PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
31981848-3	2020	Herein, a cobalt molybdate/cobalt boride (CoMoO4/Co-B) composite is constructed with cobalt boride nanoflake-like as a conductive additive in CoMoO4 nanorods using a facile water bath deposition process and liquid-phase reduction method.	Cobalt	10-16	metabolism of cobalamin associated B	Homo sapiens	49-53	
33797888-9	2021	CblD then hitches up with CblC via a unique Co-sulfur bond to cob(II)alamin at a bifurcation point, leading to the cytoplasmic methylcobalamin or mitochondrial 5"-deoxyadenosylcobalamin branch.	Cobalt	44-46	metabolism of cobalamin associated B	Homo sapiens	62-65	
7939615-17	1994	In addition, it was demonstrated that ingestion of controlled amounts of the soluble cobalt compound resulted in significantly higher concentrations of cobalt in urine and blood (Co-B) from females compared with males (P < 0.01).	Cobalt	85-91	metabolism of cobalamin associated B	Homo sapiens	179-183	
7939615-17	1994	In addition, it was demonstrated that ingestion of controlled amounts of the soluble cobalt compound resulted in significantly higher concentrations of cobalt in urine and blood (Co-B) from females compared with males (P < 0.01).	Cobalt	152-158	metabolism of cobalamin associated B	Homo sapiens	179-183	
31981848-3	2020	Herein, a cobalt molybdate/cobalt boride (CoMoO4/Co-B) composite is constructed with cobalt boride nanoflake-like as a conductive additive in CoMoO4 nanorods using a facile water bath deposition process and liquid-phase reduction method.	Cobalt	27-40	metabolism of cobalamin associated B	Homo sapiens	49-53	
31981848-3	2020	Herein, a cobalt molybdate/cobalt boride (CoMoO4/Co-B) composite is constructed with cobalt boride nanoflake-like as a conductive additive in CoMoO4 nanorods using a facile water bath deposition process and liquid-phase reduction method.	Cobalt	85-98	metabolism of cobalamin associated B	Homo sapiens	49-53	
26207564-4	2015	The EXAFS analyses reveal that upon heating, CoO is first reduced to metallic Co at 130  C and then partially combines with B to form a Co-B species.	Cobalt	45-47	metabolism of cobalamin associated B	Homo sapiens	136-140	
25741574-15	2015	In contrast, the nonplanar cob(III)alamins contain two axial ligands to the central cobalt atom.	Cobalt	84-90	metabolism of cobalamin associated B	Homo sapiens	27-30	
17567043-7	2007	Our spectroscopic data revealed that this form contains a five-coordinate cob(II)alamin species, with a water molecule as an axial ligand to the cobalt.	Cobalt	145-151	metabolism of cobalamin associated B	Homo sapiens	74-77	
17567043-9	2007	This form was found to possess an effectively four-coordinate cob(II)alamin species that has neither water nor histidine coordinated to the cobalt center.	Cobalt	140-146	metabolism of cobalamin associated B	Homo sapiens	62-65	
16304645-6	2005	In the diol dehydratases the 5"-deoxyadenosyl radical generated by homolysis of the carbon-cobalt bond of coenzyme B12 moves about 10 A away from the cobalt atom in cob(II)alamin.	Cobalt	150-156	metabolism of cobalamin associated B	Homo sapiens	91-94	
14661978-3	2003	Comparison of the rates of reaction of cobalamin, which contains a dimethylbenzimidazole nucleotide coordinated to the cobalt in the lower axial position, and cobinamide, which lacks the dimethylbenzimidazole nucleotide, allows assessment of the degree of stabilization the dimethylbenzimidazole base provides for methyl transfer between CH(3)-H(4)folate bound to MetH(2-649) and exogenous cob(I)alamin.	Cobalt	119-125	metabolism of cobalamin associated B	Homo sapiens	39-42	
10504238-2	1999	Enzyme-bound cob(II)alamin was cryotrapped after formation by substrate-initiated, thermally activated cleavage of the cobalt-carbon bond of adenosylcobalamin.	Cobalt	119-125	metabolism of cobalamin associated B	Homo sapiens	13-16	
10504238-11	1999	A 14% increase in the isotropic hyperfine coupling of the remote dimethylbenzimidazole (14)N nucleus in enzyme-bound versus free base-on cob(II)alamin shows an enhanced delocalization of unpaired spin density from Co(II) onto the axial ligand, which would contribute to the acceleration of the cobalt-carbon bond cleavage rate in situ.	Cobalt	294-300	metabolism of cobalamin associated B	Homo sapiens	137-140	
31965133-7	2020	When coupled to WO3 thin films, the CoB@CoOx nanostructures exhibit a higher catalytic enhancement than corresponding pure cobalt borate (Co-Bi) and cobalt hydroxide (Co(OH)x) electrocatalysts.	Cobalt	123-136	metabolism of cobalamin associated B	Homo sapiens	36-40	
21971012-0	2011	Amorphous tunable-size Co-B magnetic nanoparticles from the cobalt-catalyzed NaBH4 hydrolysis.	Cobalt	60-66	metabolism of cobalamin associated B	Homo sapiens	23-27	
18586770-3	2008	In the inactivation, the Co-C bond of adenosylcobalamin underwent irreversible cleavage forming unidentified radicals and cob(II)alamin that resisted oxidation even in the presence of oxygen.	Cobalt	25-27	metabolism of cobalamin associated B	Homo sapiens	46-49	
11669778-7	1997	For cob(II)inamide itself, the alpha diastereomer is enthalpically stabilized relative to the beta diastereomer in the transition state for carbon-cobalt bond formation, but an even larger entropic stabilization of the beta diastereomer causes the latter to be the predominant product.	Cobalt	147-153	metabolism of cobalamin associated B	Homo sapiens	4-7