Zobrazeno 1 - 8
of 8
pro vyhledávání: '"James A.E. Kraunsoe"'
Publikováno v:
Pesticide Science. 55:887-895
Dihydrodipicolinate synthase (DHDPS) (EC 4.2.1.52) and dihydrodipicolinate reductase (DHDPR) (EC 1.3.1.26) have attracted much recent attention as potential herbicide targets. DHDPS was feedback-inhibited by (S)-lysine; inhibition was reversible and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6d0f0fb41296790dfcb0845bfab414a7
https://doi.org/10.1002/(sici)1096-9063(199909)55:9<887::aid-ps36>3.0.co
https://doi.org/10.1002/(sici)1096-9063(199909)55:9<887::aid-ps36>3.0.co
Autor:
Robert S. Fuller, Donald A. MacKenzie, Tomoko Komiyama, Gordon Lowe, James A.E. Kraunsoe, David B. Archer, Julian A. Chesshyre
Publikováno v:
Journal of Biotechnology. 63:137-146
Bovine pancreatic trypsin inhibitor (BPTI) was secreted by Aspergillus niger at yields of up to 23 mg l−1 using a protein fusion strategy. BPTI was linked to part of the fungal glucoamylase protein (GAM) with a dibasic amino acid (KEX2) processing
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::31e2c7435a71c4345021981cfa3cebd6
https://doi.org/10.1016/s0168-1656(98)00081-9
https://doi.org/10.1016/s0168-1656(98)00081-9
Publikováno v:
FEBS Letters. 396:108-112
The binding of BPTI and SBTI with trypsin has been investigated by ESI MS, using the mutant K15V-BPTI and the chemically modified RcamBPTI as controls. Although high cone voltages (+80 V) produce sharp spectra of BPTI, RcamBPTI, SBTI and trypsin alon
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::128268c8ce64b12bbcd0c6b4663a7a9d
https://doi.org/10.1016/0014-5793(96)01081-2
https://doi.org/10.1016/0014-5793(96)01081-2
Autor:
Carolyn V. Coulter, Deborah J. Moore, Juliet A. Gerrard, Andrew J. Pratt, James A.E. Kraunsoe
Publikováno v:
Tetrahedron. 52:7127-7136
We report a novel synthesis of (S)-aspartate semi-aldehyde, (S)-ASA, 1, a key intermediate in the biosynthesis of lysine, based on hydrolysis of an enol ether precursor, (S)-2-amino-4-methoxybut-3-enoic acid, 10. (S)-ASA is conveniently and quantitat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5d6c4d749eef3f9843a165cfa4a208c0
https://doi.org/10.1016/0040-4020(96)00330-4
https://doi.org/10.1016/0040-4020(96)00330-4
Publikováno v:
Tetrahedron. 52:5983-5988
N-Nitrosochloroethyl-cephem7 was prepared via acylation and selective nitrosation of a cephalothin derivative. This cephalosporin is an efficient substrate for Enterobacter cloacae P99 β-lactamase. Kinetic parameters were determined for enzyme-catal
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a759b476dc553157e04449156e4a8445
https://doi.org/10.1016/0040-4020(96)00228-1
https://doi.org/10.1016/0040-4020(96)00228-1
Autor:
Carolyn V. Coulter, Juliet A. Gerrard, James A.E. Kraunsoe, Deborah J. Moore, Andrew J. Pratt
Publikováno v:
ChemInform. 27
We report a novel synthesis of (S)-aspartate semi-aldehyde, (S)-ASA, 1, a key intermediate in the biosynthesis of lysine, based on hydrolysis of an enol ether precursor, (S)-2-amino-4-methoxybut-3-enoic acid, 10. (S)-ASA is conveniently and quantitat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ce7e85d08760223cd54c3e3594202556
https://doi.org/10.1002/chin.199637268
https://doi.org/10.1002/chin.199637268
Publikováno v:
ChemInform. 27
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6aeaf8e510b37f9d30df4d56cbee1c1b
https://doi.org/10.1002/chin.199631215
https://doi.org/10.1002/chin.199631215
Publikováno v:
Biochemistry. 35(28)
The interactions of three BPTI homologues with human leukocyte elastase and porcine pancreatic elastase have been investigated. The principal mutation in determining the specificity of inhibition was the Lys15-Val mutation at the P1 position. An addi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c83de7400d21668be146a6eaa5242d53
http://ora.ox.ac.uk/objects/uuid:36399f53-a2e9-474f-b758-44fb30726c73
http://ora.ox.ac.uk/objects/uuid:36399f53-a2e9-474f-b758-44fb30726c73