PMID-sentid Pub_year Sent_text comp_official_name comp_offset protein_name organism prot_offset 6546848-6 1984 Cross-reactivity of AFB1-diol antibody in the competitive ELISA with AF analogs was as follows: AFB1-diol, 100%; AFB1, 200%; AFM1, 130%; AFB2a, 100%; AFG1, 6%; AFG2, 4%; aflatoxicol, 20%; AFQ1, 2%; AFB1-modified DNA, 32%; and 2,3-dihydro-2-(N7-guanyl)-3-hydroxy AFB1, 0.6%. afb1-diol 20-29 AFG1 like ATPase Homo sapiens 150-154 2519710-2 1989 Human liver microsomal cytochrome P-450NF oxidized the dihydrofurans (in the presence of calf thymus DNA) to give guanyl-N7 adducts in the order AFB1 greater than STG greater than AFG1. dihydrofurans 55-68 AFG1 like ATPase Homo sapiens 180-184 2519710-3 1989 The order of the umu response seen was STG greater than AFB1 greater than AFG1, when either the dihydrofurans were activated enzymatically or the synthetic epoxides of the dihydrofurans were added directly to the bacteria. dihydrofurans 96-109 AFG1 like ATPase Homo sapiens 74-78 2519710-3 1989 The order of the umu response seen was STG greater than AFB1 greater than AFG1, when either the dihydrofurans were activated enzymatically or the synthetic epoxides of the dihydrofurans were added directly to the bacteria. dihydrofurans 172-185 AFG1 like ATPase Homo sapiens 74-78 30952310-3 2019 Under optimized conditions (1.25 mL of 5 mg L-1 MIP-PEG-ZnS QDs solution, pH 5.0, and 12 min delay time before scanning), the prepared MIP-QDs composite was found to offer high affinity and selectivity for AFs (AFB1, AFB2, AFG1 and AFG2). Zinc 56-59 AFG1 like ATPase Homo sapiens 223-227 32983001-2 2020 Aflatoxin B1 (AFB1) and aflatoxin B2 (AFB2) as well as aflatoxin G1(AFG1) and aflatoxin G2 (AFG2) occur in the contaminated foods and feed. aflatoxin G1 55-67 AFG1 like ATPase Homo sapiens 68-72 31793394-5 2020 Aflatoxin B1was found in all positive samples and co-occurred with AFB2, AFG1, and AFG2. Aflatoxins 0-9 AFG1 like ATPase Homo sapiens 73-77 31814038-0 2019 An amino-functionalized zirconium-based metal-organic framework of type UiO-66-NH2 covered with a molecularly imprinted polymer as a sorbent for the extraction of aflatoxins AFB1, AFB2, AFG1 and AFG2 from grain. Zirconium 24-33 AFG1 like ATPase Homo sapiens 186-190 31814038-0 2019 An amino-functionalized zirconium-based metal-organic framework of type UiO-66-NH2 covered with a molecularly imprinted polymer as a sorbent for the extraction of aflatoxins AFB1, AFB2, AFG1 and AFG2 from grain. Metals 40-45 AFG1 like ATPase Homo sapiens 186-190 31814038-0 2019 An amino-functionalized zirconium-based metal-organic framework of type UiO-66-NH2 covered with a molecularly imprinted polymer as a sorbent for the extraction of aflatoxins AFB1, AFB2, AFG1 and AFG2 from grain. Polymers 120-127 AFG1 like ATPase Homo sapiens 186-190 32517894-6 2020 Aflatoxins were detected in a maximum of 13% (AFB1), 16% (AFB2), 1% (AFG1), 2% (AFG2) and 19% (AFM1) of the urine samples. Aflatoxins 0-10 AFG1 like ATPase Homo sapiens 69-73 30468840-4 2019 Basic AFs (AFB1, AFB2, AFG1, and AFG2) are metabolized in the liver or by microbes that produce hydroxylated metabolites (AFM1, AFM2, and AFP1) and aflatoxicol (AFL), soluble in water and easy to dispose. aflatoxicol 148-159 AFG1 like ATPase Homo sapiens 23-27 30478833-1 2019 Aflatoxin G1 (AFG1 ), a member of the AF family with cytotoxic and carcinogenic properties, could cause DNA damage in alveolar type II (AT-II) cells and induce lung adenocarcinoma. aflatoxin G1 0-12 AFG1 like ATPase Homo sapiens 14-18 30832301-6 2019 Trace element analysis showed that the concentrations of several metal ions differed by factors of >100, and the carbons that most effectively increased AFG1 production contained higher amounts of metal ions. Carbon 113-120 AFG1 like ATPase Homo sapiens 153-157 30832301-6 2019 Trace element analysis showed that the concentrations of several metal ions differed by factors of >100, and the carbons that most effectively increased AFG1 production contained higher amounts of metal ions. Metals 197-202 AFG1 like ATPase Homo sapiens 153-157 30832301-7 2019 Adding 5 mg L-1 Fe or Mg ions increased AFG1 production even without activated carbon. Iron 16-18 AFG1 like ATPase Homo sapiens 40-44 30832301-7 2019 Adding 5 mg L-1 Fe or Mg ions increased AFG1 production even without activated carbon. Magnesium 22-24 AFG1 like ATPase Homo sapiens 40-44 30832301-8 2019 Furthermore, co-addition of both ions increased AFG1 production stably with the addition of carbon. Carbon 92-98 AFG1 like ATPase Homo sapiens 48-52 30468840-4 2019 Basic AFs (AFB1, AFB2, AFG1, and AFG2) are metabolized in the liver or by microbes that produce hydroxylated metabolites (AFM1, AFM2, and AFP1) and aflatoxicol (AFL), soluble in water and easy to dispose. aflatoxicol 161-164 AFG1 like ATPase Homo sapiens 23-27 30468840-4 2019 Basic AFs (AFB1, AFB2, AFG1, and AFG2) are metabolized in the liver or by microbes that produce hydroxylated metabolites (AFM1, AFM2, and AFP1) and aflatoxicol (AFL), soluble in water and easy to dispose. Water 178-183 AFG1 like ATPase Homo sapiens 23-27 28844113-11 2017 We hypothesize that the formation of OH radicals initiated by UV light may have caused photolysis of AFB1, AFB2, and AFG1 molecules. oh radicals 38-49 AFG1 like ATPase Homo sapiens 118-122 28911616-5 2016 After screening, five MAbs (AFM1-1, AFM1-3, AFM1-9, AFM1-11, and AFM1-17) were obtained that showed cross-reactivity with aflatoxin B1 (AFB1) and aflatoxin G1 (AFG1) but with no other tested compounds. Aflatoxin B1 122-134 AFG1 like ATPase Homo sapiens 160-164 28801561-2 2017 Our previous study showed Aflatoxin G1 (AFG1) could induce lung adenocarcinoma in mice. Aflatoxins 26-35 AFG1 like ATPase Homo sapiens 40-44 25336278-1 2015 Recently, we discovered that Aflatoxin G1 (AFG1 ) induces chronic lung inflammatory responses, which may contribute to lung tumorigenesis in Balb/C mice. aflatoxin G1 29-41 AFG1 like ATPase Homo sapiens 43-47 27187470-2 2016 We developed a murine monoclonal antibody of immunoglobulin A (IgA) isotype with a strong binding affinity to aflatoxin B1 (AFB1), aflatoxin B2 (AFB2), aflatoxin G1 (AFG1), aflatoxin G2 (AFG2) and aflatoxin M1 (AFM1). Aflatoxin B1 110-122 AFG1 like ATPase Homo sapiens 166-170 27323408-5 2016 LACE1 physically interacts with p53 and is necessary for mitomycin c-induced translocation of p53 into mitochondria. Mitomycin 57-68 AFG1 like ATPase Homo sapiens 0-5 26133228-4 2015 The aflatoxin most frequently detected in the samples was AFG1, present in 57.9% of samples, while the other aflatoxins were rarely present. Aflatoxins 4-13 AFG1 like ATPase Homo sapiens 58-62 25603600-5 2014 The transmicivities of AFB1, AFG1 and AFG2 reached the highest at the incubation time of 60 minutes but 120 minutes for DON and AFB2. DONS 120-123 AFG1 like ATPase Homo sapiens 29-33 25606005-3 2014 Aflatoxins were found in 124 out of the 729 analyzed samples: 65 containing aflatoxin B1 (AFB1), 24 with aflatoxin B2 (AFB2), 15 with aflatoxin G1 (AFG1), and 20 samples with aflatoxin G2 (AFG2). Aflatoxins 0-10 AFG1 like ATPase Homo sapiens 148-152 25603600-5 2014 The transmicivities of AFB1, AFG1 and AFG2 reached the highest at the incubation time of 60 minutes but 120 minutes for DON and AFB2. aflatoxin B2 128-132 AFG1 like ATPase Homo sapiens 29-33 22971039-1 2012 A simple method for the reduction of aflatoxins B1 (AFB1), B2 (AFB2), G1 (AFG1), G2 (AFG2) and ochratoxin A (OTA) in white pepper was studied. Aflatoxins 37-47 AFG1 like ATPase Homo sapiens 74-78 25029403-3 2014 A positive correlation was found between four types of aflatoxins in all the tested samples (p < 0.01) and the positive correlation between AFG1 and AFG2 was significant (r(2) = 0.708). Aflatoxins 55-65 AFG1 like ATPase Homo sapiens 143-147 24090735-5 2013 Thus, we explore whether AFG1 activates the reactive oxygen species (ROS)/MAPK/apoptosis pathway to cause cell damage in human AT-II cells like the cell line (A549). Reactive Oxygen Species 44-67 AFG1 like ATPase Homo sapiens 25-29 24090735-5 2013 Thus, we explore whether AFG1 activates the reactive oxygen species (ROS)/MAPK/apoptosis pathway to cause cell damage in human AT-II cells like the cell line (A549). Reactive Oxygen Species 69-72 AFG1 like ATPase Homo sapiens 25-29 24090735-6 2013 We found AFG1 induced oxidative stress by increasing ROS generation and caused DNA double-strand breaks (DSBs) by up-regulating gammaH2AX expression. Reactive Oxygen Species 53-56 AFG1 like ATPase Homo sapiens 9-13 24090735-8 2013 Pre-treatment with antioxidant n-acetyl-l-cysteine (NAC) reduced ROS generation and DNA DSBs, inhibited apoptosis, and increased cell viability in AFG1-treated cells. Acetylcysteine 31-50 AFG1 like ATPase Homo sapiens 147-151 24090735-8 2013 Pre-treatment with antioxidant n-acetyl-l-cysteine (NAC) reduced ROS generation and DNA DSBs, inhibited apoptosis, and increased cell viability in AFG1-treated cells. dsbs 88-92 AFG1 like ATPase Homo sapiens 147-151 24090735-9 2013 Furthermore, we found AFG1 activated ROS-mediated JNK and p38 pathways to induce cell apoptosis in A549 cells. Reactive Oxygen Species 37-40 AFG1 like ATPase Homo sapiens 22-26 24090735-10 2013 In conclusion, our results indicate that AFG1 induces oxidative DNA damage and triggers apoptosis through ROS-mediated JNK and p38 signaling pathways in A549 cells, which may contribute to AFG1-induced AT-II cell damage. Reactive Oxygen Species 106-109 AFG1 like ATPase Homo sapiens 41-45 24090735-10 2013 In conclusion, our results indicate that AFG1 induces oxidative DNA damage and triggers apoptosis through ROS-mediated JNK and p38 signaling pathways in A549 cells, which may contribute to AFG1-induced AT-II cell damage. Reactive Oxygen Species 106-109 AFG1 like ATPase Homo sapiens 189-193 23907605-6 2013 In addition, AFG1 increased 8-OHdG and gammaH2AX in the nuclies and induced S phase arrest and DNA damage in B-2A13 cells, and the proteins related to DNA damage responses, such as ATM, ATR, Chk2, p53, BRCA1, and gammaH2AX, were activated. 8-ohdg 28-34 AFG1 like ATPase Homo sapiens 13-17 23907605-7 2013 All the above effects were inhibited by nicotine (a substrate of CYP2A13) or 8-MOP (an inhibitor of CYP enzymes), confirming that CYP2A13 mediated the AFG1-induced cytotoxicity and DNA damages. Nicotine 40-48 AFG1 like ATPase Homo sapiens 151-155 23907605-7 2013 All the above effects were inhibited by nicotine (a substrate of CYP2A13) or 8-MOP (an inhibitor of CYP enzymes), confirming that CYP2A13 mediated the AFG1-induced cytotoxicity and DNA damages. Methoxsalen 77-82 AFG1 like ATPase Homo sapiens 151-155 21957681-9 2011 Aflatoxin metabolites, apart from AFM1 and AFB1 present in the weaning foods, were AFG1 and AFG2. Aflatoxins 0-9 AFG1 like ATPase Homo sapiens 83-87 11938994-5 1999 The lymphocytes treated with DON and AFG1 showed characteristic "ladder" pattern in agarose gel electrophoresis. Sepharose 84-91 AFG1 like ATPase Homo sapiens 37-41 12217366-1 2002 The kinetics of reduction of AFB(1) to AFB(2) and AFG(1) to AFG(2) by lactic acid has been investigated in dilute aqueous acidic solutions (pH 3.35-4.50) as a function of the concentrations of lactic acid, AFB(1), AFG(1) and hydrogen ion at 37 degrees C. The rate of the reaction was found to be first order with respect to the concentrations of lactic acid and aflatoxins and independent on hydrogen ion concentration. Lactic Acid 70-81 AFG1 like ATPase Homo sapiens 50-56 12217366-1 2002 The kinetics of reduction of AFB(1) to AFB(2) and AFG(1) to AFG(2) by lactic acid has been investigated in dilute aqueous acidic solutions (pH 3.35-4.50) as a function of the concentrations of lactic acid, AFB(1), AFG(1) and hydrogen ion at 37 degrees C. The rate of the reaction was found to be first order with respect to the concentrations of lactic acid and aflatoxins and independent on hydrogen ion concentration. Lactic Acid 70-81 AFG1 like ATPase Homo sapiens 214-220 12217366-3 2002 The proposed mechanisms involve an overall transfer of two protons and two electrons from lactic acid to AFB(1) and AFG(1) to give the corresponding reduced less toxic products AFB(2) and AFG(2) and the oxidised product pyruvic acid. Lactic Acid 90-101 AFG1 like ATPase Homo sapiens 116-122 12217366-3 2002 The proposed mechanisms involve an overall transfer of two protons and two electrons from lactic acid to AFB(1) and AFG(1) to give the corresponding reduced less toxic products AFB(2) and AFG(2) and the oxidised product pyruvic acid. afb 177-180 AFG1 like ATPase Homo sapiens 116-122 12217366-3 2002 The proposed mechanisms involve an overall transfer of two protons and two electrons from lactic acid to AFB(1) and AFG(1) to give the corresponding reduced less toxic products AFB(2) and AFG(2) and the oxidised product pyruvic acid. Pyruvic Acid 220-232 AFG1 like ATPase Homo sapiens 116-122 12131971-6 2002 Peanuts and its products showed the highest levels of aflatoxin contamination (34.7%) with up to 1280 mg/kg of AFB1+AFG1 and 1706 mg/kg of total aflatoxins. Aflatoxins 54-63 AFG1 like ATPase Homo sapiens 116-120 11829670-6 2002 The relative cross-reactivity with aflatoxins (AF) and ochratoxin A, assessed as the amount of AFM1 necessary to cause 50% inhibition of binding, was 5% for AFB1 and much less for AFB2, AFG1, and AFG2; there was no reaction with ochratoxin A. Aflatoxins 35-45 AFG1 like ATPase Homo sapiens 186-190 20630912-0 2011 Protective effects of selenium against sister chromatid exchange induced by AFG 1 in human lymphocytes in vitro. Selenium 22-30 AFG1 like ATPase Homo sapiens 76-81 24779628-1 2010 Aflatoxins (AFB1, AFB2, AFG1 and AFG2) are immunosuppressant, mutagenic, teratogenic and carcinogenic agents with a widespread presence in foodstuffs. Aflatoxins 0-10 AFG1 like ATPase Homo sapiens 24-28 12244755-3 2002 RESULTS: DNA agarose gel electrophoresis results showed the characteristic "ladder" pattern of apoptosis in HPBLs treated with ST, DON and AFG1. Sepharose 13-20 AFG1 like ATPase Homo sapiens 139-143 11829670-6 2002 The relative cross-reactivity with aflatoxins (AF) and ochratoxin A, assessed as the amount of AFM1 necessary to cause 50% inhibition of binding, was 5% for AFB1 and much less for AFB2, AFG1, and AFG2; there was no reaction with ochratoxin A. ochratoxin A 55-67 AFG1 like ATPase Homo sapiens 186-190 11765082-4 2001 Chromatographic responses of AFB1 and AFG1 achieved using beta-CD dissolved in the mobile phase were enhanced, respectively, 8 and 12 times, and 10 and 15 times with beta-CD-Su. betadex 58-65 AFG1 like ATPase Homo sapiens 38-42 11765082-4 2001 Chromatographic responses of AFB1 and AFG1 achieved using beta-CD dissolved in the mobile phase were enhanced, respectively, 8 and 12 times, and 10 and 15 times with beta-CD-Su. beta-cd-su 166-176 AFG1 like ATPase Homo sapiens 38-42 35594247-7 2022 Then, 30 CF samples were collected and the level of aflatoxins (AFB1, AFB2, AFG1, and AFG2) was determined using a validated method. Aflatoxins 52-62 AFG1 like ATPase Homo sapiens 76-80 1899057-0 1991 Identification of an aflatoxin G1-serum albumin adduct and its relevance to the measurement of human exposure to aflatoxins. Aflatoxins 113-123 AFG1 like ATPase Homo sapiens 21-33 1899057-2 1991 The product isolated from a Pronase digest of in vivo-modified albumin was identical by chromatographic retention time to the synthetic product obtained by the acylase-catalysed deacetylation product of N alpha-acetyl-L-lysine with 8,9-dihydro-8,9-dibromo-AFG1. N(alpha)-acetyllysine 203-226 AFG1 like ATPase Homo sapiens 256-260 1899057-3 1991 The in vitro product, AFG1-lysine, was characterized by UV, fluorescence, 1H- and 13C-NMR spectroscopy and fast atom bombardment MS. A competitive enzyme-linked immunoassay for this adduct was established using polyclonal antibodies to AFB1 and this was used together with an HPLC-fluorescence technique to quantitate the in vivo formation of AFG1-albumin adducts in comparison to AFB1. Lysine 27-33 AFG1 like ATPase Homo sapiens 22-26 1899057-3 1991 The in vitro product, AFG1-lysine, was characterized by UV, fluorescence, 1H- and 13C-NMR spectroscopy and fast atom bombardment MS. A competitive enzyme-linked immunoassay for this adduct was established using polyclonal antibodies to AFB1 and this was used together with an HPLC-fluorescence technique to quantitate the in vivo formation of AFG1-albumin adducts in comparison to AFB1. Lysine 27-33 AFG1 like ATPase Homo sapiens 343-347 1899057-3 1991 The in vitro product, AFG1-lysine, was characterized by UV, fluorescence, 1H- and 13C-NMR spectroscopy and fast atom bombardment MS. A competitive enzyme-linked immunoassay for this adduct was established using polyclonal antibodies to AFB1 and this was used together with an HPLC-fluorescence technique to quantitate the in vivo formation of AFG1-albumin adducts in comparison to AFB1. Hydrogen 74-76 AFG1 like ATPase Homo sapiens 22-26 1899057-3 1991 The in vitro product, AFG1-lysine, was characterized by UV, fluorescence, 1H- and 13C-NMR spectroscopy and fast atom bombardment MS. A competitive enzyme-linked immunoassay for this adduct was established using polyclonal antibodies to AFB1 and this was used together with an HPLC-fluorescence technique to quantitate the in vivo formation of AFG1-albumin adducts in comparison to AFB1. 13c 82-85 AFG1 like ATPase Homo sapiens 22-26 1899057-5 1991 The levels of AFG1-albumin adducts were determined to be 5.7- and 2.8-fold lower than with equivalent doses of AFB1 as determined by immunoassay and HPLC fluorescence respectively. Aflatoxin B1 111-115 AFG1 like ATPase Homo sapiens 14-18 7532124-1 1994 To find out if the presumed intake of dietary aflatoxins (AFB1 and AFG1) has adverse effect on the liver of Ghanaians, the toxins were measured in serum, urine and faecal specimens obtained from a group of apparently healthy Ghanaian adults. Aflatoxins 46-56 AFG1 like ATPase Homo sapiens 67-71