INT37439

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Context Info
Confidence 0.01
First Reported 1986
Last Reported 1986
Negated 0
Speculated 0
Reported most in Abstract
Documents 1
Total Number 2
Disease Relevance 0
Pain Relevance 0.76

This is a graph with borders and nodes. Maybe there is an Imagemap used so the nodes may be linking to some Pages.

pigmentation (Tyr) cell proliferation (Tyr) oxidoreductase activity (Tyr)
cellular_component (Tyr) cytoplasm (Tyr)
Shbdp1 (Mus musculus)
Tyr (Rattus norvegicus)
Pain Link Frequency Relevance Heat
Enkephalin 14 88.64 High High
Intracerebroventricular 4 83.36 Quite High

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Sentences Mentioned In

Key: Protein Mutation Event Anatomy Negation Speculation Pain term Disease term
In contrast, Tyr-Phe-NHOH, designed to interact with S2,S1 subsites through its positively charged Tyr as the P2 component, is a highly potent (Ki = 9 nM) and selective DAP inhibitor.
S2 Binding (interact) of Tyr
1) Confidence 0.01 Published 1986 Journal Mol. Pharmacol. Section Abstract Doc Link 3531805 Disease Relevance 0 Pain Relevance 0.38
In contrast, Tyr-Phe-NHOH, designed to interact with S2,S1 subsites through its positively charged Tyr as the P2 component, is a highly potent (Ki = 9 nM) and selective DAP inhibitor.
S2 Binding (interact) of Tyr
2) Confidence 0.01 Published 1986 Journal Mol. Pharmacol. Section Abstract Doc Link 3531805 Disease Relevance 0 Pain Relevance 0.38

General Comments

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