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Admiraal, Suzanne J., Herschlag, Daniel (1999) Catalysis of Phosphoryl Transfer from ATP by Amine Nucleophiles. Journal Of The American Chemical Society, 121 (25) 5837-5845 doi:10.1021/ja990903w

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Reference TypeJournal (article/letter/editorial)
TitleCatalysis of Phosphoryl Transfer from ATP by Amine Nucleophiles
JournalJournal Of The American Chemical Society
AuthorsAdmiraal, Suzanne J.Author
Herschlag, DanielAuthor
Year1999 (June)Volume121
Issue25
PublisherAmerican Chemical Society (ACS)
DOIdoi:10.1021/ja990903wSearch in ResearchGate
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Mindat Ref. ID1546787Long-form Identifiermindat:1:5:1546787:8
GUID0
Full ReferenceAdmiraal, Suzanne J., Herschlag, Daniel (1999) Catalysis of Phosphoryl Transfer from ATP by Amine Nucleophiles. Journal Of The American Chemical Society, 121 (25) 5837-5845 doi:10.1021/ja990903w
Plain TextAdmiraal, Suzanne J., Herschlag, Daniel (1999) Catalysis of Phosphoryl Transfer from ATP by Amine Nucleophiles. Journal Of The American Chemical Society, 121 (25) 5837-5845 doi:10.1021/ja990903w
In(1999, June) Journal Of The American Chemical Society Vol. 121 (25) American Chemical Society (ACS)

See Also

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Admiraal, Suzanne J., Herschlag, Daniel (2000) The Substrate-Assisted General Base Catalysis Model for Phosphate Monoester Hydrolysis:  Evaluation Using Reactivity Comparisons. Journal Of The American Chemical Society, 122 (10) 2145-2148 doi:10.1021/ja993942g
O'Brie, Patrick J., Herschlag, Daniel (1999) Does the Active Site Arginine Change the Nature of the Transition State for Alkaline Phosphatase-Catalyzed Phosphoryl Transfer?. Journal Of The American Chemical Society, 121 (47) 11022-11023 doi:10.1021/ja9932582
Herschlag, Daniel, Jencks, William P. (1989) Phosphoryl transfer to anionic oxygen nucleophiles. Nature of the transition state and electrostatic repulsion. Journal Of The American Chemical Society, 111 (19) 7587-7596 doi:10.1021/ja00201a048
Herschlag, Daniel, Jencks, William P. (1990) Nucleophiles of high reactivity in phosphoryl transfer reactions: .alpha.-effect compounds and fluoride ion. Journal Of The American Chemical Society, 112 (5) 1951-1956 doi:10.1021/ja00161a047
Cheng, Hu, Nikolic-Hughes, Ivana, Wang, Jianghua H., Deng, Hua, O'Brien, Patrick J., Wu, Li, Zhang, Zhong-Yin, Herschlag, Daniel, Callender, Robert (2002) Environmental Effects on Phosphoryl Group Bonding Probed by Vibrational Spectroscopy:  Implications for Understanding Phosphoryl Transfer and Enzymatic Catalysis. Journal Of The American Chemical Society, 124 (38) 11295-11306 doi:10.1021/ja026481z
Herschlag, Daniel, Jencks, William P. (1987) The effect of divalent metal ions on the rate and transition-state structure of phosphoryl-transfer reactions. Journal Of The American Chemical Society, 109 (15) 4665-4674 doi:10.1021/ja00249a033
Forconi, Marcello, Herschlag, Daniel (2005) Promiscuous Catalysis by theTetrahymenaGroup I Ribozyme. Journal Of The American Chemical Society, 127 (17) 6160-6161 doi:10.1021/ja050180i
Nikolic-Hughes, Ivana, Rees, Douglas C., Herschlag, Daniel (2004) Do Electrostatic Interactions with Positively Charged Active Site Groups Tighten the Transition State for Enzymatic Phosphoryl Transfer?. Journal Of The American Chemical Society, 126 (38) 11814-11819 doi:10.1021/ja0480421
Herschlag, Daniel, Jencks, William P. (1990) The effects of magnesium2+, hydrogen bonding, and steric factors on rate and equilibrium constants for phosphoryl transfer between carboxylate ions and pyridines. Journal Of The American Chemical Society, 112 (5) 1942-1950 doi:10.1021/ja00161a046
Jencks, William P., Haber, Martin T., Herschlag, Daniel., Nazaretian, Karen L. (1986) Decreasing reactivity with increasing nucleophile basicity. The effect of solvation on .beta.nuc for phosphoryl transfer to amines. Journal Of The American Chemical Society, 108 (3) 479-483 doi:10.1021/ja00263a019
Jencks, William P., Haber, Martin T., Herschlag, Daniel., Nazaretian, Karen L. (1986) Additions and Corrections: Decreasing Reactivity with Increasing Nucleophile Basicity. The Effect of Solvation on βnucfor Phosphoryl Transfer to Amines. Journal Of The American Chemical Society, 108 (19) 6100 doi:10.1021/ja00279a603
 
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