TY - JOUR
T1 - A critical survey of average distances between catalytic carboxyl groups in glycoside hydrolases
AU - Mhlongo, Ndumiso N.
AU - Skelton, Adam A.
AU - Kruger, Gert
AU - Soliman, Mahmoud E. S.
AU - Williams, Ian H.
PY - 2014/9
Y1 - 2014/9
N2 - Published X-ray crystallographic structures for glycoside hydrolases (GHs) from 39 different families are surveyed according to some rigorous selection criteria, and the distances separating 208 pairs of catalytic carboxyl groups (20 α-retaining, 87 β-retaining, 38 α-inverting, and 63 β-inverting) are analyzed. First, the average of all four inter-carboxyl OO distances for each pair is determined; second, the mean of all the pair-averages within each GH family is determined; third, means are determined for groups of GH families. No significant differences are found for free structures compared with those complexed with a ligand in the active site of the enzyme, nor for α-GHs as compared with β-GHs. The mean and standard deviation (1σ) of the unimodal distribution of average OO distances for all families of inverting GHs is 8±2Å, with a very wide range from 5Å (GH82) to nearly 13Å (GH46). The distribution of average OO distances for all families of retaining GHs appears to be bimodal: the means and standard deviations of the two groups are 4.8±0.3Å and 6.4±0.6Å. These average values are more representative, and more likely to be meaningful, than the often-quoted literature values, which are based on a very small sample of structures. The newly-updated average values proposed here may alter perceptions about what separations between catalytic residues are "normal" or "abnormal" for GHs.
AB - Published X-ray crystallographic structures for glycoside hydrolases (GHs) from 39 different families are surveyed according to some rigorous selection criteria, and the distances separating 208 pairs of catalytic carboxyl groups (20 α-retaining, 87 β-retaining, 38 α-inverting, and 63 β-inverting) are analyzed. First, the average of all four inter-carboxyl OO distances for each pair is determined; second, the mean of all the pair-averages within each GH family is determined; third, means are determined for groups of GH families. No significant differences are found for free structures compared with those complexed with a ligand in the active site of the enzyme, nor for α-GHs as compared with β-GHs. The mean and standard deviation (1σ) of the unimodal distribution of average OO distances for all families of inverting GHs is 8±2Å, with a very wide range from 5Å (GH82) to nearly 13Å (GH46). The distribution of average OO distances for all families of retaining GHs appears to be bimodal: the means and standard deviations of the two groups are 4.8±0.3Å and 6.4±0.6Å. These average values are more representative, and more likely to be meaningful, than the often-quoted literature values, which are based on a very small sample of structures. The newly-updated average values proposed here may alter perceptions about what separations between catalytic residues are "normal" or "abnormal" for GHs.
UR - http://www.scopus.com/inward/record.url?scp=84894266356&partnerID=8YFLogxK
UR - http://dx.doi.org/10.1002/prot.24528
U2 - 10.1002/prot.24528
DO - 10.1002/prot.24528
M3 - Article
SN - 0887-3585
VL - 82
SP - 1747
EP - 1755
JO - Proteins: Structure, Function, and Bioinformatics
JF - Proteins: Structure, Function, and Bioinformatics
IS - 9
ER -