PMID-sentid Pub_year Sent_text comp_official_name comp_offset protein_name organism prot_offset 31792371-0 2020 PACSIN2 rs2413739 influence on thiopurine pharmacokinetics: validation studies in pediatric patients. 2-mercaptopyrazine 31-41 protein kinase C and casein kinase substrate in neurons 2 Homo sapiens 0-7 34720526-5 2021 In this editorial, we discuss evidence supporting the use of PACSIN2, RAC1, and ITPA genes, in addition to TPMT and NUDT15, as possible biomarkers for thiopurine-related gastrointestinal toxicity. 2-mercaptopyrazine 151-161 protein kinase C and casein kinase substrate in neurons 2 Homo sapiens 61-68 32966336-7 2020 Moreover, we demonstrate that at least 3 different asparagine-proline-phenylalanine (NPF) motif-containing EHD binding partners, Rabenosyn-5, Syndapin2 and MICAL-L1, are required for the recruitment of EHD1 to SE. npf 85-88 protein kinase C and casein kinase substrate in neurons 2 Homo sapiens 142-151 11352907-5 2001 PACSIN 2 shows enhanced binding to the mSos proline-rich domain in pull-down assays from brain extracts as compared with lung extracts, suggesting a tissue-specific regulation of the interaction. Proline 44-51 protein kinase C and casein kinase substrate in neurons 2 Homo sapiens 0-8 32878944-0 2020 Regulation of caveolae through cholesterol-depletion dependent tubulation by PACSIN2/Syndapin II. Cholesterol 31-42 protein kinase C and casein kinase substrate in neurons 2 Homo sapiens 77-84 32878944-0 2020 Regulation of caveolae through cholesterol-depletion dependent tubulation by PACSIN2/Syndapin II. Cholesterol 31-42 protein kinase C and casein kinase substrate in neurons 2 Homo sapiens 85-96 32878944-4 2020 We show that the binding of PACSIN2 to the membrane could be negatively regulated by cholesterol. Cholesterol 85-96 protein kinase C and casein kinase substrate in neurons 2 Homo sapiens 28-35 32878944-6 2020 The reconstituted membrane with cholesterol had a weaker affinity to the F-BAR domain of PACSIN2 than the membrane without cholesterol. Cholesterol 32-43 protein kinase C and casein kinase substrate in neurons 2 Homo sapiens 89-96 32878944-6 2020 The reconstituted membrane with cholesterol had a weaker affinity to the F-BAR domain of PACSIN2 than the membrane without cholesterol. Cholesterol 123-134 protein kinase C and casein kinase substrate in neurons 2 Homo sapiens 89-96 32878944-7 2020 Consistently, the depletion of cholesterol from the plasma membrane induced the PACSIN2-localized tubules with caveolin-1 at their tips, suggesting that cholesterol inhibited the membrane tubulation by PACSIN2. Cholesterol 31-42 protein kinase C and casein kinase substrate in neurons 2 Homo sapiens 80-87 32878944-7 2020 Consistently, the depletion of cholesterol from the plasma membrane induced the PACSIN2-localized tubules with caveolin-1 at their tips, suggesting that cholesterol inhibited the membrane tubulation by PACSIN2. Cholesterol 31-42 protein kinase C and casein kinase substrate in neurons 2 Homo sapiens 202-209 32878944-7 2020 Consistently, the depletion of cholesterol from the plasma membrane induced the PACSIN2-localized tubules with caveolin-1 at their tips, suggesting that cholesterol inhibited the membrane tubulation by PACSIN2. Cholesterol 153-164 protein kinase C and casein kinase substrate in neurons 2 Homo sapiens 80-87 32878944-7 2020 Consistently, the depletion of cholesterol from the plasma membrane induced the PACSIN2-localized tubules with caveolin-1 at their tips, suggesting that cholesterol inhibited the membrane tubulation by PACSIN2. Cholesterol 153-164 protein kinase C and casein kinase substrate in neurons 2 Homo sapiens 202-209 32878944-9 2020 Consistently, the removal of caveolae from the plasma membrane upon cholesterol depletion was diminished in the PACSIN2-deficient cells. Cholesterol 68-79 protein kinase C and casein kinase substrate in neurons 2 Homo sapiens 112-119 32878944-10 2020 These data suggested that PACSIN2 mediated caveolae internalization dependently on the amount of cholesterol, providing a mechanism for cholesterol-dependent regulation of caveolae. Cholesterol 97-108 protein kinase C and casein kinase substrate in neurons 2 Homo sapiens 26-33 32878944-10 2020 These data suggested that PACSIN2 mediated caveolae internalization dependently on the amount of cholesterol, providing a mechanism for cholesterol-dependent regulation of caveolae. Cholesterol 136-147 protein kinase C and casein kinase substrate in neurons 2 Homo sapiens 26-33 31792371-1 2020 The aim of the study was to validate the impact of the single-nucleotide polymorphism rs2413739 (T > C) in the PACSIN2 gene on thiopurines pharmacological parameters and clinical response in an Italian cohort of pediatric patients with acute lymphoblastic leukemia (ALL) and inflammatory bowel disease (IBD). thiopurines 127-138 protein kinase C and casein kinase substrate in neurons 2 Homo sapiens 111-118 31792371-6 2020 These results support the role of PACSIN2 polymorphism on TPMT activity and mercaptopurine adverse effects in patients with ALL. Mercaptopurine 76-90 protein kinase C and casein kinase substrate in neurons 2 Homo sapiens 34-41 31792371-7 2020 Further evidence on PBMC and pediatric patients with IBD supports an association between PACSIN2 variants, TPMT activity, and thiopurines effects, even if more studies are needed since some of these effects may be tissue specific. thiopurines 126-137 protein kinase C and casein kinase substrate in neurons 2 Homo sapiens 89-96 25248744-7 2014 Given that MICAL-L1 and the F-BAR-containing membrane-tubulating protein Syndapin2 associate selectively with phosphatidic acid, we propose a positive feedback loop in which DGKalpha generates phosphatidic acid to drive its own recruitment to TRE via its interaction with MICAL-L1. Phosphatidic Acids 110-127 protein kinase C and casein kinase substrate in neurons 2 Homo sapiens 73-82 27452984-0 2016 PACSIN2 polymorphism is associated with thiopurine-induced hematological toxicity in children with acute lymphoblastic leukaemia undergoing maintenance therapy. 2-mercaptopyrazine 40-50 protein kinase C and casein kinase substrate in neurons 2 Homo sapiens 0-7 26092940-2 2015 Here, we found that protein kinase C (PKC) phosphorylates PACSIN2 at serine 313, thereby decreasing its membrane binding and tubulation capacities. Serine 69-75 protein kinase C and casein kinase substrate in neurons 2 Homo sapiens 58-65 26092940-5 2015 Both hypotonic treatment and isotonic drug-induced PKC activation increased PACSIN2 phosphorylation at serine 313 and shortened caveolar-tracking durations. Serine 103-109 protein kinase C and casein kinase substrate in neurons 2 Homo sapiens 76-83 31801866-8 2020 Interestingly, NS5A specifically attenuated protein kinase C alpha (PKCalpha)-mediated phosphorylation of PACSIN2 at serine 313 by interrupting PACSIN2 and PKCalpha interaction. Serine 117-123 protein kinase C and casein kinase substrate in neurons 2 Homo sapiens 106-113 31801866-16 2020 Taken together, these data indicate that HCV modulates PACSIN2 via NS5A to promote virion assembly.IMPORTANCE PACSIN2 is a lipid-binding protein that triggers the tubulation of the phosphatidic acid-containing membranes. Phosphatidic Acids 181-198 protein kinase C and casein kinase substrate in neurons 2 Homo sapiens 55-62 31801866-16 2020 Taken together, these data indicate that HCV modulates PACSIN2 via NS5A to promote virion assembly.IMPORTANCE PACSIN2 is a lipid-binding protein that triggers the tubulation of the phosphatidic acid-containing membranes. Phosphatidic Acids 181-198 protein kinase C and casein kinase substrate in neurons 2 Homo sapiens 110-117 31801866-21 2020 We showed that HCV NS5A interrupted PKCalpha-mediated PACSIN2 phosphorylation at serine 313, thereby promoting NS5A-PACSIN2 interaction. Serine 81-87 protein kinase C and casein kinase substrate in neurons 2 Homo sapiens 54-61 31801866-21 2020 We showed that HCV NS5A interrupted PKCalpha-mediated PACSIN2 phosphorylation at serine 313, thereby promoting NS5A-PACSIN2 interaction. Serine 81-87 protein kinase C and casein kinase substrate in neurons 2 Homo sapiens 116-123 27189942-5 2016 Also crucial for TRE biogenesis is the generation of phosphatidic acid, an essential lipid component of TRE that serves as a docking point for MICAL-L1 and Syndapin2. Phosphatidic Acids 53-70 protein kinase C and casein kinase substrate in neurons 2 Homo sapiens 156-165 25248744-7 2014 Given that MICAL-L1 and the F-BAR-containing membrane-tubulating protein Syndapin2 associate selectively with phosphatidic acid, we propose a positive feedback loop in which DGKalpha generates phosphatidic acid to drive its own recruitment to TRE via its interaction with MICAL-L1. Phosphatidic Acids 193-210 protein kinase C and casein kinase substrate in neurons 2 Homo sapiens 73-82 22846425-0 2012 PACSIN2 polymorphism influences TPMT activity and mercaptopurine-related gastrointestinal toxicity. Mercaptopurine 50-64 protein kinase C and casein kinase substrate in neurons 2 Homo sapiens 0-7 23335936-4 2012 The use of high-throughput genomic analysis allows identification of additional candidate genetic factors associated with pharmacogenetic phenotypes, such as TPMT enzymatic activity: PACSIN2 polymorphisms have been identified by a genome-wide analysis, combining evaluation of polymorphisms and gene expression, as a significant determinant of TPMT activity in the HapMap CEU cell lines and the effects of PACSIN2 on TPMT activity and mercaptopurine induced adverse effects were confirmed in children with ALL. Mercaptopurine 435-449 protein kinase C and casein kinase substrate in neurons 2 Homo sapiens 183-190 23596323-7 2013 We demonstrate that MICAL-L1 and the BAR-domain protein syndapin2 bind to phosphatidic acid, which we identify as a novel lipid component of RE. Phosphatidic Acids 74-91 protein kinase C and casein kinase substrate in neurons 2 Homo sapiens 56-65 23596323-9 2013 Indeed, the presence of phosphatidic acid in liposomes enhances the ability of syndapin2 to tubulate membranes in vitro. Phosphatidic Acids 24-41 protein kinase C and casein kinase substrate in neurons 2 Homo sapiens 79-88 22846425-7 2012 Moreover, this PACSIN2 SNP was significantly associated with the incidence of severe gastrointestinal (GI) toxicity during consolidation therapy containing mercaptopurine, and remained significant in a multivariate analysis including TPMT and SLCO1B1 as covariates, consistent with its influence on TPMT activity. Mercaptopurine 156-170 protein kinase C and casein kinase substrate in neurons 2 Homo sapiens 15-22 22846425-9 2012 These data indicate that polymorphism in PACSIN2 significantly modulates TPMT activity and influences the risk of GI toxicity associated with mercaptopurine therapy. Mercaptopurine 142-156 protein kinase C and casein kinase substrate in neurons 2 Homo sapiens 41-48 20188097-0 2010 Mapping of the basic amino-acid residues responsible for tubulation and cellular protrusion by the EFC/F-BAR domain of pacsin2/Syndapin II. Amino Acids, Basic 15-31 protein kinase C and casein kinase substrate in neurons 2 Homo sapiens 119-126 20188097-0 2010 Mapping of the basic amino-acid residues responsible for tubulation and cellular protrusion by the EFC/F-BAR domain of pacsin2/Syndapin II. Amino Acids, Basic 15-31 protein kinase C and casein kinase substrate in neurons 2 Homo sapiens 127-138 20188097-4 2010 The hydrophobic loops and the basic amino-acid residues on the concave surface of the pacsin2 EFC/F-BAR domain are essential for both the microspike formation and tubulation. Amino Acids, Basic 30-46 protein kinase C and casein kinase substrate in neurons 2 Homo sapiens 86-93