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1 , BarA, and ArfA C2-A2-T2 but not to free HS-pantetheine.
4 based on interligand NOEs between TLM and a pantetheine analog when both are bound simultaneously to
7 However, the adducts with R-3,4-decadienoyl-pantetheine and -N-acetylcysteamine are some 9- and >100
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
16 nside, suggesting that the attachment of the pantetheine arm to ACP must occur before complete assemb
18 ue modality that mimics (R)-beta-hydroxyacyl pantetheine binding to LpxA and displays how the peptide
20 nethiol (GlyPan), with one fewer carbon than pantetheine, can rescue a mutant E. coli strain MG1655De
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
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
29 ate and then transfer the carboxylate to the pantetheine group of either coenzyme A or an acyl-carrie
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
35 The absence of long range NOEs along the pantetheine moiety is consistent with this region of the
39 Es between the adenine H8 proton and several pantetheine protons in the bound form of HD-CoA indicate
42 e that the percentage yield of pantethine to pantetheine through disulfide exchange is approximately
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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