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1ald

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{{Seed}}
 
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[[Image:1ald.png|left|200px]]
 
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==ACTIVITY AND SPECIFICITY OF HUMAN ALDOLASES==
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The line below this paragraph, containing "STRUCTURE_1ald", creates the "Structure Box" on the page.
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<StructureSection load='1ald' size='340' side='right'caption='[[1ald]], [[Resolution|resolution]] 2.00&Aring;' scene=''>
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You may change the PDB parameter (which sets the PDB file loaded into the applet)
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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'>[[1ald]] is a 1 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=1ALD OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=1ALD FirstGlance]. <br>
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or leave the SCENE parameter empty for the default display.
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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&#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=1ald FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1ald OCA], [https://pdbe.org/1ald PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=1ald RCSB], [https://www.ebi.ac.uk/pdbsum/1ald PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=1ald ProSAT]</span></td></tr>
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{{STRUCTURE_1ald| PDB=1ald | SCENE= }}
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</table>
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== Disease ==
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[https://www.uniprot.org/uniprot/ALDOA_HUMAN ALDOA_HUMAN] Defects in ALDOA are the cause of glycogen storage disease type 12 (GSD12) [MIM:[https://omim.org/entry/611881 611881]; also known as red cell aldolase deficiency. A metabolic disorder associated with increased hepatic glycogen and hemolytic anemia. It may lead to myopathy with exercise intolerance and rhabdomyolysis.<ref>PMID:14766013</ref> <ref>PMID:2825199</ref> <ref>PMID:2229018</ref> <ref>PMID:8598869</ref> <ref>PMID:14615364</ref>
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== Function ==
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[https://www.uniprot.org/uniprot/ALDOA_HUMAN ALDOA_HUMAN] Plays a key role in glycolysis and gluconeogenesis. In addition, may also function as scaffolding protein (By similarity).
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== Evolutionary Conservation ==
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[[Image:Consurf_key_small.gif|200px|right]]
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Check<jmol>
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<jmolCheckbox>
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<scriptWhenChecked>; select protein; define ~consurf_to_do selected; consurf_initial_scene = true; script "/wiki/ConSurf/al/1ald_consurf.spt"</scriptWhenChecked>
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<scriptWhenUnchecked>script /wiki/extensions/Proteopedia/spt/initialview01.spt</scriptWhenUnchecked>
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<text>to colour the structure by Evolutionary Conservation</text>
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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=1ald ConSurf].
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<div style="clear:both"></div>
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===ACTIVITY AND SPECIFICITY OF HUMAN ALDOLASES===
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==See Also==
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*[[Aldolase 3D structures|Aldolase 3D structures]]
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== References ==
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<references/>
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__TOC__
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(as it appears on PubMed at http://www.pubmed.gov), where 2056525 is the PubMed ID number.
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</StructureSection>
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{{ABSTRACT_PUBMED_2056525}}
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==About this Structure==
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1ALD is a 1 chain structure of 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=1ALD OCA].
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==Reference==
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<ref group="xtra">PMID:2056525</ref><references group="xtra"/>
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[[Category: Fructose-bisphosphate aldolase]]
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[[Category: Homo sapiens]]
[[Category: Homo sapiens]]
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[[Category: Watson, H C.]]
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[[Category: Large Structures]]
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[[Category: Watson HC]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Tue Feb 17 04:40:12 2009''
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Current revision

ACTIVITY AND SPECIFICITY OF HUMAN ALDOLASES

PDB ID 1ald

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