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2isn

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[[Image:2isn.jpg|left|200px]]<br /><applet load="2isn" size="350" color="white" frame="true" align="right" spinBox="true"
 
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caption="2isn, resolution 1.90&Aring;" />
 
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'''Crystal structure of a phosphatase from a pathogenic strain Toxoplasma gondii'''<br />
 
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==About this Structure==
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==Crystal structure of a phosphatase from a pathogenic strain Toxoplasma gondii==
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2ISN is a [http://en.wikipedia.org/wiki/Protein_complex Protein complex] structure of sequences from [http://en.wikipedia.org/wiki/Toxoplasma_gondii Toxoplasma gondii] with <scene name='pdbligand=SO4:'>SO4</scene> and <scene name='pdbligand=PR:'>PR</scene> as [http://en.wikipedia.org/wiki/ligands ligands]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2ISN OCA].
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<StructureSection load='2isn' size='340' side='right'caption='[[2isn]], [[Resolution|resolution]] 1.90&Aring;' scene=''>
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[[Category: Protein complex]]
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== Structural highlights ==
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[[Category: Toxoplasma gondii]]
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<table><tr><td colspan='2'>Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2ISN OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=2ISN FirstGlance]. <br>
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[[Category: Agarwal, R.]]
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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]] 1.9&#8491;</td></tr>
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[[Category: Burley, S K.]]
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<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=MSE:SELENOMETHIONINE'>MSE</scene>, <scene name='pdbligand=PR:PRASEODYMIUM+ION'>PR</scene>, <scene name='pdbligand=SO4:SULFATE+ION'>SO4</scene></td></tr>
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[[Category: NYSGXRC, New York Structural GenomiX Research Consortium.]]
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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=2isn FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2isn OCA], [https://pdbe.org/2isn PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2isn RCSB], [https://www.ebi.ac.uk/pdbsum/2isn PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2isn ProSAT], [https://www.topsan.org/Proteins/NYSGXRC/2isn TOPSAN]</span></td></tr>
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[[Category: Swaminathan, S.]]
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</table>
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[[Category: PR]]
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== Evolutionary Conservation ==
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[[Category: SO4]]
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[[Image:Consurf_key_small.gif|200px|right]]
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[[Category: 8828z]]
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Check<jmol>
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[[Category: new york structural genomix research consortium]]
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<jmolCheckbox>
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[[Category: nysgxrc]]
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<scriptWhenChecked>; select protein; define ~consurf_to_do selected; consurf_initial_scene = true; script "/wiki/ConSurf/is/2isn_consurf.spt"</scriptWhenChecked>
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[[Category: pathogenic strain]]
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<scriptWhenUnchecked>script /wiki/extensions/Proteopedia/spt/initialview03.spt</scriptWhenUnchecked>
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[[Category: phosphatase]]
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<text>to colour the structure by Evolutionary Conservation</text>
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[[Category: praseodymium]]
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</jmolCheckbox>
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[[Category: protein structure initiative]]
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</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/main_output.php?pdb_ID=2isn ConSurf].
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[[Category: psi-2]]
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<div style="clear:both"></div>
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[[Category: structural genomics]]
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<div style="background-color:#fffaf0;">
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[[Category: sulfate]]
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== Publication Abstract from PubMed ==
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The New York SGX Research Center for Structural Genomics (NYSGXRC) of the NIGMS Protein Structure Initiative (PSI) has applied its high-throughput X-ray crystallographic structure determination platform to systematic studies of all human protein phosphatases and protein phosphatases from biomedically-relevant pathogens. To date, the NYSGXRC has determined structures of 21 distinct protein phosphatases: 14 from human, 2 from mouse, 2 from the pathogen Toxoplasma gondii, 1 from Trypanosoma brucei, the parasite responsible for African sleeping sickness, and 2 from the principal mosquito vector of malaria in Africa, Anopheles gambiae. These structures provide insights into both normal and pathophysiologic processes, including transcriptional regulation, regulation of major signaling pathways, neural development, and type 1 diabetes. In conjunction with the contributions of other international structural genomics consortia, these efforts promise to provide an unprecedented database and materials repository for structure-guided experimental and computational discovery of inhibitors for all classes of protein phosphatases.
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 17:55:28 2008''
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Structural genomics of protein phosphatases.,Almo SC, Bonanno JB, Sauder JM, Emtage S, Dilorenzo TP, Malashkevich V, Wasserman SR, Swaminathan S, Eswaramoorthy S, Agarwal R, Kumaran D, Madegowda M, Ragumani S, Patskovsky Y, Alvarado J, Ramagopal UA, Faber-Barata J, Chance MR, Sali A, Fiser A, Zhang ZY, Lawrence DS, Burley SK J Struct Funct Genomics. 2007 Sep;8(2-3):121-40. Epub 2007 Dec 5. PMID:18058037<ref>PMID:18058037</ref>
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From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
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</div>
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<div class="pdbe-citations 2isn" style="background-color:#fffaf0;"></div>
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== References ==
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<references/>
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__TOC__
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</StructureSection>
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[[Category: Large Structures]]
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[[Category: Agarwal R]]
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[[Category: Burley SK]]
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[[Category: Swaminathan S]]

Current revision

Crystal structure of a phosphatase from a pathogenic strain Toxoplasma gondii

PDB ID 2isn

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