4c49
From Proteopedia
(Difference between revisions)
| Line 3: | Line 3: | ||
<StructureSection load='4c49' size='340' side='right'caption='[[4c49]], [[Resolution|resolution]] 2.70Å' scene=''> | <StructureSection load='4c49' size='340' side='right'caption='[[4c49]], [[Resolution|resolution]] 2.70Å' scene=''> | ||
== Structural highlights == | == Structural highlights == | ||
| - | <table><tr><td colspan='2'>[[4c49]] is a 4 chain structure with sequence from [ | + | <table><tr><td colspan='2'>[[4c49]] is a 4 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=4C49 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=4C49 FirstGlance]. <br> |
| - | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat"><scene name='pdbligand=HCY:(11ALPHA,14BETA)-11,17,21-TRIHYDROXYPREGN-4-ENE-3,20-DIONE'>HCY</scene> | + | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=HCY:(11ALPHA,14BETA)-11,17,21-TRIHYDROXYPREGN-4-ENE-3,20-DIONE'>HCY</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=4c49 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4c49 OCA], [https://pdbe.org/4c49 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4c49 RCSB], [https://www.ebi.ac.uk/pdbsum/4c49 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4c49 ProSAT]</span></td></tr> | |
| - | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[ | + | |
</table> | </table> | ||
== Disease == | == Disease == | ||
| - | [[ | + | [[https://www.uniprot.org/uniprot/CBG_HUMAN CBG_HUMAN]] Corticosteroid-binding globulin deficiency. The disease is caused by mutations affecting the gene represented in this entry. |
== Function == | == Function == | ||
| - | [[ | + | [[https://www.uniprot.org/uniprot/CBG_HUMAN CBG_HUMAN]] Major transport protein for glucocorticoids and progestins in the blood of almost all vertebrate species.<ref>PMID:18513745</ref> |
==See Also== | ==See Also== | ||
| Line 19: | Line 18: | ||
__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
| - | [[Category: | + | [[Category: Homo sapiens]] |
[[Category: Large Structures]] | [[Category: Large Structures]] | ||
| - | [[Category: Chan | + | [[Category: Chan WL]] |
| - | [[Category: Read | + | [[Category: Read RJ]] |
| - | [[Category: Zhou | + | [[Category: Zhou A]] |
| - | + | ||
| - | + | ||
| - | + | ||
| - | + | ||
Revision as of 17:25, 7 September 2022
Reactive loop cleaved human CBG in complex with cortisol
| |||||||||||
