GLUDP5
Glutamate dehydrogenase pseudogene 5, also known as GLUDP5, is a human gene.[2]
References
Further reading
- Meissner T, Beinbrech B, Mayatepek E (1999). "Congenital hyperinsulinism: molecular basis of a heterogeneous disease.". Hum. Mutat. 13 (5): 351–61. PMID 10338089. doi:10.1002/(SICI)1098-1004(1999)13:5<351::AID-HUMU3>3.0.CO;2-R.
- Julliard JH, Smith EL (1979). "Partial amino acid sequence of the glutamate dehydrogenase of human liver and a revision of the sequence of the bovine enzyme.". J. Biol. Chem. 254 (9): 3427–38. PMID 429360.
- Hochstrasser DF, Frutiger S, Paquet N, et al. (1993). "Human liver protein map: a reference database established by microsequencing and gel comparison". Electrophoresis. 13 (12): 992–1001. PMID 1286669. doi:10.1002/elps.11501301201.
- Mavrothalassitis G, Tzimagiorgis G, Mitsialis A, et al. (1988). "Isolation and characterization of cDNA clones encoding human liver glutamate dehydrogenase: evidence for a small gene family". Proc. Natl. Acad. Sci. U.S.A. 85 (10): 3494–8. PMC 280238 . PMID 3368458. doi:10.1073/pnas.85.10.3494.
- Amuro N, Yamaura M, Goto Y, Okazaki T (1988). "Molecular cloning and nucleotide sequence of the cDNA for human liver glutamate dehydrogenase precursor". Biochem. Biophys. Res. Commun. 152 (3): 1395–400. PMID 3377777. doi:10.1016/S0006-291X(88)80440-6.
- Nakatani Y, Schneider M, Banner C, Freese E (1988). "Complete nucleotide sequence of human glutamate dehydrogenase cDNA". Nucleic Acids Res. 16 (13): 6237. PMC 336872 . PMID 3399399. doi:10.1093/nar/16.13.6237.
- Nakatani Y, Banner C, von Herrath M, et al. (1988). "Comparison of human brain and liver glutamate dehydrogenase cDNAS". Biochem. Biophys. Res. Commun. 149 (2): 405–10. PMID 3426581. doi:10.1016/0006-291X(87)90381-0.
- Banner C, Silverman S, Thomas JW, et al. (1987). "Isolation of a human brain cDNA for glutamate dehydrogenase". J. Neurochem. 49 (1): 246–52. PMID 3585334. doi:10.1111/j.1471-4159.1987.tb03422.x.
- Tzimagiorgis G, Leversha MA, Chroniary K, et al. (1993). "Structure and expression analysis of a member of the human glutamate dehydrogenase (GLUD) gene family mapped to chromosome 10p11.2". Hum. Genet. 91 (5): 433–8. PMID 8314555. doi:10.1007/BF00217767.
- Goulielmos G, Angelicheva D, Kapsetaki M, et al. (1993). "A chromosome 10p11.2 Gt-dinucleotide repeat polymorphism at the GLUDP5 gene locus". Hum. Mol. Genet. 2 (8): 1328. PMID 8401522. doi:10.1093/hmg/2.8.1328-a.
- Michaelidis TM, Tzimagiorgis G, Moschonas NK, Papamatheakis J (1993). "The human glutamate dehydrogenase gene family: gene organization and structural characterization". Genomics. 16 (1): 150–60. PMID 8486350. doi:10.1006/geno.1993.1152.
- Stanley CA, Lieu YK, Hsu BY, et al. (1998). "Hyperinsulinism and hyperammonemia in infants with regulatory mutations of the glutamate dehydrogenase gene". N. Engl. J. Med. 338 (19): 1352–7. PMID 9571255. doi:10.1056/NEJM199805073381904.
- Miki Y, Taki T, Ohura T, et al. (2000). "Novel missense mutations in the glutamate dehydrogenase gene in the congenital hyperinsulinism-hyperammonemia syndrome". J. Pediatr. 136 (1): 69–72. PMID 10636977. doi:10.1016/S0022-3476(00)90052-0.
- Santer R, Kinner M, Passarge M, et al. (2001). "Novel missense mutations outside the allosteric domain of glutamate dehydrogenase are prevalent in European patients with the congenital hyperinsulinism-hyperammonemia syndrome". Hum. Genet. 108 (1): 66–71. PMID 11214910. doi:10.1007/s004390000432.
- Smith TJ, Peterson PE, Schmidt T, et al. (2001). "Structures of bovine glutamate dehydrogenase complexes elucidate the mechanism of purine regulation". J. Mol. Biol. 307 (2): 707–20. PMID 11254391. doi:10.1006/jmbi.2001.4499.
- MacMullen C, Fang J, Hsu BY, et al. (2001). "Hyperinsulinism/hyperammonemia syndrome in children with regulatory mutations in the inhibitory guanosine triphosphate-binding domain of glutamate dehydrogenase". J. Clin. Endocrinol. Metab. 86 (4): 1782–7. PMID 11297618. doi:10.1210/jc.86.4.1782.
- Fang J, Hsu BY, MacMullen CM, et al. (2002). "Expression, purification and characterization of human glutamate dehydrogenase (GDH) allosteric regulatory mutations". Biochem. J. 363 (Pt 1): 81–7. PMC 1222454 . PMID 11903050. doi:10.1042/0264-6021:3630081.
- Smith TJ, Schmidt T, Fang J, et al. (2002). "The structure of apo human glutamate dehydrogenase details subunit communication and allostery". J. Mol. Biol. 318 (3): 765–77. PMID 12054821. doi:10.1016/S0022-2836(02)00161-4.
- Banerjee S, Schmidt T, Fang J, et al. (2003). "Structural studies on ADP activation of mammalian glutamate dehydrogenase and the evolution of regulation". Biochemistry. 42 (12): 3446–56. PMID 12653548. doi:10.1021/bi0206917.