Literature DB >> 923582

The Protein Data Bank. A computer-based archival file for macromolecular structures.

F C Bernstein, T F Koetzle, G J Williams, E F Meyer, M D Brice, J R Rodgers, O Kennard, T Shimanouchi, M Tasumi.   

Abstract

The Protein Data Bank is a computer-based archival file for macromolecular structures. The Bank stores in a uniform format atomic co-ordinates and partial bond connectivities, as derived from crystallographic studies. Text included in each data entry gives pertinent information for the structure at hand (e.g. species from which the molecule has been obtained, resolution of diffraction data, literature citations and specifications of secondary structure). In addition to atomic co-ordinates and connectivities, the Protein Data Bank stores structure factors and phases, although these latter data are not placed in any uniform format. Input of data to the Bank and general maintenance functions are carried out at Brookhaven National Laboratory. All data stored in the Bank are available on magnetic tape for public distribution, from Brookhaven (to laboratories in the Americas), Tokyo (Japan), and Cambridge (Europe and worldwide). A master file is maintained at Brookhaven and duplicate copies are stored in Cambridge and Tokyo. In the future, it is hoped to expand the scope of the Protein Data Bank to make available co-ordinates for standard structural types (e.g. alpha-helix, RNA double-stranded helix) and representative computer programs of utility in the study and interpretation of macromolecular structures.

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Year:  1977        PMID: 923582     DOI: 10.1111/j.1432-1033.1977.tb11885.x

Source DB:  PubMed          Journal:  Eur J Biochem        ISSN: 0014-2956


  187 in total

1.  Thermolysin and mitochondrial processing peptidase: how far structure-functional convergence goes.

Authors:  K S Makarova; N V Grishin
Journal:  Protein Sci       Date:  1999-11       Impact factor: 6.725

2.  Structure of the Ca2+-regulated photoprotein obelin at 1.7 A resolution determined directly from its sulfur substructure.

Authors:  Z J Liu; E S Vysotski; C J Chen; J P Rose; J Lee; B C Wang
Journal:  Protein Sci       Date:  2000-11       Impact factor: 6.725

3.  A theoretical search for folding/unfolding nuclei in three-dimensional protein structures.

Authors:  O V Galzitskaya; A V Finkelstein
Journal:  Proc Natl Acad Sci U S A       Date:  1999-09-28       Impact factor: 11.205

4.  Optimal region of average side-chain entropy for fast protein folding.

Authors:  O V Galzitskaya; A K Surin; H Nakamura
Journal:  Protein Sci       Date:  2000-03       Impact factor: 6.725

5.  Two tricks in one bundle: helix-turn-helix gains enzymatic activity.

Authors:  N V Grishin
Journal:  Nucleic Acids Res       Date:  2000-06-01       Impact factor: 16.971

6.  Arg660Ser mutation in Thermus aquaticus DNA polymerase I suppresses T-->C transitions: implication of wobble base pair formation at the nucleotide incorporation step.

Authors:  K Yoshida; A Tosaka; H Kamiya; T Murate; H Kasai; Y Nimura; M Ogawa; S Yoshida; M Suzuki
Journal:  Nucleic Acids Res       Date:  2001-10-15       Impact factor: 16.971

7.  Enhanced protein fold recognition using secondary structure information from NMR.

Authors:  D J Ayers; P R Gooley; A Widmer-Cooper; A E Torda
Journal:  Protein Sci       Date:  1999-05       Impact factor: 6.725

8.  Contact order revisited: influence of protein size on the folding rate.

Authors:  Dmitry N Ivankov; Sergiy O Garbuzynskiy; Eric Alm; Kevin W Plaxco; David Baker; Alexei V Finkelstein
Journal:  Protein Sci       Date:  2003-09       Impact factor: 6.725

9.  Prediction of protein folding rates from the amino acid sequence-predicted secondary structure.

Authors:  Dmitry N Ivankov; Alexei V Finkelstein
Journal:  Proc Natl Acad Sci U S A       Date:  2004-06-07       Impact factor: 11.205

10.  In silico docking and molecular dynamics simulation of 3-dehydroquinate synthase (DHQS) from Mycobacterium tuberculosis.

Authors:  Mustafa Alhaji Isa; Rita Singh Majumdhar; Shazia Haider
Journal:  J Mol Model       Date:  2018-05-11       Impact factor: 1.810

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