1bst
From Proteopedia
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- | + | ==A HEURISTIC APPROACH TO PREDICTING THE TERTIARY STRUCTURE OF BOVINE SOMATOTROPIN== | |
+ | <StructureSection load='1bst' size='340' side='right' caption='[[1bst]]' scene=''> | ||
+ | == Structural highlights == | ||
+ | <table><tr><td colspan='2'>For a <b>guided tour on the structure components</b> use [http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1BST FirstGlance]. <br> | ||
+ | </td></tr><tr><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1bst FirstGlance], [http://www.ebi.ac.uk/pdbsum/1bst PDBsum]</span></td></tr> | ||
+ | <table> | ||
+ | <div style="background-color:#fffaf0;"> | ||
+ | == Publication Abstract from PubMed == | ||
+ | A combination of a heuristic approach and energy minimization was used to predict the three-dimensional structure of bovine somatotropin (bSt), also known as bovine growth hormone, a protein of 191 amino acids. The starting points for energy minimizations were generated from the following two types of inputs: (a) the amino acid sequence and (b) the heuristic inputs, which were derived according to physical, chemical, and biological principles by piecing together all useful information available. The predicted 3-D structure of the bSt molecule has all the features observed in four-helix bundle proteins. The four alpha-helices in bSt are intimately packed to form an assembly with an approximately square cross section. All the adjacent alpha-helices are antiparallel, with a somewhat tilted angle between each of the adjacent pairs so that the assembly of the four helices looks like a left-handed twisted bundle. There are two disulfide bonds in the bSt structure: one "hooking" the middle of a long loop with helix 4 so as to pull the long loop onto the surface of the helix bundle and the other "hooking" the C-terminal segment with the same helix so as to force the C-terminal segment to bend toward the helix bundle. As a consequence, a considerable part of the surface of the four-helix bundle is closely packed or intimately embraced by the loop segments. The predicted bSt structure has a hydrophobic core and a hydrophilic exterior surface. The energetic analysis of the predicted bSt structure indicates that the interaction between helices and loops plays a dominant role in stabilizing the four-helix bundle structure from the viewpoint of both electrostatic and nonbonded interactions. A technique called FOLD was meanwhile developed, by which one can fold a polypeptide chain into any shape as desired. This tool proved to be very useful during the heuristic model-building process. | ||
- | + | A heuristic approach to predicting the tertiary structure of bovine somatotropin.,Carlacci L, Chou KC, Maggiora GM Biochemistry. 1991 May 7;30(18):4389-98. PMID:2021631<ref>PMID:2021631</ref> | |
- | + | From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br> | |
- | + | </div> | |
- | == | + | == References == |
- | + | <references/> | |
- | + | __TOC__ | |
- | + | </StructureSection> | |
- | + | ||
- | < | + | |
[[Category: Carlacci, L]] | [[Category: Carlacci, L]] | ||
[[Category: Chou, K C]] | [[Category: Chou, K C]] | ||
[[Category: Maggiora, G M]] | [[Category: Maggiora, G M]] |
Revision as of 09:38, 13 August 2014
A HEURISTIC APPROACH TO PREDICTING THE TERTIARY STRUCTURE OF BOVINE SOMATOTROPIN
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