|  |   | 
		| Line 3: | Line 3: | 
|  | <StructureSection load='5jtf' size='340' side='right'caption='[[5jtf]], [[Resolution|resolution]] 2.16Å' scene=''> |  | <StructureSection load='5jtf' size='340' side='right'caption='[[5jtf]], [[Resolution|resolution]] 2.16Å' scene=''> | 
|  | == Structural highlights == |  | == Structural highlights == | 
| - | <table><tr><td colspan='2'>[[5jtf]] is a 2 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=5JTF OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=5JTF FirstGlance]. <br> | + | <table><tr><td colspan='2'>[[5jtf]] is a 2 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=5JTF OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=5JTF FirstGlance]. <br> | 
| - | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=TRS:2-AMINO-2-HYDROXYMETHYL-PROPANE-1,3-DIOL'>TRS</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]] 2.156Å</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=TRS:2-AMINO-2-HYDROXYMETHYL-PROPANE-1,3-DIOL'>TRS</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=5jtf FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5jtf OCA], [http://pdbe.org/5jtf PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=5jtf RCSB], [http://www.ebi.ac.uk/pdbsum/5jtf PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=5jtf 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=5jtf FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5jtf OCA], [https://pdbe.org/5jtf PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=5jtf RCSB], [https://www.ebi.ac.uk/pdbsum/5jtf PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=5jtf 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 == | 
| Line 22: | Line 24: | 
|  | </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: 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
 
 |