Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
8325651 | The International Journal of Biochemistry & Cell Biology | 2009 | 10 Pages |
Abstract
Intriguingly, the affinity of Y56F-PepT1 was found to be dramatically increased (approximately 100-fold) in comparison to that of the wild-type rabbit PepT1. Y91 mutations also affected the substrate affinity of the transporter, which increased in line with the hydrophilicity of the substituted amino acid (FÂ >Â YÂ >Â QÂ >Â R). Y167 was demonstrated to play a pivotal role in rabbit PepT1 function since Y167F, Y167R and Y167Q demonstrated very little transport function. These results are discussed with regard to a proposed mechanism for PepT1 substrate binding.
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Authors
Myrtani Pieri, Christine Gan, Patrick Bailey, David Meredith,