1bl1
From Proteopedia
(Difference between revisions)
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== Structural highlights == | == Structural highlights == | ||
<table><tr><td colspan='2'>[[1bl1]] 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=1BL1 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1BL1 FirstGlance]. <br> | <table><tr><td colspan='2'>[[1bl1]] 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=1BL1 OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1BL1 FirstGlance]. <br> | ||
| - | </td></tr><tr><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1bl1 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1bl1 OCA], [http://www.rcsb.org/pdb/explore.do?structureId=1bl1 RCSB], [http://www.ebi.ac.uk/pdbsum/1bl1 PDBsum]</span></td></tr> | + | </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=1bl1 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1bl1 OCA], [http://www.rcsb.org/pdb/explore.do?structureId=1bl1 RCSB], [http://www.ebi.ac.uk/pdbsum/1bl1 PDBsum]</span></td></tr> |
| - | <table> | + | </table> |
== Disease == | == Disease == | ||
[[http://www.uniprot.org/uniprot/PTHR1_HUMAN PTHR1_HUMAN]] Chondrodysplasia, Blomstrand type;Dental ankylosis;Eiken syndrome;Metaphyseal chondrodysplasia, Jansen type;Enchondromatosis. The disease is caused by mutations affecting the gene represented in this entry.<ref>PMID:7701349</ref> <ref>PMID:8703170</ref> <ref>PMID:9178745</ref> <ref>PMID:10487664</ref> <ref>PMID:15240651</ref> The disease is caused by mutations affecting the gene represented in this entry.<ref>PMID:9745456</ref> The disease may be caused by mutations affecting the gene represented in this entry.<ref>PMID:11850620</ref> <ref>PMID:15523647</ref> The disease is caused by mutations affecting the gene represented in this entry.<ref>PMID:15525660</ref> The disease is caused by mutations affecting the gene represented in this entry. | [[http://www.uniprot.org/uniprot/PTHR1_HUMAN PTHR1_HUMAN]] Chondrodysplasia, Blomstrand type;Dental ankylosis;Eiken syndrome;Metaphyseal chondrodysplasia, Jansen type;Enchondromatosis. The disease is caused by mutations affecting the gene represented in this entry.<ref>PMID:7701349</ref> <ref>PMID:8703170</ref> <ref>PMID:9178745</ref> <ref>PMID:10487664</ref> <ref>PMID:15240651</ref> The disease is caused by mutations affecting the gene represented in this entry.<ref>PMID:9745456</ref> The disease may be caused by mutations affecting the gene represented in this entry.<ref>PMID:11850620</ref> <ref>PMID:15523647</ref> The disease is caused by mutations affecting the gene represented in this entry.<ref>PMID:15525660</ref> The disease is caused by mutations affecting the gene represented in this entry. | ||
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</StructureSection> | </StructureSection> | ||
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
| - | [[Category: Bisello, A | + | [[Category: Bisello, A]] |
| - | [[Category: Chorev, M | + | [[Category: Chorev, M]] |
| - | [[Category: Mierke, D F | + | [[Category: Mierke, D F]] |
| - | [[Category: Pellegrini, M | + | [[Category: Pellegrini, M]] |
| - | [[Category: Rosenblatt, M | + | [[Category: Rosenblatt, M]] |
[[Category: Calciotropic hormone]] | [[Category: Calciotropic hormone]] | ||
[[Category: Hormone receptor]] | [[Category: Hormone receptor]] | ||
Revision as of 10:27, 22 December 2014
PTH RECEPTOR N-TERMINUS FRAGMENT, NMR, 1 STRUCTURE
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