6nl1

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Current revision (14:48, 13 March 2024) (edit) (undo)
 
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<StructureSection load='6nl1' size='340' side='right'caption='[[6nl1]], [[Resolution|resolution]] 2.30&Aring;' scene=''>
<StructureSection load='6nl1' size='340' side='right'caption='[[6nl1]], [[Resolution|resolution]] 2.30&Aring;' scene=''>
== Structural highlights ==
== Structural highlights ==
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<table><tr><td colspan='2'>[[6nl1]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Trypanosoma_(trypanozoon)_brucei Trypanosoma (trypanozoon) brucei]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6NL1 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6NL1 FirstGlance]. <br>
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<table><tr><td colspan='2'>[[6nl1]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Trypanosoma_brucei Trypanosoma brucei]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6NL1 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6NL1 FirstGlance]. <br>
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</td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=SO4:SULFATE+ION'>SO4</scene></td></tr>
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</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.297&#8491;</td></tr>
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<tr id='gene'><td class="sblockLbl"><b>[[Gene|Gene:]]</b></td><td class="sblockDat">MERS1 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=5691 Trypanosoma (Trypanozoon) brucei])</td></tr>
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<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=SO4:SULFATE+ION'>SO4</scene></td></tr>
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<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6nl1 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6nl1 OCA], [http://pdbe.org/6nl1 PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6nl1 RCSB], [http://www.ebi.ac.uk/pdbsum/6nl1 PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6nl1 ProSAT]</span></td></tr>
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<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=6nl1 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6nl1 OCA], [https://pdbe.org/6nl1 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6nl1 RCSB], [https://www.ebi.ac.uk/pdbsum/6nl1 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6nl1 ProSAT]</span></td></tr>
</table>
</table>
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<div style="background-color:#fffaf0;">
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== Function ==
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== Publication Abstract from PubMed ==
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[https://www.uniprot.org/uniprot/B6SBM0_9TRYP B6SBM0_9TRYP]
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Most mitochondrial mRNAs are transcribed as polycistronic precursors that are cleaved by endonucleases to produce mature mRNA transcripts. However, recent studies have shown that mitochondrial transcripts in the kinetoplastid protozoan, Trypanosoma brucei, are transcribed individually. Also unlike most mitochondrial mRNAs, the 5' end of these transcripts harbor a triphosphate that is hydrolyzed. This modification is carried out by a putative Nudix hydrolase called MERS1. The Nudix motif in MERS1 is degenerate, lacking a conserved glutamic acid, thus it is unclear how it may bind its substrates and whether it contains a Nudix fold. To obtain insight into this unusual hydrolase we determined structures of apo, GTP-bound and RNA-bound T. brucei MERS1 to 2.35 A, 2.45 A and 2.60 A respectively. The MERS1 structure has a unique fold that indeed contains a Nudix motif. The nucleotide bound structures combined with binding studies reveal that MERS1 shows preference for RNA sequences with a central guanine repeat which it binds in a single stranded conformation. The apo MERS1 structure indicates that a significant portion of its nucleotide-binding site folds upon substrate binding. Finally, a potential interaction region for a binding partner, MERS2, that activates MERS1 was identified. The MERS2-like peptide inserts a glutamate near the missing Nudix acidic residue in the RNA binding pocket, suggesting how the enzyme may be activated. Thus, the combined studies reveal insight into the structure and enzyme properties of MERS1 and its substrate binding activities.
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Structures of MERS1, the 5' processing enzyme of mitochondrial mRNAs in Trypanosoma brucei.,Schumacher MA, Zeng W, Henderson M RNA. 2019 Nov 8. pii: rna.072231.119. doi: 10.1261/rna.072231.119. PMID:31704716<ref>PMID:31704716</ref>
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From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
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</div>
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<div class="pdbe-citations 6nl1" style="background-color:#fffaf0;"></div>
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== References ==
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<references/>
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__TOC__
__TOC__
</StructureSection>
</StructureSection>
[[Category: Large Structures]]
[[Category: Large Structures]]
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[[Category: Schumacher, M A]]
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[[Category: Trypanosoma brucei]]
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[[Category: Mers1]]
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[[Category: Schumacher MA]]
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[[Category: Mrna processing]]
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[[Category: Nudix]]
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[[Category: Rna binding protein]]
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Current revision

Structure of T. brucei MERS1 protein in its apo form

PDB ID 6nl1

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