7ffs
From Proteopedia
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==Human Serum Albumin_1== | ==Human Serum Albumin_1== | ||
| - | <StructureSection load='7ffs' size='340' side='right'caption='[[7ffs]]' scene=''> | + | <StructureSection load='7ffs' size='340' side='right'caption='[[7ffs]], [[Resolution|resolution]] 2.05Å' scene=''> |
== Structural highlights == | == Structural highlights == | ||
| - | <table><tr><td colspan='2'>Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=7FFS OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=7FFS FirstGlance]. <br> | + | <table><tr><td colspan='2'>[[7ffs]] 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=7FFS OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=7FFS FirstGlance]. <br> |
</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=7ffs FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7ffs OCA], [https://pdbe.org/7ffs PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7ffs RCSB], [https://www.ebi.ac.uk/pdbsum/7ffs PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7ffs ProSAT]</span></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=7ffs FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7ffs OCA], [https://pdbe.org/7ffs PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7ffs RCSB], [https://www.ebi.ac.uk/pdbsum/7ffs PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7ffs ProSAT]</span></td></tr> | ||
</table> | </table> | ||
| + | == 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> | ||
| + | |||
| + | ==See Also== | ||
| + | *[[Albumin 3D structures|Albumin 3D structures]] | ||
| + | == References == | ||
| + | <references/> | ||
__TOC__ | __TOC__ | ||
</StructureSection> | </StructureSection> | ||
| + | [[Category: Homo sapiens]] | ||
[[Category: Large Structures]] | [[Category: Large Structures]] | ||
[[Category: Su JY]] | [[Category: Su JY]] | ||
[[Category: Xiang W]] | [[Category: Xiang W]] | ||
[[Category: Yue ZL]] | [[Category: Yue ZL]] | ||
Revision as of 04:05, 8 September 2022
Human Serum Albumin_1
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Categories: Homo sapiens | Large Structures | Su JY | Xiang W | Yue ZL
