메뉴 건너뛰기




Volumn 51, Issue 4, 2011, Pages 425-435

Alternative SAIL-Trp for robust aromatic signal assignment and determination of the χ2 conformation by intra-residue NOEs

Author keywords

2 conformation; Aromatic ring CH assignment; Intra residue NOE; SAIL Trp

Indexed keywords

AMINO ACID DERIVATIVE; PROTEIN C MYB; STEREO ARRAY ISOTOPE LABELED PROTEIN; UNCLASSIFIED DRUG;

EID: 84855284736     PISSN: 09252738     EISSN: 15735001     Source Type: Journal    
DOI: 10.1007/s10858-011-9568-3     Document Type: Article
Times cited : (25)

References (60)
  • 1
    • 34247547456 scopus 로고    scopus 로고
    • Stereochemical course of tryptophan dehydrogenation during biosynthesis of the calcium-dependent lipopeptide antibiotics
    • 10.1021/ol0701619
    • B Amir-Heidari J Thirlway J Micklefield 2007 Stereochemical course of tryptophan dehydrogenation during biosynthesis of the calcium-dependent lipopeptide antibiotics Org Lett 9 1513 1516 10.1021/ol0701619
    • (2007) Org Lett , vol.9 , pp. 1513-1516
    • Amir-Heidari, B.1    Thirlway, J.2    Micklefield, J.3
  • 2
    • 0141974397 scopus 로고
    • Hydrogen-deuterium exchange in tryptophan
    • 10.3891/acta.chem.scand.21-1674
    • B Bak C Dambmann F Nicolaisen 1967 Hydrogen-deuterium exchange in tryptophan Acta Chem Scand 21 1674 1675 10.3891/acta.chem.scand.21-1674
    • (1967) Acta Chem Scand , vol.21 , pp. 1674-1675
    • Bak, B.1    Dambmann, C.2    Nicolaisen, F.3
  • 3
    • 0345311216 scopus 로고
    • Proton and carbon-13 assignments from sensitivity-enhanced detection of heteronuclear multiple-bond connectivity by 2D multiple quantum NMR
    • 10.1021/ja00268a061
    • A Bax MF Summers 1986 Proton and carbon-13 assignments from sensitivity-enhanced detection of heteronuclear multiple-bond connectivity by 2D multiple quantum NMR J Am Chem Soc 108 2093 2094 10.1021/ja00268a061
    • (1986) J Am Chem Soc , vol.108 , pp. 2093-2094
    • Bax, A.1    Summers, M.F.2
  • 4
    • 44949288628 scopus 로고
    • Proton-proton correlation via isotropic mixing of carbon-13 magnetization, a new three-dimensional approach for assigning proton and carbon-13 spectra of carbon-13-enriched proteins
    • 10.1016/0022-2364(90)90202-K
    • A Bax GM Clore AM Gronenborn 1990 Proton-proton correlation via isotropic mixing of carbon-13 magnetization, a new three-dimensional approach for assigning proton and carbon-13 spectra of carbon-13-enriched proteins J Magn Reson 88 425 431 10.1016/0022-2364(90)90202-K
    • (1990) J Magn Reson , vol.88 , pp. 425-431
    • Bax, A.1    Clore, G.M.2    Gronenborn, A.M.3
  • 5
    • 0020475305 scopus 로고
    • 1H nuclear magnetic resonance spectra computation of sterically allowed proton-proton distances and statistical analysis of proton-proton distances in single crystal protein conformations
    • 10.1016/0022-2836(82)90008-0
    • 1H nuclear magnetic resonance spectra computation of sterically allowed proton-proton distances and statistical analysis of proton-proton distances in single crystal protein conformations J Mol Biol 155 321 346 10.1016/0022-2836(82)90008-0
    • (1982) J Mol Biol , vol.155 , pp. 321-346
    • Billeter, M.1    Braun, W.2    Wüthrich, K.3
  • 6
    • 0000195671 scopus 로고
    • Natural abundance nitrogen-15 NMR by enhanced heteronuclear spectroscopy
    • 1980CPL.69.185B 10.1016/0009-2614(80)80041-8
    • G Bodenhausen DJ Ruben 1980 Natural abundance nitrogen-15 NMR by enhanced heteronuclear spectroscopy Chem Phys Lett 69 185 189 1980CPL....69..185B 10.1016/0009-2614(80)80041-8
    • (1980) Chem Phys Lett , vol.69 , pp. 185-189
    • Bodenhausen, G.1    Ruben, D.J.2
  • 7
    • 0037700908 scopus 로고    scopus 로고
    • Enzymatic synthesis of L-tryptophan and 5′-hydroxy-L-tryptophan labeled with deuterium and tritium at the α-carbon position
    • DOI 10.1002/jlcr.708
    • E Boroda S Rakowska R Kański M Kańska 2003 Enzymatic synthesis of l-tryptophan and 5′-hydroxy-l-tryptophan labeled with deuterium and tritium at the α-carbon position J Label Compd Radiopharm 46 691 698 10.1002/jlcr.708 (Pubitemid 36890058)
    • (2003) Journal of Labelled Compounds and Radiopharmaceuticals , vol.46 , Issue.8 , pp. 691-698
    • Boroda, E.1    Rakowska, S.2    Kanski, R.3    Kanska, M.4
  • 10
    • 1842326139 scopus 로고    scopus 로고
    • Bayesian statistical analysis of protein side-chain rotamer preferences
    • RL Dunbrack Jr FE Cohen 1997 Bayesian statistical analysis of protein side-chain rotamer preferences Protein Sci 6 1661 1681 10.1002/pro.5560060807 (Pubitemid 27333069)
    • (1997) Protein Science , vol.6 , Issue.8 , pp. 1661-1681
    • Dunbrack Jr., R.L.1    Cohen, F.E.2
  • 11
    • 0027160197 scopus 로고
    • Backbone-dependent rotamer library for proteins. Application to side-chain prediction
    • DOI 10.1006/jmbi.1993.1170
    • RL Dunbrack Jr M Karplus 1993 Backbone-dependent rotamer library for proteins: applications to side-chain prediction J Mol Biol 230 543 574 10.1006/jmbi.1993.1170 (Pubitemid 23161363)
    • (1993) Journal of Molecular Biology , vol.230 , Issue.2 , pp. 543-574
    • Dunbrack Jr., R.L.1    Karplus, M.2
  • 13
    • 0001603007 scopus 로고
    • Oxindoles. New, general method of synthesis
    • 10.1021/ja00824a029
    • PG Gassman TJ Van Bergen 1974 Oxindoles. New, general method of synthesis J Am Chem Soc 96 5508 5511 10.1021/ja00824a029
    • (1974) J Am Chem Soc , vol.96 , pp. 5508-5511
    • Gassman, P.G.1    Van Bergen, T.J.2
  • 14
    • 0026844368 scopus 로고
    • Myb: A transcriptional activator linking proliferation and differentiation in hematopoietic cells
    • 10.1016/S0959-437X(05)80281-3
    • T Graf 1992 Myb: a transcriptional activator linking proliferation and differentiation in hematopoietic cells Curr Opin Genet Dev 2 249 255 10.1016/S0959-437X(05)80281-3
    • (1992) Curr Opin Genet Dev , vol.2 , pp. 249-255
    • Graf, T.1
  • 15
    • 0028803014 scopus 로고
    • Audio-Frequency NMR in a nutating frame. Application to the assignment of phenylalanine residues in isotopically enriched proteins
    • 10.1021/ja00129a016
    • S Grzesiek A Bax 1995 Audio-Frequency NMR in a nutating frame. Application to the assignment of phenylalanine residues in isotopically enriched proteins J Am Chem Soc 117 6527 6531 10.1021/ja00129a016
    • (1995) J Am Chem Soc , vol.117 , pp. 6527-6531
    • Grzesiek, S.1    Bax, A.2
  • 16
    • 33645475255 scopus 로고
    • The synthesis of Dl-tryptophan-beta-C14, indole-3-acetic acid-alpha-C14, and Dl-tryptophan-3-C14
    • C Heidelberger 1949 The synthesis of Dl-tryptophan-beta-C14, indole-3-acetic acid-alpha-C14, and Dl-tryptophan-3-C14 J Biol Chem 179 139 142
    • (1949) J Biol Chem , vol.179 , pp. 139-142
    • Heidelberger, C.1
  • 17
    • 6344277888 scopus 로고    scopus 로고
    • 13C]-isotopomers of indole and tryptophan for use in the analysis of indole-3-acetic acid biosynthesis
    • DOI 10.1002/jlcr.850
    • 13C]-isotopomers of indole and tryptophan for use in the analysis of indole-3-acetic acid biosynthesis J Label Compd Radiopharm 47 635 646 10.1002/jlcr.850 (Pubitemid 39390038)
    • (2004) Journal of Labelled Compounds and Radiopharmaceuticals , vol.47 , Issue.10 , pp. 635-646
    • Ilic, N.1    Cohen, J.D.2
  • 18
    • 0036873036 scopus 로고    scopus 로고
    • 13C labeling facilitates identification of Phe and Tyr aromatic signals in proteins
    • DOI 10.1023/A:1021662423490
    • 13C labeling facilitates identification of Phe and Tyr aromatic signals in proteins J Biomol NMR 24 231 235 10.1023/A:1021662423490 (Pubitemid 36113650)
    • (2002) Journal of Biomolecular NMR , vol.24 , Issue.3 , pp. 231-235
    • Jacob, J.1    Louis, J.M.2    Nesheiwat, I.3    Torchia, D.A.4
  • 19
    • 77952430272 scopus 로고    scopus 로고
    • SAIL-stereo-array isotope labeling
    • 10.1017/S0033583510000016
    • M Kainosho P Güntert 2009 SAIL-stereo-array isotope labeling Q Rev Biophys 42 247 300 10.1017/S0033583510000016
    • (2009) Q Rev Biophys , vol.42 , pp. 247-300
    • Kainosho, M.1    Güntert, P.2
  • 20
    • 33644774471 scopus 로고    scopus 로고
    • Optimal isotope labelling for NMR protein structure determinations
    • DOI 10.1038/nature04525, PII N04525
    • M Kainosho T Torizawa Y Iwashita T Terauchi AM Ono P Güntert 2006 Optimal isotope labelling for NMR protein structure determinations Nature 440 52 57 2006Natur.440...52K 10.1038/nature04525 (Pubitemid 43336263)
    • (2006) Nature , vol.440 , Issue.7080 , pp. 52-57
    • Kainosho, M.1    Torizawa, T.2    Iwashita, Y.3    Terauchi, T.4    Mei Ono, A.5    Guntert, P.6
  • 21
    • 0003026536 scopus 로고
    • Practical aspects of 3D heteronuclear NMR of proteins
    • LE Kay D Marion A Bax 1989 Practical aspects of 3D heteronuclear NMR of proteins J Magn Reson 84 7284
    • (1989) J Magn Reson , vol.84 , pp. 7284
    • Kay, L.E.1    Marion, D.2    Bax, A.3
  • 23
    • 0014666772 scopus 로고
    • 14C into quinine
    • 10.1021/ja01038a049
    • 14C into quinine J Am Chem Soc 91 2698 2702 10.1021/ja01038a049
    • (1969) J Am Chem Soc , vol.91 , pp. 2698-2702
    • Leete, E.1    Wemple, J.N.2
  • 24
    • 58149232616 scopus 로고    scopus 로고
    • 15N labeled anthranilic acid by fermentation of Candida utilis mutant
    • 10.1007/s00726-008-0030-0
    • 15N labeled anthranilic acid by fermentation of Candida utilis mutant Amino Acids 36 71 73 10.1007/s00726-008-0030-0
    • (2009) Amino Acids , vol.36 , pp. 71-73
    • Liu, Z.1    Yuan, Q.2    Wang, W.3
  • 25
    • 27244451944 scopus 로고    scopus 로고
    • Triple-resonance methods for complete resonance assignment of aromatic protons and directly bound heteronuclei in histidine and tryptophan residues
    • DOI 10.1007/s10858-005-1195-4
    • F Löhr VV Rogov M Shi F Bernhard V Dötsch 2005 Triple-resonance methods for complete resonance assignment of aromatic protons and directly bound heteronuclei in histidine and tryptophan residues J Biomol NMR 32 309 328 10.1007/s10858-005-1195-4 (Pubitemid 41511512)
    • (2005) Journal of Biomolecular NMR , vol.32 , Issue.4 , pp. 309-328
    • Lohr, F.1    Rogov, V.V.2    Shi, M.3    Bernhard, F.4    Dotsch, V.5
  • 26
    • 0027433604 scopus 로고
    • DNA and redox state induced conformational changes in the DNA-binding domain of the Myb oncoprotein
    • AH Myrset A Bostad N Jamin PN Lirsac F Toma OS Gabrielsen 1993 DNA and redox state induced conformational changes in the DNA-binding domain of the Myb oncoprotein EMBO J 12 4625 4633 (Pubitemid 23330268)
    • (1993) EMBO Journal , vol.12 , Issue.12 , pp. 4625-4633
    • Myrset, A.H.1    Bostad, A.2    Jamin, N.3    Lirsac, P.-N.4    Toma, F.5    Gabrielsen, O.S.6
  • 27
    • 0017160420 scopus 로고
    • Kinetics of hydrogen-deuterium exchange of tryptophan and tryptophan peptides in deutero-trifluoroacetic acid using proton magnetic resonance spectroscopy
    • 10.1007/BF01731556
    • RS Norton JH Bradbury 1976 Kinetics of hydrogen-deuterium exchange of tryptophan and tryptophan peptides in deutero-trifluoroacetic acid using proton magnetic resonance spectroscopy Molecul Cell Biochem 12 103 111 10.1007/BF01731556
    • (1976) Molecul Cell Biochem , vol.12 , pp. 103-111
    • Norton, R.S.1    Bradbury, J.H.2
  • 29
    • 0037170573 scopus 로고    scopus 로고
    • Biosynthesis of luciferin in the sea firefly, Cypridina hilgendorfii: L-tryptophan is a component in Cypridina luciferin
    • DOI 10.1016/S0040-4039(02)00257-5, PII S0040403902002575
    • Y Oba S Kato M Ojika S Inouye 2002 Biosynthesis of luciferin in the sea firefly, Cypridina hilgendorfii: l-tryptophan is a component in Cypridina luciferin Tetrahedron Lett 43 2389 2392 10.1016/S0040-4039(02)00257-5 (Pubitemid 34230462)
    • (2002) Tetrahedron Letters , vol.43 , Issue.13 , pp. 2389-2392
    • Oba, Y.1    Kato, S.-I.2    Ojika, M.3    Inouye, S.4
  • 30
    • 0028138773 scopus 로고
    • Solution structure of a specific DNA complex of the Myb DNA-binding domain with cooperative recognition helices
    • DOI 10.1016/0092-8674(94)90549-5
    • K Ogata S Morikawa H Nakamura A Sekikawa T Inoue H Kanai A Sarai S Ishii N Yoshifumi 1994 Solution structure of a specific DNA complex of the Myb DNA-binding domain with cooperative recognition helices Cell 79 639 648 10.1016/0092-8674(94)90549-5 (Pubitemid 24363807)
    • (1994) Cell , vol.79 , Issue.4 , pp. 639-648
    • Ogata, K.1    Morikawa, S.2    Nakamura, H.3    Sekikawa, A.4    Inoue, T.5    Kanai, H.6    Sarai, A.7    Ishii, S.8    Nishimura, Y.9
  • 32
    • 0030612833 scopus 로고    scopus 로고
    • 2 relaxation by mutual cancellation of dipole-dipole coupling and chemical shift anisotropy indicates an avenue to NMR structures of very large biological macromolecules in solution
    • DOI 10.1073/pnas.94.23.12366
    • K Pervushin R Riek G Wider K Wüthrich 1997 Attenuated T2 relaxation by mutual cancellation of dipole-dipole coupling and chemical shift anisotropy indicates an avenue to NMR structures of very large biological macromolecules in solution Proc Natl Acad Sci USA 94 12366 12371 1997PNAS...9412366P 10.1073/pnas.94.23.12366 (Pubitemid 27492534)
    • (1997) Proceedings of the National Academy of Sciences of the United States of America , vol.94 , Issue.23 , pp. 12366-12371
    • Pervushin, K.1    Riek, R.2    Wider, G.3    Wuthrich, K.4
  • 34
    • 0023155210 scopus 로고
    • Tertiary templates for proteins. Use of packing criteria in the enumeration of allowed sequences for different structural classes
    • DOI 10.1016/0022-2836(87)90358-5
    • JW Ponder FM Richards 1987 Tertiary templates for proteins. Use of packing criteria in the enumeration of allowed sequences for different structural classes J Mol Biol 193 775 791 10.1016/0022-2836(87)90358-5 (Pubitemid 17020078)
    • (1987) Journal of Molecular Biology , vol.193 , Issue.4 , pp. 775-791
    • Ponder, J.W.1    Richards, F.M.2
  • 37
    • 0041524233 scopus 로고    scopus 로고
    • A novel method for the biosynthesis of deuterated proteins with selective protonation at the aromatic rings of Phe, Tyr and Trp
    • DOI 10.1023/A:1024710729352
    • S Rajesh D Nietlispach H Nakayama K Takio ED Laue T Shibata Y Ito 2003 A novel method for the biosynthesis of deuterated proteins with selective protonation at the aromatic rings of Phe, Tyr and Trp J Biomol NMR 27 81 86 10.1023/A:1024710729352 (Pubitemid 36987112)
    • (2003) Journal of Biomolecular NMR , vol.27 , Issue.1 , pp. 81-86
    • Rajesh, S.1    Nietlispach, D.2    Nakayama, H.3    Takio, K.4    Laue, E.D.5    Shibata, T.6    Ito, Y.7
  • 38
    • 0000113347 scopus 로고
    • Fluorescence of cis-1-amino-2-(3-indolyl)cyclohexane-1-carboxylic acid: A single tryptophan chi(1) rotamer model
    • 10.1021/ja00327a048
    • I Saito H Sugiyama A Yamamoto S Muramatsu T Matsuda 1984 Fluorescence of cis-1-amino-2-(3-indolyl)cyclohexane-1-carboxylic acid: a single tryptophan chi(1) rotamer model J Am Chem Soc 106 4286 4287 10.1021/ja00327a048
    • (1984) J Am Chem Soc , vol.106 , pp. 4286-4287
    • Saito, I.1    Sugiyama, H.2    Yamamoto, A.3    Muramatsu, S.4    Matsuda, T.5
  • 39
    • 0027208112 scopus 로고
    • Rotamers: To be or not to be? An analysis of amino acid side-chain conformations in globular proteins
    • DOI 10.1006/jmbi.1993.1172
    • H Schrauber F Eisenhaber P Argos 1993 Rotamers: to be or not to be? An analysis of amino acid side-chain conformations in globular proteins J Mol Biol 230 592 612 10.1006/jmbi.1993.1172 (Pubitemid 23161365)
    • (1993) Journal of Molecular Biology , vol.230 , Issue.2 , pp. 592-612
    • Schrauber, H.1    Eisenhaber, F.2    Argos, P.3
  • 40
    • 32644440254 scopus 로고    scopus 로고
    • Syntheses of perdeuterated indoles and derivatives as probes for the biosyntheses of crucifer phytoalexins
    • DOI 10.1002/jlcr.1028
    • M Soledade C Pedras DPO Okinyo 2006 Syntheses of perdeuterated indoles and derivatives as probes for the biosyntheses of crucifer phytoalexins J Label Compd Radiopharm 49 33 45 10.1002/jlcr.1028 (Pubitemid 43242616)
    • (2006) Journal of Labelled Compounds and Radiopharmaceuticals , vol.49 , Issue.1 , pp. 33-45
    • Pedras, M.S.C.1    Okinyo, D.P.O.2
  • 41
    • 2242474754 scopus 로고    scopus 로고
    • Spin-state-selective coherence transfer via intermediate states of two-spin coherence in IS spin systems: Application to E.COSY-type measurement of J coupling constants
    • MD Sørensen A Meissner OW Sørensen 1997 Spin-state-selective coherence transfer via intermediate states of two-spin coherence in IS spin systems: application to E.COSY-type measurement of J coupling constants J Biomol NMR 10 181 186 10.1023/A:1018323913680 (Pubitemid 127504662)
    • (1997) Journal of Biomolecular NMR , vol.10 , Issue.2 , pp. 181-186
    • Sorensen, M.D.1    Meissner, A.2    Sorensen, O.W.3
  • 42
    • 45649085737 scopus 로고    scopus 로고
    • Solution structure of the C-terminal dimerization domain of SARS coronavirus nucleocapsid protein solved by the SAIL-NMR method
    • 10.1016/j.jmb.2007.11.093
    • M Takeda CK Chang T Ikeya P Güntert YH Chang YL Hsu TH Huang M Kainosho 2008 Solution structure of the C-terminal dimerization domain of SARS coronavirus nucleocapsid protein solved by the SAIL-NMR method J Mol Biol 380 608 622 10.1016/j.jmb.2007.11.093
    • (2008) J Mol Biol , vol.380 , pp. 608-622
    • Takeda, M.1    Chang, C.K.2    Ikeya, T.3    Güntert, P.4    Chang, Y.H.5    Hsu, Y.L.6    Huang, T.H.7    Kainosho, M.8
  • 43
    • 73249126534 scopus 로고    scopus 로고
    • Hydrogen exchange rate of tyrosine hydroxyl groups in proteins as studied by the deuterium isotope effect on C(zeta) chemical shifts
    • 10.1021/ja907911y
    • M Takeda J Jee AM Ono T Terauchi M Kainosho 2009 Hydrogen exchange rate of tyrosine hydroxyl groups in proteins as studied by the deuterium isotope effect on C(zeta) chemical shifts J Am Chem Soc 131 18556 18562 10.1021/ja907911y
    • (2009) J Am Chem Soc , vol.131 , pp. 18556-18562
    • Takeda, M.1    Jee, J.2    Ono, A.M.3    Terauchi, T.4    Kainosho, M.5
  • 44
    • 77649192422 scopus 로고    scopus 로고
    • Application of SAIL phenylalanine and tyrosine with alternative isotope-labeling patterns for protein structure determination
    • 10.1007/s10858-009-9360-9
    • M Takeda AM Ono T Terauchi M Kainosho 2010 Application of SAIL phenylalanine and tyrosine with alternative isotope-labeling patterns for protein structure determination J Biomol NMR 46 45 49 10.1007/s10858-009-9360-9
    • (2010) J Biomol NMR , vol.46 , pp. 45-49
    • Takeda, M.1    Ono, A.M.2    Terauchi, T.3    Kainosho, M.4
  • 47
    • 51649097908 scopus 로고    scopus 로고
    • Stereoselective synthesis of triply isotope-labeled Ser, Cys, and Ala: Amino acids for stereoarray isotope labeling technology
    • 10.1021/ol800970t
    • T Terauchi K Kobayashi K Okuma M Oba N Nishiyama M Kainosho 2008 Stereoselective synthesis of triply isotope-labeled Ser, Cys, and Ala: amino acids for stereoarray isotope labeling technology Org Lett 10 2785 2787 10.1021/ol800970t
    • (2008) Org Lett , vol.10 , pp. 2785-2787
    • Terauchi, T.1    Kobayashi, K.2    Okuma, K.3    Oba, M.4    Nishiyama, N.5    Kainosho, M.6
  • 48
    • 78650865398 scopus 로고    scopus 로고
    • Synthesis of stereoarray isotope labeled (SAIL) lysine via the "head-to-Tail" conversion of SAIL glutamic acid
    • 10.1021/ol1026766
    • T Terauchi T Kamikawai MG Vinogradov EV Starodubtseva M Takeda M Kainosho 2011 Synthesis of stereoarray isotope labeled (SAIL) lysine via the "Head-to-Tail" conversion of SAIL glutamic acid Org Lett 13 161 163 10.1021/ol1026766
    • (2011) Org Lett , vol.13 , pp. 161-163
    • Terauchi, T.1    Kamikawai, T.2    Vinogradov, M.G.3    Starodubtseva, E.V.4    Takeda, M.5    Kainosho, M.6
  • 49
    • 0035817362 scopus 로고    scopus 로고
    • A mild and efficient dehydrogenation of indolines
    • DOI 10.1016/S0040-4039(01)00986-8, PII S0040403901009868
    • U Tilstam M Harre T Heckrodt H Weinmann 2001 A mild and efficient dehydrogenation of indolines Tetrahedron Lett 42 5385 5387 10.1016/S0040- 4039(01)00986-8 (Pubitemid 32709789)
    • (2001) Tetrahedron Letters , vol.42 , Issue.32 , pp. 5385-5387
    • Tilstam, U.1    Harre, M.2    Heckrodt, T.3    Weinmann, H.4
  • 50
    • 24744440330 scopus 로고    scopus 로고
    • NMR assignment methods for the aromatic ring resonances of phenylalanine and tyrosine residues in proteins
    • DOI 10.1021/ja051386m
    • T Torizawa AM Ono T Terauchi M Kainosho 2005 NMR assignment methods for the aromatic ring resonances of phenylalanine and tyrosine residues in proteins J Am Chem Soc 127 12620 12626 10.1021/ja051386m (Pubitemid 41292179)
    • (2005) Journal of the American Chemical Society , vol.127 , Issue.36 , pp. 12620-12626
    • Torizawa, T.1    Ono, A.M.2    Terauchi, T.3    Kainosho, M.4
  • 52
    • 0002785189 scopus 로고
    • Synthesis of three isotopomers of L-tryptophan via a combination of organic synthesis and biotechnology
    • 10.1002/recl.19881070206
    • EMM van den Berg AU Baldew ATJW de Goede J Raap J Lugtenburg 1988 Synthesis of three isotopomers of L-tryptophan via a combination of organic synthesis and biotechnology Recl Trav Chim Pays-Bas 107 73 81 10.1002/recl.19881070206
    • (1988) Recl Trav Chim Pays-Bas , vol.107 , pp. 73-81
    • Van Den Berg, E.M.M.1    Baldew, A.U.2    De Goede Atjw3    Raap, J.4    Lugtenburg, J.5
  • 55
    • 0017814311 scopus 로고
    • Stereochemistry and mechanism of reactions catalyzed by tryptophanase from Escherichia coli
    • JC Vederas E Schleicher MD Tsai HG Floss 1978 Stereochemistry and mechanism of reactions catalyzed by tryptophanase from Escherichia coli J Biol Chem 253 5350 5354 (Pubitemid 8398249)
    • (1978) Journal of Biological Chemistry , vol.253 , Issue.15 , pp. 5350-5354
    • Vederas, J.C.1    Schleicher, E.2    Tsai, M.D.3    Floss, H.G.4
  • 58
  • 59
    • 0032802275 scopus 로고    scopus 로고
    • Deuteration of indole and N-methylindole by Raney nickel catalysis
    • DOI 10.1002/(SICI)1099-1344(199907)42:7<709::AID-JLCR235>3.0.CO;2-2
    • WM Yaw K Gawrisch 1999 Deuteration of indole and N-methylindole by Raney nickel catalysis J Label Compd Radiopharm 42 709 713 10.1002/(SICI)1099- 1344(199907)42:7<709::AID-JLCR235>3.0.CO;2-2 (Pubitemid 29371086)
    • (1999) Journal of Labelled Compounds and Radiopharmaceuticals , vol.42 , Issue.7 , pp. 709-713
    • Yau, W.-M.1    Gawrisch, K.2
  • 60
    • 0242562787 scopus 로고
    • 15N labelled (S)-Tryptophan
    • 10.1016/0040-4020(82)85150-8
    • 15N labelled (S)-Tryptophan Tetrahedron 38 2051 2053 10.1016/0040-4020(82)85150-8
    • (1982) Tetrahedron , vol.38 , pp. 2051-2053
    • Yuan, S.S.1    Ajami, A.M.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.