1997
DOI: 10.1016/s0014-5793(97)01346-x
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Representation of amino acid sequences in terms of interaction energy in protein globules

Abstract: We suggest a new simple approach for comparing the primary structure of proteins and their spatial structure. It relies on the one-to-one correspondence between each residue of the polypeptide chain and the energy of van der Waals interactions between the regions of the native globule flanking this residue. The method obviates the sophisticated geometrical criteria for estimating similarity between spatial structures. Besides, it permits one to analyze structural units of different scale.

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Cited by 30 publications
(19 citation statements)
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“…Specifically, prevalence of the nucleotide thymine in the second codon position and its strong correlation with OGT in Archaea is apparently a result of the demand on enrichement of Archaeal proteins with hydrophobic residues (Table 7). Noteworthy, a massive increase of van der Waals interactions (24,64) was found to be the cornerstone of the structure-based evolutionary strategy of protein thermostability in ancient species (29). In Bacterial proteins, however, there is an increase of the fractions of charged residues with OGT (Table 7).…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…Specifically, prevalence of the nucleotide thymine in the second codon position and its strong correlation with OGT in Archaea is apparently a result of the demand on enrichement of Archaeal proteins with hydrophobic residues (Table 7). Noteworthy, a massive increase of van der Waals interactions (24,64) was found to be the cornerstone of the structure-based evolutionary strategy of protein thermostability in ancient species (29). In Bacterial proteins, however, there is an increase of the fractions of charged residues with OGT (Table 7).…”
Section: Discussionmentioning
confidence: 99%
“…Specifically, it has been claimed that it is essentially governed by the genome replication and DNA-repair mechanisms (19), is involved into lineage- and niche-specific molecular strategies of adaptation (17), drives a codon usage (20) and even amino acid composition (12–14,16). In the case of protein structure, distinct stabilizing interactions (24–28), their structural determinants (24,29–33) and contribution from different amino acid residues (22,24,25,29,34–36) have been studied extensively (37–40). However, until recently all the studies were focused around few proteins or small set of them, individual stabilizing interactions, or considered anecdotal cases of organisms thriving under normal or extreme temperatures.…”
Section: Introductionmentioning
confidence: 99%
“…Two types of physical mechanisms that contribute to protein thermophily are distinguished as "structure-based" and "sequencebased" (19). The features associated with enhanced thermal stability include ionic interactions (20), increase in hydrophobicity and packing density (21,22), augmentation of hydrogen bonding and van der Waals interactions (23,24), and specific amino acid substitutions that stabilize protein structure at particularly critical locations (25).…”
mentioning
confidence: 99%
“…The energy of the pair-wise interactions is calculated for atoms belonging to residues separated by at least two amino acid residues. This is suf cient (Berezovskii et al, 1997a;Berezovsky et al, 1997b;Berezovskii and Tumanyan, 1995) for estimating the interactions between the adjacent regions of the globule. Only contacts between atoms were taken into consideration and appropriate energies were calculated if the distance lay in the range of values 2.5-5.0Å.…”
Section: Figmentioning
confidence: 99%