Naadp (BioDeep_00000004164)

 

Secondary id: BioDeep_00001872139

natural product PANOMIX_OTCML-2023


代谢物信息卡片


Nicotinic acid adenine dinucleotide phosphate sodium salt

化学式: [C21H28N6O18P3]+ (745.0673)
中文名称: 烟酸腺嘌呤二核苷酸磷酸
谱图信息: 最多检出来源 Chinese Herbal Medicine(otcml) 81.25%

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)O
InChI: InChI=1S/C21H27N6O18P3/c22-17-12-18(24-7-23-17)27(8-25-12)20-16(44-46(33,34)35)14(29)11(43-20)6-41-48(38,39)45-47(36,37)40-5-10-13(28)15(30)19(42-10)26-3-1-2-9(4-26)21(31)32/h1-4,7-8,10-11,13-16,19-20,28-30H,5-6H2,(H6-,22,23,24,31,32,33,34,35,36,37,38,39)/p+1/t10-,11-,13-,14-,15-,16-,19-,20-/m1/s1



数据库引用编号

14 个数据库交叉引用编号

分类词条

相关代谢途径

Reactome(3)

BioCyc(0)

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)

0 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 5 EDN1, ITPR3, JPT2, LSM12, RYR1
Endosome membrane 3 MCOLN1, TPCN1, TPCN2
Endoplasmic reticulum membrane 3 CD4, HSP90B1, ITPR3
Nucleus 2 HSP90B1, JPT2
cytosol 3 HSP90B1, JPT2, TPCN2
nucleoplasm 3 ATP2B1, ITPR3, MCOLN1
Cell membrane 4 ATP2B1, CD4, MCOLN1, TRPM2
Early endosome membrane 1 TPCN1
Multi-pass membrane protein 10 ATP2B1, CATSPER3, ITPR3, MCOLN1, RYR1, RYR2, RYR3, TPCN1, TPCN2, TRPM2
Synapse 1 ATP2B1
cell cortex 1 RYR1
cell surface 1 CD38
glutamatergic synapse 1 ATP2B1
Golgi apparatus 1 MCOLN1
Golgi membrane 1 INS
lysosomal membrane 4 MCOLN1, TPCN1, TPCN2, TRPM2
neuronal cell body 1 ITPR3
presynaptic membrane 1 ATP2B1
sarcolemma 3 RYR1, RYR2, RYR3
smooth endoplasmic reticulum 4 HSP90B1, RYR1, RYR2, RYR3
Lysosome 4 MCOLN1, TPCN1, TPCN2, TRPM2
acrosomal vesicle 1 CATSPER3
endosome 1 TPCN1
plasma membrane 12 ATP2B1, CATSPER3, CD38, CD4, F2, GCG, ITPR3, JPT2, MCOLN1, RYR1, RYR2, TRPM2
synaptic vesicle membrane 1 ATP2B1
Membrane 11 ATP2B1, CD38, HSP90B1, ITPR3, MCOLN1, RYR1, RYR2, RYR3, TPCN1, TPCN2, TRPM2
axon 1 CCK
basolateral plasma membrane 2 ATP2B1, CD38
brush border 1 ITPR3
extracellular exosome 5 ATP2B1, CD38, F2, HSP90B1, RYR1
Lysosome membrane 3 MCOLN1, TPCN1, TPCN2
endoplasmic reticulum 3 CATSPER3, HSP90B1, ITPR3
extracellular space 5 CCK, EDN1, F2, GCG, INS
perinuclear region of cytoplasm 1 HSP90B1
protein-containing complex 2 HSP90B1, RYR2
intracellular membrane-bounded organelle 2 ATP2B1, MCOLN1
Single-pass type I membrane protein 1 CD4
Secreted 5 CCK, EDN1, F2, GCG, INS
extracellular region 6 CCK, EDN1, F2, GCG, HSP90B1, INS
basal part of cell 1 EDN1
motile cilium 1 CATSPER3
Cytoplasmic vesicle, secretory vesicle, synaptic vesicle membrane 1 ATP2B1
nuclear membrane 1 CD38
external side of plasma membrane 1 CD4
perikaryon 1 TRPM2
Z disc 3 RYR1, RYR2, RYR3
cytoplasmic vesicle 1 TRPM2
nucleolus 1 ITPR3
Melanosome membrane 1 TPCN2
midbody 1 HSP90B1
Early endosome 1 CD4
apical part of cell 1 ITPR3
Single-pass type II membrane protein 1 CD38
Membrane raft 1 CD4
focal adhesion 1 HSP90B1
sarcoplasmic reticulum 3 ITPR3, RYR1, RYR2
collagen-containing extracellular matrix 2 F2, HSP90B1
lateral plasma membrane 1 ATP2B1
nuclear outer membrane 1 ITPR3
Late endosome 1 MCOLN1
receptor complex 2 ITPR3, MCOLN1
Cytoplasmic vesicle, phagosome membrane 1 MCOLN1
Late endosome membrane 2 MCOLN1, TPCN2
Cell projection, phagocytic cup 1 MCOLN1
cell projection 3 ATP2B1, MCOLN1, TRPM2
phagocytic cup 1 MCOLN1
phagocytic vesicle membrane 1 MCOLN1
blood microparticle 1 F2
Basolateral cell membrane 1 ATP2B1
[Isoform 2]: Cell membrane 1 TRPM2
organelle membrane 1 RYR1
Recycling endosome membrane 1 TPCN1
endosome lumen 1 INS
I band 1 RYR1
Cell projection, cilium, flagellum membrane 1 CATSPER3
monoatomic ion channel complex 2 TPCN1, TPCN2
Cytoplasmic vesicle membrane 2 MCOLN1, TRPM2
specific granule membrane 1 TRPM2
tertiary granule membrane 1 TRPM2
Melanosome 1 HSP90B1
Presynaptic cell membrane 1 ATP2B1
sperm plasma membrane 1 HSP90B1
secretory granule lumen 2 GCG, INS
secretory granule membrane 1 ITPR3
Golgi lumen 2 F2, INS
endoplasmic reticulum lumen 5 CD4, F2, GCG, HSP90B1, INS
transport vesicle 2 EDN1, INS
Sarcoplasmic reticulum membrane 3 RYR1, RYR2, RYR3
Endoplasmic reticulum-Golgi intermediate compartment membrane 1 INS
immunological synapse 1 ATP2B1
clathrin-coated endocytic vesicle membrane 1 CD4
Sarcoplasmic reticulum lumen 1 HSP90B1
calcium channel complex 3 RYR1, RYR2, RYR3
junctional sarcoplasmic reticulum membrane 2 RYR1, RYR2
platelet dense tubular network membrane 1 ITPR3
ficolin-1-rich granule membrane 1 TRPM2
endolysosome membrane 1 TPCN2
[Isoform 1]: Cell membrane 1 TRPM2
Cytoplasmic vesicle, secretory vesicle membrane 1 ITPR3
terminal cisterna 1 RYR1
[Isoform 3]: Cell membrane 1 TRPM2
endocytic vesicle lumen 1 HSP90B1
[Glucagon-like peptide 1]: Secreted 1 GCG
T cell receptor complex 1 CD4
transport vesicle membrane 1 ITPR3
rough endoplasmic reticulum lumen 1 EDN1
Weibel-Palade body 1 EDN1
endoplasmic reticulum chaperone complex 1 HSP90B1
photoreceptor ribbon synapse 1 ATP2B1
endolysosome 1 TPCN1
cytoplasmic side of endoplasmic reticulum membrane 1 ITPR3
ryanodine receptor complex 1 RYR1
CatSper complex 1 CATSPER3


文献列表

  • Shenghua Yang, Fan Zhang, Quanwen Li, Quanzhong Li. Niacin promotes the efflux of lysosomal cholesterol from macrophages via the CD38/NAADP signaling pathway. Experimental biology and medicine (Maywood, N.J.). 2022 06; 247(12):1047-1054. doi: 10.1177/15353702221084632. [PMID: 35369785]
  • Neel R Nabar, Christopher N Heijjer, Chong-Shan Shi, Il-Young Hwang, Sundar Ganesan, Mikael C I Karlsson, John H Kehrl. LRRK2 is required for CD38-mediated NAADP-Ca2+ signaling and the downstream activation of TFEB (transcription factor EB) in immune cells. Autophagy. 2022 01; 18(1):204-222. doi: 10.1080/15548627.2021.1954779. [PMID: 34313548]
  • Paula Maria Heister, Trevor Powell, Antony Galione. Glucose and NAADP trigger elementary intracellular β-cell Ca2+ signals. Scientific reports. 2021 05; 11(1):10714. doi: 10.1038/s41598-021-88906-0. [PMID: 34021189]
  • Gihan S Gunaratne, Eugen Brailoiu, Shijun He, Ellen M Unterwald, Sandip Patel, James T Slama, Timothy F Walseth, Jonathan S Marchant. Essential requirement for JPT2 in NAADP-evoked Ca2+ signaling. Science signaling. 2021 03; 14(675):. doi: 10.1126/scisignal.abd5605. [PMID: 33758061]
  • Sharon Negri, Pawan Faris, Francesco Moccia. Endolysosomal Ca2+ signaling in cardiovascular health and disease. International review of cell and molecular biology. 2021; 363(?):203-269. doi: 10.1016/bs.ircmb.2021.03.001. [PMID: 34392930]
  • Johannes Westman, Spencer A Freeman, Sergio Grinstein. Unconventional role of lysosomes in phagocytosis. Cell calcium. 2020 11; 91(?):102269. doi: 10.1016/j.ceca.2020.102269. [PMID: 32818767]
  • Na Xie, Lu Zhang, Wei Gao, Canhua Huang, Peter Ernst Huber, Xiaobo Zhou, Changlong Li, Guobo Shen, Bingwen Zou. NAD+ metabolism: pathophysiologic mechanisms and therapeutic potential. Signal transduction and targeted therapy. 2020 10; 5(1):227. doi: 10.1038/s41392-020-00311-7. [PMID: 33028824]
  • Andreas H Guse. 25 Years of Collaboration with A Genius: Deciphering Adenine Nucleotide Ca2+ Mobilizing Second Messengers Together with Professor Barry Potter. Molecules (Basel, Switzerland). 2020 Sep; 25(18):. doi: 10.3390/molecules25184220. [PMID: 32942537]
  • Antony Galione. NAADP Receptors. Cold Spring Harbor perspectives in biology. 2019 11; 11(11):. doi: 10.1101/cshperspect.a035071. [PMID: 31182546]
  • Jeffrey J Kelu, Sarah E Webb, Antony Galione, Andrew L Miller. Characterization of ADP-ribosyl cyclase 1-like (ARC1-like) activity and NAADP signaling during slow muscle cell development in zebrafish embryos. Developmental biology. 2019 01; 445(2):211-225. doi: 10.1016/j.ydbio.2018.11.005. [PMID: 30447180]
  • Roberto Moscatiello, Simone Sello, Michelina Ruocco, Ani Barbulova, Enrico Cortese, Sebastiano Nigris, Barbara Baldan, Maurizio Chiurazzi, Paola Mariani, Matteo Lorito, Lorella Navazio. The Hydrophobin HYTLO1 Secreted by the Biocontrol Fungus Trichoderma longibrachiatum Triggers a NAADP-Mediated Calcium Signalling Pathway in Lotus japonicus. International journal of molecular sciences. 2018 Sep; 19(9):. doi: 10.3390/ijms19092596. [PMID: 30200468]
  • V Hreniukh, S Bychkova, O Kulachkovsky, A Babsky. Effect of bafilomycin and NAADP on membrane-associated ATPases and respiration of isolated mitochondria of the murine Nemeth-Kellner lymphoma. Cell biochemistry and function. 2016 Dec; 34(8):579-587. doi: 10.1002/cbf.3231. [PMID: 27862060]
  • Felix Schuebel, Andrea Rocker, Daniel Edelmann, Julia Schessner, Clara Brieke, Anton Meinhart. 3'-NADP and 3'-NAADP, Two Metabolites Formed by the Bacterial Type III Effector AvrRxo1. The Journal of biological chemistry. 2016 10; 291(44):22868-22880. doi: 10.1074/jbc.m116.751297. [PMID: 27621317]
  • Xiaoyang Xu, Xinxu Yuan, Ningjun Li, William L Dewey, Pin-Lan Li, Fan Zhang. Lysosomal cholesterol accumulation in macrophages leading to coronary atherosclerosis in CD38(-/-) mice. Journal of cellular and molecular medicine. 2016 06; 20(6):1001-13. doi: 10.1111/jcmm.12788. [PMID: 26818887]
  • Sandip Patel, Christopher J Penny, Taufiq Rahman. Two-pore Channels Enter the Atomic Era: Structure of Plant TPC Revealed. Trends in biochemical sciences. 2016 06; 41(6):475-477. doi: 10.1016/j.tibs.2016.04.007. [PMID: 27156118]
  • G Cristina Brailoiu, Eugen Brailoiu. Modulation of Calcium Entry by the Endo-lysosomal System. Advances in experimental medicine and biology. 2016; 898(?):423-47. doi: 10.1007/978-3-319-26974-0_18. [PMID: 27161239]
  • Insa M A Wolf, Björn-Philipp Diercks, Ellen Gattkowski, Frederik Czarniak, Jan Kempski, René Werner, Daniel Schetelig, Hans-Willi Mittrücker, Valéa Schumacher, Manuel von Osten, Dimitri Lodygin, Alexander Flügel, Ralf Fliegert, Andreas H Guse. Frontrunners of T cell activation: Initial, localized Ca2+ signals mediated by NAADP and the type 1 ryanodine receptor. Science signaling. 2015 Oct; 8(398):ra102. doi: 10.1126/scisignal.aab0863. [PMID: 26462735]
  • Anthony J Morgan, Lianne C Davis, Margarida Ruas, Antony Galione. TPC: the NAADP discovery channel?. Biochemical Society transactions. 2015 Jun; 43(3):384-9. doi: 10.1042/bst20140300. [PMID: 26009180]
  • Agustin Guerrero-Hernandez, Martin Leonardo Gallegos-Gomez, Victor Hugo Sanchez-Vazquez, Maria Cristina Lopez-Mendez. Acidic intracellular Ca(2+) stores and caveolae in Ca(2+) signaling and diabetes. Cell calcium. 2014 Nov; 56(5):323-31. doi: 10.1016/j.ceca.2014.08.005. [PMID: 25182518]
  • Samantha J Pitt, Andy K M Lam, Katja Rietdorf, Antony Galione, Rebecca Sitsapesan. Reconstituted human TPC1 is a proton-permeable ion channel and is activated by NAADP or Ca2+. Science signaling. 2014 May; 7(326):ra46. doi: 10.1126/scisignal.2004854. [PMID: 24847115]
  • Anthony J Morgan, Antony Galione. Two-pore channels (TPCs): current controversies. BioEssays : news and reviews in molecular, cellular and developmental biology. 2014 Feb; 36(2):173-83. doi: 10.1002/bies.201300118. [PMID: 24277557]
  • Cristina I López Sanjurjo, Stephen C Tovey, Colin W Taylor. Rapid recycling of Ca2+ between IP3-sensitive stores and lysosomes. PloS one. 2014; 9(10):e111275. doi: 10.1371/journal.pone.0111275. [PMID: 25337829]
  • Jing Xiong, Min Xia, Ming Xu, Yang Zhang, Justine M Abais, Guangbi Li, Christopher R Riebling, Joseph K Ritter, Krishna M Boini, Pin-Lan Li. Autophagy maturation associated with CD38-mediated regulation of lysosome function in mouse glomerular podocytes. Journal of cellular and molecular medicine. 2013 Dec; 17(12):1598-607. doi: 10.1111/jcmm.12173. [PMID: 24238063]
  • Peter J Kilfoil, Srinivas M Tipparaju, Oleg A Barski, Aruni Bhatnagar. Regulation of ion channels by pyridine nucleotides. Circulation research. 2013 Feb; 112(4):721-41. doi: 10.1161/circresaha.111.247940. [PMID: 23410881]
  • Richard M Graeff, Hon Cheung Lee. Determination of ADP-ribosyl cyclase activity, cyclic ADP-ribose, and nicotinic acid adenine dinucleotide phosphate in tissue extracts. Methods in molecular biology (Clifton, N.J.). 2013; 1016(?):39-56. doi: 10.1007/978-1-62703-441-8_4. [PMID: 23681571]
  • Hong Wu. [Calcium signaling in platelet activation]. Sheng li ke xue jin zhan [Progress in physiology]. 2012 Dec; 43(6):417-21. doi: . [PMID: 23520759]
  • Volodymyr Rybalchenko, Malini Ahuja, Jessica Coblentz, Dev Churamani, Sandip Patel, Krill Kiselyov, Shmuel Muallem. Membrane potential regulates nicotinic acid adenine dinucleotide phosphate (NAADP) dependence of the pH- and Ca2+-sensitive organellar two-pore channel TPC1. The Journal of biological chemistry. 2012 Jun; 287(24):20407-16. doi: 10.1074/jbc.m112.359612. [PMID: 22500018]
  • Colin W Taylor, Philippa Dale. Intracellular Ca(2+) channels - a growing community. Molecular and cellular endocrinology. 2012 Apr; 353(1-2):21-8. doi: 10.1016/j.mce.2011.08.028. [PMID: 21889573]
  • Antony Galione, Kai-Ting Chuang. Pyridine nucleotide metabolites and calcium release from intracellular stores. Advances in experimental medicine and biology. 2012; 740(?):305-23. doi: 10.1007/978-94-007-2888-2_13. [PMID: 22453948]
  • Fan Zhang, Ming Xu, Wei-Qing Han, Pin-Lan Li. Reconstitution of lysosomal NAADP-TRP-ML1 signaling pathway and its function in TRP-ML1(-/-) cells. American journal of physiology. Cell physiology. 2011 Aug; 301(2):C421-30. doi: 10.1152/ajpcell.00393.2010. [PMID: 21613607]
  • Emyr Lloyd-Evans, Frances M Platt. Lysosomal Ca(2+) homeostasis: role in pathogenesis of lysosomal storage diseases. Cell calcium. 2011 Aug; 50(2):200-5. doi: 10.1016/j.ceca.2011.03.010. [PMID: 21724254]
  • Edgar Peiter. The plant vacuole: emitter and receiver of calcium signals. Cell calcium. 2011 Aug; 50(2):120-8. doi: 10.1016/j.ceca.2011.02.002. [PMID: 21376393]
  • Soichiro Yamaguchi, Archana Jha, Qin Li, Abigail A Soyombo, George D Dickinson, Dev Churamani, Eugen Brailoiu, Sandip Patel, Shmuel Muallem. Transient receptor potential mucolipin 1 (TRPML1) and two-pore channels are functionally independent organellar ion channels. The Journal of biological chemistry. 2011 Jul; 286(26):22934-42. doi: 10.1074/jbc.m110.210930. [PMID: 21540176]
  • S O Sage, N Pugh, M J Mason, A G S Harper. Monitoring the intracellular store Ca2+ concentration in agonist-stimulated, intact human platelets by using Fluo-5N. Journal of thrombosis and haemostasis : JTH. 2011 Mar; 9(3):540-51. doi: 10.1111/j.1538-7836.2010.04159.x. [PMID: 21143372]
  • Antony Galione. NAADP receptors. Cold Spring Harbor perspectives in biology. 2011 Jan; 3(1):a004036. doi: 10.1101/cshperspect.a004036. [PMID: 21047915]
  • Eugen Brailoiu, Taufiq Rahman, Dev Churamani, David L Prole, G Cristina Brailoiu, Robert Hooper, Colin W Taylor, Sandip Patel. An NAADP-gated two-pore channel targeted to the plasma membrane uncouples triggering from amplifying Ca2+ signals. The Journal of biological chemistry. 2010 Dec; 285(49):38511-6. doi: 10.1074/jbc.m110.162073. [PMID: 20880839]
  • Emyr Lloyd-Evans, Helen Waller-Evans, Ksenia Peterneva, Frances M Platt. Endolysosomal calcium regulation and disease. Biochemical Society transactions. 2010 Dec; 38(6):1458-64. doi: 10.1042/bst0381458. [PMID: 21118107]
  • Mira Rosenblat, Nina Volkova, Michael Aviram. Macrophage endoplasmic reticulum (ER) proteins and reducing elements stabilize paraoxonase 2 (PON2). Atherosclerosis. 2010 Dec; 213(2):408-14. doi: 10.1016/j.atherosclerosis.2010.09.029. [PMID: 21036357]
  • Xinjiang Cai, Sandip Patel. Degeneration of an intracellular ion channel in the primate lineage by relaxation of selective constraints. Molecular biology and evolution. 2010 Oct; 27(10):2352-9. doi: 10.1093/molbev/msq122. [PMID: 20463046]
  • Latha Ramakrishnan, Hélène Muller-Steffner, Christophe Bosc, Victor D Vacquier, Francis Schuber, Marie-Jo Moutin, Leslie Dale, Sandip Patel. A single residue in a novel ADP-ribosyl cyclase controls production of the calcium-mobilizing messengers cyclic ADP-ribose and nicotinic acid adenine dinucleotide phosphate. The Journal of biological chemistry. 2010 Jun; 285(26):19900-9. doi: 10.1074/jbc.m110.105312. [PMID: 20385553]
  • Sridhar R Vasudevan, Alexander M Lewis, Jennifer W Chan, Claire L Machin, Debroshi Sinha, Antony Galione, Grant C Churchill. The calcium-mobilizing messenger nicotinic acid adenine dinucleotide phosphate participates in sperm activation by mediating the acrosome reaction. The Journal of biological chemistry. 2010 Jun; 285(24):18262-9. doi: 10.1074/jbc.m109.087858. [PMID: 20400502]
  • Guey-Shyang Hwang, Szu-Tah Chen, Te-Jung Chen, Shyi-Wu Wang. Effects of hypoxia on testosterone release in rat Leydig cells. American journal of physiology. Endocrinology and metabolism. 2009 Nov; 297(5):E1039-45. doi: 10.1152/ajpendo.00010.2009. [PMID: 19690072]
  • Tiffany L Thai, Grant C Churchill, William J Arendshorst. NAADP receptors mediate calcium signaling stimulated by endothelin-1 and norepinephrine in renal afferent arterioles. American journal of physiology. Renal physiology. 2009 Aug; 297(2):F510-6. doi: 10.1152/ajprenal.00116.2009. [PMID: 19439521]
  • Dev Churamani, Michael J Boulware, Latha Ramakrishnan, Timothy J Geach, Andrew C R Martin, Victor D Vacquier, Jonathan S Marchant, Leslie Dale, Sandip Patel. Molecular characterization of a novel cell surface ADP-ribosyl cyclase from the sea urchin. Cellular signalling. 2008 Dec; 20(12):2347-55. doi: 10.1016/j.cellsig.2008.09.005. [PMID: 18824228]
  • Andreas H Guse, Hon Cheung Lee. NAADP: a universal Ca2+ trigger. Science signaling. 2008 Nov; 1(44):re10. doi: 10.1126/scisignal.144re10. [PMID: 18984909]
  • Nicholas P Kinnear, Christopher N Wyatt, Jill H Clark, Peter J Calcraft, Sidney Fleischer, Loice H Jeyakumar, Graeme F Nixon, A Mark Evans. Lysosomes co-localize with ryanodine receptor subtype 3 to form a trigger zone for calcium signalling by NAADP in rat pulmonary arterial smooth muscle. Cell calcium. 2008 Aug; 44(2):190-201. doi: 10.1016/j.ceca.2007.11.003. [PMID: 18191199]
  • Guido Gambara, Richard A Billington, Marcella Debidda, Alessio D'Alessio, Fioretta Palombi, Elio Ziparo, Armando A Genazzani, Antonio Filippini. NAADP-induced Ca(2+ signaling in response to endothelin is via the receptor subtype B and requires the integrity of lipid rafts/caveolae. Journal of cellular physiology. 2008 Aug; 216(2):396-404. doi: 10.1002/jcp.21407. [PMID: 18288637]
  • Byung-Ju Kim, Kwang-Hyun Park, Chang-Yeol Yim, Shin Takasawa, Hiroshi Okamoto, Mie-Jae Im, Uh-Hyun Kim. Generation of nicotinic acid adenine dinucleotide phosphate and cyclic ADP-ribose by glucagon-like peptide-1 evokes Ca2+ signal that is essential for insulin secretion in mouse pancreatic islets. Diabetes. 2008 Apr; 57(4):868-78. doi: 10.2337/db07-0443. [PMID: 18184929]
  • Fan Zhang, Pin-Lan Li. Reconstitution and characterization of a nicotinic acid adenine dinucleotide phosphate (NAADP)-sensitive Ca2+ release channel from liver lysosomes of rats. The Journal of biological chemistry. 2007 Aug; 282(35):25259-69. doi: 10.1074/jbc.m701614200. [PMID: 17613490]
  • Emma Heart, Gordon C Yaney, Richard F Corkey, Vera Schultz, Esthere Luc, Lihan Liu, Jude T Deeney, Orian Shirihai, Keith Tornheim, Peter J S Smith, Barbara E Corkey. Ca2+, NAD(P)H and membrane potential changes in pancreatic beta-cells by methyl succinate: comparison with glucose. The Biochemical journal. 2007 Apr; 403(1):197-205. doi: 10.1042/bj20061209. [PMID: 17181533]
  • R Fliegert, A Gasser, A H Guse. Regulation of calcium signalling by adenine-based second messengers. Biochemical Society transactions. 2007 Feb; 35(Pt 1):109-14. doi: 10.1042/bst0350109. [PMID: 17233614]
  • Julia V Gerasimenko, Sarah E Flowerdew, Svetlana G Voronina, Tatiana K Sukhomlin, Alexei V Tepikin, Ole H Petersen, Oleg V Gerasimenko. Bile acids induce Ca2+ release from both the endoplasmic reticulum and acidic intracellular calcium stores through activation of inositol trisphosphate receptors and ryanodine receptors. The Journal of biological chemistry. 2006 Dec; 281(52):40154-63. doi: 10.1074/jbc.m606402200. [PMID: 17074764]
  • F Moccia, R A Billington, Luigia Santella. Pharmacological characterization of NAADP-induced Ca2+ signals in starfish oocytes. Biochemical and biophysical research communications. 2006 Sep; 348(2):329-36. doi: 10.1016/j.bbrc.2006.05.157. [PMID: 16890912]
  • Fan Zhang, Guo Zhang, Andrew Y Zhang, Matthew J Koeberl, Eryn Wallander, Pin-Lan Li. Production of NAADP and its role in Ca2+ mobilization associated with lysosomes in coronary arterial myocytes. American journal of physiology. Heart and circulatory physiology. 2006 Jul; 291(1):H274-82. doi: 10.1152/ajpheart.01064.2005. [PMID: 16473958]
  • Stéphanie Bezin, Gilles Charpentier, Philippe Fossier, José-Manuel Cancela. The Ca2+-releasing messenger NAADP, a new player in the nervous system. Journal of physiology, Paris. 2006 Mar; 99(2-3):111-8. doi: 10.1016/j.jphysparis.2005.12.007. [PMID: 16458493]
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