CoA 10:5;O2 (BioDeep_00000630391)

Main id: BioDeep_00000004286

 


代谢物信息卡片


3-phosphoadenosine 5-{3-[(3R)-3-hydroxy-4-({3-[(2-{[(2E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]sulfanyl}ethyl)amino]-3-oxopropyl}amino)-2,2-dimethyl-4-oxobutyl] dihydrogen diphosphate}

化学式: C31H44N7O19P3S (943.1625464)
中文名称:
谱图信息: 最多检出来源 () 0%

分子结构信息

SMILES: CC(C)(COP(=O)(O)OP(=O)(O)OCC1C(C(C(O1)N2C=NC3=C(N=CN=C32)N)O)OP(=O)(O)O)C(C(=O)NCCC(=O)NCCSC(=O)C=CC4=CC(=C(C=C4)O)OC)O
InChI: InChI=1S/C31H44N7O19P3S/c1-31(2,26(43)29(44)34-9-8-21(40)33-10-11-61-22(41)7-5-17-4-6-18(39)19(12-17)52-3)14-54-60(50,51)57-59(48,49)53-13-20-25(56-58(45,46)47)24(42)30(55-20)38-16-37-23-27(32)35-15-36-28(23)38/h4-7,12,15-16,20,24-26,30,39,42-43H,8-11,13-14H2,1-3H3,(H,33,40)(H,34,44)(H,48,49)(H,50,51)(H2,32,35,36)(H2,45,46,47)/b7-5+/t20-,24-,25-,26+,30-/m1/s1

描述信息

同义名列表

4 个代谢物同义名

3-phosphoadenosine 5-{3-[(3R)-3-hydroxy-4-({3-[(2-{[(2E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]sulfanyl}ethyl)amino]-3-oxopropyl}amino)-2,2-dimethyl-4-oxobutyl] dihydrogen diphosphate}; trans-4-hydroxy-3-methoxycinnamoyl-CoA;trans-4-hydroxy-3-methoxycinnamoyl-coenzyme A;trans-feruloyl-coenzyme A; trans-feruloyl-CoA; CoA 10:5;O2



数据库引用编号

10 个数据库交叉引用编号

分类词条

相关代谢途径

Reactome(0)

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)

1 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。



文献列表

  • Xiaochong Zhu, Jieyuan Wu, Shizhong Li, La Xiang, Jian-Ming Jin, Chaoning Liang, Shuang-Yan Tang. Artificial Biosynthetic Pathway for Efficient Synthesis of Vanillin, a Feruloyl-CoA-Derived Natural Product from Eugenol. Journal of agricultural and food chemistry. 2024 Mar; 72(12):6463-6470. doi: 10.1021/acs.jafc.3c08723. [PMID: 38501643]
  • Minglei Tao, Shengzhi Liu, Yaohan Li, Amin Liu, Jingkui Tian, Yuchang Liu, Hongwei Fu, Wei Zhu. Molecular characterization of a feruloyl-CoA 6'-hydroxylase involved in coumarin biosynthesis in Clematis terniflora DC. Plant physiology and biochemistry : PPB. 2023 Jan; 196(?):162-170. doi: 10.1016/j.plaphy.2023.01.046. [PMID: 36709578]
  • Xi Liu, Shuliu Dai, Yu Zhou, Jinyue Liu, Dong Li, Jun Zhang, Yushan Zhu, Qiao Zhao, Yue Feng, Yi Zhang. Crystal structure of the plant feruloyl-coenzyme A monolignol transferase provides insights into the formation of monolignol ferulate conjugates. Biochemical and biophysical research communications. 2022 02; 594(?):8-14. doi: 10.1016/j.bbrc.2022.01.037. [PMID: 35066379]
  • Ping-Ping Wang, Hui Liu, Shuai Gao, Ai-Xia Cheng. Functional Characterization of a Hydroxyacid/Alcohol Hydroxycinnamoyl Transferase Produced by the Liverwort Marchantia emarginata. Molecules (Basel, Switzerland). 2017 Oct; 22(11):. doi: 10.3390/molecules22111854. [PMID: 29088080]
  • Steven A Sattler, Alexander M Walker, Wilfred Vermerris, Scott E Sattler, ChulHee Kang. Structural and Biochemical Characterization of Cinnamoyl-CoA Reductases. Plant physiology. 2017 02; 173(2):1031-1044. doi: 10.1104/pp.16.01671. [PMID: 27956488]
  • Mwafaq Ibdah, Anna Berim, Stefan Martens, Andrea Lorena Herrera Valderrama, Luisa Palmieri, Efraim Lewinsohn, David R Gang. Identification and cloning of an NADPH-dependent hydroxycinnamoyl-CoA double bond reductase involved in dihydrochalcone formation in Malus×domestica Borkh. Phytochemistry. 2014 Nov; 107(?):24-31. doi: 10.1016/j.phytochem.2014.07.027. [PMID: 25152451]
  • Seitaro Matsumoto, Masaharu Mizutani, Kanzo Sakata, Bun-Ichi Shimizu. Molecular cloning and functional analysis of the ortho-hydroxylases of p-coumaroyl coenzyme A/feruloyl coenzyme A involved in formation of umbelliferone and scopoletin in sweet potato, Ipomoea batatas (L.) Lam. Phytochemistry. 2012 Feb; 74(?):49-57. doi: 10.1016/j.phytochem.2011.11.009. [PMID: 22169019]
  • Isabel Molina, Yonghua Li-Beisson, Fred Beisson, John B Ohlrogge, Mike Pollard. Identification of an Arabidopsis feruloyl-coenzyme A transferase required for suberin synthesis. Plant physiology. 2009 Nov; 151(3):1317-28. doi: 10.1104/pp.109.144907. [PMID: 19759341]
  • M Baltas, C Lapeyre, F Bedos-Belval, M Maturano, P Saint-Aguet, L Roussel, H Duran, J Grima-Pettenati. Kinetic and inhibition studies of cinnamoyl-CoA reductase 1 from Arabidopsis thaliana. Plant physiology and biochemistry : PPB. 2005 Aug; 43(8):746-53. doi: 10.1016/j.plaphy.2005.06.003. [PMID: 16122934]
  • Till Beuerle, Eran Pichersky. Enzymatic synthesis and purification of aromatic coenzyme a esters. Analytical biochemistry. 2002 Mar; 302(2):305-12. doi: 10.1006/abio.2001.5574. [PMID: 11878812]
  • Scott A Harding, Jacqueline Leshkevich, Vincent L Chiang, Chung-Jui Tsai. Differential substrate inhibition couples kinetically distinct 4-coumarate:coenzyme a ligases with spatially distinct metabolic roles in quaking aspen. Plant physiology. 2002 Feb; 128(2):428-38. doi: 10.1104/pp.010603. [PMID: 11842147]
  • M J Mayer, A Narbad, A J Parr, M L Parker, N J Walton, F A Mellon, A J Michael. Rerouting the plant phenylpropanoid pathway by expression of a novel bacterial enoyl-CoA hydratase/lyase enzyme function. The Plant cell. 2001 Jul; 13(7):1669-82. doi: 10.1105/tpc.010063. [PMID: 11449058]
  • N Obel, H V Scheller. Enzymatic synthesis and purification of caffeoyl-CoA, p-coumaroyl-CoA, and feruloyl-CoA. Analytical biochemistry. 2000 Nov; 286(1):38-44. doi: 10.1006/abio.2000.4760. [PMID: 11038271]
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