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1 0) hydroxoaquocobinamide (hereinafter called cobinamide).
2 ile method to measure cyanide in blood using cobinamide.
3 a facile method for producing and purifying cobinamide.
4 everal commercially available cobalamins and cobinamide.
5 wn de novo intermediate, and did not salvage cobinamide.
6 ll depended on the assimilation of exogenous cobinamide.
7 gh binding affinity for the cobalamin analog cobinamide.
8 d for cob(II)alamin, base-off cobalamins, or cobinamides.
11 is in Drosophila melanogaster, we found that cobinamide, a B(12) analog and an effective NO scavenger
13 on the electronic properties of Cbls is Ado-cobinamide (AdoCbi(+)), an AdoCbl derivative that lacks
15 appeared to convert most of the cobalamin to cobinamide and the 4 analogues that contain the bases-2-
18 human HC in complex with cyanocobalamin and cobinamide at 2.35 and 3.0 A resolution, respectively.
21 ossible to detail the activities of purified cobinamide biosynthesis (Cbi) proteins CbiF, CbiG, CbiD,
22 ux through the 5,6-dimethylbenzimidazole and cobinamide (Cbi) activation branches of the nucleotide l
25 nents of two distinct pathways for salvaging cobinamide (Cbi), a precursor of adenosylcobalamin (AdoC
26 se distinct pathways for salvaging exogenous cobinamide (Cbi), a precursor of adenosylcobalamin (coen
27 importing an "incomplete" corrinoid, such as cobinamide (Cbi), and adding appropriate alpha- and beta
28 d cobalamin (Cbl) as a substrate better than cobinamide (Cbi; a Cbl precursor); the beta phosphate of
30 A novel cyanide analyzer based on sensitive cobinamide chemistry relies on simultaneous reagent and
31 present a new method for the preparation of cobinamide (CN)2Cbi, a vitamin B12 precursor, that shoul
32 also utilize the incomplete corrinoid Co (1+)cobinamide (Co (1+)Cbi) as an alternative substrate.
33 tronic excited states of Co(2+)Cbl and Co(2+)cobinamide (Co(2+)Cbi(+), a cobalamin derivative that la
34 (2-pic) and pyridine (py) adducts of Co(II) cobinamide (Co(II)Cbi(+)), adducts thought to have long
37 t CobU requires a nucleoside upper ligand on cobinamide for substrate recognition, with the nucleosid
39 paper reports evidence that archaea salvage cobinamide from the environment by using a pathway diffe
40 osynthesis pathway, but efficiently salvaged cobinamide from the environment, suggesting the existenc
42 allele of the cobY gene was auxotrophic for cobinamide-GDP, a known intermediate of the late steps o
45 dative stress in cells and tissues, and that cobinamide has promise as a first specific treatment for
46 are consistent with a salvaging pathway for cobinamide in which an amidohydrolase enzyme cleaves off
47 ongly support the proposal that the relevant cobinamide intermediates during de novo adenosylcobalami
49 noid substrates that are believed to include cobinamide, its precursor cobyric acid and probably othe
59 of color change increases 10 times when the cobinamide solution for filter impregnation is prepared
60 sphate guanylyltransferase needed to convert cobinamide to adenosylcobinamide-GDP during the late ste
62 not presence, of cobalamin, suggesting that cobinamide toxicity was secondary to interference with c
64 the cobalt in the lower axial position, and cobinamide, which lacks the dimethylbenzimidazole nucleo
66 yme B(12) de novo and from Cby, but not from cobinamide, which was the expected phenotype for an L-th
69 Here we show that adding sodium nitrite to cobinamide yields a stable derivative (referred to as ni
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