NCI: a server to identify non-canonical interactions in protein structures
Open Access
- 1 July 2003
- journal article
- research article
- Published by Oxford University Press (OUP) in Nucleic Acids Research
- Vol. 31 (13) , 3345-3348
- https://doi.org/10.1093/nar/gkg528
Abstract
NCI is a server for the identification of non-canonical interactions in protein structures. These interactions, which include N-H···π, Cα-H···π, Cα-H···O=C and variants of them, were first observed in small molecules and subsequently in high-resolution protein structures. Such interactions have been subjected to extensive structural analysis to elucidate the different geometric criteria required to identify them. These interactions have also recently been shown to be important for the stability of protein structures. In this work, I describe a server called NCI, which allows the user to either upload protein/peptide coordinates in Protein Data Bank (PDB) format or enter a Structural Classification of Proteins database (SCOP)/PDB identifier for which NCI identifies the different non-canonical interactions, based purely on geometric criteria. Results are presented as an HTML table, as a parseable text file and as a color-coded interaction matrix. In addition, the user can view the RasMol image highlighting the interactions in the protein structure and download the RasMol script. The NCI server is available at: http://www.mrc-lmb.cam.ac.uk/genomes/nci/.Keywords
This publication has 29 references indexed in Scilit:
- Strength and co-operativity of contributions of surface salt bridges to protein stabilityPublished by Elsevier ,2006
- Hydrogen bonding in globular proteinsPublished by Elsevier ,2003
- A C–H⋯O Hydrogen Bond Stabilized Polypeptide Chain Reversal Motif at the C Terminus of Helices in ProteinsJournal of Molecular Biology, 2002
- SCOP database in 2002: refinements accommodate structural genomicsNucleic Acids Research, 2002
- The Cα—H⋅⋅⋅O hydrogen bond: A determinant of stability and specificity in transmembrane helix interactionsProceedings of the National Academy of Sciences, 2001
- Hydrogen bonds with π-acceptors in proteins: frequencies and role in stabilizing local 3D structures11Edited by R. HuberJournal of Molecular Biology, 2001
- Cation-π interactions in structural biologyProceedings of the National Academy of Sciences, 1999
- Structure of acetylcholinesterase complexed with E2020 (Aricept®): implications for the design of new anti-Alzheimer drugsPublished by Elsevier ,1999
- (His)Cε-H···O=C< Hydrogen Bond in the Active Sites of Serine HydrolasesJournal of Molecular Biology, 1994
- The (i,i+4) Phe-His Interaction Studied in an Alanine-based α-HelixJournal of Molecular Biology, 1993