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Structure prediction of partial-length protein sequences.

Adrian Laurenzi | Ling-Hong Hung | Ram Samudrala
International journal of molecular sciences | 2013

Protein structure information is essential to understand protein function. Computational methods to accurately predict protein structure from the sequence have primarily been evaluated on protein sequences representing full-length native proteins. Here, we demonstrate that top-performing structure prediction methods can accurately predict the partial structures of proteins encoded by sequences that contain approximately 50% or more of the full-length protein sequence. We hypothesize that structure prediction may be useful for predicting functions of proteins whose corresponding genes are mapped expressed sequence tags (ESTs) that encode partial-length amino acid sequences. Additionally, we identify a confidence score representing the quality of a predicted structure as a useful means of predicting the likelihood that an arbitrary polypeptide sequence represents a portion of a foldable protein sequence ("foldability"). This work has ramifications for the prediction of protein structure with limited or noisy sequence information, as well as genome annotation.

Pubmed ID: 23867606

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Associated grants

  • Agency: NLM NIH HHS, United States
    Id: DP1 LM011509
  • Agency: NIH HHS, United States
    Id: DP1 OD006779
  • Agency: NIH HHS, United States
    Id: DP1OD006779

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I-TASSER (tool)

RRID:SCR_014627

Web server as integrated platform for automated protein structure and function prediction. Used for protein 3D structure prediction. Resource for automated protein structure prediction and structure-based function annotation.

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