سينثيز بيتا-كيتواسيل- أيه سي بي III (Arabic Wikipedia)

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4harvard.edu

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1who.int

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archive.org

"Characterization of β-Ketoacyl-Acyl Carrier Protein Synthase III from Streptomyces glaucescens and Its Role in Initiation of Fatty Acid Biosynthesis". J. Bacteriol. ج. 180 ع. 17: 4481–6. 1998. DOI:10.1128/JB.180.17.4481-4486.1998. PMC:107458. PMID:9721286.
"Alteration of the Fatty Acid Profile of Streptomyces coelicolor by Replacement of the Initiation Enzyme 3-Ketoacyl Acyl Carrier Protein Synthase III (FabH)". J. Bacteriol. ج. 187 ع. 11: 3795–9. 2005. DOI:10.1128/JB.187.11.3795-3799.2005. PMC:1112031. PMID:15901703.
"1,2-Dithiole-3-Ones as Potent Inhibitors of the Bacterial 3-Ketoacyl Acyl Carrier Protein Synthase III (FabH)". Antimicrob. Agents Chemother. ج. 48 ع. 8: 3093–102. أغسطس 2004. DOI:10.1128/AAC.48.8.3093-3102.2004. PMC:478545. PMID:15273125.
"Discovery of FabH/FabF Inhibitors from Natural Products". Antimicrob. Agents Chemother. ج. 50 ع. 2: 519–26. فبراير 2006. DOI:10.1128/AAC.50.2.519-526.2006. PMC:1366929. PMID:16436705.
"Mycolic Acid Index Susceptibility Method for Mycobacterium tuberculosis". J. Clin. Microbiol. ج. 39 ع. 7: 2642–5. يوليو 2001. DOI:10.1128/JCM.39.7.2642-2645.2001. PMC:88200. PMID:11427584.

doi.org

Davies C، Heath RJ، White SW، Rock CO (2000). "The 1.8 A crystal structure and active-site architecture of beta-ketoacyl-acyl carrier protein synthase III (FabH) from escherichia coli". Structure. ج. 8 ع. 2: 185–95. DOI:10.1016/S0969-2126(00)00094-0. PMID:10673437.
Davies C, Heath RJ, White SW, Rock CO (2000). "The 1.8 A crystal structure and active-site architecture of beta-ketoacyl-acyl carrier protein synthase III (FabH) from escherichia coli". Structure. 8 (2): 185–95. doi:10.1016/S0969-2126(00)00094-0. PMID 10673437. نسخة محفوظة 2023-02-14 على موقع واي باك مشين.
"Characterization of β-Ketoacyl-Acyl Carrier Protein Synthase III from Streptomyces glaucescens and Its Role in Initiation of Fatty Acid Biosynthesis". J. Bacteriol. ج. 180 ع. 17: 4481–6. 1998. DOI:10.1128/JB.180.17.4481-4486.1998. PMC:107458. PMID:9721286.
"Identification, substrate specificity, and inhibition of the Streptococcus pneumoniae beta-ketoacyl-acyl carrier protein synthase III (FabH)". J. Biol. Chem. ج. 276 ع. 32: 30024–30. 2001. DOI:10.1074/jbc.M101769200. PMID:11375394.{{استشهاد بدورية محكمة}}: صيانة الاستشهاد: دوي مجاني غير معلم (link)
"Alteration of the Fatty Acid Profile of Streptomyces coelicolor by Replacement of the Initiation Enzyme 3-Ketoacyl Acyl Carrier Protein Synthase III (FabH)". J. Bacteriol. ج. 187 ع. 11: 3795–9. 2005. DOI:10.1128/JB.187.11.3795-3799.2005. PMC:1112031. PMID:15901703.
"The Mycobacterium tuberculosis FAS-II condensing enzymes: their role in mycolic acid biosynthesis, acid-fastness, pathogenesis and in future drug development". Mol. Microbiol. ج. 64 ع. 6: 1442–54. يونيو 2007. DOI:10.1111/j.1365-2958.2007.05761.x. PMID:17555433.
"Flux Balance Analysis of Mycolic Acid Pathway: Targets for Anti-Tubercular Drugs". PLOS Comput. Biol. ج. 1 ع. 5: e46. أكتوبر 2005. Bibcode:2005PLSCB...1...46R. DOI:10.1371/journal.pcbi.0010046. PMC:1246807. PMID:16261191.{{استشهاد بدورية محكمة}}: صيانة الاستشهاد: دوي مجاني غير معلم (link)
"Genes required for mycobacterial growth defined by high density mutagenesis". Mol. Microbiol. ج. 48 ع. 1: 77–84. أبريل 2003. DOI:10.1046/j.1365-2958.2003.03425.x. PMID:12657046.
ببب: 1HND, 1HNH, 1HNJ; "Refined structures of beta-ketoacyl-acyl carrier protein synthase III". J. Mol. Biol. ج. 307 ع. 1: 341–56. مارس 2001. DOI:10.1006/jmbi.2000.4457. PMID:11243824.
ببب: 1HZP; "Crystal structure of the Mycobacterium tuberculosis beta-ketoacyl-acyl carrier protein synthase III". J. Biol. Chem. ج. 276 ع. 23: 20516–22. يونيو 2001. DOI:10.1074/jbc.M010762200. PMID:11278743.{{استشهاد بدورية محكمة}}: صيانة الاستشهاد: دوي مجاني غير معلم (link)
ببب: 1ZOW; "Crystal structure and substrate specificity of the β-ketoacyl-acyl carrier protein synthase III (FabH) from Staphylococcus aureus". Protein Sci. ج. 14 ع. 8: 2087–94. أغسطس 2005. DOI:10.1110/ps.051501605. PMC:2279320. PMID:15987898.
ببب: 1HN9; "Crystal structure of beta-ketoacyl-acyl carrier protein synthase III. A key condensing enzyme in bacterial fatty acid biosynthesis". J. Biol. Chem. ج. 274 ع. 51: 36465–71. ديسمبر 1999. DOI:10.1074/jbc.274.51.36465. PMID:10593943.{{استشهاد بدورية محكمة}}: صيانة الاستشهاد: دوي مجاني غير معلم (link)
"Identification and substrate specificity of beta -ketoacyl (acyl carrier protein) synthase III (mtFabH) from Mycobacterium tuberculosis". J. Biol. Chem. ج. 275 ع. 36: 28201–7. سبتمبر 2000. DOI:10.1074/jbc.M003241200. PMID:10840036.{{استشهاد بدورية محكمة}}: صيانة الاستشهاد: دوي مجاني غير معلم (link)
ببب: 1M1M, 2AJ9; "Probing the mechanism of the Mycobacterium tuberculosis beta-ketoacyl-acyl carrier protein synthase III mtFabH: factors influencing catalysis and substrate specificity". J. Biol. Chem. ج. 280 ع. 37: 32539–47. سبتمبر 2005. DOI:10.1074/jbc.M413216200. PMID:16040614.{{استشهاد بدورية محكمة}}: صيانة الاستشهاد: دوي مجاني غير معلم (link)
ببب: 1HND, 1HNH, 1HNJ; "Refined structures of beta-ketoacyl-acyl carrier protein synthase III". J. Mol. Biol. ج. 307 ع. 1: 341–56. مارس 2001. DOI:10.1006/jmbi.2000.4457. PMID:11243824.Qiu X, Janson CA, Smith WW, Head M, Lonsdale J, Konstantinidis AK (March 2001).
ببب: 1MZS; "First X-ray cocrystal structure of a bacterial FabH condensing enzyme and a small molecule inhibitor achieved using rational design and homology modeling". J. Med. Chem. ج. 46 ع. 1: 5–8. يناير 2003. DOI:10.1021/jm025571b. PMID:12502353.
"Structure-based design, synthesis, and study of potent inhibitors of beta-ketoacyl-acyl carrier protein synthase III as potential antimicrobial agents". J. Med. Chem. ج. 48 ع. 5: 1596–609. مارس 2005. DOI:10.1021/jm049141s. PMID:15743201.
"A combined approach of docking and 3D QSAR study of beta-ketoacyl-acyl carrier protein synthase III (FabH) inhibitors". Bioorg. Med. Chem. ج. 14 ع. 5: 1474–82. مارس 2006. DOI:10.1016/j.bmc.2005.10.001. PMID:16275103.
ببب: 1U6S; "Crystal structure of a substrate complex of Mycobacterium tuberculosis beta-ketoacyl-acyl carrier protein synthase III (FabH) with lauroyl-coenzyme A". J. Mol. Biol. ج. 346 ع. 5: 1313–21. مارس 2005. DOI:10.1016/j.jmb.2004.12.044. PMID:15713483.
"The Mycobacterium tuberculosis β-Ketoacyl-Acyl Carrier Protein Synthase III Activity Is Inhibited by Phosphorylation on a Single Threonine Residue". J. Biol. Chem. ج. 284 ع. 10: 6414–24. مارس 2009. DOI:10.1074/jbc.M806537200. PMC:2649087. PMID:19074144.{{استشهاد بدورية محكمة}}: صيانة الاستشهاد: دوي مجاني غير معلم (link)
"Drugs that inhibit mycolic acid biosynthesis in Mycobacterium tuberculosis". Curr Pharm Biotechnol. ج. 3 ع. 3: 197–225. سبتمبر 2002. DOI:10.2174/1389201023378328. PMID:12164478.
"Biphenyl-based analogues of thiolactomycin, active against Mycobacterium tuberculosis mtFabH fatty acid condensing enzyme". Bioorg. Med. Chem. Lett. ج. 13 ع. 21: 3685–8. نوفمبر 2003. DOI:10.1016/j.bmcl.2003.08.015. PMID:14552758.
"Acetylene-based analogues of thiolactomycin, active against Mycobacterium tuberculosis mtFabH fatty acid condensing enzyme". Bioorg. Med. Chem. Lett. ج. 14 ع. 2: 373–6. يناير 2004. DOI:10.1016/j.bmcl.2003.10.061. PMID:14698162.
"1,2-Dithiole-3-Ones as Potent Inhibitors of the Bacterial 3-Ketoacyl Acyl Carrier Protein Synthase III (FabH)". Antimicrob. Agents Chemother. ج. 48 ع. 8: 3093–102. أغسطس 2004. DOI:10.1128/AAC.48.8.3093-3102.2004. PMC:478545. PMID:15273125.
Todd، Matthew H.، المحرر (2009). "Identification of 2-Aminothiazole-4-Carboxylate Derivatives Active against Mycobacterium tuberculosis H37Rv and the β-Ketoacyl-ACP Synthase mtFabH". PLOS ONE. ج. 4 ع. 5: e5617. Bibcode:2009PLoSO...4.5617A. DOI:10.1371/journal.pone.0005617. PMC:2680598. PMID:19440303.{{استشهاد بدورية محكمة}}: صيانة الاستشهاد: دوي مجاني غير معلم (link)
"The Mycobacterium tuberculosis β-Ketoacyl-Acyl Carrier Protein Synthase III Activity Is Inhibited by Phosphorylation on a Single Threonine Residue". J. Biol. Chem. ج. 284 ع. 10: 6414–24. مارس 2009. DOI:10.1074/jbc.M806537200. PMC:2649087. PMID:19074144.{{استشهاد بدورية محكمة}}: صيانة الاستشهاد: دوي مجاني غير معلم (link)Veyron-Churlet R, Molle V, Taylor RC, Brown AK, Besra GS, Zanella-Cléon I, Fütterer K, Kremer L (March 2009).
"Discovery of FabH/FabF Inhibitors from Natural Products". Antimicrob. Agents Chemother. ج. 50 ع. 2: 519–26. فبراير 2006. DOI:10.1128/AAC.50.2.519-526.2006. PMC:1366929. PMID:16436705.
"Discovery of bacterial fatty acid synthase inhibitors from a Phoma species as antimicrobial agents using a new antisense-based strategy". J. Nat. Prod. ج. 69 ع. 3: 377–80. مارس 2006. DOI:10.1021/np050416w. PMID:16562839.
"Discovery of platencin, a dual FabF and FabH inhibitor with in vivo antibiotic properties". Proceedings of the National Academy of Sciences of the United States of America. ج. 104 ع. 18: 7612–6. مايو 2007. Bibcode:2007PNAS..104.7612W. DOI:10.1073/pnas.0700746104. PMC:1863502. PMID:17456595.
Ahmed، Niyaz، المحرر (2009). "Platensimycin Activity against Mycobacterial β-Ketoacyl-ACP Synthases". PLOS ONE. ج. 4 ع. 7: e6306. Bibcode:2009PLoSO...4.6306B. DOI:10.1371/journal.pone.0006306. PMC:2707616. PMID:19609444.{{استشهاد بدورية محكمة}}: صيانة الاستشهاد: دوي مجاني غير معلم (link)
"Mycolic Acid Index Susceptibility Method for Mycobacterium tuberculosis". J. Clin. Microbiol. ج. 39 ع. 7: 2642–5. يوليو 2001. DOI:10.1128/JCM.39.7.2642-2645.2001. PMC:88200. PMID:11427584.
"Development of a scintillation proximity assay for beta-ketoacyl-acyl carrier protein synthase III". Anal. Biochem. ج. 282 ع. 1: 107–14. يونيو 2000. DOI:10.1006/abio.2000.4594. PMID:10860506.
"The growing burden of tuberculosis: global trends and interactions with the HIV epidemic". Arch. Intern. Med. ج. 163 ع. 9: 1009–21. مايو 2003. DOI:10.1001/archinte.163.9.1009. PMID:12742798.

harvard.edu

ui.adsabs.harvard.edu

"Flux Balance Analysis of Mycolic Acid Pathway: Targets for Anti-Tubercular Drugs". PLOS Comput. Biol. ج. 1 ع. 5: e46. أكتوبر 2005. Bibcode:2005PLSCB...1...46R. DOI:10.1371/journal.pcbi.0010046. PMC:1246807. PMID:16261191.{{استشهاد بدورية محكمة}}: صيانة الاستشهاد: دوي مجاني غير معلم (link)
Todd، Matthew H.، المحرر (2009). "Identification of 2-Aminothiazole-4-Carboxylate Derivatives Active against Mycobacterium tuberculosis H37Rv and the β-Ketoacyl-ACP Synthase mtFabH". PLOS ONE. ج. 4 ع. 5: e5617. Bibcode:2009PLoSO...4.5617A. DOI:10.1371/journal.pone.0005617. PMC:2680598. PMID:19440303.{{استشهاد بدورية محكمة}}: صيانة الاستشهاد: دوي مجاني غير معلم (link)
"Discovery of platencin, a dual FabF and FabH inhibitor with in vivo antibiotic properties". Proceedings of the National Academy of Sciences of the United States of America. ج. 104 ع. 18: 7612–6. مايو 2007. Bibcode:2007PNAS..104.7612W. DOI:10.1073/pnas.0700746104. PMC:1863502. PMID:17456595.
Ahmed، Niyaz، المحرر (2009). "Platensimycin Activity against Mycobacterial β-Ketoacyl-ACP Synthases". PLOS ONE. ج. 4 ع. 7: e6306. Bibcode:2009PLoSO...4.6306B. DOI:10.1371/journal.pone.0006306. PMC:2707616. PMID:19609444.{{استشهاد بدورية محكمة}}: صيانة الاستشهاد: دوي مجاني غير معلم (link)

nih.gov

pubmed.ncbi.nlm.nih.gov

Davies C، Heath RJ، White SW، Rock CO (2000). "The 1.8 A crystal structure and active-site architecture of beta-ketoacyl-acyl carrier protein synthase III (FabH) from escherichia coli". Structure. ج. 8 ع. 2: 185–95. DOI:10.1016/S0969-2126(00)00094-0. PMID:10673437.
Davies C, Heath RJ, White SW, Rock CO (2000). "The 1.8 A crystal structure and active-site architecture of beta-ketoacyl-acyl carrier protein synthase III (FabH) from escherichia coli". Structure. 8 (2): 185–95. doi:10.1016/S0969-2126(00)00094-0. PMID 10673437. نسخة محفوظة 2023-02-14 على موقع واي باك مشين.
"Characterization of β-Ketoacyl-Acyl Carrier Protein Synthase III from Streptomyces glaucescens and Its Role in Initiation of Fatty Acid Biosynthesis". J. Bacteriol. ج. 180 ع. 17: 4481–6. 1998. DOI:10.1128/JB.180.17.4481-4486.1998. PMC:107458. PMID:9721286.
"Identification, substrate specificity, and inhibition of the Streptococcus pneumoniae beta-ketoacyl-acyl carrier protein synthase III (FabH)". J. Biol. Chem. ج. 276 ع. 32: 30024–30. 2001. DOI:10.1074/jbc.M101769200. PMID:11375394.{{استشهاد بدورية محكمة}}: صيانة الاستشهاد: دوي مجاني غير معلم (link)
"Alteration of the Fatty Acid Profile of Streptomyces coelicolor by Replacement of the Initiation Enzyme 3-Ketoacyl Acyl Carrier Protein Synthase III (FabH)". J. Bacteriol. ج. 187 ع. 11: 3795–9. 2005. DOI:10.1128/JB.187.11.3795-3799.2005. PMC:1112031. PMID:15901703.
"The Mycobacterium tuberculosis FAS-II condensing enzymes: their role in mycolic acid biosynthesis, acid-fastness, pathogenesis and in future drug development". Mol. Microbiol. ج. 64 ع. 6: 1442–54. يونيو 2007. DOI:10.1111/j.1365-2958.2007.05761.x. PMID:17555433.
"Flux Balance Analysis of Mycolic Acid Pathway: Targets for Anti-Tubercular Drugs". PLOS Comput. Biol. ج. 1 ع. 5: e46. أكتوبر 2005. Bibcode:2005PLSCB...1...46R. DOI:10.1371/journal.pcbi.0010046. PMC:1246807. PMID:16261191.{{استشهاد بدورية محكمة}}: صيانة الاستشهاد: دوي مجاني غير معلم (link)
"Genes required for mycobacterial growth defined by high density mutagenesis". Mol. Microbiol. ج. 48 ع. 1: 77–84. أبريل 2003. DOI:10.1046/j.1365-2958.2003.03425.x. PMID:12657046.
ببب: 1HND, 1HNH, 1HNJ; "Refined structures of beta-ketoacyl-acyl carrier protein synthase III". J. Mol. Biol. ج. 307 ع. 1: 341–56. مارس 2001. DOI:10.1006/jmbi.2000.4457. PMID:11243824.
ببب: 1HZP; "Crystal structure of the Mycobacterium tuberculosis beta-ketoacyl-acyl carrier protein synthase III". J. Biol. Chem. ج. 276 ع. 23: 20516–22. يونيو 2001. DOI:10.1074/jbc.M010762200. PMID:11278743.{{استشهاد بدورية محكمة}}: صيانة الاستشهاد: دوي مجاني غير معلم (link)
ببب: 1ZOW; "Crystal structure and substrate specificity of the β-ketoacyl-acyl carrier protein synthase III (FabH) from Staphylococcus aureus". Protein Sci. ج. 14 ع. 8: 2087–94. أغسطس 2005. DOI:10.1110/ps.051501605. PMC:2279320. PMID:15987898.
ببب: 1HN9; "Crystal structure of beta-ketoacyl-acyl carrier protein synthase III. A key condensing enzyme in bacterial fatty acid biosynthesis". J. Biol. Chem. ج. 274 ع. 51: 36465–71. ديسمبر 1999. DOI:10.1074/jbc.274.51.36465. PMID:10593943.{{استشهاد بدورية محكمة}}: صيانة الاستشهاد: دوي مجاني غير معلم (link)
"Identification and substrate specificity of beta -ketoacyl (acyl carrier protein) synthase III (mtFabH) from Mycobacterium tuberculosis". J. Biol. Chem. ج. 275 ع. 36: 28201–7. سبتمبر 2000. DOI:10.1074/jbc.M003241200. PMID:10840036.{{استشهاد بدورية محكمة}}: صيانة الاستشهاد: دوي مجاني غير معلم (link)
ببب: 1M1M, 2AJ9; "Probing the mechanism of the Mycobacterium tuberculosis beta-ketoacyl-acyl carrier protein synthase III mtFabH: factors influencing catalysis and substrate specificity". J. Biol. Chem. ج. 280 ع. 37: 32539–47. سبتمبر 2005. DOI:10.1074/jbc.M413216200. PMID:16040614.{{استشهاد بدورية محكمة}}: صيانة الاستشهاد: دوي مجاني غير معلم (link)
ببب: 1HND, 1HNH, 1HNJ; "Refined structures of beta-ketoacyl-acyl carrier protein synthase III". J. Mol. Biol. ج. 307 ع. 1: 341–56. مارس 2001. DOI:10.1006/jmbi.2000.4457. PMID:11243824.Qiu X, Janson CA, Smith WW, Head M, Lonsdale J, Konstantinidis AK (March 2001).
ببب: 1MZS; "First X-ray cocrystal structure of a bacterial FabH condensing enzyme and a small molecule inhibitor achieved using rational design and homology modeling". J. Med. Chem. ج. 46 ع. 1: 5–8. يناير 2003. DOI:10.1021/jm025571b. PMID:12502353.
"Structure-based design, synthesis, and study of potent inhibitors of beta-ketoacyl-acyl carrier protein synthase III as potential antimicrobial agents". J. Med. Chem. ج. 48 ع. 5: 1596–609. مارس 2005. DOI:10.1021/jm049141s. PMID:15743201.
"A combined approach of docking and 3D QSAR study of beta-ketoacyl-acyl carrier protein synthase III (FabH) inhibitors". Bioorg. Med. Chem. ج. 14 ع. 5: 1474–82. مارس 2006. DOI:10.1016/j.bmc.2005.10.001. PMID:16275103.
ببب: 1U6S; "Crystal structure of a substrate complex of Mycobacterium tuberculosis beta-ketoacyl-acyl carrier protein synthase III (FabH) with lauroyl-coenzyme A". J. Mol. Biol. ج. 346 ع. 5: 1313–21. مارس 2005. DOI:10.1016/j.jmb.2004.12.044. PMID:15713483.
"The Mycobacterium tuberculosis β-Ketoacyl-Acyl Carrier Protein Synthase III Activity Is Inhibited by Phosphorylation on a Single Threonine Residue". J. Biol. Chem. ج. 284 ع. 10: 6414–24. مارس 2009. DOI:10.1074/jbc.M806537200. PMC:2649087. PMID:19074144.{{استشهاد بدورية محكمة}}: صيانة الاستشهاد: دوي مجاني غير معلم (link)
"Drugs that inhibit mycolic acid biosynthesis in Mycobacterium tuberculosis". Curr Pharm Biotechnol. ج. 3 ع. 3: 197–225. سبتمبر 2002. DOI:10.2174/1389201023378328. PMID:12164478.
"Biphenyl-based analogues of thiolactomycin, active against Mycobacterium tuberculosis mtFabH fatty acid condensing enzyme". Bioorg. Med. Chem. Lett. ج. 13 ع. 21: 3685–8. نوفمبر 2003. DOI:10.1016/j.bmcl.2003.08.015. PMID:14552758.
"Acetylene-based analogues of thiolactomycin, active against Mycobacterium tuberculosis mtFabH fatty acid condensing enzyme". Bioorg. Med. Chem. Lett. ج. 14 ع. 2: 373–6. يناير 2004. DOI:10.1016/j.bmcl.2003.10.061. PMID:14698162.
"1,2-Dithiole-3-Ones as Potent Inhibitors of the Bacterial 3-Ketoacyl Acyl Carrier Protein Synthase III (FabH)". Antimicrob. Agents Chemother. ج. 48 ع. 8: 3093–102. أغسطس 2004. DOI:10.1128/AAC.48.8.3093-3102.2004. PMC:478545. PMID:15273125.
Todd، Matthew H.، المحرر (2009). "Identification of 2-Aminothiazole-4-Carboxylate Derivatives Active against Mycobacterium tuberculosis H37Rv and the β-Ketoacyl-ACP Synthase mtFabH". PLOS ONE. ج. 4 ع. 5: e5617. Bibcode:2009PLoSO...4.5617A. DOI:10.1371/journal.pone.0005617. PMC:2680598. PMID:19440303.{{استشهاد بدورية محكمة}}: صيانة الاستشهاد: دوي مجاني غير معلم (link)
"The Mycobacterium tuberculosis β-Ketoacyl-Acyl Carrier Protein Synthase III Activity Is Inhibited by Phosphorylation on a Single Threonine Residue". J. Biol. Chem. ج. 284 ع. 10: 6414–24. مارس 2009. DOI:10.1074/jbc.M806537200. PMC:2649087. PMID:19074144.{{استشهاد بدورية محكمة}}: صيانة الاستشهاد: دوي مجاني غير معلم (link)Veyron-Churlet R, Molle V, Taylor RC, Brown AK, Besra GS, Zanella-Cléon I, Fütterer K, Kremer L (March 2009).
"Discovery of FabH/FabF Inhibitors from Natural Products". Antimicrob. Agents Chemother. ج. 50 ع. 2: 519–26. فبراير 2006. DOI:10.1128/AAC.50.2.519-526.2006. PMC:1366929. PMID:16436705.
"Discovery of bacterial fatty acid synthase inhibitors from a Phoma species as antimicrobial agents using a new antisense-based strategy". J. Nat. Prod. ج. 69 ع. 3: 377–80. مارس 2006. DOI:10.1021/np050416w. PMID:16562839.
"Discovery of platencin, a dual FabF and FabH inhibitor with in vivo antibiotic properties". Proceedings of the National Academy of Sciences of the United States of America. ج. 104 ع. 18: 7612–6. مايو 2007. Bibcode:2007PNAS..104.7612W. DOI:10.1073/pnas.0700746104. PMC:1863502. PMID:17456595.
Ahmed، Niyaz، المحرر (2009). "Platensimycin Activity against Mycobacterial β-Ketoacyl-ACP Synthases". PLOS ONE. ج. 4 ع. 7: e6306. Bibcode:2009PLoSO...4.6306B. DOI:10.1371/journal.pone.0006306. PMC:2707616. PMID:19609444.{{استشهاد بدورية محكمة}}: صيانة الاستشهاد: دوي مجاني غير معلم (link)
"Mycolic Acid Index Susceptibility Method for Mycobacterium tuberculosis". J. Clin. Microbiol. ج. 39 ع. 7: 2642–5. يوليو 2001. DOI:10.1128/JCM.39.7.2642-2645.2001. PMC:88200. PMID:11427584.
"Development of a scintillation proximity assay for beta-ketoacyl-acyl carrier protein synthase III". Anal. Biochem. ج. 282 ع. 1: 107–14. يونيو 2000. DOI:10.1006/abio.2000.4594. PMID:10860506.
"The growing burden of tuberculosis: global trends and interactions with the HIV epidemic". Arch. Intern. Med. ج. 163 ع. 9: 1009–21. مايو 2003. DOI:10.1001/archinte.163.9.1009. PMID:12742798.

ncbi.nlm.nih.gov

"Characterization of β-Ketoacyl-Acyl Carrier Protein Synthase III from Streptomyces glaucescens and Its Role in Initiation of Fatty Acid Biosynthesis". J. Bacteriol. ج. 180 ع. 17: 4481–6. 1998. DOI:10.1128/JB.180.17.4481-4486.1998. PMC:107458. PMID:9721286.
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rcsb.org

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web.archive.org

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who.int

"Global Tuberculosis Control 2007". World Health Organization. 2007. مؤرشف من الأصل في 2010-02-02. اطلع عليه بتاريخ 2010-01-02.