Literature DB >> 11050234

Anatomy of protein structures: visualizing how a one-dimensional protein chain folds into a three-dimensional shape.

C J Tsai1, J V Maizel, R Nussinov.   

Abstract

Here, we depict the anatomy of protein structures in terms of the protein folding process. Via an iterative, top-down dissecting procedure, tertiary structures are spliced down to reveal their anatomy: first, to produce domains (defined by visual three-dimensional inspection criteria); then, hydrophobic folding units (HFU); and, at the end of a multilevel process, a set of building blocks. The resulting anatomy tree organization not only clearly depicts the organization of a one-dimensional polypeptide chain in three-dimensional space but also straightforwardly describes the most likely folding pathway(s). Comparison of the tree with the formation of the hydrophobic folding units through combinatorial assembly of the building blocks illustrates how the chain folds in a sequential or a complex folding pathway. Further, the tree points to the kinetics of the folding, whether the chain is a fast or a slow folder, and the probability of misfolding. Our ability to successfully dissect the protein into an anatomy tree illustrates that protein folding is a hierarchical process and further validates a building blocks protein folding model.

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Year:  2000        PMID: 11050234      PMCID: PMC17290          DOI: 10.1073/pnas.97.22.12038

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  42 in total

1.  Solution structure of a peptide model of a region important for the folding of alpha-lactalbumin provides evidence for the formation of nonnative structure in the denatured state.

Authors:  S J Demarest; D P Raleigh
Journal:  Proteins       Date:  2000-02-01

2.  Energetic basis of structural stability in the molten globule state: alpha-lactalbumin.

Authors:  Y V Griko
Journal:  J Mol Biol       Date:  2000-04-14       Impact factor: 5.469

3.  Molecular dynamics simulations of a beta-hairpin fragment of protein G: balance between side-chain and backbone forces.

Authors:  B Ma; R Nussinov
Journal:  J Mol Biol       Date:  2000-03-03       Impact factor: 5.469

4.  Limited proteolysis of bovine alpha-lactalbumin: isolation and characterization of protein domains.

Authors:  P Polverino de Laureto; E Scaramella; M Frigo; F G Wondrich; V De Filippis; M Zambonin; A Fontana
Journal:  Protein Sci       Date:  1999-11       Impact factor: 6.725

5.  Structural patterns in globular proteins.

Authors:  M Levitt; C Chothia
Journal:  Nature       Date:  1976-06-17       Impact factor: 49.962

6.  Initial hydrophobic collapse is not necessary for folding RNase A.

Authors:  A Nöppert; K Gast; D Zirwer; G Damaschun
Journal:  Fold Des       Date:  1998

7.  Alpha-lactalbumin forms a compact molten globule in the absence of disulfide bonds.

Authors:  C Redfield; B A Schulman; M A Milhollen; P S Kim; C M Dobson
Journal:  Nat Struct Biol       Date:  1999-10

Review 8.  The anatomy and taxonomy of protein structure.

Authors:  J S Richardson
Journal:  Adv Protein Chem       Date:  1981

9.  Folding units in globular proteins.

Authors:  A M Lesk; G D Rose
Journal:  Proc Natl Acad Sci U S A       Date:  1981-07       Impact factor: 11.205

10.  Location of structural domains in protein.

Authors:  S J Wodak; J Janin
Journal:  Biochemistry       Date:  1981-11-10       Impact factor: 3.162

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  26 in total

1.  Protein folding and function: the N-terminal fragment in adenylate kinase.

Authors:  S Kumar; Y Y Sham; C J Tsai; R Nussinov
Journal:  Biophys J       Date:  2001-05       Impact factor: 4.033

2.  Molecular dynamics simulation of Escherichia coli dihydrofolate reductase and its protein fragments: relative stabilities in experiment and simulations.

Authors:  Y Y Sham; B Ma; C J Tsai; R Nussinov
Journal:  Protein Sci       Date:  2001-01       Impact factor: 6.725

3.  Point mutations and sequence variability in proteins: redistributions of preexisting populations.

Authors:  N Sinha; R Nussinov
Journal:  Proc Natl Acad Sci U S A       Date:  2001-03-13       Impact factor: 11.205

4.  Comparison of protein fragments identified by limited proteolysis and by computational cutting of proteins.

Authors:  Chung-Jung Tsai; Patrizia Polverino de Laureto; Angelo Fontana; Ruth Nussinov
Journal:  Protein Sci       Date:  2002-07       Impact factor: 6.725

5.  Reducing the computational complexity of protein folding via fragment folding and assembly.

Authors:  Nurit Haspel; Chung-Jung Tsai; Haim Wolfson; Ruth Nussinov
Journal:  Protein Sci       Date:  2003-06       Impact factor: 6.725

6.  In silico protein design by combinatorial assembly of protein building blocks.

Authors:  Hui-Hsu Gavin Tsai; Chung-Jung Tsai; Buyong Ma; Ruth Nussinov
Journal:  Protein Sci       Date:  2004-10       Impact factor: 6.725

7.  CONTSOR--a new knowledge-based fold recognition potential, based on side chain orientation and contacts between residue terminal groups.

Authors:  Boris Vishnepolsky; Malak Pirtskhalava
Journal:  Protein Sci       Date:  2011-11-23       Impact factor: 6.725

8.  Reducing the dimensionality of the protein-folding search problem.

Authors:  George D Chellapa; George D Rose
Journal:  Protein Sci       Date:  2012-07-06       Impact factor: 6.725

9.  A thermodynamic definition of protein domains.

Authors:  Lauren L Porter; George D Rose
Journal:  Proc Natl Acad Sci U S A       Date:  2012-05-25       Impact factor: 11.205

10.  The implications of higher (or lower) success in secondary structure prediction of chain fragments.

Authors:  Chung-Jung Tsai; Ruth Nussinov
Journal:  Protein Sci       Date:  2005-08       Impact factor: 6.725

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