4c49: Difference between revisions

Line 1:

'''~~Unreleased structure~~'''

==Reactive loop cleaved human CBG in complex with cortisol==

~~The entry~~ 4c49 is ~~ON HOLD~~

== 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 guided tour on the structure components use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=4C49 FirstGlance].

~~Authors~~: ~~Chan~~, W.L., ~~Zhou~~, A., Read, R.J.

</td></tr><tr><td class="sblockLbl">[[Ligand|Ligands:]]</td><td class="sblockDat"><scene name='pdbligand=HCY:(11ALPHA,14BETA)-11,17,21-TRIHYDROXYPREGN-4-ENE-3,20-DIONE'>HCY</scene>

<tr><td class="sblockLbl">[[Related_structure|Related:]]</td><td class="sblockDat">[[4c41|4c41]]</td></tr>

~~Description~~: ~~Reactive loop cleaved human CBG in complex with cortisol~~

<tr><td class="sblockLbl">Resources:</td><td class="sblockDat">[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]</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 ==

__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]]

Navigation menu

Page actions

Page actions

Personal tools

Navigation

Search

Tools

@@ Line 1: / Line 1: @@
-'''Unreleased structure'''
+==Reactive loop cleaved human CBG in complex with cortisol==
+<StructureSection load='4c49' size='340' side='right' caption='[[4c49]], [[Resolution|resolution]] 2.70&Aring;' scene=''>
-The entry 4c49 is ON HOLD
+== 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>
-Authors: Chan, W.L., Zhou, A., Read, R.J.
+</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>
-Description: Reactive loop cleaved human CBG in complex with cortisol
+<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]]