Annotation inferences using phylogenetic trees
UniProtKB/Swiss-Prot entry Q93099 (HGD_HUMAN)
Falcon (Edison Scientific) deep research report on human HGD
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HGD is a cytosolic enzyme of the tyrosine catabolic pathway.
"HGD functions as a cytosolic enzyme."
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The functional enzyme is a hexamer organized as a dimer of trimers.
"The crystal structure of human HGD reveals that the functional enzyme is a hexamer organized as a dimer of trimers"
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A 2026 report describes a non-canonical tryptophan-oxidizing activity of HGD in small cell lung cancer; this is not yet independently replicated and is not annotated here.
"HGD is highly upregulated under chemotherapeutic stress and catalyzes the oxidation of tryptophan to N-formylkynurenine (FK)"
PAINT IBD nodes for PTHR11056
Combined Automated Annotation using Multiple IEA Methods
The molecular basis of alkaptonuria.
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HGD (originally HGO) is the alkaptonuria gene; alkaptonuria results from loss of homogentisate 1,2-dioxygenase activity, causing accumulation of homogentisic acid, an intermediary product of tyrosine and phenylalanine catabolism.
Untargeted NMR Metabolomics Reveals Alternative Biomarkers and Pathways in Alkaptonuria.
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Homogentisic acid, the substrate of HGD, is an intermediate of phenylalanine and tyrosine degradation; the aromatic ring is opened and oxidized by the hexameric homogentisate 1,2-dioxygenase, and reduced HGD catalytic activity causes HGA accumulation in alkaptonuria.
Crystal structure of human homogentisate dioxygenase.
Genome-wide YFP fluorescence complementation screen identifies new regulators for telomere signaling in human cells.
A proteome-scale map of the human interactome network.
A reference map of the human binary protein interactome.
In-depth proteomic analyses of exosomes isolated from expressed prostatic secretions in urine.
Large-scale proteomics and phosphoproteomics of urinary exosomes.
HGD dioxygenates homogentisate