6oeu: Difference between revisions
Jump to navigation
Jump to search
m Protected "6oeu" [edit=sysop:move=sysop] |
No edit summary |
||
| (4 intermediate revisions by the same user not shown) | |||
| Line 1: | Line 1: | ||
The entry | ==Structure of human Patched1== | ||
<SX load='6oeu' size='340' side='right' viewer='molstar' caption='[[6oeu]], [[Resolution|resolution]] 3.50Å' scene=''> | |||
== Structural highlights == | |||
<table><tr><td colspan='2'>[[6oeu]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. This structure supersedes the now removed PDB entry [http://oca.weizmann.ac.il/oca-bin/send-pdb?obs=1&id=6d4h 6d4h]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6OEU OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6OEU FirstGlance]. <br> | |||
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Electron Microscopy, [[Resolution|Resolution]] 3.5Å</td></tr> | |||
<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'>[https://proteopedia.org/fgij/fg.htm?mol=6oeu FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6oeu OCA], [https://pdbe.org/6oeu PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6oeu RCSB], [https://www.ebi.ac.uk/pdbsum/6oeu PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6oeu ProSAT]</span></td></tr> | |||
</table> | |||
== 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 == | |||
[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> | |||
==See Also== | |||
*[[Protein patched homolog 1|Protein patched homolog 1]] | |||
== References == | |||
[[Category: | <references/> | ||
[[Category: Li | __TOC__ | ||
[[Category: Qi | </SX> | ||
[[Category: Wang | [[Category: Homo sapiens]] | ||
[[Category: Large Structures]] | |||
[[Category: Li X]] | |||
[[Category: Qi X]] | |||
[[Category: Wang J]] | |||
Latest revision as of 17:51, 13 March 2024
Structure of human Patched1Structure of human Patched1
| |||||||||