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  • 11.0 [archived version]
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FAM150A FAM150A FAM150B FAM150B GPBAR1 GPBAR1 UGT2B11 UGT2B11 DIO3 DIO3 DIO1 DIO1 UGT2B10 UGT2B10 SEPHS2 SEPHS2 SEPHS1 SEPHS1 SULT1A1 SULT1A1 SULT1A2 SULT1A2
"DIO1" - Type I iodothyronine deiodinase in Homo sapiens
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Predicted Interactions
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textmining
co-expression
protein homology
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DIO1Type I iodothyronine deiodinase; Responsible for the deiodination of T4 (3,5,3’,5’- tetraiodothyronine) into T3 (3,5,3’-triiodothyronine) and of T3 into T2 (3,3’-diiodothyronine). Plays a role in providing a source of plasma T3 by deiodination of T4 in peripheral tissues such as liver and kidney (249 aa)    
Predicted Functional Partners:
UGT2B10
UDP-glucuronosyltransferase 2B10; UDPGT is of major importance in the conjugation and subsequent elimination of potentially toxic xenobiotics and endogenous compounds; Belongs to the UDP-glycosyltransferase family (528 aa)
     
 
    0.913
DIO3
Thyroxine 5-deiodinase; Responsible for the deiodination of T4 (3,5,3’,5’- tetraiodothyronine) into RT3 (3,3’,5’-triiodothyronine) and of T3 (3,5,3’-triiodothyronine) into T2 (3,3’-diiodothyronine). RT3 and T2 are inactive metabolites. May play a role in preventing premature exposure of developing fetal tissues to adult levels of thyroid hormones. Can regulate circulating fetal thyroid hormone concentrations throughout gestation. Essential role for regulation of thyroid hormone inactivation during embryological development (304 aa)
         
0.911
UGT2B11
UDP-glucuronosyltransferase 2B11; UDPGT is of major importance in the conjugation and subsequent elimination of potentially toxic xenobiotics and endogenous compounds; Belongs to the UDP-glycosyltransferase family (529 aa)
     
 
    0.907
SULT1A1
Sulfotransferase 1A1; Sulfotransferase that utilizes 3’-phospho-5’-adenylyl sulfate (PAPS) as sulfonate donor to catalyze the sulfate conjugation of catecholamines, phenolic drugs and neurotransmitters. Has also estrogen sulfotransferase activity. responsible for the sulfonation and activation of minoxidil. Is Mediates the metabolic activation of carcinogenic N- hydroxyarylamines to DNA binding products and could so participate as modulating factor of cancer risk; Sulfotransferases, cytosolic (295 aa)
     
 
  0.906
SULT1A2
Sulfotransferase 1A2; Sulfotransferase that utilizes 3’-phospho-5’-adenylyl sulfate (PAPS) as sulfonate donor to catalyze the sulfate conjugation of catecholamines, phenolic drugs and neurotransmitters. Is also responsible for the sulfonation and activation of minoxidil. Mediates the metabolic activation of carcinogenic N-hydroxyarylamines to DNA binding products and could so participate as modulating factor of cancer risk; Sulfotransferases, cytosolic (295 aa)
     
 
    0.902
SEPHS2
Selenide, water dikinase 2; Synthesizes selenophosphate from selenide and ATP; Selenoproteins (483 aa)
     
   
  0.804
SEPHS1
Selenide, water dikinase 1; Synthesizes selenophosphate from selenide and ATP (392 aa)
     
   
  0.804
GPBAR1
G-protein coupled bile acid receptor 1; Receptor for bile acid. Bile acid-binding induces its internalization, activation of extracellular signal-regulated kinase and intracellular cAMP production. May be involved in the suppression of macrophage functions by bile acids (330 aa)
           
  0.715
FAM150B
ALK and LTK ligand 2; Ligand for receptor tyrosine kinases LTK and ALK. Stimulation of ALK signaling may be involved in regulation of cell proliferation and transformation (152 aa)
           
  0.712
FAM150A
ALK and LTK ligand 1; Ligand for receptor tyrosine kinase LTK and perhaps receptor tyrosine kinase ALK; activation of ALK is reported conflictingly (129 aa)
           
  0.712
Your Current Organism:
Homo sapiens
NCBI taxonomy Id: 9606
Other names: H. sapiens, Homo sapiens, human, man
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