2lu7
From Proteopedia
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==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 | + | <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/ | + | <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> | + | </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> | |
| + | == Function == | ||
| + | [https://www.uniprot.org/uniprot/OBSL1_HUMAN OBSL1_HUMAN] | ||
==See Also== | ==See Also== | ||
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__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
| - | [[Category: | + | [[Category: Homo sapiens]] |
[[Category: Large Structures]] | [[Category: Large Structures]] | ||
| - | [[Category: Acton | + | [[Category: Acton TB]] |
| - | [[Category: Eletsky | + | [[Category: Eletsky A]] |
| - | [[Category: Everett | + | [[Category: Everett JK]] |
| - | [[Category: Janjua | + | [[Category: Janjua H]] |
| - | [[Category: Kohan | + | [[Category: Kohan E]] |
| - | [[Category: Lee | + | [[Category: Lee D]] |
| - | [[Category: Montelione | + | [[Category: Montelione GT]] |
| - | + | [[Category: Pulavarti S]] | |
| - | [[Category: Pulavarti | + | [[Category: Satyamoorthy B]] |
| - | [[Category: Satyamoorthy | + | [[Category: Sukumaran DK]] |
| - | [[Category: Sukumaran | + | [[Category: Szyperski T]] |
| - | [[Category: Szyperski | + | [[Category: Xiao R]] |
| - | [[Category: Xiao | + | |
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Revision as of 13:10, 22 February 2023
Solution NMR Structure of Ig like domain (1277-1357) of Obscurin-like protein 1 from Homo sapiens, Northeast Structural Genomics Consortium (NESG) Target HR8578D
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Categories: Homo sapiens | Large Structures | Acton TB | Eletsky A | Everett JK | Janjua H | Kohan E | Lee D | Montelione GT | Pulavarti S | Satyamoorthy B | Sukumaran DK | Szyperski T | Xiao R
