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UniProtKB/Swiss-Prot variant pages

UniProtKB/Swiss-Prot P07101: Variant p.Ile394Thr

Tyrosine 3-monooxygenase
Gene: TH
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Variant information Variant position: help 394 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Type of variant: help LP/P [Disclaimer] The variants are classified into three categories: LP/P, LB/B and US.
  • LP/P: likely pathogenic or pathogenic.
  • LB/B: likely benign or benign.
  • US: uncertain significance

Residue change: help From Isoleucine (I) to Threonine (T) at position 394 (I394T, p.Ile394Thr). Indicates the amino acid change of the variant. The one-letter and three-letter codes for amino acids used in UniProtKB/Swiss-Prot are those adopted by the commission on Biochemical Nomenclature of the IUPAC-IUB.
Physico-chemical properties: help Change from medium size and hydrophobic (I) to medium size and polar (T) The physico-chemical property of the reference and variant residues and the change implicated.
BLOSUM score: help -1 The score within a Blosum matrix for the corresponding wild-type to variant amino acid change. The log-odds score measures the logarithm for the ratio of the likelihood of two amino acids appearing by chance. The Blosum62 substitution matrix is used. This substitution matrix contains scores for all possible exchanges of one amino acid with another:
  • Lowest score: -4 (low probability of substitution).
  • Highest score: 11 (high probability of substitution).
More information can be found on the following page

Variant description: help In ARSEGS; complete loss of tyrosine 3-monooxygenase activity. Any additional useful information about the variant.


Sequence information Variant position: help 394 The position of the amino-acid change on the UniProtKB canonical protein sequence.
Protein sequence length: help 528 The length of the canonical sequence.
Location on the sequence: help TFAQFSQDIGLASLGASDEE I EKLSTLYWFTVEFGLCKQNG The residue change on the sequence. Unless the variant is located at the beginning or at the end of the protein sequence, both residues upstream (20) and downstream (20) of the variant will be shown.
Residue conservation: help The multiple alignment of the region surrounding the variant against various orthologous sequences.
Human                         TFAQFSQDIGLASLGASDEEIEKLSTLYWFTVEFGLCKQNG

                              TFAQFSQDIGLASLGASDEEIEKLSTLYWFTVEFGLCKQNG

Mouse                         TFAQFSQDIGLASLGASDEEIEKLSTVYWFTVEFGLCKQNG

Rat                           TFAQFSQDIGLASLGASDEEIEKLSTVYWFTVEFGLCKQNG

Bovine                        TFAQFSQDIGLASLGVSDEEIEKLSTLYWFTVEFGLCKQNG

Caenorhabditis elegans        LLAQMSQDIGLMSLGASDEHIEKLSTVYWFIVEFGLCKEDG

Drosophila                    SFAQFSQEIGLASLGASDEEIEKLSTVYWFTVEFGLCKEHG

Sequence annotation in neighborhood: help The regions or sites of interest surrounding the variant. In general the features listed are posttranslational modifications, binding sites, enzyme active sites, local secondary structure or other characteristics reported in the cited references. The "Sequence annotation in neighborhood" lines have a fixed format:
  • Type: the type of sequence feature.
  • Positions: endpoints of the sequence feature.
  • Description: contains additional information about the feature.
TypePositionsDescription
Chain 1 – 528 Tyrosine 3-monooxygenase
Binding site 406 – 406
Helix 391 – 403



Literature citations
Tyrosine hydroxylase deficiency: a treatable disorder of brain catecholamine biosynthesis.
Willemsen M.A.; Verbeek M.M.; Kamsteeg E.J.; de Rijk-van Andel J.F.; Aeby A.; Blau N.; Burlina A.; Donati M.A.; Geurtz B.; Grattan-Smith P.J.; Haeussler M.; Hoffmann G.F.; Jung H.; de Klerk J.B.; van der Knaap M.S.; Kok F.; Leuzzi V.; de Lonlay P.; Megarbane A.; Monaghan H.; Renier W.O.; Rondot P.; Ryan M.M.; Seeger J.; Smeitink J.A.; Steenbergen-Spanjers G.C.; Wassmer E.; Weschke B.; Wijburg F.A.; Wilcken B.; Zafeiriou D.I.; Wevers R.A.;
Brain 133:1810-1822(2010)
Cited for: VARIANTS ARSEGS TYR-207; GLY-227; THR-241; GLY-259 AND THR-394; Biochemical and molecular characterization of tyrosine hydroxylase deficiency in Hong Kong Chinese.
Mak C.M.; Lam C.W.; Siu T.S.; Chan K.Y.; Siu W.K.; Yeung W.L.; Hui J.; Wong V.C.; Low L.C.; Ko C.H.; Fung C.W.; Chen S.P.; Yuen Y.P.; Lee H.C.; Yau E.; Chan B.; Tong S.F.; Tam S.; Chan Y.W.;
Mol. Genet. Metab. 99:431-433(2010)
Cited for: VARIANTS ARSEGS ARG-294; SER-315; VAL-385; THR-394 AND ARG-408; Functional studies of tyrosine hydroxylase missense variants reveal distinct patterns of molecular defects in Dopa-responsive dystonia.
Fossbakk A.; Kleppe R.; Knappskog P.M.; Martinez A.; Haavik J.;
Hum. Mutat. 35:880-890(2014)
Cited for: FUNCTION; CATALYTIC ACTIVITY; BIOPHYSICOCHEMICAL PROPERTIES; CHARACTERIZATION OF VARIANTS ARSEGS TYR-207; GLY-227; HIS-233; PRO-236; THR-241; TYR-246; SER-247; GLY-259; PRO-276; ALA-301; SER-309; MET-314; PRO-319; TRP-328; HIS-337; PHE-359; LEU-375; VAL-376; MET-387; THR-394; MET-399; LYS-412; ARG-414; PRO-441; GLY-467; LEU-492; MET-494; GLY-498 AND GLN-510;
Disclaimer: Any medical or genetic information present in this entry is provided for research, educational and informational purposes only. They are not in any way intended to be used as a substitute for professional medical advice, diagnostic, treatment or care.