2lu7 - Revision history

OCA at 05:52, 15 May 2024

OCA — Wed, 15 May 2024 05:52:10 GMT

←Older revision		Revision as of 05:52, 15 May 2024
Line 4:		Line 4:
	== Structural highlights ==		== Structural highlights ==
	<table><tr><td colspan='2'>[[2lu7]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2LU7 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=2LU7 FirstGlance]. <br>		<table><tr><td colspan='2'>[[2lu7]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2LU7 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=2LU7 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=2lu7 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2lu7 OCA], [https://pdbe.org/2lu7 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2lu7 RCSB], [https://www.ebi.ac.uk/pdbsum/2lu7 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2lu7 ProSAT]</span></td></tr>	+	</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models\|Method:]]</b></td><td class="sblockDat" id="methodDat">Solution NMR</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=2lu7 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2lu7 OCA], [https://pdbe.org/2lu7 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2lu7 RCSB], [https://www.ebi.ac.uk/pdbsum/2lu7 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2lu7 ProSAT]</span></td></tr>
	</table>		</table>
	== Disease ==		== Disease ==

OCA at 13:10, 22 February 2023

OCA — Wed, 22 Feb 2023 13:10:55 GMT

←Older revision		Revision as of 13:10, 22 February 2023
Line 1:		Line 1:

	==Solution NMR Structure of Ig like domain (1277-1357) of Obscurin-like protein 1 from Homo sapiens, Northeast Structural Genomics Consortium (NESG) Target HR8578D==		==Solution NMR Structure of Ig like domain (1277-1357) of Obscurin-like protein 1 from Homo sapiens, Northeast Structural Genomics Consortium (NESG) Target HR8578D==
-	<StructureSection load='2lu7' size='340' side='right'caption='[[2lu7~~]], [[NMR_Ensembles_of_Models \| 20 NMR models~~]]' scene=''>	+	<StructureSection load='2lu7' size='340' side='right'caption='[[2lu7]]' scene=''>
	== Structural highlights ==		== Structural highlights ==
-	<table><tr><td colspan='2'>[[2lu7]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/~~Human Human~~]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2LU7 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=2LU7 FirstGlance]. <br>	+	<table><tr><td colspan='2'>[[2lu7]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2LU7 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=2LU7 FirstGlance]. <br>
-	</td></tr><tr id='gene'><td class="sblockLbl"><b>[[Gene\|Gene:]]</b></td><td class="sblockDat">KIAA0657, OBSL1 ([https://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 HUMAN])</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=2lu7 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2lu7 OCA], [https://pdbe.org/2lu7 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2lu7 RCSB], [https://www.ebi.ac.uk/pdbsum/2lu7 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2lu7 ProSAT]</span></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=2lu7 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2lu7 OCA], [https://pdbe.org/2lu7 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2lu7 RCSB], [https://www.ebi.ac.uk/pdbsum/2lu7 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2lu7 ProSAT]</span></td></tr>	+
	</table>		</table>
	== Disease ==		== Disease ==
-	[[https://www.uniprot.org/uniprot/OBSL1_HUMAN OBSL1_HUMAN]] Defects in OBSL1 are the cause of 3M syndrome type 2 (3M2) [MIM:[https://omim.org/entry/612921 612921]]. An autosomal recessive disorder characterized by severe pre- and postnatal growth retardation, facial dysmorphism, large head circumference, and normal intelligence and endocrine function. Skeletal changes include long slender tubular bones and tall vertebral bodies.<ref>PMID:19481195</ref>	+	[https://www.uniprot.org/uniprot/OBSL1_HUMAN OBSL1_HUMAN] Defects in OBSL1 are the cause of 3M syndrome type 2 (3M2) [MIM:[https://omim.org/entry/612921 612921]. An autosomal recessive disorder characterized by severe pre- and postnatal growth retardation, facial dysmorphism, large head circumference, and normal intelligence and endocrine function. Skeletal changes include long slender tubular bones and tall vertebral bodies.<ref>PMID:19481195</ref>
		+	== Function ==
		+	[https://www.uniprot.org/uniprot/OBSL1_HUMAN OBSL1_HUMAN]

	==See Also==		==See Also==
Line 16:		Line 17:
	__TOC__		__TOC__
	</StructureSection>		</StructureSection>
-	[[Category: ~~Human~~]]	+	[[Category: Homo sapiens]]
	[[Category: Large Structures]]		[[Category: Large Structures]]
-	[[Category: Acton~~, T B~~]]	+	[[Category: Acton TB]]
-	[[Category: Eletsky, A]]	+	[[Category: Eletsky A]]
-	[[Category: Everett~~, J K~~]]	+	[[Category: Everett JK]]
-	[[Category: Janjua, H]]	+	[[Category: Janjua H]]
-	[[Category: Kohan, E]]	+	[[Category: Kohan E]]
-	[[Category: Lee, D]]	+	[[Category: Lee D]]
-	[[Category: Montelione~~, G T]]~~	+	[[Category: Montelione GT]]
-	~~[[Category: Structural genomic~~]]	+	[[Category: Pulavarti S]]
-	[[Category: Pulavarti, S]]	+	[[Category: Satyamoorthy B]]
-	[[Category: Satyamoorthy, B]]	+	[[Category: Sukumaran DK]]
-	[[Category: Sukumaran~~, D K~~]]	+	[[Category: Szyperski T]]
-	[[Category: Szyperski, T]]	+	[[Category: Xiao R]]
-	[[Category: Xiao, R]]	+
-	~~[[Category: Nesg]]~~	+
-	~~[[Category: PSI, Protein structure initiative]]~~	+
-	~~[[Category: Psi-biology]]~~	+
-	~~[[Category: Structural protein~~]]	+

OCA at 10:53, 19 May 2021

OCA — Wed, 19 May 2021 10:53:32 GMT

←Older revision		Revision as of 10:53, 19 May 2021
Line 1:		Line 1:

	==Solution NMR Structure of Ig like domain (1277-1357) of Obscurin-like protein 1 from Homo sapiens, Northeast Structural Genomics Consortium (NESG) Target HR8578D==		==Solution NMR Structure of Ig like domain (1277-1357) of Obscurin-like protein 1 from Homo sapiens, Northeast Structural Genomics Consortium (NESG) Target HR8578D==
-	<StructureSection load='2lu7' size='340' side='right' caption='[[2lu7]], [[NMR_Ensembles_of_Models \| 20 NMR models]]' scene=''>	+	<StructureSection load='2lu7' size='340' side='right'caption='[[2lu7]], [[NMR_Ensembles_of_Models \| 20 NMR models]]' scene=''>
	== Structural highlights ==		== Structural highlights ==
-	<table><tr><td colspan='2'>[[2lu7]] is a 1 chain structure with sequence from [~~http~~://en.wikipedia.org/wiki/Human Human]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2LU7 OCA]. For a <b>guided tour on the structure components</b> use [~~http~~://~~oca~~.~~weizmann.ac.il/oca-docs~~/fgij/fg.htm?mol=2LU7 FirstGlance]. <br>	+	<table><tr><td colspan='2'>[[2lu7]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Human Human]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2LU7 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=2LU7 FirstGlance]. <br>
-	</td></tr><tr id='gene'><td class="sblockLbl"><b>[[Gene\|Gene:]]</b></td><td class="sblockDat">KIAA0657, OBSL1 ([~~http~~://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 HUMAN])</td></tr>	+	</td></tr><tr id='gene'><td class="sblockLbl"><b>[[Gene\|Gene:]]</b></td><td class="sblockDat">KIAA0657, OBSL1 ([https://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 HUMAN])</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=2lu7 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2lu7 OCA], [~~http~~://pdbe.org/2lu7 PDBe], [~~http~~://www.rcsb.org/pdb/explore.do?structureId=2lu7 RCSB], [~~http~~://www.ebi.ac.uk/pdbsum/2lu7 PDBsum], [~~http~~://prosat.h-its.org/prosat/prosatexe?pdbcode=2lu7 ProSAT]</span></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=2lu7 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2lu7 OCA], [https://pdbe.org/2lu7 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2lu7 RCSB], [https://www.ebi.ac.uk/pdbsum/2lu7 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2lu7 ProSAT]</span></td></tr>
	</table>		</table>
	== Disease ==		== Disease ==
-	[[~~http~~://www.uniprot.org/uniprot/OBSL1_HUMAN OBSL1_HUMAN]] Defects in OBSL1 are the cause of 3M syndrome type 2 (3M2) [MIM:[~~http~~://omim.org/entry/612921 612921]]. An autosomal recessive disorder characterized by severe pre- and postnatal growth retardation, facial dysmorphism, large head circumference, and normal intelligence and endocrine function. Skeletal changes include long slender tubular bones and tall vertebral bodies.<ref>PMID:19481195</ref>	+	[[https://www.uniprot.org/uniprot/OBSL1_HUMAN OBSL1_HUMAN]] Defects in OBSL1 are the cause of 3M syndrome type 2 (3M2) [MIM:[https://omim.org/entry/612921 612921]]. An autosomal recessive disorder characterized by severe pre- and postnatal growth retardation, facial dysmorphism, large head circumference, and normal intelligence and endocrine function. Skeletal changes include long slender tubular bones and tall vertebral bodies.<ref>PMID:19481195</ref>
		+
		+	==See Also==
		+	*[[Obscurin\|Obscurin]]
	== References ==		== References ==
	<references/>		<references/>
Line 14:		Line 17:
	</StructureSection>		</StructureSection>
	[[Category: Human]]		[[Category: Human]]
		+	[[Category: Large Structures]]
	[[Category: Acton, T B]]		[[Category: Acton, T B]]
	[[Category: Eletsky, A]]		[[Category: Eletsky, A]]

OCA at 22:40, 9 August 2018

OCA — Thu, 09 Aug 2018 22:40:49 GMT

←Older revision		Revision as of 22:40, 9 August 2018
Line 1:		Line 1:
		+
	==Solution NMR Structure of Ig like domain (1277-1357) of Obscurin-like protein 1 from Homo sapiens, Northeast Structural Genomics Consortium (NESG) Target HR8578D==		==Solution NMR Structure of Ig like domain (1277-1357) of Obscurin-like protein 1 from Homo sapiens, Northeast Structural Genomics Consortium (NESG) Target HR8578D==
	<StructureSection load='2lu7' size='340' side='right' caption='[[2lu7]], [[NMR_Ensembles_of_Models \| 20 NMR models]]' scene=''>		<StructureSection load='2lu7' size='340' side='right' caption='[[2lu7]], [[NMR_Ensembles_of_Models \| 20 NMR models]]' scene=''>
Line 4:		Line 5:
	<table><tr><td colspan='2'>[[2lu7]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Human Human]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2LU7 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2LU7 FirstGlance]. <br>		<table><tr><td colspan='2'>[[2lu7]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Human Human]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2LU7 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2LU7 FirstGlance]. <br>
	</td></tr><tr id='gene'><td class="sblockLbl"><b>[[Gene\|Gene:]]</b></td><td class="sblockDat">KIAA0657, OBSL1 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 HUMAN])</td></tr>		</td></tr><tr id='gene'><td class="sblockLbl"><b>[[Gene\|Gene:]]</b></td><td class="sblockDat">KIAA0657, OBSL1 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 HUMAN])</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=2lu7 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2lu7 OCA], [http://pdbe.org/2lu7 PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=2lu7 RCSB], [http://www.ebi.ac.uk/pdbsum/2lu7 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=2lu7 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2lu7 OCA], [http://pdbe.org/2lu7 PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=2lu7 RCSB], [http://www.ebi.ac.uk/pdbsum/2lu7 PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=2lu7 ProSAT]</span></td></tr>
	</table>		</table>
	== Disease ==		== Disease ==

OCA at 19:59, 10 September 2015

OCA — Thu, 10 Sep 2015 19:59:34 GMT

←Older revision		Revision as of 19:59, 10 September 2015
Line 2:		Line 2:
	<StructureSection load='2lu7' size='340' side='right' caption='[[2lu7]], [[NMR_Ensembles_of_Models \| 20 NMR models]]' scene=''>		<StructureSection load='2lu7' size='340' side='right' caption='[[2lu7]], [[NMR_Ensembles_of_Models \| 20 NMR models]]' scene=''>
	== Structural highlights ==		== Structural highlights ==
-	<table><tr><td colspan='2'>[[2lu7]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/~~Homo_sapiens Homo sapiens~~]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2LU7 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2LU7 FirstGlance]. <br>	+	<table><tr><td colspan='2'>[[2lu7]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Human Human]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2LU7 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2LU7 FirstGlance]. <br>
-	</td></tr><tr id='gene'><td class="sblockLbl"><b>[[Gene\|Gene:]]</b></td><td class="sblockDat">KIAA0657, OBSL1 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 ~~Homo sapiens~~])</td></tr>	+	</td></tr><tr id='gene'><td class="sblockLbl"><b>[[Gene\|Gene:]]</b></td><td class="sblockDat">KIAA0657, OBSL1 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 HUMAN])</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=2lu7 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2lu7 OCA], [http://www.rcsb.org/pdb/explore.do?structureId=2lu7 RCSB], [http://www.ebi.ac.uk/pdbsum/2lu7 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=2lu7 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2lu7 OCA], [http://pdbe.org/2lu7 PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=2lu7 RCSB], [http://www.ebi.ac.uk/pdbsum/2lu7 PDBsum]</span></td></tr>
	</table>		</table>
	== Disease ==		== Disease ==
Line 12:		Line 12:
	__TOC__		__TOC__
	</StructureSection>		</StructureSection>
-	[[Category: ~~Homo sapiens~~]]	+	[[Category: Human]]
	[[Category: Acton, T B]]		[[Category: Acton, T B]]
	[[Category: Eletsky, A]]		[[Category: Eletsky, A]]

OCA at 05:22, 25 December 2014

OCA — Thu, 25 Dec 2014 05:22:32 GMT

←Older revision		Revision as of 05:22, 25 December 2014
Line 8:		Line 8:
	== Disease ==		== Disease ==
	[[http://www.uniprot.org/uniprot/OBSL1_HUMAN OBSL1_HUMAN]] Defects in OBSL1 are the cause of 3M syndrome type 2 (3M2) [MIM:[http://omim.org/entry/612921 612921]]. An autosomal recessive disorder characterized by severe pre- and postnatal growth retardation, facial dysmorphism, large head circumference, and normal intelligence and endocrine function. Skeletal changes include long slender tubular bones and tall vertebral bodies.<ref>PMID:19481195</ref>		[[http://www.uniprot.org/uniprot/OBSL1_HUMAN OBSL1_HUMAN]] Defects in OBSL1 are the cause of 3M syndrome type 2 (3M2) [MIM:[http://omim.org/entry/612921 612921]]. An autosomal recessive disorder characterized by severe pre- and postnatal growth retardation, facial dysmorphism, large head circumference, and normal intelligence and endocrine function. Skeletal changes include long slender tubular bones and tall vertebral bodies.<ref>PMID:19481195</ref>
-	== Function ==
-
	== References ==		== References ==
	<references/>		<references/>

OCA at 11:48, 18 December 2014

OCA — Thu, 18 Dec 2014 11:48:16 GMT

←Older revision		Revision as of 11:48, 18 December 2014
Line 1:		Line 1:
-	~~{{STRUCTURE_2lu7\| PDB=2lu7 \| SCENE= }}~~	+	==Solution NMR Structure of Ig like domain (1277-1357) of Obscurin-like protein 1 from Homo sapiens, Northeast Structural Genomics Consortium (NESG) Target HR8578D==
-	===Solution NMR Structure of Ig like domain (1277-1357) of Obscurin-like protein 1 from Homo sapiens, Northeast Structural Genomics Consortium (NESG) Target HR8578D===	+	<StructureSection load='2lu7' size='340' side='right' caption='[[2lu7]], [[NMR_Ensembles_of_Models \| 20 NMR models]]' scene=''>
		+	== Structural highlights ==
		+	<table><tr><td colspan='2'>[[2lu7]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2LU7 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=2LU7 FirstGlance]. <br>
		+	</td></tr><tr id='gene'><td class="sblockLbl"><b>[[Gene\|Gene:]]</b></td><td class="sblockDat">KIAA0657, OBSL1 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 Homo sapiens])</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=2lu7 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2lu7 OCA], [http://www.rcsb.org/pdb/explore.do?structureId=2lu7 RCSB], [http://www.ebi.ac.uk/pdbsum/2lu7 PDBsum]</span></td></tr>
		+	</table>
		+	== Disease ==
		+	[[http://www.uniprot.org/uniprot/OBSL1_HUMAN OBSL1_HUMAN]] Defects in OBSL1 are the cause of 3M syndrome type 2 (3M2) [MIM:[http://omim.org/entry/612921 612921]]. An autosomal recessive disorder characterized by severe pre- and postnatal growth retardation, facial dysmorphism, large head circumference, and normal intelligence and endocrine function. Skeletal changes include long slender tubular bones and tall vertebral bodies.<ref>PMID:19481195</ref>
		+	== Function ==

-	==~~Disease~~==	+	== References ==
-	[[http://www.uniprot.org/uniprot/OBSL1_HUMAN OBSL1_HUMAN]] Defects in OBSL1 are the cause of 3M syndrome type 2 (3M2) [MIM:[http://omim.org/entry/612921 612921]]. An autosomal recessive disorder characterized by severe pre- and postnatal growth retardation, facial dysmorphism, large head circumference, and normal intelligence and endocrine function. Skeletal changes include long slender tubular bones and tall vertebral bodies.<ref>PMID:19481195</~~ref~~>	+	<references/>
-		+	__TOC__
-	~~==About this Structure==~~	+	</StructureSection>
-	[[2lu7]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2LU7 OCA].	+
-		+
-	~~==Reference==~~	+
-	<~~references group="xtra"/><references~~/>	+
	[[Category: Homo sapiens]]		[[Category: Homo sapiens]]
-	[[Category: Acton, T B.]]	+	[[Category: Acton, T B]]
-	[[Category: Eletsky, A.]]	+	[[Category: Eletsky, A]]
-	[[Category: Everett, J K.]]	+	[[Category: Everett, J K]]
-	[[Category: Janjua, H.]]	+	[[Category: Janjua, H]]
-	[[Category: Kohan, E.]]	+	[[Category: Kohan, E]]
-	[[Category: Lee, D.]]	+	[[Category: Lee, D]]
-	[[Category: Montelione, G T.]]	+	[[Category: Montelione, G T]]
-	[[Category: ~~NESG, Northeast~~ Structural ~~Genomics Consortium.~~]]	+	[[Category: Structural genomic]]
-	[[Category: Pulavarti, S.]]	+	[[Category: Pulavarti, S]]
-	[[Category: Satyamoorthy, B.]]	+	[[Category: Satyamoorthy, B]]
-	[[Category: Sukumaran, D K.]]	+	[[Category: Sukumaran, D K]]
-	[[Category: Szyperski, T.]]	+	[[Category: Szyperski, T]]
-	[[Category: Xiao, R.]]	+	[[Category: Xiao, R]]
	[[Category: Nesg]]		[[Category: Nesg]]
-	[[Category: ~~Northeast structural genomics consortium]]~~	+	[[Category: PSI, Protein structure initiative]]
-	~~[[Category:~~ Protein structure initiative]]	+
	[[Category: Psi-biology]]		[[Category: Psi-biology]]
-	[[Category: Structural genomic]]
	[[Category: Structural protein]]		[[Category: Structural protein]]

OCA at 04:25, 25 March 2013

OCA — Mon, 25 Mar 2013 04:25:57 GMT

←Older revision		Revision as of 04:25, 25 March 2013
Line 1:		Line 1:
-	[[Image:2lu7.jpg\|left\|200px]]
-
	{{STRUCTURE_2lu7\| PDB=2lu7 \| SCENE= }}		{{STRUCTURE_2lu7\| PDB=2lu7 \| SCENE= }}
-
	===Solution NMR Structure of Ig like domain (1277-1357) of Obscurin-like protein 1 from Homo sapiens, Northeast Structural Genomics Consortium (NESG) Target HR8578D===		===Solution NMR Structure of Ig like domain (1277-1357) of Obscurin-like protein 1 from Homo sapiens, Northeast Structural Genomics Consortium (NESG) Target HR8578D===

		+	==Disease==
		+	[[http://www.uniprot.org/uniprot/OBSL1_HUMAN OBSL1_HUMAN]] Defects in OBSL1 are the cause of 3M syndrome type 2 (3M2) [MIM:[http://omim.org/entry/612921 612921]]. An autosomal recessive disorder characterized by severe pre- and postnatal growth retardation, facial dysmorphism, large head circumference, and normal intelligence and endocrine function. Skeletal changes include long slender tubular bones and tall vertebral bodies.<ref>PMID:19481195</ref>

	==About this Structure==		==About this Structure==
	[[2lu7]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2LU7 OCA].		[[2lu7]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2LU7 OCA].
		+
		+	==Reference==
		+	<references group="xtra"/><references/>
	[[Category: Homo sapiens]]		[[Category: Homo sapiens]]
	[[Category: Acton, T B.]]		[[Category: Acton, T B.]]

OCA at 06:00, 22 August 2012

OCA — Wed, 22 Aug 2012 06:00:10 GMT

←Older revision		Revision as of 06:00, 22 August 2012
Line 1:		Line 1:
-	~~'''Unreleased structure'''~~	+	[[Image:2lu7.jpg\|left\|200px]]

-	~~The entry~~ 2lu7 ~~is ON HOLD~~ ~~until Aug 16 2013~~	+	{{STRUCTURE_2lu7\| PDB=2lu7 \| SCENE= }}

-	~~Authors: Pulavarti, S., Eletsky, A., Satyamoorthy, B., Sukumaran, D.K., Lee, D., Kohan, E., Janjua, H., Xiao, R., Acton, T.B., Everett, J.K., Montelione, G.T., Szyperski, T.~~, Northeast Structural Genomics Consortium (NESG)	+	===Solution NMR Structure of Ig like domain (1277-1357) of Obscurin-like protein 1 from Homo sapiens, Northeast Structural Genomics Consortium (NESG) Target HR8578D===

-	~~Description: Solution NMR~~ Structure ~~of Ig like domain (1277-1357) of Obscurin-like protein~~ 1 from Homo sapiens, Northeast Structural Genomics Consortium ~~(NESG) Target HR8578D~~	+
		+	==About this Structure==
		+	[[2lu7]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2LU7 OCA].
		+	[[Category: Homo sapiens]]
		+	[[Category: Acton, T B.]]
		+	[[Category: Eletsky, A.]]
		+	[[Category: Everett, J K.]]
		+	[[Category: Janjua, H.]]
		+	[[Category: Kohan, E.]]
		+	[[Category: Lee, D.]]
		+	[[Category: Montelione, G T.]]
		+	[[Category: NESG, Northeast Structural Genomics Consortium.]]
		+	[[Category: Pulavarti, S.]]
		+	[[Category: Satyamoorthy, B.]]
		+	[[Category: Sukumaran, D K.]]
		+	[[Category: Szyperski, T.]]
		+	[[Category: Xiao, R.]]
		+	[[Category: Nesg]]
		+	[[Category: Northeast structural genomics consortium]]
		+	[[Category: Protein structure initiative]]
		+	[[Category: Psi-biology]]
		+	[[Category: Structural genomic]]
		+	[[Category: Structural protein]]

OCA at 07:00, 4 July 2012

OCA — Wed, 04 Jul 2012 07:00:52 GMT

←Older revision		Revision as of 07:00, 4 July 2012
Line 1:		Line 1:
	'''Unreleased structure'''		'''Unreleased structure'''

-	The entry 2lu7 is ON HOLD	+	The entry 2lu7 is ON HOLD until Aug 16 2013

	Authors: Pulavarti, S., Eletsky, A., Satyamoorthy, B., Sukumaran, D.K., Lee, D., Kohan, E., Janjua, H., Xiao, R., Acton, T.B., Everett, J.K., Montelione, G.T., Szyperski, T., Northeast Structural Genomics Consortium (NESG)		Authors: Pulavarti, S., Eletsky, A., Satyamoorthy, B., Sukumaran, D.K., Lee, D., Kohan, E., Janjua, H., Xiao, R., Acton, T.B., Everett, J.K., Montelione, G.T., Szyperski, T., Northeast Structural Genomics Consortium (NESG)

	Description: Solution NMR Structure of Ig like domain (1277-1357) of Obscurin-like protein 1 from Homo sapiens, Northeast Structural Genomics Consortium (NESG) Target HR8578D		Description: Solution NMR Structure of Ig like domain (1277-1357) of Obscurin-like protein 1 from Homo sapiens, Northeast Structural Genomics Consortium (NESG) Target HR8578D