4unk - Revision history

OCA at 10:31, 10 January 2024

OCA — Wed, 10 Jan 2024 10:31:12 GMT

←Older revision		Revision as of 10:31, 10 January 2024
Line 4:		Line 4:
	== Structural highlights ==		== Structural highlights ==
	<table><tr><td colspan='2'>[[4unk]] 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=4UNK OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=4UNK FirstGlance]. <br>		<table><tr><td colspan='2'>[[4unk]] 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=4UNK OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=4UNK FirstGlance]. <br>
-	</td></tr><tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=4unk FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4unk OCA], [https://pdbe.org/4unk PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4unk RCSB], [https://www.ebi.ac.uk/pdbsum/4unk PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4unk ProSAT]</span></td></tr>	+	</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models\|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution\|Resolution]] 2Å</td></tr>
		+	<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=4unk FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4unk OCA], [https://pdbe.org/4unk PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4unk RCSB], [https://www.ebi.ac.uk/pdbsum/4unk PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4unk ProSAT]</span></td></tr>
	</table>		</table>
	== Disease ==		== Disease ==

OCA at 07:27, 29 March 2023

OCA — Wed, 29 Mar 2023 07:27:05 GMT

←Older revision		Revision as of 07:27, 29 March 2023
Line 3:		Line 3:
	<StructureSection load='4unk' size='340' side='right'caption='[[4unk]], [[Resolution\|resolution]] 2.00Å' scene=''>		<StructureSection load='4unk' size='340' side='right'caption='[[4unk]], [[Resolution\|resolution]] 2.00Å' scene=''>
	== Structural highlights ==		== Structural highlights ==
-	<table><tr><td colspan='2'>[[4unk]] is a 2 chain structure with sequence from [~~http~~://en.wikipedia.org/wiki/~~Human Human~~]. 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>	+	<table><tr><td colspan='2'>[[4unk]] 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=4UNK OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=4UNK FirstGlance]. <br>
-	</td></tr>~~<tr id='related'><td class="sblockLbl"><b>[[Related_structure\|Related:]]</b></td><td class="sblockDat">[[4unl\|4unl]]</td></tr>~~	+	</td></tr><tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=4unk FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4unk OCA], [https://pdbe.org/4unk PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4unk RCSB], [https://www.ebi.ac.uk/pdbsum/4unk PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4unk ProSAT]</span></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=4unk FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4unk OCA], [~~http~~://pdbe.org/4unk PDBe], [~~http~~://www.rcsb.org/pdb/explore.do?structureId=4unk RCSB], [~~http~~://www.ebi.ac.uk/pdbsum/4unk PDBsum], [~~http~~://prosat.h-its.org/prosat/prosatexe?pdbcode=4unk ProSAT]</span></td></tr>	+
	</table>		</table>
	== Disease ==		== 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.	+	[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.
		+	== Function ==
		+	[https://www.uniprot.org/uniprot/TPIS_HUMAN TPIS_HUMAN]

	==See Also==		==See Also==
-	*[[Triose ~~Phosphate Isomerase~~\|Triose ~~Phosphate Isomerase~~]]	+	*[[Triose phosphate isomerase 3D structures\|Triose phosphate isomerase 3D structures]]
	__TOC__		__TOC__
	</StructureSection>		</StructureSection>
-	[[Category: ~~Human~~]]	+	[[Category: Homo sapiens]]
	[[Category: Large Structures]]		[[Category: Large Structures]]
-	~~[[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: Lopez-Velazquez G]]
-	[[Category: Lopez-Velazquez, G]]	+	[[Category: Marcial-Quino J]]
-	[[Category: Marcial-Quino, J]]	+	[[Category: Mendez ST]]
-	[[Category: Mendez~~, S T~~]]	+	[[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: Deamidation]]~~	+
-	~~[[Category: Isomerase~~]]	+

OCA at 09:21, 21 May 2019

OCA — Tue, 21 May 2019 09:21:43 GMT

←Older revision		Revision as of 09:21, 21 May 2019
Line 1:		Line 1:

	==Crystal structure of human triosephosphate isomerase (mutant N15D)==		==Crystal structure of human triosephosphate isomerase (mutant N15D)==
-	<StructureSection load='4unk' size='340' side='right' caption='[[4unk]], [[Resolution\|resolution]] 2.00Å' scene=''>	+	<StructureSection load='4unk' size='340' side='right'caption='[[4unk]], [[Resolution\|resolution]] 2.00Å' scene=''>
	== Structural highlights ==		== Structural highlights ==
-	<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>	+	<table><tr><td colspan='2'>[[4unk]] is a 2 chain structure with sequence from [http://en.wikipedia.org/wiki/Human Human]. 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>
	</td></tr><tr id='related'><td class="sblockLbl"><b>[[Related_structure\|Related:]]</b></td><td class="sblockDat">[[4unl\|4unl]]</td></tr>		</td></tr><tr id='related'><td class="sblockLbl"><b>[[Related_structure\|Related:]]</b></td><td class="sblockDat">[[4unl\|4unl]]</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='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>
Line 15:		Line 15:
	__TOC__		__TOC__
	</StructureSection>		</StructureSection>
		+	[[Category: Human]]
		+	[[Category: Large Structures]]
	[[Category: Triose-phosphate isomerase]]		[[Category: Triose-phosphate isomerase]]
	[[Category: Castillo-Villanueva, A]]		[[Category: Castillo-Villanueva, A]]

OCA at 11:22, 11 August 2016

OCA — Thu, 11 Aug 2016 11:22:20 GMT

←Older revision		Revision as of 11:22, 11 August 2016
Line 1:		Line 1:
		+
	==Crystal structure of human triosephosphate isomerase (mutant N15D)==		==Crystal structure of human triosephosphate isomerase (mutant N15D)==
	<StructureSection load='4unk' size='340' side='right' caption='[[4unk]], [[Resolution\|resolution]] 2.00Å' scene=''>		<StructureSection load='4unk' size='340' side='right' caption='[[4unk]], [[Resolution\|resolution]] 2.00Å' scene=''>
Line 5:		Line 6:
	</td></tr><tr id='related'><td class="sblockLbl"><b>[[Related_structure\|Related:]]</b></td><td class="sblockDat">[[4unl\|4unl]]</td></tr>		</td></tr><tr id='related'><td class="sblockLbl"><b>[[Related_structure\|Related:]]</b></td><td class="sblockDat">[[4unl\|4unl]]</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='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=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>	+	<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://pdbe.org/4unk PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=4unk RCSB], [http://www.ebi.ac.uk/pdbsum/4unk PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=4unk ProSAT]</span></td></tr>
	</table>		</table>
	== Disease ==		== 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.		[[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.
		+
		+	==See Also==
		+	*[[Triose Phosphate Isomerase\|Triose Phosphate Isomerase]]
	__TOC__		__TOC__
	</StructureSection>		</StructureSection>

OCA at 15:59, 7 February 2015

OCA — Sat, 07 Feb 2015 15:59:59 GMT

←Older revision		Revision as of 15:59, 7 February 2015
Line 1:		Line 1:
-	'''~~Unreleased structure~~'''	+	==Crystal structure of human triosephosphate isomerase (mutant N15D)==
-		+	<StructureSection load='4unk' size='340' side='right' caption='[[4unk]], [[Resolution\|resolution]] 2.00Å' scene=''>
-	~~The entry~~ 4unk is ~~ON HOLD until Paper Publication~~	+	== Structural highlights ==
-		+	<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>
-	~~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~~.	+	</td></tr><tr id='related'><td class="sblockLbl"><b>[[Related_structure\|Related:]]</b></td><td class="sblockDat">[[4unl\|4unl]]</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>
-	~~Description~~: ~~Crystal structure~~ of ~~human~~ triosephosphate isomerase (~~mutant N15D~~)	+	<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>
-	[~~[Category~~: ~~Unreleased Structures]]~~	+	</table>
-	[~~[Category~~: ~~Oria-Hernandez, J~~]]	+	== Disease ==
-	[[Category: ~~Lopez~~-~~Velazquez, G~~]]	+	[[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.
		+	__TOC__
		+	</StructureSection>
		+	[[Category: Triose-phosphate isomerase]]
	[[Category: Castillo-Villanueva, A]]		[[Category: Castillo-Villanueva, A]]
-	[[Category: ~~Reyes~~-~~Vivas, H]]~~	+	[[Category: DeLaMora-DeLaMora, I]]
-	~~[[Category: Delamora-Delamora, I]]~~	+
-	~~[[Category: Mendez, S.T]]~~	+
-	~~[[Category: Gomez-Manzo, S]]~~	+
-	~~[[Category: Garcia-Torres~~, I]]	+
	[[Category: Enriquez-Flores, S]]		[[Category: Enriquez-Flores, S]]
-	[[Category: Torres-~~Larios~~, A]]	+	[[Category: Garcia-Torres, I]]
		+	[[Category: Gomez-Manzo, S]]
		+	[[Category: Lopez-Velazquez, G]]
	[[Category: Marcial-Quino, J]]		[[Category: Marcial-Quino, J]]
		+	[[Category: Mendez, S T]]
		+	[[Category: Oria-Hernandez, J]]
		+	[[Category: Reyes-Vivas, H]]
	[[Category: Torres-Arroyo, A]]		[[Category: Torres-Arroyo, A]]
		+	[[Category: Torres-Larios, A]]
		+	[[Category: Deamidation]]
		+	[[Category: Isomerase]]

OCA at 18:32, 24 December 2014

OCA — Wed, 24 Dec 2014 18:32:38 GMT

←Older revision		Revision as of 18:32, 24 December 2014
Line 6:		Line 6:

	Description: Crystal structure of human triosephosphate isomerase (mutant N15D)		Description: Crystal structure of human triosephosphate isomerase (mutant N15D)
		+	[[Category: Unreleased Structures]]
		+	[[Category: Oria-Hernandez, J]]
		+	[[Category: Lopez-Velazquez, G]]
		+	[[Category: Castillo-Villanueva, A]]
		+	[[Category: Reyes-Vivas, H]]
		+	[[Category: Delamora-Delamora, I]]
		+	[[Category: Mendez, S.T]]
		+	[[Category: Gomez-Manzo, S]]
		+	[[Category: Garcia-Torres, I]]
		+	[[Category: Enriquez-Flores, S]]
		+	[[Category: Torres-Larios, A]]
		+	[[Category: Marcial-Quino, J]]
		+	[[Category: Torres-Arroyo, A]]

OCA: Protected "4unk" [edit=sysop:move=sysop]

OCA — Wed, 04 Jun 2014 05:00:50 GMT

Protected "4unk" [edit=sysop:move=sysop]

←Older revision

Revision as of 05:00, 4 June 2014

OCA: New page: '''Unreleased structure''' The entry 4unk is ON HOLD until Paper Publication Authors: DeLaMora-DeLaMora, I., Torres-Larios, A., Enriquez-Flores, S., Mendez, S.T., Castillo-Villanueva, A...

OCA — Wed, 04 Jun 2014 05:00:49 GMT

New page: '''Unreleased structure''' The entry 4unk is ON HOLD until Paper Publication Authors: DeLaMora-DeLaMora, I., Torres-Larios, A., Enriquez-Flores, S., Mendez, S.T., Castillo-Villanueva, A...

New page

'''Unreleased structure'''

The entry 4unk is ON HOLD until Paper Publication

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.

Description: Crystal structure of human triosephosphate isomerase (mutant N15D)