2na9: Difference between revisions
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==Transmembrane Structure of the P441A Mutant of the Cytokine Receptor Common Subunit beta== | ==Transmembrane Structure of the P441A Mutant of the Cytokine Receptor Common Subunit beta== | ||
<StructureSection load='2na9' size='340' side='right'caption='[[2na9 | <StructureSection load='2na9' size='340' side='right'caption='[[2na9]]' scene=''> | ||
== Structural highlights == | == Structural highlights == | ||
<table><tr><td colspan='2'>[[2na9]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/ | <table><tr><td colspan='2'>[[2na9]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full experimental information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=2NA9 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=2NA9 FirstGlance]. <br> | ||
</td></tr> | </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=2na9 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2na9 OCA], [https://pdbe.org/2na9 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2na9 RCSB], [https://www.ebi.ac.uk/pdbsum/2na9 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2na9 ProSAT]</span></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=2na9 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=2na9 OCA], [https://pdbe.org/2na9 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=2na9 RCSB], [https://www.ebi.ac.uk/pdbsum/2na9 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=2na9 ProSAT]</span></td></tr> | |||
</table> | </table> | ||
== Disease == | == Disease == | ||
[https://www.uniprot.org/uniprot/IL3RB_HUMAN IL3RB_HUMAN] Defects in CSF2RB are the cause of pulmonary surfactant metabolism dysfunction type 5 (SMDP5) [MIM:[https://omim.org/entry/614370 614370]. SMDP5 is a rare lung disorder due to impaired surfactant homeostasis. It is characterized by alveolar filling with floccular material that stains positive using the periodic acid-Schiff method and is derived from surfactant phospholipids and protein components. Excessive lipoproteins accumulation in the alveoli results in severe respiratory distress.<ref>PMID:21075760</ref> | |||
== Function == | == Function == | ||
[https://www.uniprot.org/uniprot/IL3RB_HUMAN IL3RB_HUMAN] High affinity receptor for interleukin-3, interleukin-5 and granulocyte-macrophage colony-stimulating factor. | |||
<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: | [[Category: Homo sapiens]] | ||
[[Category: Large Structures]] | [[Category: Large Structures]] | ||
[[Category: An | [[Category: An W]] | ||
[[Category: Ginsberg | [[Category: Ginsberg MH]] | ||
[[Category: Schmidt | [[Category: Schmidt T]] | ||
[[Category: Situ | [[Category: Situ AJ]] | ||
[[Category: Ulmer | [[Category: Ulmer TS]] | ||
[[Category: Ye | [[Category: Ye F]] | ||