Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

The human L-threonine 3-dehydrogenase gene is an expressed pseudogene.

BMC genetics - 2 Oct 2002

Edgar Alasdair J

Abstract excerpt

BACKGROUND: L-threonine is an indispensable amino acid. One of the major L-threonine degradation pathways is the conversion of L-threonine via 2-amino-3-ketobutyrate to glycine. L-threonine dehydrogenase (EC 1.1.1.103) is the first enzyme in the pathway and catalyses the reaction: L-threonine + NAD+ = 2-amino-3-ketobutyrate + NADH. The murine and porcine L-threonine dehydrogenase genes (TDH) have been identified...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Alcohol Oxidoreductases
Share to Codon, Terminator
Share to DNA Restriction Enzymes

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Protein Structure, Secondary

Share to Pseudogenes

Share to RNA Splice Sites

Share to Sequence Alignment

Share to Tissue Distribution

Source

Open in PubMed Open full text

Identifiers

PMID: 12361482
DOI: 10.1186/1471-2156-3-18
PMCID: PMC131051

Genes

CGA

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 8 closest

The human L-threonine 3-dehydrogenase gene is an expressed pseudogene.PMID 12361482Read ↗

Gains, Losses and Changes of Function after Gene Duplication: Study of the Metallothionein FamilySemantic proximity Read ↗

Clinical and molecular characterization of a novel selenocysteine insertion sequence-binding protein 2 (SBP2) gene mutation (R128X).Semantic proximity Read ↗

Isolation and characterization of a rat delta-aminolevulinate dehydratase processed pseudogene.Semantic proximity Read ↗

Mitochondrial acetoacetyl-coenzyme A thiolase gene: a novel 68-bp deletion involving 3' splice site of intron 7, causing exon 8 skipping in a Caucasian patient with beta-ketothiolase deficiency.Semantic proximity Read ↗

The human cytochrome P450 3A locus. Gene evolution by capture of downstream exons.Semantic proximity Read ↗

Molecular cloning and expression of novel sulphotransferase-like cDNAs from human and rat brainSemantic proximity Read ↗

Conserved nucleotide sequences in the open reading frame and 3' untranslated region of selenoprotein P mRNA.Semantic proximity Read ↗

Inherited defects of thyroxine-binding proteins.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.