Molibdopterin (Hungarian Wikipedia)

Analysis of information sources in references of the Wikipedia article "Molibdopterin" in Hungarian language version.

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archive.org

(2015. május 1.) „Mechanism of pyranopterin ring formation in molybdenum cofactor biosynthesis”. Proc Natl Acad Sci USA 112 (20), 6347–52. o. DOI:10.1073/pnas.1500697112. PMID 25941396. PMC 4443348.
(2013. április 1.) „Identification of a cyclic nucleotide as a cryptic intermediate in molybdenum cofactor biosynthesis”. J Am Chem Soc 135 (18), 7019–32. o. DOI:10.1021/ja401781t. PMID 23627491. PMC 3777439.
(2015) „The biosynthesis of the molybdenum cofactors”. J. Biol. Inorg. Chem. 20 (2), 337–347. o. DOI:10.1007/s00775-014-1173-y. PMID 24980677.
(2006) „Molybdenum cofactor biosynthesis and molybdenum enzymes”. Annual Review of Plant Biology 57, 623–647. o. DOI:10.1146/annurev.arplant.57.032905.105437. PMID 16669776.
(1999) „A structural comparison of molybdenum cofactor-containing enzymes”. FEMS Microbiol. Rev. 22 (5), 503–521. o. DOI:10.1111/j.1574-6976.1998.tb00384.x. PMID 9990727.
Stiefel, E. I. (1998). „Transition metal sulfur chemistry and its relevance to molybdenum and tungsten enzymes”. Pure Appl. Chem. 70 (4), 889–896. o. DOI:10.1351/pac199870040889.
(1999. szeptember 1.) „Selenium-containing xanthine dehydrogenase from Eubacterium barkeri”. Eur. J. Biochem. 264 (3), 862–71. o. DOI:10.1046/j.1432-1327.1999.00678.x. PMID 10491134.

(2015. május 1.) „Mechanism of pyranopterin ring formation in molybdenum cofactor biosynthesis”. Proc Natl Acad Sci USA 112 (20), 6347–52. o. DOI:10.1073/pnas.1500697112. PMID 25941396. PMC 4443348.
(2013. április 1.) „Identification of a cyclic nucleotide as a cryptic intermediate in molybdenum cofactor biosynthesis”. J Am Chem Soc 135 (18), 7019–32. o. DOI:10.1021/ja401781t. PMID 23627491. PMC 3777439.
(2015) „The biosynthesis of the molybdenum cofactors”. J. Biol. Inorg. Chem. 20 (2), 337–347. o. DOI:10.1007/s00775-014-1173-y. PMID 24980677.
(2006) „Molybdenum cofactor biosynthesis and molybdenum enzymes”. Annual Review of Plant Biology 57, 623–647. o. DOI:10.1146/annurev.arplant.57.032905.105437. PMID 16669776.
(1999) „A structural comparison of molybdenum cofactor-containing enzymes”. FEMS Microbiol. Rev. 22 (5), 503–521. o. DOI:10.1111/j.1574-6976.1998.tb00384.x. PMID 9990727.
(1999. szeptember 1.) „Selenium-containing xanthine dehydrogenase from Eubacterium barkeri”. Eur. J. Biochem. 264 (3), 862–71. o. DOI:10.1046/j.1432-1327.1999.00678.x. PMID 10491134.

HPEUEJRPDGMIMY-UHFFFAOYSA-N (angol nyelven). pubchem.ncbi.nlm.nih.gov . (Hozzáférés: 2019. február 4.) „IUPAC Name [2-amino-4-oxo-6,7-bis(sulfanyl)-3,5,5~{a},8,9~{a},10-hexahydropyrano[3,2-g]pteridin-8-yl]methyl dihydrogen phosphate”
HPEUEJRPDGMIMY-UHFFFAOYSA-N (angol nyelven). pubchem.ncbi.nlm.nih.gov . (Hozzáférés: 2019. február 4.) „InChI InChI=1S/C10H14N5O6PS2/c11-10-14-7-4(8(16)15-10)12-3-6(24)5(23)2(21-9(3)13-7)1-20-22(17,18)19/h2-3,9,12,23-24H,1H2,(H2,17,18,19)(H4,11,13,14,15,16)”
[2-Amino-4-oxo-6,7-bis(sulfanyl)-3,5,5a,8,9a,10-hexahydropyrano[3,2-g]pteridin-8-yl]methyl dihydrogen phosphate (angol nyelven). pubchem.ncbi.nlm.nih.gov . (Hozzáférés: 2019. február 4.) „InChI=1S/C10H14N5O6PS2/c11-10-14-7-4(8(16)15-10)12-3-6(24)5(23)2(21-9(3)13-7)1-20-22(17,18)19/h2-3,9,12,23-24H,1H2,(H2,17,18,19)(H4,11,13,14,15,16)”
HPEUEJRPDGMIMY-UHFFFAOYSA-N (angol nyelven). pubchem.ncbi.nlm.nih.gov . (Hozzáférés: 2019. február 4.) „InChI Key HPEUEJRPDGMIMY-UHFFFAOYSA-N”

(2015. május 1.) „Mechanism of pyranopterin ring formation in molybdenum cofactor biosynthesis”. Proc Natl Acad Sci USA 112 (20), 6347–52. o. DOI:10.1073/pnas.1500697112. PMID 25941396. PMC 4443348.
(2013. április 1.) „Identification of a cyclic nucleotide as a cryptic intermediate in molybdenum cofactor biosynthesis”. J Am Chem Soc 135 (18), 7019–32. o. DOI:10.1021/ja401781t. PMID 23627491. PMC 3777439.