Maximum Allowed Solvent Accessibilites of Residues in Proteins
University of Chicago · Texas Tech University · +2 more institutions
Abstract
The relative solvent accessibility (RSA) of a residue in a protein measures the extent of burial or exposure of that residue in the 3D structure. RSA is frequently used to describe a protein's biophysical or evolutionary properties. To calculate RSA, a residue's solvent accessibility (ASA) needs to be normalized by a suitable reference value for the given amino acid; several normalization scales have previously been proposed. However, these scales do not provide tight upper bounds on ASA values frequently observed in empirical crystal structures. Instead, they underestimate the largest allowed ASA values, by up to 20%. As a result, many empirical crystal structures contain residues that seem to have RSA values…
Citation impact
- FWCI
- 7.78
- Percentile
- 100%
- References
- 42
Authors
5- MTMatthew Tien
University of Chicago
- AGAustin G. Meyer
Texas Tech University, Texas Tech University Health Sciences Center, The University of Texas at Austin
- DKDariya K. Sydykova
The University of Texas at Austin
- SJStephanie J. Spielman
The University of Texas at Austin
- COClaus O. WilkeCorresponding
The University of Texas at Austin
Topics & keywords
- Normalization (sociology)
- Tripeptide
- Residue (chemistry)
- Amino acid residue
- Solvent
- Enumeration
- Mathematics
- Chemistry