8h0o
From Proteopedia
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| - | '''Unreleased structure''' | ||
| - | + | ==Crystal structure of human serum albumin and ruthenium PZA complex adduct== | |
| - | + | <StructureSection load='8h0o' size='340' side='right'caption='[[8h0o]], [[Resolution|resolution]] 2.48Å' scene=''> | |
| - | + | == Structural highlights == | |
| - | + | <table><tr><td colspan='2'>[[8h0o]] 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=8H0O OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=8H0O FirstGlance]. <br> | |
| - | + | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.479Å</td></tr> | |
| - | [[Category:  | + | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=CL:CHLORIDE+ION'>CL</scene>, <scene name='pdbligand=NO:NITRIC+OXIDE'>NO</scene>, <scene name='pdbligand=PLM:PALMITIC+ACID'>PLM</scene>, <scene name='pdbligand=PZA:PYRAZINE-2-CARBOXAMIDE'>PZA</scene>, <scene name='pdbligand=RU:RUTHENIUM+ION'>RU</scene></td></tr> | 
| - | [[Category:  | + | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=8h0o FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8h0o OCA], [https://pdbe.org/8h0o PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8h0o RCSB], [https://www.ebi.ac.uk/pdbsum/8h0o PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8h0o ProSAT]</span></td></tr> | 
| - | [[Category:  | + | </table> | 
| - | [[Category: Wang | + | == Disease == | 
| - | [[Category:  | + | [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>  | 
| - | [[Category:  | + | == 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: Bai HH]] | ||
| + | [[Category: Gong WJ]] | ||
| + | [[Category: Wang HF]] | ||
| + | [[Category: Wang WM]] | ||
| + | [[Category: Wang Y]] | ||
Current revision
Crystal structure of human serum albumin and ruthenium PZA complex adduct
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Categories: Homo sapiens | Large Structures | Bai HH | Gong WJ | Wang HF | Wang WM | Wang Y
