GLUDP5

From Wikipedia, the free encyclopedia

Glutamate dehydrogenase pseudogene 5

Identifiers

Gene ontology

Orthologs

Human

Mouse

Entrez

2751

n/a

Pubmed search

[1]

n/a

Glutamate dehydrogenase pseudogene 5, also known as GLUDP5, is a human gene.^[1]

[edit] References

^ Entrez Gene: GLUDP5 glutamate dehydrogenase pseudogene 5.

[edit] Further reading

Meissner T, Beinbrech B, Mayatepek E (1999). "Congenital hyperinsulinism: molecular basis of a heterogeneous disease.". Hum. Mutat. 13 (5): 351-61. doi:10.1002/(SICI)1098-1004(1999)13:5<351::AID-HUMU3>3.0.CO;2-R. PMID 10338089.
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.
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. PMID 3368458.
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.
Nakatani Y, Schneider M, Banner C, Freese E (1988). "Complete nucleotide sequence of human glutamate dehydrogenase cDNA.". Nucleic Acids Res. 16 (13): 6237. PMID 3399399.
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.
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.
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.
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.
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. doi:10.1006/geno.1993.1152. PMID 8486350.
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.
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.
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.
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. doi:10.1006/jmbi.2001.4499. PMID 11254391.
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.
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. PMID 11903050.
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. doi:10.1016/S0022-2836(02)00161-4. PMID 12054821.
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. doi:10.1021/bi0206917. PMID 12653548.