EC Number | Inhibitors | Comment | Organism | Structure |
---|---|---|---|---|
3.1.2.22 | additional information | no inhibition by EDTA | Homo sapiens |
EC Number | Localization | Comment | Organism | GeneOntology No. | Textmining |
---|---|---|---|---|---|
3.1.2.22 | lysosome | - |
Homo sapiens | 5764 | - |
EC Number | Natural Substrates | Organism | Comment (Nat. Sub.) | Natural Products | Comment (Nat. Pro.) | Rev. | Reac. |
---|---|---|---|---|---|---|---|
3.1.2.22 | additional information | Homo sapiens | PPT1 deficiency causes, together with tripeptidyl peptidase 1 deficiency, progressive neurological disorder infantile neuronal ceroid lipofuscinosis, a group of at least 8 inherited, progressive encephalopathies that are characterized by lipofuscin-like inclusions in various tissues and have been classified as CNL1-CNL8 | ? | - |
? |
EC Number | Organism | UniProt | Comment | Textmining |
---|---|---|---|---|
3.1.2.22 | Homo sapiens | - |
lysosomal enzyme forms PPT1 | - |
EC Number | Reaction | Comment | Organism | Reaction ID |
---|---|---|---|---|
3.1.2.22 | palmitoyl[protein] + H2O = palmitate + protein | specific for long-chain thioesters of fatty acids from S-acylated residues in proteins, palmitoyl cysteine and palmitoyl-CoA | Homo sapiens |
EC Number | Source Tissue | Comment | Organism | Textmining |
---|---|---|---|---|
3.1.2.22 | blood | - |
Homo sapiens | - |
3.1.2.22 | leukocyte | - |
Homo sapiens | - |
3.1.2.22 | skin fibroblast | very low or no activity | Homo sapiens | - |
EC Number | Specific Activity Minimum [µmol/min/mg] | Specific Activity Maximum [µmol/min/mg] | Comment | Organism |
---|---|---|---|---|
3.1.2.22 | additional information | - |
- |
Homo sapiens |
EC Number | Substrates | Comment Substrates | Organism | Products | Comment (Products) | Rev. | Reac. |
---|---|---|---|---|---|---|---|
3.1.2.22 | 4-methylumbelliferyl 6-S-palmitoyl-6-thio-beta-D-glucoside + H2O | - |
Homo sapiens | 4-methylumbelliferyl 6-thio-beta-D-glucoside + palmitate | - |
? | |
3.1.2.22 | additional information | enzyme assay development | Homo sapiens | ? | - |
? | |
3.1.2.22 | additional information | PPT1 deficiency causes, together with tripeptidyl peptidase 1 deficiency, progressive neurological disorder infantile neuronal ceroid lipofuscinosis, a group of at least 8 inherited, progressive encephalopathies that are characterized by lipofuscin-like inclusions in various tissues and have been classified as CNL1-CNL8 | Homo sapiens | ? | - |
? |
EC Number | Synonyms | Comment | Organism |
---|---|---|---|
3.1.2.22 | palmitoyl protein thioesterase 1 | - |
Homo sapiens |
3.1.2.22 | PPT1 | - |
Homo sapiens |
EC Number | Temperature Optimum [°C] | Temperature Optimum Maximum [°C] | Comment | Organism |
---|---|---|---|---|
3.1.2.22 | 22 | - |
assay at, room temperature | Homo sapiens |
EC Number | pH Optimum Minimum | pH Optimum Maximum | Comment | Organism |
---|---|---|---|---|
3.1.2.22 | 4 | - |
assay at | Homo sapiens |