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
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
cDNA sequence and kinetic properties of human lung fructose(1, 6)bisphosphatase.
A human protein-protein interaction network: a resource for annotating the proteome.
Towards a proteome-scale map of the human protein-protein interaction network.
Identification of VCP/p97, carboxyl terminus of Hsp70-interacting protein (CHIP), and amphiphysin II interaction partners using membrane-based human proteome arrays.
Benzoxazole benzenesulfonamides are novel allosteric inhibitors of fructose-1,6-bisphosphatase with a distinct binding mode.
Glu 69 is essential for the high sensitivity of muscle fructose-1,6-bisphosphatase inhibition by calcium ions.
Allosteric FBPase inhibitors gain 10(5) times in potency when simultaneously binding two neighboring AMP sites.
Large-scale proteomics and phosphoproteomics of urinary exosomes.
Novel FBP1 gene mutations in Arab patients with fructose-1,6-bisphosphatase deficiency.
Warburg effect revisited: an epigenetic link between glycolysis and gastric carcinogenesis.
Novel compound heterozygous mutations in the fructose-1,6-bisphosphatase gene cause hypoglycemia and lactic acidosis.
Next-generation sequencing to generate interactome datasets.
In-depth proteomic analyses of exosomes isolated from expressed prostatic secretions in urine.
Fructose-1,6-bisphosphatase opposes renal carcinoma progression.
A proteome-scale map of the human interactome network.
A massively parallel pipeline to clone DNA variants and examine molecular phenotypes of human disease mutations.
Widespread macromolecular interaction perturbations in human genetic disorders.
Architecture of the human interactome defines protein communities and disease networks.
Extensive disruption of protein interactions by genetic variants across the allele frequency spectrum in human populations.
A reference map of the human binary protein interactome.
Interactome Mapping Provides a Network of Neurodegenerative Disease Proteins and Uncovers Widespread Protein Aggregation in Affected Brains.
Dual proteome-scale networks reveal cell-specific remodeling of the human interactome.
Human fructose-1,6-bisphosphatase gene (FBP1): exon-intron organization, localization to chromosome bands 9q22.2-q22.3, and mutation screening in subjects with fructose-1,6-bisphosphatase deficiency.
Isolation of a human liver fructose-1,6-bisphosphatase cDNA and expression of the protein in Escherichia coli. Role of ASP-118 and ASP-121 in catalysis.
FBP tetramers hydrolyze F1,6PP to Fru(6)P
TCF19:NuRD represses FBP1 gene expression
Fructose 1,6-bisphosphatase deficiency: clinical, biochemical and genetic features in French patients.
Identification of genetic mutations in Japanese patients with fructose-1,6-bisphosphatase deficiency.
Expression of human fructose-1,6-bisphosphatase in the liver of transgenic mice results in increased glycerol gluconeogenesis.
Hepatic but not Intestinal FBP1 Is Required for Fructose Metabolism and Tolerance.
Identification of genotype-biochemical phenotype correlations associated with fructose 1,6-bisphosphatase deficiency.
UniProt entry P09467 (FBP1_HUMAN)