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| <StructureSection load='7kes' size='340' side='right'caption='[[7kes]], [[Resolution|resolution]] 2.36Å' scene=''> | | <StructureSection load='7kes' size='340' side='right'caption='[[7kes]], [[Resolution|resolution]] 2.36Å' scene=''> |
| == Structural highlights == | | == Structural highlights == |
- | <table><tr><td colspan='2'>[[7kes]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/Uncultivated_bacterium Uncultivated bacterium]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=7KES OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=7KES FirstGlance]. <br> | + | <table><tr><td colspan='2'>[[7kes]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/Uncultured_bacterium Uncultured bacterium]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=7KES OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=7KES FirstGlance]. <br> |
- | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=AM2:APRAMYCIN'>AM2</scene>, <scene name='pdbligand=CL:CHLORIDE+ION'>CL</scene>, <scene name='pdbligand=COA:COENZYME+A'>COA</scene>, <scene name='pdbligand=GOL:GLYCEROL'>GOL</scene></td></tr> | + | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.36Å</td></tr> |
- | <tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat"><div style='overflow: auto; max-height: 3em;'>[[5ht0|5ht0]], [[6mmz|6mmz]], [[6mn0|6mn0]], [[6mn1|6mn1]], [[6mn2|6mn2]]</div></td></tr> | + | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=AM2:APRAMYCIN'>AM2</scene>, <scene name='pdbligand=CL:CHLORIDE+ION'>CL</scene>, <scene name='pdbligand=COA:COENZYME+A'>COA</scene>, <scene name='pdbligand=GOL:GLYCEROL'>GOL</scene></td></tr> |
- | <tr id='activity'><td class="sblockLbl"><b>Activity:</b></td><td class="sblockDat"><span class='plainlinks'>[https://en.wikipedia.org/wiki/Aminoglycoside_N(3')-acetyltransferase Aminoglycoside N(3')-acetyltransferase], with EC number [https://www.brenda-enzymes.info/php/result_flat.php4?ecno=2.3.1.81 2.3.1.81] </span></td></tr> | + | |
| <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=7kes FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7kes OCA], [https://pdbe.org/7kes PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7kes RCSB], [https://www.ebi.ac.uk/pdbsum/7kes PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7kes ProSAT]</span></td></tr> | | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=7kes FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7kes OCA], [https://pdbe.org/7kes PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7kes RCSB], [https://www.ebi.ac.uk/pdbsum/7kes PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7kes ProSAT]</span></td></tr> |
| </table> | | </table> |
| + | == Function == |
| + | [https://www.uniprot.org/uniprot/A0A059X981_9BACT A0A059X981_9BACT] |
| <div style="background-color:#fffaf0;"> | | <div style="background-color:#fffaf0;"> |
| == Publication Abstract from PubMed == | | == Publication Abstract from PubMed == |
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| </StructureSection> | | </StructureSection> |
| [[Category: Large Structures]] | | [[Category: Large Structures]] |
- | [[Category: Uncultivated bacterium]] | + | [[Category: Uncultured bacterium]] |
- | [[Category: Structural genomic]]
| + | [[Category: Joachimiak A]] |
- | [[Category: Joachimiak, A]] | + | [[Category: Michalska K]] |
- | [[Category: Michalska, K]] | + | [[Category: Satchell KJ]] |
- | [[Category: Satchell, K J]] | + | [[Category: Savchenko A]] |
- | [[Category: Savchenko, A]] | + | [[Category: Skarina T]] |
- | [[Category: Skarina, T]] | + | [[Category: Stogios PJ]] |
- | [[Category: Stogios, P J]] | + | [[Category: Xu Z]] |
- | [[Category: Xu, Z]] | + | [[Category: Yim V]] |
- | [[Category: Yim, V]] | + | |
- | [[Category: Acetyltransferase]]
| + | |
- | [[Category: Aminoglycoside]]
| + | |
- | [[Category: Antibiotic resistance]]
| + | |
- | [[Category: Antibiotic_nat family]]
| + | |
- | [[Category: Csgid]]
| + | |
- | [[Category: Metagenome]]
| + | |
- | [[Category: National institute of allergy and infectious disease]]
| + | |
- | [[Category: Niaid]]
| + | |
- | [[Category: Soil]]
| + | |
- | [[Category: Transferase]]
| + | |
- | [[Category: Transferase-antibiotic complex]]
| + | |
| Structural highlights
Function
A0A059X981_9BACT
Publication Abstract from PubMed
The environmental microbiome harbors a vast repertoire of antibiotic resistance genes (ARGs) which can serve as evolutionary predecessors for ARGs found in pathogenic bacteria, or can be directly mobilized to pathogens in the presence of selection pressures. Thus, ARGs from benign environmental bacteria are an important resource for understanding clinically relevant resistance. Here, we conduct a comprehensive functional analysis of the Antibiotic_NAT family of aminoglycoside acetyltransferases. We determined a pan-family antibiogram of 21 Antibiotic_NAT enzymes, including 8 derived from clinical isolates and 13 from environmental metagenomic samples. We find that environment-derived representatives confer high-level, broad-spectrum resistance, including against the atypical aminoglycoside apramycin, and that a metagenome-derived gene likely is ancestral to an aac(3) gene found in clinical isolates. Through crystallographic analysis, we rationalize the molecular basis for diversification of substrate specificity across the family. This work provides critical data on the molecular mechanism underpinning resistance to established and emergent aminoglycoside antibiotics and broadens our understanding of ARGs in the environment.
Structural and molecular rationale for the diversification of resistance mediated by the Antibiotic_NAT family.,Stogios PJ, Bordeleau E, Xu Z, Skarina T, Evdokimova E, Chou S, Diorio-Toth L, D'Souza AW, Patel S, Dantas G, Wright GD, Savchenko A Commun Biol. 2022 Mar 25;5(1):263. doi: 10.1038/s42003-022-03219-w. PMID:35338238[1]
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.
References
- ↑ Stogios PJ, Bordeleau E, Xu Z, Skarina T, Evdokimova E, Chou S, Diorio-Toth L, D'Souza AW, Patel S, Dantas G, Wright GD, Savchenko A. Structural and molecular rationale for the diversification of resistance mediated by the Antibiotic_NAT family. Commun Biol. 2022 Mar 25;5(1):263. doi: 10.1038/s42003-022-03219-w. PMID:35338238 doi:http://dx.doi.org/10.1038/s42003-022-03219-w
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