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  2. Methylcobalamin - Wikipedia

    en.wikipedia.org/wiki/Methylcobalamin

    Methylcobalamin (mecobalamin, MeCbl, or MeB 12) is a cobalamin, a form of vitamin B 12. It differs from cyanocobalamin in that the cyano group at the cobalt is replaced with a methyl group. [1] Methylcobalamin features an octahedral cobalt(III) centre and can be obtained as bright red crystals. [2]

  3. Vitamin B12 - Wikipedia

    en.wikipedia.org/wiki/Vitamin_B12

    Methylcobalamin (shown) is a form of vitamin B 12. Physically it resembles the other forms of vitamin B 12, occurring as dark red crystals that freely form cherry-colored transparent solutions in water. Vitamin B 12 is the most chemically complex of all the vitamins. [6]

  4. Organocobalt chemistry - Wikipedia

    en.wikipedia.org/wiki/Organocobalt_chemistry

    In methylcobalamin the ligand is a methyl group, which is electrophilic. in vitamin B12, the alkyl ligand is an adenosyl group. Related to vitamin B12 are cobalt porphyrins, dimethylglyoximates, and related complexes of Schiff base ligands. These synthetic compounds also form alkyl derivatives that undergo diverse reactions reminiscent of the ...

  5. Cobalamin biosynthesis - Wikipedia

    en.wikipedia.org/wiki/Cobalamin_biosynthesis

    Adenosylcobalamin Methylcobalamin, another biologically active form. The dark red crystals dissolve in water giving cherry-colored solutions. Cobalamin biosynthesis is the process by which bacteria and archea make cobalamin, vitamin B 12.

  6. Vitamin B12-binding domain - Wikipedia

    en.wikipedia.org/wiki/Vitamin_B12-binding_domain

    In molecular biology, the vitamin B12-binding domain is a protein domain which binds to cobalamin (vitamin B12). It can bind two different forms of the cobalamin cofactor, with cobalt bonded either to a methyl group (methylcobalamin) or to 5'-deoxyadenosine (adenosylcobalamin).

  7. Methionine synthase - Wikipedia

    en.wikipedia.org/wiki/Methionine_synthase

    Mutations in the MTR gene have been identified as the underlying cause of methylcobalamin deficiency complementation group G, or methylcobalamin deficiency cblG-type. [5] Deficiency or deregulation of the enzyme due to deficient methionine synthase reductase can directly result in elevated levels of homocysteine ( hyperhomocysteinemia ), which ...

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