Target intelligence / Profile preview

Tubulin-folding cofactor B (TBCB)

Target
TBCB
Molecular classification
Other, Molecular chaperone
01

Overview

Tubulin-folding cofactor B (TBCB) is a molecular chaperone involved in the biogenesis and regulation of α/β-tubulin heterodimers, acting downstream of cytosolic chaperonins to bind α-tubulin folding intermediates and guide proper tubulin assembly. TBCB forms complexes with other tubulin-folding cofactors, especially TBCE, regulating both the folding and dissociation of tubulin heterodimers. These activities are essential for microtubule organization, cell integrity, and proper cell division and growth. Disruption or altered expression of TBCB is associated with disorders of cytoskeletal dynamics, neurodevelopment, and diseases such as Kenny-Caffey syndrome[1][2][3][6][7].

Other names
Cytoskeleton-associated protein 1CKAP1CKAPITubulin-specific chaperone BCG22
02

Mechanism of action

Tubulin folding cofactors like TBCB participate in the biogenesis and homeostasis of tubulin dimers and can modulate microtubule stability, potentially affecting sensitivity to microtubule-modulating drugs like paclitaxel.

03

Biological functions

Microtubule organizationTubulin foldingRegulation of tubulin heterodimer dissociationRegulation of microtubule dynamicsNegative regulation of axonal growthCell divisionCell growth
04

Disease associations

Neurodevelopmental diseaseNeurodegenerative diseaseOther
05

Safety considerations

Disruption of TBCB activity may cause neurodevelopmental or cytoskeletal abnormalities, but not a direct therapeutic target
06

Interacting drugs

Paclitaxel (indirect, as a tubulin modulator)

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