Nicotinamide adenine dinucleotide phosphate (BioDeep_00001868340)

Main id: BioDeep_00000003514

 

PANOMIX_OTCML-2023 BioNovoGene_Lab2019 natural product


代谢物信息卡片


NADP nicotinamide-adenine-dinucleotide phosphATE

化学式: C21H29N7O17P3+ (744.0833)
中文名称: β-烟酰胺腺嘌呤二核苷酸磷酸(NADP)水合物, β-烟酰胺腺嘌呤二核苷酸磷酸 水合物
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: C1=CC(=C[N+](=C1)C2C(C(C(O2)COP(=O)(O)OP(=O)(O)OCC3C(C(C(O3)N4C=NC5=C(N=CN=C54)N)OP(=O)(O)O)O)O)O)C(=O)N
InChI: InChI=1S/C21H28N7O17P3/c22-17-12-19(25-7-24-17)28(8-26-12)21-16(44-46(33,34)35)14(30)11(43-21)6-41-48(38,39)45-47(36,37)40-5-10-13(29)15(31)20(42-10)27-3-1-2-9(4-27)18(23)32/h1-4,7-8,10-11,13-16,20-21,29-31H,5-6H2,(H7-,22,23,24,25,32,33,34,35,36,37,38,39)/p+1/t10-,11-,13-,14-,15-,16-,20-,21-/m1/s1

描述信息

COVID info from COVID-19 Disease Map
Corona-virus
Coronavirus
SARS-CoV-2
COVID-19
SARS-CoV
COVID19
SARS2
SARS

同义名列表

3 个代谢物同义名

NADP nicotinamide-adenine-dinucleotide phosphATE; Nicotinamide adenine dinucleotide phosphate; NADP+



数据库引用编号

19 个数据库交叉引用编号

分类词条

相关代谢途径

Reactome(82)

BioCyc(68)

PlantCyc(0)

代谢反应

0 个相关的代谢反应过程信息。

Reactome(0)

BioCyc(0)

WikiPathways(0)

Plant Reactome(0)

INOH(0)

PlantCyc(0)

COVID-19 Disease Map(0)

PathBank(0)

PharmGKB(0)

11 个相关的物种来源信息

在这里通过桑基图来展示出与当前的这个代谢物在我们的BioDeep知识库中具有相关联信息的其他代谢物。在这里进行关联的信息来源主要有：

  • PubMed: 来源于PubMed文献库中的文献信息，我们通过自然语言数据挖掘得到的在同一篇文献中被同时提及的相关代谢物列表，这个列表按照代谢物同时出现的文献数量降序排序，取前10个代谢物作为相关研究中关联性很高的代谢物集合展示在桑基图中。
  • NCBI Taxonomy: 通过文献数据挖掘，得到的代谢物物种来源信息关联。这个关联信息同样按照出现的次数降序排序，取前10个代谢物作为高关联度的代谢物集合展示在桑吉图上。
  • Chemical Taxonomy: 在物质分类上处于同一个分类集合中的其他代谢物
  • Chemical Reaction: 在化学反应过程中，存在为当前代谢物相关联的生化反应过程中的反应底物或者反应产物的关联代谢物信息。

点击图上的相关代谢物的名称，可以跳转到相关代谢物的信息页面。

亚细胞结构定位 关联基因列表
Cytoplasm 10 AKR1B1, AKT1, CAT, DHFR, IDH1, MAPK14, NCF1, NOX4, RAC1, TXN
Peripheral membrane protein 2 FDXR, NCF1
Endoplasmic reticulum membrane 4 CYBA, CYBB, NOX4, RAC1
Nucleus 6 AKT1, MAPK14, MPO, NOX4, RAC1, TXN
cytosol 12 AKR1B1, AKT1, CAT, DHFR, GSR, IDH1, IDH2, MAPK14, NCF1, NCF2, RAC1, TXN
dendrite 3 CYBB, NCF1, RAC1
phagocytic vesicle 1 CYBB
trans-Golgi network 1 RAC1
nucleoplasm 5 AKR1B1, AKT1, MAPK14, MPO, TXN
Cell membrane 6 AKT1, CYBA, CYBB, NOX1, NOX4, RAC1
Lipid-anchor 1 RAC1
Cytoplasmic side 2 NCF1, RAC1
lamellipodium 2 AKT1, RAC1
ruffle membrane 1 RAC1
Multi-pass membrane protein 4 CYBB, DUOX1, NOX1, NOX4
Synapse 1 RAC1
cell cortex 2 AKT1, RAC1
cell surface 1 DUOX1
glutamatergic synapse 3 AKT1, MAPK14, RAC1
mitochondrial inner membrane 1 FDXR
neuronal cell body 2 CYBB, NCF1
postsynapse 2 AKT1, RAC1
Cytoplasm, cytosol 2 IDH1, NCF1
Lysosome 1 MPO
acrosomal vesicle 1 NCF2
endosome 1 CYBA
plasma membrane 9 AKT1, CYBA, CYBB, DUOX1, NCF1, NCF2, NOX1, NOX4, RAC1
Membrane 10 AKT1, CAT, CYBA, CYBB, DUOX1, NCF1, NCF2, NOX1, NOX4, RAC1
apical plasma membrane 1 DUOX1
extracellular exosome 8 AKR1B1, CAT, GSR, IDH1, IDH2, MPO, RAC1, TXN
endoplasmic reticulum 3 DUOX1, H6PD, NOX4
extracellular space 2 AKR1B1, MPO
perinuclear region of cytoplasm 1 NOX4
mitochondrion 9 AKR1B1, CAT, DHFR, FDXR, GSR, IDH1, IDH2, MAPK14, NOX4
protein-containing complex 2 AKT1, CAT
intracellular membrane-bounded organelle 2 CAT, MPO
Secreted 2 RAC1, TXN
extracellular region 6 CAT, IDH1, MAPK14, MPO, RAC1, TXN
cytoplasmic side of plasma membrane 1 NCF1
mitochondrial matrix 4 CAT, FDXR, GSR, IDH2
anchoring junction 1 NOX1
external side of plasma membrane 1 GSR
dendritic spine 1 RAC1
cytoplasmic vesicle 1 RAC1
microtubule cytoskeleton 1 AKT1
nucleolus 1 NOX4
Early endosome 1 NOX1
cell-cell junction 1 AKT1
vesicle 1 AKT1
Apical cell membrane 1 DUOX1
Cell projection, lamellipodium 1 RAC1
Cytoplasm, perinuclear region 1 NOX4
Mitochondrion inner membrane 1 FDXR
Cell junction, focal adhesion 1 NOX4
focal adhesion 3 CAT, NOX4, RAC1
spindle 1 AKT1
Peroxisome 3 CAT, IDH1, IDH2
Peroxisome matrix 1 CAT
peroxisomal matrix 2 CAT, IDH1
peroxisomal membrane 1 CAT
Mitochondrion intermembrane space 1 AKT1
mitochondrial intermembrane space 1 AKT1
secretory granule 2 CYBA, MPO
nuclear speck 1 MAPK14
ciliary basal body 1 AKT1
cell leading edge 1 DUOX1
cell projection 1 NOX1
phagocytic vesicle membrane 2 CYBA, CYBB
cytoskeleton 1 RAC1
cytoplasmic ribonucleoprotein granule 1 RAC1
[Isoform 5]: Cytoplasm 1 NOX4
Nucleus, nucleolus 1 NOX4
spindle pole 1 MAPK14
nuclear envelope 1 CYBB
Recycling endosome membrane 1 RAC1
monoatomic ion channel complex 1 CYBB
Cell projection, dendrite 1 RAC1
specific granule membrane 2 CYBA, CYBB
tertiary granule membrane 2 CYBA, CYBB
Melanosome 1 RAC1
azurophil granule 1 MPO
[Isoform 3]: Cytoplasm 1 NOX4
ficolin-1-rich granule lumen 3 CAT, IDH1, MAPK14
secretory granule lumen 3 CAT, IDH1, MAPK14
secretory granule membrane 1 RAC1
endoplasmic reticulum lumen 1 H6PD
tertiary granule lumen 1 IDH1
azurophil granule lumen 1 MPO
perinuclear endoplasmic reticulum 2 CYBB, NOX4
phagocytic vesicle lumen 1 MPO
ficolin-1-rich granule membrane 1 RAC1
[Isoform 4]: Nucleus 1 NOX4
catalase complex 1 CAT
NADPH oxidase complex 8 CYBA, CYBB, DUOX1, NCF1, NCF2, NOX1, NOX4, RAC1
Cell projection, invadopodium membrane 1 NOX1
[Isoform 6]: Cytoplasm 1 NOX4
phagolysosome 2 NCF1, NCF2


文献列表

  • Lara Vogelsang, Jürgen Eirich, Iris Finkemeier, Karl-Josef Dietz. Specificity and dynamics of H2O2 detoxification by the cytosolic redox regulatory network as revealed by in vitro reconstitution. Redox biology. 2024 Jun; 72(?):103141. doi: 10.1016/j.redox.2024.103141. [PMID: 38599017]
  • Ashley E Maloney, Sebastian H Kopf, Zhaoyue Zhang, Jamie McFarlin, Daniel B Nelson, Andrew L Masterson, Xinning Zhang. Large enrichments in fatty acid 2H/1H ratios distinguish respiration from aerobic fermentation in yeast Saccharomyces cerevisiae. Proceedings of the National Academy of Sciences of the United States of America. 2024 May; 121(20):e2310771121. doi: 10.1073/pnas.2310771121. [PMID: 38709917]
  • Jia Wang, Xiao Zhou, Kexin Li, Herong Wang, Chenglong Zhang, Yi Shi, Mingdong Yao, Ying Wang, Wenhai Xiao. Systems Metabolic Engineering for Efficient Violaxanthin Production in Yeast. Journal of agricultural and food chemistry. 2024 May; 72(18):10459-10468. doi: 10.1021/acs.jafc.4c01240. [PMID: 38666490]
  • Xiangpeng Meng, Fang Peng, Shijie Yu, Xinming Chi, Wenchi Wang, Shujuan Shao. Knockdown of NADK promotes LUAD ferroptosis via NADPH/FSP1 axis. Journal of cancer research and clinical oncology. 2024 May; 150(5):228. doi: 10.1007/s00432-024-05752-z. [PMID: 38700533]
  • Xue Bai, Shuling Wang, Qin Zhang, Yuhan Hu, Jiawei Zhou, Lianhui Men, Dengyu Li, Jing Ma, Qiuhui Wei, Mengdie Xu, Xiaopu Yin, Tianyuan Hu. Reprogramming the Metabolism of Yeast for High-Level Production of Miltiradiene. Journal of agricultural and food chemistry. 2024 Apr; 72(15):8704-8714. doi: 10.1021/acs.jafc.4c01203. [PMID: 38572931]
  • Wenjing Ouyang, Emilie Wientjes, Peter E L van der Putten, Ludovico Caracciolo, Ruixuan Zhao, Collins Agho, Maurizio Junior Chiurazzi, Marius Bongers, Paul C Struik, Herbert van Amerongen, Xinyou Yin. Roles for leakiness and O2 evolution in explaining lower-than-theoretical quantum yields of photosynthesis in the PEP-CK subtype of C4 plants. The New phytologist. 2024 Apr; 242(2):431-443. doi: 10.1111/nph.19614. [PMID: 38406986]
  • Mingming Sun, Qi Feng, Qi Yan, Huifang Zhao, Haiyan Wang, Shuai Zhang, Changliang Shan, Shuangping Liu, Jiyan Wang, Hongyan Zhai. Malate, a natural inhibitor of 6PGD, improves the efficacy of chemotherapy in lung cancer. Lung cancer (Amsterdam, Netherlands). 2024 Apr; 190(?):107541. doi: 10.1016/j.lungcan.2024.107541. [PMID: 38531154]
  • Xinxin Wang, Mei Li, Fan Wang, Guanghui Mao, Junchao Wu, Rong Han, Rui Sheng, Zhenghong Qin, Hong Ni. TIGAR reduces neuronal ferroptosis by inhibiting succinate dehydrogenase activity in cerebral ischemia. Free radical biology & medicine. 2024 Apr; 216(?):89-105. doi: 10.1016/j.freeradbiomed.2024.03.011. [PMID: 38494143]
  • Ray Singh Rathore, Manjari Mishra, Ashwani Pareek, Sneh Lata Singla-Pareek. A glutathione-independent DJ-1/Pfp1 domain containing glyoxalase III, OsDJ-1C, functions in abiotic stress adaptation in rice. Planta. 2024 Mar; 259(4):81. doi: 10.1007/s00425-023-04315-9. [PMID: 38438662]
  • Parisa Taghvimi, Mohammad Mohsenzadeh Golfazani, Mohammad Mahdi Taghvaei, Habibollah Samizadeh Lahiji. Investigating the effect of drought stress and methanol spraying on the influential genes in the Calvin cycle and photorespiration of rapeseed (Brassica napus). Functional plant biology : FPB. 2024 03; 51(?):. doi: 10.1071/fp23280. [PMID: 38467163]
  • Mingyu Yue, Mengsu Liu, Song Gao, Xuefeng Ren, Shenghu Zhou, Yijian Rao, Jingwen Zhou. High-Level De Novo Production of (2S)-Eriodictyol in Yarrowia Lipolytica by Metabolic Pathway and NADPH Regeneration Engineering. Journal of agricultural and food chemistry. 2024 Feb; 72(8):4292-4300. doi: 10.1021/acs.jafc.3c08861. [PMID: 38364826]
  • Yangzhen Liao, Wenmin Du, Jingqiong Wan, Jiahe Fan, Jilan Pi, Min Wu, Yuan Wei, Zhen Ouyang. Mining and functional characterization of NADPH-cytochrome P450 reductases of the DNJ biosynthetic pathway in mulberry leaves. BMC plant biology. 2024 Feb; 24(1):133. doi: 10.1186/s12870-024-04815-0. [PMID: 38395770]
  • Jaroslaw Szponar, Agnieszka Gorska, Marta Ostrowska-Lesko, Agnieszka Korga-Plewko, Michal Tchorz, Erwin Ciechanski, Anna Dabrowska, Ewa Poleszak, Franciszek Burdan, Jaroslaw Dudka, Marek Murias, Slawomir Mandziuk. Assessment of the Impact of Carvedilol Administered Together with Dexrazoxan and Doxorubicin on Liver Structure and Function, Iron Metabolism, and Myocardial Redox System in Rats. International journal of molecular sciences. 2024 Feb; 25(4):. doi: 10.3390/ijms25042219. [PMID: 38396896]
  • Jing Li, Wei Wang, Bingze Li, Yunzhuan Xue, Xinxin Wang, Shihui Liu, Shuwei Hu, Jiaxuan Tang, Bo Yan, Tong Li, Jiao Xue. NADP+-dependent isocitrate dehydrogenase as a novel target for altering carbon flux to lipid accumulation and enhancing antioxidant capacity in Tetradesmus obliquus. Bioresource technology. 2024 Jan; 395(?):130365. doi: 10.1016/j.biortech.2024.130365. [PMID: 38266784]
  • Ildefonso Rodriguez-Ramiro, Andrés Pastor-Fernández, José Luis López-Aceituno, Esther Garcia-Dominguez, Aranzazu Sierra-Ramirez, Angela M Valverde, Bárbara Martinez-Pastor, Alejo Efeyan, Mari Carmen Gomez-Cabrera, José Viña, Pablo J Fernandez-Marcos. Pharmacological and genetic increases in liver NADPH levels ameliorate NASH progression in female mice. Free radical biology & medicine. 2024 Jan; 210(?):448-461. doi: 10.1016/j.freeradbiomed.2023.11.019. [PMID: 38036067]
  • Chaomurilege, Atsuko Miyagi, Toshiki Ishikawa, Masatoshi Yamaguchi, Hideki Murayama, Maki Kawai-Yamada. Metabolic changes associated with dark-induced leaf senescence in Arabidopsis nadk2 mutants. Plant signaling & behavior. 2023 12; 18(1):2215618. doi: 10.1080/15592324.2023.2215618. [PMID: 37272565]
  • Dong-Oh Moon. NADPH Dynamics: Linking Insulin Resistance and β-Cells Ferroptosis in Diabetes Mellitus. International journal of molecular sciences. 2023 Dec; 25(1):. doi: 10.3390/ijms25010342. [PMID: 38203517]
  • Shaojie Cheng, Xueying Wan, Liping Yang, Yilu Qin, Shanchun Chen, Yongcan Liu, Yan Sun, Yuxiang Qiu, Luyi Huang, Qizhong Qin, Xiaojiang Cui, Mingjun Wu, Manran Liu. RGCC-mediated PLK1 activity drives breast cancer lung metastasis by phosphorylating AMPKα2 to activate oxidative phosphorylation and fatty acid oxidation. Journal of experimental & clinical cancer research : CR. 2023 Dec; 42(1):342. doi: 10.1186/s13046-023-02928-2. [PMID: 38102722]
  • Judith Scharte, Sebastian Hassa, Cornelia Herrfurth, Ivo Feussner, Giuseppe Forlani, Engelbert Weis, Antje von Schaewen. Metabolic priming in G6PDH isoenzyme-replaced tobacco lines improves stress tolerance and seed yields via altering assimilate partitioning. The Plant journal : for cell and molecular biology. 2023 Dec; 116(6):1696-1716. doi: 10.1111/tpj.16460. [PMID: 37713307]
  • Xin Lin, Xiaoxia Zhao, Qingfeng Chen, Xiaoyue Wang, Yongya Wu, Hao Zhao. Quercetin ameliorates ferroptosis of rat cardiomyocytes via activation of the SIRT1/p53/SLC7A11 signaling pathway to alleviate sepsis‑induced cardiomyopathy. International journal of molecular medicine. 2023 Dec; 52(6):. doi: 10.3892/ijmm.2023.5319. [PMID: 37859612]
  • Mengnan Zhao, Tao Lu, Guoshu Bi, Zhengyang Hu, Jiaqi Liang, Yunyi Bian, Mingxiang Feng, Cheng Zhan. PLK1 regulating chemoradiotherapy sensitivity of esophageal squamous cell carcinoma through pentose phosphate pathway/ferroptosis. Biomedicine & pharmacotherapy = Biomedecine & pharmacotherapie. 2023 Dec; 168(?):115711. doi: 10.1016/j.biopha.2023.115711. [PMID: 37879213]
  • Akiko Yoshihara, Keiko Kobayashi, Noriko Nagata, Sho Fujii, Hajime Wada, Koichi Kobayashi. Anionic lipids facilitate membrane development and protochlorophyllide biosynthesis in etioplasts. Plant physiology. 2023 Nov; ?(?):. doi: 10.1093/plphys/kiad604. [PMID: 37962588]
  • Shoki Ito, Atsuko Watanabe, Takashi Osanai. Regulation of l-aspartate oxidase contributes to NADP+ biosynthesis in Synechocystis sp. PCC 6803. Plant physiology. 2023 Nov; ?(?):. doi: 10.1093/plphys/kiad580. [PMID: 37936332]
  • Jingping Cheng, Guodong Li, Xue Wang, Congwei Yang, Furong Xu, Zigang Qian, Xiaohui Ma. Cloning and Functional Characterization of NADPH-Cytochrome P450 Reductases in Aconitum vilmorinianum. Molecules (Basel, Switzerland). 2023 Nov; 28(21):. doi: 10.3390/molecules28217409. [PMID: 37959828]
  • Konosuke Takemoto, Akiho Tsurugi-Sakurada, Ryota Moriuchi, Yuko Yoneda, Shingo Kawai. Cloning and characterization of NADPH-dependent double-bond reductases from Alnus sieboldiana that recognize linear diarylheptanoids as substrates. Phytochemistry. 2023 Nov; 215(?):113850. doi: 10.1016/j.phytochem.2023.113850. [PMID: 37659705]
  • Agata Jacewicz, Swathi Dantuluri, Stewart Shuman. Structural basis for Tpt1-catalyzed 2'-PO4 transfer from RNA and NADP(H) to NAD. Proceedings of the National Academy of Sciences of the United States of America. 2023 Oct; 120(44):e2312999120. doi: 10.1073/pnas.2312999120. [PMID: 37883434]
  • Alka Jangra, Siddhant Chaturvedi, Sonia Sihag, Garima Sharma, Siddharth Tiwari, Vinod Chhokar. Identification and functional characterization of a novel aldo-keto reductase from Aloe vera. Planta. 2023 Oct; 258(6):107. doi: 10.1007/s00425-023-04256-3. [PMID: 37897513]
  • Qiqi Zhang, Shilong Tian, Genyun Chen, Qiming Tang, Yijing Zhang, Andrew J Fleming, Xin-Guang Zhu, Peng Wang. Regulatory NADH dehydrogenase-like complex optimizes C4 photosynthetic carbon flow and cellular redox in maize. The New phytologist. 2023 Oct; ?(?):. doi: 10.1111/nph.19332. [PMID: 37872738]
  • Eda Dagsuyu, Refiye Yanardag. Purification and characterization of thioredoxin reductase enzyme from commercial Spirulina platensis tablets by affinity chromatography and investigation of the effects of some chemicals and drugs on enzyme activity. Biotechnology and applied biochemistry. 2023 Oct; ?(?):. doi: 10.1002/bab.2530. [PMID: 37864368]
  • Binyan Wu, Fan Qi, Yan Liang. Fuels for ROS signaling in plant immunity. Trends in plant science. 2023 10; 28(10):1124-1131. doi: 10.1016/j.tplants.2023.04.007. [PMID: 37188557]
  • Kenneth K Y Ting, Pei Yu, Riley Dow, Eric Floro, Hisham Ibrahim, Corey A Scipione, Sharon J Hyduk, Chanele K Polenz, Olga Zaslaver, Peer W F Karmaus, Michael B Fessler, Hannes L Röst, Michael Ohh, Sue Tsai, Daniel A Winer, Minna Woo, Jonathan Rocheleau, Jenny Jongstra-Bilen, Myron I Cybulsky. Oxidized Low-Density Lipoprotein Accumulation Suppresses Glycolysis and Attenuates the Macrophage Inflammatory Response by Diverting Transcription from the HIF-1α to the Nrf2 Pathway. Journal of immunology (Baltimore, Md. : 1950). 2023 Sep; ?(?):. doi: 10.4049/jimmunol.2300293. [PMID: 37756544]
  • Ivan Kushkevych, Dani Dordević, Mohammad I Alberfkani, Márió Gajdács, Eszter Ostorházi, Monika Vítězová, Simon K-M R Rittmann. NADH and NADPH peroxidases as antioxidant defense mechanisms in intestinal sulfate-reducing bacteria. Scientific reports. 2023 08; 13(1):13922. doi: 10.1038/s41598-023-41185-3. [PMID: 37626119]
  • Yanqiu Yang, Tingyu Hao, Xiaohu Yao, Yue Che, Yueyang Liu, Mingxia Fang, Yingjie Wang, Di Zhou, Huifang Chai, Ning Li, Yue Hou. Crebanine ameliorates ischemia-reperfusion brain damage by inhibiting oxidative stress and neuroinflammation mediated by NADPH oxidase 2 in microglia. Phytomedicine : international journal of phytotherapy and phytopharmacology. 2023 Aug; 120(?):155044. doi: 10.1016/j.phymed.2023.155044. [PMID: 37634486]
  • Deepika Kandoi, Baishnab C Tripathy. Overexpression of chloroplastic Zea mays NADP-malic enzyme (ZmNADP-ME) confers tolerance to salt stress in Arabidopsis thaliana. Photosynthesis research. 2023 Aug; ?(?):. doi: 10.1007/s11120-023-01041-x. [PMID: 37561272]
  • Jihye Yang, Yoontae Lee, Cheol-Sang Hwang. The ubiquitin-proteasome system links NADPH metabolism to ferroptosis. Trends in cell biology. 2023 Aug; ?(?):. doi: 10.1016/j.tcb.2023.07.003. [PMID: 37558595]
  • Moges A Retta, Xinyou Yin, Quang Tri Ho, Rodrigo Watté, Herman N C Berghuijs, Pieter Verboven, Wouter Saeys, Francisco Javier Cano, Oula Ghannoum, Paul C Struik, Bart M Nicolaï. The role of chloroplast movement in C4 photosynthesis: a theoretical analysis using a three-dimensional reaction-diffusion model for maize. Journal of experimental botany. 2023 08; 74(14):4125-4142. doi: 10.1093/jxb/erad138. [PMID: 37083863]
  • Ruiyuan Liu, Leng Wang, Yue Meng, Yiyi Tian, Fang Li, Huizhe Lu. Theoretical and Experimental Studies on Plant Light-Dependent Protochlorophyllide Oxidoreductase as a Novel Target for Searching Potential Herbicides. Journal of agricultural and food chemistry. 2023 Aug; 71(30):11654-11666. doi: 10.1021/acs.jafc.3c01783. [PMID: 37467369]
  • Sai Krishna Talla, Bobba Sunil, Duvvarapu Easwar Rao, Pidakala Rajsheel, Deepak Saini, Agepati S Raghavendra. Redox basis of photosynthesis inhibition at supra-optimal bicarbonate in mesophyll protoplasts of Arabidopsis thaliana. Journal of plant physiology. 2023 Aug; 287(?):154047. doi: 10.1016/j.jplph.2023.154047. [PMID: 37393886]
  • Karen Zinzius, Giulia Maria Marchetti, Ronja Fischer, Yuval Milrad, Anne Oltmanns, Simon Kelterborn, Iftach Yacoby, Peter Hegemann, Martin Scholz, Michael Hippler. Calredoxin regulates the chloroplast NADPH-dependent thioredoxin reductase in Chlamydomonas reinhardtii. Plant physiology. 2023 Jul; ?(?):. doi: 10.1093/plphys/kiad426. [PMID: 37474113]
  • Maria Pilarska, Ewa Niewiadomska, Jerzy Kruk. Salinity-induced changes in plastoquinone pool redox state in halophytic Mesembryanthemum crystallinum L. Scientific reports. 2023 07; 13(1):11160. doi: 10.1038/s41598-023-38194-7. [PMID: 37430104]
  • Toshitaka Nakamura, Clara Hipp, André Santos Dias Mourão, Jan Borggräfe, Maceler Aldrovandi, Bernhard Henkelmann, Jonas Wanninger, Eikan Mishima, Elena Lytton, David Emler, Bettina Proneth, Michael Sattler, Marcus Conrad. Phase separation of FSP1 promotes ferroptosis. Nature. 2023 Jul; 619(7969):371-377. doi: 10.1038/s41586-023-06255-6. [PMID: 37380771]
  • Ziyu Zhu, Xiaoqian Chen, Wenhao Li, Yingping Zhuang, Yuzheng Zhao, Guan Wang. Understanding the effect of temperature downshift on CHO cell growth, antibody titer and product quality by intracellular metabolite profiling and in vivo monitoring of redox state. Biotechnology progress. 2023 Jul; 39(4):e3352. doi: 10.1002/btpr.3352. [PMID: 37141532]
  • Tomasz Piechowiak, Bartosz Skóra, Maciej Balawejder. Effect of postharvest nicotinamide treatment on NAD+ metabolism and redox status in strawberry fruit during storage. Phytochemistry. 2023 Jun; 213(?):113766. doi: 10.1016/j.phytochem.2023.113766. [PMID: 37343736]
  • Miriam Ferrer, Nicholas Mourikis, Emma E Davidson, Sam O Kleeman, Marta Zaccaria, Jill Habel, Rachel Rubino, Qing Gao, Thomas R Flint, Lisa Young, Claire M Connell, Michael J Lukey, Marcus D Goncalves, Eileen P White, Ashok R Venkitaraman, Tobias Janowitz. Ketogenic diet promotes tumor ferroptosis but induces relative corticosterone deficiency that accelerates cachexia. Cell metabolism. 2023 Jun; ?(?):. doi: 10.1016/j.cmet.2023.05.008. [PMID: 37311455]
  • Pamela E Molinari, Adriana R Krapp, Andrea Weiner, Hannes M Beyer, Arun Kumar Kondadi, Tim Blomeier, Melina López, Pilar Bustos-Sanmamed, Evelyn Tevere, Wilfried Weber, Andreas S Reichert, Nora B Calcaterra, Mathias Beller, Nestor Carrillo, Matias D Zurbriggen. NERNST: a genetically-encoded ratiometric non-destructive sensing tool to estimate NADP(H) redox status in bacterial, plant and animal systems. Nature communications. 2023 06; 14(1):3277. doi: 10.1038/s41467-023-38739-4. [PMID: 37280202]
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