Target intelligence / Profile preview

ABL1 and Src family tyrosine kinases (ABL1 and Src family)

Target
ABL1 and Src family
Molecular classification
Enzyme, Protein kinase (specifically: non-receptor tyrosine kinase), Signal transducer
01

Overview

The ABL1 tyrosine kinase is a non-receptor enzyme, encoded by the ABL1 gene on chromosome 9, involved in cell signaling pathways regulating proliferation, differentiation, survival, apoptosis, migration, and cytoskeletal dynamics through actin modulation. In its mutant or fusion form (BCR-ABL1), it drives chronic myeloid leukemia and other cancers by constitutive activation. The kinase possesses multiple functional domains (KD, SH2, SH3), with tightly regulated activity and complex structural dynamics. The Src family tyrosine kinases are related enzymes, each with unique cellular roles but sharing mechanisms of signal transduction and oncogenesis, implicated in various cancer types and also targeted by kinase inhibitor drugs.\n\nNote: The target "ABL1 and Src family tyrosine kinases" collectively refers to multiple individual proteins rather than a single molecule, and information should be parsed for either ABL1 or each Src family member for specific experimental or clinical use.

Other names
Abelson murine leukemia viral oncogene homolog 1Abelson tyrosine-protein kinase 1c-Ablproto-oncogene c-AblJTK7p150Proto-oncogene tyrosine-protein kinase SrcFynYesLynLckHckBlkFgrYrkSrc kinases
02

Mechanism of action

TKIs (Tyrosine kinase inhibitors) bind to kinase domain, blocking ATP-binding and kinase activity, thereby inhibiting downstream signaling critical for cell proliferation and survival. Allosteric inhibitors (e.g., asciminib for ABL1) bind outside the ATP site, further modulating kinase activity.

03

Biological functions

Signal transductionCell proliferationCell differentiationCell survival and apoptosisCell migration and adhesionCytoskeletal organization (especially actin polymerization)DNA damage responseTranscriptional regulation
04

Disease associations

Cancer (especially chronic myeloid leukemia, acute lymphoblastic leukemia, and multiple solid tumors)InflammationInfection (pathogen manipulation of kinase signaling)Neurodegenerative disease (increasingly recognized for ABL1)Other proliferative disorders
05

Safety considerations

Off-target inhibition of other kinases leading to toxicity (e.g., myelosuppression, cardiovascular effects, fluid retention, QT prolongation, hepatotoxicity)Resistance mutations (such as T315I in BCR-ABL1)Immunosuppression and infection risk with prolonged therapy
06

Interacting drugs

6 more in the full profile.

07

Biomarkers

BCR-ABL1 fusion gene or protein expression (for CML diagnosis/monitoring)Phosphorylated substrates (e.g., Tyr412 autophosphorylation for ABL1 activity)Src activation/phosphorylation status (used in oncology research and some clinical contexts)

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