2vg5
From Proteopedia
(Difference between revisions)
Line 1: | Line 1: | ||
- | [[ | + | ==CRYSTAL STRUCTURES OF HIV-1 REVERSE TRANSCRIPTASE COMPLEXES WITH THIOCARBAMATE NON-NUCLEOSIDE INHIBITORS== |
+ | <StructureSection load='2vg5' size='340' side='right' caption='[[2vg5]], [[Resolution|resolution]] 2.80Å' scene=''> | ||
+ | == Structural highlights == | ||
+ | <table><tr><td colspan='2'>[[2vg5]] is a 2 chain structure with sequence from [http://en.wikipedia.org/wiki/Human_immunodeficiency_virus_1 Human immunodeficiency virus 1]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2VG5 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2VG5 FirstGlance]. <br> | ||
+ | </td></tr><tr><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=NNC:O-[2-(1,3-DIOXO-1,3-DIHYDRO-2H-ISOINDOL-2-YL)ETHYL]+(4-CHLOROPHENYL)THIOCARBAMATE'>NNC</scene><br> | ||
+ | <tr><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[1ajv|1ajv]], [[1hps|1hps]], [[1d4j|1d4j]], [[1r0a|1r0a]], [[1hpz|1hpz]], [[1hqe|1hqe]], [[1qe1|1qe1]], [[1ajx|1ajx]], [[1tvr|1tvr]], [[1ebk|1ebk]], [[1s6p|1s6p]], [[1bqm|1bqm]], [[1ikv|1ikv]], [[1w5y|1w5y]], [[1hos|1hos]], [[1s6q|1s6q]], [[1ikw|1ikw]], [[3hvt|3hvt]], [[1ec1|1ec1]], [[1ec0|1ec0]], [[1t05|1t05]], [[1rvq|1rvq]], [[1d4i|1d4i]], [[1meu|1meu]], [[2be2|2be2]], [[1s9g|1s9g]], [[1hnv|1hnv]], [[1rvr|1rvr]], [[1ikx|1ikx]], [[1w5w|1w5w]], [[1iky|1iky]], [[1qmc|1qmc]], [[1n6q|1n6q]], [[1rvn|1rvn]], [[1d4h|1d4h]], [[1hbv|1hbv]], [[1rtd|1rtd]], [[1htf|1htf]], [[1ec2|1ec2]], [[1w5v|1w5v]], [[2hmi|2hmi]], [[2uy0|2uy0]], [[1sv5|1sv5]], [[1hmv|1hmv]], [[1s9e|1s9e]], [[1n5y|1n5y]], [[1dlo|1dlo]], [[1heg|1heg]], [[1rvp|1rvp]], [[1rvl|1rvl]], [[1dw6|1dw6]], [[1eet|1eet]], [[2b6a|2b6a]], [[1w5x|1w5x]], [[1hvu|1hvu]], [[1htg|1htg]], [[1ebw|1ebw]], [[2ban|2ban]], [[1rdh|1rdh]], [[1eby|1eby]], [[1j5o|1j5o]], [[1hvp|1hvp]], [[1rvo|1rvo]], [[1mes|1mes]], [[1ec3|1ec3]], [[1hih|1hih]], [[1hef|1hef]], [[1hni|1hni]], [[1tv6|1tv6]], [[2b5j|2b5j]], [[1ebz|1ebz]], [[1hys|1hys]], [[1met|1met]], [[1t03|1t03]], [[1axa|1axa]], [[1mer|1mer]], [[3tlh|3tlh]], [[2uxz|2uxz]], [[1sbg|1sbg]], [[1hvk|1hvk]], [[1bqn|1bqn]], [[1suq|1suq]], [[1uwb|1uwb]], [[1rvm|1rvm]], [[1hte|1hte]], [[1hrh|1hrh]], [[1hqu|1hqu]], [[2vg6|2vg6]], [[2vg7|2vg7]]</td></tr> | ||
+ | <tr><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2vg5 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2vg5 OCA], [http://www.rcsb.org/pdb/explore.do?structureId=2vg5 RCSB], [http://www.ebi.ac.uk/pdbsum/2vg5 PDBsum]</span></td></tr> | ||
+ | <table> | ||
+ | == Evolutionary Conservation == | ||
+ | [[Image:Consurf_key_small.gif|200px|right]] | ||
+ | Check<jmol> | ||
+ | <jmolCheckbox> | ||
+ | <scriptWhenChecked>select protein; define ~consurf_to_do selected; consurf_initial_scene = true; script "/wiki/ConSurf/vg/2vg5_consurf.spt"</scriptWhenChecked> | ||
+ | <scriptWhenUnchecked>script /wiki/extensions/Proteopedia/spt/initialview01.spt</scriptWhenUnchecked> | ||
+ | <text>to colour the structure by Evolutionary Conservation</text> | ||
+ | </jmolCheckbox> | ||
+ | </jmol>, as determined by [http://consurfdb.tau.ac.il/ ConSurfDB]. You may read the [[Conservation%2C_Evolutionary|explanation]] of the method and the full data available from [http://bental.tau.ac.il/new_ConSurfDB/chain_selection.php?pdb_ID=2ata ConSurf]. | ||
+ | <div style="clear:both"></div> | ||
+ | <div style="background-color:#fffaf0;"> | ||
+ | == Publication Abstract from PubMed == | ||
+ | O-Phthalimidoethyl-N-arylthiocarbamates (TCs) have been recently identified as a new class of potent HIV-1 reverse transcriptase (RT) non-nucleoside inhibitors (NNRTIs), by means of computer-aided drug design techniques [Ranise A. Spallarossa, S. Cesarini, F. Bondavalli, S. Schenone, O. Bruno, G. Menozzi, P. Fossa, L. Mosti, M. La Colla, et al., Structure-based design, parallel synthesis, structure-activity relationship, and molecular modeling studies of thiocarbamates, new potent non-nucleoside HIV-1 reverse transcriptase inhibitor isosteres of phenethylthiazolylthiourea derivatives, J. Med. Chem. 48 (2005) 3858-3873]. To elucidate the atomic details of RT/TC interaction and validate an earlier TC docking model, the structures of three RT/TC complexes were determined at 2.8-3.0A resolution by X-ray crystallography. The conformations adopted by the enzyme-bound TCs were analyzed and compared with those of bioisosterically related NNRTIs. | ||
- | + | Crystal structures of HIV-1 reverse transcriptase complexes with thiocarbamate non-nucleoside inhibitors.,Spallarossa A, Cesarini S, Ranise A, Ponassi M, Unge T, Bolognesi M Biochem Biophys Res Commun. 2008 Jan 25;365(4):764-70. Epub 2007 Nov 21. PMID:18035053<ref>PMID:18035053</ref> | |
- | + | From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br> | |
- | + | </div> | |
- | + | ||
- | + | ||
- | + | ||
- | + | ||
==See Also== | ==See Also== | ||
*[[Reverse transcriptase|Reverse transcriptase]] | *[[Reverse transcriptase|Reverse transcriptase]] | ||
- | + | == References == | |
- | == | + | <references/> |
- | < | + | __TOC__ |
+ | </StructureSection> | ||
[[Category: Human immunodeficiency virus 1]] | [[Category: Human immunodeficiency virus 1]] | ||
[[Category: Bolognesi, M.]] | [[Category: Bolognesi, M.]] |
Revision as of 06:16, 29 September 2014
CRYSTAL STRUCTURES OF HIV-1 REVERSE TRANSCRIPTASE COMPLEXES WITH THIOCARBAMATE NON-NUCLEOSIDE INHIBITORS
|
Categories: Human immunodeficiency virus 1 | Bolognesi, M. | Cesarini, S. | Ponassi, M. | Ranise, A. | Spallarossa, A. | Unge, T. | Aid | Aspartyl protease | Capsid maturation | Core protein | Dna integration | Dna recombination | Dna-directed dna polymerase | Endonuclease | Hiv-1 | Hydrolase | Lipoprotein | Magnesium | Membrane | Metal-binding | Multifunctional enzyme | Myristate | Non-nucleoside reverse transcriptase inhibitor | Nuclease | Nucleotidyltransferase | Nucleus | Phosphorylation | Protease | Reverse transcriptase | Rna-binding | Rna-directed dna polymerase | Thiocarbamate | Transferase | Viral nucleoprotein | Virion | Zinc-finger