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PDBsum entry 1acp
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Fatty acid synthesis protein
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PDB id
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1acp
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References listed in PDB file
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Key reference
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Title
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Refinement of the nmr structures for acyl carrier protein with scalar coupling data.
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Authors
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Y.Kim,
J.H.Prestegard.
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Ref.
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Proteins, 1990,
8,
377-385.
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PubMed id
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Abstract
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Structure determination of small proteins using NMR data is most commonly
pursued by combining NOE derived distance constraints with inherent constraints
based on chemical bonding. Ideally, one would make use of a variety of
experimental observations, not just distance constraints. Here, coupling
constant constraints have been added to molecular mechanics and molecular
dynamics protocols for structure determination in the form of a psuedoenergy
function that is minimized in a search for an optimum molecular conformation.
Application is made to refinement of a structure for a 77 amino acid protein
involved in fatty acid synthesis, Escherichia coli acyl carrier protein (ACP).
54 3JHN alpha coupling constants, 12 coupling constants for stereospecifically
assigned side chain protons, and 450 NOE distance constraints were used to
calculate the 3-D structure of ACP. A three-step protocol for a molecular
dynamics calculation is described, in analogy to the protocol previously used in
molecular mechanics calculations. The structures calculated with the molecular
mechanics approach and the molecular dynamics approach using a rigid model for
the protein show similar molecular energies and similar agreement with
experimental distance and coupling constant constraints. The molecular dynamics
approach shows some advantage in overcoming local minimum problems, but only
when a two-state averaging model for the protein was used, did molecular
energies drop significantly.
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Secondary reference #1
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Title
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A dynamic model for the structure of acyl carrier protein in solution.
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Authors
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Y.Kim,
J.H.Prestegard.
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Ref.
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Biochemistry, 1989,
28,
8792-8797.
[DOI no: ]
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PubMed id
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Secondary reference #2
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Title
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Three-Dimensional structure of acyl carrier protein determined by nmr pseudoenergy and distance geometry calculations.
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Authors
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T.A.Holak,
S.K.Kearsley,
Y.Kim,
J.H.Prestegard.
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Ref.
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Biochemistry, 1988,
27,
6135-6142.
[DOI no: ]
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PubMed id
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