-
1
-
-
0025183708
-
Basic local alignment search tool
-
Altschul, S.F., Gish, W., Miller, W., Myers, E.W., and Lipman, D.J. 1990. Basic local alignment search tool. J. Mol. Biol. 215: 403-410.
-
(1990)
J. Mol. Biol
, vol.215
, pp. 403-410
-
-
Altschul, S.F.1
Gish, W.2
Miller, W.3
Myers, E.W.4
Lipman, D.J.5
-
2
-
-
0030452311
-
A mechanism of drug action revealed by structural studies of enoyl reductase
-
Baldock, C., Rafferty, J.B., Sedelnikova, S.E., Baker, P.J., Stuitje, A.R., Slabas, A.R., Hawkes, T.R., and Rice, D.W. 1996. A mechanism of drug action revealed by structural studies of enoyl reductase. Science 274: 2107-2110.
-
(1996)
Science
, vol.274
, pp. 2107-2110
-
-
Baldock, C.1
Rafferty, J.B.2
Sedelnikova, S.E.3
Baker, P.J.4
Stuitje, A.R.5
Slabas, A.R.6
Hawkes, T.R.7
Rice, D.W.8
-
3
-
-
0031894382
-
Community-acquired pneumonia in adults: Guidelines for management. The Infectious Diseases Society of America
-
Bartlett, J.G., Breiman, R.F., Mandell, L.A., and File Jr., T.M. 1998. Community-acquired pneumonia in adults: Guidelines for management. The Infectious Diseases Society of America. Clin. Infect. Dis. 26: 811-838.
-
(1998)
Clin. Infect. Dis
, vol.26
, pp. 811-838
-
-
Bartlett, J.G.1
Breiman, R.F.2
Mandell, L.A.3
File Jr., T.M.4
-
4
-
-
0026705492
-
Epidemiology of drug resistance: Implications for a post-antimicrobial era
-
Cohen, M.L. 1992. Epidemiology of drug resistance: Implications for a post-antimicrobial era. Science 257: 1050-1055.
-
(1992)
Science
, vol.257
, pp. 1050-1055
-
-
Cohen, M.L.1
-
5
-
-
0028988237
-
Crystal structure and function of the isoniazid target of Mycobacterium tuberculosis
-
Dessen, A., Quemard, A., Blanchard, J.S., Jacobs Jr., W.R., and Sacchettini, J.C. 1995. Crystal structure and function of the isoniazid target of Mycobacterium tuberculosis. Science 267: 1638-1641.
-
(1995)
Science
, vol.267
, pp. 1638-1641
-
-
Dessen, A.1
Quemard, A.2
Blanchard, J.S.3
Jacobs Jr., W.R.4
Sacchettini, J.C.5
-
7
-
-
33745859340
-
Crystal structure of 2-nitropropane dioxygenase complexed with FMN and substrate. Identification of the catalytic base
-
Ha, J.Y., Min, J.Y., Lee, S.K., Kim, H.S., Kim do, J., Kim, K.H., Lee, H.H., Kim, H.K., Yoon, H.J., and Suh, S.W. 2006. Crystal structure of 2-nitropropane dioxygenase complexed with FMN and substrate. Identification of the catalytic base. J. Biol. Chem. 281: 18660-18667.
-
(2006)
J. Biol. Chem
, vol.281
, pp. 18660-18667
-
-
Ha, J.Y.1
Min, J.Y.2
Lee, S.K.3
Kim, H.S.4
Kim do, J.5
Kim, K.H.6
Lee, H.H.7
Kim, H.K.8
Yoon, H.J.9
Suh, S.W.10
-
8
-
-
0028855972
-
Enoyl-acyl carrier protein reductase (fabI) plays a determinant role in completing cycles of fatty acid elongation in Escherichia coli
-
Heath, R.J. and Rock, C.O. 1995. Enoyl-acyl carrier protein reductase (fabI) plays a determinant role in completing cycles of fatty acid elongation in Escherichia coli. J. Biol. Chem. 270: 26538-26542.
-
(1995)
J. Biol. Chem
, vol.270
, pp. 26538-26542
-
-
Heath, R.J.1
Rock, C.O.2
-
9
-
-
0030033704
-
Regulation of fatty acid elongation and initiation by acyl-acyl carrier protein in Escherichia coli
-
Heath, R.J. and Rock, C.O. 1996. Regulation of fatty acid elongation and initiation by acyl-acyl carrier protein in Escherichia coli. J. Biol. Chem. 271: 1833-1836.
-
(1996)
J. Biol. Chem
, vol.271
, pp. 1833-1836
-
-
Heath, R.J.1
Rock, C.O.2
-
10
-
-
0034644010
-
A triclosan-resistant bacterial enzyme
-
Heath, R.J. and Rock, C.O. 2000. A triclosan-resistant bacterial enzyme. Nature 406: 145-146.
-
(2000)
Nature
, vol.406
, pp. 145-146
-
-
Heath, R.J.1
Rock, C.O.2
-
11
-
-
0032515066
-
Broad spectrum antimicrobial biocides target the FabI component of fatty acid synthesis
-
Heath, R.J., Yu, Y.T., Shapiro, M.A., Olson, E., and Rock, C.O. 1998. Broad spectrum antimicrobial biocides target the FabI component of fatty acid synthesis. J. Biol. Chem. 273: 30316-30320.
-
(1998)
J. Biol. Chem
, vol.273
, pp. 30316-30320
-
-
Heath, R.J.1
Yu, Y.T.2
Shapiro, M.A.3
Olson, E.4
Rock, C.O.5
-
12
-
-
0034681329
-
Inhibition of the Staphylococcus aureus NADPH-dependent enoyl-acyl carrier protein reductase by triclosan and hexachlorophene
-
Heath, R.J., Li, J., Roland, G.E., and Rock, C.O. 2000. Inhibition of the Staphylococcus aureus NADPH-dependent enoyl-acyl carrier protein reductase by triclosan and hexachlorophene. J. Biol. Chem. 275: 4654-4659.
-
(2000)
J. Biol. Chem
, vol.275
, pp. 4654-4659
-
-
Heath, R.J.1
Li, J.2
Roland, G.E.3
Rock, C.O.4
-
13
-
-
0034804919
-
Lipid biosynthesis as a target for antibacterial agents
-
Heath, R.J., White, S.W., and Rock, C.O. 2001. Lipid biosynthesis as a target for antibacterial agents. Prog. Lipid Res. 40: 467-497.
-
(2001)
Prog. Lipid Res
, vol.40
, pp. 467-497
-
-
Heath, R.J.1
White, S.W.2
Rock, C.O.3
-
14
-
-
17944376779
-
1,4-Disubstituted imidazoles are potential antibacterial agents functioning as inhibitors of enoyl-acyl carrier protein reductase (FabI)
-
Heerding, D.A., Chan, G., DeWolf, W.E., Fosberry, A.P., Janson, C.A., Jaworski, D.D., McManus, E., Miller, W.H., Moore, T.D., Payne, D.J., et al. 2001. 1,4-Disubstituted imidazoles are potential antibacterial agents functioning as inhibitors of enoyl-acyl carrier protein reductase (FabI). Bioorg. Med. Chem. Lett. 11: 2061-2065.
-
(2001)
Bioorg. Med. Chem. Lett
, vol.11
, pp. 2061-2065
-
-
Heerding, D.A.1
Chan, G.2
DeWolf, W.E.3
Fosberry, A.P.4
Janson, C.A.5
Jaworski, D.D.6
McManus, E.7
Miller, W.H.8
Moore, T.D.9
Payne, D.J.10
-
15
-
-
34247383568
-
Structure of fungal fatty acid synthase and implications for iterative substrate shuttling
-
Jenni, S., Leibundgut, M., Boehringer, D., Frick, C., Mikolasek, B., and Ban, N. 2007. Structure of fungal fatty acid synthase and implications for iterative substrate shuttling. Science 316: 254-261.
-
(2007)
Science
, vol.316
, pp. 254-261
-
-
Jenni, S.1
Leibundgut, M.2
Boehringer, D.3
Frick, C.4
Mikolasek, B.5
Ban, N.6
-
16
-
-
19344368130
-
Relative fitness of fluoroquinolone-resistant Streptococcus pneumoniae
-
Johnson, C.N., Briles, D.E., Benjamin Jr., W.H., Hollingshead, S.K., and Waites, K.B. 2005. Relative fitness of fluoroquinolone-resistant Streptococcus pneumoniae. Emerg. Infect. Dis. 11: 814-820.
-
(2005)
Emerg. Infect. Dis
, vol.11
, pp. 814-820
-
-
Johnson, C.N.1
Briles, D.E.2
Benjamin Jr., W.H.3
Hollingshead, S.K.4
Waites, K.B.5
-
17
-
-
33845298658
-
4-Pyridone derivatives as new inhibitors of bacterial enoyl-ACP reductase FabI
-
Kitagawa, H., Kumura, K., Takahata, S., Iida, M., and Atsumi, K. 2007a. 4-Pyridone derivatives as new inhibitors of bacterial enoyl-ACP reductase FabI. Bioorg. Med. Chem. Lett. 15: 1106-1116.
-
(2007)
Bioorg. Med. Chem. Lett
, vol.15
, pp. 1106-1116
-
-
Kitagawa, H.1
Kumura, K.2
Takahata, S.3
Iida, M.4
Atsumi, K.5
-
18
-
-
34547553734
-
Phenylimidazole derivatives as new inhibitors of bacterial enoyl-ACP reductase FabK
-
Kitagawa, H., Ozawa, T., Takahata, S., and Iida, M. 2007b. Phenylimidazole derivatives as new inhibitors of bacterial enoyl-ACP reductase FabK. Bioorg. Med. Chem. Lett. 17: 4982-4986.
-
(2007)
Bioorg. Med. Chem. Lett
, vol.17
, pp. 4982-4986
-
-
Kitagawa, H.1
Ozawa, T.2
Takahata, S.3
Iida, M.4
-
19
-
-
34648833337
-
Phenylimidazole derivatives of 4-pyridone as dual inhibitors of bacterial enoyl-acyl carrier protein reductases FabI and FabK
-
Kitagawa, H., Ozawa, T., Takahata, S., Iida, M., Saito, J., and Yamada, M. 2007c. Phenylimidazole derivatives of 4-pyridone as dual inhibitors of bacterial enoyl-acyl carrier protein reductases FabI and FabK. J. Med. Chem. 50: 4710-4720.
-
(2007)
J. Med. Chem
, vol.50
, pp. 4710-4720
-
-
Kitagawa, H.1
Ozawa, T.2
Takahata, S.3
Iida, M.4
Saito, J.5
Yamada, M.6
-
20
-
-
4444265496
-
Kinetic mechanism of quinone oxidoreductase 2 and its inhibition by the antimalarial quinolines
-
Kwiek, J.J., Haystead, T.A., and Rudolph, J. 2004. Kinetic mechanism of quinone oxidoreductase 2 and its inhibition by the antimalarial quinolines. Biochemistry (Mosc.) 43: 4538-4547.
-
(2004)
Biochemistry (Mosc.)
, vol.43
, pp. 4538-4547
-
-
Kwiek, J.J.1
Haystead, T.A.2
Rudolph, J.3
-
21
-
-
0000243829
-
PROCHECK: A program to check the stereochemical quality of protein structures
-
Laskowski, R.A., MacArthur, M.W., Moss, D.S., and Thornton, J.M. 1993. PROCHECK: A program to check the stereochemical quality of protein structures. J. Appl. Crystallogr. 26: 283-291.
-
(1993)
J. Appl. Crystallogr
, vol.26
, pp. 283-291
-
-
Laskowski, R.A.1
MacArthur, M.W.2
Moss, D.S.3
Thornton, J.M.4
-
22
-
-
11144356444
-
Identification and characterization of inhibitors of bacterial enoyl-acyl carrier protein reductase
-
Ling, L.L., Xian, J., Ali, S., Geng, B., Fan, J., Mills, D.M., Arvanites, A.C., Orgueira, H., Ashwell, M.A., Carmel, G., et al. 2004. Identification and characterization of inhibitors of bacterial enoyl-acyl carrier protein reductase. Antimicrob. Agents Chemother. 48: 1541-1547.
-
(2004)
Antimicrob. Agents Chemother
, vol.48
, pp. 1541-1547
-
-
Ling, L.L.1
Xian, J.2
Ali, S.3
Geng, B.4
Fan, J.5
Mills, D.M.6
Arvanites, A.C.7
Orgueira, H.8
Ashwell, M.A.9
Carmel, G.10
-
23
-
-
33644697200
-
Architecture of mammalian fatty acid synthase at 4.5 Å resolution
-
Maier, T., Jenni, S., and Ban, N. 2006. Architecture of mammalian fatty acid synthase at 4.5 Å resolution. Science 311: 1258-1262.
-
(2006)
Science
, vol.311
, pp. 1258-1262
-
-
Maier, T.1
Jenni, S.2
Ban, N.3
-
24
-
-
0037444822
-
Characterization of Streptococcus pneumoniae enoyl-(acyl-carrier protein) reductase (FabK)
-
Marrakchi, H., Dewolf Jr., W.E., Quinn, C., West, J., Polizzi, B.J., So, C.Y., Holmes, D.J., Reed, S.L., Heath, R.J., Payne, D.J., et al. 2003. Characterization of Streptococcus pneumoniae enoyl-(acyl-carrier protein) reductase (FabK). Biochem. J. 370: 1055-1062.
-
(2003)
Biochem. J
, vol.370
, pp. 1055-1062
-
-
Marrakchi, H.1
Dewolf Jr., W.E.2
Quinn, C.3
West, J.4
Polizzi, B.J.5
So, C.Y.6
Holmes, D.J.7
Reed, S.L.8
Heath, R.J.9
Payne, D.J.10
-
25
-
-
0346494932
-
TOPS: An enhanced database of protein structural topology
-
Michalopoulos, I., Torrance, G.M., Gilbert, D.R., and Westhead, D.R. 2004. TOPS: An enhanced database of protein structural topology. Nucleic Acids Res. 32: D251-D254.
-
(2004)
Nucleic Acids Res
, vol.32
-
-
Michalopoulos, I.1
Torrance, G.M.2
Gilbert, D.R.3
Westhead, D.R.4
-
26
-
-
0030924992
-
Refinement of macromolecular structures by the maximum-likelihood method
-
Murshudov, G.N., Vagin, A.A., and Dodson, E.J. 1997. Refinement of macromolecular structures by the maximum-likelihood method. Acta Crystallogr. D Biol. Crystallogr. 53: 240-255.
-
(1997)
Acta Crystallogr. D Biol. Crystallogr
, vol.53
, pp. 240-255
-
-
Murshudov, G.N.1
Vagin, A.A.2
Dodson, E.J.3
-
27
-
-
0036384350
-
One fold with many functions: The evolutionary relationships between TIM barrel families based on their sequences, structures and functions
-
Nagano, N., Orengo, C.A., and Thornton, J.M. 2002. One fold with many functions: The evolutionary relationships between TIM barrel families based on their sequences, structures and functions. J. Mol. Biol. 321: 741-765.
-
(2002)
J. Mol. Biol
, vol.321
, pp. 741-765
-
-
Nagano, N.1
Orengo, C.A.2
Thornton, J.M.3
-
28
-
-
0036783668
-
Discovery of a novel and potent class of FabI-directed antibacterial agents
-
Payne, D.J., Miller, W.H., Berry, V., Brosky, J., Burgess, W.J., Chen, E., DeWolf Jr., W.E., Fosberry, A.P., Greenwood, R., Head, M.S., et al. 2002. Discovery of a novel and potent class of FabI-directed antibacterial agents. Antimicrob. Agents Chemother. 46: 3118-3124.
-
(2002)
Antimicrob. Agents Chemother
, vol.46
, pp. 3118-3124
-
-
Payne, D.J.1
Miller, W.H.2
Berry, V.3
Brosky, J.4
Burgess, W.J.5
Chen, E.6
DeWolf Jr., W.E.7
Fosberry, A.P.8
Greenwood, R.9
Head, M.S.10
-
29
-
-
16644397843
-
Developments in the CCP4 molecular-graphics project
-
Potterton, L., McNicholas, S., Krissinel, E., Gruber, J., Cowtan, K., Emsley, P., Murshudov, G.N., Cohen, S., Perrakis, A., and Noble, M. 2004. Developments in the CCP4 molecular-graphics project. Acta Crystallogr. D Biol. Crystallogr. 60: 2288-2294.
-
(2004)
Acta Crystallogr. D Biol. Crystallogr
, vol.60
, pp. 2288-2294
-
-
Potterton, L.1
McNicholas, S.2
Krissinel, E.3
Gruber, J.4
Cowtan, K.5
Emsley, P.6
Murshudov, G.N.7
Cohen, S.8
Perrakis, A.9
Noble, M.10
-
30
-
-
0029000868
-
Enzymatic characterization of the target for isoniazid in Mycobacterium tuberculosis
-
Quemard, A., Sacchettini, J.C., Dessen, A., Vilcheze, C., Bittman, R., Jacobs Jr., W.R., and Blanchard, J.S. 1995. Enzymatic characterization of the target for isoniazid in Mycobacterium tuberculosis. Biochemistry 34: 8235-8241.
-
(1995)
Biochemistry
, vol.34
, pp. 8235-8241
-
-
Quemard, A.1
Sacchettini, J.C.2
Dessen, A.3
Vilcheze, C.4
Bittman, R.5
Jacobs Jr., W.R.6
Blanchard, J.S.7
-
31
-
-
0030581109
-
Escherichia coli as a model for the regulation of dissociable (type II) fatty acid biosynthesis
-
Rock, C.O. and Cronan, J.E. 1996. Escherichia coli as a model for the regulation of dissociable (type II) fatty acid biosynthesis. Biochim. Biophys. Acta 1302: 1-16.
-
(1996)
Biochim. Biophys. Acta
, vol.1302
, pp. 1-16
-
-
Rock, C.O.1
Cronan, J.E.2
-
32
-
-
33745127323
-
Crystallization and preliminary X-ray analysis of enoyl-acyl carrier protein reductase (FabK) from Streptococcus pneumoniae
-
Saito, J., Yamada, M., Watanabe, T., Kitagawa, H., and Takeuchi, Y. 2006. Crystallization and preliminary X-ray analysis of enoyl-acyl carrier protein reductase (FabK) from Streptococcus pneumoniae. Acta Crystallograph. F Struct. Biol. Cryst. Commun. 62: 576-578.
-
(2006)
Acta Crystallograph. F Struct. Biol. Cryst. Commun
, vol.62
, pp. 576-578
-
-
Saito, J.1
Yamada, M.2
Watanabe, T.3
Kitagawa, H.4
Takeuchi, Y.5
-
33
-
-
17944379321
-
Inhibitors of bacterial enoyl-acyl carrier protein reductase (FabI): 2,9-Disubstituted 1,2,3,4-tetrahydropyrido[3,4-b]indoles as potential antibacterial agents
-
Seefeld, M.A., Miller, W.H., Newlander, K.A., Burgess, W.J., Payne, D.J., Rittenhouse, S.F., Moore, T.D., DeWolf Jr., W.E., Keller, P.M., Qiu, X., et al. 2001. Inhibitors of bacterial enoyl-acyl carrier protein reductase (FabI): 2,9-Disubstituted 1,2,3,4-tetrahydropyrido[3,4-b]indoles as potential antibacterial agents. Bioorg. Med. Chem. Lett. 11: 2241-2244.
-
(2001)
Bioorg. Med. Chem. Lett
, vol.11
, pp. 2241-2244
-
-
Seefeld, M.A.1
Miller, W.H.2
Newlander, K.A.3
Burgess, W.J.4
Payne, D.J.5
Rittenhouse, S.F.6
Moore, T.D.7
DeWolf Jr., W.E.8
Keller, P.M.9
Qiu, X.10
-
34
-
-
0037464456
-
Indole naphthyridinones as inhibitors of bacterial enoyl-ACP reductases FabI and FabK
-
Seefeld, M.A., Miller, W.H., Newlander, K.A., Burgess, W.J., DeWolf Jr., W.E., Elkins, P.A., Head, M.S., Jakas, D.R., Janson, C.A., Keller, P.M., et al. 2003. Indole naphthyridinones as inhibitors of bacterial enoyl-ACP reductases FabI and FabK. J. Med. Chem. 46: 1627-1635.
-
(2003)
J. Med. Chem
, vol.46
, pp. 1627-1635
-
-
Seefeld, M.A.1
Miller, W.H.2
Newlander, K.A.3
Burgess, W.J.4
DeWolf Jr., W.E.5
Elkins, P.A.6
Head, M.S.7
Jakas, D.R.8
Janson, C.A.9
Keller, P.M.10
-
35
-
-
0034922477
-
Biochemical and genetic characterization of the action of triclosan on Staphylococcus aureus
-
Slater-Radosti, C., Van Aller, G., Greenwood, R., Nicholas, R., Keller, P.M., DeWolf Jr., W.E., Fan, F., Payne, D.J., and Jaworski, D.D. 2001. Biochemical and genetic characterization of the action of triclosan on Staphylococcus aureus. J. Antimicrob. Chemother. 48: 1-6.
-
(2001)
J. Antimicrob. Chemother
, vol.48
, pp. 1-6
-
-
Slater-Radosti, C.1
Van Aller, G.2
Greenwood, R.3
Nicholas, R.4
Keller, P.M.5
DeWolf Jr., W.E.6
Fan, F.7
Payne, D.J.8
Jaworski, D.D.9
-
36
-
-
33746892678
-
AG205, a novel agent directed against FabK of Streptococcus pneumoniae
-
Takahata, S., Iida, M., Osaki, Y., Saito, J., Kitagawa, H., Ozawa, T., Yoshida, T., and Hoshiko, S. 2006. AG205, a novel agent directed against FabK of Streptococcus pneumoniae. Antimicrob. Agents Chemother. 50: 2869-2871.
-
(2006)
Antimicrob. Agents Chemother
, vol.50
, pp. 2869-2871
-
-
Takahata, S.1
Iida, M.2
Osaki, Y.3
Saito, J.4
Kitagawa, H.5
Ozawa, T.6
Yoshida, T.7
Hoshiko, S.8
-
37
-
-
34249739592
-
Discovery of 4-pyridone derivatives as specific inhibitors of enoyl-acyl carrier protein reductase (FabI) with antibacterial activity against Staphylococcus aureus
-
Takahata, S., Iida, M., Yoshida, T., Kumura, K., Kitagawa, H., and Hoshiko, S. 2007. Discovery of 4-pyridone derivatives as specific inhibitors of enoyl-acyl carrier protein reductase (FabI) with antibacterial activity against Staphylococcus aureus. J. Antibiot. (Tokyo) 60: 123-128.
-
(2007)
J. Antibiot. (Tokyo)
, vol.60
, pp. 123-128
-
-
Takahata, S.1
Iida, M.2
Yoshida, T.3
Kumura, K.4
Kitagawa, H.5
Hoshiko, S.6
-
39
-
-
0037237545
-
Automated main-chain model building by template matching and iterative fragment extension
-
Terwilliger, T.C. 2003a. Automated main-chain model building by template matching and iterative fragment extension. Acta Crystallogr. D Biol. Crystallogr. 59: 38-44.
-
(2003)
Acta Crystallogr. D Biol. Crystallogr
, vol.59
, pp. 38-44
-
-
Terwilliger, T.C.1
-
40
-
-
0037242985
-
Automated side-chain model building and sequence assignment by template matching
-
Terwilliger, T.C. 2003b. Automated side-chain model building and sequence assignment by template matching. Acta Crystallogr. D Biol. Crystallogr. 59: 45-49.
-
(2003)
Acta Crystallogr. D Biol. Crystallogr
, vol.59
, pp. 45-49
-
-
Terwilliger, T.C.1
-
42
-
-
0035325778
-
Kinetic characterization of the rotenoneinsensitive internal NADH: Ubiquinone oxidoreductase of mitochondria from Saccharomyces cerevisiae
-
Velazquez, I. and Pardo, J.P. 2001. Kinetic characterization of the rotenoneinsensitive internal NADH: Ubiquinone oxidoreductase of mitochondria from Saccharomyces cerevisiae. Arch. Biochem. Biophys. 389: 7-14.
-
(2001)
Arch. Biochem. Biophys
, vol.389
, pp. 7-14
-
-
Velazquez, I.1
Pardo, J.P.2
-
43
-
-
34447263022
-
In vitro activities of CG400549, a novel FabI inhibitor, against recent clinical staphylococcal isolates in Korea
-
Yum, J.H., Kim, C.K., Yong, D., Lee, K., Chong, Y., Kim, C.M., Kim, J.M., Ro, S., and Cho, J.M. 2007. In vitro activities of CG400549, a novel FabI inhibitor, against recent clinical staphylococcal isolates in Korea. Antimicrob. Agents Chemother. 51: 2591-2593.
-
(2007)
Antimicrob. Agents Chemother
, vol.51
, pp. 2591-2593
-
-
Yum, J.H.1
Kim, C.K.2
Yong, D.3
Lee, K.4
Chong, Y.5
Kim, C.M.6
Kim, J.M.7
Ro, S.8
Cho, J.M.9
-
44
-
-
33846811742
-
Atromentin and leucomelone, the first inhibitors specific to enoyl-ACP reductase (FabK) of Streptococcus pneumoniae
-
Zheng, C.J., Sohn, M.J., and Kim, W.G. 2006. Atromentin and leucomelone, the first inhibitors specific to enoyl-ACP reductase (FabK) of Streptococcus pneumoniae. J. Antibiot. (Tokyo) 59: 808-812.
-
(2006)
J. Antibiot. (Tokyo)
, vol.59
, pp. 808-812
-
-
Zheng, C.J.1
Sohn, M.J.2
Kim, W.G.3
|