9eod

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Current revision (21:45, 26 March 2025) (edit) (undo)
 
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'''Unreleased structure'''
 
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The entry 9eod is ON HOLD until Paper Publication
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==Human serum albumin with adamantene carboxylic acid==
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<StructureSection load='9eod' size='340' side='right'caption='[[9eod]], [[Resolution|resolution]] 1.90&Aring;' scene=''>
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Authors: Freitag-Pohl, S., Pohl, E.
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== Structural highlights ==
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<table><tr><td colspan='2'>[[9eod]] is a 2 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=9EOD OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=9EOD FirstGlance]. <br>
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Description: Human serum albumin with adamantene carboxylic acid
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</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 1.9&#8491;</td></tr>
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[[Category: Unreleased Structures]]
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<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=A1H6A:adamantane-1-carboxylic+acid'>A1H6A</scene>, <scene name='pdbligand=MYR:MYRISTIC+ACID'>MYR</scene>, <scene name='pdbligand=PEG:DI(HYDROXYETHYL)ETHER'>PEG</scene>, <scene name='pdbligand=PGE:TRIETHYLENE+GLYCOL'>PGE</scene></td></tr>
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[[Category: Pohl, E]]
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<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=9eod FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=9eod OCA], [https://pdbe.org/9eod PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=9eod RCSB], [https://www.ebi.ac.uk/pdbsum/9eod PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=9eod ProSAT]</span></td></tr>
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[[Category: Freitag-Pohl, S]]
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</table>
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== Disease ==
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[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>
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== Function ==
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[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>
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== References ==
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<references/>
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__TOC__
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</StructureSection>
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[[Category: Homo sapiens]]
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[[Category: Large Structures]]
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[[Category: Freitag-Pohl S]]
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[[Category: Pohl E]]

Current revision

Human serum albumin with adamantene carboxylic acid

PDB ID 9eod

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