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GoPubMed Proteins lists recent and important papers and reviews for proteins. Page last changed on 19 Aug 2016.

PRKR interacting protein 1

Top mentioned proteins: CAN, HAD, ACID, OUT, C43
Papers on C114
Feasibility of halogen determination in noncombustible inorganic matrices by ion chromatography after a novel volatilization method using microwave-induced combustion.
Mesko et al., Pelotas, Brazil. In Talanta, Feb 2016
Results were also compared to those using the procedure recommended by the American Society of Testing and Materials (ASTM) for the determination of total chlorides (C114-13), and no difference was found.
Expression characterization and activity analysis of a cathepsin B from Pacific abalone Haliotis discus hannai.
Sun et al., Qingdao, China. In Fish Shellfish Immunol, 2013
HdCatB possesses typical domain architecture of cathepsin B and contains a propeptide region and a cysteine protease domain, the latter containing the four active site residues (Q108, C114, H282, and N302) that are conserved in many different organisms.
Protein microarrays discover angiotensinogen and PRKRIP1 as novel targets for autoantibodies in chronic renal disease.
Sarwal et al., Stanford, United States. In Mol Cell Proteomics, 2011
Significant elevations in the titer of novel auto-Ab were noted against angiotensinogen and PRKRIP1 in renal insufficiency.
Identification and molecular characterization of a SpƤtzle-like protein from Chinese shrimp (Fenneropenaeus chinensis).
Wang et al., Jinan, China. In Fish Shellfish Immunol, 2009
The recombinant Fc-Spz C-114 was injected into crayfish (Procambarus clarkii) to determine the expression levels of several antimicrobial peptide genes.
Zinc binding to the HCCH motif of HIV-1 virion infectivity factor induces a conformational change that mediates protein-protein interactions.
Maynard et al., Bethesda, United States. In Proc Natl Acad Sci U S A, 2007
Cysteine modification studies with the HCCH peptide suggest that C114 is critical for stabilizing the fold of the apopeptide, and that C133 is located in a solvent-exposed region with no definite secondary structure.
Protection of susceptible potato cultivars against late blight in mixtures increases with decreasing disease pressure.
Andrivon et al., In Phytopathology, 2006
Cecilia in 2000 and LBr37 in 2001, as well as C114 (moderately resistant) and PAN (highly resistant), planted as pure stands and as the three possible two-way combinations.
Characterization of the neutralizing activity of three anti-human TNF monoclonal antibodies and prediction of their TNF epitopes by molecular modeling and mutant protein approach.
Jin et al., Xi'an, China. In Immunol Lett, 2006
In the structures, the TNF epitopes of D2, E6, and F6 were predicted at amino acids of (A109, A111-A112, C19, C21-C29, C44-C46, C66-C75, C77, C79, C90, C101, C103, C105, C114, C134-C148), (C18-C19, C21-C30, C32, C37, C43-C47, C67-C75, C83, C105-C106, C131, C135-C141), and (C21-C32, C45-C47, C65, C67-C72, C74, C81, C83, C90-C95, C105-C113, C133-C147), respectively, and the affinities of D2, E6, and F6 to TNF were predicted as -252.69,
Selective extraction of higher fullerenes using cyclic dimers of zinc porphyrins.
Aida et al., Tokyo, Japan. In J Am Chem Soc, 2004
Sequential three-stage extraction of the fullerene mixture with the best-behaved 2C6 resulted in considerable enrichment in very rare fullerenes C102-C110 (<0.1 abs %) up to 82 abs % (C76-C114, 99 abs %) (356 nm) of total fullerenes.
C114 is a novel IL-11-inducible nuclear double-stranded RNA-binding protein that inhibits protein kinase R.
Yang et al., Cleveland, United States. In J Biol Chem, 2003
C114 binds to protein kinase R (PKR), via dsRNA-binding domains of PKR and the N-terminal region of the C114 protein
Lactobacillus salivarius CTC2197 prevents Salmonella enteritidis colonization in chickens.
Garriga et al., Spain. In Appl Environ Microbiol, 1999
A rifampin-resistant Lactobacillus salivarius strain, CTC2197, was assessed as a probiotic in poultry, by studying its ability to prevent Salmonella enteritidis C-114 colonization in chickens.
Contributions of cysteine 114 of the human D3 dopamine receptor to ligand binding and sensitivity to external oxidizing agents.
Im et al., Kalamazoo, United States. In Br J Pharmacol, 1998
1. Cysteine 114 (C114) of the human dopamine D3 receptor is located at the helical face of transmembrane segment III (TMIII) near aspartate 110, a counterion for the amine group of catecholamines.
Characterization of human immunodeficiency virus type 1 Vif particle incorporation.
Trono et al., Los Angeles, United States. In J Virol, 1996
Furthermore, mutating several highly conserved residues (H-108, C-114, C-133, L-145, and Q-146) or deleting the C-terminal 18 amino acids of Vif, either of which severely impairs Vif function, does not abolish its incorporation into virions.
Substitution of serine for glycine-91 in the HXGH motif of CTP:phosphocholine cytidylyltransferase implicates this motif in CTP binding.
Cornell et al., Canada. In Biochemistry, 1996
The effect of mutations in the proposed catalytic domain of CTP:phosphocholine cytidylyltransferase was investigated by constructing the single mutants CT-S91 and CT-C114 from the double mutant CT-S91C114, previously shown to have 4-fold lower than wild-type activity [Walkey, C.R., Kalmar, G. B., & Cornell, R. B. (1994) J. Biol.
Differential binding of the NFE3 and CP1/NFY transcription factors to the human gamma- and epsilon-globin CCAAT boxes.
Santoro et al., Milano, Italy. In J Biol Chem, 1995
Although the distal CCAAT box is the target of several factors, including CP1/NFY, CDP, GATA-1 and NFE3, only NFE3 binding activity is consistently sensitive to well characterized mutations in this region such as G-117-->A, C-114-->T, and delta 13 hereditary persistence of fetal hemoglobin.
Evidence for vasopressin activation of adenylate cyclase by subunit dissociation.
Ausiello et al., In Am J Physiol, 1986
19): C103-C114, 1986].
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