NCI: a server to identify non-canonical interactions in protein structures

被引:66
作者
Babu, MM [1 ]
机构
[1] MRC, Mol Biol Lab, Cambridge CB2 2QH, England
基金
英国医学研究理事会;
关键词
D O I
10.1093/nar/gkg528
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
NCI is a server for the identification of non-canonical interactions in protein structures. These interactions, which include N-H...pi, C-alpha-H...pi, C-alpha-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/.
引用
收藏
页码:3345 / 3348
页数:4
相关论文
共 37 条
  • [1] THE (I, I+4) PHE-HIS INTERACTION STUDIED IN AN ALANINE-BASED ALPHA-HELIX
    ARMSTRONG, KM
    FAIRMAN, R
    BALDWIN, RL
    [J]. JOURNAL OF MOLECULAR BIOLOGY, 1993, 230 (01) : 284 - 291
  • [2] A C-H•••O hydrogen bond stabilized polypeptide chain reversal motif at the C terminus of helices in proteins
    Babu, MM
    Singh, SK
    Balaram, P
    [J]. JOURNAL OF MOLECULAR BIOLOGY, 2002, 322 (04) : 871 - 880
  • [3] HYDROGEN-BONDING IN GLOBULAR-PROTEINS
    BAKER, EN
    HUBBARD, RE
    [J]. PROGRESS IN BIOPHYSICS & MOLECULAR BIOLOGY, 1984, 44 (02) : 97 - 179
  • [4] Crystallographic evidence for C-alpha-H center dot center dot center dot O=C hydrogen bonds in a collagen triple helix
    Bella, J
    Berman, HM
    [J]. JOURNAL OF MOLECULAR BIOLOGY, 1996, 264 (04) : 734 - 742
  • [5] C-H•••π-interactions in proteins
    Brandl, M
    Weiss, MS
    Jabs, A
    Sühnel, J
    Hilgenfeld, R
    [J]. JOURNAL OF MOLECULAR BIOLOGY, 2001, 307 (01) : 357 - 377
  • [6] C-H•••O hydrogen bond involving proline residues in α-helices
    Chakrabarti, P
    Chakrabarti, S
    [J]. JOURNAL OF MOLECULAR BIOLOGY, 1998, 284 (04) : 867 - 873
  • [7] ASTRAL compendium enhancements
    Chandonia, JM
    Walker, NS
    Conte, LL
    Koehl, P
    Levitt, M
    Brenner, SE
    [J]. NUCLEIC ACIDS RESEARCH, 2002, 30 (01) : 260 - 263
  • [8] Creighton TE, 1993, PROTEINS STRUCTURES
  • [9] THE OCCURRENCE OF C-H-CENTER-DOT-CENTER-DOT-CENTER-DOT-O HYDROGEN-BONDS IN PROTEINS
    DEREWENDA, ZS
    LEE, L
    DEREWENDA, U
    [J]. JOURNAL OF MOLECULAR BIOLOGY, 1995, 252 (02) : 248 - 262
  • [10] (HIS)C-EPSILON-H...O=C HYDROGEN-BOND IN THE ACTIVE-SITES OF SERINE HYDROLASES
    DEREWENDA, ZS
    DEREWENDA, U
    KOBOS, PM
    [J]. JOURNAL OF MOLECULAR BIOLOGY, 1994, 241 (01) : 83 - 93