KEGG    Network variation - Dopamine and serotonin metabolism
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ENTRYnt06028
NameDopamine and serotonin metabolism
CategoryPathway view; Amino acid metabolism
Pathwayhsa00350 Tyrosine metabolism
hsa00380 Tryptophan metabolism
hsa00790 Folate biosynthesis
hsa04728 Dopaminergic synapse
Modulehsa_M00842 Tetrahydrobiopterin biosynthesis, GTP => BH4
Display drug-target relation   disease type
N01530    Tyr+BH4−TH→L-Dopa−DDC→Dopamine−MAO→DOPAL
    Dopa-responsive dystonia   TH*
       D1
 |
    AADC deficiency       DDC*
    Brunner syndrome           MAOA*
 
N01037    PD SNCA*⌿TH→L-Dopa
N01039    PD         PRKN*⌿MAO→DOPAL
N01040            Dopamine−VMAT→Dopamine(SV)
N01041    PD         SNCA*⊣VMAT2
    PKDYS2           VMAT2*
N01790            Dopamine(outer)−DAT→Dopamine(inner)
    PKDYS1           DAT*
 
N01550    Dopamine−DBH→Noradrenaline−PNMT→Adrenaline−MAO→DOPEGAL
    DBH deficiency   DBH*
    Brunner syndrome           MAOA*
 
N01551      Trp−TPH1/2⇉DDC→Serotonin−MAO→5-HIAL
    MDD/ADHD     TPH2*
       D1
 |
    AADC deficiency       DDC*
    Brunner syndrome           MAOA*
 
N01552    Tyr−TYR→Dopaquinone−DCT⇉TYRP1→Eumelanin
    OCA1   TYR*
    OCA8       DCT*
    OCA3         TYRP1*
 
N00702    GTP−GCH1⇉PTS⇉SPR→BH4
    Dopa-responsive dystonia   GCH1*
    SPR deficiency       SPR*

Disease nameDisease category
Dopa-responsive dystonia H02557Dopa-responsive dystoniaNervous system disease
AADC deficiencyH01161Aromatic L-amino acid decarboxylase deficiencyNervous system disease
Brunner syndromeH00548Brunner syndromeInherited metabolic disorder
PDH00057Parkinson diseaseNeurodegenerative disease
PKDYS2H02676Infantile-onset parkinsonism-dystoniaNervous system disease
PKDYS1H02676Infantile-onset parkinsonism-dystoniaNervous system disease
DBH deficiencyH01005Dopamine beta-hydroxylase deficiencyNervous system disease
MDD/ADHDH01646Major depressive disorderMental and behavioural disorder
H01895Attention deficit hyperactivity disorder (ADHD)Mental and behavioural disorder
OCA1H00168Oculocutaneous albinismInherited metabolic disorder
OCA8H00168Oculocutaneous albinismInherited metabolic disorder
OCA3H00168Oculocutaneous albinismInherited metabolic disorder
Dopa-responsive dystoniaH02557Dopa-responsive dystoniaNervous system disease
SPR deficiencyH02597Sepiapterin reductase deficiencyInherited metabolic disorder


Drug name
D1D12407Eladocagene exuparvovec (USAN/INN)