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1 , BarA, and ArfA C2-A2-T2 but not to free HS-pantetheine.
2                             The K(m) of free pantetheine (30-50 mM) was 3 orders of magnitude larger
3                                              Pantetheine also serves as an amino acid acceptor in rea
4  based on interligand NOEs between TLM and a pantetheine analog when both are bound simultaneously to
5                          A detailed study of pantetheine analogues was performed in order to identify
6                        Finally bioorthogonal pantetheine analogues were shown to target carrier prote
7  However, the adducts with R-3,4-decadienoyl-pantetheine and -N-acetylcysteamine are some 9- and >100
8                                              Pantetheine and its corresponding disulfide pantethine p
9 e truncation of CoA to 4-phosphopantetheine, pantetheine, and finally cysteamine was observed with Th
10 hin the phosphopantetheine arm overlaps, the pantetheine arm binds to the same pocket in two distinct
11 of CoASH, but the absence of density for the pantetheine arm indicates that it is flexible within the
12 of the 4'-phosphate at the distal end of the pantetheine arm is demonstrated to both facilitate deliv
13 the same as in the binary complex, while the pantetheine arm is more extended and approaches close to
14                            Specifically, the pantetheine arm of CoA bound to one protomer within the
15 ng equivalents to the RHD, with the swinging pantetheine arm serving as a ca. 20 A bridge.
16 nside, suggesting that the attachment of the pantetheine arm to ACP must occur before complete assemb
17                 In the region of the phospho-pantetheine attachment site, significant similarity betw
18 ue modality that mimics (R)-beta-hydroxyacyl pantetheine binding to LpxA and displays how the peptide
19 the phenyl moiety partially fills the enzyme pantetheine binding tunnel.
20 nethiol (GlyPan), with one fewer carbon than pantetheine, can rescue a mutant E. coli strain MG1655De
21 ere shown to be effective substrates for the pantetheine-cleaving enzyme ThnT.
22  molecule and covalently transfers it to the pantetheine cofactor of an aryl-carrier protein of BasF,
23 in a three-step sequence in which a farnesyl-pantetheine conjugate is phosphorylated, adenylated, and
24 ingle-turnover reaction of 4-CBA, MgATP, and pantetheine corresponded to one-half of the starting 4-C
25                                         Free pantetheine could capture cysteinyl adenylate with a 25-
26  Substitution of CoA with the slow substrate pantetheine did not significantly alter the rate of the
27 f CoA docks to the PAPS domain, and the acyl-pantetheine group docks to the hydrophobic phenol bindin
28                                          The pantetheine group of CoA partially obstructs the active
29 ate and then transfer the carboxylate to the pantetheine group of either coenzyme A or an acyl-carrie
30                                    ThnT is a pantetheine hydrolase from the DmpA/OAT superfamily invo
31 elevance of these transitions, we designed a pantetheine-like chloromethyl ketone inactivator and co-
32 l reversibility of post-translational custom pantetheine modification of Escherichia coli acyl carrie
33 yme has shown that the benzoyl thioester and pantetheine moieties of the substrate ligand are bound i
34 crystal structure of this complex, while the pantetheine moiety is clearly less extended.
35     The absence of long range NOEs along the pantetheine moiety is consistent with this region of the
36                               Docking of the pantetheine moiety of the substrate identifies the loop
37                            When L-threonyl-S-pantetheine or L-threonyl-S-(N-acetyl)cysteamine was use
38                  We exploited solvatochromic pantetheine probes attached to ACP that fluoresce when s
39 Es between the adenine H8 proton and several pantetheine protons in the bound form of HD-CoA indicate
40                       Unexpectedly, the acyl-pantetheine thioester carbonyl is not hydrogen-bonded to
41 and MetRS, forming corresponding aminoacyl-S-pantetheine thioesters.
42 e that the percentage yield of pantethine to pantetheine through disulfide exchange is approximately
43 pha is the percentage yield of pantethine to pantetheine through disulfide exchange.
44 ntetheinase that catalyzes the hydrolysis of pantetheine to produce pantothenic acid (vitamin B5) and
45  acyl chain is transferred back from the ACP pantetheine to the KS cysteine before dissociation can o

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