View source for 1ee7


==NMR STRUCTURE OF THE PEPTAIBOL CHRYSOSPERMIN C BOUND TO DPC MICELLES==
<StructureSection load='1ee7' size='340' side='right' caption='[[1ee7]], [[NMR_Ensembles_of_Models | 1 NMR models]]' scene=''>
== Structural highlights ==
<table><tr><td colspan='2'>[[1ee7]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Hypomyces_chrysospermus Hypomyces chrysospermus]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1EE7 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1EE7 FirstGlance]. <br>
</td></tr><tr id='NonStdRes'><td class="sblockLbl"><b>[[Non-Standard_Residue|NonStd Res:]]</b></td><td class="sblockDat"><scene name='pdbligand=ACE:ACETYL+GROUP'>ACE</scene>, <scene name='pdbligand=AIB:ALPHA-AMINOISOBUTYRIC+ACID'>AIB</scene>, <scene name='pdbligand=DIV:D-ISOVALINE'>DIV</scene>, <scene name='pdbligand=TPL:TRYPTOPHANOL'>TPL</scene></td></tr>
<tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[1m24|1m24]], [[1r9u|1r9u]], [[1dlz|1dlz]], [[1ih9|1ih9]], [[1gq0|1gq0]], [[1joh|1joh]], [[1amt|1amt]], [[1ob7|1ob7]], [[1ob6|1ob6]], [[1ob4|1ob4]]</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=1ee7 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1ee7 OCA], [http://pdbe.org/1ee7 PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=1ee7 RCSB], [http://www.ebi.ac.uk/pdbsum/1ee7 PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=1ee7 ProSAT]</span></td></tr>
</table>
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== Publication Abstract from PubMed ==
Chrysospermin C is a 19-residue peptaibol capable of forming transmembrane ion channels in phospholipid bilayers. The conformation of chrysospermin C bound to dodecylphosphocholine micelles has been solved using heteronuclear NMR spectroscopy. Selective 15N-labeling and 13C-labeling of specific alpha-aminoisobutyric acid residues was used to obtain complete stereospecific assignments for all eight alpha-aminoisobutyric acid residues. Structures were calculated using 339 distance constraints and 40 angle constraints obtained from NMR data. The NMR structures superimpose with mean global rmsd values to the mean structure of 0. 27 A (backbone heavy atoms) and 0.42 A (all heavy atoms). Chrysospermin C bound to decylphosphocholine micelles displays two well-defined helices at the N-terminus (residues Phe1-Aib9) and C-terminus (Aib13-Trp-ol19). A slight bend preceding Pro14, i.e. encompassing residues 10-12, results in an angle of approximately 38 degrees between the mean axes of the two helical regions. The bend structure observed for chrysospermin C is compatible with the sequences of all 18 long peptaibols and may represent a common 'active' conformation. The structure of chrysospermin C shows clear hydrophobic and hydrophilic surfaces which would be appropriate for the formation of oligomeric ion channels.

The NMR solution structure of the ion channel peptaibol chrysospermin C bound to dodecylphosphocholine micelles.,Anders R, Ohlenschlager O, Soskic V, Wenschuh H, Heise B, Brown LR Eur J Biochem. 2000 Mar;267(6):1784-94. PMID:10712611<ref>PMID:10712611</ref>

From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
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== References ==
<references/>
__TOC__
</StructureSection>
[[Category: Hypomyces chrysospermus]]
[[Category: Anders, R]]
[[Category: Brown, L R]]
[[Category: Heise, B]]
[[Category: Ohlenschlager, O]]
[[Category: Soskic, V]]
[[Category: Wenschuh, H]]
[[Category: Antibacterial]]
[[Category: Antibiotic]]
[[Category: Antifungal]]
[[Category: Chrysospermin c]]
[[Category: Peptaibol]]