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Gene analysis determined a novel GRK1 mutation c.923T>C, which caused Oguchi disease in all siblings. This mutation, was demonstrated by amino acid alignment analysis to be in a phylogenetically conserved region and resulted in an amino acid change from leucine to proline at position 308. Thus, the present study reports a novel missense mutation of GRK1 in the affected members of a consanguineous Turkish family.
AAMP (zeige AAMP ELISA Kits) Regulates Endothelial Cell Migration and Angiogenesis Through RhoA (zeige RHOA ELISA Kits)/Rho Kinase (zeige ROCK1 ELISA Kits) Signaling.
In the Ca(2 (zeige CA2 ELISA Kits)+)/NCS-1 (zeige NCS1 ELISA Kits).D2R (zeige DRD2 ELISA Kits) peptide complex, the C-terminal region adopts a 310 helix-turn-310 helix, whereas in the GRK1 peptide complex it forms an a-helix
Rho-kinase (zeige ROCK1 ELISA Kits) activity exhibits distinct circadian variation associated with alterations in coronary vasomotor responses and autonomic activity in VSA patients.
The selective thinning of the inner retinal layers in patients with GRM6 (zeige GRM6 ELISA Kits) mutations suggests either reduced bipolar or ganglion cell numbers or altered synaptic structure in the inner retina.
Defects in GRK1 or GRK7 (zeige GRK7 ELISA Kits) cause patients to suffer from an inability to properly deactivate rhodopsin (zeige RHO ELISA Kits) leading to problems with recovery and dark adaptation.
There are two genes that cause Oguchi disease: the G protein-coupled receptor kinase 1 gene and the S antigen (zeige SAG ELISA Kits) gene. There is evidence that Oguchi disease and retinitis pigmentosa (RP) can coexist in the same family or even in the same individual
Phosphorylation of GRK1 and GRK7 by PKA occurs in the dark, when cAMP levels in photoreceptor cells are elevated.
The disease in the Pakistani family localizes to 13q34 and is caused by a novel deletion including Exon 3 of the GRK1 gene.
G protein-coupled receptor kinase site serine cluster has a role in beta2-adrenergic receptor internalization, desensitization, and beta-arrestin translocation
The C-terminal segment in GCAP2 (zeige GUCA1B ELISA Kits) confers target selectivity, facilitates membrane binding and provides sensitivity of the membrane localization of the protein to phosphorylation by rhodopsin kinase.
The methylation status of GRK1 is affected by nucleotide binding and by the levels of free Ca2 (zeige CA2 ELISA Kits) + via recoverin (zeige RCVRN ELISA Kits).
crystalline dimer interface was disrupted with a L166K mutation and the structure of GRK1-L166K was determined in complex with Mg(2 (zeige MCOLN1 ELISA Kits)+) . ATP to 2.5 A resolution
A novel rhodopsin-kinase-binding site within the C-terminal region of recoverin (zeige RCVRN ELISA Kits).
similar to transducin (zeige GNAT1 ELISA Kits) activation, rhodopsin (zeige RHO ELISA Kits) phosphorylation by GRK1 and high affinity arrestin-1 (zeige SAG ELISA Kits) binding only requires a rhodopsin (zeige RHO ELISA Kits) monomer
Recoverin (zeige RCVRN ELISA Kits) and rhodopsin kinase have roles in a Ca2 (zeige CA2 ELISA Kits)+-dependent feedback loop in membrane rafts from rod outer segments
an interaction surface for the recoverin (zeige RCVRN ELISA Kits) target rhodopsin kinase is constituted upon Ca2 (zeige CA2 ELISA Kits)+ binding to the non-acylated mutant
Recoverin (zeige RCVRN ELISA Kits) binds exclusively to an amphipathic peptide at the N terminus of rhodopsin kinase
Ca(2 (zeige CA2 ELISA Kits)+)-bound recoverin (zeige RCVRN ELISA Kits) is bound between rhodopsin (zeige RHO ELISA Kits) and RK in a ternary complex on rod outer segment disk membranes, thereby blocking RK interaction with rhodopsin (zeige RHO ELISA Kits) at high Ca(2 (zeige CA2 ELISA Kits)+)
key elements of rhodopsin kinase in different ligand states are involved in G protein-coupled receptor (zeige GPBAR1 ELISA Kits) kinase activation
We conclude that, in addition to their well-established roles in Meta II inactivation, Grk1 and Arr1 can modulate the kinetics of Meta III decay and rod dark adaptation in vivo.
The retinal phenotype of Grk1-/- mice is compromised by a Crb1 (zeige CRB1 ELISA Kits) rd8 mutation.
Rods and cones share the same isoforms of recoverin (zeige RCVRN ELISA Kits) and GRK1, and photoactivation also triggers a calcium decline in cones
Knockout of Unc119 (zeige UNC119 ELISA Kits) partially reversed the transport defect of GRK1 in cone photoreceptors caused by deletion of Pde6d (zeige PDE6D ELISA Kits).
rhodopsin kinase may modulate the decay of light-activated PDE (zeige TWIST1 ELISA Kits)*, which may be responsible for the quickening of response recovery in background light.
Altering the expression of GRK1 from 0.3- to 3-fold that in wild-type rods had little effect on the single photon response amplitude.
phototransduction does not play a direct role in the light-dependent dephosphorylation of GRK1.
PLCdelta3 negatively regulates RhoA (zeige RHOA ELISA Kits) expression, inhibits RhoA (zeige RHOA ELISA Kits)/Rho kinase (zeige ROCK2 ELISA Kits) signaling, and thereby promotes neurite extension.
The results of this study demonstrated a light-independent mechanism for retinal degeneration in the absence of GRK1, suggesting a second, not previously recognized role for that kinase.
Nrl (zeige NRL ELISA Kits) and Grk1 have roles in photoresponse recovery and age-related degeneration
Specifically phosphorylates the activated forms of G protein-coupled receptors (By similarity).
, rhodopsin kinase
, G-protein-coupled receptor kinase 1a
, G-protein coupled receptor kinase 1
, G-protein receptor kinase 1
, G protein-coupled receptpr kinase 1