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1ghg

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(New page: 200px<br /><applet load="1ghg" size="450" color="white" frame="true" align="right" spinBox="true" caption="1ghg, resolution 0.98&Aring;" /> '''CRYSTAL STRUCTURE OF...)
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[[Image:1ghg.gif|left|200px]]<br /><applet load="1ghg" size="450" color="white" frame="true" align="right" spinBox="true"
 
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caption="1ghg, resolution 0.98&Aring;" />
 
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'''CRYSTAL STRUCTURE OF VANCOMYCIN AGLYCON'''<br />
 
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==Overview==
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==CRYSTAL STRUCTURE OF VANCOMYCIN AGLYCON==
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The sugar residues of the glycopeptide antibiotic vancomycin contribute to, the cooperativity of ligand binding, thereby increasing ligand affinity, and enhancing antimicrobial activity. To assess the structural basis for, these effects, we determined a 0.98 A X-ray crystal structure of the, vancomycin aglycon and compared it to structures of several intact, vancomycin:ligand complexes. The crystal structure reveals that the, aglycon binds acetate anions and forms back-to-back dimeric complexes in a, manner similar to that of intact vancomycin. However, the four independent, copies of the aglycon in each asymmetric unit of the crystal exhibit a, high degree of conformational heterogeneity. These results suggest that, the sugar residues, in addition to enlarging and strengthening the dimer, interface, provide steric constraints that limit the vancomycin molecule, to a relatively small number of productive conformations.
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<StructureSection load='1ghg' size='340' side='right'caption='[[1ghg]], [[Resolution|resolution]] 0.98&Aring;' scene=''>
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== Structural highlights ==
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<table><tr><td colspan='2'>[[1ghg]] is a 4 chain structure with sequence from [https://en.wikipedia.org/wiki/Amycolatopsis_orientalis Amycolatopsis orientalis]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1GHG OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=1GHG 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">X-ray diffraction, [[Resolution|Resolution]] 0.98&#8491;</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=3FG:(2S)-AMINO(3,5-DIHYDROXYPHENYL)ETHANOIC+ACID'>3FG</scene>, <scene name='pdbligand=ACY:ACETIC+ACID'>ACY</scene>, <scene name='pdbligand=DMS:DIMETHYL+SULFOXIDE'>DMS</scene>, <scene name='pdbligand=GHP:(2R)-AMINO(4-HYDROXYPHENYL)ETHANOIC+ACID'>GHP</scene>, <scene name='pdbligand=MLU:N-METHYL-D-LEUCINE'>MLU</scene>, <scene name='pdbligand=OMY:(BETAR)-3-CHLORO-BETA-HYDROXY-L-TYROSINE'>OMY</scene>, <scene name='pdbligand=OMZ:(BETAR)-3-CHLORO-BETA-HYDROXY-D-TYROSINE'>OMZ</scene>, <scene name='pdbligand=PRD_000206:VANCOMYCIN+AGLYCON'>PRD_000206</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=1ghg FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1ghg OCA], [https://pdbe.org/1ghg PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=1ghg RCSB], [https://www.ebi.ac.uk/pdbsum/1ghg PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=1ghg ProSAT]</span></td></tr>
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</table>
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<div style="background-color:#fffaf0;">
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== Publication Abstract from PubMed ==
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The sugar residues of the glycopeptide antibiotic vancomycin contribute to the cooperativity of ligand binding, thereby increasing ligand affinity and enhancing antimicrobial activity. To assess the structural basis for these effects, we determined a 0.98 A X-ray crystal structure of the vancomycin aglycon and compared it to structures of several intact vancomycin:ligand complexes. The crystal structure reveals that the aglycon binds acetate anions and forms back-to-back dimeric complexes in a manner similar to that of intact vancomycin. However, the four independent copies of the aglycon in each asymmetric unit of the crystal exhibit a high degree of conformational heterogeneity. These results suggest that the sugar residues, in addition to enlarging and strengthening the dimer interface, provide steric constraints that limit the vancomycin molecule to a relatively small number of productive conformations.
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==About this Structure==
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The role of sugar residues in molecular recognition by vancomycin.,Kaplan J, Korty BD, Axelsen PH, Loll PJ J Med Chem. 2001 May 24;44(11):1837-40. PMID:11356118<ref>PMID:11356118</ref>
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1GHG is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/ ] with VAG, DMS and ACY as [http://en.wikipedia.org/wiki/ligands ligands]. Full crystallographic information is available from [http://ispc.weizmann.ac.il/oca-bin/ocashort?id=1GHG 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 role of sugar residues in molecular recognition by vancomycin., Kaplan J, Korty BD, Axelsen PH, Loll PJ, J Med Chem. 2001 May 24;44(11):1837-40. PMID:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=11356118 11356118]
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</div>
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[[Category: Protein complex]]
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<div class="pdbe-citations 1ghg" style="background-color:#fffaf0;"></div>
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[[Category: Axelsen, P.H.]]
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== References ==
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[[Category: Kaplan, J.]]
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<references/>
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[[Category: Korty, B.D.]]
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__TOC__
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[[Category: Loll, P.J.]]
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</StructureSection>
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[[Category: ACY]]
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[[Category: Amycolatopsis orientalis]]
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[[Category: DMS]]
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[[Category: Large Structures]]
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[[Category: VAG]]
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[[Category: Axelsen PH]]
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[[Category: aglycon]]
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[[Category: Kaplan J]]
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[[Category: glycopeptide antibiotic]]
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[[Category: Korty BD]]
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[[Category: Loll PJ]]
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''Page seeded by [http://ispc.weizmann.ac.il/oca OCA ] on Sun Nov 25 01:20:30 2007''
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Current revision

CRYSTAL STRUCTURE OF VANCOMYCIN AGLYCON

PDB ID 1ghg

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