9ik6

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
Current revision (05:29, 3 July 2025) (edit) (undo)
 
Line 1: Line 1:
-
'''Unreleased structure'''
 
-
The entry 9ik6 is ON HOLD until Paper Publication
+
==Human Serum Albumin crystallized with T4, pH 6.5==
-
 
+
<StructureSection load='9ik6' size='340' side='right'caption='[[9ik6]], [[Resolution|resolution]] 1.69&Aring;' scene=''>
-
Authors: Xiang, W., Yue, Z.L., Su, J.Y.
+
== Structural highlights ==
-
 
+
<table><tr><td colspan='2'>[[9ik6]] is a 1 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=9IK6 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=9IK6 FirstGlance]. <br>
-
Description: Human Serum Albumin crystallized with T4, pH 6.5
+
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 1.69&#8491;</td></tr>
-
[[Category: Unreleased Structures]]
+
<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=T44:3,5,3,5-TETRAIODO-L-THYRONINE'>T44</scene></td></tr>
-
[[Category: Xiang, W]]
+
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=9ik6 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=9ik6 OCA], [https://pdbe.org/9ik6 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=9ik6 RCSB], [https://www.ebi.ac.uk/pdbsum/9ik6 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=9ik6 ProSAT]</span></td></tr>
-
[[Category: Yue, Z.L]]
+
</table>
-
[[Category: Su, J.Y]]
+
== Disease ==
 +
[https://www.uniprot.org/uniprot/ALBU_HUMAN ALBU_HUMAN] Defects in ALB are a cause of familial dysalbuminemic hyperthyroxinemia (FDH) [MIM:[https://omim.org/entry/103600 103600]. FDH is a form of euthyroid hyperthyroxinemia that is due to increased affinity of ALB for T(4). It is the most common cause of inherited euthyroid hyperthyroxinemia in Caucasian population.<ref>PMID:8048949</ref> <ref>PMID:7852505</ref> <ref>PMID:9329347</ref> <ref>PMID:9589637</ref>
 +
== Function ==
 +
[https://www.uniprot.org/uniprot/ALBU_HUMAN ALBU_HUMAN] Serum albumin, the main protein of plasma, has a good binding capacity for water, Ca(2+), Na(+), K(+), fatty acids, hormones, bilirubin and drugs. Its main function is the regulation of the colloidal osmotic pressure of blood. Major zinc transporter in plasma, typically binds about 80% of all plasma zinc.<ref>PMID:19021548</ref>
 +
== References ==
 +
<references/>
 +
__TOC__
 +
</StructureSection>
 +
[[Category: Homo sapiens]]
 +
[[Category: Large Structures]]
 +
[[Category: Su JY]]
 +
[[Category: Xiang W]]
 +
[[Category: Yue ZL]]

Current revision

Human Serum Albumin crystallized with T4, pH 6.5

PDB ID 9ik6

Drag the structure with the mouse to rotate

Proteopedia Page Contributors and Editors (what is this?)

OCA

Personal tools