Target intelligence / Profile preview

Leucine-rich repeat-containing protein 49 (LRRC49)

Target
LRRC49
Molecular classification
Other (leucine-rich repeat-containing protein), Structural/regulatory protein involved in centriolar satellite and tubulin polyglutamylase complexes
01

Overview

Leucine-rich repeat-containing protein 49 (LRRC49) is a protein encoded by the LRRC49 gene in humans and is primarily localized in centriolar satellites within the cytoplasm[1][7]. It serves as a subunit of the tubulin polyglutamylase complex (TPGC), which plays an essential role in microtubule polyglutamylation—critical for cilia and flagella biogenesis and motility[2][7]. LRRC49 has context-dependent roles in cellular architecture and signaling: it regulates microtubule polymerization, cilium disassembly, and nuclear shape. In breast cancer, LRRC49 transcript levels are influenced by estrogen receptor status and epigenetic regulation; its down-regulation via promoter hypermethylation is common in tumors, suggesting a role in carcinogenesis[1]. LRRC49 is also highly expressed in podocytes, supporting functions in kidney filtration barrier maintenance, and is genetically linked to cardiovascular disease risk[1]. There are no known drug interactions or therapeutic targeting for LRRC49 at present. LRRC49 is not currently regarded as a classic therapeutic target such as a receptor or enzyme but is recognized as an important multifunctional regulatory protein in human cellular biology[1][2][7].

Other names
Leucine-rich repeat-containing protein 49LRRC49CSTPP2PGs4FLJ20156Centriolar satellite-associated tubulin polyglutamylase complex regulator 2Tubulin polyglutamylase complex subunit 4Leucine rich repeat containing 49Polyglutamylase subunit 4LRC49_HUMAND430025H09RikLOC100504571p79RGD1309466
02

Biological functions

Cilium disassemblyMicrotubule polymerizationNuclear morphology regulationPolyglutamylation of tubulinCytoskeleton organization
03

Disease associations

Cancer (especially breast cancer, where promoter methylation is implicated)Cardiovascular disease (genetic associations in coronary artery disease)Koolen-De Vries Syndrome (associated disease per OMIM)Renal biology (podocyte-enriched, potential glomerular barrier function)

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