메뉴 건너뛰기




Volumn , Issue , 2003, Pages 141-1-141-22

DNA damage and repair: Photochemistry

Author keywords

[No Author keywords available]

Indexed keywords


EID: 85056326230     PISSN: None     EISSN: None     Source Type: Book    
DOI: None     Document Type: Chapter
Times cited : (2)

References (122)
  • 2
  • 3
    • 34547239649 scopus 로고
    • Reduction of stratospheric ozone by nitrogen oxide catalysts from supersonic transport exhaust
    • Johnston, H., Reduction of stratospheric ozone by nitrogen oxide catalysts from supersonic transport exhaust, Science, 173, 517, 1971.
    • (1971) Science , vol.173 , pp. 517
    • Johnston, H.1
  • 4
    • 0016322177 scopus 로고
    • Stratospheric sink for chlorofluoromethanes: Chlorine atom catalysed destruction of ozone
    • Molina, M.J. and Rowland, F.S., Stratospheric sink for chlorofluoromethanes: chlorine atom catalysed destruction of ozone, Nature, 249, 810, 1974.
    • (1974) Nature , vol.249 , pp. 810
    • Molina, M.J.1    Rowland, F.S.2
  • 6
    • 0000177002 scopus 로고
    • The photochemistry of nucleic acids
    • chap. 1, Morrison, H., Ed., Wiley, New York
    • Cadet, J. and Vigny, P., The photochemistry of nucleic acids, in Bioorganic Photochemistry, vol. 1, chap. 1, Morrison, H., Ed., Wiley, New York, 1990.
    • (1990) Bioorganic Photochemistry , vol.1
    • Cadet, J.1    Vigny, P.2
  • 7
    • 0029198754 scopus 로고
    • UV and nucleic acids
    • Jollés, P. and Jörnvall, H., Eds., Birkhäuser Verlag, Basel
    • Douki, T. and Cadet, J., UV and nucleic acids, in Interface between Chemistry and Biochemistry, Jollés, P. and Jörnvall, H., Eds., Birkhäuser Verlag, Basel, 1995, p. 173.
    • (1995) Interface between Chemistry and Biochemistry , pp. 173
    • Douki, T.1    Cadet, J.2
  • 8
    • 0025582036 scopus 로고
    • Molecular mechanisms of ultraviolet radiation carcinogenesis
    • Ananthaswamy, H.N. and Pierceall, W.E., Molecular mechanisms of ultraviolet radiation carcinogenesis, Photochem. Photobiol., 52, 1119, 1990.
    • (1990) Photochem. Photobiol , vol.52 , pp. 1119
    • Ananthaswamy, H.N.1    Pierceall, W.E.2
  • 9
    • 33751553234 scopus 로고
    • DNA, sunlight and skin cancer
    • Taylor, J.-S., DNA, sunlight and skin cancer, J. Chem. Ed., 67, 835, 1990.
    • (1990) J. Chem. Ed , vol.67 , pp. 835
    • Taylor, J.-S.1
  • 10
    • 0002622056 scopus 로고
    • Unraveling the molecular pathway from sunlight to skin cancer
    • Taylor, J.-S., Unraveling the molecular pathway from sunlight to skin cancer, Acc. Chem. Res., 27, 76, 1994.
    • (1994) Acc. Chem. Res , vol.27 , pp. 76
    • Taylor, J.-S.1
  • 11
    • 0000723716 scopus 로고
    • DNA, sunlight and skin-cancer
    • Taylor, J.-S., DNA, sunlight and skin-cancer, Pure Appl. Chem., 67, 183, 1995.
    • (1995) Pure Appl. Chem , vol.67 , pp. 183
    • Taylor, J.-S.1
  • 14
    • 0029036342 scopus 로고
    • The specificity of p53 mutation spectra in sunlight induced human cancers
    • Daya-Grosjean, L., Dumaz, N., and Sarasin, A., The specificity of p53 mutation spectra in sunlight induced human cancers, J. Photochem. Photobiol. B: Biol., 28, 115, 1995.
    • (1995) J. Photochem. Photobiol. B: Biol , vol.28 , pp. 115
    • Daya-Grosjean, L.1    Dumaz, N.2    Sarasin, A.3
  • 15
    • 85056351099 scopus 로고    scopus 로고
    • Globocan 2000: http://www-dep.iarc.fr/globocan/globocan.html.
  • 16
    • 85056323316 scopus 로고    scopus 로고
    • WHO cancer mortality database: http://www-depdb.iarc.fr/who/menu.htm.
  • 17
    • 0037011949 scopus 로고    scopus 로고
    • The prize of tumor suppression
    • Ferbeyre, G. and Lowe, S.W., The prize of tumor suppression, Nature, 415, 26, 2002.
    • (2002) Nature , vol.415 , pp. 26
    • Ferbeyre, G.1    Lowe, S.W.2
  • 18
    • 0028215974 scopus 로고
    • Slow repair of pyrimidine dimers at p53 mutation hotspots in skin cancer
    • Tornaletti, S. and Pfeifer, G.P., Slow repair of pyrimidine dimers at p53 mutation hotspots in skin cancer, Science, 163, 1436, 1994.
    • (1994) Science , vol.163 , pp. 1436
    • Tornaletti, S.1    Pfeifer, G.P.2
  • 23
    • 0027223848 scopus 로고
    • Identification and structure determination of a third cyclobutane photodimer of thymidylyl-(3' →5')-thymidine: The trans-syn-II product
    • Kao, J.F.L., Nadji, S., and Taylor, J.-S., Identification and structure determination of a third cyclobutane photodimer of thymidylyl-(3' →5')-thymidine: the trans-syn-II product, Chem. Res. Toxicol., 6, 561, 1993.
    • (1993) Chem. Res. Toxicol , vol.6 , pp. 561
    • Kao, J.F.L.1    Nadji, S.2    Taylor, J.-S.3
  • 24
    • 0034282907 scopus 로고    scopus 로고
    • Distribution and repair of bipyrimidine photoproducts in solar UV-irradiated mammalian cells -possible role of Dewar photoproducts in solar mutagenesis
    • Perdiz, D., Grof, P., Mezzina, M., Nikaido, O., Moustacchi, E., and Sage, E., Distribution and repair of bipyrimidine photoproducts in solar UV-irradiated mammalian cells -possible role of Dewar photoproducts in solar mutagenesis, J. Biol. Chem., 275, 26732, 2000.
    • (2000) J. Biol. Chem , vol.275 , pp. 26732
    • Perdiz, D.1    Grof, P.2    Mezzina, M.3    Nikaido, O.4    Moustacchi, E.5    Sage, E.6
  • 26
    • 0025649381 scopus 로고
    • Saturation photodimerization of thymines in DNA
    • Texter, J., Saturation photodimerization of thymines in DNA, Biopolymers, 30, 797, 1990.
    • (1990) Biopolymers , vol.30 , pp. 797
    • Texter, J.1
  • 27
    • 0035957120 scopus 로고    scopus 로고
    • Individual determination of the yield of the main UV-induced dimeric pyrimidine photoproducts in DNA suggests a high mutagenicity of CC photolesions
    • Douki, T. and Cadet, J., Individual determination of the yield of the main UV-induced dimeric pyrimidine photoproducts in DNA suggests a high mutagenicity of CC photolesions, Biochemistry, 40, 2495, 2001.
    • (2001) Biochemistry , vol.40 , pp. 2495
    • Douki, T.1    Cadet, J.2
  • 28
    • 0025196845 scopus 로고
    • 1H-NMR assignment and melting temperature study of cis-syn and trans-syn thymine dimer containing duplexes of d(CGTATTATGC)·d(GCATAATACG)
    • 1H-NMR assignment and melting temperature study of cis-syn and trans-syn thymine dimer containing duplexes of d(CGTATTATGC)·d(GCATAATACG), Biochemistry, 29, 8858, 1990.
    • (1990) Biochemistry , vol.29 , pp. 8858
    • Taylor, J.-S.1    Garett, D.S.2    Brockie, I.R.3    Svoboda, D.L.4    Telser, J.5
  • 29
    • 0021760450 scopus 로고
    • The structure of d(CGCGAAT[]TCGCG) ·d(CGCGAATTCGCG): He incorporation of a thymine photodimer into a B-DNA helix
    • Rao, S.N., Keepers, J.W., and Kollman, P., The structure of d(CGCGAAT[]TCGCG) ·d(CGCGAATTCGCG): he incorporation of a thymine photodimer into a B-DNA helix, Nucl. Acids Res., 12, 4789, 1984.
    • (1984) Nucl. Acids Res , vol.12 , pp. 4789
    • Rao, S.N.1    Keepers, J.W.2    Kollman, P.3
  • 30
    • 0029804674 scopus 로고    scopus 로고
    • Computational simulations of DNA distortions by a cis-syn-cyclobutane thymine dimer lesion
    • Miaskiewicz, K., Miller, J., Cooney, M., and Osman, R., Computational simulations of DNA distortions by a cis-syn-cyclobutane thymine dimer lesion, J. Am. Chem. Soc., 118, 9156, 1996.
    • (1996) J. Am. Chem. Soc , vol.118 , pp. 9156
    • Miaskiewicz, K.1    Miller, J.2    Cooney, M.3    Osman, R.4
  • 31
    • 0030745348 scopus 로고    scopus 로고
    • Unrestrained molecular dynamics of photodamaged DNA in aqueous solution
    • Spector, T.I., Cheatham, T.E., III, and Kollman, P.A., Unrestrained molecular dynamics of photodamaged DNA in aqueous solution, J. Am. Chem. Soc., 119, 7095, 1997.
    • (1997) J. Am. Chem. Soc , vol.119 , pp. 7095
    • Spector, T.I.1    Cheatham, T.E.2    Kollman, P.A.3
  • 32
    • 0023641840 scopus 로고
    • Conformational changes in the oligonucleotide duplex d(GCGTTGCG) ·d(CGCAACGC) induced by formation of a cis-syn thymine dimer
    • Kemmink, J., Boelens, R., Koning, T.M.G., Kaptein, R., van der Marel, G.A., and van Boom, J.H., Conformational changes in the oligonucleotide duplex d(GCGTTGCG) ·d(CGCAACGC) induced by formation of a cis-syn thymine dimer, Eur.J. Biochem., 162, 37, 1987.
    • (1987) Eur.J. Biochem , vol.162 , pp. 37
    • Kemmink, J.1    Boelens, R.2    Koning, T.M.G.3    Kaptein, R.4    van der Marel, G.A.5    van Boom, J.H.6
  • 34
    • 0032500623 scopus 로고    scopus 로고
    • Solution-state structure of a DNA dodecamer duplex containing a cis-syn thymine cyclobutane dimer, the major UV photoproduct of DNA
    • McAteer, K., Jing, Y., Kao, J., Taylor, J.-S., and Kennedy, M.A., Solution-state structure of a DNA dodecamer duplex containing a cis-syn thymine cyclobutane dimer, the major UV photoproduct of DNA, J. Mol. Biol., 282, 1013, 1998.
    • (1998) J. Mol. Biol , vol.282 , pp. 1013
    • McAteer, K.1    Jing, Y.2    Kao, J.3    Taylor, J.-S.4    Kennedy, M.A.5
  • 35
    • 0031860433 scopus 로고    scopus 로고
    • Synthesis, crystal-structure and enzymatic evaluation of a DNA-photolesion isostere
    • Butenandt, J., Eker, A.P.M., and Carell, T., Synthesis, crystal-structure and enzymatic evaluation of a DNA-photolesion isostere, Chem. Eur.J., 4, 642, 1998.
    • (1998) Chem. Eur.J , vol.4 , pp. 642
    • Butenandt, J.1    Eker, A.P.M.2    Carell, T.3
  • 36
    • 0033105505 scopus 로고    scopus 로고
    • “Base Flipping”: Photodamaged DNA-RNA duplexes are poor substrates for photoreactivating DNA-repair enzymes
    • Butenandt, J., Burgdorf, L.T., and Carell, T., “Base Flipping”: photodamaged DNA-RNA duplexes are poor substrates for photoreactivating DNA-repair enzymes, Angew. Chem. Int. Ed., 38, 708, 1999.
    • (1999) Angew. Chem. Int. Ed , vol.38 , pp. 708
    • Butenandt, J.1    Burgdorf, L.T.2    Carell, T.3
  • 37
    • 0027234732 scopus 로고
    • The trans-syn-I thymine dimer bends DNA by -22° and unwinds DNA by -15°
    • Wang, C.-I. and Taylor, J.-S., The trans-syn-I thymine dimer bends DNA by -22° and unwinds DNA by -15°, Chem. Res. Toxicol., 6, 519, 1993.
    • (1993) Chem. Res. Toxicol , vol.6 , pp. 519
    • Wang, C.-I.1    Taylor, J.-S.2
  • 39
    • 0030657472 scopus 로고    scopus 로고
    • Base pair conformationdependent excision of benzo[a]pyrene diol epoxideguanine adducts by human nucleotide excision repair enzymes
    • Hess, M.T., Gunz, D., Luneva, N., Geacintov, N.E., and Naegeli, H., Base pair conformationdependent excision of benzo[a]pyrene diol epoxideguanine adducts by human nucleotide excision repair enzymes, Mol. Cell. Biol., 17, 7069, 1997.
    • (1997) Mol. Cell. Biol , vol.17 , pp. 7069
    • Hess, M.T.1    Gunz, D.2    Luneva, N.3    Geacintov, N.E.4    Naegeli, H.5
  • 40
    • 0029840823 scopus 로고    scopus 로고
    • Recognition of DNA adducts by human nucleotide excision repair -evidence for a thermodynamic probing mechanism
    • Gunz, D., Hess, M.T., and Naegeli, H., Recognition of DNA adducts by human nucleotide excision repair -evidence for a thermodynamic probing mechanism, J. Biol. Chem., 271, 41, 25089, 1996.
    • (1996) J. Biol. Chem , vol.271 , Issue.41 , pp. 25089
    • Gunz, D.1    Hess, M.T.2    Naegeli, H.3
  • 41
    • 0027469125 scopus 로고
    • In vivo evidence that UV-induced C →T mutations at dipyrimidine sites could result from the replicative bypass of cis-syn cyclobutane dimers or their deamination products
    • Jiang, N. and Taylor, J.-S., In vivo evidence that UV-induced C →T mutations at dipyrimidine sites could result from the replicative bypass of cis-syn cyclobutane dimers or their deamination products, Biochemistry, 32, 472, 1993.
    • (1993) Biochemistry , vol.32 , pp. 472
    • Jiang, N.1    Taylor, J.-S.2
  • 42
    • 0032573433 scopus 로고    scopus 로고
    • Sequence and time-dependent deamination of cytosine bases in UVB-induced cyclobutane pyrimidine dimers in vivo
    • Tu, Y., Dammann, R., and Pfeifer, G.P., Sequence and time-dependent deamination of cytosine bases in UVB-induced cyclobutane pyrimidine dimers in vivo, J. Mol. Biol., 284, 297, 1998.
    • (1998) J. Mol. Biol , vol.284 , pp. 297
    • Tu, Y.1    Dammann, R.2    Pfeifer, G.P.3
  • 43
    • 0019347263 scopus 로고
    • The rmal resistance to photoreactivation of specific mutations potentiated in E. coli B/r ung by ultraviolet light
    • Fix, D. and Bockrath, R., The rmal resistance to photoreactivation of specific mutations potentiated in E. coli B/r ung by ultraviolet light, Mol. Gen. Genet., 182, 7, 1981.
    • (1981) Mol. Gen. Genet , vol.182 , pp. 7
    • Fix, D.1    Bockrath, R.2
  • 44
    • 0026093232 scopus 로고
    • Unraveling the origin of the major mutation induced by ultraviolet light, the C →T transition at dTpdC sites. A DNA synthesis building block for the cis-syn cyclobutane dimer of dTpdU
    • Taylor, J.-S. and Nadji, S., Unraveling the origin of the major mutation induced by ultraviolet light, the C →T transition at dTpdC sites. A DNA synthesis building block for the cis-syn cyclobutane dimer of dTpdU, Tetrahedron, 47, 2579, 1991.
    • (1991) Tetrahedron , vol.47 , pp. 2579
    • Taylor, J.-S.1    Nadji, S.2
  • 45
    • 0024101976 scopus 로고
    • Models for the solution structure of the (6-4) photoproduct of thymidylyl-(3' →5')-thymidine derived via a distance-and angle-constrained conformation search procedure
    • Taylor, J.-S., Garett, D.S., and Wang, M.J., Models for the solution structure of the (6-4) photoproduct of thymidylyl-(3' →5')-thymidine derived via a distance-and angle-constrained conformation search procedure, Biopolymers, 27, 1571, 1988.
    • (1988) Biopolymers , vol.27 , pp. 1571
    • Taylor, J.-S.1    Garett, D.S.2    Wang, M.J.3
  • 46
    • 84989665761 scopus 로고
    • Characterization of the (6-4) photoproduct of 2'-deoxycytidylyl-(3' →5')-thymidine and of its Dewar valence isomer
    • Douki, T., Voituriez, L., and Cadet, J., Characterization of the (6-4) photoproduct of 2'-deoxycytidylyl-(3' →5')-thymidine and of its Dewar valence isomer, Photochem. Photobiol., 53, 293, 1991.
    • (1991) Photochem. Photobiol , vol.53 , pp. 293
    • Douki, T.1    Voituriez, L.2    Cadet, J.3
  • 47
    • 0030050520 scopus 로고    scopus 로고
    • NMR structural studies of DNA decamer duplex containing the Dewar photoproduct of thymidylyl(3' →5')thymidine. Conformational changes of the oligonucleotide duplex by photoconversion of a (6-4) adduct to its Dewar valence isomer
    • Hwang, G.S., Kim, J.-K., and Choi, B.S., NMR structural studies of DNA decamer duplex containing the Dewar photoproduct of thymidylyl(3' →5')thymidine. Conformational changes of the oligonucleotide duplex by photoconversion of a (6-4) adduct to its Dewar valence isomer, Eur. J. Biochem., 235, 359, 1996.
    • (1996) Eur. J. Biochem , vol.235 , pp. 359
    • Hwang, G.S.1    Kim, J.-K.2    Choi, B.S.3
  • 48
    • 0028927254 scopus 로고
    • The solution structure of DNA duplex-decamer containing the (6-4) photoproduct of thymidylyl(3' →5')thymidine by NMR and relaxation matrix refinement
    • Kim, J.-K. and Choi, B.S., The solution structure of DNA duplex-decamer containing the (6-4) photoproduct of thymidylyl(3' →5')thymidine by NMR and relaxation matrix refinement, Eur. J. Biochem., 228, 849, 1995.
    • (1995) Eur. J. Biochem , vol.228 , pp. 849
    • Kim, J.-K.1    Choi, B.S.2
  • 49
    • 0029338999 scopus 로고
    • Contrasting structural impacts induced by cis-syn cyclobutane dimer and (6-4) adduct in DNA duplex decamers: Implication in mutagenesis and repair activity
    • Kim, J.-K., Patel, D., and Choi, B.-S., Contrasting structural impacts induced by cis-syn cyclobutane dimer and (6-4) adduct in DNA duplex decamers: implication in mutagenesis and repair activity, Photochem. Photobiol., 62, 44, 1995.
    • (1995) Photochem. Photobiol , vol.62 , pp. 44
    • Kim, J.-K.1    Patel, D.2    Choi, B.-S.3
  • 50
    • 0035945250 scopus 로고    scopus 로고
    • Structural study of DNA duplexes containing the (6-4) photoproduct by fluorescence resonance energy transfer
    • Mizukoshi, T., Kodama, T.S., Fujiwara, Y., Furuno, T., Nakanishi, M., and Iwai, S., Structural study of DNA duplexes containing the (6-4) photoproduct by fluorescence resonance energy transfer, Nucl. Acids Res., 29, 4948, 2001.
    • (2001) Nucl. Acids Res , vol.29 , pp. 4948
    • Mizukoshi, T.1    Kodama, T.S.2    Fujiwara, Y.3    Furuno, T.4    Nakanishi, M.5    Iwai, S.6
  • 51
    • 0030826228 scopus 로고    scopus 로고
    • The rmodynamic studies of the hybridization properties of photolesions in DNA
    • Fujiwara, Y. and Iwai, S., The rmodynamic studies of the hybridization properties of photolesions in DNA, Biochemistry, 36, 11050, 1997.
    • (1997) Biochemistry , vol.36 , pp. 11050
    • Fujiwara, Y.1    Iwai, S.2
  • 52
    • 0032529296 scopus 로고    scopus 로고
    • The rmodynamic and base-pairing studies of matched and mismatched DNA dodecamer duplexes containing cis-syn, (6-4) and Dewar photoproducts of TT
    • Jing, Y.Q., Kao, J.F.L., and Taylor, J.-S., The rmodynamic and base-pairing studies of matched and mismatched DNA dodecamer duplexes containing cis-syn, (6-4) and Dewar photoproducts of TT, Nucleic Acids Res., 26, 3845, 1998.
    • (1998) Nucleic Acids Res , vol.26 , pp. 3845
    • Jing, Y.Q.1    Kao, J.F.L.2    Taylor, J.-S.3
  • 53
    • 0025950131 scopus 로고
    • The thymine-thymine pyrimidine-pyrimidone(6-4) ultraviolet light photoproduct is highly mutagenic and specifically induces 3' thymine-to-cytosine transitions in Escherichia coli
    • LeClerc, E.J., Borden, A., and Lawrence, C.W., The thymine-thymine pyrimidine-pyrimidone(6-4) ultraviolet light photoproduct is highly mutagenic and specifically induces 3' thymine-to-cytosine transitions in Escherichia coli, Proc. Natl. Acad. Sci. USA, 88, 9685, 1991.
    • (1991) Proc. Natl. Acad. Sci. USA , vol.88 , pp. 9685
    • LeClerc, E.J.1    Borden, A.2    Lawrence, C.W.3
  • 54
    • 0033535936 scopus 로고    scopus 로고
    • Solution structure of a DNA decamer duplex containing the stable 3' T: Base pair of the pyrimidine(6-4)pyrimidone photoproduct [(6-4) adduct]: Implications for the highly specific 3' T →C transition of the (6-4) adduct
    • Lee, J.H., Hwang, G.S., and Choi, B.S., Solution structure of a DNA decamer duplex containing the stable 3' T: base pair of the pyrimidine(6-4)pyrimidone photoproduct [(6-4) adduct]: implications for the highly specific 3' T →C transition of the (6-4) adduct, Proc. Natl. Acad. Sci. USA, 96, 6632, 1999.
    • (1999) Proc. Natl. Acad. Sci. USA , vol.96 , pp. 6632
    • Lee, J.H.1    Hwang, G.S.2    Choi, B.S.3
  • 55
    • 0025382059 scopus 로고
    • Quantitative conversion of the (6-4) photoproduct of TpdC to its Dewar valence isomer upon exposure to simulated sunlight
    • Taylor, J.-S., Lu, H.-F., and Kotyk, J.J., Quantitative conversion of the (6-4) photoproduct of TpdC to its Dewar valence isomer upon exposure to simulated sunlight, Photochem. Photobiol., 51, 161, 1990.
    • (1990) Photochem. Photobiol , vol.51 , pp. 161
    • Taylor, J.-S.1    Lu, H.-F.2    Kotyk, J.J.3
  • 56
    • 0001731948 scopus 로고
    • DNA, light, and Dewar pyrimidones: The structure and biological significance of TpT3
    • Taylor, J.-S. and Cohrs, M.P., DNA, light, and Dewar pyrimidones: the structure and biological significance of TpT3, J. Am. Chem. Soc., 109, 2834, 1987.
    • (1987) J. Am. Chem. Soc , vol.109 , pp. 2834
    • Taylor, J.-S.1    Cohrs, M.P.2
  • 57
    • 0024293229 scopus 로고
    • Solution-state structure of the Dewar pyrimidinone photoproduct of thymidylyl-(3'-5')-thymidine
    • Taylor, J.-S., Garett, D.S., and Cohrs, M.P., Solution-state structure of the Dewar pyrimidinone photoproduct of thymidylyl-(3'-5')-thymidine, Biochemistry, 27, 7206, 1988.
    • (1988) Biochemistry , vol.27 , pp. 7206
    • Taylor, J.-S.1    Garett, D.S.2    Cohrs, M.P.3
  • 58
    • 0026607962 scopus 로고
    • The Dewar valence isomer of the (6-4) photoadduct of thymidylyl-(3'-5')-thymidine monophosphate: Formation, alkaline lability and conformational properties
    • Kan, L.-S., Voituriez, L., and Cadet, J., The Dewar valence isomer of the (6-4) photoadduct of thymidylyl-(3'-5')-thymidine monophosphate: formation, alkaline lability and conformational properties, J. Photochem. Photobiol. B: Biol., 12, 339, 1992.
    • (1992) J. Photochem. Photobiol. B: Biol , vol.12 , pp. 339
    • Kan, L.-S.1    Voituriez, L.2    Cadet, J.3
  • 59
    • 0034712856 scopus 로고    scopus 로고
    • The Dewar photoproduct of thymidylyl(3'→5')-thymidine (Dewar product) exhibits mutagenic behavior in accordance with the “A rule,”
    • Lee, J.H., Bae, S.H., and Choi, B.S., The Dewar photoproduct of thymidylyl(3'→5')-thymidine (Dewar product) exhibits mutagenic behavior in accordance with the “A rule,” Proc. Natl. Acad. Sci. USA, 97, 4591, 2000.
    • (2000) Proc. Natl. Acad. Sci. USA , vol.97 , pp. 4591
    • Lee, J.H.1    Bae, S.H.2    Choi, B.S.3
  • 60
    • 0024152866 scopus 로고
    • Small, acid-soluble spore proteins of Bacillus species: Structure, synthesis, genetics, function and degradation
    • Setlow, P., Small, acid-soluble spore proteins of Bacillus species: Structure, synthesis, genetics, function and degradation, Ann. Rev. Microbiol., 42, 319, 1988.
    • (1988) Ann. Rev. Microbiol , vol.42 , pp. 319
    • Setlow, P.1
  • 61
    • 0025965910 scopus 로고
    • Binding of small acid-soluble spore proteins from Bacillus subtilis changes the conformation of DNA from B to A
    • Mohr, S.C., Sokolov, N.V.H.A., He, C., and Setlow, P., Binding of small acid-soluble spore proteins from Bacillus subtilis changes the conformation of DNA from B to A, Proc. Natl. Acad. Sci. USA, 88, 77, 1991.
    • (1991) Proc. Natl. Acad. Sci. USA , vol.88 , pp. 77
    • Mohr, S.C.1    Sokolov, N.V.H.A.2    He, C.3    Setlow, P.4
  • 62
    • 0026556134 scopus 로고
    • DNA in dormant spores of Bacillus species is in an A-like conformation
    • Setlow, P., DNA in dormant spores of Bacillus species is in an A-like conformation, Mol. Microbiol., 6, 563, 1992.
    • (1992) Mol. Microbiol , vol.6 , pp. 563
    • Setlow, P.1
  • 63
    • 0000454531 scopus 로고
    • Thymine photoproducts but not thymine dimers found in ultraviolet-irradiated bacterial spores
    • Donnellan, J.E. and Setlow, R.B., Thymine photoproducts but not thymine dimers found in ultraviolet-irradiated bacterial spores, Science, 149, 308, 1965.
    • (1965) Science , vol.149 , pp. 308
    • Donnellan, J.E.1    Setlow, R.B.2
  • 64
    • 0014934488 scopus 로고
    • 5-Thyminyl-5,6-dihydrothymine from DNA irradiated with ultraviolet light
    • Varghese, A.J., 5-Thyminyl-5,6-dihydrothymine from DNA irradiated with ultraviolet light, Biochem. Biophys. Res. Commun., 38, 484, 1970.
    • (1970) Biochem. Biophys. Res. Commun , vol.38 , pp. 484
    • Varghese, A.J.1
  • 65
    • 0041900460 scopus 로고
    • Photoproduct formation in DNA at low temperatures
    • Rahn, R.O. and Hosszu, J.L., Photoproduct formation in DNA at low temperatures, Photochem. Photobiol., 8, 53, 1968.
    • (1968) Photochem. Photobiol , vol.8 , pp. 53
    • Rahn, R.O.1    Hosszu, J.L.2
  • 66
    • 0014682361 scopus 로고
    • Influence of relative humidity on the photochemistry of DNA films
    • Rahn, R.O. and Hosszu, J.L., Influence of relative humidity on the photochemistry of DNA films, Biochim. Biophys. Acta, 190, 126, 1969.
    • (1969) Biochim. Biophys. Acta , vol.190 , pp. 126
    • Rahn, R.O.1    Hosszu, J.L.2
  • 67
    • 0014961163 scopus 로고
    • Photochemistry of thymidine in ice
    • Varghese, A.J., Photochemistry of thymidine in ice, Biochemistry, 9, 4781, 1970.
    • (1970) Biochemistry , vol.9 , pp. 4781
    • Varghese, A.J.1
  • 68
    • 84981632809 scopus 로고
    • Photochemistry of thymidine as a thin solid film
    • Varghese, A.J., Photochemistry of thymidine as a thin solid film, Photochem. Photobiol., 13, 357, 1971.
    • (1971) Photochem. Photobiol , vol.13 , pp. 357
    • Varghese, A.J.1
  • 69
    • 0034689864 scopus 로고    scopus 로고
    • Synthesis and UV photolysis of oligodeoxynucleotides that contain 5-(phenylthiomethyl)-2'-deoxyuridine: A specific photolabile precursor of 5-(2 '-deoxyuridilyl)methyl radical
    • Romieu, A., Bellon, S., Gasparutto, D., and Cadet, J., Synthesis and UV photolysis of oligodeoxynucleotides that contain 5-(phenylthiomethyl)-2'-deoxyuridine: a specific photolabile precursor of 5-(2 '-deoxyuridilyl)methyl radical, Org. Lett., 2, 1085, 2000.
    • (2000) Org. Lett , vol.2 , pp. 1085
    • Romieu, A.1    Bellon, S.2    Gasparutto, D.3    Cadet, J.4
  • 70
    • 0034051701 scopus 로고    scopus 로고
    • Electrospray-mass spectrometry characterization and measurement of far-UV-induced thymine photoproducts
    • Douki, T., Court, M., and Cadet, J., Electrospray-mass spectrometry characterization and measurement of far-UV-induced thymine photoproducts, J. Photochem. Photobiol. B: Biol., 54, 145, 2000.
    • (2000) J. Photochem. Photobiol. B: Biol , vol.54 , pp. 145
    • Douki, T.1    Court, M.2    Cadet, J.3
  • 71
    • 0037139601 scopus 로고    scopus 로고
    • Further insight in the photochemistry of DNA: Structure of a 2-imidazolone (5-4) pyrimidone adduct from the mutagenic pyrimidine (6-4) pyrimidone photolesion by UV irradiation
    • Thomas, M., Guillaume, D., Fourrey, J.L., and Clivio, P., Further insight in the photochemistry of DNA: structure of a 2-imidazolone (5-4) pyrimidone adduct from the mutagenic pyrimidine (6-4) pyrimidone photolesion by UV irradiation, J. Am. Chem. Soc., 124, 2400, 2002.
    • (2002) J. Am. Chem. Soc , vol.124 , pp. 2400
    • Thomas, M.1    Guillaume, D.2    Fourrey, J.L.3    Clivio, P.4
  • 72
    • 0030831112 scopus 로고    scopus 로고
    • Molecular evolution of the photolyase-blue light photoreceptor familiy
    • Kanai, S., Kikuna, R., Toh, H., Ryo, H., and Todo, T., Molecular evolution of the photolyase-blue light photoreceptor familiy, J. Mol. Evol., 45, 535, 1997.
    • (1997) J. Mol. Evol , vol.45 , pp. 535
    • Kanai, S.1    Kikuna, R.2    Toh, H.3    Ryo, H.4    Todo, T.5
  • 73
    • 0028117141 scopus 로고
    • Structure and function of DNA photolyase
    • Sancar, A., Structure and function of DNA photolyase, Biochemistry, 33, 2, 1994.
    • (1994) Biochemistry , vol.33 , pp. 2
    • Sancar, A.1
  • 75
    • 0043215375 scopus 로고
    • Photoenzymatic repair of UV-damaged DNA: A chemist’s perspective
    • Heelis, P.F., Hartman, R.F., and Rose, S.D., Photoenzymatic repair of UV-damaged DNA: a chemist’s perspective, Chem. Soc. Rev., 289, 1995.
    • (1995) Chem. Soc. Rev , pp. 289
    • Heelis, P.F.1    Hartman, R.F.2    Rose, S.D.3
  • 76
    • 0028812143 scopus 로고
    • Crystal-structure of DNA photolyase from Escherichia coli
    • Park, H.W., Kim, S.T., Sancar, A., and Deisenhofer, J., Crystal-structure of DNA photolyase from Escherichia coli, Science, 268, 1866, 1995.
    • (1995) Science , vol.268 , pp. 1866
    • Park, H.W.1    Kim, S.T.2    Sancar, A.3    Deisenhofer, J.4
  • 79
    • 0029068245 scopus 로고
    • On base flipping
    • Roberts, R.J., On base flipping, Cell, 82, 9, 1995.
    • (1995) Cell , vol.82 , pp. 9
    • Roberts, R.J.1
  • 80
    • 0034708226 scopus 로고    scopus 로고
    • Structural basis for recognition and repair of the endogenous mutagen 8-oxoguanine in DNA
    • Bruner, S.D., Norman, D.P.G., and Verdine, G.L., Structural basis for recognition and repair of the endogenous mutagen 8-oxoguanine in DNA, Nature, 403, 859, 2000.
    • (2000) Nature , vol.403 , pp. 859
    • Bruner, S.D.1    Norman, D.P.G.2    Verdine, G.L.3
  • 81
    • 33745160351 scopus 로고    scopus 로고
    • Mechanistic link between DNA methyltransferases and DNA repair enzymes by base flipping
    • Lloyd, R.S. and Cheng, X., Mechanistic link between DNA methyltransferases and DNA repair enzymes by base flipping, Curr. Op. Chem. Biol., 4, 139, 1998.
    • (1998) Curr. Op. Chem. Biol , vol.4 , pp. 139
    • Lloyd, R.S.1    Cheng, X.2
  • 82
    • 0037178070 scopus 로고    scopus 로고
    • Base flipping in DNA: Pathways and energetics studied with molecular dynamics simulations
    • Varnai, P. and Lavery, R., Base flipping in DNA: pathways and energetics studied with molecular dynamics simulations, J. Am. Chem. Soc., 124, 7272, 2002.
    • (2002) J. Am. Chem. Soc , vol.124 , pp. 7272
    • Varnai, P.1    Lavery, R.2
  • 83
    • 0032493753 scopus 로고    scopus 로고
    • Evidence for dinucleotide flipping by DNA photolyase
    • van de Berg, B.J. and Sancar, G.B., Evidence for dinucleotide flipping by DNA photolyase, J. Biol. Chem., 273, 20276, 1998.
    • (1998) J. Biol. Chem , vol.273 , pp. 20276
    • van de Berg, B.J.1    Sancar, G.B.2
  • 85
    • 0033215330 scopus 로고    scopus 로고
    • DNA bending by photolyase in specific and non-specific complexes studied by atomic force microscopy
    • van Noort, J., Orsini, F., Eker, A., Wyman, C., de Grooth, B., and Greve, J., DNA bending by photolyase in specific and non-specific complexes studied by atomic force microscopy, Nucl. Acids Res., 27, 3875, 1999.
    • (1999) Nucl. Acids Res , vol.27 , pp. 3875
    • van Noort, J.1    Orsini, F.2    Eker, A.3    Wyman, C.4    de Grooth, B.5    Greve, J.6
  • 86
    • 0033538279 scopus 로고    scopus 로고
    • A model for the enzyme-substrate complex of DNA photolyase and photodamaged DNA
    • Sanders, D.B. and Wiest, O., A model for the enzyme-substrate complex of DNA photolyase and photodamaged DNA, J. Am. Chem. Soc., 121, 5127, 1999.
    • (1999) J. Am. Chem. Soc , vol.121 , pp. 5127
    • Sanders, D.B.1    Wiest, O.2
  • 88
    • 0034896579 scopus 로고    scopus 로고
    • Substrate binding to DNA photolyase studied by electron paramagnetic resonance spectroscopy
    • Weber, S., Richter, G., Schleicher, E., Bacher, A., Möbius, K., and Kay, C.W.M., Substrate binding to DNA photolyase studied by electron paramagnetic resonance spectroscopy, Biophys. J., 81, 1195, 2001.
    • (2001) Biophys. J , vol.81 , pp. 1195
    • Weber, S.1    Richter, G.2    Schleicher, E.3    Bacher, A.4    Möbius, K.5    Kay, C.W.M.6
  • 89
    • 2742612470 scopus 로고    scopus 로고
    • Repair of UV light induced DNA lesions: A comparative study with model compounds
    • Carell, T. and Epple, R., Repair of UV light induced DNA lesions: a comparative study with model compounds, Eur. J. Org. Chem., 1245, 1998.
    • (1998) Eur. J. Org. Chem , pp. 1245
    • Carell, T.1    Epple, R.2
  • 90
    • 0030795004 scopus 로고    scopus 로고
    • Investigation of flavin-containing DNA-repair model compounds
    • Epple, R., Wallenborn, E.-U., and Carell, T., Investigation of flavin-containing DNA-repair model compounds, J. Am. Chem. Soc., 119, 7440, 1997.
    • (1997) J. Am. Chem. Soc , vol.119 , pp. 7440
    • Epple, R.1    Wallenborn, E.-U.2    Carell, T.3
  • 91
    • 0034831016 scopus 로고    scopus 로고
    • DFT study of the [2 + 2] cycloreversion of uracil dimer anion radical: Aters matter
    • Saettel, N.J. and Wiest, O., DFT study of the [2 + 2] cycloreversion of uracil dimer anion radical: aters matter, J. Am. Chem. Soc., 123, 2693, 2001.
    • (2001) J. Am. Chem. Soc , vol.123 , pp. 2693
    • Saettel, N.J.1    Wiest, O.2
  • 92
    • 0031959870 scopus 로고    scopus 로고
    • Flavin and deazaflavin containing model compounds mimic the energytransfer step in type II DNA-photolyases
    • Epple, R. and Carell, T., Flavin and deazaflavin containing model compounds mimic the energytransfer step in type II DNA-photolyases, Angew. Chem. Int. Ed., 37, 938, 1998.
    • (1998) Angew. Chem. Int. Ed , vol.37 , pp. 938
    • Epple, R.1    Carell, T.2
  • 93
    • 0033581149 scopus 로고    scopus 로고
    • Efficient light-dependent DNA repair requires a large cofactor separation
    • Epple, R. and Carell, T., Efficient light-dependent DNA repair requires a large cofactor separation, J. Am. Chem. Soc., 121, 7318, 1999.
    • (1999) J. Am. Chem. Soc , vol.121 , pp. 7318
    • Epple, R.1    Carell, T.2
  • 94
    • 0033545878 scopus 로고    scopus 로고
    • Intraprotein electron transfer between tyrosine and tryptophan in DNA photolyase from Anacystis nidulans
    • Aubert, C., Mathis, P., Eker, A.P.M., and Brettel, K., Intraprotein electron transfer between tyrosine and tryptophan in DNA photolyase from Anacystis nidulans, Proc. Natl. Acad. Sci. USA, 96, 5423, 1999.
    • (1999) Proc. Natl. Acad. Sci. USA , vol.96 , pp. 5423
    • Aubert, C.1    Mathis, P.2    Eker, A.P.M.3    Brettel, K.4
  • 95
    • 0033595465 scopus 로고    scopus 로고
    • EPR detection of the transient tyrosyl radical in DNA photolyase from Anacystis nidulans
    • Aubert, C., Brettel, K., Mathis, P., Eker, A.P.M., and Boussac, A., EPR detection of the transient tyrosyl radical in DNA photolyase from Anacystis nidulans, J. Am. Chem. Soc., 121, 8659, 1999.
    • (1999) J. Am. Chem. Soc , vol.121 , pp. 8659
    • Aubert, C.1    Brettel, K.2    Mathis, P.3    Eker, A.P.M.4    Boussac, A.5
  • 97
    • 0032023777 scopus 로고    scopus 로고
    • Protein radicals in enzyme catalysis
    • Stubbe, J. and van der Donk, W.A., Protein radicals in enzyme catalysis, Chem. Rev., 98, 705, 1998.
    • (1998) Chem. Rev , vol.98 , pp. 705
    • Stubbe, J.1    van der Donk, W.A.2
  • 98
    • 0027439741 scopus 로고
    • A new photoreactivating enzyme that specifically repairs ultraviolet light-induced (6-4)photoproducts
    • Todo, T., A new photoreactivating enzyme that specifically repairs ultraviolet light-induced (6-4)photoproducts, Nature, 361, 371, 1993.
    • (1993) Nature , vol.361 , pp. 371
    • Todo, T.1
  • 99
    • 0037022384 scopus 로고    scopus 로고
    • Photoreactivation of the flavin cofactor in Xenopus laevis (6-4) photolyase: Observation of a transient tyrosyl radical by timeresolved electron paramagnetic resonance
    • Weber, S., Kay, C.W.M., Mögling, H., Hitomi, K., and Todo, T., Photoreactivation of the flavin cofactor in Xenopus laevis (6-4) photolyase: observation of a transient tyrosyl radical by timeresolved electron paramagnetic resonance, Proc. Natl. Acad. Sci. USA, 99, 1319, 2002.
    • (2002) Proc. Natl. Acad. Sci. USA , vol.99 , pp. 1319
    • Weber, S.1    Kay, C.W.M.2    Mögling, H.3    Hitomi, K.4    Todo, T.5
  • 103
    • 0034647226 scopus 로고    scopus 로고
    • Quantum chemical study of the electron-transfer-catalyzed splitting of oxetane and azetidine intermediates proposed in the photoenzymatic repair of (6-4) photoproducts of DNA
    • Wang, Y.S., Gaspar, P.P., and Taylor, J.-S., Quantum chemical study of the electron-transfer-catalyzed splitting of oxetane and azetidine intermediates proposed in the photoenzymatic repair of (6-4) photoproducts of DNA, J. Am. Chem. Soc., 122, 5510, 2000.
    • (2000) J. Am. Chem. Soc , vol.122 , pp. 5510
    • Wang, Y.S.1    Gaspar, P.P.2    Taylor, J.-S.3
  • 104
    • 0028870985 scopus 로고
    • Model studies of the (6-4)-photoproduct DNA photolyase -synthesis and photosensitized splitting of a thymine-5,6-oxetane
    • Prakash, G. and Falvey, D.E., Model studies of the (6-4)-photoproduct DNA photolyase -synthesis and photosensitized splitting of a thymine-5,6-oxetane, J. Am. Chem. Soc., 117, 11375, 1995.
    • (1995) J. Am. Chem. Soc , vol.117 , pp. 11375
    • Prakash, G.1    Falvey, D.E.2
  • 105
    • 0034669483 scopus 로고    scopus 로고
    • Model studies of the (6-4) photoproduct photolyase enzyme: Laser flash photolysis experiments confirm radical ion intermediates in the sensitized repair of thymine oxetane adducts
    • Joseph, A., Prakash, G., and Falvey, D.E., Model studies of the (6-4) photoproduct photolyase enzyme: laser flash photolysis experiments confirm radical ion intermediates in the sensitized repair of thymine oxetane adducts, J. Am. Chem. Soc., 122, 11219, 2000.
    • (2000) J. Am. Chem. Soc , vol.122 , pp. 11219
    • Joseph, A.1    Prakash, G.2    Falvey, D.E.3
  • 106
    • 0036494784 scopus 로고    scopus 로고
    • A (6-4) photolyase model: Repair of DNA (6-4) lesions requires a reduced and deprotonated flavin
    • Cichon, M.K., Arnold, S., and Carell, T., A (6-4) photolyase model: repair of DNA (6-4) lesions requires a reduced and deprotonated flavin, Angew. Chem. Int. Ed., 41, 767, 2002.
    • (2002) Angew. Chem. Int. Ed , vol.41 , pp. 767
    • Cichon, M.K.1    Arnold, S.2    Carell, T.3
  • 107
    • 0037067119 scopus 로고    scopus 로고
    • Stepwise cycloreversion of oxetane radical cations with initial C-O bond cleavage
    • Miranda, M.A. and Izquierdo, M.A., Stepwise cycloreversion of oxetane radical cations with initial C-O bond cleavage, J. Am. Chem. Soc., 124, 6532, 2002.
    • (2002) J. Am. Chem. Soc , vol.124 , pp. 6532
    • Miranda, M.A.1    Izquierdo, M.A.2
  • 108
    • 0037077079 scopus 로고    scopus 로고
    • Involvement of triplet excited states and olefin radical cations in electron-transfer cycloreversion of four-membered ring compounds photosensitized by (thia)pyrylium salts
    • Miranda, M.A., Izquierdo, M.A., and Galindo, F., Involvement of triplet excited states and olefin radical cations in electron-transfer cycloreversion of four-membered ring compounds photosensitized by (thia)pyrylium salts, J. Org. Chem., 67, 4138, 2002.
    • (2002) J. Org. Chem , vol.67 , pp. 4138
    • Miranda, M.A.1    Izquierdo, M.A.2    Galindo, F.3
  • 109
    • 15644383272 scopus 로고
    • DNA photodamage mechanistic studies: Characterization of a thietane intermediate in a model reaction relevant to "(6-4) lesions,”
    • Clivio, P. and Fourrey, J.-L., DNA photodamage mechanistic studies: characterization of a thietane intermediate in a model reaction relevant to "(6-4) lesions,” J. Am. Chem. Soc., 113, 5481, 1991.
    • (1991) J. Am. Chem. Soc , vol.113 , pp. 5481
    • Clivio, P.1    Fourrey, J.-L.2
  • 111
    • 0030567374 scopus 로고    scopus 로고
    • Remarkable photoreversal of a thio analog of the Dewar valence isomer of the (6-4) photoproduct of DNA to the parent nucleotides
    • Liu, J.Q. and Taylor, J.-S., Remarkable photoreversal of a thio analog of the Dewar valence isomer of the (6-4) photoproduct of DNA to the parent nucleotides, J. Am. Chem. Soc., 118, 3287, 1996.
    • (1996) J. Am. Chem. Soc , vol.118 , pp. 3287
    • Liu, J.Q.1    Taylor, J.-S.2
  • 112
    • 0030887567 scopus 로고    scopus 로고
    • Photoenzymic repair of the DNA (6-4) photoproduct -a density functional theory and semiempirical study
    • Heelis, P.F. and Liu, S.B., Photoenzymic repair of the DNA (6-4) photoproduct -a density functional theory and semiempirical study, J. Am. Chem. Soc., 119, 2936, 1997.
    • (1997) J. Am. Chem. Soc , vol.119 , pp. 2936
    • Heelis, P.F.1    Liu, S.B.2
  • 114
    • 0028868465 scopus 로고
    • Mechanisms for the prevention of damage to DNA in spores of Bacillus species
    • Setlow, P., Mechanisms for the prevention of damage to DNA in spores of Bacillus species, Ann. Rev. Microbiol., 49, 29, 1995.
    • (1995) Ann. Rev. Microbiol , vol.49 , pp. 29
    • Setlow, P.1
  • 115
    • 0028332201 scopus 로고
    • Temporal regulation and foresporespecific expression of the spore photoproduct lyase gene by σ-G RNA-polymerase during Bacillus subtilis sporulation
    • Pedraza-Reyes, M., Gutierrez-Corona, F., and Nicholson, W.L., Temporal regulation and foresporespecific expression of the spore photoproduct lyase gene by σ-G RNA-polymerase during Bacillus subtilis sporulation, J. Bacteriol., 176, 3983, 1994.
    • (1994) J. Bacteriol , vol.176 , pp. 3983
    • Pedraza-Reyes, M.1    Gutierrez-Corona, F.2    Nicholson, W.L.3
  • 116
    • 0033818517 scopus 로고    scopus 로고
    • Resistance of Bacillus endospores to extreme terrestrial and extraterrestrial environments
    • Nicholson, W.L., Munakata, N., Horneck, G., Melosh, H.J., and Setlow, P., Resistance of Bacillus endospores to extreme terrestrial and extraterrestrial environments, Microbiol. Mol. Biol. Rev., 64, 548, 2000.
    • (2000) Microbiol. Mol. Biol. Rev , vol.64 , pp. 548
    • Nicholson, W.L.1    Munakata, N.2    Horneck, G.3    Melosh, H.J.4    Setlow, P.5
  • 117
    • 0027453081 scopus 로고
    • Molecular cloning and characterization of the Bacilllus subtilis spore photoproduct lyase (spl) gene, which is involved in repair of UV radiation-induced DNA damage during spore germination
    • Fajardo-Cavazos, P., Salazar, C., and Nicholson, W.L., Molecular cloning and characterization of the Bacilllus subtilis spore photoproduct lyase (spl) gene, which is involved in repair of UV radiation-induced DNA damage during spore germination, J. Bacteriol., 175, 1735, 1993.
    • (1993) J. Bacteriol , vol.175 , pp. 1735
    • Fajardo-Cavazos, P.1    Salazar, C.2    Nicholson, W.L.3
  • 118
    • 0031679414 scopus 로고    scopus 로고
    • Spore photoproduct lyase from Bacillus subtilis spores is a novel iron-sulfur DNA repair enzyme which shares features with proteins such as class III anaerobic ribonucleotide reductases and pyruvate-formate lyases
    • Rebeil, R., Sun, Y.B., Chooback, L., Pedraza-Reyes, M., Kinsland, C., Begley, T.P., and Nicholson, W.L., Spore photoproduct lyase from Bacillus subtilis spores is a novel iron-sulfur DNA repair enzyme which shares features with proteins such as class III anaerobic ribonucleotide reductases and pyruvate-formate lyases, J. Bacteriol., 180, 4879, 1998.
    • (1998) J. Bacteriol , vol.180 , pp. 4879
    • Rebeil, R.1    Sun, Y.B.2    Chooback, L.3    Pedraza-Reyes, M.4    Kinsland, C.5    Begley, T.P.6    Nicholson, W.L.7
  • 119
    • 0035979231 scopus 로고    scopus 로고
    • The subunit structure and catalytic mechanism of the Bacillus subtilis DNA repair enzyme spore photoproduct lyase
    • Rebeil, R. and Nicholson, W.L., The subunit structure and catalytic mechanism of the Bacillus subtilis DNA repair enzyme spore photoproduct lyase, Proc. Natl. Acad. Sci. USA, 98, 9038, 2001.
    • (2001) Proc. Natl. Acad. Sci. USA , vol.98 , pp. 9038
    • Rebeil, R.1    Nicholson, W.L.2
  • 120
    • 0033533642 scopus 로고    scopus 로고
    • Mechanistic studies on the repair of a novel DNA photolesion: The spore photoproduct
    • Mehl, R.A. and Begley, T.P., Mechanistic studies on the repair of a novel DNA photolesion: the spore photoproduct, Org. Lett., 1, 1065, 1999.
    • (1999) Org. Lett , vol.1 , pp. 1065
    • Mehl, R.A.1    Begley, T.P.2
  • 121
    • 0034841061 scopus 로고    scopus 로고
    • Adenosylmethionine-dependent iron-sulfur enzymes: Versatile clusters in a radical new role
    • Cheek, J. and Broderick, J.B., Adenosylmethionine-dependent iron-sulfur enzymes: versatile clusters in a radical new role, J. Biol. Inorg. Chem., 6, 209, 2001.
    • (2001) J. Biol. Inorg. Chem , vol.6 , pp. 209
    • Cheek, J.1    Broderick, J.B.2
  • 122
    • 0037181382 scopus 로고    scopus 로고
    • Direct H atom abstraction from spore photoproduct C-6 initiates DNA repair in the reaction catalyzed by spore photoproduct lyase: Evidence for a reversibly generated adenosyl radical intermediate
    • Cheek, J. and Broderick, J.B., Direct H atom abstraction from spore photoproduct C-6 initiates DNA repair in the reaction catalyzed by spore photoproduct lyase: evidence for a reversibly generated adenosyl radical intermediate, J. Am. Chem. Soc., 124, 2860, 2002.
    • (2002) J. Am. Chem. Soc , vol.124 , pp. 2860
    • Cheek, J.1    Broderick, J.B.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.