1toz
From Proteopedia
(Difference between revisions)
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== Structural highlights == | == Structural highlights == | ||
<table><tr><td colspan='2'>[[1toz]] 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=1TOZ OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1TOZ FirstGlance]. <br> | <table><tr><td colspan='2'>[[1toz]] 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=1TOZ OCA]. For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1TOZ FirstGlance]. <br> | ||
- | </td></tr><tr><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[1emo|1emo]], [[1lmj|1lmj]], [[1hj7|1hj7]]</td></tr> | + | </td></tr><tr id='related'><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[1emo|1emo]], [[1lmj|1lmj]], [[1hj7|1hj7]]</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=1toz FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1toz OCA], [http://www.rcsb.org/pdb/explore.do?structureId=1toz RCSB], [http://www.ebi.ac.uk/pdbsum/1toz 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=1toz FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1toz OCA], [http://www.rcsb.org/pdb/explore.do?structureId=1toz RCSB], [http://www.ebi.ac.uk/pdbsum/1toz PDBsum]</span></td></tr> |
- | <table> | + | </table> |
== Disease == | == Disease == | ||
[[http://www.uniprot.org/uniprot/NOTC1_HUMAN NOTC1_HUMAN]] Defects in NOTCH1 are a cause of aortic valve disease 1 (AOVD1) [MIM:[http://omim.org/entry/109730 109730]]. A common defect in the aortic valve in which two rather than three leaflets are present. It is often associated with aortic valve calcification and insufficiency. In extreme cases, the blood flow may be so restricted that the left ventricle fails to grow, resulting in hypoplastic left heart syndrome.<ref>PMID:16025100</ref> | [[http://www.uniprot.org/uniprot/NOTC1_HUMAN NOTC1_HUMAN]] Defects in NOTCH1 are a cause of aortic valve disease 1 (AOVD1) [MIM:[http://omim.org/entry/109730 109730]]. A common defect in the aortic valve in which two rather than three leaflets are present. It is often associated with aortic valve calcification and insufficiency. In extreme cases, the blood flow may be so restricted that the left ventricle fails to grow, resulting in hypoplastic left heart syndrome.<ref>PMID:16025100</ref> | ||
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</StructureSection> | </StructureSection> | ||
[[Category: Homo sapiens]] | [[Category: Homo sapiens]] | ||
- | [[Category: Downing, A K | + | [[Category: Downing, A K]] |
- | [[Category: Hambleton, S | + | [[Category: Hambleton, S]] |
- | [[Category: Handford, P A | + | [[Category: Handford, P A]] |
- | [[Category: Knott, V | + | [[Category: Knott, V]] |
- | [[Category: Mcmichael, A J | + | [[Category: Mcmichael, A J]] |
- | [[Category: Muranyi, A | + | [[Category: Muranyi, A]] |
- | [[Category: Valeyev, N Y | + | [[Category: Valeyev, N Y]] |
- | [[Category: Werner, J M | + | [[Category: Werner, J M]] |
[[Category: Calcium binding]] | [[Category: Calcium binding]] | ||
[[Category: Egf]] | [[Category: Egf]] |
Revision as of 14:06, 6 January 2015
NMR structure of the human NOTCH-1 ligand binding region
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Categories: Homo sapiens | Downing, A K | Hambleton, S | Handford, P A | Knott, V | Mcmichael, A J | Muranyi, A | Valeyev, N Y | Werner, J M | Calcium binding | Egf | Ligand binding | Module | Notch | Signaling protein