Performance of a neural-network-based determination of amino acid class and secondary structure from 1H-15N NMR data
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Michael Andrec | James H. Prestegard | J. Prestegard | M. Andrec | S. Heald | Kai Huang | Sarah Heald | Paul Blake | K. Huang | Paul Blake
[1] L. Kay,et al. Overcoming the overlap problem in the assignment of 1H NMR spectra of larger proteins by use of three-dimensional heteronuclear 1H-15N Hartmann-Hahn-multiple quantum coherence and nuclear Overhauser-multiple quantum coherence spectroscopy: application to interleukin 1 beta. , 1989, Biochemistry.
[2] E. Oldfield,et al. Secondary and tertiary structural effects on protein NMR chemical shifts: an ab initio approach. , 1993, Science.
[3] Gerhard Wider,et al. Sequence-Corrected 15N "Random Coil" Chemical Shifts , 1994 .
[4] H Oschkinat,et al. Assignment of protein nmr spectra in the light of homonuclear 3D spectroscopy: An automatable procedure based on 3D TOCSY‐TOCSY and 3D TOCSY‐NOESY , 1991, Biopolymers.
[5] Paul A. Keifer,et al. Pure absorption gradient enhanced heteronuclear single quantum correlation spectroscopy with improved sensitivity , 1992 .
[6] Ad Bax,et al. Quantitative J correlation: a new approach for measuring homonuclear three-bond J(HNH.alpha.) coupling constants in 15N-enriched proteins , 1993 .
[7] F. Richards,et al. Relationship between nuclear magnetic resonance chemical shift and protein secondary structure. , 1991, Journal of molecular biology.
[8] James L. McClelland. Explorations In Parallel Distributed Processing , 1988 .
[9] S. Brown,et al. Sequential 1H NMR assignments and secondary structure identification of human ubiquitin. , 1987, Biochemistry.
[10] J. Simorre,et al. 1H, 13C, 15N-NMR resonance assignments of oxidized thioredoxin h from the eukaryotic green alga Chlamydomonas reinhardtii using new methods based on two-dimensional triple-resonance NMR spectroscopy and computer-assisted backbone assignment. , 1995, European journal of biochemistry.
[11] D. Cowburn,et al. Nitrogen-15 chemical shifts of backbone amides in bovine pancreatic trypsin inhibitor and apamin [Erratum to document cited in CA111(17):149076x] , 1990 .
[12] K Wüthrich,et al. Sequential resonance assignments in protein 1H nuclear magnetic resonance spectra. Basic pancreatic trypsin inhibitor. , 1982, Journal of molecular biology.
[13] M. Karplus. Contact Electron‐Spin Coupling of Nuclear Magnetic Moments , 1959 .
[14] Timothy Masters,et al. Practical neural network recipes in C , 1993 .
[15] J. Prestegard,et al. NMR investigations of the structural properties of the nodulation protein, NodF, from Rhizobium leguminosarum and its homology with Escherichia coli acyl carrier protein , 1996, FEBS letters.
[16] K. Wüthrich. NMR of proteins and nucleic acids , 1988 .
[17] J. Prestegard,et al. 1H and 15N magnetic resonance assignments, secondary structure, and tertiary fold of Escherichia coli DnaJ(1-78). , 1995, Biochemistry.
[18] J H Prestegard,et al. Secondary structure of acyl carrier protein as derived from two-dimensional 1H NMR spectroscopy. , 1986, Biochemistry.
[19] D. Cowburn,et al. 15N Chemical Shifts of Backbone Amides in Bovine Pancreatic Trypsin Inhibitor and Apamin , 1989 .
[20] Frank J. M. Van De Ven,et al. PROSPECT, a program for automated interpretation of 2D NMR spectra of proteins , 1990 .
[21] D. Fry,et al. Chemical shift assignments and folding topology of the Ras-binding domain of human Raf-1 as determined by heteronuclear three-dimensional NMR spectroscopy. , 1994, Biochemistry.