Molybdopteriny (Czech Wikipedia)

Analysis of information sources in references of the Wikipedia article "Molybdopteriny" in Czech language version.

refsWebsite

Global rank Czech rank

7doi.org

2^nd place

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6nih.gov

4^th place

8^th place

1web.archive.org

1^st place

1gramene.org

low place

1harvard.edu

18^th place

99^th place

1iupac.org

538^th place

244^th place

doi.org

dx.doi.org

B. M. Hover; N. K. Tonthat; M. A. Schumacher; K. Yokoyama. Mechanism of pyranopterin ring formation in molybdenum cofactor biosynthesis. Proceedings of the National Academy of Sciences of the United States of America. 2015, s. 6347–6352. DOI 10.1073/pnas.1500697112. PMID 25941396. Bibcode 2015PNAS..112.6347H.
B. M. Hover; A. Loksztejn; A. A. Ribeiro; K. Yokoyama. Identification of a cyclic nucleotide as a cryptic intermediate in molybdenum cofactor biosynthesis. Journal of the American Chemical Society. 2013, s. 7019–7032. DOI 10.1021/ja401781t. PMID 236274919.
R. R. Mendel; S. Leimkuehler. The biosynthesis of the molybdenum cofactors. Journal of Biological Inorganic Chemistry. 2015, s. 337–347. DOI 10.1007/s00775-014-1173-y. PMID 24980677.
G. Schwarz; R. R. Mendel. Molybdenum cofactor biosynthesis and molybdenum enzymes. Annual Review of Plant Biology. 2006, s. 623–647. DOI 10.1146/annurev.arplant.57.032905.105437. PMID 16669776.
C. Kisker; H. Schindelin; D. Baas; J. Rétey; R. U. Meckenstock; P. M. H. Kroneck. A structural comparison of molybdenum cofactor-containing enzymes. FEMS Microbiology Reviews. 1999, s. 503–521. DOI 10.1111/j.1574-6976.1998.tb00384.x. PMID 9990727.
Erik Lassner. Transition metal sulfur chemistry and its relevance to molybdenum and tungsten enzymes. Pure and Applied Chemistry. 1998, s. 889–896. Dostupné online. DOI 10.1351/pac199870040889.
T. Schräder; A. Rienhöfer; J. R. Andreesen. Selenium-containing xanthine dehydrogenase from Eubacterium barkeri. European Journal of Biochemistry. 1999, s. 862–871. DOI 10.1046/j.1432-1327.1999.00678.x. PMID 10491134.

gramene.org

pathway.gramene.org

Structure, synthesis, empirical formula for the di-sulfhydryl. pathway.gramene.org [online]. [cit. 2024-02-08]. Dostupné v archivu pořízeném z originálu dne 2016-06-04.

harvard.edu

adsabs.harvard.edu

B. M. Hover; N. K. Tonthat; M. A. Schumacher; K. Yokoyama. Mechanism of pyranopterin ring formation in molybdenum cofactor biosynthesis. Proceedings of the National Academy of Sciences of the United States of America. 2015, s. 6347–6352. DOI 10.1073/pnas.1500697112. PMID 25941396. Bibcode 2015PNAS..112.6347H.

iupac.org

media.iupac.org

Erik Lassner. Transition metal sulfur chemistry and its relevance to molybdenum and tungsten enzymes. Pure and Applied Chemistry. 1998, s. 889–896. Dostupné online. DOI 10.1351/pac199870040889.

nih.gov

ncbi.nlm.nih.gov

B. M. Hover; N. K. Tonthat; M. A. Schumacher; K. Yokoyama. Mechanism of pyranopterin ring formation in molybdenum cofactor biosynthesis. Proceedings of the National Academy of Sciences of the United States of America. 2015, s. 6347–6352. DOI 10.1073/pnas.1500697112. PMID 25941396. Bibcode 2015PNAS..112.6347H.
B. M. Hover; A. Loksztejn; A. A. Ribeiro; K. Yokoyama. Identification of a cyclic nucleotide as a cryptic intermediate in molybdenum cofactor biosynthesis. Journal of the American Chemical Society. 2013, s. 7019–7032. DOI 10.1021/ja401781t. PMID 236274919.
R. R. Mendel; S. Leimkuehler. The biosynthesis of the molybdenum cofactors. Journal of Biological Inorganic Chemistry. 2015, s. 337–347. DOI 10.1007/s00775-014-1173-y. PMID 24980677.
G. Schwarz; R. R. Mendel. Molybdenum cofactor biosynthesis and molybdenum enzymes. Annual Review of Plant Biology. 2006, s. 623–647. DOI 10.1146/annurev.arplant.57.032905.105437. PMID 16669776.
C. Kisker; H. Schindelin; D. Baas; J. Rétey; R. U. Meckenstock; P. M. H. Kroneck. A structural comparison of molybdenum cofactor-containing enzymes. FEMS Microbiology Reviews. 1999, s. 503–521. DOI 10.1111/j.1574-6976.1998.tb00384.x. PMID 9990727.
T. Schräder; A. Rienhöfer; J. R. Andreesen. Selenium-containing xanthine dehydrogenase from Eubacterium barkeri. European Journal of Biochemistry. 1999, s. 862–871. DOI 10.1046/j.1432-1327.1999.00678.x. PMID 10491134.

web.archive.org

Structure, synthesis, empirical formula for the di-sulfhydryl. pathway.gramene.org [online]. [cit. 2024-02-08]. Dostupné v archivu pořízeném z originálu dne 2016-06-04.