Continuum secondary structure captures protein flexibility

被引:125
作者
Anderson, CAF
Palmer, AG
Brunak, S
Rost, B
机构
[1] Columbia Univ, Dept Biochem & Mol Biophys, New York, NY 10032 USA
[2] Tech Univ Denmark, Bioctr, Ctr Biol Sequence Anal, DK-2800 Lyngby, Denmark
[3] Columbia Univ, Ctr Computat Biol & Bioinformat C2B2, New York, NY 10032 USA
关键词
protein secondary structure assignment; evaluation; protein motion; protein structure prediction; protein function; NMR spectroscopy; structure comparison;
D O I
10.1016/S0969-2126(02)00700-1
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
The DSSP program assigns protein secondary structure to one of eight states. This discrete assignment cannot describe the continuum of thermal fluctuations. Hence, a continuous assignment is proposed. Technically, the continuum results from averaging over ten discrete DSSP assignments with different hydrogen bond thresholds. The final continuous assignment for a single NMR model successfully reflected the structural variations observed between all NMR models in the ensemble. The structural variations between NMR models were verified to correlate with thermal motion; these variations were captured by the continuous assignments. Because the continuous assignment reproduces the structural variation between many NMR models from one single model, functionally important variation can be extracted from a single X-ray structure. Thus, continuous assignments of secondary structure may affect future protein structure analysis, comparison, and prediction.
引用
收藏
页码:175 / 184
页数:10
相关论文
共 63 条
  • [1] SOLUTION STRUCTURE OF (CD2+)(1)-CALBINDIN D-9K REVEALS DETAILS OF THE STEPWISE STRUCTURAL-CHANGES ALONG THE APO-](CA2+)(1)(II)-](CA2+)(2)(I,II) BINDING PATHWAY
    AKKE, M
    FORSEN, S
    CHAZIN, WJ
    [J]. JOURNAL OF MOLECULAR BIOLOGY, 1995, 252 (01) : 102 - 121
  • [2] ANDERSEN CA, 1998, THESIS TU DENMARK LY
  • [3] Helix capping
    Aurora, R
    Rose, GD
    [J]. PROTEIN SCIENCE, 1998, 7 (01) : 21 - 38
  • [4] BARBATO G, 2000, BIOCHEMISTRY-US, V31, P5269
  • [5] Are proteins even floppier than we thought?
    Bax, A
    Tjandra, N
    [J]. NATURE STRUCTURAL BIOLOGY, 1997, 4 (04) : 254 - 256
  • [6] The three-dimensional solution structure and dynamic properties of the human FADD death domain
    Berglund, H
    Olerenshaw, D
    Sankar, A
    Federwisch, M
    McDonald, NQ
    Driscoll, PC
    [J]. JOURNAL OF MOLECULAR BIOLOGY, 2000, 302 (01) : 171 - 188
  • [7] The Protein Data Bank
    Berman, HM
    Westbrook, J
    Feng, Z
    Gilliland, G
    Bhat, TN
    Weissig, H
    Shindyalov, IN
    Bourne, PE
    [J]. NUCLEIC ACIDS RESEARCH, 2000, 28 (01) : 235 - 242
  • [8] Bonvin AMJJ, 1996, J BIOMOL NMR, V7, P72
  • [9] CONFORMATIONAL VARIABILITY OF SOLUTION NUCLEAR-MAGNETIC-RESONANCE STRUCTURES
    BONVIN, AMJJ
    BRUNGER, AT
    [J]. JOURNAL OF MOLECULAR BIOLOGY, 1995, 250 (01) : 80 - 93
  • [10] Brunak S, 1996, PROTEINS, V25, P237, DOI 10.1002/(SICI)1097-0134(199606)25:2<237::AID-PROT9>3.3.CO