Literature DB >> 4627755

Thyroxine-binding globulin: specificity for the hormonally active conformation of triiodothyronine.

G C Schussler.   

Abstract

The conformational requirements for binding of triiodothyronine to thyroxine-binding globulin were investigated with triiodothyronine analogs having restricted rotation at the ether bond. Although it has been reported that the predominant conformation of triiodothyronine carries the 3' iodine in a position proximal to the phenylalanine ring, the analog for the distal, hormonally active orientation of the 3' iodine is more effective in displacing triiodothyronine and thyroxine from thyroxine-binding globulin. The lower binding affinity of thyroxine-binding globulin for triiodothyronine as compared to thyroxine may be explained by specificity of the binding site for the less abundant conformation of triiodothyronine.

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Year:  1972        PMID: 4627755     DOI: 10.1126/science.178.4057.172

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  1 in total

1.  Phenothiazine drugs: structure-activity relationships explained by a conformation that mimics dopamine.

Authors:  A P Feinberg; S H Snyder
Journal:  Proc Natl Acad Sci U S A       Date:  1975-05       Impact factor: 11.205

  1 in total

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