2v0c: Difference between revisions

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[[Image:2v0c.jpg|left|200px]]
[[Image:2v0c.jpg|left|200px]]


{{Structure
<!--
|PDB= 2v0c |SIZE=350|CAPTION= <scene name='initialview01'>2v0c</scene>, resolution 1.85&Aring;
The line below this paragraph, containing "STRUCTURE_2v0c", creates the "Structure Box" on the page.
|SITE= <scene name='pdbsite=AC1:Binding+Site+For+Residue+LEU+A+1501'>AC1</scene>, <scene name='pdbsite=AC2:Binding+Site+For+Residue+Lms+A+1814'>AC2</scene>, <scene name='pdbsite=AC3:Binding+Site+For+Residue+Zn+A+1815'>AC3</scene>, <scene name='pdbsite=AC4:Binding+Site+For+Residue+Zn+A+1816'>AC4</scene>, <scene name='pdbsite=AC5:Binding+Site+For+Residue+Anz+A+1817'>AC5</scene>, <scene name='pdbsite=AC6:Binding+Site+For+Residue+So4+A+1818'>AC6</scene>, <scene name='pdbsite=AC7:Binding+Site+For+Residue+So4+A+1819'>AC7</scene>, <scene name='pdbsite=AC8:Binding+Site+For+Residue+So4+A+1820'>AC8</scene>, <scene name='pdbsite=AC9:Binding+Site+For+Residue+So4+A+1821'>AC9</scene> and <scene name='pdbsite=BC1:Binding+Site+For+Residue+So4+A+1822'>BC1</scene>
You may change the PDB parameter (which sets the PDB file loaded into the applet)  
|LIGAND= <scene name='pdbligand=ANZ:[(6-AMINO-9H-PURIN-9-YL)-[5-FLUORO-1,3-DIHYDRO-1-HYDROXY-2,1-BENZOXABOROLE]-4&#39;YL]METHYL+DIHYDROGEN+PHOSPHATE'>ANZ</scene>, <scene name='pdbligand=LEU:LEUCINE'>LEU</scene>, <scene name='pdbligand=LMS:[(2R,3S,4R,5R)-5-(6-AMINO-9H-PURIN-9-YL)-3,4-DIHYDROXYTETRAHYDRO-2-FURANYL]METHYL+SULFAMATE'>LMS</scene>, <scene name='pdbligand=SO4:SULFATE+ION'>SO4</scene>, <scene name='pdbligand=ZN:ZINC+ION'>ZN</scene>
or the SCENE parameter (which sets the initial scene displayed when the page is loaded),
|ACTIVITY=  
or leave the SCENE parameter empty for the default display.
|GENE=  
-->
|DOMAIN=<span class='plainlinks'>[http://www.ncbi.nlm.nih.gov/Structure/cdd/cddsrv.cgi?uid=pfam08264 Anticodon_1], [http://www.ncbi.nlm.nih.gov/Structure/cdd/cddsrv.cgi?uid=PRK00390 leuS], [http://www.ncbi.nlm.nih.gov/Structure/cdd/cddsrv.cgi?uid=cd00812 LeuRS_core]</span>
{{STRUCTURE_2v0c| PDB=2v0c  | SCENE= }}  
|RELATEDENTRY=[[1h3n|1H3N]], [[1obc|1OBC]], [[1obh|1OBH]], [[2bte|2BTE]], [[2byt|2BYT]]
|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2v0c FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2v0c OCA], [http://www.ebi.ac.uk/pdbsum/2v0c PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=2v0c RCSB]</span>
}}


'''LEUCYL-TRNA SYNTHETASE FROM THERMUS THERMOPHILUS COMPLEXED WITH A SULPHAMOYL ANALOGUE OF LEUCYL-ADENYLATE IN THE SYNTHETIC SITE AND AN ADDUCT OF AMP WITH 5-FLUORO-1,3-DIHYDRO-1-HYDROXY-2,1-BENZOXABOROLE (AN2690) IN THE EDITING SITE'''
'''LEUCYL-TRNA SYNTHETASE FROM THERMUS THERMOPHILUS COMPLEXED WITH A SULPHAMOYL ANALOGUE OF LEUCYL-ADENYLATE IN THE SYNTHETIC SITE AND AN ADDUCT OF AMP WITH 5-FLUORO-1,3-DIHYDRO-1-HYDROXY-2,1-BENZOXABOROLE (AN2690) IN THE EDITING SITE'''
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[[Category: Zhang, Y.]]
[[Category: Zhang, Y.]]
[[Category: Zhou, H.]]
[[Category: Zhou, H.]]
[[Category: aminoacyl-trna synthetase]]
[[Category: Aminoacyl-trna synthetase]]
[[Category: atp + l-leucine + trna (leu) gives amp + ppi + l-leucyl-trna(leu)]]
[[Category: Atp-binding]]
[[Category: atp-binding]]
[[Category: Clss i aminoacyl-trna synthetase]]
[[Category: clss i aminoacyl-trna synthetase]]
[[Category: Ligase]]
[[Category: ligase]]
[[Category: Metal-binding]]
[[Category: metal-binding]]
[[Category: Nucleotide-binding]]
[[Category: nucleotide-binding]]
[[Category: Protein biosynthesis]]
[[Category: protein biosynthesis]]
[[Category: Zinc]]
[[Category: zinc]]
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun May 4 17:57:11 2008''
 
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Apr 2 11:32:12 2008''

Revision as of 17:57, 4 May 2008

File:2v0c.jpg

Template:STRUCTURE 2v0c

LEUCYL-TRNA SYNTHETASE FROM THERMUS THERMOPHILUS COMPLEXED WITH A SULPHAMOYL ANALOGUE OF LEUCYL-ADENYLATE IN THE SYNTHETIC SITE AND AN ADDUCT OF AMP WITH 5-FLUORO-1,3-DIHYDRO-1-HYDROXY-2,1-BENZOXABOROLE (AN2690) IN THE EDITING SITE


OverviewOverview

Aminoacyl-transfer RNA (tRNA) synthetases, which catalyze the attachment of the correct amino acid to its corresponding tRNA during translation of the genetic code, are proven antimicrobial drug targets. We show that the broad-spectrum antifungal 5-fluoro-1,3-dihydro-1-hydroxy-2,1-benzoxaborole (AN2690), in development for the treatment of onychomycosis, inhibits yeast cytoplasmic leucyl-tRNA synthetase by formation of a stable tRNA(Leu)-AN2690 adduct in the editing site of the enzyme. Adduct formation is mediated through the boron atom of AN2690 and the 2'- and 3'-oxygen atoms of tRNA's3'-terminal adenosine. The trapping of enzyme-bound tRNA(Leu) in the editing site prevents catalytic turnover, thus inhibiting synthesis of leucyl-tRNA(Leu) and consequentially blocking protein synthesis. This result establishes the editing site as a bona fide target for aminoacyl-tRNA synthetase inhibitors.

About this StructureAbout this Structure

2V0C is a Single protein structure of sequence from Thermus thermophilus. Full crystallographic information is available from OCA.

ReferenceReference

An antifungal agent inhibits an aminoacyl-tRNA synthetase by trapping tRNA in the editing site., Rock FL, Mao W, Yaremchuk A, Tukalo M, Crepin T, Zhou H, Zhang YK, Hernandez V, Akama T, Baker SJ, Plattner JJ, Shapiro L, Martinis SA, Benkovic SJ, Cusack S, Alley MR, Science. 2007 Jun 22;316(5832):1759-61. PMID:17588934 Page seeded by OCA on Sun May 4 17:57:11 2008

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