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| <StructureSection load='6m7g' size='340' side='right'caption='[[6m7g]], [[Resolution|resolution]] 2.66Å' scene=''> | | <StructureSection load='6m7g' size='340' side='right'caption='[[6m7g]], [[Resolution|resolution]] 2.66Å' scene=''> |
| == Structural highlights == | | == Structural highlights == |
- | <table><tr><td colspan='2'>[[6m7g]] is a 12 chain structure with sequence from [http://en.wikipedia.org/wiki/Psepk Psepk]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6M7G OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=6M7G FirstGlance]. <br> | + | <table><tr><td colspan='2'>[[6m7g]] is a 12 chain structure with sequence from [https://en.wikipedia.org/wiki/Pseudomonas_putida_KT2440 Pseudomonas putida KT2440]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6M7G OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6M7G FirstGlance]. <br> |
- | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=PPQ:PHOSPHINOTHRICIN'>PPQ</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]] 2.657Å</td></tr> |
- | <tr id='gene'><td class="sblockLbl"><b>[[Gene|Gene:]]</b></td><td class="sblockDat">PP_1924 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=160488 PSEPK])</td></tr> | + | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=PPQ:PHOSPHINOTHRICIN'>PPQ</scene></td></tr> |
- | <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=6m7g FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6m7g OCA], [http://pdbe.org/6m7g PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6m7g RCSB], [http://www.ebi.ac.uk/pdbsum/6m7g PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6m7g 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=6m7g FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6m7g OCA], [https://pdbe.org/6m7g PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6m7g RCSB], [https://www.ebi.ac.uk/pdbsum/6m7g PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6m7g ProSAT]</span></td></tr> |
| </table> | | </table> |
| + | == Function == |
| + | [https://www.uniprot.org/uniprot/Q88LK7_PSEPK Q88LK7_PSEPK] |
| <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: Psepk]] | + | [[Category: Pseudomonas putida KT2440]] |
- | [[Category: Dheeman, D S]] | + | [[Category: Dheeman DS]] |
- | [[Category: Kandavelu, P]] | + | [[Category: Kandavelu P]] |
- | [[Category: Rosen, B P]] | + | [[Category: Rosen BP]] |
- | [[Category: Venkadesh, S]] | + | [[Category: Venkadesh S]] |
- | [[Category: Yoshinaga, M]] | + | [[Category: Yoshinaga M]] |
- | [[Category: N-acetyltransferase]]
| + | |
- | [[Category: Pseudomonas putida]]
| + | |
- | [[Category: Transferase]]
| + | |
| Structural highlights
Function
Q88LK7_PSEPK
Publication Abstract from PubMed
The emergence and spread of antimicrobial resistance highlights the urgent need for new antibiotics. Organoarsenicals have been used as antimicrobials since Paul Ehrlich's salvarsan. Recently a soil bacterium was shown to produce the organoarsenical arsinothricin. We demonstrate that arsinothricin, a non-proteinogenic analog of glutamate that inhibits glutamine synthetase, is an effective broad-spectrum antibiotic against both Gram-positive and Gram-negative bacteria, suggesting that bacteria have evolved the ability to utilize the pervasive environmental toxic metalloid arsenic to produce a potent antimicrobial. With every new antibiotic, resistance inevitably arises. The arsN1 gene, widely distributed in bacterial arsenic resistance (ars) operons, selectively confers resistance to arsinothricin by acetylation of the alpha-amino group. Crystal structures of ArsN1 N-acetyltransferase, with or without arsinothricin, shed light on the mechanism of its substrate selectivity. These findings have the potential for development of a new class of organoarsenical antimicrobials and ArsN1 inhibitors.
Arsinothricin, an arsenic-containing non-proteinogenic amino acid analog of glutamate, is a broad-spectrum antibiotic.,Nadar VS, Chen J, Dheeman DS, Galvan AE, Yoshinaga-Sakurai K, Kandavelu P, Sankaran B, Kuramata M, Ishikawa S, Rosen BP, Yoshinaga M Commun Biol. 2019 Apr 15;2:131. doi: 10.1038/s42003-019-0365-y. eCollection 2019. PMID:30993215[1]
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.
References
- ↑ Nadar VS, Chen J, Dheeman DS, Galvan AE, Yoshinaga-Sakurai K, Kandavelu P, Sankaran B, Kuramata M, Ishikawa S, Rosen BP, Yoshinaga M. Arsinothricin, an arsenic-containing non-proteinogenic amino acid analog of glutamate, is a broad-spectrum antibiotic. Commun Biol. 2019 Apr 15;2:131. doi: 10.1038/s42003-019-0365-y. eCollection 2019. PMID:30993215 doi:http://dx.doi.org/10.1038/s42003-019-0365-y
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