4iw2: Difference between revisions

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OCA

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-'''Unreleased structure'''
+{{STRUCTURE_4iw2|  PDB=4iw2  |  SCENE=  }}
+===HSA-glucose complex===
-The entry 4iw2 is ON HOLD  until Paper Publication
+==Disease==
+[[http://www.uniprot.org/uniprot/ALBU_HUMAN ALBU_HUMAN]] Defects in ALB are a cause of familial dysalbuminemic hyperthyroxinemia (FDH) [MIM:[http://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>
-Authors: Wang, Y., Yu, H., Shi, X., Luo, Z., Huang, M.
+==Function==
+[[http://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>
-Description: HSA-glucose complex
+==About this Structure==
+[[4iw2]] is a 1 chain structure with sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4IW2 OCA].
+==Reference==
+<references group="xtra"/><references/>
+[[Category: Homo sapiens]]
+[[Category: Huang, M.]]
+[[Category: Luo, Z.]]
+[[Category: Shi, X.]]
+[[Category: Wang, Y.]]
+[[Category: Yu, H.]]
+[[Category: Heart shape]]
+[[Category: Tansport]]
+[[Category: Transport protein]]