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1 ucture and primary sequence only in nematode astacins.
2 this hypothesis of zymogen activation of the astacins.
3 with a Glu residue that is conserved in all astacins.
5 It is proposed that prosequence removal of astacins allows the formation of hydrogen bonds involvin
8 s with thrombospondin domains (ADAM-TS), and Astacins are now recognized as key signaling "scissors"
10 lpha and beta protease domains, based on the astacin crystal structure, revealed active site differen
11 gen activation mechanism of meprin and other astacins differs from that of the trypsin family of enzy
18 tween gene and protein structures within the astacin family provide novel information on the evolutio
19 these, SpAN, which encodes a protease in the astacin family related to Drosophila tolloid and vertebr
24 sion of key gene families--families encoding astacin-like and SCP/TAPS proteins--is associated with t
25 1 (BMP-1), which is a tolloid member of the astacin-like family of zinc metalloproteinases, is a hig
27 dog hookworm Ancylostoma caninum secretes an astacin-like metalloprotease, Ac-MTP-1, upon activation
29 ), a selective inhibitor of a small group of astacin-like metalloproteinases, which includes bone mor
30 NA sequences encoding the active site of the astacin-like protease domain common to all splice varian
31 ed protein domain structure: an NH2-terminal astacin-like protease domain, followed by a fixed order
34 ha(2)-macroglobulin is unable to inhibit the astacin-like proteinases meprin alpha and meprin beta, w
35 etic protein1 (Bmp1) gene encodes a secreted astacin metalloprotease that cleaves the COOH-propeptide
39 ese results suggest that HMP-1 is a secreted astacin metalloproteinase that has an important role in
42 roles in other systems-BMP-1/TLD (tolloid) (astacins), MMPs (matrix metalloproteases) and the ADAMs
43 cessed HMP-1 is composed of a characteristic astacin proteinase domain and a unique Cys-rich C-termin
45 inase 1 (HMP-1), a developmentally important astacin proteinase that functions in head regeneration a
48 tase mu) that is only present in meprin-like astacin proteinases; and a unique C-terminal domain (TH
50 sed on the crystal structure of the crayfish astacin, showed electrostatic differences within the mep
51 ion of patristacin and found conservation of astacin-specific motifs but also several positively sele
52 ith protease domains structurally related to astacin, the prototype of the "astacin family" of metall
54 of the more structurally complex members of astacin-type enzymes in deuterostomes, which can add sup
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