2lvc
From Proteopedia
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==Solution NMR Structure of Ig like domain (805-892) of Obscurin-like protein 1 from Homo sapiens, Northeast Structural Genomics Consortium (NESG) Target HR8578K== | ==Solution NMR Structure of Ig like domain (805-892) of Obscurin-like protein 1 from Homo sapiens, Northeast Structural Genomics Consortium (NESG) Target HR8578K== | ||
| - | <StructureSection load='2lvc' size='340' side='right' caption='[[2lvc | + | <StructureSection load='2lvc' size='340' side='right'caption='[[2lvc]]' scene=''> |
== Structural highlights == | == Structural highlights == | ||
| - | <table><tr><td colspan='2'>[[2lvc]] is a 1 chain structure with sequence from [ | + | <table><tr><td colspan='2'>[[2lvc]] 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=2LVC OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=2LVC FirstGlance]. <br> |
| - | </td></tr><tr id=' | + | </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'>[ | + | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=2lvc FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2lvc OCA], [https://pdbe.org/2lvc PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2lvc RCSB], [https://www.ebi.ac.uk/pdbsum/2lvc PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2lvc 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> |
| + | == Function == | ||
| + | [https://www.uniprot.org/uniprot/OBSL1_HUMAN OBSL1_HUMAN] | ||
| + | |||
| + | ==See Also== | ||
| + | *[[Obscurin|Obscurin]] | ||
== References == | == References == | ||
<references/> | <references/> | ||
__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
| - | [[Category: | + | [[Category: Homo sapiens]] |
| - | [[Category: Acton | + | [[Category: Large Structures]] |
| - | [[Category: Eletsky | + | [[Category: Acton TB]] |
| - | [[Category: Everett | + | [[Category: Eletsky A]] |
| - | [[Category: Janjua | + | [[Category: Everett JK]] |
| - | [[Category: Kohan | + | [[Category: Janjua H]] |
| - | [[Category: Lee | + | [[Category: Kohan E]] |
| - | [[Category: Montelione | + | [[Category: Lee D]] |
| - | + | [[Category: Montelione GT]] | |
| - | [[Category: Pederson | + | [[Category: Pederson K]] |
| - | [[Category: Prestegard | + | [[Category: Prestegard J]] |
| - | [[Category: Pulavarti | + | [[Category: Pulavarti S]] |
| - | [[Category: Sukumaran | + | [[Category: Sukumaran DK]] |
| - | [[Category: Szyperski | + | [[Category: Szyperski T]] |
| - | [[Category: Xiao | + | [[Category: Xiao R]] |
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Current revision
Solution NMR Structure of Ig like domain (805-892) of Obscurin-like protein 1 from Homo sapiens, Northeast Structural Genomics Consortium (NESG) Target HR8578K
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Categories: Homo sapiens | Large Structures | Acton TB | Eletsky A | Everett JK | Janjua H | Kohan E | Lee D | Montelione GT | Pederson K | Prestegard J | Pulavarti S | Sukumaran DK | Szyperski T | Xiao R
