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'''6-pyruvoyltetrahydropterin synthase''', also known as '''PTS''', is a human [[gene]] which facilitates [[Folic acid|folate biosynthesis]].<ref name="entrez">{{cite web | title = Entrez Gene: PTS 6-pyruvoyltetrahydropterin synthase| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=5805| accessdate = }}</ref> | |||
}} | |||
'''6-pyruvoyltetrahydropterin synthase''', also known as '''PTS''', is a human [[gene]].<ref name="entrez">{{cite web | title = Entrez Gene: PTS 6-pyruvoyltetrahydropterin synthase| url = | |||
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==See also== | |||
* [[6-pyruvoyltetrahydropterin synthase]] | |||
* [[6-Pyruvoyltetrahydropterin synthase deficiency]] | |||
==References== | ==References== | ||
{{reflist | {{reflist}} | ||
==Further reading== | ==Further reading== | ||
{{refbegin | 2}} | {{refbegin | 2}} | ||
{{PBB_Further_reading | {{PBB_Further_reading | ||
| citations = | | citations = | ||
*{{cite journal | author=Werner ER | *{{cite journal | author=Werner ER |title=Biochemistry and function of pteridine synthesis in human and murine macrophages |journal=Pathobiology |volume=59 |issue= 4 |pages= 276–9 |year= 1991 |pmid= 1883524 |doi=10.1159/000163662 |name-list-format=vanc| author2=Werner-Felmayer G | author3=Fuchs D | display-authors=3 | last4=Hausen | first4=A. | last5=Reibnegger | first5=R. | last6=Yim | first6=J.J. | last7=Wachter | first7=H. }} | ||
*{{cite journal |vauthors=Thöny B, Blau N |title=Mutations in the GTP cyclohydrolase I and 6-pyruvoyl-tetrahydropterin synthase genes |journal=Hum. Mutat. |volume=10 |issue= 1 |pages= 11–20 |year= 1997 |pmid= 9222755 |doi= 10.1002/(SICI)1098-1004(1997)10:1<11::AID-HUMU2>3.0.CO;2-P }} | |||
*{{cite journal | | *{{cite journal |vauthors=Thöny B, Auerbach G, Blau N |title=Tetrahydrobiopterin biosynthesis, regeneration and functions |journal=Biochem. J. |volume=347 | issue = 1 |pages= 1–16 |year= 2000 |pmid= 10727395 |doi=10.1042/0264-6021:3470001 | pmc=1220924 }} | ||
*{{cite journal |vauthors=Thöny B, Leimbacher W, Bürgisser D, Heizmann CW |title=Human 6-pyruvoyltetrahydropterin synthase: cDNA cloning and heterologous expression of the recombinant enzyme |journal=Biochem. Biophys. Res. Commun. |volume=189 |issue= 3 |pages= 1437–43 |year= 1993 |pmid= 1282802 |doi=10.1016/0006-291X(92)90235-D }} | |||
*{{cite journal | | *{{cite journal |vauthors=Scriver CR, Clow CL, Kaplan P, Niederwieser A |title=Hyperphenylalaninemia due to deficiency of 6-pyruvoyl tetrahydropterin synthase. Unusual gene dosage effect in heterozygotes |journal=Hum. Genet. |volume=77 |issue= 2 |pages= 168–71 |year= 1987 |pmid= 3308682 |doi=10.1007/BF00272386 }} | ||
*{{cite journal | | *{{cite journal | author=Oppliger T |title=Structural and functional consequences of mutations in 6-pyruvoyltetrahydropterin synthase causing hyperphenylalaninemia in humans. Phosphorylation is a requirement for in vivo activity |journal=J. Biol. Chem. |volume=270 |issue= 49 |pages= 29498–506 |year= 1996 |pmid= 7493990 |doi=10.1074/jbc.270.49.29498 |name-list-format=vanc| author2=Thöny B | author3=Nar H | display-authors=3 | last4=Bürgisser | first4=D | last5=Huber | first5=R | last6=Heizmann | first6=CW | last7=Blau | first7=N }} | ||
*{{cite journal | author= | *{{cite journal |vauthors=Ashida A, Owada M, Hatakeyama K |title=A missense mutation (A to G) of 6-pyruvoyltetrahydropterin synthase in tetrahydrobiopterin-deficient form of hyperphenylalaninemia |journal=Genomics |volume=24 |issue= 2 |pages= 408–10 |year= 1995 |pmid= 7698774 |doi= 10.1006/geno.1994.1642 }} | ||
*{{cite journal | author=Thöny B |title=Hyperphenylalaninemia due to defects in tetrahydrobiopterin metabolism: molecular characterization of mutations in 6-pyruvoyl-tetrahydropterin synthase |journal=Am. J. Hum. Genet. |volume=54 |issue= 5 |pages= 782–92 |year= 1994 |pmid= 8178819 |doi= | pmc=1918260 |name-list-format=vanc| author2=Leimbacher W | author3=Blau N | display-authors=3 | last4=Harvie | first4=A | last5=Heizmann | first5=CW }} | |||
*{{cite journal | | *{{cite journal |vauthors=Thöny B, Heizmann CW, Mattei MG |title=Chromosomal location of two human genes encoding tetrahydrobiopterin-metabolizing enzymes: 6-pyruvoyl-tetrahydropterin synthase maps to 11q22.3-q23.3, and pterin-4 alpha-carbinolamine dehydratase maps to 10q22 |journal=Genomics |volume=19 |issue= 2 |pages= 365–8 |year= 1994 |pmid= 8188266 |doi= 10.1006/geno.1994.1071 }} | ||
*{{cite journal | author= | *{{cite journal |vauthors=Ashida A, Hatakeyama K, Kagamiyama H |title=cDNA cloning, expression in Escherichia coli and purification of human 6-pyruvoyl-tetrahydropterin synthase |journal=Biochem. Biophys. Res. Commun. |volume=195 |issue= 3 |pages= 1386–93 |year= 1993 |pmid= 8216273 |doi= 10.1006/bbrc.1993.2197 }} | ||
*{{cite journal |vauthors=Liu TT, Hsiao KJ |title=Identification of a common 6-pyruvoyl-tetrahydropterin synthase mutation at codon 87 in Chinese phenylketonuria caused by tetrahydrobiopterin synthesis deficiency |journal=Hum. Genet. |volume=98 |issue= 3 |pages= 313–6 |year= 1996 |pmid= 8707300 |doi=10.1007/s004390050213 }} | |||
*{{cite journal | | *{{cite journal | author=Kluge C |title=Chromosomal localization, genomic structure and characterization of the human gene and a retropseudogene for 6-pyruvoyltetrahydropterin synthase |journal=Eur. J. Biochem. |volume=240 |issue= 2 |pages= 477–84 |year= 1996 |pmid= 8841415 |doi=10.1111/j.1432-1033.1996.0477h.x |name-list-format=vanc| author2=Brecevic L | author3=Heizmann CW | display-authors=3 | last4=Blau | first4=Nenad | last5=Thony | first5=Beat }} | ||
*{{cite journal | | *{{cite journal | author=Hanihara T |title=6-Pyruvoyl-tetrahydropterin synthase deficiency with generalized dystonia and diurnal fluctuation of symptoms: a clinical and molecular study |journal=Mov. Disord. |volume=12 |issue= 3 |pages= 408–11 |year= 1997 |pmid= 9159737 |doi= 10.1002/mds.870120321 |name-list-format=vanc| author2=Inoue K | author3=Kawanishi C | display-authors=3 | last4=Sugiyama | first4=N. | last5=Miyakawa | first5=T. | last6=Onishi | first6=H. | last7=Yamada | first7=Y. | last8=Osaka | first8=H. | last9=Kosaka | first9=K. }} | ||
*{{cite journal | | *{{cite journal | author=Oppliger T |title=Identification of mutations causing 6-pyruvoyl-tetrahydropterin synthase deficiency in four Italian families |journal=Hum. Mutat. |volume=10 |issue= 1 |pages= 25–35 |year= 1997 |pmid= 9222757 |doi= 10.1002/(SICI)1098-1004(1997)10:1<25::AID-HUMU4>3.0.CO;2-L |name-list-format=vanc| author2=Thöny B | author3=Kluge C | display-authors=3 | last4=Matasovic | first4=Ana | last5=Heizmann | first5=Claus W. | last6=Ponzone | first6=Alberto | last7=Spada | first7=Marco | last8=Blau | first8=Nenad }} | ||
*{{cite journal | author=Liu TT |title=Mutation analysis of the 6-pyruvoyl-tetrahydropterin synthase gene in Chinese hyperphenylalaninemia caused by tetrahydrobiopterin synthesis deficiency |journal=Hum. Mutat. |volume=11 |issue= 1 |pages= 76–83 |year= 1998 |pmid= 9450907 |doi= 10.1002/(SICI)1098-1004(1998)11:1<76::AID-HUMU12>3.0.CO;2-W |name-list-format=vanc| author2=Hsiao KJ | author3=Lu SF | display-authors=3 | last4=Wu | first4=Sheu-Jen | last5=Wu | first5=Kuei-Fen | last6=Chiang | first6=Szu-Hui | last7=Liu | first7=Xiao-Quing | last8=Chen | first8=Rui-Guan | last9=Yu | first9=Wei-Min }} | |||
*{{cite journal | author=Scherer-Oppliger T |title=Dominant negative allele (N47D) in a compound heterozygote for a variant of 6-pyruvoyltetrahydropterin synthase deficiency causing transient hyperphenylalaninemia |journal=Hum. Mutat. |volume=13 |issue= 4 |pages= 286–9 |year= 1999 |pmid= 10220141 |doi= 10.1002/(SICI)1098-1004(1999)13:4<286::AID-HUMU4>3.0.CO;2-C |name-list-format=vanc| author2=Matasovic A | author3=Laufs S | display-authors=3 | last4=Levy | first4=Harvey L. | last5=Quackenbush | first5=Elisabeth J. | last6=Blau | first6=Nenad | last7=Thöny | first7=Beat }} | |||
*{{cite journal |vauthors=Scherer-Oppliger T, Leimbacher W, Blau N, Thöny B |title=Serine 19 of human 6-pyruvoyltetrahydropterin synthase is phosphorylated by cGMP protein kinase II |journal=J. Biol. Chem. |volume=274 |issue= 44 |pages= 31341–8 |year= 1999 |pmid= 10531334 |doi=10.1074/jbc.274.44.31341 }} | |||
*{{cite journal | author= | *{{cite journal |vauthors=Kim ST, Lim DS, Canman CE, Kastan MB |title=Substrate specificities and identification of putative substrates of ATM kinase family members |journal=J. Biol. Chem. |volume=274 |issue= 53 |pages= 37538–43 |year= 2000 |pmid= 10608806 |doi=10.1074/jbc.274.53.37538 }} | ||
}} | }} | ||
{{refend}} | {{refend}} | ||
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{{Metabolism of vitamins, coenzymes, and cofactors}} | |||
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Latest revision as of 15:28, 14 January 2018
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Species | Human | Mouse | |||||
Entrez |
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Ensembl |
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UniProt |
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RefSeq (mRNA) |
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RefSeq (protein) |
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Location (UCSC) | n/a | n/a | |||||
PubMed search | n/a | n/a | |||||
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6-pyruvoyltetrahydropterin synthase, also known as PTS, is a human gene which facilitates folate biosynthesis.[1]
See also
References
Further reading
- Werner ER, Werner-Felmayer G, Fuchs D, et al. (1991). "Biochemistry and function of pteridine synthesis in human and murine macrophages". Pathobiology. 59 (4): 276–9. doi:10.1159/000163662. PMID 1883524.
- Thöny B, Blau N (1997). "Mutations in the GTP cyclohydrolase I and 6-pyruvoyl-tetrahydropterin synthase genes". Hum. Mutat. 10 (1): 11–20. doi:10.1002/(SICI)1098-1004(1997)10:1<11::AID-HUMU2>3.0.CO;2-P. PMID 9222755.
- Thöny B, Auerbach G, Blau N (2000). "Tetrahydrobiopterin biosynthesis, regeneration and functions". Biochem. J. 347 (1): 1–16. doi:10.1042/0264-6021:3470001. PMC 1220924. PMID 10727395.
- Thöny B, Leimbacher W, Bürgisser D, Heizmann CW (1993). "Human 6-pyruvoyltetrahydropterin synthase: cDNA cloning and heterologous expression of the recombinant enzyme". Biochem. Biophys. Res. Commun. 189 (3): 1437–43. doi:10.1016/0006-291X(92)90235-D. PMID 1282802.
- Scriver CR, Clow CL, Kaplan P, Niederwieser A (1987). "Hyperphenylalaninemia due to deficiency of 6-pyruvoyl tetrahydropterin synthase. Unusual gene dosage effect in heterozygotes". Hum. Genet. 77 (2): 168–71. doi:10.1007/BF00272386. PMID 3308682.
- Oppliger T, Thöny B, Nar H, et al. (1996). "Structural and functional consequences of mutations in 6-pyruvoyltetrahydropterin synthase causing hyperphenylalaninemia in humans. Phosphorylation is a requirement for in vivo activity". J. Biol. Chem. 270 (49): 29498–506. doi:10.1074/jbc.270.49.29498. PMID 7493990.
- Ashida A, Owada M, Hatakeyama K (1995). "A missense mutation (A to G) of 6-pyruvoyltetrahydropterin synthase in tetrahydrobiopterin-deficient form of hyperphenylalaninemia". Genomics. 24 (2): 408–10. doi:10.1006/geno.1994.1642. PMID 7698774.
- Thöny B, Leimbacher W, Blau N, et al. (1994). "Hyperphenylalaninemia due to defects in tetrahydrobiopterin metabolism: molecular characterization of mutations in 6-pyruvoyl-tetrahydropterin synthase". Am. J. Hum. Genet. 54 (5): 782–92. PMC 1918260. PMID 8178819.
- Thöny B, Heizmann CW, Mattei MG (1994). "Chromosomal location of two human genes encoding tetrahydrobiopterin-metabolizing enzymes: 6-pyruvoyl-tetrahydropterin synthase maps to 11q22.3-q23.3, and pterin-4 alpha-carbinolamine dehydratase maps to 10q22". Genomics. 19 (2): 365–8. doi:10.1006/geno.1994.1071. PMID 8188266.
- Ashida A, Hatakeyama K, Kagamiyama H (1993). "cDNA cloning, expression in Escherichia coli and purification of human 6-pyruvoyl-tetrahydropterin synthase". Biochem. Biophys. Res. Commun. 195 (3): 1386–93. doi:10.1006/bbrc.1993.2197. PMID 8216273.
- Liu TT, Hsiao KJ (1996). "Identification of a common 6-pyruvoyl-tetrahydropterin synthase mutation at codon 87 in Chinese phenylketonuria caused by tetrahydrobiopterin synthesis deficiency". Hum. Genet. 98 (3): 313–6. doi:10.1007/s004390050213. PMID 8707300.
- Kluge C, Brecevic L, Heizmann CW, et al. (1996). "Chromosomal localization, genomic structure and characterization of the human gene and a retropseudogene for 6-pyruvoyltetrahydropterin synthase". Eur. J. Biochem. 240 (2): 477–84. doi:10.1111/j.1432-1033.1996.0477h.x. PMID 8841415.
- Hanihara T, Inoue K, Kawanishi C, et al. (1997). "6-Pyruvoyl-tetrahydropterin synthase deficiency with generalized dystonia and diurnal fluctuation of symptoms: a clinical and molecular study". Mov. Disord. 12 (3): 408–11. doi:10.1002/mds.870120321. PMID 9159737.
- Oppliger T, Thöny B, Kluge C, et al. (1997). "Identification of mutations causing 6-pyruvoyl-tetrahydropterin synthase deficiency in four Italian families". Hum. Mutat. 10 (1): 25–35. doi:10.1002/(SICI)1098-1004(1997)10:1<25::AID-HUMU4>3.0.CO;2-L. PMID 9222757.
- Liu TT, Hsiao KJ, Lu SF, et al. (1998). "Mutation analysis of the 6-pyruvoyl-tetrahydropterin synthase gene in Chinese hyperphenylalaninemia caused by tetrahydrobiopterin synthesis deficiency". Hum. Mutat. 11 (1): 76–83. doi:10.1002/(SICI)1098-1004(1998)11:1<76::AID-HUMU12>3.0.CO;2-W. PMID 9450907.
- Scherer-Oppliger T, Matasovic A, Laufs S, et al. (1999). "Dominant negative allele (N47D) in a compound heterozygote for a variant of 6-pyruvoyltetrahydropterin synthase deficiency causing transient hyperphenylalaninemia". Hum. Mutat. 13 (4): 286–9. doi:10.1002/(SICI)1098-1004(1999)13:4<286::AID-HUMU4>3.0.CO;2-C. PMID 10220141.
- Scherer-Oppliger T, Leimbacher W, Blau N, Thöny B (1999). "Serine 19 of human 6-pyruvoyltetrahydropterin synthase is phosphorylated by cGMP protein kinase II". J. Biol. Chem. 274 (44): 31341–8. doi:10.1074/jbc.274.44.31341. PMID 10531334.
- Kim ST, Lim DS, Canman CE, Kastan MB (2000). "Substrate specificities and identification of putative substrates of ATM kinase family members". J. Biol. Chem. 274 (53): 37538–43. doi:10.1074/jbc.274.53.37538. PMID 10608806.
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