This old version of Proteopedia is provided for student assignments while the new version is undergoing repairs. Content and edits done in this old version of Proteopedia after March 1, 2026 will eventually be lost when it is retired in about June of 2026.

Apply for new accounts at the new Proteopedia. Your logins will work in both the old and new versions.


1swg

From Proteopedia

(Difference between revisions)
Jump to: navigation, search
Line 1: Line 1:
-
[[Image:1swg.gif|left|200px]]
+
{{Seed}}
 +
[[Image:1swg.png|left|200px]]
<!--
<!--
Line 9: Line 10:
{{STRUCTURE_1swg| PDB=1swg | SCENE= }}
{{STRUCTURE_1swg| PDB=1swg | SCENE= }}
-
'''CIRCULAR PERMUTED STREPTAVIDIN E51/A46 IN COMPLEX WITH BIOTIN'''
+
===CIRCULAR PERMUTED STREPTAVIDIN E51/A46 IN COMPLEX WITH BIOTIN===
-
==Overview==
+
<!--
-
A circularly permuted streptavidin (CP51/46) has been designed to remove the flexible polypeptide loop that undergoes an open to closed conformational change when biotin is bound. The original termini have been joined by a tetrapeptide linker, and four loop residues have been removed, resulting in the creation of new N- and C-termini. Isothermal titration calorimetric studies show that the association constant has been reduced approximately six orders of magnitude below that of wild-type streptavidin to 10(7) M(-1). The deltaH degrees of biotin association for CP51/46 is reduced by 11.1 kcal/mol. Crystal structures of CP51/46 and its biotin complex show no significant alterations in the binding site upon removal of the loop. A hydrogen bond between Ser45 and Ser52 found in the absence of biotin is broken in the closed conformation as the side-chain hydroxyl of Ser45 moves to hydrogen bond to a ureido nitrogen of biotin. This is true in both the wild-type and CP51/46 forms of the protein, and the hydrogen bonding interaction might thus help nucleate closure of the loop. The reduced entropic cost of binding biotin to CP51/46 is consistent with the removal of this loop and a reduction in entropic costs associated with loop closure and immobilization. The reduced enthalpic contribution to the free energy of binding is not readily explainable in terms of the molecular structure, as the binding contacts are nearly entirely conserved, and only small differences in solvent accessible surfaces are observed relative to wild-type streptavidin.
+
The line below this paragraph, {{ABSTRACT_PUBMED_9568892}}, adds the Publication Abstract to the page
 +
(as it appears on PubMed at http://www.pubmed.gov), where 9568892 is the PubMed ID number.
 +
-->
 +
{{ABSTRACT_PUBMED_9568892}}
==About this Structure==
==About this Structure==
Line 31: Line 35:
[[Category: Circular permutation]]
[[Category: Circular permutation]]
[[Category: Signal]]
[[Category: Signal]]
-
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sat May 3 09:13:08 2008''
+
 
 +
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Jul 28 13:22:41 2008''

Revision as of 10:22, 28 July 2008

Image:1swg.png

Template:STRUCTURE 1swg

CIRCULAR PERMUTED STREPTAVIDIN E51/A46 IN COMPLEX WITH BIOTIN

Template:ABSTRACT PUBMED 9568892

About this Structure

1SWG is a Single protein structure of sequence from Streptomyces avidinii. Full crystallographic information is available from OCA.

Reference

Thermodynamic and structural consequences of flexible loop deletion by circular permutation in the streptavidin-biotin system., Chu V, Freitag S, Le Trong I, Stenkamp RE, Stayton PS, Protein Sci. 1998 Apr;7(4):848-59. PMID:9568892

Page seeded by OCA on Mon Jul 28 13:22:41 2008

Proteopedia Page Contributors and Editors (what is this?)

OCA

Retrieved from "http://52.214.119.220/wiki/index.php/1swg"
Personal tools