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CAMKMT encodes a class I protein methyltransferase that acts in the formation of trimethyllysine in calmodulin. Additionally we are shipping Calmodulin-Lysine N-Methyltransferase Antibodies (2) and many more products for this protein.
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Deletion of CAMKMT is associated with Hypotonia-cystinuria syndrome.
The CaM KMT is the major, possibly the single, methyltransferase of calmodulin (show CALM1 Proteins) in human cells with a wide tissue distribution and is a novel Hsp90 (show HSP90 Proteins) client protein.
Calmodulin (show CALM1 Proteins) methyltransferase is an evolutionarily conserved enzyme that trimethylates Lys (show LYZ Proteins)-115 in calmodulin (show CALM1 Proteins).
a deletion of C2orf34 causes atypical hypotonia-cystinuria syndrome
Two key transcription factors, NRF-2 (show GABPA Proteins) and YY-1 (show YY1 Proteins), were further identified to coordinately participate in driving gene expressions of PREPL (show PREPL Proteins)-C2ORF34 genes pairin an additive manner.
CaM (show Calm2 Proteins) methylation appears to have a role in growth, muscle strength, somatosensory development and brain function.
This gene encodes a class I protein methyltransferase that acts in the formation of trimethyllysine in calmodulin. The protein contains a AdoMet-binding motif and may play a role in calcium-dependent signaling.