Substitution of aromatic and nonaromatic amino acids for the Phe3 residue in the δ-selective opioid peptide deltorphin I: Effects on binding affinity and selectivity-Reference-Cited by-同舟云学术

Substitution of aromatic and nonaromatic amino acids for the Phe3 residue in the δ-selective opioid peptide deltorphin I: Effects on binding affinity and selectivity

Published:2009-01-12 Issue:5 Volume:44 Page:420-426
ISSN:0367-8377
Container-title:International Journal of Peptide and Protein Research
language:en
Short-container-title:

Author:

HEYL DEBORAH L.,SCHMITTER SHARON J.,BOUZIT HASSIBA,JOHNSON THOMAS W.,HEPP ANGELA M.,KURTZ KATHLEEN R.,MOUSIGIAN CAROL

Publisher

Wiley

Subject

Biochemistry

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1399-3011.1994.tb00177.x/fullpdf

Reference27 articles.

1. Endogenous opioid peptides: multiple agonists and receptors

2. Endogenous opiates: 1989

3. Opiate receptor subclasses differ in their conformational requirements

4. Identification of two related pentapeptides from the brain with potent opiate agonist activity

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4. pKa and Volume of residue one influence δ/μ opioid binding: QSAR analysis of tyrosine replacement in a nonselective deltorphin analogue;Bioorganic & Medicinal Chemistry;2003-08

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