4unk

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'''Unreleased structure'''
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==Crystal structure of human triosephosphate isomerase (mutant N15D)==
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<StructureSection load='4unk' size='340' side='right' caption='[[4unk]], [[Resolution|resolution]] 2.00&Aring;' scene=''>
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The entry 4unk is ON HOLD until Paper Publication
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== Structural highlights ==
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<table><tr><td colspan='2'>[[4unk]] is a 2 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4UNK OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4UNK FirstGlance]. <br>
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Authors: DeLaMora-DeLaMora, I., Torres-Larios, A., Enriquez-Flores, S., Mendez, S.T., Castillo-Villanueva, A., Gomez-Manzo, S., Lopez-Velazquez, G., Marcial-Quino, J., Torres-Arroyo, A., Garcia-Torres, I., Reyes-Vivas, H., Oria-Hernandez, J.
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</td></tr><tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[4unl|4unl]]</td></tr>
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<tr id='activity'><td class="sblockLbl"><b>Activity:</b></td><td class="sblockDat"><span class='plainlinks'>[http://en.wikipedia.org/wiki/Triose-phosphate_isomerase Triose-phosphate isomerase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=5.3.1.1 5.3.1.1] </span></td></tr>
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Description: Crystal structure of human triosephosphate isomerase (mutant N15D)
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<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4unk FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4unk OCA], [http://www.rcsb.org/pdb/explore.do?structureId=4unk RCSB], [http://www.ebi.ac.uk/pdbsum/4unk PDBsum]</span></td></tr>
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[[Category: Unreleased Structures]]
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</table>
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[[Category: Oria-Hernandez, J]]
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== Disease ==
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[[Category: Lopez-Velazquez, G]]
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[[http://www.uniprot.org/uniprot/TPIS_HUMAN TPIS_HUMAN]] Defects in TPI1 are the cause of triosephosphate isomerase deficiency (TPI deficiency) [MIM:[http://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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__TOC__
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</StructureSection>
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[[Category: Triose-phosphate isomerase]]
[[Category: Castillo-Villanueva, A]]
[[Category: Castillo-Villanueva, A]]
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[[Category: Reyes-Vivas, H]]
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[[Category: DeLaMora-DeLaMora, I]]
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[[Category: Delamora-Delamora, I]]
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[[Category: Mendez, S.T]]
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[[Category: Gomez-Manzo, S]]
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[[Category: Garcia-Torres, I]]
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[[Category: Enriquez-Flores, S]]
[[Category: Enriquez-Flores, S]]
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[[Category: Torres-Larios, A]]
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[[Category: Garcia-Torres, I]]
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[[Category: Gomez-Manzo, S]]
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[[Category: Lopez-Velazquez, G]]
[[Category: Marcial-Quino, J]]
[[Category: Marcial-Quino, J]]
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[[Category: Mendez, S T]]
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[[Category: Oria-Hernandez, J]]
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[[Category: Reyes-Vivas, H]]
[[Category: Torres-Arroyo, A]]
[[Category: Torres-Arroyo, A]]
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[[Category: Torres-Larios, A]]
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[[Category: Deamidation]]
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[[Category: Isomerase]]

Revision as of 15:59, 7 February 2015

Crystal structure of human triosephosphate isomerase (mutant N15D)

4unk, resolution 2.00Å

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