Year |
Citation |
Score |
2023 |
Scully TW, Jiao W, Mittelstädt G, Parker EJ. Structure, mechanism and inhibition of anthranilate phosphoribosyltransferase. Philosophical Transactions of the Royal Society of London. Series B, Biological Sciences. 378: 20220039. PMID 36633281 DOI: 10.1098/rstb.2022.0039 |
0.421 |
|
2022 |
Bai Y, Jiao W, Vörster J, Parker EJ. Conformational interdomain flexibility in a bacterial α-isopropylmalate synthase is necessary for leucine biosynthesis. The Journal of Biological Chemistry. 102789. PMID 36509144 DOI: 10.1016/j.jbc.2022.102789 |
0.311 |
|
2022 |
Jiao W, Mittelstädt G, Parker EJ. Precise Positioning of Water Is Critical for Hydrolysis Catalyzed by 5'-Methylthioadenosine Nucleosidase. Biochemistry. PMID 35969806 DOI: 10.1021/acs.biochem.2c00351 |
0.365 |
|
2021 |
Bai Y, Parker EJ. Reciprocal allostery arising from a bi-enzyme assembly controls aromatic amino acid biosynthesis in Prevotella nigrescens. The Journal of Biological Chemistry. 101038. PMID 34343567 DOI: 10.1016/j.jbc.2021.101038 |
0.433 |
|
2020 |
Jiao W, Lang EJ, Bai Y, Fan Y, Parker EJ. Diverse allosteric componentry and mechanisms control entry into aromatic metabolite biosynthesis. Current Opinion in Structural Biology. 65: 159-167. PMID 32739636 DOI: 10.1016/J.Sbi.2020.06.015 |
0.454 |
|
2020 |
Jiao W, Fan Y, Blackmore NJ, Parker EJ. A single amino acid substitution uncouples catalysis and allostery in an essential biosynthetic enzyme in Mycobacterium tuberculosis. The Journal of Biological Chemistry. PMID 32217694 DOI: 10.1074/Jbc.Ra120.012605 |
0.486 |
|
2019 |
Van de Bittner KC, Cameron RC, Bustamante LY, Bundela R, Kessans SA, Vorster J, Nicholson MJ, Parker EJ. Nodulisporic acid E biosynthesis: characterisation of NodD1, an indole-diterpene prenyltransferase that acts on an emindole SB derived indole-diterpene scaffold. Medchemcomm. 10: 1160-1164. PMID 31391888 DOI: 10.1039/C9Md00143C |
0.453 |
|
2019 |
Jiao W, Mittelstädt G, Moggré GJ, Parker EJ. Hinge Twists and Population Shifts Deliver Regulated Catalysis for ATP-PRT in Histidine Biosynthesis. Biophysical Journal. PMID 31053263 DOI: 10.1016/J.Bpj.2019.03.040 |
0.47 |
|
2019 |
Bai Y, Lang EJM, Nazmi AR, Parker EJ. Domain cross-talk within a bifunctional enzyme provides catalytic and allosteric functionality in the biosynthesis of aromatic amino acids. The Journal of Biological Chemistry. PMID 30670586 DOI: 10.1074/Jbc.Ra118.005220 |
0.453 |
|
2018 |
Sterritt OW, Lang EJM, Kessans SA, Ryan TM, Demeler B, Jameson GB, Parker EJ. The short-form type II DAH7PS from , associated with phenazine biosynthesis, suggests reclassification of type II enzymes. Bioscience Reports. PMID 30242059 DOI: 10.1042/Bsr20181605 |
0.397 |
|
2018 |
Heikal A, Nakatani Y, Jiao W, Wilson C, Rennison D, Weimar MR, Parker EJ, Brimble MA, Cook GM. 'Tethering' fragment-based drug discovery to identify inhibitors of the essential respiratory membrane protein type II NADH dehydrogenase. Bioorganic & Medicinal Chemistry Letters. PMID 29859905 DOI: 10.1016/J.Bmcl.2018.05.048 |
0.346 |
|
2018 |
Petri J, Shimaki Y, Jiao W, Bridges HR, Russell ER, Parker EJ, Aragão D, Cook GM, Nakatani Y. Structure of the NDH-2 - HQNO inhibited complex provides molecular insight into quinone-binding site inhibitors. Biochimica Et Biophysica Acta. PMID 29621505 DOI: 10.1016/J.Bbabio.2018.03.014 |
0.393 |
|
2018 |
Sterritt O, Kessans SA, Jameson GB, Parker EJ. A pseudo-isostructural type II DAH7PS enzyme from Pseudomonas aeruginosa: alternative evolutionary strategies to control shikimate pathway flux. Biochemistry. PMID 29608284 DOI: 10.1021/Acs.Biochem.8B00082 |
0.459 |
|
2018 |
Fan Y, Cross PJ, Jameson GB, Parker EJ. Exploring modular allostery via interchangeable regulatory domains. Proceedings of the National Academy of Sciences of the United States of America. PMID 29507215 DOI: 10.1073/Pnas.1717621115 |
0.357 |
|
2017 |
Mittelstädt G, Jiao W, Livingstone E, Moggré GJ, Nazmi AR, Parker EJ. A dimeric catalytic core relates the short and long forms of ATP-phosphoribosyltransferase. The Biochemical Journal. PMID 29208762 DOI: 10.1042/Bcj20170762 |
0.401 |
|
2017 |
Evans GL, Furkert DP, Abermil N, Kundu P, de Lange KM, Parker EJ, Brimble MA, Baker EN, Lott JS. Datasets, processing and refinement details for Mtb-AnPRT: inhibitor structures with various space groups. Data in Brief. 15: 1019-1029. PMID 29167811 DOI: 10.1016/J.Dib.2017.10.051 |
0.341 |
|
2017 |
Nakatani Y, Jiao W, Aragão D, Shimaki Y, Petri J, Parker EJ, Cook GM. Crystal structure of type II NADH:quinone oxidoreductase from Caldalkalibacillus thermarum with an improved resolution of 2.15 Å. Acta Crystallographica. Section F, Structural Biology Communications. 73: 541-549. PMID 28994401 DOI: 10.1107/S2053230X17013073 |
0.372 |
|
2017 |
Moggré GJ, Poulin MB, Tyler PC, Schramm VL, Parker EJ. Transition state analysis of adenosine triphosphate phosphoribosyltransferase. Acs Chemical Biology. PMID 28872824 DOI: 10.1021/Acschembio.7B00484 |
0.459 |
|
2017 |
Evans GL, Furkert DP, Abermil N, Kundu P, de Lange KM, Parker EJ, Brimble MA, Baker EN, Shaun Lott J. Anthranilate phosphoribosyltransferase: Binding determinants for 5'-phospho-alpha-d-ribosyl-1'-pyrophosphate (PRPP) and the implications for inhibitor design. Biochimica Et Biophysica Acta. PMID 28844746 DOI: 10.1016/J.Bbapap.2017.08.018 |
0.414 |
|
2017 |
Jiao W, Blackmore NJ, Nazmi AR, Parker EJ. Quaternary structure is an essential component that contributes to the sophisticated allosteric regulation mechanism in a key enzyme from Mycobacterium tuberculosis. Plos One. 12: e0180052. PMID 28665948 DOI: 10.1371/Journal.Pone.0180052 |
0.506 |
|
2016 |
Nazmi AR, Lang EJ, Bai Y, Allison TM, Othman MH, Panjikar S, Arcus VL, Parker EJ. Interdomain Conformational Changes Provide Allosteric Regulation En Route To Chorismate. The Journal of Biological Chemistry. PMID 27502275 DOI: 10.1074/Jbc.M116.741637 |
0.449 |
|
2016 |
Livingstone EK, Mittelstädt G, Given FM, Parker EJ. Independent catalysis of the short form HisG from Lactococcus lactis. Febs Letters. PMID 27393206 DOI: 10.1002/1873-3468.12277 |
0.352 |
|
2016 |
Mittelstädt G, Moggré GJ, Panjikar S, Nazmi AR, Parker EJ. Campylobacter jejuni adenosine triphosphate phosphoribosyltransferase is an active hexamer which is allosterically controlled by the twisting of a regulatory tail. Protein Science : a Publication of the Protein Society. PMID 27191057 DOI: 10.1002/Pro.2948 |
0.449 |
|
2016 |
Reichau S, Blackmore NJ, Jiao W, Parker EJ. Probing the Sophisticated Synergistic Allosteric Regulation of Aromatic Amino Acid Biosynthesis in Mycobacterium tuberculosis Using ᴅ-Amino Acids. Plos One. 11: e0152723. PMID 27128682 DOI: 10.1371/Journal.Pone.0152723 |
0.458 |
|
2016 |
Arturo EC, Gupta K, Héroux A, Stith L, Cross PJ, Parker EJ, Loll PJ, Jaffe EK. First structure of full-length mammalian phenylalanine hydroxylase reveals the architecture of an autoinhibited tetramer. Proceedings of the National Academy of Sciences of the United States of America. PMID 26884182 DOI: 10.1073/Pnas.1516967113 |
0.383 |
|
2016 |
Arcus VL, Prentice EJ, Hobbs JK, Mulholland AJ, van der Kamp MW, Pudney CR, Parker EJ, Schipper LA. On the Temperature Dependence of Enzyme-catalyzed Rates. Biochemistry. PMID 26881922 DOI: 10.1021/Acs.Biochem.5B01094 |
0.44 |
|
2016 |
Cross PJ, Heyes LC, Zhang S, Nazmi AR, Parker EJ. The Functional Unit of Neisseria meningitidis 3-Deoxy-ᴅ-Arabino-Heptulosonate 7-Phosphate Synthase Is Dimeric. Plos One. 11: e0145187. PMID 26828675 DOI: 10.1371/Journal.Pone.0145187 |
0.471 |
|
2016 |
Lang EJ, Heyes LC, Jameson GB, Parker EJ. Calculated pKa variations expose dynamic allosteric communication networks. Journal of the American Chemical Society. PMID 26794122 DOI: 10.1021/Jacs.5B13134 |
0.424 |
|
2015 |
Cookson TV, Evans GL, Castell A, Baker EN, Lott JS, Parker EJ. Structures of Mycobacterium tuberculosis Anthranilate Phosphoribosyltransferase Variants Reveal the Conformational Changes That Facilitate Delivery of the Substrate to the Active Site. Biochemistry. 54: 6082-92. PMID 26356348 DOI: 10.1021/Acs.Biochem.5B00612 |
0.466 |
|
2015 |
Blackmore NJ, Nazmi AR, Hutton RD, Webby MN, Baker EN, Jameson GB, Parker EJ. Complex Formation between Two Biosynthetic Enzymes Modifies the Allosteric Regulatory Properties of Both: AN EXAMPLE OF MOLECULAR SYMBIOSIS. The Journal of Biological Chemistry. 290: 18187-98. PMID 26032422 DOI: 10.1074/Jbc.M115.638700 |
0.732 |
|
2015 |
Parker EJ. The molecular basis for the substrate specificity of protein tyrosine phosphatase PTPN3. Structure (London, England : 1993). 23: 608-9. PMID 25862931 DOI: 10.1016/J.Str.2015.03.005 |
0.346 |
|
2014 |
Lang EJ, Cross PJ, Mittelstädt G, Jameson GB, Parker EJ. Allosteric ACTion: the varied ACT domains regulating enzymes of amino-acid metabolism. Current Opinion in Structural Biology. 29: 102-11. PMID 25543886 DOI: 10.1016/J.Sbi.2014.10.007 |
0.404 |
|
2014 |
Naismith JH, Parker EJ. Editorial overview: Catalysis and regulation: enzyme catalysis, biosynthetic pathways and regulation. Current Opinion in Structural Biology. 29: iv-v. PMID 25480465 DOI: 10.1016/J.Sbi.2014.11.004 |
0.415 |
|
2014 |
Heyes LC, Reichau S, Cross PJ, Jameson GB, Parker EJ. Structural analysis of substrate-mimicking inhibitors in complex with Neisseria meningitidis 3-deoxy-d-arabino-heptulosonate 7-phosphate synthase - The importance of accommodating the active site water. Bioorganic Chemistry. 57: 242-50. PMID 25245459 DOI: 10.1016/J.Bioorg.2014.08.003 |
0.523 |
|
2014 |
Cotton TR, Joseph DD, Jiao W, Parker EJ. Probing the determinants of phosphorylated sugar-substrate binding for human sialic acid synthase. Biochimica Et Biophysica Acta. 1844: 2257-2264. PMID 25242570 DOI: 10.1016/J.Bbapap.2014.09.014 |
0.481 |
|
2014 |
Cookson TV, Castell A, Bulloch EM, Evans GL, Short FL, Baker EN, Lott JS, Parker EJ. Alternative substrates reveal catalytic cycle and key binding events in the reaction catalysed by anthranilate phosphoribosyltransferase from Mycobacterium tuberculosis. The Biochemical Journal. 461: 87-98. PMID 24712732 DOI: 10.1042/Bj20140209 |
0.444 |
|
2014 |
Joseph DD, Jiao W, Kessans SA, Parker EJ. Substrate-mediated control of the conformation of an ancillary domain delivers a competent catalytic site for N-acetylneuraminic acid synthase. Proteins. 82: 2054-66. PMID 24633984 DOI: 10.1002/Prot.24558 |
0.398 |
|
2014 |
Hunter MF, Parker EJ. Modifying the determinants of α-ketoacid substrate selectivity in mycobacterium tuberculosis α-isopropylmalate synthase. Febs Letters. 588: 1603-7. PMID 24613923 DOI: 10.1016/J.Febslet.2014.02.053 |
0.336 |
|
2014 |
Nazmi AR, Schofield LR, Dobson RC, Jameson GB, Parker EJ. Destabilization of the homotetrameric assembly of 3-deoxy-D-arabino-heptulosonate-7-phosphate synthase from the hyperthermophile Pyrococcus furiosus enhances enzymatic activity. Journal of Molecular Biology. 426: 656-73. PMID 24239948 DOI: 10.1016/J.Jmb.2013.11.008 |
0.477 |
|
2013 |
Hobbs JK, Jiao W, Easter AD, Parker EJ, Schipper LA, Arcus VL. Change in heat capacity for enzyme catalysis determines temperature dependence of enzyme catalyzed rates. Acs Chemical Biology. 8: 2388-93. PMID 24015933 DOI: 10.1021/Cb4005029 |
0.366 |
|
2013 |
Cross PJ, Parker EJ. Allosteric inhibitor specificity of Thermotoga maritima 3-deoxy-D-arabino-heptulosonate 7-phosphate synthase. Febs Letters. 587: 3063-8. PMID 23916814 DOI: 10.1016/J.Febslet.2013.07.044 |
0.383 |
|
2013 |
Mittelstädt G, Negron L, Schofield LR, Marsh K, Parker EJ. Biochemical and structural characterisation of dehydroquinate synthase from the New Zealand kiwifruit Actinidia chinensis. Archives of Biochemistry and Biophysics. 537: 185-91. PMID 23916589 DOI: 10.1016/J.Abb.2013.07.022 |
0.474 |
|
2013 |
Cross PJ, Pietersma AL, Allison TM, Wilson-Coutts SM, Cochrane FC, Parker EJ. Neisseria meningitidis expresses a single 3-deoxy-d-arabino-heptulosonate 7-phosphate synthase that is inhibited primarily by phenylalanine. Protein Science : a Publication of the Protein Society. 22: 1087-99. PMID 23754471 DOI: 10.1002/Pro.2293 |
0.486 |
|
2013 |
Allison TM, Cochrane FC, Jameson GB, Parker EJ. Examining the role of intersubunit contacts in catalysis by 3-deoxy-d-manno-octulosonate 8-phosphate synthase. Biochemistry. 52: 4676-86. PMID 23746359 DOI: 10.1021/Bi400521F |
0.518 |
|
2013 |
Joseph DD, Jiao W, Parker EJ. Arg314 is essential for catalysis by N-acetyl neuraminic acid synthase from Neisseria meningitidis. Biochemistry. 52: 2609-19. PMID 23534460 DOI: 10.1021/Bi400062C |
0.502 |
|
2013 |
Huisman FH, Squire CJ, Parker EJ. Amino-acid substitutions at the domain interface affect substrate and allosteric inhibitor binding in α-isopropylmalate synthase from Mycobacterium tuberculosis. Biochemical and Biophysical Research Communications. 433: 249-54. PMID 23500460 DOI: 10.1016/J.Bbrc.2013.02.092 |
0.445 |
|
2013 |
Castell A, Short FL, Evans GL, Cookson TV, Bulloch EM, Joseph DD, Lee CE, Parker EJ, Baker EN, Lott JS. The substrate capture mechanism of Mycobacterium tuberculosis anthranilate phosphoribosyltransferase provides a mode for inhibition. Biochemistry. 52: 1776-87. PMID 23363292 DOI: 10.1021/Bi301387M |
0.483 |
|
2013 |
Cross PJ, Allison TM, Dobson RC, Jameson GB, Parker EJ. Engineering allosteric control to an unregulated enzyme by transfer of a regulatory domain. Proceedings of the National Academy of Sciences of the United States of America. 110: 2111-6. PMID 23345433 DOI: 10.1073/Pnas.1217923110 |
0.449 |
|
2013 |
Blackmore NJ, Reichau S, Jiao W, Hutton RD, Baker EN, Jameson GB, Parker EJ. Three sites and you are out: ternary synergistic allostery controls aromatic amino acid biosynthesis in Mycobacterium tuberculosis. Journal of Molecular Biology. 425: 1582-92. PMID 23274137 DOI: 10.1016/J.Jmb.2012.12.019 |
0.733 |
|
2013 |
Reichau S, Parker EJ. Active site plasticity of a critical enzyme from Mycobacterium tuberculosis Rsc Advances. 3: 3209-3212. DOI: 10.1039/C3Ra00037K |
0.478 |
|
2012 |
Huisman FH, Koon N, Bulloch EM, Baker HM, Baker EN, Squire CJ, Parker EJ. Removal of the C-terminal regulatory domain of α-isopropylmalate synthase disrupts functional substrate binding. Biochemistry. 51: 2289-97. PMID 22352945 DOI: 10.1021/Bi201717J |
0.505 |
|
2012 |
Harrison AN, Reichau S, Parker EJ. Synthesis and evaluation of tetrahedral intermediate mimic inhibitors of 3-deoxy-d-manno-octulosonate 8-phosphate synthase. Bioorganic & Medicinal Chemistry Letters. 22: 907-11. PMID 22204912 DOI: 10.1016/J.Bmcl.2011.12.025 |
0.487 |
|
2012 |
Jiao W, Hutton RD, Cross PJ, Jameson GB, Parker EJ. Dynamic cross-talk among remote binding sites: the molecular basis for unusual synergistic allostery. Journal of Molecular Biology. 415: 716-26. PMID 22154807 DOI: 10.1016/J.Jmb.2011.11.037 |
0.712 |
|
2011 |
Tran D, Pietersma AL, Schofield LR, Rost M, Jameson GB, Parker EJ. Investigating the role of the hydroxyl groups of substrate erythrose 4-phosphate in the reaction catalysed by the first enzyme of the shikimate pathway. Bioorganic & Medicinal Chemistry Letters. 21: 6838-41. PMID 21978677 DOI: 10.1016/J.Bmcl.2011.09.017 |
0.495 |
|
2011 |
Allison TM, Hutton RD, Jiao W, Gloyne BJ, Nimmo EB, Jameson GB, Parker EJ. An extended β7α7 substrate-binding loop is essential for efficient catalysis by 3-deoxy-D-manno-octulosonate 8-phosphate synthase. Biochemistry. 50: 9318-27. PMID 21942786 DOI: 10.1021/Bi201231E |
0.738 |
|
2011 |
Negron L, Patchett ML, Parker EJ. Expression, Purification, and Characterisation of Dehydroquinate Synthase from Pyrococcus furiosus. Enzyme Research. 2011: 134893. PMID 21603259 DOI: 10.4061/2011/134893 |
0.417 |
|
2011 |
Walker SR, Jiao W, Parker EJ. Synthesis and evaluation of dual site inhibitors of 3-deoxy-D-arabino-heptulosonate 7-phosphate synthase. Bioorganic & Medicinal Chemistry Letters. 21: 5092-7. PMID 21493065 DOI: 10.1016/J.Bmcl.2011.03.071 |
0.481 |
|
2011 |
Reichau S, Jiao W, Walker SR, Hutton RD, Baker EN, Parker EJ. Potent inhibitors of a shikimate pathway enzyme from Mycobacterium tuberculosis: combining mechanism- and modeling-based design. The Journal of Biological Chemistry. 286: 16197-207. PMID 21454647 DOI: 10.1074/Jbc.M110.211649 |
0.733 |
|
2011 |
Allison TM, Hutton RD, Cochrane FC, Yeoman JA, Jameson GB, Parker EJ. Targeting the role of a key conserved motif for substrate selection and catalysis by 3-deoxy-D-manno-octulosonate 8-phosphate synthase. Biochemistry. 50: 3686-95. PMID 21438567 DOI: 10.1021/Bi200251F |
0.722 |
|
2011 |
Negron L, Parker EJ. Fluorinated substrates result in variable leakage of a reaction intermediate during catalysis by dehydroquinate synthase. Organic & Biomolecular Chemistry. 9: 2861-7. PMID 21387027 DOI: 10.1039/C0Ob01141J |
0.419 |
|
2011 |
Cross PJ, Dobson RC, Patchett ML, Parker EJ. Tyrosine latching of a regulatory gate affords allosteric control of aromatic amino acid biosynthesis. The Journal of Biological Chemistry. 286: 10216-24. PMID 21282100 DOI: 10.1074/Jbc.M110.209924 |
0.496 |
|
2010 |
Webby CJ, Jiao W, Hutton RD, Blackmore NJ, Baker HM, Baker EN, Jameson GB, Parker EJ. Synergistic allostery, a sophisticated regulatory network for the control of aromatic amino acid biosynthesis in Mycobacterium tuberculosis. The Journal of Biological Chemistry. 285: 30567-76. PMID 20667835 DOI: 10.1074/Jbc.M110.111856 |
0.754 |
|
2010 |
Allison TM, Yeoman JA, Hutton RD, Cochrane FC, Jameson GB, Parker EJ. Specificity and mutational analysis of the metal-dependent 3-deoxy-D-manno-octulosonate 8-phosphate synthase from Acidithiobacillus ferrooxidans. Biochimica Et Biophysica Acta. 1804: 1526-36. PMID 20406700 DOI: 10.1016/J.Bbapap.2010.04.005 |
0.717 |
|
2010 |
Huisman FH, Hunter MF, Devenish SR, Gerrard JA, Parker EJ. The C-terminal regulatory domain is required for catalysis by Neisseria meningitidis alpha-isopropylmalate synthase. Biochemical and Biophysical Research Communications. 393: 168-73. PMID 20117081 DOI: 10.1016/J.Bbrc.2010.01.114 |
0.358 |
|
2009 |
Cochrane FC, Cookson TV, Jameson GB, Parker EJ. Reversing evolution: re-establishing obligate metal ion dependence in a metal-independent KDO8P synthase. Journal of Molecular Biology. 390: 646-61. PMID 19447118 DOI: 10.1016/J.Jmb.2009.05.014 |
0.371 |
|
2009 |
Devenish SR, Huisman FH, Parker EJ, Hadfield AT, Gerrard JA. Cloning and characterisation of dihydrodipicolinate synthase from the pathogen Neisseria meningitidis. Biochimica Et Biophysica Acta. 1794: 1168-74. PMID 19236959 DOI: 10.1016/J.Bbapap.2009.02.003 |
0.443 |
|
2009 |
Walker SR, Cumming H, Parker EJ. Substrate and reaction intermediate mimics as inhibitors of 3-deoxy-d-arabino-heptulosonate 7-phosphate synthase Organic and Biomolecular Chemistry. 7: 3031-3035. DOI: 10.1039/B909241B |
0.481 |
|
2008 |
Ahn M, Cochrane FC, Patchett ML, Parker EJ. Arabinose 5-phosphate analogues as mechanistic probes for Neisseria meningitidis 3-deoxy-D-manno-octulosonate 8-phosphate synthase. Bioorganic & Medicinal Chemistry. 16: 9830-6. PMID 18930408 DOI: 10.1016/J.Bmc.2008.09.056 |
0.428 |
|
2007 |
Saikia S, Parker EJ, Koulman A, Scott B. Defining paxilline biosynthesis in Penicillium paxilli: functional characterization of two cytochrome P450 monooxygenases. The Journal of Biological Chemistry. 282: 16829-37. PMID 17428785 DOI: 10.1074/Jbc.M701626200 |
0.307 |
|
2006 |
Walker SR, Parker EJ. Synthesis and evaluation of a mechanism-based inhibitor of a 3-deoxy-D-arabino heptulosonate 7-phosphate synthase. Bioorganic & Medicinal Chemistry Letters. 16: 2951-4. PMID 16563755 DOI: 10.1016/J.Bmcl.2006.02.073 |
0.409 |
|
2006 |
Saikia S, Parker EJ, Koulman A, Scott B. Four gene products are required for the fungal synthesis of the indole-diterpene, paspaline. Febs Letters. 580: 1625-30. PMID 16494875 DOI: 10.1016/J.Febslet.2006.02.008 |
0.305 |
|
2005 |
Webby CJ, Lott JS, Baker HM, Baker EN, Parker EJ. Crystallization and preliminary X-ray crystallographic analysis of 3-deoxy-D-arabino-heptulosonate-7-phosphate synthase from Mycobacterium tuberculosis. Acta Crystallographica. Section F, Structural Biology and Crystallization Communications. 61: 403-6. PMID 16511053 DOI: 10.1107/S1744309105007931 |
0.412 |
|
2005 |
Webby CJ, Baker HM, Lott JS, Baker EN, Parker EJ. The structure of 3-deoxy-d-arabino-heptulosonate 7-phosphate synthase from Mycobacterium tuberculosis reveals a common catalytic scaffold and ancestry for type I and type II enzymes. Journal of Molecular Biology. 354: 927-39. PMID 16288916 DOI: 10.1016/J.Jmb.2005.09.093 |
0.456 |
|
2005 |
Ahn M, Pietersma AL, Schofield LR, Parker EJ. Mechanistic divergence of two closely related aldol-like enzyme-catalysed reactions. Organic & Biomolecular Chemistry. 3: 4046-9. PMID 16267580 DOI: 10.1039/B511661A |
0.475 |
|
2005 |
Schofield LR, Anderson BF, Patchett ML, Norris GE, Jameson GB, Parker EJ. Substrate ambiguity and crystal structure of Pyrococcus furiosus 3-deoxy-D-arabino-heptulosonate-7-phosphate synthase: an ancestral 3-deoxyald-2-ulosonate-phosphate synthase? Biochemistry. 44: 11950-62. PMID 16142893 DOI: 10.1021/Bi050577Z |
0.484 |
|
2005 |
Tanaka A, Tapper BA, Popay A, Parker EJ, Scott B. A symbiosis expressed non-ribosomal peptide synthetase from a mutualistic fungal endophyte of perennial ryegrass confers protection to the symbiotum from insect herbivory. Molecular Microbiology. 57: 1036-50. PMID 16091042 DOI: 10.1111/J.1365-2958.2005.04747.X |
0.323 |
|
2005 |
Webby CJ, Patchett ML, Parker EJ. Characterization of a recombinant type II 3-deoxy-D-arabino-heptulosonate-7-phosphate synthase from Helicobacter pylori. The Biochemical Journal. 390: 223-30. PMID 15853768 DOI: 10.1042/Bj20050259 |
0.468 |
|
2005 |
Williamson RM, Pietersma AL, Jameson GB, Parker EJ. Stereospecific deuteration of 2-deoxyerythrose 4-phosphate using 3-deoxy-D-arabino-heptulosonate 7-phosphate synthase. Bioorganic & Medicinal Chemistry Letters. 15: 2339-42. PMID 15837321 DOI: 10.1016/J.Bmcl.2005.02.080 |
0.489 |
|
2004 |
Bulloch EM, Jones MA, Parker EJ, Osborne AP, Stephens E, Davies GM, Coggins JR, Abell C. Identification of 4-amino-4-deoxychorismate synthase as the molecular target for the antimicrobial action of (6s)-6-fluoroshikimate. Journal of the American Chemical Society. 126: 9912-3. PMID 15303852 DOI: 10.1021/Ja048312F |
0.528 |
|
2004 |
Schofield LR, Patchett ML, Parker EJ. Expression, purification, and characterization of 3-deoxy-D-arabino-heptulosonate 7-phosphate synthase from Pyrococcus furiosus. Protein Expression and Purification. 34: 17-27. PMID 14766297 DOI: 10.1016/J.Pep.2003.11.008 |
0.429 |
|
2003 |
Frederickson M, Parker EJ, Coggins JR, Abell C. Enzymic synthesis of 3-[3- 13C]dehydroquinic acid. Organic & Biomolecular Chemistry. 1: 3271-3. PMID 14584789 DOI: 10.1039/B309666A |
0.584 |
|
2003 |
McMillan LK, Carr RL, Young CA, Astin JW, Lowe RG, Parker EJ, Jameson GB, Finch SC, Miles CO, McManus OB, Schmalhofer WA, Garcia ML, Kaczorowski GJ, Goetz M, Tkacz JS, et al. Molecular analysis of two cytochrome P450 monooxygenase genes required for paxilline biosynthesis in Penicillium paxilli, and effects of paxilline intermediates on mammalian maxi-K ion channels. Molecular Genetics and Genomics : Mgg. 270: 9-23. PMID 12884010 DOI: 10.1007/S00438-003-0887-2 |
0.428 |
|
2003 |
Frederickson M, Parker EJ, Coggins JR, Abell C. Enzymic synthesis of 3-[3-13C]dehydroquinic acid Organic and Biomolecular Chemistry. 1: 3271-3273. DOI: 10.1039/b309666a |
0.521 |
|
2001 |
Parker EJ, Bulloch EM, Jameson GB, Abell C. Substrate deactivation of phenylalanine-sensitive 3-deoxy-D-arabino-heptulosonate 7-phosphate synthase by erythrose 4-phosphate. Biochemistry. 40: 14821-8. PMID 11732901 DOI: 10.1021/Bi010928J |
0.632 |
|
2000 |
Parker EJ, González Bello C, Coggins JR, Hawkins AR, Abell C. Mechanistic studies on type I and type II dehydroquinase with (6R)- and (6S)-6-fluoro-3-dehydroquinic acids. Bioorganic & Medicinal Chemistry Letters. 10: 231-4. PMID 10698442 DOI: 10.1016/S0960-894X(99)00660-5 |
0.56 |
|
1999 |
Frederickson M, Parker EJ, Hawkins AR, Coggins JR, Abell C. Selective Inhibition of Type II Dehydroquinases. The Journal of Organic Chemistry. 64: 2612-2613. PMID 11674325 DOI: 10.1021/Jo990004Q |
0.451 |
|
1997 |
Parker EJ, Coggins JR, Abell C. Derailing Dehydroquinate Synthase by Introducing a Stabilizing Stereoelectronic Effect in a Reaction Intermediate. The Journal of Organic Chemistry. 62: 8582-8585. PMID 11672011 DOI: 10.1021/Jo9713060 |
0.488 |
|
1995 |
Duggan PJ, Parker E, Coggins J, Abell C. Enzymatic synthesis of (6R)- and (6S)-fluoroshikimic acids Bioorganic and Medicinal Chemistry Letters. 5: 2347-2352. DOI: 10.1016/0960-894X(95)00405-I |
0.472 |
|
Show low-probability matches. |