Gene Ontology annotation through association of InterPro records with GO terms
Manual transfer of experimentally-verified manual GO annotation data to orthologs by curator judgment of sequence similarity
Annotation inferences using phylogenetic trees
Gene Ontology annotation based on UniProtKB/Swiss-Prot Subcellular Location vocabulary mapping, accompanied by conservative changes to GO terms applied by UniProt
Gene Ontology annotation based on curation of immunofluorescence data
Automatic transfer of experimentally verified manual GO annotation data to orthologs using Ensembl Compara
Electronic Gene Ontology annotations created by ARBA machine learning models
Combined Automated Annotation using Multiple IEA Methods
Novel raf kinase protein-protein interactions found by an exhaustive yeast two-hybrid analysis.
Relationship between carbamoyl-phosphate synthetase genotype and systemic vascular function.
Comprehensive proteomic analysis of interphase and mitotic 14-3-3-binding proteins.
Release of the mitochondrial enzyme carbamoyl phosphate synthase under septic conditions.
The layered structure of human mitochondrial DNA nucleoids.
Cloning and sequence of a cDNA encoding human carbamyl phosphate synthetase I: molecular analysis of hyperammonemia.
Novel associations of CPS1, MUT, NOX4, and DPEP1 with plasma homocysteine in a healthy population: a genome-wide evaluation of 13 974 participants in the Women's Genome Health Study.
Proteomic and biochemical analysis of 14-3-3-binding proteins during C2-ceramide-induced apoptosis.
Molecular defects in human carbamoy phosphate synthetase I: mutational spectrum, diagnostic and protein structure considerations.
Molecular characterization of carbamoyl-phosphate synthetase (CPS1) deficiency using human recombinant CPS1 as a key tool.
Understanding carbamoyl phosphate synthetase (CPS1) deficiency by using the recombinantly purified human enzyme: effects of CPS1 mutations that concentrate in a central domain of unknown function.
Structure of human carbamoyl phosphate synthetase: deciphering the on/off switch of human ureagenesis.
Quantitative high-confidence human mitochondrial proteome and its dynamics in cellular context.
Human carbamylphosphate synthetase I. Stabilization, purification, and partial characterization of the enzyme from human liver.
Detection of carbamyl phosphate synthetase 1 deficiency using duodenal biopsy samples.
Carbamyl phosphate synthetase I deficiency. One base substitution in an exon of the CPS I gene causes a 9-basepair deletion due to aberrant splicing.
Prenatal diagnosis of carbamoyl phosphate synthetase I deficiency by identification of a missense mutation in CPS1.
2 ATP + NH4+ + HCO3- => 2 ADP + orthophosphate + carbamoyl phosphate [mitochondrial]
SIRT5 deglutarylates CPS1
CPS1 variants don't synthesize carbamoyl phosphate