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1 n the genus Conus (known as "conotoxins" or "conopeptides").
2 which together define a new P-superfamily of conopeptides.
3 notably different from other Gla-containing conopeptides.
4 onses to hydroxylated versus nonhydroxylated conopeptides and the relative susceptibility of proteins
7 (V)1.2 and that further engineering of micro-conopeptides belonging to the KIIIA group may provide su
13 somally expressed polypeptide chains of four conopeptides from the venoms of Conus gladiator and Conu
16 because (i) they are not constrained as most conopeptides, (ii) they are extremely short in length, (
18 at are functionally linked to the targets of conopeptides) is another determinant of the elicited beh
21 selection; the magnitude depends on which A-conopeptide lineage and amino-acid locus is analyzed.
22 ustelinus, conolysin-Mt, we expand the known conopeptide mechanisms to include association with and d
23 inding site for the N-channel-specific omega-conopeptide MVIIA, but also a distinct high-affinity sit
24 istinct high-affinity site for another omega-conopeptide (MVIIC), which affects both N- and P/Q-chann
27 o-conotoxin KIIIA is representative of micro-conopeptides previously characterized as inhibitors of t
33 he venom of Conus purpurascens, is the first conopeptide shown to inhibit the Shaker K(+) channel.
34 C-PrXA is strikingly different from the many conopeptides shown to be nicotinic antagonists; it is mo
36 s might help improve the design of analgesic conopeptides that selectively "avoid" nAChR receptors wh
38 to help identify the allosteric site for rho-conopeptide TIA, an inverse agonist at this receptor.
41 ypeptides stabilized by disulfide bonds, and conopeptides, which have no or only one disulfide bond.
44 rmatic tools, we found the highest number of conopeptides yet discovered in a single Conus specimen,
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