Literature DB >> 9385654

The partial charge of the nitrogen atom in peptide bonds.

E J Milner-White1.   

Abstract

A majority of the standard texts dealing with proteins portray the peptide link as a mixture of two resonance forms, in one of which the nitrogen atom has a positive charge. As a consequence, it is often believed that the nitrogen atom has a net positive charge. This is in apparent contradiction with the partial negative charge on the nitrogen that is used in force fields for molecular modeling. However, charges on resonance forms are best regarded as formal rather than actual charges and current evidence clearly favors a net negative charge for the nitrogen atom. In the course of the discussion, new ideas about the electronic structure of amides and the peptide bond are presented.

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Year:  1997        PMID: 9385654      PMCID: PMC2143592          DOI: 10.1002/pro.5560061125

Source DB:  PubMed          Journal:  Protein Sci        ISSN: 0961-8368            Impact factor:   6.725


  9 in total

1.  Experimentally observed conformation-dependent geometry and hidden strain in proteins.

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Journal:  Protein Sci       Date:  1996-07       Impact factor: 6.725

2.  Dominant role of local dipoles in stabilizing uncompensated charges on a sulfate sequestered in a periplasmic active transport protein.

Authors:  J J He; F A Quiocho
Journal:  Protein Sci       Date:  1993-10       Impact factor: 6.725

3.  Helix stop signals in proteins and peptides: the capping box.

Authors:  E T Harper; G D Rose
Journal:  Biochemistry       Date:  1993-08-03       Impact factor: 3.162

4.  Dictionary of protein secondary structure: pattern recognition of hydrogen-bonded and geometrical features.

Authors:  W Kabsch; C Sander
Journal:  Biopolymers       Date:  1983-12       Impact factor: 2.505

5.  Structures of N-termini of helices in proteins.

Authors:  A J Doig; M W MacArthur; B J Stapley; J M Thornton
Journal:  Protein Sci       Date:  1997-01       Impact factor: 6.725

6.  Anion binding sites in protein structures.

Authors:  P Chakrabarti
Journal:  J Mol Biol       Date:  1993-11-20       Impact factor: 5.469

7.  A new look at proton transfer dynamics along the hydrogen bonds in amides and peptides.

Authors:  G J Kearley; F Fillaux; M H Baron; S Bennington; J Tomkinson
Journal:  Science       Date:  1994-05-27       Impact factor: 47.728

8.  Coulombic interactions between partially charged main-chain atoms not hydrogen-bonded to each other influence the conformations of alpha-helices and antiparallel beta-sheet. A new method for analysing the forces between hydrogen bonding groups in proteins includes all the Coulombic interactions.

Authors:  P H Maccallum; R Poet; E J Milner-White
Journal:  J Mol Biol       Date:  1995-04-28       Impact factor: 5.469

9.  Acyl-transfer reactions of amides and esters with alcohols and thiols. A reference system for the serine and cysteine proteinases. Concerning the N protonation of amides and amide-imidate equilibria.

Authors:  A R Fersht
Journal:  J Am Chem Soc       Date:  1971-07-14       Impact factor: 15.419

  9 in total
  18 in total

1.  H-bonding mediates polarization of peptide groups in folded proteins.

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Journal:  Protein Sci       Date:  2003-11       Impact factor: 6.725

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3.  2005 Emil Thomas Kaiser Award.

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6.  On contribution of known atomic partial charges of protein backbone in electrostatic potential density maps.

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Journal:  Protein Sci       Date:  2017-04-07       Impact factor: 6.725

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Journal:  PLoS One       Date:  2017-09-18       Impact factor: 3.240

8.  On the involvement of electron transfer reactions in the fluorescence decay kinetics heterogeneity of proteins.

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Journal:  Protein Sci       Date:  2001-10       Impact factor: 6.725

9.  Dependence of the AmII'p proline Raman band on peptide conformation.

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Journal:  J Phys Chem B       Date:  2009-08-13       Impact factor: 2.991

10.  The dead-end elimination method, tryptophan rotamers, and fluorescence lifetimes.

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