Proteomics of vitamin B12 processing

L Hannibal, PM DiBello, DW Jacobsen - Clinical chemistry and …, 2013 - degruyter.com
The causes of cobalamin (B12, Cbl) deficiency are multifactorial. Whether nutritional due to
poor dietary intake, or functional due to impairments in absorption or intracellular processing …

Biomarkers and Algorithms for the Diagnosis of Vitamin B12 Deficiency

L Hannibal, V Lysne, AL Bjørke-Monsen… - Frontiers in molecular …, 2016 - frontiersin.org
Vitamin B12 (cobalamin, Cbl, B12) is an indispensable water-soluble micronutrient that
serves as a coenzyme for cytosolic methionine synthase (MS) and mitochondrial …

Intracellular processing of vitamin B12 by MMACHC (CblC)

L Hannibal, DW Jacobsen - Vitamins and hormones, 2022 - Elsevier
Abstract Vitamin B 12 (cobalamin, Cbl, B 12) is a water-soluble micronutrient synthesized
exclusively by a group of microorganisms. Human beings are unable to make B 12 and thus …

Versatile enzymology and heterogeneous phenotypes in cobalamin complementation type C disease

AJ Esser, S Mukherjee, IA Dereven'kov, SV Makarov… - Iscience, 2022 - cell.com
Nutritional deficiency and genetic errors that impair the transport, absorption, and utilization
of vitamin B 12 (B 12) lead to hematological and neurological manifestations. The cblC …

The MMACHC proteome: hallmarks of functional cobalamin deficiency in humans

L Hannibal, PM DiBello, M Yu, A Miller, S Wang… - Molecular genetics and …, 2011 - Elsevier
Abstract Cobalamin (Cbl, B 12) is an essential micronutrient required to fulfill the enzymatic
reactions of cytosolic methylcobalamin-dependent methionine synthase and mitochondrial …

[HTML][HTML] Vitamin B12 Metabolism: A Network of Multi-Protein Mediated Processes

P Mucha, F Kus, D Cysewski, RT Smolenski… - International Journal of …, 2024 - mdpi.com
The water-soluble vitamin, vitamin B 12, also known as cobalamin, plays a crucial role in
cellular metabolism, particularly in DNA synthesis, methylation, and mitochondrial …

The proteome of cblC defect: in vivo elucidation of altered cellular pathways in humans

M Caterino, A Pastore, MG Strozziero… - Journal of Inherited …, 2015 - Wiley Online Library
Methylmalonic acidemia with homocystinuria, cobalamin deficiency type C
(cblC)(MMACHC) is the most common inborn error of cobalamin metabolism. Despite a …

Thiolatocobalamins repair the activity of pathogenic variants of the human cobalamin processing enzyme CblC

V Wingert, S Mukherjee, AJ Esser, S Behringer… - Biochimie, 2021 - Elsevier
Thiolatocobalamins are a class of cobalamins comprised of naturally occurring and synthetic
ligands. Glutathionylcobalamin (GSCbl) occurs naturally in mammalian cells, and also as an …

Absence of an intracellular cobalamin-binding protein in cultured fibroblasts from patients with defective synthesis of 5′-deoxyadenosylcobalamin and …

LE Rosenberg, L Patel… - Proceedings of the …, 1975 - National Acad Sciences
Three distinct classes of human mutations (cbl A, cbl B, and cbl C) cause defective synthesis
of cobalamin (Cbl; vitamin B12) coenzymes. Cultured fibroblasts from that unique class (cbl …

Gene Identification for the cblD Defect of Vitamin B12 Metabolism

D Coelho, T Suormala, M Stucki… - … England Journal of …, 2008 - Mass Medical Soc
Background Vitamin B12 (cobalamin) is an essential cofactor in several metabolic pathways.
Intracellular conversion of cobalamin to its two coenzymes, adenosylcobalamin in …