8ylx

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m (Protected "8ylx" [edit=sysop:move=sysop])
Current revision (06:25, 19 March 2025) (edit) (undo)
 
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'''Unreleased structure'''
 
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The entry 8ylx is ON HOLD
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==Single particle cryo-EM reconstruction of Oryza sativa recombinant human serum albumin==
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<StructureSection load='8ylx' size='340' side='right'caption='[[8ylx]], [[Resolution|resolution]] 3.18&Aring;' scene=''>
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Authors: Dong, C.J., Yang, D.C., Duan, B.R.
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== Structural highlights ==
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<table><tr><td colspan='2'>[[8ylx]] 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=8YLX OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=8YLX FirstGlance]. <br>
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Description: Single particle cryo-EM reconstruction of Oryza sativa recombinant human serum albumin
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</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">Electron Microscopy, [[Resolution|Resolution]] 3.18&#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=OCA:OCTANOIC+ACID+(CAPRYLIC+ACID)'>OCA</scene></td></tr>
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[[Category: Yang, D.C]]
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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=8ylx FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8ylx OCA], [https://pdbe.org/8ylx PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8ylx RCSB], [https://www.ebi.ac.uk/pdbsum/8ylx PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8ylx ProSAT]</span></td></tr>
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[[Category: Duan, B.R]]
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</table>
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[[Category: Dong, C.J]]
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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: Dong CJ]]
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[[Category: Duan BR]]
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[[Category: Yang DC]]

Current revision

Single particle cryo-EM reconstruction of Oryza sativa recombinant human serum albumin

PDB ID 8ylx

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