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References from Generation and characterization of two acid-resistant macrocin O -methyltransferase variants with a higher enzyme activity at 30 °C from Streptomyces fradiae. Local targets link to admitted publications; unresolved targets remain external evidence.
Biological methylation: selected aspects
10.1146/annurev.bi.44.070175.002251 · 1975 · External reference
10.1039/c3np70045c
10.1039/c3np70045c · External reference
Progress in the microbial production of S-adenosyl-L-methionine
10.1007/s11274-016-2102-8 · 2016 · External reference
Structural basis for substrate recognition in the salicylic acid carboxyl methyltransferase family
10.1105/tpc.014548 · 2003 · External reference
10.1074/jbc.m111698200
10.1074/jbc.m111698200 · External reference
Highly divergent methyltransferases catalyze a conserved reaction in tocopherol and plastoquinone synthesis in cyanobacteria and photosynthetic eukaryotes
10.1105/tpc.013656 · 2003 · External reference
10.1038/nchembio.482
10.1038/nchembio.482 · External reference
10.1038/nrd3674
10.1038/nrd3674 · External reference
10.1007/s12035-016-0357-6
10.1007/s12035-016-0357-6 · External reference
10.1007/s00018-015-1847-9
10.1007/s00018-015-1847-9 · External reference
Fluorescent probes for bioactive detection and imaging of phase II metabolic enzymes
10.1016/j.ccr.2019.213026 · 2019 · External reference
Site-specific bioalkylation of rapamycin by the RapM 16-O-methyltransferase
10.1039/c5sc00164a · 2015 · External reference
Expanding the structural diversity of polyketides by exploring the cofactor tolerance of an inline methyltransferase domain
10.1021/ol401723h · 2013 · External reference
10.1002/anie.201308272
10.1002/anie.201308272 · External reference
Methyltransferases: functions and applications
10.1002/cbic.202200212 · 2022 · External reference
Comprehensive structural and substrate specificity classification of the Saccharomyces cerevisiae methyltransferome
10.1371/journal.pone.0023168 · 2011 · External reference
The enzymatic synthesis of S-adenosyl-l-homocysteine from adenosine and homocysteine
10.1016/s0021-9258(18)70253-6 · 1959 · External reference
Characterization of SafC, a catechol 4-O-methyltransferase involved in saframycin biosynthesis
10.1128/aem.00011-07 · 2007 · External reference
10.1039/b703488c
10.1039/b703488c · External reference
Production of 7-O-methyl aromadendrin, a medicinally valuable flavonoid, in Escherichia coli
10.1128/aem.06274-11 · 2012 · External reference
10.1517/13543776.2012.667403
10.1517/13543776.2012.667403 · External reference
Recent advances in methyltransferase biocatalysis
10.1016/j.cbpa.2017.01.020 · 2017 · External reference
Aerobic degradation of tylosin in cattle, chicken, and swine excreta
10.1016/s0013-9351(02)00086-5 · 2003 · External reference
Stability of Tylosin A in manure containing test systems determined by high performance liquid chromatography
10.1016/s0045-6535(99)00450-6 · 2000 · External reference
Terminal stages in the biosynthesis of tylosin
10.1128/aac.11.3.455 · 1977 · External reference
Biosynthesis of the macrolide antibiotic tylosin. A preferred pathway from tylactone to tylosin
10.7164/antibiotics.36.131 · 1983 · External reference
S-Adenosyl-L-methionine: macrocin O-methyltransferase activities in a series of Streptomyces fradiae mutants that produce different levels of the macrolide antibiotic tylosin
10.1128/aac.21.5.758 · 1982 · External reference
Properties of S-adenosyl-L-methionine:macrocin O-methyltransferase in extracts of Streptomyces fradiae strains which produce normal or elevated levels of tylosin and in mutants blocked in specific O-methylations
10.1128/aac.20.3.370 · 1981 · External reference
Purification, characterization, and kinetic mechanism of S-adenosyl-L-methionine:macrocin O-methyltransferase from Streptomyces fradiae
10.1016/s0021-9258(19)37633-1 · 1988 · External reference
10.1016/j.biotechadv.2015.02.014
10.1016/j.biotechadv.2015.02.014 · External reference
Thermostability improvement of Aspergillus awamori glucoamylase via directed evolution of its gene located on episomal expression vector in Pichia pastoris cells
10.1093/protein/gzz048 · 2019 · External reference
Enzyme engineering: current trends and future perspectives
10.1080/87559129.2019.1695835 · 2019 · External reference
Native to designed: microbial-amylases for industrial applications
2021 · External reference
Improvement of thermostability and catalytic efficiency of glucoamylase from Talaromyces leycettanus JCM12802 via site-directed mutagenesis to enhance industrial saccharification applications
10.1186/s13068-021-02052-3 · 2021 · External reference
Directed evolution 2.0: improving and deciphering enzyme properties
10.1039/c5cc01594d · 2015 · External reference
Directed evolution of TetR for constructing sensitive and broad-spectrum tetracycline antibiotics whole-cell biosensor
2023 · External reference
Hot spots-making directed evolution easier
2022 · External reference
An efficient one-step site-directed and site-saturation mutagenesis protocol
10.1093/nar/gnh110 · 2004 · External reference
10.1002/anie.201901491
10.1002/anie.201901491 · External reference
10.1016/j.csbj.2023.04.005 · Admitted local publication
A high-throughput method based on microculture technology for screening of high-yield strains of tylosin-producing Streptomyces fradiae
10.4014/jmb.2210.10023 · 2023 · External reference
Consistency evaluation between matrix components ratio and microbiological potency of tylosin major components
10.1007/s40199-018-0220-6 · 2018 · External reference
Deciphering key features in protein structures with the new ENDscript server
10.1093/nar/gku316 · 2014 · External reference
The I-TASSER suite: protein structure and function prediction
10.1038/nmeth.3213 · 2015 · External reference
10.1038/nprot.2010.5
10.1038/nprot.2010.5 · External reference
AutoDock4 and AutoDockTools4: automated docking with selective receptor flexibility
10.1002/jcc.21256 · 2009 · External reference
AutoDock4 and AutoDockTools4: automated docking with selective receptor flexibility
10.1002/jcc.21256 · 2009 · External reference
Yield-determining factors in high-solids enzymatic hydrolysis of lignocellulose
10.1186/1754-6834-2-11 · 2009 · External reference
Kinetic study of batch and fed-batch enzymatic saccharification of pretreated substrate and subsequent fermentation to ethanol
10.1186/1754-6834-5-16 · 2012 · External reference
Characterization of NovP and NovN: completion of novobiocin biosynthesis by sequential tailoring of the noviosyl ring
10.1002/anie.200352626 · 2004 · External reference
Structural basis of substrate specificity and regiochemistry in the MycF/TylF family of sugar O-methyltransferases
10.1021/cb5009348 · 2015 · External reference
SAM (dependent) I AM: the S-adenosylmethionine-dependent methyltransferase fold
10.1016/s0959-440x(02)00391-3 · 2002 · External reference
The crystal structure of the novobiocin biosynthetic enzyme NovP: the first representative structure for the TylF O-methyltransferase superfamily
10.1016/j.jmb.2009.10.045 · 2010 · External reference
Adaptive steered molecular dynamics combined with protein structure networks revealing the mechanism of Y68I/G109P mutations that enhance the catalytic activity of d-psicose 3-epimerase from Clostridium bolteae
10.3389/fchem.2018.00437 · 2018 · External reference
Role of heme in structural organization of cytochrome c probed by semisynthesis
10.1021/bi9919089 · 1999 · External reference
Some like it hot, some like it cold: temperature dependent biotechnological applications and improvements in extremophilic enzymes
10.1016/j.biotechadv.2015.11.001 · 2015 · External reference
Thermostability improvement of a streptomyces xylanase by introducing proline and glutamic acid residues
10.1128/aem.03458-13 · 2014 · External reference
Enzymatic biodiesel synthesis – key factors affecting efficiency of the process
10.1016/j.renene.2008.11.013 · 2008 · External reference
Ultrasound enhanced butyric acid-lauric acid designer lipid synthesis: based on artificial neural network and changes in enzymatic structure
2022 · External reference
Select human cancer mutants of NRMT1 alter its catalytic activity and decrease N-terminal trimethylation
10.1002/pro.3202 · 2017 · External reference