8ew4
From Proteopedia
(Difference between revisions)
(New page: '''Unreleased structure''' The entry 8ew4 is ON HOLD Authors: Gucwa, M., Cooper, D.R., Unciano, J., Lea, K., Kim, L., Lenkiewicz, J., Starban, I., Stewart, A.J., Minor, W., Center for S...) |
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| - | '''Unreleased structure''' | ||
| - | + | ==Human Serum Albumin with Cobalt (II) and Myristic Acid - crystal 1== | |
| - | + | <StructureSection load='8ew4' size='340' side='right'caption='[[8ew4]], [[Resolution|resolution]] 2.40Å' scene=''> | |
| - | + | == Structural highlights == | |
| - | + | <table><tr><td colspan='2'>[[8ew4]] 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=8EW4 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=8EW4 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]] 2.4Å</td></tr> | |
| - | [[Category: | + | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=CO:COBALT+(II)+ION'>CO</scene>, <scene name='pdbligand=MYR:MYRISTIC+ACID'>MYR</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=8ew4 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=8ew4 OCA], [https://pdbe.org/8ew4 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=8ew4 RCSB], [https://www.ebi.ac.uk/pdbsum/8ew4 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=8ew4 ProSAT]</span></td></tr> |
| - | [[Category: | + | </table> |
| - | [[Category: | + | == 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: Lea | + | == Function == |
| - | [[Category: | + | [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> |
| - | [[Category: | + | == References == |
| - | [[Category: | + | <references/> |
| - | [[Category: | + | __TOC__ |
| - | [[Category: Unciano | + | </StructureSection> |
| + | [[Category: Homo sapiens]] | ||
| + | [[Category: Large Structures]] | ||
| + | [[Category: Cooper DR]] | ||
| + | [[Category: Gucwa M]] | ||
| + | [[Category: Kim L]] | ||
| + | [[Category: Lea K]] | ||
| + | [[Category: Lenkiewicz J]] | ||
| + | [[Category: Minor W]] | ||
| + | [[Category: Starban I]] | ||
| + | [[Category: Stewart AJ]] | ||
| + | [[Category: Unciano J]] | ||
Current revision
Human Serum Albumin with Cobalt (II) and Myristic Acid - crystal 1
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Categories: Homo sapiens | Large Structures | Cooper DR | Gucwa M | Kim L | Lea K | Lenkiewicz J | Minor W | Starban I | Stewart AJ | Unciano J
