Tag | Content |
---|---|
UniProt Accession | TY3H_HUMAN; P07101; |
Entrez ID | 7054 |
GenBank Protein ID | NM_000360.3; NM_199292.2; NM_199293.2; XM_011520335.2; |
GenBank Nucleotide ID | NP_000351.2; NP_954986.2; NP_954987.2; XP_011518637.1; |
Protein Name | Tyrosine 3-monooxygenase (EC 1.14.16.2) (Tyrosine 3-hydroxylase) (TH) |
Gene Name | TH; TYH |
Organism | Homo sapiens |
NCBI Taxa ID | 9606 |
Functional Description | Plays an important role in the physiology of adrenergic neurons. |
Sequence (Fasta) | MPTPDATTPQ AKGFRRAVSE LDAKQAEAIM VRGQGAPGPS LTGSPWPGTA APAASYTPTP 60 RSPRFIGRRQ SLIEDARKER EAAVAAAAAA VPSEPGDPLE AVAFEEKEGK AVLNLLFSPR 120 ATKPSALSRA VKVFETFEAK IHHLETRPAQ RPRAGGPHLE YFVRLEVRRG DLAALLSGVR 180 QVSEDVRSPA GPKVPWFPRK VSELDKCHHL VTKFDPDLDL DHPGFSDQVY RQRRKLIAEI 240 AFQYRHGDPI PRVEYTAEEI ATWKEVYTTL KGLYATHACG EHLEAFALLE RFSGYREDNI 300 PQLEDVSRFL KERTGFQLRP VAGLLSARDF LASLAFRVFQ CTQYIRHASS PMHSPEPDCC 360 HELLGHVPML ADRTFAQFSQ DIGLASLGAS DEEIEKLSTL YWFTVEFGLC KQNGEVKAYG 420 AGLLSSYGEL LHCLSEEPEI RAFDPEAAAV QPYQDQTYQS VYFVSESFSD AKDKLRSYAS 480 RIQRPFSVKF DPYTLAIDVL DSPQAVRRSL EGVQDELDTL AHALSAIG 529 |
|
Database | Annotation |
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CTD (Curated) (count: 15) (view all) | MESH:D001927
; Brain Diseases MESH:D006528 ; Carcinoma, Hepatocellular MESH:D002375 ; Catalepsy MESH:D004409 ; Dyskinesia, Drug-Induced MESH:D004421 ; Dystonia MESH:D006331 ; Heart Diseases |
GWASdb (count: 5) | rs2070762; Coronary heart disease; coronary artery disease
rs6356; Type 1 diabetes; type 1 diabetes mellitus rs7950050; LDL cholesterol; atherosclerosis|coronary artery disease rs10770141; Type 1 diabetes; type 1 diabetes mellitus rs10770141; Type 2 diabetes; type 2 diabetes mellitus |
PTM | Modification Sites |
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Phosphorylation (count: 10) (view all) | 118 AVLNLLFSPRATKPS dbPAF
19 KGFRRAVSELDAKQA dbPAF 230 PGFSDQVYRQRRKLI dbPAF 3 *****MPTPDATTPQ dbPAF 40 GQGAPGPSLTGSPWP dbPAF 419 QNGEVKAYGAGLLSS dbPAF |
Sumoylation (count: 1) | 474 SFSDAKDKLRSYASR PLMD |
Network | Interaction | ||
---|---|---|---|
A | B | Source | |