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5azz

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(New page: '''Unreleased structure''' The entry 5azz is ON HOLD until Paper Publication Authors: Watanabe, S., Okumura, M., Arai, K., Takei, T., Asahina, Y., Hojo, H., Iwaoka, M., Inaba, K. Descr...)
Current revision (06:33, 31 May 2023) (edit) (undo)
 
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'''Unreleased structure'''
 
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The entry 5azz is ON HOLD until Paper Publication
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==Crystal structure of seleno-insulin==
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<StructureSection load='5azz' size='340' side='right'caption='[[5azz]], [[Resolution|resolution]] 1.45&Aring;' scene=''>
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== Structural highlights ==
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<table><tr><td colspan='2'>[[5azz]] is a 2 chain structure with sequence from [https://en.wikipedia.org/wiki/Bos_taurus Bos taurus]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=5AZZ OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=5AZZ FirstGlance]. <br>
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</td></tr><tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=5azz FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=5azz OCA], [https://pdbe.org/5azz PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=5azz RCSB], [https://www.ebi.ac.uk/pdbsum/5azz PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=5azz ProSAT]</span></td></tr>
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</table>
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== Function ==
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[https://www.uniprot.org/uniprot/INS_BOVIN INS_BOVIN] Insulin decreases blood glucose concentration. It increases cell permeability to monosaccharides, amino acids and fatty acids. It accelerates glycolysis, the pentose phosphate cycle, and glycogen synthesis in liver.
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<div style="background-color:#fffaf0;">
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== Publication Abstract from PubMed ==
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Synthetic insulin analogues with a long lifetime are current drug targets for the therapy of diabetic patients. The replacement of the interchain disulfide with a diselenide bridge, which is more resistant to reduction and internal bond rotation, can enhance the lifetime of insulin in the presence of the insulin-degrading enzyme (IDE) without impairing the hormonal function. The [C7UA ,C7UB ] variant of bovine pancreatic insulin (BPIns) was successfully prepared by using two selenocysteine peptides (i.e., the C7U analogues of A- and B-chains, respectively). In a buffer solution at pH 10 they spontaneously assembled under thermodynamic control to the correct insulin fold. The selenoinsulin (Se-Ins) exhibited a bioactivity comparable to that of BPIns. Interestingly, degradation of Se-Ins with IDE was significantly decelerated (tau1/2 approximately 8 h vs. approximately 1 h for BPIns). The lifetime enhancement could be due to both the intrinsic stability of the diselenide bond and local conformational changes induced by the substitution.
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Authors: Watanabe, S., Okumura, M., Arai, K., Takei, T., Asahina, Y., Hojo, H., Iwaoka, M., Inaba, K.
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Preparation of Selenoinsulin as a Long-Lasting Insulin Analogue.,Arai K, Takei T, Okumura M, Watanabe S, Amagai Y, Asahina Y, Moroder L, Hojo H, Inaba K, Iwaoka M Angew Chem Int Ed Engl. 2017 May 8;56(20):5522-5526. doi: 10.1002/anie.201701654., Epub 2017 Apr 10. PMID:28394477<ref>PMID:28394477</ref>
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Description: Crystal structure of seleno-insulin
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From MEDLINE&reg;/PubMed&reg;, a database of the U.S. National Library of Medicine.<br>
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[[Category: Unreleased Structures]]
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</div>
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[[Category: Inaba, K]]
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<div class="pdbe-citations 5azz" style="background-color:#fffaf0;"></div>
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[[Category: Takei, T]]
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[[Category: Iwaoka, M]]
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==See Also==
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[[Category: Arai, K]]
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*[[Insulin 3D Structures|Insulin 3D Structures]]
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[[Category: Hojo, H]]
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== References ==
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[[Category: Okumura, M]]
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<references/>
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[[Category: Asahina, Y]]
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__TOC__
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[[Category: Watanabe, S]]
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</StructureSection>
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[[Category: Bos taurus]]
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[[Category: Large Structures]]
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[[Category: Arai K]]
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[[Category: Asahina Y]]
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[[Category: Hojo H]]
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[[Category: Inaba K]]
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[[Category: Iwaoka M]]
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[[Category: Okumura M]]
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[[Category: Takei T]]
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[[Category: Watanabe S]]

Current revision

Crystal structure of seleno-insulin

PDB ID 5azz

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