Protein family
Protein sequence
Protein function
Catalytic activity
EC number
EC number description
3.5.4.4
Hydrolases;
Acting on carbon-nitrogen bonds, other than peptide bonds;
In cyclic amidines;
adenosine deaminase
GO ontology | GO term | GO description |
---|---|---|
Biological Process | GO:0006196 | AMP catabolic process |
Biological Process | GO:0044209 | AMP salvage |
Biological Process | GO:0042100 | B cell proliferation |
Biological Process | GO:0032263 | GMP salvage |
Biological Process | GO:0048541 | Peyer's patch development |
Biological Process | GO:0042110 | T cell activation |
Biological Process | GO:0033077 | T cell differentiation in thymus |
Biological Process | GO:0050852 | T cell receptor signaling pathway |
Biological Process | GO:0006154 | adenosine catabolic process |
Biological Process | GO:0046085 | adenosine metabolic process |
Biological Process | GO:0000255 | allantoin metabolic process |
Biological Process | GO:0046632 | alpha-beta T cell differentiation |
Biological Process | GO:0043605 | amide catabolic process |
Biological Process | GO:0019722 | calcium-mediated signaling |
Biological Process | GO:0007155 | cell adhesion |
Biological Process | GO:0046059 | dAMP catabolic process |
Biological Process | GO:0046061 | dATP catabolic process |
Biological Process | GO:0006157 | deoxyadenosine catabolic process |
Biological Process | GO:0048566 | embryonic digestive tract development |
Biological Process | GO:0002314 | germinal center B cell differentiation |
Biological Process | GO:0002467 | germinal center formation |
Biological Process | GO:0043103 | hypoxanthine salvage |
Biological Process | GO:0046103 | inosine biosynthetic process |
Biological Process | GO:0050900 | leukocyte migration |
Biological Process | GO:0001889 | liver development |
Biological Process | GO:0048286 | lung alveolus development |
Biological Process | GO:0002901 | mature B cell apoptotic process |
Biological Process | GO:0070254 | mucus secretion |
Biological Process | GO:0060169 | negative regulation of adenosine receptor signaling pathway |
Biological Process | GO:0050728 | negative regulation of inflammatory response |
Biological Process | GO:0002686 | negative regulation of leukocyte migration |
Biological Process | GO:0002906 | negative regulation of mature B cell apoptotic process |
Biological Process | GO:0070256 | negative regulation of mucus secretion |
Biological Process | GO:0060407 | negative regulation of penile erection |
Biological Process | GO:0070244 | negative regulation of thymocyte apoptotic process |
Biological Process | GO:0043084 | penile erection |
Biological Process | GO:0001890 | placenta development |
Biological Process | GO:0030890 | positive regulation of B cell proliferation |
Biological Process | GO:0033089 | positive regulation of T cell differentiation in thymus |
Biological Process | GO:0050862 | positive regulation of T cell receptor signaling pathway |
Biological Process | GO:0046638 | positive regulation of alpha-beta T cell differentiation |
Biological Process | GO:0050850 | positive regulation of calcium-mediated signaling |
Biological Process | GO:0002636 | positive regulation of germinal center formation |
Biological Process | GO:0010460 | positive regulation of heart rate |
Biological Process | GO:0045987 | positive regulation of smooth muscle contraction |
Biological Process | GO:0032261 | purine nucleotide salvage |
Biological Process | GO:0043101 | purine-containing compound salvage |
Biological Process | GO:0033632 | regulation of cell-cell adhesion mediated by integrin |
Biological Process | GO:0001666 | response to hypoxia |
Biological Process | GO:0010035 | response to inorganic substance |
Biological Process | GO:0014074 | response to purine-containing compound |
Biological Process | GO:0006939 | smooth muscle contraction |
Biological Process | GO:0070242 | thymocyte apoptotic process |
Biological Process | GO:0001829 | trophectodermal cell differentiation |
Biological Process | GO:0046111 | xanthine biosynthetic process |
Biological Process | GO:0006805 | xenobiotic metabolic process |
Molecular Function | GO:0046936 | 2'-deoxyadenosine deaminase activity |
Molecular Function | GO:0004000 | adenosine deaminase activity |
Molecular Function | GO:0019239 | deaminase activity |
Molecular Function | GO:0008270 | zinc ion binding |
Cellular Component | GO:0070161 | anchoring junction |
Cellular Component | GO:0009986 | cell surface |
Cellular Component | GO:0060205 | cytoplasmic vesicle lumen |
Cellular Component | GO:0005829 | cytosol |
Cellular Component | GO:0009897 | external side of plasma membrane |
Cellular Component | GO:0005764 | lysosome |
Cellular Component | GO:0016020 | membrane |
Cellular Component | GO:0005886 | plasma membrane |
Reactome | Reactome Name | Node type | Reactome Root | Reactome Root Name |
---|---|---|---|---|
R-HSA-74217 | Purine salvage | Leaf | R-HSA-1430728 | Metabolism |
R-HSA-9734735 | Defective ADA disrupts (deoxy)adenosine deamination | Leaf | R-HSA-1643685 | Disease |
R-HSA-9755088 | Ribavirin ADME | Leaf | R-HSA-9748784 | Drug ADME |
Location | ECO term | Pubmed |
---|---|---|
Cell junction | ECO:0000269 | PubMed:11772392 |
Cell membrane | ECO:0000269 | PubMed:11772392 |
Cell membrane | ECO:0000269 | PubMed:8101391 |
Cytoplasm | ECO:0000250 | |
Cytoplasmic vesicle lumen | ECO:0000250 | |
Lysosome | ECO:0000269 | PubMed:8452534 |
HPO ID | HPO name |
---|---|
HP:0000007 | Autosomal recessive inheritance |
HP:0000100 | Nephrotic syndrome |
HP:0000246 | Sinusitis |
HP:0000403 | Recurrent otitis media |
HP:0000821 | Hypothyroidism |
HP:0000907 | Anterior rib cupping |
HP:0000926 | Platyspondyly |
HP:0000944 | Abnormal metaphysis morphology |
HP:0000958 | Dry skin |
HP:0000969 | Edema |
HP:0000988 | Skin rash |
HP:0000989 | Pruritus |
HP:0001019 | Erythroderma |
HP:0001072 | Thickened skin |
HP:0001270 | Motor delay |
HP:0001442 | Somatic mosaicism |
HP:0001508 | Failure to thrive |
HP:0001596 | Alopecia |
HP:0001744 | Splenomegaly |
HP:0001831 | Short toe |
HP:0001880 | Eosinophilia |
HP:0001888 | Lymphopenia |
HP:0001890 | Autoimmune hemolytic anemia |
HP:0001903 | Anemia |
HP:0001945 | Fever |
HP:0001954 | Recurrent fever |
HP:0001967 | Diffuse mesangial sclerosis |
HP:0001973 | Autoimmune thrombocytopenia |
HP:0001974 | Leukocytosis |
HP:0002014 | Diarrhea |
HP:0002028 | Chronic diarrhea |
HP:0002090 | Pneumonia |
HP:0002099 | Asthma |
HP:0002240 | Hepatomegaly |
HP:0002644 | Abnormal pelvic girdle bone morphology |
HP:0002665 | Lymphoma |
HP:0002716 | Lymphadenopathy |
HP:0002718 | Recurrent bacterial infections |
HP:0002720 | Decreased circulating IgA level |
HP:0002728 | Chronic mucocutaneous candidiasis |
HP:0002788 | Recurrent upper respiratory tract infections |
HP:0002841 | Recurrent fungal infections |
HP:0002849 | Absence of lymph node germinal center |
HP:0002850 | Decreased circulating total IgM |
HP:0002960 | Autoimmunity |
HP:0003212 | Increased circulating IgE level |
HP:0003593 | Infantile onset |
HP:0003623 | Neonatal onset |
HP:0004332 | Abnormal lymphocyte morphology |
HP:0004429 | Recurrent viral infections |
HP:0004430 | Severe combined immunodeficiency |
HP:0005354 | Lack of T cell function |
HP:0005359 | Aplasia of the thymus |
HP:0005365 | Severe B lymphocytopenia |
HP:0005368 | Abnormality of humoral immunity |
HP:0005390 | Recurrent opportunistic infections |
HP:0005403 | T lymphocytopenia |
HP:0005424 | Absent specific antibody response |
HP:0006532 | Recurrent pneumonia |
HP:0007549 | Desquamation of skin soon after birth |
HP:0008348 | Decreased circulating IgG2 level |
HP:0010444 | Pulmonary insufficiency |
HP:0010976 | B lymphocytopenia |
HP:0011123 | Inflammatory abnormality of the skin |
HP:0012191 | B-cell lymphoma |
HP:0012393 | Allergy |
HP:0025379 | Anti-thyroid peroxidase antibody positivity |
HP:0030273 | Reduced red cell adenosine deaminase level |
HP:0030813 | Absent tonsils |
HP:0031164 | Growth arrest lines |
HP:0031233 | Horizontal inferior border of scapula |
HP:0100646 | Thyroiditis |
HP:0100806 | Sepsis |
HP:0100840 | Aplasia/Hypoplasia of the eyebrow |
Disease name | MONDO ID | ICD10 | ICD10 chapter | OMIM | Orphanet |
---|---|---|---|---|---|
severe combined immunodeficiency, autosomal recessive, t cell-negative, b cell-negative, nk cell-negative, due to adenosine deaminase deficiency | MONDO:0007064 | D81 | chapter3, Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism | OMIM:102700 | Orphanet:277 |
severe combined immunodeficiency, autosomal recessive, t cell-negative, b cell-negative, nk cell-positive | MONDO:0011086 | D81 | chapter3, Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism | OMIM:601457 | Orphanet:331206 |
omenn syndrome | MONDO:0011338 | D81 | chapter3, Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism | OMIM:603554 | Orphanet:39041 |