Target intelligence / Profile preview

Calcineurin-binding protein cabin-1 (CABIN1)

Target
CABIN1
Molecular classification
Other (protein phosphatase inhibitor), Transcriptional regulator
01

Overview

Calcineurin-binding protein cabin-1 (CABIN1) is a nuclear protein encoded by the CABIN1 gene, which specifically binds to the activated form of the protein phosphatase calcineurin and inhibits its signal transduction, especially in the T-cell receptor pathway[1][2][5]. CABIN1 contains a leucine zipper domain and PEST motifs associated with protein-protein interactions and degradation, respectively[2]. It acts as a negative regulator of T-cell signaling, and has additional roles in regulating transcription factors such as MEF2 and p53, chromatin assembly, and cellular apoptosis[1][2][4][6]. CABIN1 associates with diseases involving immune dysregulation and neuronal development[2][4][6].\n\nNote: No drugs are currently known to specifically target CABIN1 for therapeutic modulation; clinically relevant immunosuppressants inhibit calcineurin directly, not CABIN1[3]. CABIN1 is a research target with potential implications in immune diseases, cancer, and neurological function.

Other names
CABIN1CAINPPP3INKIAA0330KB-318B8.7calcineurin inhibitorcalcineurin binding protein 1calcineurin-binding protein cabin-1
02

Mechanism of action

Theoretically, a drug could block CABIN1/calcineurin binding. It is involved in the inhibition of calcineurin-mediated dephosphorylation pathways.

03

Biological functions

Negative regulation of calcineurin-mediated signal transductionNegative regulation of T-cell receptor signalingChromatin assembly (replication-independent)Negative regulation of MEF2 transcriptional activityRegulation of p53/TP53 transcriptional functionApoptosisNeuronal development
04

Disease associations

SchwannomatosisLegius syndromeOther (implicated in immune regulation, apoptosis, and possibly cancer/autoimmune diseases due to role in signal transduction)
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Safety considerations

Therapeutic targeting may risk immune dysregulation or impact apoptosis, chromatin assembly, or neuronal development due to role in multiple pathways[2][4]

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