-
1
-
-
0017652901
-
New antibiotics saframycins A, B, C, D and e
-
T. Arai, K. Takahashi, and A. Kubo New antibiotics saframycins A, B, C, D and E J. Antibiot. (Tokyo) 30 1977 1015 1018
-
(1977)
J. Antibiot. (Tokyo)
, vol.30
, pp. 1015-1018
-
-
Arai, T.1
Takahashi, K.2
Kubo, A.3
-
2
-
-
80855147553
-
Function of MbtH homologs in nonribosomal peptide biosynthesis and applications in secondary metabolite discovery
-
R.H. Baltz Function of MbtH homologs in nonribosomal peptide biosynthesis and applications in secondary metabolite discovery J. Ind. Microbiol. Biotechnol. 38 2011 1747 1760
-
(2011)
J. Ind. Microbiol. Biotechnol.
, vol.38
, pp. 1747-1760
-
-
Baltz, R.H.1
-
3
-
-
0035032074
-
New naphthyridinomycin-type antibiotics, aclidinomycins A and B, from Streptomyces halstedi
-
S. Cang, S. Ohta, H. Chiba, O. Johdo, H. Nomura, Y. Nagamatsu, and A. Yoshimoto New naphthyridinomycin-type antibiotics, aclidinomycins A and B, from Streptomyces halstedi J. Antibiot. (Tokyo) 54 2001 304 307
-
(2001)
J. Antibiot. (Tokyo)
, vol.54
, pp. 304-307
-
-
Cang, S.1
Ohta, S.2
Chiba, H.3
Johdo, O.4
Nomura, H.5
Nagamatsu, Y.6
Yoshimoto, A.7
-
4
-
-
0034013269
-
Predictive, structure-based model of amino acid recognition by nonribosomal peptide synthetase adenylation domains
-
G.L. Challis, J. Ravel, and C.A. Townsend Predictive, structure-based model of amino acid recognition by nonribosomal peptide synthetase adenylation domains Chem. Biol. 7 2000 211 224
-
(2000)
Chem. Biol.
, vol.7
, pp. 211-224
-
-
Challis, G.L.1
Ravel, J.2
Townsend, C.A.3
-
5
-
-
84857559505
-
In vivo characterization of nonribosomal peptide synthetases NocA and NocB in the biosynthesis of nocardicin A
-
J.M. Davidsen, and C.A. Townsend In vivo characterization of nonribosomal peptide synthetases NocA and NocB in the biosynthesis of nocardicin A Chem. Biol. 19 2012 297 306
-
(2012)
Chem. Biol.
, vol.19
, pp. 297-306
-
-
Davidsen, J.M.1
Townsend, C.A.2
-
6
-
-
31444456167
-
ET-743: A novel agent with activity in soft tissue sarcomas
-
J. Fayette, I.R. Coquard, L. Alberti, D. Ranchère, H. Boyle, and J.Y. Blay ET-743: a novel agent with activity in soft tissue sarcomas Oncologist 10 2005 827 832
-
(2005)
Oncologist
, vol.10
, pp. 827-832
-
-
Fayette, J.1
Coquard, I.R.2
Alberti, L.3
Ranchère, D.4
Boyle, H.5
Blay, J.Y.6
-
7
-
-
77957920621
-
MbtH-like proteins as integral components of bacterial nonribosomal peptide synthetases
-
E.A. Felnagle, J.J. Barkei, H. Park, A.M. Podevels, M.D. McMahon, D.W. Drott, and M.G. Thomas MbtH-like proteins as integral components of bacterial nonribosomal peptide synthetases Biochemistry 49 2010 8815 8817
-
(2010)
Biochemistry
, vol.49
, pp. 8815-8817
-
-
Felnagle, E.A.1
Barkei, J.J.2
Park, H.3
Podevels, A.M.4
McMahon, M.D.5
Drott, D.W.6
Thomas, M.G.7
-
9
-
-
33748631825
-
Assembly-line enzymology for polyketide and nonribosomal peptide antibiotics: Logic, machinery, and mechanisms
-
M.A. Fischbach, and C.T. Walsh Assembly-line enzymology for polyketide and nonribosomal peptide antibiotics: logic, machinery, and mechanisms Chem. Rev. 106 2006 3468 3496
-
(2006)
Chem. Rev.
, vol.106
, pp. 3468-3496
-
-
Fischbach, M.A.1
Walsh, C.T.2
-
10
-
-
67649437201
-
Biosynthesis of 3-hydroxy-5-methyl-O-methyltyrosine in the saframycin/safracin biosynthetic pathway
-
C.Y. Fu, M.C. Tang, C. Peng, L. Li, Y.L. He, W. Liu, and G.L. Tang Biosynthesis of 3-hydroxy-5-methyl-O-methyltyrosine in the saframycin/safracin biosynthetic pathway J. Microbiol. Biotechnol. 19 2009 439 446
-
(2009)
J. Microbiol. Biotechnol.
, vol.19
, pp. 439-446
-
-
Fu, C.Y.1
Tang, M.C.2
Peng, C.3
Li, L.4
He, Y.L.5
Liu, W.6
Tang, G.L.7
-
11
-
-
0028226896
-
Analysis of core sequences in the D-Phe activating domain of the multifunctional peptide synthetase TycA by site-directed mutagenesis
-
M. Gocht, and M.A. Marahiel Analysis of core sequences in the D-Phe activating domain of the multifunctional peptide synthetase TycA by site-directed mutagenesis J. Bacteriol. 176 1994 2654 2662
-
(1994)
J. Bacteriol.
, vol.176
, pp. 2654-2662
-
-
Gocht, M.1
Marahiel, M.A.2
-
12
-
-
27744534400
-
Investigating β-hydroxyenduracididine formation in the biosynthesis of the mannopeptimycins
-
B. Haltli, Y. Tan, N.A. Magarvey, M. Wagenaar, X.H. Yin, M. Greenstein, J.A. Hucul, and T.M. Zabriskie Investigating β-hydroxyenduracididine formation in the biosynthesis of the mannopeptimycins Chem. Biol. 12 2005 1163 1168
-
(2005)
Chem. Biol.
, vol.12
, pp. 1163-1168
-
-
Haltli, B.1
Tan, Y.2
Magarvey, N.A.3
Wagenaar, M.4
Yin, X.H.5
Greenstein, M.6
Hucul, J.A.7
Zabriskie, T.M.8
-
13
-
-
0034719702
-
Structural elucidation of lemonomycin, a potent antibiotic from Streptomyces candidus
-
H.Y. He, B. Shen, and G.T. Carter Structural elucidation of lemonomycin, a potent antibiotic from Streptomyces candidus Tetrahedron Lett. 41 2000 2067 2071
-
(2000)
Tetrahedron Lett.
, vol.41
, pp. 2067-2071
-
-
He, H.Y.1
Shen, B.2
Carter, G.T.3
-
14
-
-
67650489064
-
Structural basis for the erythro-stereospecificity of the L-arginine oxygenase VioC in viomycin biosynthesis
-
V. Helmetag, S.A. Samel, M.G. Thomas, M.A. Marahiel, and L.O. Essen Structural basis for the erythro-stereospecificity of the L-arginine oxygenase VioC in viomycin biosynthesis FEBS J. 276 2009 3669 3682
-
(2009)
FEBS J.
, vol.276
, pp. 3669-3682
-
-
Helmetag, V.1
Samel, S.A.2
Thomas, M.G.3
Marahiel, M.A.4
Essen, L.O.5
-
16
-
-
0347232737
-
Synthetic studies toward gelsemine 2. Preparation of the tetracyclic skeletal part by way of a highly stereospecific intramolecular reaction of a silyl enol ether with an N-acyliminium ion
-
H. Hiemstra, R.J. Vijn, and W.N. Speckamp Synthetic studies toward gelsemine 2. Preparation of the tetracyclic skeletal part by way of a highly stereospecific intramolecular reaction of a silyl enol ether with an N-acyliminium ion J. Org. Chem. 53 1988 3882 3884
-
(1988)
J. Org. Chem.
, vol.53
, pp. 3882-3884
-
-
Hiemstra, H.1
Vijn, R.J.2
Speckamp, W.N.3
-
17
-
-
0019952742
-
New semisynthetic antitumor antibiotics, SF-1739 HP and naphthocyanidine
-
J. Itoh, S. Omoto, S. Inouye, Y. Kodama, T. Hisamatsu, T. Niida, and Y. Ogawa New semisynthetic antitumor antibiotics, SF-1739 HP and naphthocyanidine J. Antibiot. (Tokyo) 35 1982 642 644
-
(1982)
J. Antibiot. (Tokyo)
, vol.35
, pp. 642-644
-
-
Itoh, J.1
Omoto, S.2
Inouye, S.3
Kodama, Y.4
Hisamatsu, T.5
Niida, T.6
Ogawa, Y.7
-
18
-
-
33748558778
-
Quinocarmycin analog DX-52-1 inhibits cell migration and targets radixin, disrupting interactions of radixin with actin and CD44
-
A.W. Kahsai, S. Zhu, D.J. Wardrop, W.S. Lane, and G. Fenteany Quinocarmycin analog DX-52-1 inhibits cell migration and targets radixin, disrupting interactions of radixin with actin and CD44 Chem. Biol. 13 2006 973 983
-
(2006)
Chem. Biol.
, vol.13
, pp. 973-983
-
-
Kahsai, A.W.1
Zhu, S.2
Wardrop, D.J.3
Lane, W.S.4
Fenteany, G.5
-
19
-
-
79551520607
-
Identification of a napsamycin biosynthesis gene cluster by genome mining
-
L. Kaysser, X.Y. Tang, E. Wemakor, K. Sedding, S. Hennig, S. Siebenberg, and B. Gust Identification of a napsamycin biosynthesis gene cluster by genome mining ChemBioChem 12 2011 477 487
-
(2011)
ChemBioChem
, vol.12
, pp. 477-487
-
-
Kaysser, L.1
Tang, X.Y.2
Wemakor, E.3
Sedding, K.4
Hennig, S.5
Siebenberg, S.6
Gust, B.7
-
20
-
-
77952542213
-
Reconstruction of the saframycin core scaffold defines dual Pictet-Spengler mechanisms
-
K. Koketsu, K. Watanabe, H. Suda, H. Oguri, and H. Oikawa Reconstruction of the saframycin core scaffold defines dual Pictet-Spengler mechanisms Nat. Chem. Biol. 6 2010 408 410
-
(2010)
Nat. Chem. Biol.
, vol.6
, pp. 408-410
-
-
Koketsu, K.1
Watanabe, K.2
Suda, H.3
Oguri, H.4
Oikawa, H.5
-
21
-
-
84859633428
-
Pictet-Spenglerase involved in tetrahydroisoquinoline antibiotic biosynthesis
-
K. Koketsu, A. Minami, K. Watanabe, H. Oguri, and H. Oikawa Pictet-Spenglerase involved in tetrahydroisoquinoline antibiotic biosynthesis Curr. Opin. Chem. Biol. 16 2012 142 149
-
(2012)
Curr. Opin. Chem. Biol.
, vol.16
, pp. 142-149
-
-
Koketsu, K.1
Minami, A.2
Watanabe, K.3
Oguri, H.4
Oikawa, H.5
-
22
-
-
84867008854
-
The Pictet-Spengler mechanism involved in the biosynthesis of tetrahydroisoquinoline antitumor antibiotics: A novel function for a nonribosomal peptide synthetase
-
K. Koketsu, A. Minami, K. Watanabe, H. Oguri, and H. Oikawa The Pictet-Spengler mechanism involved in the biosynthesis of tetrahydroisoquinoline antitumor antibiotics: a novel function for a nonribosomal peptide synthetase Methods Enzymol. 516 2012 79 98
-
(2012)
Methods Enzymol.
, vol.516
, pp. 79-98
-
-
Koketsu, K.1
Minami, A.2
Watanabe, K.3
Oguri, H.4
Oikawa, H.5
-
23
-
-
37549065124
-
Characterization of the saframycin A gene cluster from Streptomyces lavendulae NRRL 11002 revealing a nonribosomal peptide synthetase system for assembling the unusual tetrapeptidyl skeleton in an iterative manner
-
L. Li, W. Deng, J. Song, W. Ding, Q.F. Zhao, C. Peng, W.W. Song, G.L. Tang, and W. Liu Characterization of the saframycin A gene cluster from Streptomyces lavendulae NRRL 11002 revealing a nonribosomal peptide synthetase system for assembling the unusual tetrapeptidyl skeleton in an iterative manner J. Bacteriol. 190 2008 251 263
-
(2008)
J. Bacteriol.
, vol.190
, pp. 251-263
-
-
Li, L.1
Deng, W.2
Song, J.3
Ding, W.4
Zhao, Q.F.5
Peng, C.6
Song, W.W.7
Tang, G.L.8
Liu, W.9
-
24
-
-
24744436189
-
Synthesis of the tetrahydroisoquinoline alkaloid (±)-renieramycin G and A (±)-lemonomycinone analogue from a common intermediate
-
P. Magnus, and K.S. Matthews Synthesis of the tetrahydroisoquinoline alkaloid (±)-renieramycin G and A (±)-lemonomycinone analogue from a common intermediate J. Am. Chem. Soc. 127 2005 12476 12477
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 12476-12477
-
-
Magnus, P.1
Matthews, K.S.2
-
25
-
-
9444278428
-
Modular peptide synthetases involved in nonribosomal peptide synthesis
-
M.A. Marahiel, T. Stachelhaus, and H.D. Mootz Modular peptide synthetases involved in nonribosomal peptide synthesis Chem. Rev. 97 1997 2651 2674
-
(1997)
Chem. Rev.
, vol.97
, pp. 2651-2674
-
-
Marahiel, M.A.1
Stachelhaus, T.2
Mootz, H.D.3
-
26
-
-
0036917889
-
SAM (dependent) i AM: The S-adenosylmethionine-dependent methyltransferase fold
-
J.L. Martin, and F.M. McMillan SAM (dependent) I AM: the S-adenosylmethionine-dependent methyltransferase fold Curr. Opin. Struct. Biol. 12 2002 783 793
-
(2002)
Curr. Opin. Struct. Biol.
, vol.12
, pp. 783-793
-
-
Martin, J.L.1
McMillan, F.M.2
-
27
-
-
84860796933
-
Sequential enzymatic epoxidation involved in polyether lasalocid biosynthesis
-
A. Minami, M. Shimaya, G. Suzuki, A. Migita, S.S. Shinde, K. Sato, K. Watanabe, T. Tamura, H. Oguri, and H. Oikawa Sequential enzymatic epoxidation involved in polyether lasalocid biosynthesis J. Am. Chem. Soc. 134 2012 7246 7249
-
(2012)
J. Am. Chem. Soc.
, vol.134
, pp. 7246-7249
-
-
Minami, A.1
Shimaya, M.2
Suzuki, G.3
Migita, A.4
Shinde, S.S.5
Sato, K.6
Watanabe, K.7
Tamura, T.8
Oguri, H.9
Oikawa, H.10
-
28
-
-
4644233997
-
Isolation and characterization of a rolling-circle-type plasmid from Rhodococcus erythropolis and application of the plasmid to multiple-recombinant- protein expression
-
N. Nakashima, and T. Tamura Isolation and characterization of a rolling-circle-type plasmid from Rhodococcus erythropolis and application of the plasmid to multiple-recombinant-protein expression Appl. Environ. Microbiol. 70 2004 5557 5568
-
(2004)
Appl. Environ. Microbiol.
, vol.70
, pp. 5557-5568
-
-
Nakashima, N.1
Tamura, T.2
-
29
-
-
0022545734
-
The incorporation of 3′-methyltyrosine and 5′-methyl DOPA into naphthyridinomycin
-
V.A. Palaniswamy, and S.J. Gould The incorporation of 3′-methyltyrosine and 5′-methyl DOPA into naphthyridinomycin J. Am. Chem. Soc. 108 1986 5651 5652
-
(1986)
J. Am. Chem. Soc.
, vol.108
, pp. 5651-5652
-
-
Palaniswamy, V.A.1
Gould, S.J.2
-
30
-
-
84861914244
-
Hijacking a hydroxyethyl unit from a central metabolic ketose into a nonribosomal peptide assembly line
-
C. Peng, J.Y. Pu, L.Q. Song, X.H. Jian, M.C. Tang, and G.L. Tang Hijacking a hydroxyethyl unit from a central metabolic ketose into a nonribosomal peptide assembly line Proc. Natl. Acad. Sci. USA 109 2012 8540 8545
-
(2012)
Proc. Natl. Acad. Sci. USA
, vol.109
, pp. 8540-8545
-
-
Peng, C.1
Pu, J.Y.2
Song, L.Q.3
Jian, X.H.4
Tang, M.C.5
Tang, G.L.6
-
31
-
-
0029996171
-
Two multifunctional peptide synthetases and an O-methyltransferase are involved in the biosynthesis of the DNA-binding antibiotic and antitumour agent saframycin Mx1 from Myxococcus xanthus
-
A. Pospiech, J. Bietenhader, and T. Schupp Two multifunctional peptide synthetases and an O-methyltransferase are involved in the biosynthesis of the DNA-binding antibiotic and antitumour agent saframycin Mx1 from Myxococcus xanthus Microbiology 142 1996 741 746
-
(1996)
Microbiology
, vol.142
, pp. 741-746
-
-
Pospiech, A.1
Bietenhader, J.2
Schupp, T.3
-
32
-
-
81555208983
-
Meta-omic characterization of the marine invertebrate microbial consortium that produces the chemotherapeutic natural product ET-743
-
C.M. Rath, B. Janto, J. Earl, A. Ahmed, F.Z. Hu, L. Hiller, M. Dahlgren, R. Kreft, F. Yu, and J.J. Wolff et al. Meta-omic characterization of the marine invertebrate microbial consortium that produces the chemotherapeutic natural product ET-743 ACS Chem. Biol. 6 2011 1244 1256
-
(2011)
ACS Chem. Biol.
, vol.6
, pp. 1244-1256
-
-
Rath, C.M.1
Janto, B.2
Earl, J.3
Ahmed, A.4
Hu, F.Z.5
Hiller, L.6
Dahlgren, M.7
Kreft, R.8
Yu, F.9
Wolff, J.J.10
-
33
-
-
0026474576
-
Additional antitumor ecteinascidins from a Caribbean tunicate: Crystal structures and activities in vivo
-
R. Sakai, K.L. Rinehart, Y. Guan, and A.H. Wang Additional antitumor ecteinascidins from a Caribbean tunicate: crystal structures and activities in vivo Proc. Natl. Acad. Sci. USA 89 1992 11456 11460
-
(1992)
Proc. Natl. Acad. Sci. USA
, vol.89
, pp. 11456-11460
-
-
Sakai, R.1
Rinehart, K.L.2
Guan, Y.3
Wang, A.H.4
-
34
-
-
0026314999
-
A new alkaloid antibiotic tetrazomine. Structure determination
-
T. Sato, F. Hirayama, T. Saito, and H. Kaniwa A new alkaloid antibiotic tetrazomine. Structure determination J. Antibiot. (Tokyo) 44 1991 1367 1370
-
(1991)
J. Antibiot. (Tokyo)
, vol.44
, pp. 1367-1370
-
-
Sato, T.1
Hirayama, F.2
Saito, T.3
Kaniwa, H.4
-
35
-
-
0036558479
-
Chemistry and biology of the tetrahydroisoquinoline antitumor antibiotics
-
J.D. Scott, and R.M. Williams Chemistry and biology of the tetrahydroisoquinoline antitumor antibiotics Chem. Rev. 102 2002 1669 1730
-
(2002)
Chem. Rev.
, vol.102
, pp. 1669-1730
-
-
Scott, J.D.1
Williams, R.M.2
-
36
-
-
0033179468
-
The specificity-conferring code of adenylation domains in nonribosomal peptide synthetases
-
T. Stachelhaus, H.D. Mootz, and M.A. Marahiel The specificity-conferring code of adenylation domains in nonribosomal peptide synthetases Chem. Biol. 6 1999 493 505
-
(1999)
Chem. Biol.
, vol.6
, pp. 493-505
-
-
Stachelhaus, T.1
Mootz, H.D.2
Marahiel, M.A.3
-
37
-
-
34248576162
-
Mechanistic and structural basis of stereospecific Cβ-hydroxylation in calcium-dependent antibiotic, a daptomycin-type lipopeptide
-
M. Strieker, F. Kopp, C. Mahlert, L.O. Essen, and M.A. Marahiel Mechanistic and structural basis of stereospecific Cβ-hydroxylation in calcium-dependent antibiotic, a daptomycin-type lipopeptide ACS Chem. Biol. 2 2007 187 196
-
(2007)
ACS Chem. Biol.
, vol.2
, pp. 187-196
-
-
Strieker, M.1
Kopp, F.2
Mahlert, C.3
Essen, L.O.4
Marahiel, M.A.5
-
38
-
-
75349085414
-
In vitro reconstruction of tetronate RK-682 biosynthesis
-
Y.H. Sun, F. Hahn, Y. Demydchuk, J. Chettle, M. Tosin, H. Osada, and P.F. Leadlay In vitro reconstruction of tetronate RK-682 biosynthesis Nat. Chem. Biol. 6 2010 99 101
-
(2010)
Nat. Chem. Biol.
, vol.6
, pp. 99-101
-
-
Sun, Y.H.1
Hahn, F.2
Demydchuk, Y.3
Chettle, J.4
Tosin, M.5
Osada, H.6
Leadlay, P.F.7
-
39
-
-
0016259782
-
The molecular structure of naphthyridinomycin: A broad spectrum antibiotic
-
J. Sygusch, F. Brisse, S. Hanessia, and D. Kluepfel The molecular structure of naphthyridinomycin: a broad spectrum antibiotic Tetrahedron Lett. 46 1974 4021 4023
-
(1974)
Tetrahedron Lett.
, vol.46
, pp. 4021-4023
-
-
Sygusch, J.1
Brisse, F.2
Hanessia, S.3
Kluepfel, D.4
-
40
-
-
0020577808
-
DC-52, a novel antitumor antibiotic. 2. Isolation, physico-chemical characteristics and structure determination
-
K. Takahashi, and F. Tomita DC-52, a novel antitumor antibiotic. 2. Isolation, physico-chemical characteristics and structure determination J. Antibiot. (Tokyo) 36 1983 468 470
-
(1983)
J. Antibiot. (Tokyo)
, vol.36
, pp. 468-470
-
-
Takahashi, K.1
Tomita, F.2
-
41
-
-
84856866295
-
Characterization of SfmD as a Heme peroxidase that catalyzes the regioselective hydroxylation of 3-methyltyrosine to 3-hydroxy-5-methyltyrosine in saframycin A biosynthesis
-
M.C. Tang, C.Y. Fu, and G.L. Tang Characterization of SfmD as a Heme peroxidase that catalyzes the regioselective hydroxylation of 3-methyltyrosine to 3-hydroxy-5-methyltyrosine in saframycin A biosynthesis J. Biol. Chem. 287 2012 5112 5121
-
(2012)
J. Biol. Chem.
, vol.287
, pp. 5112-5121
-
-
Tang, M.C.1
Fu, C.Y.2
Tang, G.L.3
-
42
-
-
0020539981
-
DC-52, a novel antitumor antibiotic. 1. Taxonomy, fermentation and biological activity
-
F. Tomita, K. Takahashi, and K. Shimizu DC-52, a novel antitumor antibiotic. 1. Taxonomy, fermentation and biological activity J. Antibiot. (Tokyo) 36 1983 463 467
-
(1983)
J. Antibiot. (Tokyo)
, vol.36
, pp. 463-467
-
-
Tomita, F.1
Takahashi, K.2
Shimizu, K.3
-
43
-
-
20144389257
-
Molecular characterization of the safracin biosynthetic pathway from Pseudomonas fluorescens A2-2: Designing new cytotoxic compounds
-
A. Velasco, P. Acebo, A. Gomez, C. Schleissner, P. Rodríguez, T. Aparicio, S. Conde, R. Muñoz, F. de la Calle, J.L. Garcia, and J.M. Sánchez-Puelles Molecular characterization of the safracin biosynthetic pathway from Pseudomonas fluorescens A2-2: designing new cytotoxic compounds Mol. Microbiol. 56 2005 144 154
-
(2005)
Mol. Microbiol.
, vol.56
, pp. 144-154
-
-
Velasco, A.1
Acebo, P.2
Gomez, A.3
Schleissner, C.4
Rodríguez, P.5
Aparicio, T.6
Conde, S.7
Muñoz, R.8
De La Calle, F.9
Garcia, J.L.10
Sánchez-Puelles, J.M.11
-
44
-
-
0011556599
-
Isolation and characterization of a new antibiotic, SF-1739 substance
-
H. Watanabe, T. Shomura, Y. Ogawa, Y. Kondo, K. Oba, J. Yoshiba, C. Moriyama, T. Tsuruoka, M. Kojima, and S. Inouye et al. Isolation and characterization of a new antibiotic, SF-1739 substance Sci. Rep. Meiji Seika Kaisha 16 1976 20 28
-
(1976)
Sci. Rep. Meiji Seika Kaisha
, vol.16
, pp. 20-28
-
-
Watanabe, H.1
Shomura, T.2
Ogawa, Y.3
Kondo, Y.4
Oba, K.5
Yoshiba, J.6
Moriyama, C.7
Tsuruoka, T.8
Kojima, M.9
Inouye, S.10
-
45
-
-
44449121406
-
Asymmetric total synthesis of (-)-quinocarcin
-
Y.C. Wu, M. Liron, and J.P. Zhu Asymmetric total synthesis of (-)-quinocarcin J. Am. Chem. Soc. 130 2008 7148 7152
-
(2008)
J. Am. Chem. Soc.
, vol.130
, pp. 7148-7152
-
-
Wu, Y.C.1
Liron, M.2
Zhu, J.P.3
-
46
-
-
4644343748
-
VioC is a non-heme iron, α-ketoglutarate-dependent oxygenase that catalyzes the formation of 3S-hydroxy-L-arginine during viomycin biosynthesis
-
X.H. Yin, and T.M. Zabriskie VioC is a non-heme iron, α-ketoglutarate-dependent oxygenase that catalyzes the formation of 3S-hydroxy-L-arginine during viomycin biosynthesis ChemBioChem 5 2004 1274 1277
-
(2004)
ChemBioChem
, vol.5
, pp. 1274-1277
-
-
Yin, X.H.1
Zabriskie, T.M.2
-
47
-
-
57749097690
-
Crystal structure of DltA: Implications for the reaction mechanism of non-ribosomal peptide synthetase adenylation domains
-
H. Yonus, P. Neumann, S. Zimmermann, J.J. May, M.A. Marahiel, and M.T. Stubbs Crystal structure of DltA: implications for the reaction mechanism of non-ribosomal peptide synthetase adenylation domains J. Biol. Chem. 283 2008 32484 32491
-
(2008)
J. Biol. Chem.
, vol.283
, pp. 32484-32491
-
-
Yonus, H.1
Neumann, P.2
Zimmermann, S.3
May, J.J.4
Marahiel, M.A.5
Stubbs, M.T.6
-
48
-
-
78649307586
-
Activation of the pacidamycin PacL adenylation domain by MbtH-like proteins
-
W. Zhang, J.R. Heemstra Jr., C.T. Walsh, and H.J. Imker Activation of the pacidamycin PacL adenylation domain by MbtH-like proteins Biochemistry 49 2010 9946 9947
-
(2010)
Biochemistry
, vol.49
, pp. 9946-9947
-
-
Zhang, W.1
Heemstra, Jr.J.R.2
Walsh, C.T.3
Imker, H.J.4
-
49
-
-
79959251862
-
Identification of phenylalanine 3-hydroxylase for meta-tyrosine biosynthesis
-
W. Zhang, B.D. Ames, and C.T. Walsh Identification of phenylalanine 3-hydroxylase for meta-tyrosine biosynthesis Biochemistry 50 2011 5401 5403
-
(2011)
Biochemistry
, vol.50
, pp. 5401-5403
-
-
Zhang, W.1
Ames, B.D.2
Walsh, C.T.3
-
50
-
-
0034828607
-
Spectroscopic studies of substrate interactions with clavaminate synthase 2, a multifunctional α-KG-dependent non-heme iron enzyme: Correlation with mechanisms and reactivities
-
J. Zhou, W.L. Kelly, B.O. Bachmann, M. Gunsior, C.A. Townsend, and E.I. Solomon Spectroscopic studies of substrate interactions with clavaminate synthase 2, a multifunctional α-KG-dependent non-heme iron enzyme: correlation with mechanisms and reactivities J. Am. Chem. Soc. 123 2001 7388 7398
-
(2001)
J. Am. Chem. Soc.
, vol.123
, pp. 7388-7398
-
-
Zhou, J.1
Kelly, W.L.2
Bachmann, B.O.3
Gunsior, M.4
Townsend, C.A.5
Solomon, E.I.6
-
51
-
-
0021955850
-
Naphthyridinomycin biosynthesis: The involvement of ornithine and the origin of the oxazolidine nitrogen
-
M.J. Zmijewski, V.A. Palaniswamy, and S.J. Gould Naphthyridinomycin biosynthesis: the involvement of ornithine and the origin of the oxazolidine nitrogen J. Chem. Soc. Chem. Commun. 18 1985 1261 1262
-
(1985)
J. Chem. Soc. Chem. Commun.
, vol.18
, pp. 1261-1262
-
-
Zmijewski, M.J.1
Palaniswamy, V.A.2
Gould, S.J.3
-
52
-
-
0021844935
-
Biosynthetic origin of carbons 1 and 2 of naphthyridinomycin
-
M.J. Zmijewski Jr. Biosynthetic origin of carbons 1 and 2 of naphthyridinomycin J. Antibiot. (Tokyo) 38 1985 819 820
-
(1985)
J. Antibiot. (Tokyo)
, vol.38
, pp. 819-820
-
-
Zmijewski, Jr.M.J.1
|