Molybdopterin (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "Molybdopterin" in English language version.

refsWebsite

Global rank English rank

12nih.gov

4^th place

7doi.org

2^nd place

2semanticscholar.org

11^th place

8^th place

1gramene.org

low place

1web.archive.org

1^st place

1harvard.edu

18^th place

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1books.google.com

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1iupac.org

538^th place

863^rd place

books.google.com

Lassner, Erik (1999). Tungsten: Properties, Chemistry, Technology of the Element, Alloys and Chemical Compounds. Springer. pp. 409–411. ISBN 978-0-306-45053-2.

doi.org

Hover BM, Tonthat NK, Schumacher MA, Yokoyama K (May 2015). "Mechanism of pyranopterin ring formation in molybdenum cofactor biosynthesis". Proc Natl Acad Sci USA. 112 (20): 6347–52. Bibcode:2015PNAS..112.6347H. doi:10.1073/pnas.1500697112. PMC 4443348. PMID 25941396.
Hover BM, Loksztejn A, Ribeiro AA, Yokoyama K (April 2013). "Identification of a cyclic nucleotide as a cryptic intermediate in molybdenum cofactor biosynthesis". J Am Chem Soc. 135 (18): 7019–32. doi:10.1021/ja401781t. PMC 3777439. PMID 23627491.
Mendel, R. R.; Leimkuehler, S. (2015). "The biosynthesis of the molybdenum cofactors". J. Biol. Inorg. Chem. 20 (2): 337–347. doi:10.1007/s00775-014-1173-y. PMID 24980677. S2CID 2638550.
Schwarz, G. & Mendel, R. R. (2006). "Molybdenum cofactor biosynthesis and molybdenum enzymes". Annual Review of Plant Biology. 57: 623–647. doi:10.1146/annurev.arplant.57.032905.105437. PMID 16669776.
Kisker, C.; Schindelin, H.; Baas, D.; Rétey, J.; Meckenstock, R.U.; Kroneck, P.M.H. (1999). "A structural comparison of molybdenum cofactor-containing enzymes". FEMS Microbiol. Rev. 22 (5): 503–521. 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" (PDF). Pure Appl. Chem. 70 (4): 889–896. doi:10.1351/pac199870040889. S2CID 98647064.
Schräder T, Rienhöfer A, Andreesen JR (September 1999). "Selenium-containing xanthine dehydrogenase from Eubacterium barkeri". Eur. J. Biochem. 264 (3): 862–71. doi:10.1046/j.1432-1327.1999.00678.x. PMID 10491134.

gramene.org

pathway.gramene.org

Structure, synthesis, empirical formula for the di-sulfhydryl. Archived 2016-06-04 at the Wayback Machine Accessed Nov. 16, 2009.

harvard.edu

ui.adsabs.harvard.edu

Hover BM, Tonthat NK, Schumacher MA, Yokoyama K (May 2015). "Mechanism of pyranopterin ring formation in molybdenum cofactor biosynthesis". Proc Natl Acad Sci USA. 112 (20): 6347–52. Bibcode:2015PNAS..112.6347H. doi:10.1073/pnas.1500697112. PMC 4443348. PMID 25941396.

iupac.org

media.iupac.org

Stiefel, E. I. (1998). "Transition metal sulfur chemistry and its relevance to molybdenum and tungsten enzymes" (PDF). Pure Appl. Chem. 70 (4): 889–896. doi:10.1351/pac199870040889. S2CID 98647064.

nih.gov

pubmed.ncbi.nlm.nih.gov

Hover BM, Tonthat NK, Schumacher MA, Yokoyama K (May 2015). "Mechanism of pyranopterin ring formation in molybdenum cofactor biosynthesis". Proc Natl Acad Sci USA. 112 (20): 6347–52. Bibcode:2015PNAS..112.6347H. doi:10.1073/pnas.1500697112. PMC 4443348. PMID 25941396.
Hover BM, Loksztejn A, Ribeiro AA, Yokoyama K (April 2013). "Identification of a cyclic nucleotide as a cryptic intermediate in molybdenum cofactor biosynthesis". J Am Chem Soc. 135 (18): 7019–32. doi:10.1021/ja401781t. PMC 3777439. PMID 23627491.
Mendel, R. R.; Leimkuehler, S. (2015). "The biosynthesis of the molybdenum cofactors". J. Biol. Inorg. Chem. 20 (2): 337–347. doi:10.1007/s00775-014-1173-y. PMID 24980677. S2CID 2638550.
Schwarz, G. & Mendel, R. R. (2006). "Molybdenum cofactor biosynthesis and molybdenum enzymes". Annual Review of Plant Biology. 57: 623–647. doi:10.1146/annurev.arplant.57.032905.105437. PMID 16669776.
Kisker, C.; Schindelin, H.; Baas, D.; Rétey, J.; Meckenstock, R.U.; Kroneck, P.M.H. (1999). "A structural comparison of molybdenum cofactor-containing enzymes". FEMS Microbiol. Rev. 22 (5): 503–521. doi:10.1111/j.1574-6976.1998.tb00384.x. PMID 9990727.
Schräder T, Rienhöfer A, Andreesen JR (September 1999). "Selenium-containing xanthine dehydrogenase from Eubacterium barkeri". Eur. J. Biochem. 264 (3): 862–71. doi:10.1046/j.1432-1327.1999.00678.x. PMID 10491134.

pubchem.ncbi.nlm.nih.gov

"HPEUEJRPDGMIMY-UHFFFAOYSA-N". pubchem.ncbi.nlm.nih.gov. Retrieved 4 February 2019. 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". pubchem.ncbi.nlm.nih.gov. Retrieved 4 February 2019. 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". pubchem.ncbi.nlm.nih.gov. Retrieved 4 February 2019. 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". pubchem.ncbi.nlm.nih.gov. Retrieved 4 February 2019. InChI Key HPEUEJRPDGMIMY-UHFFFAOYSA-N

ncbi.nlm.nih.gov

Hover BM, Tonthat NK, Schumacher MA, Yokoyama K (May 2015). "Mechanism of pyranopterin ring formation in molybdenum cofactor biosynthesis". Proc Natl Acad Sci USA. 112 (20): 6347–52. Bibcode:2015PNAS..112.6347H. doi:10.1073/pnas.1500697112. PMC 4443348. PMID 25941396.
Hover BM, Loksztejn A, Ribeiro AA, Yokoyama K (April 2013). "Identification of a cyclic nucleotide as a cryptic intermediate in molybdenum cofactor biosynthesis". J Am Chem Soc. 135 (18): 7019–32. doi:10.1021/ja401781t. PMC 3777439. PMID 23627491.

semanticscholar.org

api.semanticscholar.org

Mendel, R. R.; Leimkuehler, S. (2015). "The biosynthesis of the molybdenum cofactors". J. Biol. Inorg. Chem. 20 (2): 337–347. doi:10.1007/s00775-014-1173-y. PMID 24980677. S2CID 2638550.
Stiefel, E. I. (1998). "Transition metal sulfur chemistry and its relevance to molybdenum and tungsten enzymes" (PDF). Pure Appl. Chem. 70 (4): 889–896. doi:10.1351/pac199870040889. S2CID 98647064.

web.archive.org

Structure, synthesis, empirical formula for the di-sulfhydryl. Archived 2016-06-04 at the Wayback Machine Accessed Nov. 16, 2009.