METHODS FOR COMPARISON OF PROTEIN THREE DIMENSIONAL STRUCTURE

蛋白质三维结构比较方法

基本信息

  • 批准号:
    2578631
  • 负责人:
  • 金额:
    --
  • 依托单位:
  • 依托单位国家:
    美国
  • 项目类别:
  • 财政年份:
  • 资助国家:
    美国
  • 起止时间:
  • 项目状态:
    未结题

项目摘要

We have developed algorithms for comparison and alignment of protein three dimensional structures. VAST (vector alignment search tool) identifies substructure similarities by comparing the types, connectivity, and relative orientations of SSE's (secondary structure elements). Surprising similarities are identified objectively, by considering the number and scores of superimposable SSE-pairs in the best alignment, and the number of alternative alignments sampled. An optimal residue-by-residue alignments are also identified objectively, as that with the most surprising combination of superposition residual and number of aligned residues. Work this year has focused in three areas: 1) refinement of the rapid search heuristic, 2) refinement of the statistical significance calculation, and 3) calculation of a complete structural neighbor database for Entrez. VAST is an exhaustive search method in that it considers all possible SSE-pair alignments via a clique detection algorithm, and ranks them according to superposition score. We have found that sensitivity is improved to over 99.5% of BLAST similarities by two simple modifications, relaxation of the geometrical criteria defining edges in the clique graph, and prior parsing of 3D structure into compact domains. The significance test statistic for VAST is the product of the chance-occurrence likelihood of the best SSE alignment, and the number of possible alignments in a given domain-pair comparison. We have found that accuracy is improved by use of explicit convolution of the empirical score distribution for SSE pairs, up to substructure sizes found in practice, and by exact calculation of the number of alternative alignments, via a dynamic programming algorithm. The Entrez neighbor database contains results of an all-against-all comparison of the 10,000 domain structures in the current 3D database. We have found that VAST requires approximately .5 seconds per comparison, a value which makes this calculation possible for the first time. Maintenance of the complete structure neighbor database is also feasible, and we expect that this will be a useful resource for comparative analysis.
我们已经开发了比较和对齐的算法

项目成果

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S H BRYANT其他文献

S H BRYANT的其他文献

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{{ truncateString('S H BRYANT', 18)}}的其他基金

STRUCTURE PREDICTION BY PROTEIN THREADING
通过蛋白质螺纹进行结构预测
  • 批准号:
    5203626
  • 财政年份:
  • 资助金额:
    --
  • 项目类别:
DATABASES FOR MOLECULAR MODELING
分子建模数据库
  • 批准号:
    5203627
  • 财政年份:
  • 资助金额:
    --
  • 项目类别:
THREADING PROTIEN SEQUENCE THROUGH FOLDING MOTIF
将蛋白质序列穿过折叠基序
  • 批准号:
    3845098
  • 财政年份:
  • 资助金额:
    --
  • 项目类别:
ANALYSIS OF PACKING CONTACTS IN PROTEIN CRYSTALS
蛋白质晶体中堆积接触的分析
  • 批准号:
    3781258
  • 财政年份:
  • 资助金额:
    --
  • 项目类别:
DATABASES FOR MOLECULAR MODELING
分子建模数据库
  • 批准号:
    3781279
  • 财政年份:
  • 资助金额:
    --
  • 项目类别:
ANALYSIS OF PACKING CONTACTS IN PROTEIN CRYSTALS
蛋白质晶体中堆积接触的分析
  • 批准号:
    3759296
  • 财政年份:
  • 资助金额:
    --
  • 项目类别:
PROTEIN THREADING METHODS
蛋白质穿线方法
  • 批准号:
    6162796
  • 财政年份:
  • 资助金额:
    --
  • 项目类别:
INTERNET RESOURCES FOR MOLECULAR 3D STRUCTURE
分子 3D 结构的互联网资源
  • 批准号:
    6162797
  • 财政年份:
  • 资助金额:
    --
  • 项目类别:
EMPIRICAL ENERGY FUNCTIONS FOR MOLECULAR MODELING
分子建模的经验能量函数
  • 批准号:
    3845097
  • 财政年份:
  • 资助金额:
    --
  • 项目类别:
METHODS FOR COMPARISON OF PROTEIN THREE DIMENSIONAL STRUCTURE
蛋白质三维结构比较方法
  • 批准号:
    5203629
  • 财政年份:
  • 资助金额:
    --
  • 项目类别:

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