Tryptophan 5-hydroxylase 2
Also known as: NTPH, TPH2
Classification
- Family (Pfam)
- PF00351 Biopterin_H
- InterPro
- ACT-like_dom_sf, ACT_dom, ArAA_hydroxylase, ArAA_hydroxylase_Fe/CU_BS, ArAA_hydroxylase_sf, Aro-AA_hydroxylase_C_sf, Aromatic-AA_hydroxylase_C, Trp_5_mOase, TrpOH_cat, Tyrosine_3-monooxygenase-like
- Functional cluster
- Oxidoreductases, Catalases & Peroxidases
Experimental structures · PDB · 5
A predicted model is available from AlphaFold.
Gene Ontology · 6
Disease associations
- major depressive disorder MONDO:0002009
- attention deficit-hyperactivity disorder, susceptibility to, 7 MONDO:0013076
Drugs targeting this protein · 3
- TELOTRISTAT inhibitor
- TELOTRISTAT ETHYL inhibitor
- TELOTRISTAT ETIPRATE inhibitor
Related proteins · sequence + function similarity
- Tryptophan 5-hydroxylase 2 0.99
- Tryptophan 5-hydroxylase 2 0.99
- Tryptophan 5-hydroxylase 2 0.99
- Tryptophan 5-hydroxylase 2 0.99
- Tryptophan 5-hydroxylase 0.94
- Tryptophan 5-hydroxylase 1 0.93
- Tryptophan 5-hydroxylase 1 0.93
- Tryptophan 5-hydroxylase 1 0.91
- Tryptophan 5-hydroxylase 1 0.90
- Tryptophan 5-hydroxylase 1 0.90
- Protein henna 0.89
- Phenylalanine-4-hydroxylase 0.88
Co-cited proteins · studied together in the literature
- Tryptophan 5-hydroxylase 2 1 shared papers
- Tryptophan 5-hydroxylase 2 1 shared papers
Literature · 9 cited papers
- The A328 V/E (rs2887147) polymorphisms in human tryptophan hydroxylase 2 compromise enzyme activity. Biochem. Biophys. Rep. · 2023
- Alternative splicing and extensive RNA editing of human TPH2 transcripts. PLoS ONE · 2010
- Functional properties of missense variants of human tryptophan hydroxylase 2. Hum. Mutat. · 2009
- A loss-of-function mutation in tryptophan hydroxylase 2 segregating with attention-deficit/hyperactivity disorder. Mol. Psychiatry · 2008
- Brain-specific tryptophan hydroxylase 2 (TPH2): a functional Pro206Ser substitution and variation in the 5'-region are associated with bipolar affective disorder. Hum. Mol. Genet. · 2008
- The finished DNA sequence of human chromosome 12. Nature · 2006
- Loss-of-function mutation in tryptophan hydroxylase-2 identified in unipolar major depression. Neuron · 2005
- The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). Genome Res. · 2004
- Synthesis of serotonin by a second tryptophan hydroxylase isoform. Science · 2003
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