1aj1

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[[Image:1aj1.gif|left|200px]]
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{{Structure
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|PDB= 1aj1 |SIZE=350|CAPTION= <scene name='initialview01'>1aj1</scene>
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|SITE= <scene name='pdbsite=MER:Homology+Region+To+Mersacidin'>MER</scene>
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|LIGAND= <scene name='pdbligand=ABA:ALPHA-AMINOBUTYRIC+ACID'>ABA</scene>, <scene name='pdbligand=DAL:D-ALANINE'>DAL</scene>
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|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1aj1 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1aj1 OCA], [http://www.ebi.ac.uk/pdbsum/1aj1 PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=1aj1 RCSB]</span>
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'''NMR STRUCTURE OF THE LANTIBIOTIC ACTAGARDINE, 15 STRUCTURES'''
'''NMR STRUCTURE OF THE LANTIBIOTIC ACTAGARDINE, 15 STRUCTURES'''
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[[Category: Jung, G.]]
[[Category: Jung, G.]]
[[Category: Zimmermann, N.]]
[[Category: Zimmermann, N.]]
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[[Category: glycosyltransferase]]
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[[Category: Glycosyltransferase]]
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[[Category: lantibiotic]]
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[[Category: Lantibiotic]]
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[[Category: murein biosynthesis inhibitor]]
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[[Category: Murein biosynthesis inhibitor]]
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[[Category: peptide antibiotic]]
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[[Category: Peptide antibiotic]]
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[[Category: transglycosylase inhibitor]]
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[[Category: Transglycosylase inhibitor]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Fri May 2 10:19:59 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Mar 30 18:41:17 2008''
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Revision as of 07:20, 2 May 2008

Template:STRUCTURE 1aj1

NMR STRUCTURE OF THE LANTIBIOTIC ACTAGARDINE, 15 STRUCTURES


Overview

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.

About this Structure

1AJ1 is a Single protein structure of sequence from Actinoplanes liguriae and actinoplanes garbadinensis. Full crystallographic information is available from OCA.

Reference

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 Page seeded by OCA on Fri May 2 10:19:59 2008

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