-
1
-
-
0028073170
-
Pyrroindomycins, novel antibiotics produced by Streptomyces rugosporus sp LL-42D005. I. Isolation and structure determination
-
(Tokyo
-
Ding, W. et al. Pyrroindomycins, novel antibiotics produced by Streptomyces rugosporus sp. LL-42D005. I. Isolation and structure determination. J. Antibiot. (Tokyo) 47, 1250-1257 (1994).
-
(1994)
J. Antibiot.
, vol.47
, pp. 1250-1257
-
-
Ding, W.1
-
2
-
-
0028102973
-
Pyrroindomycins, novel antibiotics produced by Streptomyces rugosporus LL-42D005. II
-
Singh, M.P. et al. Pyrroindomycins, novel antibiotics produced by Streptomyces rugosporus LL-42D005. II. Biological activities. J. Antibiot. (Tokyo) 47, 1258-1265 (1994).
-
(1994)
Biological Activities. J. Antibiot. (Tokyo
, vol.47
, pp. 1258-1265
-
-
Singh, M.P.1
-
3
-
-
84907884996
-
Recent advances in the field of bioactive tetronates
-
Vieweg, L., Reichau, S., Schobert, R., Leadlay, P.F. & Sussmuth, R.D. Recent advances in the field of bioactive tetronates. Nat. Prod. Rep. 31, 1554-1584 (2014).
-
(2014)
Nat. Prod. Rep.
, vol.31
, pp. 1554-1584
-
-
Vieweg, L.1
Reichau, S.2
Schobert, R.3
Leadlay, P.F.4
Sussmuth, R.D.5
-
4
-
-
3042745794
-
Enzymatic catalysis of the Diels-Alder reaction in the biosynthesis of natural products
-
Oikawa, H. & Tokiwano, T. Enzymatic catalysis of the Diels-Alder reaction in the biosynthesis of natural products. Nat. Prod. Rep. 21, 321-352 (2004).
-
(2004)
Nat. Prod. Rep.
, vol.21
, pp. 321-352
-
-
Oikawa, H.1
Tokiwano, T.2
-
5
-
-
84862786646
-
Current developments and challenges in the search for a naturally selected Diels-Alderase
-
Kim, H.J., Ruszczycky, M.W. & Liu, H.W. Current developments and challenges in the search for a naturally selected Diels-Alderase. Curr. Opin. Chem. Biol. 16, 124-131 (2012).
-
(2012)
Curr. Opin. Chem. Biol.
, vol.16
, pp. 124-131
-
-
Kim, H.J.1
Ruszczycky, M.W.2
Liu, H.W.3
-
6
-
-
57049138419
-
Intramolecular cyclizations of polyketide biosynthesis: Mining for a "diels-Alderase"?
-
Kelly, W.L. Intramolecular cyclizations of polyketide biosynthesis: mining for a "Diels-Alderase"? Org. Biomol. Chem. 6, 4483-4493 (2008).
-
(2008)
Org. Biomol. Chem.
, vol.6
, pp. 4483-4493
-
-
Kelly, W.L.1
-
7
-
-
80053598148
-
Diels-Alderase at last
-
Townsend, C.A.A. "Diels-Alderase" at last. ChemBioChem 12, 2267-2269 (2011).
-
(2011)
ChemBioChem
, vol.12
, pp. 2267-2269
-
-
Townsend, C.A.A.1
-
8
-
-
79955621903
-
Biochemistry life imitates art
-
Kelly, W.L. Biochemistry: life imitates art. Nature 473, 35-36 (2011).
-
(2011)
Nature
, vol.473
, pp. 35-36
-
-
Kelly, W.L.1
-
9
-
-
84867826620
-
Insights into pyrroindomycin biosynthesis reveal a uniform paradigm for tetramate/tetronate formation
-
Wu, Q., Wu, Z., Qu, X. & Liu, W. Insights into pyrroindomycin biosynthesis reveal a uniform paradigm for tetramate/tetronate formation. J. Am. Chem. Soc. 134, 17342-17345 (2012).
-
(2012)
J. Am. Chem. Soc.
, vol.134
, pp. 17342-17345
-
-
Wu, Q.1
Wu, Z.2
Qu, X.3
Liu, W.4
-
10
-
-
33745184421
-
Genetic characterization of the chlorothricin gene cluster as a model for spirotetronate antibiotic biosynthesis
-
Jia, X.Y. et al. Genetic characterization of the chlorothricin gene cluster as a model for spirotetronate antibiotic biosynthesis. Chem. Biol. 13, 575-585 (2006).
-
(2006)
Chem. Biol.
, vol.13
, pp. 575-585
-
-
Jia, X.Y.1
-
11
-
-
50249101630
-
Cloning and characterization of the tetrocarcin A gene cluster from Micromonospora chalcea NRRL 11289 reveals a highly conserved strategy for tetronate biosynthesis in spirotetronate antibiotics
-
Fang, J. et al. Cloning and characterization of the tetrocarcin A gene cluster from Micromonospora chalcea NRRL 11289 reveals a highly conserved strategy for tetronate biosynthesis in spirotetronate antibiotics. J. Bacteriol. 190, 6014-6025 (2008).
-
(2008)
J. Bacteriol.
, vol.190
, pp. 6014-6025
-
-
Fang, J.1
-
12
-
-
36749055680
-
Elucidation of the kijanimicin gene cluster: Insights into the biosynthesis of spirotetronate antibiotics and nitrosugars
-
Zhang, H. et al. Elucidation of the kijanimicin gene cluster: insights into the biosynthesis of spirotetronate antibiotics and nitrosugars. J. Am. Chem. Soc. 129, 14670-14683 (2007).
-
(2007)
J. Am. Chem. Soc.
, vol.129
, pp. 14670-14683
-
-
Zhang, H.1
-
13
-
-
84875208701
-
Dissecting glycosylation steps in lobophorin biosynthesis implies an iterative glycosyltransferase
-
Li, S. et al. Dissecting glycosylation steps in lobophorin biosynthesis implies an iterative glycosyltransferase. Org. Lett. 15, 1374-1377 (2013).
-
(2013)
Org. Lett.
, vol.15
, pp. 1374-1377
-
-
Li, S.1
-
14
-
-
0034887171
-
Polyketide biosyn thesis: A millennium review
-
Staunton, J. & Weissman, K.J. Polyketide biosynthesis: a millennium review. Nat. Prod. Rep. 18, 380-416 (2001).
-
(2001)
Nat. Prod. Rep.
, vol.18
, pp. 380-416
-
-
Staunton, J.1
Weissman, K.J.2
-
15
-
-
1642304143
-
Polyketide and nonribosomal peptide antibiotics: Modularity and versatility
-
Walsh, C.T. Polyketide and nonribosomal peptide antibiotics: modularity and versatility. Science 303, 1805-1810 (2004).
-
(2004)
Science
, vol.303
, pp. 1805-1810
-
-
Walsh, C.T.1
-
16
-
-
30544434619
-
Combinatorial biosynthesis of reduced polyketides
-
Weissman, K.J. & Leadlay, P.F. Combinatorial biosynthesis of reduced polyketides. Nat. Rev. Microbiol. 3, 925-936 (2005).
-
(2005)
Nat. Rev. Microbiol.
, vol.3
, pp. 925-936
-
-
Weissman, K.J.1
Leadlay, P.F.2
-
17
-
-
75349085414
-
In vitro reconstruction of tetronate RK-682 biosynthesis
-
Sun, Y. et al. In vitro reconstruction of tetronate RK-682 biosynthesis. Nat. Chem. Biol. 6, 99-101 (2010).
-
(2010)
Nat. Chem. Biol.
, vol.6
, pp. 99-101
-
-
Sun, Y.1
-
18
-
-
84878027011
-
Unusual acetylation-elimination in the formation of tetronate antibiotics
-
Kanchanabanca, C. et al. Unusual acetylation-elimination in the formation of tetronate antibiotics. Angew. Chem. Int. Ed. Engl. 52, 5785-5788 (2013).
-
(2013)
Angew. Chem. Int. Ed. Engl.
, vol.52
, pp. 5785-5788
-
-
Kanchanabanca, C.1
-
19
-
-
34548172398
-
Crystal structures of two aromatic hydroxylases involved in the early tailoring steps of angucycline biosynthesis
-
Koskiniemi, H. et al. Crystal structures of two aromatic hydroxylases involved in the early tailoring steps of angucycline biosynthesis. J. Mol. Biol. 372, 633-648 (2007).
-
(2007)
J. Mol. Biol.
, vol.372
, pp. 633-648
-
-
Koskiniemi, H.1
-
20
-
-
84880164381
-
Tracing the evolution of angucyclinone monooxygenases: Structural determinants for C-12b hydroxylation and substrate inhibition in PgaE
-
Kallio, P. et al. Tracing the evolution of angucyclinone monooxygenases: structural determinants for C-12b hydroxylation and substrate inhibition in PgaE. Biochemistry 52, 4507-4516 (2013).
-
(2013)
Biochemistry
, vol.52
, pp. 4507-4516
-
-
Kallio, P.1
-
21
-
-
84877830592
-
Uncovering the enzymes that catalyze the final steps in oxytetracycline biosynthesis
-
Wang, P. et al. Uncovering the enzymes that catalyze the final steps in oxytetracycline biosynthesis. J. Am. Chem. Soc. 135, 7138-7141 (2013).
-
(2013)
J. Am. Chem. Soc.
, vol.135
, pp. 7138-7141
-
-
Wang, P.1
-
22
-
-
79958756737
-
Abyssomicin biosynthesis formation of an unusual polyketide, antibiotic-feeding studies and genetic analysis
-
Gottardi, E.M. et al. Abyssomicin biosynthesis: formation of an unusual polyketide, antibiotic-feeding studies and genetic analysis. ChemBioChem 12, 1401-1410 (2011).
-
(2011)
ChemBioChem
, vol.12
, pp. 1401-1410
-
-
Gottardi, E.M.1
-
23
-
-
84868028202
-
Quartromicin biosyn thesis: Two alternative polyketide chains produced by one polyketide synthase assembly line
-
He, H.Y. et al. Quartromicin biosynthesis: two alternative polyketide chains produced by one polyketide synthase assembly line. Chem. Biol. 19, 1313-1323 (2012).
-
(2012)
Chem. Biol.
, vol.19
, pp. 1313-1323
-
-
He, H.Y.1
-
24
-
-
0033619244
-
A chain initiation factor common to both modular and aromatic polyketide synthases
-
Bisang, C. et al. A chain initiation factor common to both modular and aromatic polyketide synthases. Nature 401, 502-505 (1999).
-
(1999)
Nature
, vol.401
, pp. 502-505
-
-
Bisang, C.1
-
25
-
-
0035951074
-
Alteration of the substrate specificity of a modular polyketide synthase acyltransferase domain through site-specific mutations
-
Reeves, C.D. et al. Alteration of the substrate specificity of a modular polyketide synthase acyltransferase domain through site-specific mutations. Biochemistry 40, 15464-15470 (2001).
-
(2001)
Biochemistry
, vol.40
, pp. 15464-15470
-
-
Reeves, C.D.1
-
26
-
-
34547945950
-
A tylosin ketoreductase reveals how chirality is determined in polyketides
-
Keatinge-Clay, A.T. A tylosin ketoreductase reveals how chirality is determined in polyketides. Chem. Biol. 14, 898-908 (2007).
-
(2007)
Chem. Biol.
, vol.14
, pp. 898-908
-
-
Keatinge-Clay, A.T.1
-
27
-
-
29044437969
-
Polyketide double bond biosynthesis. Mechanistic analysis of the dehydratase-containing module 2 of the picromycin/methylmycin synthase
-
Wu, J., Zaleski, T.J., Valenzano, C., Khosla, C. & Cane, D.E. Polyketide double bond biosynthesis. Mechanistic analysis of the dehydratase-containing module 2 of the picromycin/methylmycin synthase. J. Am. Chem. Soc. 127, 17393-17404 (2005).
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 17393-17404
-
-
Wu, J.1
Zaleski, T.J.2
Valenzano, C.3
Khosla, C.4
Cane, D.E.5
-
28
-
-
56049119642
-
Prediction and manipulation of the stereochemistry of enoylreduction in modular polyketide synthases
-
Kwan, D.H. et al. Prediction and manipulation of the stereochemistry of enoylreduction in modular polyketide synthases. Chem. Biol. 15, 1231-1240 (2008).
-
(2008)
Chem. Biol.
, vol.15
, pp. 1231-1240
-
-
Kwan, D.H.1
-
29
-
-
0036919327
-
Flavoenzymes that catalyse reactions with no net redox change
-
Bornemann, S. Flavoenzymes that catalyse reactions with no net redox change. Nat. Prod. Rep. 19, 761-772 (2002).
-
(2002)
Nat. Prod. Rep.
, vol.19
, pp. 761-772
-
-
Bornemann, S.1
-
30
-
-
84921516173
-
Biosynthesis of versipelostatin: Identification of an enzyme-catalyzed [4+2]-cycloaddition required for macrocyclization of spirotetronate-containing polyketides
-
Hashimoto, T. et al. Biosynthesis of versipelostatin: identification of an enzyme-catalyzed [4+2]-cycloaddition required for macrocyclization of spirotetronate-containing polyketides. J. Am. Chem. Soc. 137, 572-575 (2015).
-
(2015)
J. Am. Chem. Soc.
, vol.137
, pp. 572-575
-
-
Hashimoto, T.1
-
31
-
-
0037434992
-
Insight into a natural Diels-Alder reaction from the structure of macrophomate synthase
-
Ose, T. et al. Insight into a natural Diels-Alder reaction from the structure of macrophomate synthase. Nature 422, 185-189 (2003).
-
(2003)
Nature
, vol.422
, pp. 185-189
-
-
Ose, T.1
-
32
-
-
37049086431
-
Enzymatic activity catalysing exo-selective Diels-Alder reaction in solanapyrone biosynthesis
-
Oikawa, H., Katayama, K., Suzuki, Y. & Ichihara, A. Enzymatic activity catalysing exo-selective Diels-Alder reaction in solanapyrone biosynthesis. J. Chem. Soc. Chem. Commun.##1321-1322 (1995).
-
(1995)
J. Chem. Soc. Chem. Commun.
, pp. 1321-1322
-
-
Oikawa, H.1
Katayama, K.2
Suzuki, Y.3
Ichihara, A.4
-
33
-
-
0034703754
-
Lovastatin nonaketide synthase catalyzes an intramolecular Diels-Alder reaction of a substrate analogue
-
Auclair, K. et al. Lovastatin nonaketide synthase catalyzes an intramolecular Diels-Alder reaction of a substrate analogue. J. Am. Chem. Soc. 122, 11519-11520 (2000).
-
(2000)
J. Am. Chem. Soc.
, vol.122
, pp. 11519-11520
-
-
Auclair, K.1
-
34
-
-
70350493673
-
Complete reconstitution of a highly reducing iterative polyketide synthase
-
Ma, S.M. et al. Complete reconstitution of a highly reducing iterative polyketide synthase. Science 326, 589-592 (2009).
-
(2009)
Science
, vol.326
, pp. 589-592
-
-
Ma, S.M.1
-
35
-
-
77949358978
-
Mechanistic insights on riboflavin synthase inspired by selective binding of the 6,7-dimethyl-8-ribityllumazine exomethylene anion
-
Kim, R.R. et al. Mechanistic insights on riboflavin synthase inspired by selective binding of the 6,7-dimethyl-8-ribityllumazine exomethylene anion. J. Am. Chem. Soc. 132, 2983-2990 (2010).
-
(2010)
J. Am. Chem. Soc.
, vol.132
, pp. 2983-2990
-
-
Kim, R.R.1
-
36
-
-
79955642774
-
Enzyme-catalysed [4+2] cycloaddition is a key step in the biosynthesis of spinosyn A
-
Kim, H.J., Ruszczycky, M.W., Choi, S.H., Liu, Y.N. & Liu, H.W. Enzyme-catalysed [4+2] cycloaddition is a key step in the biosynthesis of spinosyn A. Nature 473, 109-112 (2011).
-
(2011)
Nature
, vol.473
, pp. 109-112
-
-
Kim, H.J.1
Ruszczycky, M.W.2
Choi, S.H.3
Liu, Y.N.4
Liu, H.W.5
-
37
-
-
0003954817
-
-
4th edn. Mcgraw-Hill Higher Education, New York
-
Carey, F.A. in Organic Chemistry 4th edn. 365-397 (Mcgraw-Hill Higher Education, New York, 2000).
-
(2000)
Organic Chemistry
, pp. 365-397
-
-
Carey, F.A.1
-
38
-
-
0001371159
-
A formal total synthesis of (+)-tetronolide, the aglycon of the tetrocarcins: Enantio-and diastereoselective syntheses of the octahydronaphthalene (bottom-half) and spirotetronate (top-half) fragments
-
Roush, W.R., Reilly, M.L., Koyama, K. & Brown, B.B. A formal total synthesis of (+)-tetronolide, the aglycon of the tetrocarcins: enantio-and diastereoselective syntheses of the octahydronaphthalene (bottom-half) and spirotetronate (top-half) fragments. J. Org. Chem. 62, 8708-8721 (1997).
-
(1997)
J. Org. Chem.
, vol.62
, pp. 8708-8721
-
-
Roush, W.R.1
Reilly, M.L.2
Koyama, K.3
Brown, B.B.4
-
39
-
-
0032486756
-
Enantioselective total synthesis of (?)-chlorothricolide via the tandem inter-and intramolecular Diels?Alder reaction of a hexaenoate intermediate
-
Roush, W.R. & Sciotti, R.J. Enantioselective total synthesis of (?)-chlorothricolide via the tandem inter-and intramolecular Diels?Alder reaction of a hexaenoate intermediate. J. Am. Chem. Soc. 120, 7411-7419 (1998).
-
(1998)
J. Am. Chem. Soc.
, vol.120
, pp. 7411-7419
-
-
Roush, W.R.1
Sciotti, R.J.2
-
40
-
-
79959378209
-
Reveromycin A biosynthesis uses RevG and RevJ for stereospecific spiroacetal formation
-
Takahashi, S. et al. Reveromycin A biosynthesis uses RevG and RevJ for stereospecific spiroacetal formation. Nat. Chem. Biol. 7, 461-468 (2011).
-
(2011)
Nat. Chem. Biol.
, vol.7
, pp. 461-468
-
-
Takahashi, S.1
-
41
-
-
84873878536
-
Spiroketal formation and modification in avermectin biosynthesis involves a dual activity of AveC
-
Sun, P. et al. Spiroketal formation and modification in avermectin biosynthesis involves a dual activity of AveC. J. Am. Chem. Soc. 135, 1540-1548 (2013).
-
(2013)
J. Am. Chem. Soc.
, vol.135
, pp. 1540-1548
-
-
Sun, P.1
-
43
-
-
0003869903
-
-
John Innes Foundation
-
Keiser, T., Bibb, M.J., Buttner, M.J., Chater, K.F. & Hopwood, D.A. Practical Streptomyces Genetics (John Innes Foundation, 2000).
-
(2000)
Practical Streptomyces Genetics
-
-
Keiser, T.1
Bibb, M.J.2
Buttner, M.J.3
Chater, K.F.4
Hopwood, D.A.5
-
45
-
-
74749097612
-
ECD Cotton effect approximated by the Gaussian curve and other methods
-
Stephens, P.J. & Harada, N. ECD Cotton effect approximated by the Gaussian curve and other methods. Chirality 22, 229-233 (2010).
-
(2010)
Chirality
, vol.22
, pp. 229-233
-
-
Stephens, P.J.1
Harada, N.2
-
46
-
-
78651325180
-
-
Swiss National Supercomputing Centre: Manno, Switzerland
-
Varetto, U. MOLEKEL 5.4. (Swiss National Supercomputing Centre: Manno, Switzerland, 2009).
-
(2009)
MOLEKEL 5.4
-
-
Varetto, U.1
-
47
-
-
77954065271
-
I-TASSER a unified platform for automated protein structure and function prediction
-
Roy, A., Kucukural, A. & Zhang, Y. I-TASSER: a unified platform for automated protein structure and function prediction. Nat. Protoc. 5, 725-738 (2010).
-
(2010)
Nat. Protoc.
, vol.5
, pp. 725-738
-
-
Roy, A.1
Kucukural, A.2
Zhang, Y.3
|