6vm6

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==Structure of Acinetobacter baumannii Cap4 SAVED/CARF-domain containing receptor with the cyclic trinucleotide 2'3'3'-cAAA==
==Structure of Acinetobacter baumannii Cap4 SAVED/CARF-domain containing receptor with the cyclic trinucleotide 2'3'3'-cAAA==
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<StructureSection load='6vm6' size='340' side='right'caption='[[6vm6]]' scene=''>
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<StructureSection load='6vm6' size='340' side='right'caption='[[6vm6]], [[Resolution|resolution]] 2.10&Aring;' scene=''>
== Structural highlights ==
== Structural highlights ==
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<table><tr><td colspan='2'>Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6VM6 OCA]. For a <b>guided tour on the structure components</b> use [http://proteopedia.org/fgij/fg.htm?mol=6VM6 FirstGlance]. <br>
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<table><tr><td colspan='2'>[[6vm6]] is a 11 chain structure with sequence from [https://en.wikipedia.org/wiki/Acinetobacter_sp._ATCC_27244 Acinetobacter sp. ATCC 27244] and [https://en.wikipedia.org/wiki/Synthetic_construct Synthetic construct]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6VM6 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6VM6 FirstGlance]. <br>
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</td></tr><tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://proteopedia.org/fgij/fg.htm?mol=6vm6 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6vm6 OCA], [http://pdbe.org/6vm6 PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6vm6 RCSB], [http://www.ebi.ac.uk/pdbsum/6vm6 PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6vm6 ProSAT]</span></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]] 2.1&#8491;</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'>[https://proteopedia.org/fgij/fg.htm?mol=6vm6 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6vm6 OCA], [https://pdbe.org/6vm6 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6vm6 RCSB], [https://www.ebi.ac.uk/pdbsum/6vm6 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6vm6 ProSAT]</span></td></tr>
</table>
</table>
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== Function ==
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[https://www.uniprot.org/uniprot/CAP4_ACIS2 CAP4_ACIS2] CBASS (cyclic oligonucleotide-based antiphage signaling system) provides immunity against bacteriophage. The CD-NTase protein synthesizes cyclic nucleotides in response to infection; these serve as specific second messenger signals. The signals activate a diverse range of effectors, leading to bacterial cell death and thus abortive phage infection. A type II-C(AAAA) CBASS system (PubMed:32839535).<ref>PMID:32839535</ref> <ref>PMID:32544385</ref> Binds cyclic nucleotide second messengers (synthesized by CdnD, the cognate CD-NTase in the CBASS operon). Ligand binding activates it to endonucleolytically degrade dsDNA to approximately 6 bp length fragments, with a preference for 5'-C or 5'-G cleavage site. The minor product of CdnD is the activating nucleotide; also binds the major product (2',3',3'-cyclic AMP-AMP-AMP) but is not activated by it. Only binds DNA in the presence of ligand. Is not activated by c-di-AMP, c-di-GMP, 3'3'-cyclic GMP-AMP (3'3'-cGAMP) or 3',3',3'-cyclic AMP-AMP-GMP.<ref>PMID:32544385</ref>
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== References ==
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<references/>
__TOC__
__TOC__
</StructureSection>
</StructureSection>
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[[Category: Acinetobacter sp. ATCC 27244]]
[[Category: Large Structures]]
[[Category: Large Structures]]
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[[Category: Synthetic construct]]
[[Category: Antine SP]]
[[Category: Antine SP]]
[[Category: Cabrera V]]
[[Category: Cabrera V]]

Current revision

Structure of Acinetobacter baumannii Cap4 SAVED/CARF-domain containing receptor with the cyclic trinucleotide 2'3'3'-cAAA

PDB ID 6vm6

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