::</details>
    </map>
</emd>