1aj1

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[[Image:1aj1.gif|left|200px]]<br />
 
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<applet load="1aj1" size="450" color="white" frame="true" align="right" spinBox="true"
 
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caption="1aj1" />
 
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'''NMR STRUCTURE OF THE LANTIBIOTIC ACTAGARDINE, 15 STRUCTURES'''<br />
 
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==Overview==
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==NMR STRUCTURE OF THE LANTIBIOTIC ACTAGARDINE==
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The three-dimensional solution structure of the lantibiotic actagardine, was determined at high resolution by homonuclear and heteronuclear, two-dimensional and three-dimensional NMR spectroscopy in, [2H3]acetonitrile/H2O (7:3). 133 non-trivial distance and 22, torsional-angle constraints were derived from the NMR data. An ensemble of, 15 low-energy structures was calculated by distance geometry followed by, an iterative relaxation-matrix-refinement procedure. The rmsd of the, backbone coordinates with respect to the average structure was 17 pm. The, two distinct thioether ring systems 1-6 and 7-19 were even better defined, with backbone rmsd of 10 pm and 14 pm, respectively. Actagardine shows a, rigid compact globular shape based on the constraining bridging pattern, which is composed of an N-terminal lanthionine ring from residues 1-6 and, three intertwined C-terminal methyllanthionine rings comprising residues, 7-12, 9-17 and 14-19. In addition, this C-terminal ring system is, stabilised by a short antiparallel beta sheet. A feature of the, actagardine structure is the presence of two putative binding pockets. A, pocket is generated by the covalent constraints of the C-terminal, thioether ring system. The rim of this pocket is built up by a loop, structure comprising residues 12-19, whose backbone amide protons are all, directed to the centre of the pocket. The second pocket is formed by an, L-shaped orientation of the N-terminal and C-terminal thioether ring, systems. The only two hydrophilic amino acid residues of actagardine, Glu11 and Ser2, are directed to this pocket. A region of high sequence, similarity with the related lantibiotic mersacidin is located exactly at, the position of the second pocket (residues 3-12). This suggests that the, second pocket is responsible for the antibiotic mode of action of, actagardine and mersacidin as inhibitors of the murein biosynthesis of, gram-positive bacteria.
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<StructureSection load='1aj1' size='340' side='right'caption='[[1aj1]]' scene=''>
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== Structural highlights ==
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<table><tr><td colspan='2'>[[1aj1]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Actinoplanes_liguriensis Actinoplanes liguriensis]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1AJ1 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=1AJ1 FirstGlance]. <br>
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</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Solution NMR, 15 models</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=DAL:D-ALANINE'>DAL</scene>, <scene name='pdbligand=DBB:D-ALPHA-AMINOBUTYRIC+ACID'>DBB</scene>, <scene name='pdbligand=PRD_000194:ACTAGARDINE'>PRD_000194</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=1aj1 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1aj1 OCA], [https://pdbe.org/1aj1 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=1aj1 RCSB], [https://www.ebi.ac.uk/pdbsum/1aj1 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=1aj1 ProSAT]</span></td></tr>
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</table>
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== Function ==
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[https://www.uniprot.org/uniprot/LANA_ACTGA LANA_ACTGA] Has potent antibacterial activity against some Gram-positive bacteria (PubMed:19400806). Has good antistreptococcal activity. Inhibits cell wall biosynthesis by binding to lipid II and blocking transglycosylation (PubMed:9449277).<ref>PMID:19400806</ref> <ref>PMID:9449277</ref>
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<div style="background-color:#fffaf0;">
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== Publication Abstract from PubMed ==
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The three-dimensional solution structure of the lantibiotic actagardine was determined at high resolution by homonuclear and heteronuclear two-dimensional and three-dimensional NMR spectroscopy in [2H3]acetonitrile/H2O (7:3). 133 non-trivial distance and 22 torsional-angle constraints were derived from the NMR data. An ensemble of 15 low-energy structures was calculated by distance geometry followed by an iterative relaxation-matrix-refinement procedure. The rmsd of the backbone coordinates with respect to the average structure was 17 pm. The two distinct thioether ring systems 1-6 and 7-19 were even better defined, with backbone rmsd of 10 pm and 14 pm, respectively. Actagardine shows a rigid compact globular shape based on the constraining bridging pattern, which is composed of an N-terminal lanthionine ring from residues 1-6 and three intertwined C-terminal methyllanthionine rings comprising residues 7-12, 9-17 and 14-19. In addition, this C-terminal ring system is stabilised by a short antiparallel beta sheet. A feature of the actagardine structure is the presence of two putative binding pockets. A pocket is generated by the covalent constraints of the C-terminal thioether ring system. The rim of this pocket is built up by a loop structure comprising residues 12-19, whose backbone amide protons are all directed to the centre of the pocket. The second pocket is formed by an L-shaped orientation of the N-terminal and C-terminal thioether ring systems. The only two hydrophilic amino acid residues of actagardine, Glu11 and Ser2, are directed to this pocket. A region of high sequence similarity with the related lantibiotic mersacidin is located exactly at the position of the second pocket (residues 3-12). This suggests that the second pocket is responsible for the antibiotic mode of action of actagardine and mersacidin as inhibitors of the murein biosynthesis of gram-positive bacteria.
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==About this Structure==
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The three-dimensional solution structure of the lantibiotic murein-biosynthesis-inhibitor actagardine determined by NMR.,Zimmermann N, Jung G Eur J Biochem. 1997 Jun 15;246(3):809-19. PMID:9219543<ref>PMID:9219543</ref>
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1AJ1 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Actinoplanes_liguriae_and_actinoplanes_garbadinensis Actinoplanes liguriae and actinoplanes garbadinensis]. Structure known Active Site: MER. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1AJ1 OCA].
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==Reference==
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From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
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The three-dimensional solution structure of the lantibiotic murein-biosynthesis-inhibitor actagardine determined by NMR., Zimmermann N, Jung G, Eur J Biochem. 1997 Jun 15;246(3):809-19. PMID:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=9219543 9219543]
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</div>
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[[Category: Actinoplanes liguriae and actinoplanes garbadinensis]]
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<div class="pdbe-citations 1aj1" style="background-color:#fffaf0;"></div>
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[[Category: Single protein]]
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== References ==
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[[Category: Jung, G.]]
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<references/>
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[[Category: Zimmermann, N.]]
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__TOC__
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[[Category: glycosyltransferase]]
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</StructureSection>
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[[Category: lantibiotic]]
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[[Category: Actinoplanes liguriensis]]
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[[Category: murein biosynthesis inhibitor]]
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[[Category: Large Structures]]
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[[Category: peptide antibiotic]]
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[[Category: Jung G]]
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[[Category: transglycosylase inhibitor]]
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[[Category: Zimmermann N]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Mon Nov 5 13:33:10 2007''
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Current revision

NMR STRUCTURE OF THE LANTIBIOTIC ACTAGARDINE

PDB ID 1aj1

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