about
Insights into molecular interactions between CaM and its inhibitors from molecular dynamics simulations and experimental data.A score of the ability of a three-dimensional protein model to retrieve its own sequence as a quantitative measure of its quality and appropriatenessA novel motif in the NaTrxh N-terminus promotes its secretion, whereas the C-terminus participates in its interaction with S-RNase in vitro.Expression of recombinant SnRK1 in E. coli. Characterization of adenine nucleotide binding to the SnRK1.1/AKINβγ-β3 complex.Evidence for a non-overlapping subcellular localization of the family I isoforms of soluble inorganic pyrophosphatase in Arabidopsis thaliana.Synthesis, cytotoxic evaluation, and DNA binding of novel thiazolo[5,4-b]quinoline derivatives.Synthesis and evaluation of 9-anilinothiazolo[5,4-b]quinoline derivatives as potential antitumorals.Synthesis, cytotoxic activity, DNA topoisomerase-II inhibition, molecular modeling and structure-activity relationship of 9-anilinothiazolo[5,4-b]quinoline derivatives.The treatment of purified maize oil bodies with organic solvents and exogenous diacylglycerol allows the detection and solubilization of diacylglycerol acyltransferase.Importance of the interaction protein-protein of the CaM-PDE1A and CaM-MLCK complexes in the development of new anti-CaM drugs.Antineoplastic activity of the thiazolo[5,4-b]quinoline derivative D3CLP in K-562 cells is mediated through effector caspases activation.An alternative assay to discover potential calmodulin inhibitors using a human fluorophore-labeled CaM protein.Calmodulin inhibitors from the fungus Emericella sp.Smooth muscle relaxant action of benzyl benzoates and salicylic acid derivatives from Brickellia veronicaefolia on isolated guinea-pig ileum.SIPP, a Novel Mitochondrial Phosphate Carrier, Mediates in Self-Incompatibility.Effect of natural and synthetic benzyl benzoates on calmodulin.Proteomic Profiling Reveals the Induction of UPR in Addition to DNA Damage Response in HeLa Cells Treated With the Thiazolo[5,4-b]Quinoline Derivative D3ClP.Kinetic evidence of the existence of a regulatory phosphoenolpyruvate binding site in maize leaf phosphoenolpyruvate carboxylase.Changes in expression of soluble inorganic pyrophosphatases of Phaseolus vulgaris under phosphate starvation.Bona fide choline monoxygenases evolved in Amaranthaceae plants from oxygenases of unknown function: Evidence from phylogenetics, homology modeling and docking studiesComparison of plasma membrane H+-ATPase activity in vesicles obtained from dry and hydrated maize embryosSynthesis and biological activity of furostanic analogues of brassinosteroids bearing the 5alpha-hydroxy-6-oxo moietySynthesis and plant growth promoting activity of polyhydroxylated ketones bearing the 5α-hydroxy-6-oxo moiety and cholestane side chainDevelopment of the fluorescent biosensor hCalmodulin (hCaM)L39C-monobromobimane(mBBr)/V91C-mBBr, a novel tool for discovering new calmodulin inhibitors and detecting calciumSynthesis and plant growth promoting activity of dinorcholanic lactones bearing the 5α-hydroxy-6-oxo moietyNaStEP: a proteinase inhibitor essential to self-incompatibility and a positive regulator of HT-B stability in Nicotiana alata pollen tubesReview: "Pyrophosphate and pyrophosphatases in plants, their involvement in stress responses and their possible relationship to secondary metabolism"
P50
Q30897301-08306379-2B42-468F-B918-785F96F85CAFQ33689338-47B2E254-EAB2-4B0F-874E-B31C9DF5B27BQ33786323-186BDEE4-2B05-4158-BEFA-51D71470E612Q38619522-BB2F83C6-B654-4350-8228-7B14F7EA5E0DQ39101847-13ED93D8-59A9-4E72-AA3F-1CDED55876D0Q40045568-6F01383D-65F6-4FBB-BD31-2EEE36E04F5AQ40585177-BF00D326-6DC0-4EF3-A902-148DCD3CFB3DQ43762586-13C526F6-E570-4228-93ED-D5867C25699EQ43828884-68BFF9D9-4E3C-434A-A423-3AA2AF3254D0Q44327186-F57D8D23-DFF4-455D-AF3E-5070A5C0A468Q45764517-351A9D7D-1F6C-47B0-A2DF-4A9EDCB8BAE1Q46137400-D29F616F-BDF9-4C28-A557-C08D4DFB6AB2Q46242599-4BFE2D25-E9C4-4852-9C7C-3FC882738EBDQ46459604-C44C1738-FE51-46AE-92C3-A4FA100CC1DFQ47852165-8BB161E7-8368-4724-A61B-52F36760E6CDQ48222049-AAE13CA0-FFE8-44DF-95C4-ED1E35B4C22AQ51450173-2AFD9943-F75A-4BE3-BB57-8D029585C4EFQ52504276-98EC384C-5635-44B7-8FC5-7CB9527DDCCFQ53134014-81B2D5CA-F191-4F46-B387-C2B635D33369Q58695899-408A732E-1CF5-4F06-A1EA-709AC914FEDCQ77521310-20E0219C-3C32-440A-947B-5886579E47BAQ81373674-8AD3FFC9-B456-4324-A331-8AE68006871DQ83316523-37B46865-1877-4F37-9C68-CB9512221118Q83873952-E6A00050-8D81-4741-BAFD-FE1F38F5D010Q85241011-77BD748F-F062-4002-9C13-60D67436E33CQ85430200-D183C92F-6AC9-4F3E-8C27-0340082E7AA9Q87593379-A7E97333-E1CE-43B5-A745-71CBF9AFC8E4
P50
description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Rogelio Rodríguez-Sotres
@ast
Rogelio Rodríguez-Sotres
@en
Rogelio Rodríguez-Sotres
@es
Rogelio Rodríguez-Sotres
@nl
Rogelio Rodríguez-Sotres
@sl
type
label
Rogelio Rodríguez-Sotres
@ast
Rogelio Rodríguez-Sotres
@en
Rogelio Rodríguez-Sotres
@es
Rogelio Rodríguez-Sotres
@nl
Rogelio Rodríguez-Sotres
@sl
prefLabel
Rogelio Rodríguez-Sotres
@ast
Rogelio Rodríguez-Sotres
@en
Rogelio Rodríguez-Sotres
@es
Rogelio Rodríguez-Sotres
@nl
Rogelio Rodríguez-Sotres
@sl
P106
P1153
6603133914
P21
P31
P3835
rogelio-rodriguez-sotres
P496
0000-0002-9443-3207