Tham khảo Ribose-phosphate diphosphokinase

  1. 1 2 Visentin LP, Hasnain S, Gallin W (tháng 7 năm 1977). “Ribosomal protein S1/S1A in bacteria”. FEBS Lett. 79 (2): 258–63. PMID 330231. doi:10.1016/0014-5793(77)80799-0. 
  2. 1 2 3 4 5 6 Li S, Lu Y, Peng B, Ding J (tháng 1 năm 2007). “Crystal structure of human phosphoribosylpyrophosphate synthetase 1 reveals a novel allosteric site”. Biochem. J. 401 (1): 39–47. PMC 1698673. PMID 16939420. doi:10.1042/BJ20061066. 
  3. ↑ Tang W, Li X, Zhu Z, Tong S, Li X, Zhang X, Teng M, Niu L (tháng 5 năm 2006). “Expression, purification, crystallization and preliminary X-ray diffraction analysis of human phosphoribosyl pyrophosphate synthetase 1 (PRS1)”. Acta Crystallographica Section F 62 (Pt 5): 432–4. PMC 2219982. PMID 16682768. doi:10.1107/S1744309106009067. 
  4. ↑ Fox IH, Kelley WN (tháng 4 năm 1972). “Human phosphoribosylpyrophosphate synthetase. Kinetic mechanism and end product inhibition”. J. Biol. Chem. 247 (7): 2126–31. PMID 4335863. 
  5. ↑ Miller GA, Rosenzweig S, Switzer RL (tháng 12 năm 1975). “Oxygen-18 studies of the mechanism of pyrophosphoryl group transfer catalyzed by phosphoribosylpyrophosphate synthetase”. Arch. Biochem. Biophys. 171 (2): 732–6. PMID 173242. doi:10.1016/0003-9861(75)90086-7. 
  6. ↑ Eriksen TA, Kadziola A, Bentsen AK, Harlow KW, Larsen S (tháng 4 năm 2000). “Structural basis for the function of Bacillus subtilis phosphoribosyl-pyrophosphate synthetase”. Nat. Struct. Biol. 7 (4): 303–8. PMID 10742175. doi:10.1038/74069. 
  7. ↑ Fox IH, Kelley WN (tháng 3 năm 1971). “Phosphoribosylpyrophosphate in man: biochemical and clinical significance”. Ann. Intern. Med. 74 (3): 424–33. PMID 4324023. doi:10.7326/0003-4819-74-3-424. 
  8. ↑ Jeremy M. Berg; John L. Tymoczko; Lubert Stryer; Gregory J. Gatto Jr. (2012). Biochemistry (ấn bản 7). New York: W.H. Freeman. ISBN 1429229365. 
  9. ↑ Rongvaux A, Andris F, Van Gool F, Leo O (tháng 7 năm 2003). “Reconstructing eukaryotic NAD metabolism”. BioEssays 25 (7): 683–90. PMID 12815723. doi:10.1002/bies.10297. 
  10. ↑ Liu X, Han D, Li J, Han B, Ouyang X, Cheng J, Li X, Jin Z, Wang Y, Bitner-Glindzicz M, Kong X, Xu H, Kantardzhieva A, Eavey RD, Seidman CE, Seidman JG, Du LL, Chen ZY, Dai P, Teng M, Yan D, Yuan H (tháng 1 năm 2010). “Loss-of-function mutations in the PRPS1 gene cause a type of nonsyndromic X-linked sensorineural deafness, DFN2”. Am. J. Hum. Genet. 86 (1): 65–71. PMC 2801751. PMID 20021999. doi:10.1016/j.ajhg.2009.11.015. 
  11. ↑ Kim HJ, Sohn KM, Shy ME, Krajewski KM, Hwang M, Park JH, Jang SY, Won HH, Choi BO, Hong SH, Kim BJ, Suh YL, Ki CS, Lee SY, Kim SH, Kim JW (tháng 9 năm 2007). “Mutations in PRPS1, which encodes the phosphoribosyl pyrophosphate synthetase enzyme critical for nucleotide biosynthesis, cause hereditary peripheral neuropathy with hearing loss and optic neuropathy (cmtx5)”. Am. J. Hum. Genet. 81 (3): 552–8. PMC 1950833. PMID 17701900. doi:10.1086/519529. 
  12. ↑ Becker MA, Smith PR, Taylor W, Mustafi R, Switzer RL (tháng 11 năm 1995). “The genetic and functional basis of purine nucleotide feedback-resistant phosphoribosylpyrophosphate synthetase superactivity”. J. Clin. Invest. 96 (5): 2133–41. PMC 185862. PMID 7593598. doi:10.1172/JCI118267. 
  13. ↑ Zoref E, De Vries A, Sperling O (tháng 11 năm 1975). “Mutant feedback-resistant phosphoribosylpyrophosphate synthetase associated with purine overproduction and gout. Phosphoribosylpyrophosphate and purine metabolism in cultured fibroblasts”. J. Clin. Invest. 56 (5): 1093–9. PMC 301970. PMID 171280. doi:10.1172/JCI108183. 
  14. ↑ “Phosphoribosylpyrophosphate synthetase superactivity”. Lister Hill National Center for Biomedical Communications. Truy cập ngày 25 tháng 2 năm 2014. 
  15. ↑ Synofzik M, Müller Vom Hagen J, Haack TB, Wilhelm C, Lindig T, Beck-Wödl S, Nabuurs SB, van Kuilenburg AB, de Brouwer AP, Schöls L (2014). “X-linked Charcot-Marie-Tooth disease, Arts syndrome, and prelingual non-syndromic deafness form a disease continuum: evidence from a family with a novel PRPS1 mutation”. Orphanet J Rare Dis 9 (1): 24. PMC 3931488. PMID 24528855. doi:10.1186/1750-1172-9-24. 

Tài liệu tham khảo

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