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PMID: 9242908 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S. Review

Structure-based perspectives on B12-dependent enzymes.

Annual review of biochemistry ·Vol. 66 ·1997-00-00 ·Pages 269-313

Ludwig ML, Matthews RG

Abstract

Two X-ray structures of cobalamin (B12) bound to proteins have now been determined. These structures reveal that the B12 cofactor undergoes a major conformational change on binding to the apoenzymes of methionine synthase and methylmalonyl-coenzyme A mutase: The dimethylbenzimidazole ligand to the cobalt is displaced by a histidine residue from the protein. Two methyltransferases from archaebacteria that catalyze methylation of mercaptoethanesulfonate (coenzyme M) during methanogenesis have also been shown to contain histidine-ligated cobamides. In corrinoid iron-sulfur methyltransferases from acetogenic and methanogenic organisms, benzimidazole is dissociated from cobalt, but without replacement by histidine. Thus, dimethylbenzimidazole displacement appears to be an emerging theme in cobamide-containing methyltransferases. In methionine synthase, the best studied of the methyltransferases, the histidine ligand appears to be required for competent methyl transfer between methyl-tetrahydrofolate and homocysteine but dissociates for reductive reactivation of the inactive oxidized enzyme. Replacement of dimethylbenzimidazole by histidine may allow switching between the catalytic and activation cycles. The best-characterized B12-dependent mutases that catalyze carbon skeleton rearrangement, for which methylmalonyl-coenzyme A mutase is the prototype, also bind cobalamin cofactors with histidine as the cobalt ligand, although other cobalamin-dependent mutases do not appear to utilize histidine ligation. It is intriguing to find that mutases, which catalyze homolytic rather than heterolytic cleavage of the carbon-cobalt bond, can use this structural motif. In methylmalonylCoA mutase a significant feature, which may be important in facilitating homolytic cleavage, is the long cobalt-nitrogen bond linking histidine to the co-factor. The intermediate radical species generated in catalysis are sequestered in the relatively hydrophilic core of an alpha/beta barrel domain of the mutase.

MeSH Terms
5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase/chemistry Animals Cobamides/chemistry Humans Methylmalonyl-CoA Mutase/chemistry Molecular Sequence Data Protein Conformation Vitamin B 12/chemistry
Chemicals
Cobamides 5-Methyltetrahydrofolate-Homocysteine S-Methyltransferase Methylmalonyl-CoA Mutase cobamamide Vitamin B 12
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Ludwig M L
Biophysics Research Division, University of Michigan, Ann Arbor 48109-1055, USA.
Matthews R G
Article Info
Journal
Annual review of biochemistry
Abbr.
Annu Rev Biochem
ISSN
0066-4154
Published
1997-00-00
Pages
269-313
Language
English
Region
United States
NLM ID
2985150R
Subset
IM
Grants
NIGMS NIH HHS · GM 16429 · United States
NIGMS NIH HHS · GM 24908 · United States
Databases
GENBANK
D64002, H11042, J04774, J04975, L07099, L10064, L30136, M22990, M37508, M65022, M65131, U00017, U30484, U36337, W33307, X14965, X57941, X75890, X77484, X80997, Z46828
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