-
1
-
-
42549160616
-
Nonribosomal peptide synthetases involved in the production of medically relevant natural products
-
DOI 10.1021/mp700137g
-
Felnagle EA, et al. (2008) Nonribosomal peptide synthetases involved in the production of medically relevant natural products. Mol Pharm 5:191-211. (Pubitemid 351579124)
-
(2008)
Molecular Pharmaceutics
, vol.5
, Issue.2
, pp. 191-211
-
-
Felnagle, E.A.1
Jackson, E.E.2
Chan, Y.A.3
Podevels, A.M.4
Berti, A.D.5
McMahon, M.D.6
Thomas, M.G.7
-
2
-
-
14844362054
-
Molecular mechanisms underlying nonribosomal peptide synthesis: Approaches to new antibiotics
-
DOI 10.1021/cr0301191
-
Sieber SAM, Marahiel MA (2005) Molecular mechanisms underlying nonribosomal peptide synthesis: Approaches to new antibiotics. Chem Rev 105:715-738. (Pubitemid 40351638)
-
(2005)
Chemical Reviews
, vol.105
, Issue.2
, pp. 715-738
-
-
Sieber, S.A.1
Marahiel, M.A.2
-
3
-
-
33748631825
-
Assembly-line enzymology for polyketide and nonribosomal peptide antibiotics: Logic machinery, and mechanisms
-
DOI 10.1021/cr0503097
-
Fischbach MA, Walsh CT (2006) Assembly-line enzymology for polyketide and nonribosomal Peptide antibiotics: Logic, machinery, and mechanisms. Chem Rev 106:3468-3496. (Pubitemid 44376945)
-
(2006)
Chemical Reviews
, vol.106
, Issue.8
, pp. 3468-3496
-
-
Fischbach, M.A.1
Walsh, C.T.2
-
4
-
-
38949083855
-
The chemical versatility of natural-product assembly lines
-
Walsh CT (2008) The chemical versatility of natural-product assembly lines. Acc Chem Res 41:4-10.
-
(2008)
Acc Chem Res
, vol.41
, pp. 4-10
-
-
Walsh, C.T.1
-
5
-
-
64249157718
-
Chapter 14. Biosynthesis of nonribosomal peptide precursors
-
Wilkinson B, Micklefield J (2009) Chapter 14. Biosynthesis of nonribosomal peptide precursors. Methods Enzymol 458:353-378.
-
(2009)
Methods Enzymol
, vol.458
, pp. 353-378
-
-
Wilkinson, B.1
Micklefield, J.2
-
6
-
-
77649305354
-
Natural products version 2.0: Connecting genes to molecules
-
Walsh CT, Fischbach MA (2010) Natural products version 2.0: Connecting genes to molecules. J Am Chem Soc 132:2469-2493.
-
(2010)
J Am Chem Soc
, vol.132
, pp. 2469-2493
-
-
Walsh, C.T.1
Fischbach, M.A.2
-
7
-
-
48249137414
-
Total biosynthesis: In vitro reconstitution of polyketide and nonribosomal peptide pathways
-
Sattely ES, Fischbach MA, Walsh CT (2008) Total biosynthesis: In vitro reconstitution of polyketide and nonribosomal peptide pathways. Nat Prod Rep 25:757-793.
-
(2008)
Nat Prod Rep
, vol.25
, pp. 757-793
-
-
Sattely, E.S.1
Fischbach, M.A.2
Walsh, C.T.3
-
8
-
-
0036558479
-
Chemistry and biology of the tetrahydroisoquinoline antitumor antibiotics
-
DOI 10.1021/cr010212u
-
Scott JD, Williams RM (2002) Chemistry and biology of the tetrahydroisoquinoline antitumor antibiotics. Chem Rev 102:1669-1730. (Pubitemid 35377652)
-
(2002)
Chemical Reviews
, vol.102
, Issue.5
, pp. 1669-1730
-
-
Scott, J.D.1
Williams, R.M.2
-
9
-
-
0028567845
-
Bioxalomycins, new antibiotics produced by the marine Streptomyces sp. LL-31F508: Taxonomy and fermentation
-
Bernan VS, et al. (1994) Bioxalomycins, new antibiotics produced by the marine Streptomyces sp. LL-31F508: Taxonomy and fermentation. J Antibiot (Tokyo) 47:1417-1424.
-
(1994)
J Antibiot (Tokyo)
, vol.47
, pp. 1417-1424
-
-
Bernan, V.S.1
-
11
-
-
61549104994
-
Development of Yondelis (trabectedin, ET-743). A semisynthetic process solves the supply problem
-
Cuevas C, Francesch A (2009) Development of Yondelis (trabectedin, ET-743). A semisynthetic process solves the supply problem. Nat Prod Rep 26:322-337.
-
(2009)
Nat Prod Rep
, vol.26
, pp. 322-337
-
-
Cuevas, C.1
Francesch, A.2
-
12
-
-
56549110286
-
Recent progress in the total synthesis of naphthyridinomycin and lemonomycin tetrahydroisoquinoline antitumor antibiotics (TAAs)
-
Siengalewicz P, Rinner U, Mulzer J (2008) Recent progress in the total synthesis of naphthyridinomycin and lemonomycin tetrahydroisoquinoline antitumor antibiotics (TAAs). Chem Soc Rev 37:2676-2690.
-
(2008)
Chem Soc Rev
, vol.37
, pp. 2676-2690
-
-
Siengalewicz, P.1
Rinner, U.2
Mulzer, J.3
-
13
-
-
77953552216
-
Synthetic progress of the tetrahydroisoquinoline antitumor alkaloids
-
Liao XW, et al. (2010) Synthetic progress of the tetrahydroisoquinoline antitumor alkaloids. Chinese J Org Chem 30:317-329.
-
(2010)
Chinese J Org Chem
, vol.30
, pp. 317-329
-
-
Liao, X.W.1
-
14
-
-
0029113877
-
A new Myxococcus xanthus gene cluster for the biosynthesis of the antibiotic saframycin Mx1 encoding a peptide synthetase
-
Pospiech A, Cluzel B, Bietenhader J, Schupp T (1995) A new Myxococcus xanthus gene cluster for the biosynthesis of the antibiotic saframycin Mx1 encoding a peptide synthetase. Microbiology 141:1793-1803.
-
(1995)
Microbiology
, vol.141
, pp. 1793-1803
-
-
Pospiech, A.1
Cluzel, B.2
Bietenhader, J.3
Schupp, T.4
-
15
-
-
20144389257
-
Molecular characterization of the safracin biosynthetic pathway from Pseudomonas fluorescens A2-2: Designing new cytotoxic compounds
-
DOI 10.1111/j.1365-2958.2004.04433.x
-
Velasco A, et al. (2005) Molecular characterization of the safracin biosynthetic pathway from Pseudomonas fluorescens A2-2: Designing new cytotoxic compounds. Mol Microbiol 56:144-154. (Pubitemid 40461494)
-
(2005)
Molecular Microbiology
, vol.56
, Issue.1
, pp. 144-154
-
-
Velasco, A.1
Acebo, P.2
Gomez, A.3
Schleissner, C.4
Rodriguez, P.5
Aparicio, T.6
Conde, S.7
Munoz, R.8
De La, C.F.9
Garcia, J.L.10
Sanchez-Puelles, J.M.11
-
16
-
-
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
-
Li L, et al. (2008) 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 190:251-263.
-
(2008)
J Bacteriol
, vol.190
, pp. 251-263
-
-
Li, L.1
-
17
-
-
77952542213
-
Reconstruction of the saframycin core scaffold defines dual Pictet-Spengler mechanisms
-
Koketsu K, Watanabe K, Suda H, Oguri H, Oikawa H (2010) Reconstruction of the saframycin core scaffold defines dual Pictet-Spengler mechanisms. Nat Chem Biol 6: 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
-
18
-
-
81555208983
-
Meta-omic characterization of the marine invertebrate microbial consortium that produces the chemotherapeutic natural product ET-743
-
Rath CM, et al. (2011) Meta-omic characterization of the marine invertebrate microbial consortium that produces the chemotherapeutic natural product ET-743. ACS Chem Biol 6:1244-1256.
-
(2011)
ACS Chem Biol
, vol.6
, pp. 1244-1256
-
-
Rath, C.M.1
-
19
-
-
0020409521
-
Biosynthesis of the antitumor antibiotic naphthyridinomycin
-
Zmijewski M, Jr., Mikolajczak M, Viswanatha V, Hruby VJ (1982) Biosynthesis of the antitumor antibiotic naphthyridinomycin. J Am Chem Soc 104:4969-4971.
-
(1982)
J Am Chem Soc
, vol.104
, pp. 4969-4971
-
-
Zmijewski Jr., M.1
Mikolajczak, M.2
Viswanatha, V.3
Hruby, V.J.4
-
21
-
-
0022545734
-
Incorporation of 3'-methyltyrosine and 5'-methyl-DOPA into naphthyridinomycin
-
Palaniswamy VA, Gould SJ (1986) The incorporation of 3′- methyltyrosine and 5′-methyl DOPA into naphthyridinomycin. J Am Chem Soc 108:5651-5652. (Pubitemid 16023310)
-
(1986)
Journal of the American Chemical Society
, vol.108
, Issue.18
, pp. 5651-5652
-
-
Palaniswamy, V.A.1
Gould, S.J.2
-
22
-
-
67649437201
-
Biosynthesis of 3-hydroxy-5-methyl-O-methyltyrosine in the saframycin/ safracin biosynthetic pathway
-
Fu C-Y, et al. (2009) Biosynthesis of 3-hydroxy-5-methyl-O-methyltyrosine in the saframycin/ safracin biosynthetic pathway. J Microbiol Biotechnol 19:439-446.
-
(2009)
J Microbiol Biotechnol
, vol.19
, pp. 439-446
-
-
Fu, C.-Y.1
-
23
-
-
84856359083
-
2 in saframycin A biosynthesis by structural characterization of the analogue saframycin O
-
2 in saframycin A biosynthesis by structural characterization of the analogue saframycin O. Sci China Chem 55:90-97.
-
(2012)
Sci China Chem
, vol.55
, pp. 90-97
-
-
Peng, C.1
-
24
-
-
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
-
Tang M-C, Fu C-Y, Tang G-L (2012) 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 287:5112-5121.
-
(2012)
J Biol Chem
, vol.287
, pp. 5112-5121
-
-
Tang, M.-C.1
Fu, C.-Y.2
Tang, G.-L.3
-
25
-
-
0032537589
-
The pyruvate dehydrogenase multi-enzyme complex from Gram-negative bacteria
-
DOI 10.1016/S0167-4838(98)00079-X, PII S016748389800079X
-
de Kok A, Hengeveld AF, Martin A, Westphal AH (1998) The pyruvate dehydrogenase multi-enzyme complex from Gram-negative bacteria. Biochim Biophys Acta 1385:353-366. (Pubitemid 28310799)
-
(1998)
Biochimica et Biophysica Acta - Protein Structure and Molecular Enzymology
, vol.1385
, Issue.2
, pp. 353-366
-
-
De Kok, A.1
Hengeveld, A.F.2
Martin, A.3
Westphal, A.H.4
-
26
-
-
0032545041
-
Biosynthesis of yersiniose: Attachment of the two-carbon branched-chain is catalyzed by a thiamine pyrophosphate-dependent flavoprotein [1]
-
DOI 10.1021/ja983071v
-
Chen H, Guo Z, Liu HW (1998) Biosynthesis of Yersiniose: Attachment of the two-carbon branched-chain is catalyzed by a thiamine pyrophosphate-dependent flavoprotein. J Am Chem Soc 120:11796-11797. (Pubitemid 28543593)
-
(1998)
Journal of the American Chemical Society
, vol.120
, Issue.45
, pp. 11796-11797
-
-
Chen, H.1
Guo, Z.2
Liu, H.-W.3
-
27
-
-
23444437665
-
Binding of the coenzyme and formation of the transketolase active center
-
DOI 10.1080/15216540500167203
-
Kochetov GA, Sevostyanova IA (2005) Binding of the coenzyme and formation of the transketolase active center. IUBMB Life 57:491-497. (Pubitemid 41112987)
-
(2005)
IUBMB Life
, vol.57
, Issue.7
, pp. 491-497
-
-
Kochetov, G.A.1
Sevostyanova, I.A.2
-
28
-
-
0035844254
-
Examination of donor substrate conversion in yeast transketolase
-
Fiedler E, et al. (2001) Examination of donor substrate conversion in yeast transketolase. J Biol Chem 276:16051-16058.
-
(2001)
J Biol Chem
, vol.276
, pp. 16051-16058
-
-
Fiedler, E.1
-
29
-
-
35348938266
-
In vitro synthesis of new enniatins: Probing the α-D-hydroxy carboxylic acid binding pocket of the multienzyme enniatin synthetase
-
DOI 10.1002/cbic.200700377
-
Feifel SC, et al. (2007) In vitro synthesis of new enniatins: Probing the α-D-hydroxy carboxylic acid binding pocket of the multienzyme enniatin synthetase. Chem- BioChem 8:1767-1770. (Pubitemid 47612862)
-
(2007)
ChemBioChem
, vol.8
, Issue.15
, pp. 1767-1770
-
-
Feifel, S.C.1
Schmiederer, T.2
Hornbogen, T.3
Berg, H.4
Sussmuth, R.D.5
Zocher, R.6
-
30
-
-
33747799012
-
Characterization of the cereulide NRPS α-hydroxy acid specifying modules: Activation of α-keto acids and chiral reduction on the assembly line
-
DOI 10.1021/ja0640187
-
Magarvey NA, Ehling-Schulz M, Walsh CT (2006) Characterization of the cereulide NRPS α-hydroxy acid specifying modules: Activation of α-keto acids and chiral reduction on the assembly line. J Am Chem Soc 128:10698-10699. (Pubitemid 44277756)
-
(2006)
Journal of the American Chemical Society
, vol.128
, Issue.33
, pp. 10698-10699
-
-
Magarvey, N.A.1
Ehling-Schulz, M.2
Walsh, C.T.3
-
31
-
-
51349154318
-
A ketoreductase domain in the PksJ protein of the bacillaene assembly line carries out both α- and β-ketone reduction during chain growth
-
Calderone CT, Bumpus SB, Kelleher NL, Walsh CT, Magarvey NA (2008) A ketoreductase domain in the PksJ protein of the bacillaene assembly line carries out both α- and β-ketone reduction during chain growth. Proc Natl Acad Sci USA 105:12809-12814.
-
(2008)
Proc Natl Acad Sci USA
, vol.105
, pp. 12809-12814
-
-
Calderone, C.T.1
Bumpus, S.B.2
Kelleher, N.L.3
Walsh, C.T.4
Magarvey, N.A.5
-
32
-
-
33749249749
-
Hydroxymalonyl-acyl carrier protein (ACP) and aminomalonyl-ACP are two additional type I polyketide synthase extender units
-
DOI 10.1073/pnas.0603748103
-
Chan YA, et al. (2006) Hydroxymalonyl-acyl carrier protein (ACP) and aminomalonyl-ACP are two additional type I polyketide synthase extender units. Proc Natl Acad Sci USA 103:14349-14354. (Pubitemid 44484753)
-
(2006)
Proceedings of the National Academy of Sciences of the United States of America
, vol.103
, Issue.39
, pp. 14349-14354
-
-
Chan, Y.A.1
Boyne II, M.T.2
Podevels, A.M.3
Klimowicz, A.K.4
Handelsman, J.5
Kelleher, N.L.6
Thomas, M.G.7
-
33
-
-
79961105202
-
Discovery of a metagenome-derived enzyme that produces branched-chain acyl-(acyl-carrier-protein)s from branched-chain α-keto acids
-
Craig JW, Brady SF (2011) Discovery of a metagenome-derived enzyme that produces branched-chain acyl-(acyl-carrier-protein)s from branched-chain α-keto acids. Chem-BioChem 12:1849-1853.
-
(2011)
Chem-BioChem
, vol.12
, pp. 1849-1853
-
-
Craig, J.W.1
Brady, S.F.2
-
35
-
-
83455210375
-
Beyond ethylmalonyl-CoA: The functional role of crotonyl-CoA carboxylase/reductase homologs in expanding polyketide diversity
-
Wilson MC, Moore BS (2012) Beyond ethylmalonyl-CoA: The functional role of crotonyl-CoA carboxylase/reductase homologs in expanding polyketide diversity. Nat Prod Rep 29:72-86.
-
(2012)
Nat Prod Rep
, vol.29
, pp. 72-86
-
-
Wilson, M.C.1
Moore, B.S.2
|