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glycine catabolic process

Known as: glycine breakdown, glycine catabolism, glycine degradation 
The chemical reactions and pathways resulting in the breakdown of glycine, aminoethanoic acid. [GOC:go_curators]
National Institutes of Health

Papers overview

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Review
2012
Review
2012
The glycine deportation system and its pharmacological consequences.
The glycine deportation system is an essential component of glycine catabolism in man whereby 400 to 800mg glycine per day are… Expand
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2012
2012
The Purine-Utilizing Bacterium Clostridium acidurici 9a: A Genome-Guided Metabolic Reconsideration
Clostridium acidurici is an anaerobic, homoacetogenic bacterium, which is able to use purines such as uric acid as sole carbon… Expand
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2006
2006
Clinical variability in glycine encephalopathy
Glycine encephalopathy (GCE) is an autosomal recessive error of glycine degradation, resulting in a poor outcome with severe… Expand
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2002
2002
Pitfalls in the diagnosis of glycine encephalopathy (non-ketotic hyperglycinemia).
Non-ketotic hyperglycinemia (NKH), also termed glycine encephalopathy (MIM 605899), is an autosomal recessive inborn error of… Expand
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2000
2000
Pulmonary hypertension associated with nonketotic hyperglycinaemia
Nonketotic hyperglycinaemia (NKH) is an autosomal recessive disorder characterized by defective glycine degradation by the… Expand
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1996
1996
Efficacy of low-dose dextromethorphan in the treatment of nonketotic hyperglycinemia.
Nonketotic hyperglycinemia (NKH) is an inborn error of glycine degradation causing muscular hypotonia, seizures, apnea, and… Expand
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1989
1989
Regulation of hepatic glycine catabolism by glucagon.
Glucagon stimulates 14CO2 production from [1-14C] glycine by isolated rat hepatocytes. Maximal stimulation (70%) of… Expand
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1984
1984
Effects of Glycolate Pathway Intermediates on Glycine Decarboxylation and Serine Synthesis in Pea (Pisum sativum L.).
Glycine decarboxylation and serine synthesis were studied in pea (Pisum sativum L.) leaf discs, in metabolically active intact… Expand
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1981
1981
Prenatal brain damage in nonketotic hyperglycinemia.
Nonketotic hyperglycinemia (NKH) is a rare disorder of glycine degradation with autosomal recessive inheritance. 1 There are… Expand
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1978
1978
Glyoxylate decarboxylation during photorespiration
At 25° C under aerobic conditions with or without gluamate 10% of the [1-14C]glycollate oxidised in spinach leaf peroxisomes was… Expand
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