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1 yridoxal 5'-phosphate (PLP), and the product phosphonoacetaldehyde.
2 hiff-base intermediate formed from Lys53 and phosphonoacetaldehyde.
3 ethyl-phosphonate, which is synthesized from phosphonoacetaldehyde by a distinct family of metal-depe
4 nY and PhnA proteins verified their roles as phosphonoacetaldehyde dehydrogenase and phosphonoacetate
5 d out using Mg(II)-activated Bacillus cereus phosphonoacetaldehyde hydrolase (phosphonatase) as an ex
10 e mechanism was demonstrated with the enzyme phosphonoacetaldehyde hydrolase (trivial name phosphonat
11 p domain loop of the HAD superfamily members phosphonoacetaldehyde hydrolase and beta-phosphoglucomut
12 the X-ray crystal structure of the Gly50Pro phosphonoacetaldehyde hydrolase mutant was determined.
13 the coupled actions of P-pyr decarboxylase, phosphonoacetaldehyde hydrolase, and alcohol dehydrogena
14 osphonopyruvate (Km = 3.2 +/- 0.2 microm) to phosphonoacetaldehyde (Ki = 15 +/- 2 microm) and carbon
15 ersible reaction of AEP and pyruvate to form phosphonoacetaldehyde (P-Ald) and L-alanine (L-Ala).
17 atalyzes the hydrolytic P-C bond cleavage of phosphonoacetaldehyde (Pald) to form orthophosphate and
18 us catalyzes hydrolytic P-C bond cleavage of phosphonoacetaldehyde (Pald) via a Schiff base intermedi
19 D12A mutant in the presence of the substrate phosphonoacetaldehyde showed that replacement of the loo
20 as verified for the S. typhimurium enzyme by phosphonoacetaldehyde-sodium borohydride-induced inactiv
21 (phosphonatase) catalyzes the hydrolysis of phosphonoacetaldehyde to acetaldehyde and inorganic phos
22 (phosphonatase) catalyzes the hydrolysis of phosphonoacetaldehyde to acetaldehyde and phosphate usin
24 e in the reaction, yet the methylene analog, phosphonoacetaldehyde, was not an inhibitor or substrate
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