Dirigent protein (English Wikipedia)

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

refsWebsite

Global rank English rank

11doi.org

2^nd place

9nih.gov

4^th place

4semanticscholar.org

11^th place

8^th place

3harvard.edu

18^th place

17^th place

1archive.org

6^th place

1rsc.org

2,020^th place

1,872^nd place

archive.org

Nicholson, Ralph L.; Wilfred Vermerris; Vermerris Wilfred (2006). Phenolic compound biochemistry. Berlin: Springer. pp. 107–108. ISBN 1-4020-5163-8.

doi.org

Davin LB, Wang HB, Crowell AL, et al. (1997). "Stereoselective bimolecular phenoxy radical coupling by an auxiliary (dirigent) protein without an active center". Science. 275 (5298): 362–6. doi:10.1126/science.275.5298.362. PMID 8994027. S2CID 41957412.
Ward R.S. (1982). "The synthesis of lignans and neolignans". Chemical Society Reviews. 11 (2): 75–125. doi:10.1039/CS9821100075.
Fournand D, Cathala B, Lapierre C (January 2003). "Initial steps of the peroxidase-catalyzed polymerization of coniferyl alcohol and/or sinapyl aldehyde: capillary zone electrophoresis study of pH effect". Phytochemistry. 62 (2): 139–46. Bibcode:2003PChem..62..139F. doi:10.1016/S0031-9422(02)00573-3. PMID 12482448.
Davin L.B.; Lewis N.G. (August 2005). "Dirigent phenoxy radical coupling: advances and challenges". Current Opinion in Biotechnology. 16 (4): 398–406. doi:10.1016/j.copbio.2005.06.010. PMID 16023845.
Pickel B, Constantin M-A, Pfannsteil J, Conrad J, Beifuss U, Schaffer A (March 2007). "An Enantiocomplementary Dirigent Protein for the Enantioselective Laccase-Catalyzed Oxidative Coupling of Phenols". Angewandte Chemie. 53 (4): 273–284. doi:10.1007/s10086-007-0892-x. S2CID 195313754.
Fournand D, Cathala B, Lapierre C (January 2003). "Initial steps of the peroxidase-catalyzed polymerization of coniferyl alcohol and/or sinapyl aldehyde: capillary zone electrophoresis study of pH effect". Phytochemistry. 62 (2): 139–46. Bibcode:2003PChem..62..139F. doi:10.1016/S0031-9422(02)00573-3. PMID 12482448.
Halls SC, Davin LB, Kramer DM, Lewis NG (2004). "Kinetic study of coniferyl alcohol radical binding to the (+)-pinoresinol forming dirigent protein". Biochemistry. 43 (9): 2587–95. doi:10.1021/bi035959o. PMID 14992596.
Kim, M.K.; Jeon J.-H.; Fujita M.; Davin L.B.; Lewis N.G. (2002). "The western red cedar (Thuja plicata) 8-8′ DIRIGENT family displays diverse expression patterns and conserved monolignol coupling specificity". Plant Molecular Biology. 49 (2): 199–214. doi:10.1023/A:1014940930703. PMID 11999375. S2CID 8042373.
Halls SC, Lewis NG (July 2002). "Secondary and quaternary structures of the (+)-pinoresinol-forming dirigent protein". Biochemistry. 41 (30): 9455–61. doi:10.1021/bi0259709. PMID 12135368.
Schroeder FC, del Campo ML, Grant JB, et al. (October 2006). "Pinoresinol: A lignol of plant origin serving for defense in a caterpillar". Proc. Natl. Acad. Sci. U.S.A. 103 (42): 15497–501. Bibcode:2006PNAS..10315497S. doi:10.1073/pnas.0605921103. PMC 1622851. PMID 17030818.
Schmitt J, Peterson M (2002). "Pinoresinol and matairesinol accumulation in a Forsythia × intermedia cell suspension culture". Plant Cell, Tissue and Organ Culture. 68 (1): 91–98. doi:10.1023/A:1012909131741. S2CID 19282302.

harvard.edu

ui.adsabs.harvard.edu

Fournand D, Cathala B, Lapierre C (January 2003). "Initial steps of the peroxidase-catalyzed polymerization of coniferyl alcohol and/or sinapyl aldehyde: capillary zone electrophoresis study of pH effect". Phytochemistry. 62 (2): 139–46. Bibcode:2003PChem..62..139F. doi:10.1016/S0031-9422(02)00573-3. PMID 12482448.
Fournand D, Cathala B, Lapierre C (January 2003). "Initial steps of the peroxidase-catalyzed polymerization of coniferyl alcohol and/or sinapyl aldehyde: capillary zone electrophoresis study of pH effect". Phytochemistry. 62 (2): 139–46. Bibcode:2003PChem..62..139F. doi:10.1016/S0031-9422(02)00573-3. PMID 12482448.
Schroeder FC, del Campo ML, Grant JB, et al. (October 2006). "Pinoresinol: A lignol of plant origin serving for defense in a caterpillar". Proc. Natl. Acad. Sci. U.S.A. 103 (42): 15497–501. Bibcode:2006PNAS..10315497S. doi:10.1073/pnas.0605921103. PMC 1622851. PMID 17030818.

nih.gov

pubmed.ncbi.nlm.nih.gov

Davin LB, Wang HB, Crowell AL, et al. (1997). "Stereoselective bimolecular phenoxy radical coupling by an auxiliary (dirigent) protein without an active center". Science. 275 (5298): 362–6. doi:10.1126/science.275.5298.362. PMID 8994027. S2CID 41957412.
Fournand D, Cathala B, Lapierre C (January 2003). "Initial steps of the peroxidase-catalyzed polymerization of coniferyl alcohol and/or sinapyl aldehyde: capillary zone electrophoresis study of pH effect". Phytochemistry. 62 (2): 139–46. Bibcode:2003PChem..62..139F. doi:10.1016/S0031-9422(02)00573-3. PMID 12482448.
Davin L.B.; Lewis N.G. (August 2005). "Dirigent phenoxy radical coupling: advances and challenges". Current Opinion in Biotechnology. 16 (4): 398–406. doi:10.1016/j.copbio.2005.06.010. PMID 16023845.
Fournand D, Cathala B, Lapierre C (January 2003). "Initial steps of the peroxidase-catalyzed polymerization of coniferyl alcohol and/or sinapyl aldehyde: capillary zone electrophoresis study of pH effect". Phytochemistry. 62 (2): 139–46. Bibcode:2003PChem..62..139F. doi:10.1016/S0031-9422(02)00573-3. PMID 12482448.
Halls SC, Davin LB, Kramer DM, Lewis NG (2004). "Kinetic study of coniferyl alcohol radical binding to the (+)-pinoresinol forming dirigent protein". Biochemistry. 43 (9): 2587–95. doi:10.1021/bi035959o. PMID 14992596.
Kim, M.K.; Jeon J.-H.; Fujita M.; Davin L.B.; Lewis N.G. (2002). "The western red cedar (Thuja plicata) 8-8′ DIRIGENT family displays diverse expression patterns and conserved monolignol coupling specificity". Plant Molecular Biology. 49 (2): 199–214. doi:10.1023/A:1014940930703. PMID 11999375. S2CID 8042373.
Halls SC, Lewis NG (July 2002). "Secondary and quaternary structures of the (+)-pinoresinol-forming dirigent protein". Biochemistry. 41 (30): 9455–61. doi:10.1021/bi0259709. PMID 12135368.
Schroeder FC, del Campo ML, Grant JB, et al. (October 2006). "Pinoresinol: A lignol of plant origin serving for defense in a caterpillar". Proc. Natl. Acad. Sci. U.S.A. 103 (42): 15497–501. Bibcode:2006PNAS..10315497S. doi:10.1073/pnas.0605921103. PMC 1622851. PMID 17030818.

ncbi.nlm.nih.gov

Schroeder FC, del Campo ML, Grant JB, et al. (October 2006). "Pinoresinol: A lignol of plant origin serving for defense in a caterpillar". Proc. Natl. Acad. Sci. U.S.A. 103 (42): 15497–501. Bibcode:2006PNAS..10315497S. doi:10.1073/pnas.0605921103. PMC 1622851. PMID 17030818.

rsc.org

pubs.rsc.org

Ward R.S. (1982). "The synthesis of lignans and neolignans". Chemical Society Reviews. 11 (2): 75–125. doi:10.1039/CS9821100075.

semanticscholar.org

api.semanticscholar.org

Davin LB, Wang HB, Crowell AL, et al. (1997). "Stereoselective bimolecular phenoxy radical coupling by an auxiliary (dirigent) protein without an active center". Science. 275 (5298): 362–6. doi:10.1126/science.275.5298.362. PMID 8994027. S2CID 41957412.
Pickel B, Constantin M-A, Pfannsteil J, Conrad J, Beifuss U, Schaffer A (March 2007). "An Enantiocomplementary Dirigent Protein for the Enantioselective Laccase-Catalyzed Oxidative Coupling of Phenols". Angewandte Chemie. 53 (4): 273–284. doi:10.1007/s10086-007-0892-x. S2CID 195313754.
Kim, M.K.; Jeon J.-H.; Fujita M.; Davin L.B.; Lewis N.G. (2002). "The western red cedar (Thuja plicata) 8-8′ DIRIGENT family displays diverse expression patterns and conserved monolignol coupling specificity". Plant Molecular Biology. 49 (2): 199–214. doi:10.1023/A:1014940930703. PMID 11999375. S2CID 8042373.
Schmitt J, Peterson M (2002). "Pinoresinol and matairesinol accumulation in a Forsythia × intermedia cell suspension culture". Plant Cell, Tissue and Organ Culture. 68 (1): 91–98. doi:10.1023/A:1012909131741. S2CID 19282302.