1wyi

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(New page: 200px <!-- The line below this paragraph, containing "STRUCTURE_1wyi", creates the "Structure Box" on the page. You may change the PDB parameter (which sets the PD...)
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[[Image:1wyi.png|left|200px]]
 
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==human triosephosphate isomerase of new crystal form==
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The line below this paragraph, containing "STRUCTURE_1wyi", creates the "Structure Box" on the page.
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<StructureSection load='1wyi' size='340' side='right'caption='[[1wyi]], [[Resolution|resolution]] 2.20&Aring;' scene=''>
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== Structural highlights ==
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or the SCENE parameter (which sets the initial scene displayed when the page is loaded),
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<table><tr><td colspan='2'>[[1wyi]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1WYI OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=1WYI 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]] 2.2&#8491;</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=1wyi FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1wyi OCA], [https://pdbe.org/1wyi PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=1wyi RCSB], [https://www.ebi.ac.uk/pdbsum/1wyi PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=1wyi ProSAT]</span></td></tr>
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{{STRUCTURE_1wyi| PDB=1wyi | SCENE= }}
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</table>
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== Disease ==
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===human triosephosphate isomerase of new crystal form===
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[https://www.uniprot.org/uniprot/TPIS_HUMAN TPIS_HUMAN] Defects in TPI1 are the cause of triosephosphate isomerase deficiency (TPI deficiency) [MIM:[https://omim.org/entry/190450 190450]. TPI deficiency is an autosomal recessive disorder. It is the most severe clinical disorder of glycolysis. It is associated with neonatal jaundice, chronic hemolytic anemia, progressive neuromuscular dysfunction, cardiomyopathy and increased susceptibility to infection.
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== Function ==
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[https://www.uniprot.org/uniprot/TPIS_HUMAN TPIS_HUMAN]
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== Evolutionary Conservation ==
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[[Image:Consurf_key_small.gif|200px|right]]
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(as it appears on PubMed at http://www.pubmed.gov), where 16511037 is the PubMed ID number.
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Check<jmol>
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{{ABSTRACT_PUBMED_16511037}}
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<scriptWhenChecked>; select protein; define ~consurf_to_do selected; consurf_initial_scene = true; script "/wiki/ConSurf/wy/1wyi_consurf.spt"</scriptWhenChecked>
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<scriptWhenUnchecked>script /wiki/extensions/Proteopedia/spt/initialview01.spt</scriptWhenUnchecked>
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==About this Structure==
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<text>to colour the structure by Evolutionary Conservation</text>
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[[1wyi]] is a 2 chain structure of [[Triose Phosphate Isomerase]] with sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1WYI OCA].
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</jmolCheckbox>
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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=1wyi ConSurf].
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<div style="clear:both"></div>
==See Also==
==See Also==
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*[[Triose Phosphate Isomerase|Triose Phosphate Isomerase]]
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*[[Triose phosphate isomerase 3D structures|Triose phosphate isomerase 3D structures]]
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__TOC__
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==Reference==
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</StructureSection>
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<ref group="xtra">PMID:016511037</ref><references group="xtra"/>
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[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
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[[Category: Triose-phosphate isomerase]]
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[[Category: Large Structures]]
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[[Category: Kinoshita, T.]]
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[[Category: Kinoshita T]]
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[[Category: Isomerase]]
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[[Category: Microgravity]]
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[[Category: New crystal form]]
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[[Category: Tim]]
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Current revision

human triosephosphate isomerase of new crystal form

PDB ID 1wyi

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