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5glh
From Proteopedia
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==Human endothelin receptor type-B in complex with ET-1== | ==Human endothelin receptor type-B in complex with ET-1== | ||
| - | <StructureSection load='5glh' size='340' side='right' caption='[[5glh]], [[Resolution|resolution]] 2.80Å' scene=''> | + | <StructureSection load='5glh' size='340' side='right'caption='[[5glh]], [[Resolution|resolution]] 2.80Å' scene=''> |
== Structural highlights == | == Structural highlights == | ||
| - | <table><tr><td colspan='2'>[[5glh]] is a 2 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5GLH OCA]. For a <b>guided tour on the structure components</b> use [ | + | <table><tr><td colspan='2'>[[5glh]] is a 2 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=5GLH OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=5GLH 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">X-ray diffraction, [[Resolution|Resolution]] 2.8Å</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=5glh FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5glh OCA], [https://pdbe.org/5glh PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=5glh RCSB], [https://www.ebi.ac.uk/pdbsum/5glh PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=5glh ProSAT]</span></td></tr> |
</table> | </table> | ||
| + | == Disease == | ||
| + | [https://www.uniprot.org/uniprot/EDNRB_HUMAN EDNRB_HUMAN] Hirschsprung disease;Waardenburg-Shah syndrome. 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. The disease is caused by mutations affecting the gene represented in this entry. Defects in EDNRB are associated with Waardenburg syndrome 2, with ocular albinism, autosomal recessive: A disorder characterized by the association of features typical of Waardenburg syndrome type 2 with ocular albinism. Patients manifest reduced visual acuity, albinotic fundus, deafness, hypomelanosis.<ref>PMID:28236341</ref> | ||
== Function == | == Function == | ||
| - | [[ | + | [https://www.uniprot.org/uniprot/ENLYS_BPT4 ENLYS_BPT4] Endolysin with lysozyme activity that degrades host peptidoglycans and participates with the holin and spanin proteins in the sequential events which lead to the programmed host cell lysis releasing the mature viral particles. Once the holin has permeabilized the host cell membrane, the endolysin can reach the periplasm and break down the peptidoglycan layer.<ref>PMID:22389108</ref> [https://www.uniprot.org/uniprot/EDNRB_HUMAN EDNRB_HUMAN] Non-specific receptor for endothelin 1, 2, and 3. Mediates its action by association with G proteins that activate a phosphatidylinositol-calcium second messenger system.<ref>PMID:7536888</ref> |
<div style="background-color:#fffaf0;"> | <div style="background-color:#fffaf0;"> | ||
== Publication Abstract from PubMed == | == Publication Abstract from PubMed == | ||
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__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
| - | [[Category: Dohmae | + | [[Category: Homo sapiens]] |
| - | [[Category: Doi | + | [[Category: Large Structures]] |
| - | [[Category: Fujiyoshi | + | [[Category: Dohmae N]] |
| - | [[Category: Nishizawa | + | [[Category: Doi T]] |
| - | [[Category: Nureki | + | [[Category: Fujiyoshi Y]] |
| - | [[Category: Okuta | + | [[Category: Nishizawa T]] |
| - | [[Category: Shihoya | + | [[Category: Nureki O]] |
| - | [[Category: Tani | + | [[Category: Okuta A]] |
| - | + | [[Category: Shihoya W]] | |
| - | + | [[Category: Tani K]] | |
Current revision
Human endothelin receptor type-B in complex with ET-1
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Categories: Homo sapiens | Large Structures | Dohmae N | Doi T | Fujiyoshi Y | Nishizawa T | Nureki O | Okuta A | Shihoya W | Tani K
