EC Number | Activating Compound | Comment | Organism | Structure |
---|---|---|---|---|
3.4.22.49 | cyclinB1 | - |
Homo sapiens | |
3.4.22.49 | imatinib | activation of separase proteolytic activity occurs exclusively in BCR-ABL-positive cells during imatinib treatment (0.00025-0.01 mM for 24 h) | Homo sapiens | |
3.4.22.49 | PP2A | - |
Homo sapiens | |
3.4.22.49 | securing | - |
Homo sapiens |
EC Number | Localization | Comment | Organism | GeneOntology No. | Textmining |
---|---|---|---|---|---|
3.4.22.49 | centrosome | - |
Homo sapiens | 5813 | - |
EC Number | Natural Substrates | Organism | Comment (Nat. Sub.) | Natural Products | Comment (Nat. Pro.) | Rev. | Reac. |
---|---|---|---|---|---|---|---|
3.4.22.49 | cohesin + H2O | Homo sapiens | - |
? | - |
? |
EC Number | Organism | UniProt | Comment | Textmining |
---|---|---|---|---|
3.4.22.49 | Homo sapiens | Q14674 | - |
- |
EC Number | Posttranslational Modification | Comment | Organism |
---|---|---|---|
3.4.22.49 | phosphoprotein | the enzyme is phosphorylated at serine residue 1126 | Homo sapiens |
EC Number | Source Tissue | Comment | Organism | Textmining |
---|---|---|---|---|
3.4.22.49 | fibroblast | - |
Homo sapiens | - |
3.4.22.49 | HL-60 cell | - |
Homo sapiens | - |
3.4.22.49 | K-562 cell | - |
Homo sapiens | - |
3.4.22.49 | LAMA-84 cell | - |
Homo sapiens | - |
3.4.22.49 | U-937 cell | - |
Homo sapiens | - |
3.4.22.49 | urothelial cell | - |
Homo sapiens | - |
3.4.22.49 | UROtsa cell | - |
Homo sapiens | - |
EC Number | Substrates | Comment Substrates | Organism | Products | Comment (Products) | Rev. | Reac. |
---|---|---|---|---|---|---|---|
3.4.22.49 | cohesin + H2O | - |
Homo sapiens | ? | - |
? |
EC Number | Organism | Comment | Expression |
---|---|---|---|
3.4.22.49 | Homo sapiens | decreased separase protein levels are observed in BCR-ABL-positive and -negative cells treated with imatinib in a dose dependent manner | down |
EC Number | General Information | Comment | Organism |
---|---|---|---|
3.4.22.49 | physiological function | separase is required for the separation of sister-chromatides in mitotic anaphase, triggers centriole disengagement during centrosome duplication. In cancer, separase is frequently overexpressed, pointing to a functional role as an aneuploidy promoter associated with centrosomal amplification and genomic instability | Homo sapiens |