Abstract Proline cis-trans isomerisation is a regulatory mechanism used in a range of biological processes, and is related to various diseases such as Alzheimers disease and cancer. However, the details of the exact molecular mechanism by which it occurs are not known. Using X-ray crystallography, proline isomerisation has been shown to occur following formation of an antigen-antibody complex between the target epiregulin (EPR) and the antibody 9E5, at proline (Pro103), located in the third complementarity-determining region (CDR) of the heavy chain of 9E5. To obtain an accurate description of the pathway involved in cis-trans isomerisation in this system, we performed ten independent long molecular dynamics (MD) simulations starting at a s...
Abstract The finding that cis/trans isomerization of proline peptide bonds can provide the basis for...
International audiencePeptide bonds in protein structures are mainly found in trans conformation wit...
There are four peptidyl-proline bonds in the 64-residue protein chymotrypsin inhibitor 2 (CI2), all ...
Conformational rearrangements in antibody antigen recognition are essential events where kinetic dis...
Molecular chaperones often possess functional modules that are specialized in assisting the formatio...
none4noThe peptidyl-proyl isomerase Pin1 plays a key role in the regulation of phospho(p)-Ser/Thr-Pr...
ArkA12 is a proline rich intrinsically disordered protein (IDP) region within a larger, more structu...
In cellular signaling cascades, protein activity can be controlled by molecular-switch directed liga...
The protein β2-microglobulin (β2-m) can aggregate in insoluble amyloid fibrils, which deposit in the...
The interactions of intrinsically disordered proteins (IDPs) with their molecular targets are essent...
AbstractPolypeptides often display proline-mediated conformational substates that are prone to isome...
Pin1 is an enzyme that specifically catalyzes the cis-trans isomerization of proline amide bonds in ...
Pin1 is a peptidyl-prolyl cis/trans isomerase that isomerizes phospho-Serine/Threonine-Proline motif...
As the dominant constituents of the active sites, complementarity-determining regions (CDRs) and par...
Peptidyl-prolyl isomerase, Pin1, is an extremely important cell regulatory enzyme, participating in ...
Abstract The finding that cis/trans isomerization of proline peptide bonds can provide the basis for...
International audiencePeptide bonds in protein structures are mainly found in trans conformation wit...
There are four peptidyl-proline bonds in the 64-residue protein chymotrypsin inhibitor 2 (CI2), all ...
Conformational rearrangements in antibody antigen recognition are essential events where kinetic dis...
Molecular chaperones often possess functional modules that are specialized in assisting the formatio...
none4noThe peptidyl-proyl isomerase Pin1 plays a key role in the regulation of phospho(p)-Ser/Thr-Pr...
ArkA12 is a proline rich intrinsically disordered protein (IDP) region within a larger, more structu...
In cellular signaling cascades, protein activity can be controlled by molecular-switch directed liga...
The protein β2-microglobulin (β2-m) can aggregate in insoluble amyloid fibrils, which deposit in the...
The interactions of intrinsically disordered proteins (IDPs) with their molecular targets are essent...
AbstractPolypeptides often display proline-mediated conformational substates that are prone to isome...
Pin1 is an enzyme that specifically catalyzes the cis-trans isomerization of proline amide bonds in ...
Pin1 is a peptidyl-prolyl cis/trans isomerase that isomerizes phospho-Serine/Threonine-Proline motif...
As the dominant constituents of the active sites, complementarity-determining regions (CDRs) and par...
Peptidyl-prolyl isomerase, Pin1, is an extremely important cell regulatory enzyme, participating in ...
Abstract The finding that cis/trans isomerization of proline peptide bonds can provide the basis for...
International audiencePeptide bonds in protein structures are mainly found in trans conformation wit...
There are four peptidyl-proline bonds in the 64-residue protein chymotrypsin inhibitor 2 (CI2), all ...