Use your antibodies-online credentials, if available.
Autism spectrum disorder patient with the smallest inactivating deletion in the collybistin gene.
Collybistin forms a complex with mTOR (显示 FRAP1 ELISA试剂盒) and eIF3 (显示 EIF3A ELISA试剂盒) and by sequestering these proteins downregulates mTORC1 signaling and protein synthesis potentially contributing to intellectual disability and autism.
Impairment of the membrane lipid binding activity of Collybistin R290H and a consequent defect in inhibitory synapse maturation represent a likely molecular pathomechanism of epilepsy and mental retardation in humans.
The enhancement of Cb-induced gephyrin (显示 GPHN ELISA试剂盒) clustering by GTP (显示 AK3 ELISA试剂盒)-TC10 (显示 RHOQ ELISA试剂盒) does not depend on the guanine nucleotide exchange activity of Cb but involves an interaction that resembles reported interactions of other small GTPases with their effectors
Phosphorylation of gephyrin (显示 GPHN ELISA试剂盒) in hippocampal neurons by cyclin-dependent kinase (显示 CDK1 ELISA试剂盒) CDK5 (显示 CDK5 ELISA试剂盒) at Ser (显示 SIGLEC1 ELISA试剂盒)-270 is dependent on collybistin.
Data indicate that ARHGEF9 is likely to be responsible for syndromic X-linked mental retardation associated with epilepsy.
These results reveal that G(s) and G(q) signalings regulate hPEM-2 functions through PKA and c-Src (显示 SRC ELISA试剂盒) in Neuro-2a neuroblastoma (显示 ARHGEF16 ELISA试剂盒) cells, respectively.
major regulator of GABAergic postsynaptic gephyrin (显示 GPHN ELISA试剂盒) clustering
Study propose that the collybistin-gephyrin (显示 GPHN ELISA试剂盒) complex has an intimate role in the clustering of GABA(A)Rs containing the alpha2 subunit.
Here we identified residues critical for interaction with gephyrin (显示 GPHN ELISA试剂盒) in the linker region between the SH3 and the DH domains of collybistin.
Results uncover previously unexpected role for CB isoforms downstream of alpha2-containing GABAARs during neuron maturation in a Cdc42 (显示 CDC42 ELISA试剂盒) dependent mechanism.
Within this network, collybistin can adopt open/active and closed/inactive conformations to act as a switchable adaptor that links gephyrin (显示 GPHN ELISA试剂盒) to plasma membrane phosphoinositides.
data show that collybistin co-clusters with gephyrin (显示 GPHN ELISA试剂盒) and GABA(A) Rs in synaptic puncta and is recruited to postsynaptic specializations early during synapse development; it co-localizes with GABA(A) Rs containing the alpha1, alpha2, or alpha3 subunits
The results of this study provided evidence that the formation of gephyrin (显示 GPHN ELISA试剂盒) scaffolds at inhibitory synapses requires an intact Cb II PH-domain but is Cdc42 (显示 CDC42 ELISA试剂盒)-independent.
The resolution crystal structure of the Cdc42 (显示 CDC42 ELISA试剂盒)-collybistin II complex reveals a novel conformation of the switch I region of Cdc42 (显示 CDC42 ELISA试剂盒), and biochemical data indicate that gephyrin (显示 GPHN ELISA试剂盒) negatively regulates collybistin activity.
Cb is essential for gephyrin (显示 GPHN ELISA试剂盒)-dependent clustering of a specific set of GABA(A) receptors, but not required for glycine receptor (显示 GLRB ELISA试剂盒) postsynaptic localization.
Data provide the first evidence that collybistin deficiency leads to significant changes of GABAergic inhibition, network excitability and synaptic plasticity in vivo.
The protein encoded by this gene is a Rho-like GTPase that switches between the active (GTP-bound) state and inactive (GDP-bound) state to regulate CDC42 and other genes. Defects in this gene are a cause of startle disease with epilepsy (STHEE), also known as hyperekplexia with epilepsy. Three transcript variants encoding different isoforms have been found for this gene.
Cdc42 guanine nucleotide exchange factor (GEF) 9
, Cdc42 guanine nucleotide exchange factor 9
, Cdc42 guanine exchange factor 9
, rho guanine nucleotide exchange factor 9-like
, PEM-2 homolog
, hPEM-2 collybistin
, rac/Cdc42 guanine nucleotide exchange factor 9
, rho guanine nucleotide exchange factor 9
, collybistin I