4c49: Difference between revisions
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''' | ==Reactive loop cleaved human CBG in complex with cortisol== | ||
<StructureSection load='4c49' size='340' side='right' caption='[[4c49]], [[Resolution|resolution]] 2.70Å' scene=''> | |||
== Structural highlights == | |||
<table><tr><td colspan='2'>[[4c49]] is a 4 chain structure. 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 [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4C49 FirstGlance]. <br> | |||
</td></tr><tr><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><br> | |||
<tr><td class="sblockLbl"><b>[[Related_structure|Related:]]</b></td><td class="sblockDat">[[4c41|4c41]]</td></tr> | |||
<tr><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4c49 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4c49 OCA], [http://www.rcsb.org/pdb/explore.do?structureId=4c49 RCSB], [http://www.ebi.ac.uk/pdbsum/4c49 PDBsum]</span></td></tr> | |||
<table> | |||
== Disease == | |||
[[http://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 == | |||
[[http://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> | |||
== References == | |||
<references/> | |||
__TOC__ | |||
</StructureSection> | |||
[[Category: Chan, W L.]] | |||
[[Category: Read, R J.]] | |||
[[Category: Zhou, A.]] | |||
[[Category: Corticosteroid binding globulin]] | |||
[[Category: Hormone carrier]] | |||
[[Category: Serpin]] | |||
[[Category: Transport protein]] |
Revision as of 03:20, 2 October 2014
Reactive loop cleaved human CBG in complex with cortisolReactive loop cleaved human CBG in complex with cortisol
Structural highlights
Disease[CBG_HUMAN] Corticosteroid-binding globulin deficiency. The disease is caused by mutations affecting the gene represented in this entry. Function[CBG_HUMAN] Major transport protein for glucocorticoids and progestins in the blood of almost all vertebrate species.[1] References
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