4br1: Difference between revisions

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-{{STRUCTURE_4br1|  PDB=4br1  |  SCENE=  }}
+==Protease-induced heterodimer of human triosephosphate isomerase.==
-===Protease-induced heterodimer of human triosephosphate isomerase.===
+<StructureSection load='4br1' size='340' side='right' caption='[[4br1]], [[Resolution|resolution]] 1.90&Aring;' scene=''>
+== Structural highlights ==
+<table><tr><td colspan='2'>[[4br1]] is a 2 chain structure 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=4BR1 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4BR1 FirstGlance]. <br>
+</td></tr><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>
+<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=4br1 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4br1 OCA], [http://www.rcsb.org/pdb/explore.do?structureId=4br1 RCSB], [http://www.ebi.ac.uk/pdbsum/4br1 PDBsum]</span></td></tr>
+</table>
+== Disease ==
+[[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.
+== Function ==
-==Disease==
-[[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.
-==About this Structure==
+==See Also==
-[[4br1]] is a 2 chain structure 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=4BR1 OCA].
+*[[Triose Phosphate Isomerase|Triose Phosphate Isomerase]]
+__TOC__
+</StructureSection>
 [[Category: Homo sapiens]]
 [[Category: Triose-phosphate isomerase]]
-[[Category: Castillo-Villanueva, A.]]
+[[Category: Castillo-Villanueva, A]]
-[[Category: DeLaMora-DeLaMora, I.]]
+[[Category: DeLaMora-DeLaMora, I]]
-[[Category: Enriquez-Flores, S.]]
+[[Category: Enriquez-Flores, S]]
-[[Category: Garcia-Torres, I.]]
+[[Category: Garcia-Torres, I]]
-[[Category: Gomez-Manzo, S.]]
+[[Category: Gomez-Manzo, S]]
-[[Category: Hernandez-Alcantara, G.]]
+[[Category: Hernandez-Alcantara, G]]
-[[Category: Lopez-Velazquez, G.]]
+[[Category: Lopez-Velazquez, G]]
-[[Category: Marcial-Quino, J.]]
+[[Category: Marcial-Quino, J]]
-[[Category: Mendez, S T.]]
+[[Category: Mendez, S T]]
-[[Category: Mendoza-Hernandez, G.]]
+[[Category: Mendoza-Hernandez, G]]
-[[Category: Oria-Hernandez, J.]]
+[[Category: Oria-Hernandez, J]]
-[[Category: Reyes-Vivas, H.]]
+[[Category: Reyes-Vivas, H]]
-[[Category: Torres-Arroyo, A.]]
+[[Category: Torres-Arroyo, A]]
-[[Category: Torres-Larios, A.]]
+[[Category: Torres-Larios, A]]
 [[Category: Hydrolase]]
 [[Category: Protease degradation]]