Pyranopterin (BioDeep_00000006000)
Secondary id: BioDeep_00001869546
代谢物信息卡片
[(5aR,8R,9aR)-2-amino-4-oxo-6,7-bis(sulfanyl)-1,5,5a,8,9a, 10-hexahydropyrano[3,2-g]pteridin-8-yl]methyl dihydrogen phosphate
化学式: C10H14N5O6PS2 (395.0123)
中文名称:
谱图信息:
最多检出来源 Homo sapiens(blood) 8.24%
分子结构信息
SMILES: C(C1C(=C(C2C(O1)NC3=C(N2)C(=O)NC(=N3)N)S)S)OP(=O)(O)O
InChI: InChI=1S/C10H14N5O6PS2/c11-10-14-7-4(8(16)15-10)12-3-6(24)5(23)2(21-9(3)13-7)1-20-22(17,18)19/h2-3,9,12,23-24H,1H2,(H2,17,18,19)(H4,11,13,14,15,16)
数据库引用编号
14 个数据库交叉引用编号
- ChEBI: CHEBI:44074
- KEGG: C05924
- PubChem: 135398581
- PubChem: 135402014
- PubChem: 444331
- Metlin: METLIN6546
- MetaCyc: CPD-4
- CAS: 220399-50-8
- PMhub: MS000018920
- PubChem: 8212
- KNApSAcK: C00000774
- PDB-CCD: MTE
- 3DMET: B05139
- NIKKAJI: J1.100.870D
分类词条
相关代谢途径
Reactome(9)
BioCyc(0)
PlantCyc(0)
代谢反应
2 个相关的代谢反应过程信息。
Reactome(0)
BioCyc(1)
- molybdenum cofactor biosynthesis:
molybdate + molybdopterin-AMP ⟶ AMP + H2O + molybdenum cofactor
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。
文献列表
- Simon Julius Mayr, Jörn Oliver Sass, Julia Vry, Janbernd Kirschner, Irina Mader, Jan-Bernd Hövener, Jochen Reiss, José Angel Santamaria-Araujo, Günter Schwarz, Sarah Catharina Grünert. A mild case of molybdenum cofactor deficiency defines an alternative route of MOCS1 protein maturation.
Journal of inherited metabolic disease.
2018 03; 41(2):187-196. doi:
10.1007/s10545-018-0138-7. [PMID: 29368224] - Joanna Jakubiczka-Smorag, Jose Angel Santamaria-Araujo, Imke Metz, Avadh Kumar, Samy Hakroush, Wolfgang Brueck, Guenter Schwarz, Peter Burfeind, Jochen Reiss, Lukasz Smorag. Mouse model for molybdenum cofactor deficiency type B recapitulates the phenotype observed in molybdenum cofactor deficient patients.
Human genetics.
2016 07; 135(7):813-26. doi:
10.1007/s00439-016-1676-4. [PMID: 27138983] - Philippa B Mills, Emma J Footitt, Serkan Ceyhan, Paula J Waters, Cornelis Jakobs, Peter T Clayton, Eduard A Struys. Urinary AASA excretion is elevated in patients with molybdenum cofactor deficiency and isolated sulphite oxidase deficiency.
Journal of inherited metabolic disease.
2012 Nov; 35(6):1031-6. doi:
10.1007/s10545-012-9466-1. [PMID: 22403017] - L H Ngu, B Afroze, B C Chen, O Affandi, M Y Zabedah. Molybdenum cofactor deficiency in a Malaysian child.
Singapore medical journal.
2009 Oct; 50(10):e365-7. doi:
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Journal of inherited metabolic disease.
2009 Aug; 32(4):560-9. doi:
10.1007/s10545-009-1151-7. [PMID: 19544009] - Birthe Smolinsky, Sabrina A Eichler, Sabine Buchmeier, Jochen C Meier, Guenter Schwarz. Splice-specific functions of gephyrin in molybdenum cofactor biosynthesis.
The Journal of biological chemistry.
2008 Jun; 283(25):17370-9. doi:
10.1074/jbc.m800985200. [PMID: 18411266] - Hava Peretz, Meirav Shtauber Naamati, David Levartovsky, Ayala Lagziel, Esther Shani, Ivona Horn, Hanna Shalev, Daniel Landau. Identification and characterization of the first mutation (Arg776Cys) in the C-terminal domain of the Human Molybdenum Cofactor Sulfurase (HMCS) associated with type II classical xanthinuria.
Molecular genetics and metabolism.
2007 May; 91(1):23-9. doi:
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Nucleosides, nucleotides & nucleic acids.
2006; 25(9-11):1087-91. doi:
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Neuropediatrics.
2005 Dec; 36(6):389-94. doi:
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American journal of medical genetics. Part A.
2005 Jul; 136(2):205-9. doi:
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2005 Apr; 19(3):223-30. doi:
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Human molecular genetics.
2002 Dec; 11(26):3309-17. doi:
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Biochimica et biophysica acta.
2002 Nov; 1588(2):135-8. doi:
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2001 Sep; 16(9):657-60. doi:
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2001 Apr; 16(4):264-70. doi:
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The Journal of biological chemistry.
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The Journal of biological chemistry.
2000 Nov; 275(45):35086-90. doi:
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The Journal of biological chemistry.
2000 Jul; 275(29):21789-92. doi:
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2000 May; 48(5):430-6. doi:
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Pediatric research.
2000 Apr; 47(4 Pt 1):492-4. doi:
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Journal of inherited metabolic disease.
1999 Oct; 22(7):842-3. doi:
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European journal of biochemistry.
1999 Aug; 264(1):176-82. doi:
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Lancet (London, England).
1999 Feb; 353(9153):675-6. doi:
10.1016/s0140-6736(05)75474-x. [PMID: 10030364] - H A Simmonds, G F Hoffmann, J L Pérignon, V Micheli, A H van Gennip. Diagnosis of molybdenum cofactor deficiency.
Lancet (London, England).
1999 Feb; 353(9153):675. doi:
10.1016/s0140-6736(05)75473-8. [PMID: 10030363] - H Koch. Dipsticks and convulsions.
Lancet (London, England).
1998 Dec; 352(9143):1824. doi:
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1998 Dec; 25(4):281-9. doi:
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Neurology.
1998 Sep; 51(3):860-2. doi:
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Molecular microbiology.
1998 May; 28(3):435-47. doi:
10.1046/j.1365-2958.1998.00795.x. [PMID: 9632249] - K Ichida, T Hosoya. [Classical xanthinuria (type I and II)].
Ryoikibetsu shokogun shirizu.
1998; ?(18 Pt 1):470-3. doi:
NULL. [PMID: 9590104] - T Matsuishi, S Ishibashi, M Nakashima, M Satoi. [Molybdenum cofactor deficiency].
Ryoikibetsu shokogun shirizu.
1998; ?(19 Pt 2):185-8. doi:
NULL. [PMID: 9645039] - K Ichida, Y Amaya, N Kamatani, T Nishino, T Hosoya, O Sakai. Identification of two mutations in human xanthine dehydrogenase gene responsible for classical type I xanthinuria.
The Journal of clinical investigation.
1997 May; 99(10):2391-7. doi:
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Nihon rinsho. Japanese journal of clinical medicine.
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Biochemical and molecular medicine.
1996 Aug; 58(2):199-203. doi:
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Journal of inherited metabolic disease.
1996; 19(5):700-1. doi:
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Clinical chemistry.
1995 Jul; 41(7):1056-7. doi:
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Journal of inherited metabolic disease.
1995; 18(3):283-90. doi:
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1995; 18(1):86-7. doi:
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Journal of inherited metabolic disease.
1995; 18(1):40-7. doi:
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European journal of biochemistry.
1994 Nov; 225(3):1063-71. doi:
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1994; 17(1):142-5. doi:
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Annales de pediatrie.
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Journal of inherited metabolic disease.
1983; 6 Suppl 1(?):78-83. doi:
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Proceedings of the National Academy of Sciences of the United States of America.
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