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Survival motor neuron domain containing 1

SPF30, SMN-related protein
This gene is a paralog of SMN1 gene, which encodes the survival motor neuron protein, mutations in which are cause of autosomal recessive proximal spinal muscular atrophy. The protein encoded by this gene is a nuclear protein that has been identified as a constituent of the spliceosome complex. This gene is differentially expressed, with abundant levels in skeletal muscle, and may share similar cellular function as the SMN1 gene. [provided by RefSeq, Jul 2008] (from NCBI)
Top mentioned proteins: SmaI, HAD, ACID, CAN, dis3
Papers on SPF30
Effective photoprotection of human skin against infrared A radiation by topically applied antioxidants: results from a vehicle controlled, double-blind, randomized study.
Krutmann et al., Düsseldorf, Germany. In Photochem Photobiol, 2015
As expected, exposure to IRA radiation significantly upregulated MMP-1 expression, as compared to unirradiated skin, and this response was significantly reduced, if the SPF30 sunscreen plus the antioxidant cocktail had been applied prior to IRA radiation.
Molecular evolution of the moonlighting protein SMN in metazoans.
Gu et al., Garden City, United States. In Comp Biochem Physiol Part D Genomics Proteomics, 2013
To test this hypothesis, we investigated sequence conservation and dN/dS, which reflects the selection acting on a coding sequence, in SMN and a related protein, splicing factor 30 (SPF30), which is not currently known to be multifunctional.
The likelihood of sunburn in sunscreen users is disproportionate to the SPF.
Diffey et al., Monte-Carlo, Monaco. In Photodermatol Photoimmunol Photomed, 2013
The purpose of this paper is to estimate the expected frequency and magnitude of sunburn resulting from typical use of sunscreens labelled SPF15 and SPF30 by people spending long periods outdoors in strong summer sunshine.
Fungal Smn and Spf30 homologues are mainly present in filamentous fungi and genomes with many introns: implications for spinal muscular atrophy.
Pérez-Pulido et al., Sevilla, Spain. In Gene, 2012
SMN binding partners and the SPF30 SMN paralogue, which are all involved in mRNA splicing, were found to be present in a similar but non-identical subset of fungal genomes.
Crystal structure of TDRD3 and methyl-arginine binding characterization of TDRD3, SMN and SPF30.
Min et al., Wuhan, China. In Plos One, 2011
The binding specificity and affinity of the Tudor domains of TDRD3, SMN and SPF30 proteins were characterized quantitatively.
Structural basis for dimethylarginine recognition by the Tudor domains of human SMN and SPF30 proteins.
Sattler et al., München, Germany. In Nat Struct Mol Biol, 2011
The structures of SMN and SPF30 Tudor domains bound to symmetric and asymmetric dimethylated arginine (DMA) are presented.
Efficacy of a novel rosacea treatment system: an investigator-blind, randomized, parallel-group study.
Leyden, United States. In J Drugs Dermatol, 2011
INTRODUCTION: A rosacea treatment system (cleanser, metronidazole 0.75% gel, hydrating complexion corrector, and sunscreen SPF30) has been developed to treat rosacea.
Topical liposomal DNA-repair enzymes in polymorphic light eruption.
Wolf et al., Graz, Austria. In Photochem Photobiol Sci, 2011
The test fields were treated with (i) active AS lotion or (ii) a placebo lotion immediately after each UV exposure, or (iii) an SPF30 sunscreen before UV exposure or left untreated.
Splicing factor Spf30 assists exosome-mediated gene silencing in fission yeast.
Javerzat et al., Bordeaux, France. In Mol Cell Biol, 2010
Spf30, bound to nascent centromeric transcripts, perhaps with other splicing factors, assists their processing by the exosome. Splicing factor intercession may thus be a common feature of gene silencing pathways.
Splicing factor SPF30 bridges an interaction between the prespliceosome protein U2AF35 and tri-small nuclear ribonucleoprotein protein hPrp3.
Jurica et al., Santa Cruz, United States. In J Biol Chem, 2008
U2AF35 and hPrp3 interactions with SPF30 can occur simultaneously, thereby potentially linking 3' splice site recognition with tri-small nuclear ribonucleoprotein addition
[Spectroscopic analysis of sun protection factor (SPF) of sunscreen cosmetic].
Fang et al., Hangzhou, China. In Guang Pu Xue Yu Guang Pu Fen Xi, 2007
Three kinds of Dingjiayi brand sunscreen cosmetics, which is SPF15, SPF20 and SPF30, were chosen as experimental material.
Tudor domains bind symmetrical dimethylated arginines.
Richard et al., Montréal, Canada. In J Biol Chem, 2005
Herein we show that the Tudor domains of the spinal muscular atrophy gene product SMN, the splicing factor 30 kDa (SPF30), and the Tudor domain-containing 3 (TDRD3) proteins interacted with arginine-glycine-rich motifs in a methylarginine-dependent manner.
Comparative efficacy of IR3535 and deet as repellents against adult Aedes aegypti and Culex quinquefasciatus.
Hallmon et al., Panama City, United States. In J Am Mosq Control Assoc, 2004
active ingredient [AI], Bug Guard Plus with SPF30 sunscreen 7.5% AI, Bug Guard Plus with SPF15 sunscreen 7.5% AI, and Bug Guard Plus 7.5% AI) were tested.
Application of sunscreen preparations among young Polish people.
Melon et al., Wrocław, Poland. In J Cosmet Dermatol, 2004
Two agents were applied: emulsion with SPF30 and a fatty cream with SPF > 60.
SMNrp is an essential pre-mRNA splicing factor required for the formation of the mature spliceosome.
Fischer et al., Göttingen, Germany. In Embo J, 2001
SMNrp, also termed SPF30, has recently been identified in spliceosomes assembled in vitro.
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