6dmo: Difference between revisions
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<SX load='6dmo' size='340' side='right' viewer='molstar' caption='[[6dmo]], [[Resolution|resolution]] 4.10Å' scene=''> | <SX load='6dmo' size='340' side='right' viewer='molstar' caption='[[6dmo]], [[Resolution|resolution]] 4.10Å' scene=''> | ||
== Structural highlights == | == Structural highlights == | ||
<table><tr><td colspan='2'>[[6dmo]] is a 1 chain structure with sequence from [ | <table><tr><td colspan='2'>[[6dmo]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6DMO OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6DMO 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">Electron Microscopy, [[Resolution|Resolution]] 4.1Å</td></tr> | ||
<tr id=' | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=NAG:N-ACETYL-D-GLUCOSAMINE'>NAG</scene></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=6dmo FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6dmo OCA], [https://pdbe.org/6dmo PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6dmo RCSB], [https://www.ebi.ac.uk/pdbsum/6dmo PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6dmo ProSAT]</span></td></tr> | ||
</table> | </table> | ||
== Disease == | == Disease == | ||
[ | [https://www.uniprot.org/uniprot/PTC1_HUMAN PTC1_HUMAN] Semilobar holoprosencephaly;Monosomy 9q22.3;Alobar holoprosencephaly;Microform holoprosencephaly;Septopreoptic holoprosencephaly;Gorlin syndrome;Lobar holoprosencephaly;Midline interhemispheric variant of holoprosencephaly. The disease may be caused by mutations affecting the gene represented in this entry. The disease is caused by mutations affecting the gene represented in this entry. The disease is caused by mutations affecting the gene represented in this entry. | ||
== Function == | == Function == | ||
[ | [https://www.uniprot.org/uniprot/PTC1_HUMAN PTC1_HUMAN] Acts as a receptor for sonic hedgehog (SHH), indian hedgehog (IHH) and desert hedgehog (DHH). Associates with the smoothened protein (SMO) to transduce the hedgehog's proteins signal. Seems to have a tumor suppressor function, as inactivation of this protein is probably a necessary, if not sufficient step for tumorigenesis.<ref>PMID:21537345</ref> | ||
<div style="background-color:#fffaf0;"> | <div style="background-color:#fffaf0;"> | ||
== Publication Abstract from PubMed == | == Publication Abstract from PubMed == | ||
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</div> | </div> | ||
<div class="pdbe-citations 6dmo" style="background-color:#fffaf0;"></div> | <div class="pdbe-citations 6dmo" style="background-color:#fffaf0;"></div> | ||
==See Also== | |||
*[[Protein patched homolog 1|Protein patched homolog 1]] | |||
== References == | == References == | ||
<references/> | <references/> | ||
__TOC__ | __TOC__ | ||
</SX> | </SX> | ||
[[Category: | [[Category: Homo sapiens]] | ||
[[Category: Large Structures]] | [[Category: Large Structures]] | ||
[[Category: Gong | [[Category: Gong X]] | ||
[[Category: Qian | [[Category: Qian HW]] | ||
[[Category: Yan | [[Category: Yan N]] | ||
Latest revision as of 08:09, 21 November 2024
Cryo-EM structure of human Ptch1 with three mutations L282Q/T500F/P504LCryo-EM structure of human Ptch1 with three mutations L282Q/T500F/P504L
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