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1 ncluding ferredoxin and the nickel-dependent carbon monoxide dehydrogenase.
2 dye P1 and the reversible CO2 cycling enzyme carbon monoxide dehydrogenase.
3 ed structure of the A-Cluster in clostridial carbon monoxide dehydrogenase.
4 ond subgroup mature the [Ni4Fe4S] cluster of carbon monoxide dehydrogenases.
5 lear sites in hydrogenases, nitrogenase, and carbon monoxide dehydrogenases.
6 pression of the cooS gene, which encodes for carbon monoxide dehydrogenase, a key enzyme in the acety
7 and nickel has been discovered in the enzyme carbon monoxide dehydrogenase/acetyl-CoA (coenzyme A) sy
10 ediate and, subsequently, is demethylated by carbon monoxide dehydrogenase/acetyl-CoA synthase (CODH/
11 the bifunctional multisubunit enzyme complex carbon monoxide dehydrogenase/acetyl-CoA synthase (CODH/
13 strate that two well-studied metalloenzymes, carbon monoxide dehydrogenase/acetyl-CoA synthase (CODH/
16 ly indicate that transfer of methyl group to carbon monoxide dehydrogenase/acetyl-CoA synthase occurs
18 of a synthetic analogue of the A-cluster of carbon monoxide dehydrogenase/acetylcoenzyme synthase, t
19 i-containing alpha2beta2 acetyl-CoA synthase/carbon monoxide dehydrogenase (ACS/CODH) catalyzes the s
20 ilm electrochemical studies of Ni-containing carbon monoxide dehydrogenase and [NiFeSe]-hydrogenase,
21 for other oxygen-sensitive enzymes, such as carbon monoxide dehydrogenase and formate dehydrogenase.
22 e, the iron-only hydrogenase, and the nickel-carbon monoxide dehydrogenase, and for the copper-sulfid
24 eterologous coexpression of a membrane-bound carbon monoxide dehydrogenase, CO was used as a reductan
25 hia coli, and CO oxidation is catalyzed by a carbon monoxide dehydrogenase (CODH I) from Carboxydothe
28 O(2) nanoparticles modified by attachment of carbon monoxide dehydrogenase (CODH) and a Ru photosensi
30 d at the active site of the NiFeS-containing carbon monoxide dehydrogenase (CODH) converts the enzyme
34 A crystal structure of the anaerobic Ni-Fe-S carbon monoxide dehydrogenase (CODH) from Rhodospirillum
35 he Fe atom of the proposed [FeNi] cluster of carbon monoxide dehydrogenase (CODH) from Rhodospirillum
37 lved in normal in vivo Ni insertion into the carbon monoxide dehydrogenase (CODH) of Rhodospirillum r
42 alpha subunit of acetyl-coenzyme A synthase/carbon monoxide dehydrogenase from Moorella thermoacetic
48 ngular feature of the catalytic C-cluster of carbon monoxide dehydrogenase is a sulfide-bridged Ni...
50 fide, are potent inhibitors of Ni-containing carbon monoxide dehydrogenases (Ni-CODH) that catalyze v
52 s of CO2- and NCO(-)-bound nickel-containing carbon monoxide dehydrogenases (Ni-CODHs) reveal that th
53 esis, whereas the presence of single-subunit carbon monoxide dehydrogenases raises the possibility of
54 ogue of the C-cluster of C. hydrogenoformans carbon monoxide dehydrogenase requires formation of a pl
55 pectroscopic information on the A-cluster of carbon monoxide dehydrogenase, was chosen as the target
56 ally in the C-cluster of C. hydrogenoformans carbon monoxide dehydrogenase whose NiFe(4)S(4) core con
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