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==Crystal structure of protein of unknown function (DUF1255,PF06865) from Acinetobacter sp. ADP1== | ==Crystal structure of protein of unknown function (DUF1255,PF06865) from Acinetobacter sp. ADP1== | ||
<StructureSection load='3hqx' size='340' side='right' caption='[[3hqx]], [[Resolution|resolution]] 1.66Å' scene=''> | <StructureSection load='3hqx' size='340' side='right'caption='[[3hqx]], [[Resolution|resolution]] 1.66Å' scene=''> | ||
== Structural highlights == | == Structural highlights == | ||
<table><tr><td colspan='2'>[[3hqx]] is a 1 chain structure with sequence from [ | <table><tr><td colspan='2'>[[3hqx]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Acinetobacter_baylyi_ADP1 Acinetobacter baylyi ADP1]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=3HQX OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=3HQX FirstGlance]. <br> | ||
</td></tr><tr id=' | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 1.66Å</td></tr> | ||
<tr id=' | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=MSE:SELENOMETHIONINE'>MSE</scene></td></tr> | ||
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[ | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=3hqx FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=3hqx OCA], [https://pdbe.org/3hqx PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=3hqx RCSB], [https://www.ebi.ac.uk/pdbsum/3hqx PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=3hqx ProSAT], [https://www.topsan.org/Proteins/MCSG/3hqx TOPSAN]</span></td></tr> | ||
</table> | </table> | ||
== Function == | |||
[https://www.uniprot.org/uniprot/PPNP_ACIAD PPNP_ACIAD] Catalyzes the phosphorolysis of diverse nucleosides, yielding D-ribose 1-phosphate and the respective free bases. Can use uridine, adenosine, guanosine, cytidine, thymidine, inosine and xanthosine as substrates. Also catalyzes the reverse reactions.[HAMAP-Rule:MF_01537] | |||
== Evolutionary Conservation == | == Evolutionary Conservation == | ||
[[Image:Consurf_key_small.gif|200px|right]] | [[Image:Consurf_key_small.gif|200px|right]] | ||
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<jmolCheckbox> | <jmolCheckbox> | ||
<scriptWhenChecked>; select protein; define ~consurf_to_do selected; consurf_initial_scene = true; script "/wiki/ConSurf/hq/3hqx_consurf.spt"</scriptWhenChecked> | <scriptWhenChecked>; select protein; define ~consurf_to_do selected; consurf_initial_scene = true; script "/wiki/ConSurf/hq/3hqx_consurf.spt"</scriptWhenChecked> | ||
<scriptWhenUnchecked>script /wiki/extensions/Proteopedia/spt/ | <scriptWhenUnchecked>script /wiki/extensions/Proteopedia/spt/initialview03.spt</scriptWhenUnchecked> | ||
<text>to colour the structure by Evolutionary Conservation</text> | <text>to colour the structure by Evolutionary Conservation</text> | ||
</jmolCheckbox> | </jmolCheckbox> | ||
| Line 20: | Line 22: | ||
__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
[[Category: | [[Category: Acinetobacter baylyi ADP1]] | ||
[[Category: Dauter | [[Category: Large Structures]] | ||
[[Category: Freeman | [[Category: Dauter Z]] | ||
[[Category: Hatzos | [[Category: Freeman L]] | ||
[[Category: Joachimiak | [[Category: Hatzos C]] | ||
[[Category: Joachimiak A]] | |||
[[Category: Nocek | [[Category: Nocek B]] | ||
Latest revision as of 08:53, 17 October 2024
Crystal structure of protein of unknown function (DUF1255,PF06865) from Acinetobacter sp. ADP1Crystal structure of protein of unknown function (DUF1255,PF06865) from Acinetobacter sp. ADP1
Structural highlights
FunctionPPNP_ACIAD Catalyzes the phosphorolysis of diverse nucleosides, yielding D-ribose 1-phosphate and the respective free bases. Can use uridine, adenosine, guanosine, cytidine, thymidine, inosine and xanthosine as substrates. Also catalyzes the reverse reactions.[HAMAP-Rule:MF_01537] Evolutionary Conservation Check, as determined by ConSurfDB. You may read the explanation of the method and the full data available from ConSurf. |
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