Alpha-aminoadipic semialdehyde synthase (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Alpha-aminoadipic semialdehyde synthase" in English language version.

refsWebsite

Global rank English rank

26nih.gov

4^th place

16doi.org

2^nd place

3web.archive.org

1^st place

2ensembl.org

1,626^th place

1,007^th place

2semanticscholar.org

11^th place

8^th place

1uniprot.org

5,673^rd place

6,418^th place

1nutrition.org

7,878^th place

low place

1stanford.edu

179^th place

183^rd place

1elmhurst.edu

low place

1rcsb.org

8,838^th place

8,783^rd place

doi.org

Sacksteder KA, Biery BJ, Morrell JC, Goodman BK, Geisbrecht BV, Cox RP, Gould SJ, Geraghty MT (June 2000). "Identification of the alpha-aminoadipic semialdehyde synthase gene, which is defective in familial hyperlysinemia". American Journal of Human Genetics. 66 (6): 1736–43. doi:10.1086/302919. PMC 1378037. PMID 10775527.
Zhu X, Tang G, Galili G (December 2002). "The activity of the Arabidopsis bifunctional lysine-ketoglutarate reductase/saccharopine dehydrogenase enzyme of lysine catabolism is regulated by functional interaction between its two enzyme domains". The Journal of Biological Chemistry. 277 (51): 49655–61. doi:10.1074/jbc.M205466200. PMID 12393892.
Houten SM, Te Brinke H, Denis S, Ruiter JP, Knegt AC, de Klerk JB, Augoustides-Savvopoulou P, Häberle J, Baumgartner MR, Coşkun T, Zschocke J, Sass JO, Poll-The BT, Wanders RJ, Duran M (April 2013). "Genetic basis of hyperlysinemia". Orphanet Journal of Rare Diseases. 8: 57. doi:10.1186/1750-1172-8-57. PMC 3626681. PMID 23570448.
Papes F, Kemper EL, Cord-Neto G, Langone F, Arruda P (December 1999). "Lysine degradation through the saccharopine pathway in mammals: involvement of both bifunctional and monofunctional lysine-degrading enzymes in mouse". The Biochemical Journal. 344 (2): 555–63. doi:10.1042/0264-6021:3440555. PMC 1220675. PMID 10567240.
Danhauser K, Sauer SW, Haack TB, Wieland T, Staufner C, Graf E, Zschocke J, Strom TM, Traub T, Okun JG, Meitinger T, Hoffmann GF, Prokisch H, Kölker S (December 2012). "DHTKD1 mutations cause 2-aminoadipic and 2-oxoadipic aciduria". American Journal of Human Genetics. 91 (6): 1082–7. doi:10.1016/j.ajhg.2012.10.006. PMC 3516599. PMID 23141293.
Meldrum BS (April 2000). "Glutamate as a neurotransmitter in the brain: review of physiology and pathology". The Journal of Nutrition. 130 (4S Suppl): 1007S–15S. doi:10.1093/jn/130.4.1007s. PMID 10736372. Archived from the original on 2017-05-16. Retrieved 2017-03-05.
Markovitz PJ, Chuang DT, Cox RP (October 1984). "Familial hyperlysinemias. Purification and characterization of the bifunctional aminoadipic semialdehyde synthase with lysine-ketoglutarate reductase and saccharopine dehydrogenase activities". The Journal of Biological Chemistry. 259 (19): 11643–6. doi:10.1016/S0021-9258(20)71252-4. PMID 6434529.
Jones EE, Broquist HP (June 1965). "Saccharopine, an intermediate of the aminoadipic acid pathway of lysine biosynthesis. Ii. studies in Saccharomyces cereviseae [sic]". The Journal of Biological Chemistry. 240 (6): 2531–6. doi:10.1016/S0021-9258(18)97358-8. PMID 14304864.
Trupin JS, Broquist HP (June 1965). "Saccharopine, an intermediate of the aminoadipic acid pathway of lysine biosynthesis. I. studies in neurospora crassa". The Journal of Biological Chemistry. 240 (6): 2524–30. doi:10.1016/S0021-9258(18)97357-6. PMID 14304863.
Johansson E, Steffens JJ, Lindqvist Y, Schneider G (October 2000). "Crystal structure of saccharopine reductase from Magnaporthe grisea, an enzyme of the alpha-aminoadipate pathway of lysine biosynthesis". Structure. 8 (10): 1037–47. doi:10.1016/s0969-2126(00)00512-8. PMID 11080625.
Saudubray JM, Rabier D (June 2007). "Biomarkers identified in inborn errors for lysine, arginine, and ornithine". The Journal of Nutrition. 137 (6 Suppl 2): 1669S–1672S. doi:10.1093/jn/137.6.1669S. PMID 17513445.
vd Heiden C, Brink M, de Bree PK, v Sprang FJ, Wadman SK, de Pater JM, van Biervliet JP (1978). "Familial hyperlysinaemia due to L-lysine alpha-ketoglutarate reductase deficiency: results of attempted treatment". Journal of Inherited Metabolic Disease. 1 (3): 89–94. doi:10.1007/bf01805679. PMID 116084. S2CID 35326745.
Mills PB, Struys E, Jakobs C, Plecko B, Baxter P, Baumgartner M, Willemsen MA, Omran H, Tacke U, Uhlenberg B, Weschke B, Clayton PT (March 2006). "Mutations in antiquitin in individuals with pyridoxine-dependent seizures". Nature Medicine. 12 (3): 307–9. doi:10.1038/nm1366. PMID 16491085. S2CID 27940375.
Goodman SI, Kratz LE, DiGiulio KA, Biery BJ, Goodman KE, Isaya G, Frerman FE (September 1995). "Cloning of glutaryl-CoA dehydrogenase cDNA, and expression of wild type and mutant enzymes in Escherichia coli". Human Molecular Genetics. 4 (9): 1493–8. doi:10.1093/hmg/4.9.1493. PMID 8541831.
Cederbaum SD, Shaw KN, Dancis J, Hutzler J, Blaskovics JC (August 1979). "Hyperlysinemia with saccharopinuria due to combined lysine-ketoglutarate reductase and saccharopine dehydrogenase deficiencies presenting as cystinuria". The Journal of Pediatrics. 95 (2): 234–8. doi:10.1016/s0022-3476(79)80657-5. PMID 571908.
Houten SM, Denis S, Te Brinke H, Jongejan A, van Kampen AH, Bradley EJ, Baas F, Hennekam RC, Millington DS, Young SP, Frazier DM, Gucsavas-Calikoglu M, Wanders RJ (September 2014). "Mitochondrial NADP(H) deficiency due to a mutation in NADK2 causes dienoyl-CoA reductase deficiency with hyperlysinemia". Human Molecular Genetics. 23 (18): 5009–16. doi:10.1093/hmg/ddu218. PMID 24847004.

elmhurst.edu

chemistry.elmhurst.edu

Ophardt CE (2003). "Acetyl CoA Crossroads Compound". Virtual ChemBook. Elmhurst College. Archived from the original on 2016-11-15. Retrieved 2017-03-05.

ensembl.org

May2017.archive.ensembl.org

GRCh38: Ensembl release 89: ENSG00000008311 – Ensembl, May 2017
GRCm38: Ensembl release 89: ENSMUSG00000029695 – Ensembl, May 2017

nih.gov

pubmed.ncbi.nlm.nih.gov

Sacksteder KA, Biery BJ, Morrell JC, Goodman BK, Geisbrecht BV, Cox RP, Gould SJ, Geraghty MT (June 2000). "Identification of the alpha-aminoadipic semialdehyde synthase gene, which is defective in familial hyperlysinemia". American Journal of Human Genetics. 66 (6): 1736–43. doi:10.1086/302919. PMC 1378037. PMID 10775527.
Zhu X, Tang G, Galili G (December 2002). "The activity of the Arabidopsis bifunctional lysine-ketoglutarate reductase/saccharopine dehydrogenase enzyme of lysine catabolism is regulated by functional interaction between its two enzyme domains". The Journal of Biological Chemistry. 277 (51): 49655–61. doi:10.1074/jbc.M205466200. PMID 12393892.
Houten SM, Te Brinke H, Denis S, Ruiter JP, Knegt AC, de Klerk JB, Augoustides-Savvopoulou P, Häberle J, Baumgartner MR, Coşkun T, Zschocke J, Sass JO, Poll-The BT, Wanders RJ, Duran M (April 2013). "Genetic basis of hyperlysinemia". Orphanet Journal of Rare Diseases. 8: 57. doi:10.1186/1750-1172-8-57. PMC 3626681. PMID 23570448.
Papes F, Kemper EL, Cord-Neto G, Langone F, Arruda P (December 1999). "Lysine degradation through the saccharopine pathway in mammals: involvement of both bifunctional and monofunctional lysine-degrading enzymes in mouse". The Biochemical Journal. 344 (2): 555–63. doi:10.1042/0264-6021:3440555. PMC 1220675. PMID 10567240.
Danhauser K, Sauer SW, Haack TB, Wieland T, Staufner C, Graf E, Zschocke J, Strom TM, Traub T, Okun JG, Meitinger T, Hoffmann GF, Prokisch H, Kölker S (December 2012). "DHTKD1 mutations cause 2-aminoadipic and 2-oxoadipic aciduria". American Journal of Human Genetics. 91 (6): 1082–7. doi:10.1016/j.ajhg.2012.10.006. PMC 3516599. PMID 23141293.
Meldrum BS (April 2000). "Glutamate as a neurotransmitter in the brain: review of physiology and pathology". The Journal of Nutrition. 130 (4S Suppl): 1007S–15S. doi:10.1093/jn/130.4.1007s. PMID 10736372. Archived from the original on 2017-05-16. Retrieved 2017-03-05.
Markovitz PJ, Chuang DT, Cox RP (October 1984). "Familial hyperlysinemias. Purification and characterization of the bifunctional aminoadipic semialdehyde synthase with lysine-ketoglutarate reductase and saccharopine dehydrogenase activities". The Journal of Biological Chemistry. 259 (19): 11643–6. doi:10.1016/S0021-9258(20)71252-4. PMID 6434529.
Jones EE, Broquist HP (June 1965). "Saccharopine, an intermediate of the aminoadipic acid pathway of lysine biosynthesis. Ii. studies in Saccharomyces cereviseae [sic]". The Journal of Biological Chemistry. 240 (6): 2531–6. doi:10.1016/S0021-9258(18)97358-8. PMID 14304864.
Trupin JS, Broquist HP (June 1965). "Saccharopine, an intermediate of the aminoadipic acid pathway of lysine biosynthesis. I. studies in neurospora crassa". The Journal of Biological Chemistry. 240 (6): 2524–30. doi:10.1016/S0021-9258(18)97357-6. PMID 14304863.
Johansson E, Steffens JJ, Lindqvist Y, Schneider G (October 2000). "Crystal structure of saccharopine reductase from Magnaporthe grisea, an enzyme of the alpha-aminoadipate pathway of lysine biosynthesis". Structure. 8 (10): 1037–47. doi:10.1016/s0969-2126(00)00512-8. PMID 11080625.
Saudubray JM, Rabier D (June 2007). "Biomarkers identified in inborn errors for lysine, arginine, and ornithine". The Journal of Nutrition. 137 (6 Suppl 2): 1669S–1672S. doi:10.1093/jn/137.6.1669S. PMID 17513445.
vd Heiden C, Brink M, de Bree PK, v Sprang FJ, Wadman SK, de Pater JM, van Biervliet JP (1978). "Familial hyperlysinaemia due to L-lysine alpha-ketoglutarate reductase deficiency: results of attempted treatment". Journal of Inherited Metabolic Disease. 1 (3): 89–94. doi:10.1007/bf01805679. PMID 116084. S2CID 35326745.
Mills PB, Struys E, Jakobs C, Plecko B, Baxter P, Baumgartner M, Willemsen MA, Omran H, Tacke U, Uhlenberg B, Weschke B, Clayton PT (March 2006). "Mutations in antiquitin in individuals with pyridoxine-dependent seizures". Nature Medicine. 12 (3): 307–9. doi:10.1038/nm1366. PMID 16491085. S2CID 27940375.
Goodman SI, Kratz LE, DiGiulio KA, Biery BJ, Goodman KE, Isaya G, Frerman FE (September 1995). "Cloning of glutaryl-CoA dehydrogenase cDNA, and expression of wild type and mutant enzymes in Escherichia coli". Human Molecular Genetics. 4 (9): 1493–8. doi:10.1093/hmg/4.9.1493. PMID 8541831.
Dancis J, Hutzler J, Cox RP (May 1979). "Familial hyperlysinemia: enzyme studies, diagnostic methods, comments on terminology". American Journal of Human Genetics. 31 (3): 290–9. PMC 1685795. PMID 463877.
Cederbaum SD, Shaw KN, Dancis J, Hutzler J, Blaskovics JC (August 1979). "Hyperlysinemia with saccharopinuria due to combined lysine-ketoglutarate reductase and saccharopine dehydrogenase deficiencies presenting as cystinuria". The Journal of Pediatrics. 95 (2): 234–8. doi:10.1016/s0022-3476(79)80657-5. PMID 571908.
Houten SM, Denis S, Te Brinke H, Jongejan A, van Kampen AH, Bradley EJ, Baas F, Hennekam RC, Millington DS, Young SP, Frazier DM, Gucsavas-Calikoglu M, Wanders RJ (September 2014). "Mitochondrial NADP(H) deficiency due to a mutation in NADK2 causes dienoyl-CoA reductase deficiency with hyperlysinemia". Human Molecular Genetics. 23 (18): 5009–16. doi:10.1093/hmg/ddu218. PMID 24847004.

ncbi.nlm.nih.gov

"Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
"Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
Sacksteder KA, Biery BJ, Morrell JC, Goodman BK, Geisbrecht BV, Cox RP, Gould SJ, Geraghty MT (June 2000). "Identification of the alpha-aminoadipic semialdehyde synthase gene, which is defective in familial hyperlysinemia". American Journal of Human Genetics. 66 (6): 1736–43. doi:10.1086/302919. PMC 1378037. PMID 10775527.
"Entrez Gene: AASS aminoadipate-semialdehyde synthase".
Houten SM, Te Brinke H, Denis S, Ruiter JP, Knegt AC, de Klerk JB, Augoustides-Savvopoulou P, Häberle J, Baumgartner MR, Coşkun T, Zschocke J, Sass JO, Poll-The BT, Wanders RJ, Duran M (April 2013). "Genetic basis of hyperlysinemia". Orphanet Journal of Rare Diseases. 8: 57. doi:10.1186/1750-1172-8-57. PMC 3626681. PMID 23570448.
Papes F, Kemper EL, Cord-Neto G, Langone F, Arruda P (December 1999). "Lysine degradation through the saccharopine pathway in mammals: involvement of both bifunctional and monofunctional lysine-degrading enzymes in mouse". The Biochemical Journal. 344 (2): 555–63. doi:10.1042/0264-6021:3440555. PMC 1220675. PMID 10567240.
Danhauser K, Sauer SW, Haack TB, Wieland T, Staufner C, Graf E, Zschocke J, Strom TM, Traub T, Okun JG, Meitinger T, Hoffmann GF, Prokisch H, Kölker S (December 2012). "DHTKD1 mutations cause 2-aminoadipic and 2-oxoadipic aciduria". American Journal of Human Genetics. 91 (6): 1082–7. doi:10.1016/j.ajhg.2012.10.006. PMC 3516599. PMID 23141293.
Dancis J, Hutzler J, Cox RP (May 1979). "Familial hyperlysinemia: enzyme studies, diagnostic methods, comments on terminology". American Journal of Human Genetics. 31 (3): 290–9. PMC 1685795. PMID 463877.

ghr.nlm.nih.gov

"hyperlysinemia". Genetics Home Reference. Retrieved 2017-03-04.

nutrition.org

jn.nutrition.org

Meldrum BS (April 2000). "Glutamate as a neurotransmitter in the brain: review of physiology and pathology". The Journal of Nutrition. 130 (4S Suppl): 1007S–15S. doi:10.1093/jn/130.4.1007s. PMID 10736372. Archived from the original on 2017-05-16. Retrieved 2017-03-05.

rcsb.org

"AASS - aminoadipate-semialdehyde synthase". RCSB Protein Data Bank. Archived from the original on 2017-11-07. Retrieved 2017-03-06 – via PDB.

semanticscholar.org

api.semanticscholar.org

vd Heiden C, Brink M, de Bree PK, v Sprang FJ, Wadman SK, de Pater JM, van Biervliet JP (1978). "Familial hyperlysinaemia due to L-lysine alpha-ketoglutarate reductase deficiency: results of attempted treatment". Journal of Inherited Metabolic Disease. 1 (3): 89–94. doi:10.1007/bf01805679. PMID 116084. S2CID 35326745.
Mills PB, Struys E, Jakobs C, Plecko B, Baxter P, Baumgartner M, Willemsen MA, Omran H, Tacke U, Uhlenberg B, Weschke B, Clayton PT (March 2006). "Mutations in antiquitin in individuals with pyridoxine-dependent seizures". Nature Medicine. 12 (3): 307–9. doi:10.1038/nm1366. PMID 16491085. S2CID 27940375.

stanford.edu

web.stanford.edu

"About Glutamate Toxicity". Huniting Disease Outreach for Education at Stanford (HOPES). Huntington’s Disease Society of America. 26 June 2011. Retrieved 2017-03-05.

uniprot.org

"Alpha-aminoadipic semialdehyde synthase, mitochondrial". UniProt. Retrieved 2017-03-04.

web.archive.org

Meldrum BS (April 2000). "Glutamate as a neurotransmitter in the brain: review of physiology and pathology". The Journal of Nutrition. 130 (4S Suppl): 1007S–15S. doi:10.1093/jn/130.4.1007s. PMID 10736372. Archived from the original on 2017-05-16. Retrieved 2017-03-05.
Ophardt CE (2003). "Acetyl CoA Crossroads Compound". Virtual ChemBook. Elmhurst College. Archived from the original on 2016-11-15. Retrieved 2017-03-05.
"AASS - aminoadipate-semialdehyde synthase". RCSB Protein Data Bank. Archived from the original on 2017-11-07. Retrieved 2017-03-06 – via PDB.