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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
19
|
pubmed:dateCreated |
1999-2-2
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pubmed:abstractText |
We report a high affinity, mu opioid receptor selective enkephalin analogue in which the N-terminal tyrosine residue thought to be required for such high affinity is replaced by phenylalanine. The high affinity can be traced to a shift of the ligand's N-terminal residue within the mu receptor binding pocket, which diminishes the importance of the usual hydrogen bond between the tyrosine phenolic moiety and the receptor.
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pubmed:grant | |
pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:month |
Oct
|
pubmed:issn |
0960-894X
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pubmed:author | |
pubmed:issnType |
Print
|
pubmed:day |
6
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pubmed:volume |
8
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
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pubmed:pagination |
2681-4
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading | |
pubmed:year |
1998
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pubmed:articleTitle |
A high affinity, mu-opioid receptor-selective enkephalin analogue lacking an N-terminal tyrosine.
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pubmed:affiliation |
College of Pharmacy, University of Michigan, Ann Arbor 48109, USA.
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pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.
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