Figure 1.
Model of cellobiohydrolase CelS structure in complex with celloheptaose (green), and cellobiose, colored in white (hydrogen), red (oxygen), and cyan (carbon).
The sugar unit at subsite −1 was modelled manually. The substrate, celloheptaose, spans between subsites −1 to −7 in the substrate-binding tunnel, and cellobiose is bound in the cleft region between subsites +1 and +2. This figure was made using the VMD software [66].
Figure 2.
Structural comparison of active sites of (A) family 8 CelA and (B) family 48 CelS.
Substrate is shown in Gray.
Figure 3.
Schematic representation of inverting reaction mechanism in CelS for hydrolysis of glycosidic bond C1-O4.
The catalytic residues Glu87, Asp255, and nucleophilic water molecule (W1) are shown. Anomeric carbon atom at subsite −1 and leaving group oxygen atom at subsite +1 are C1 and O4, respectively. The thin arrows represent electron transfer between atoms. Distances between atoms are shown in red.
Figure 4.
Potential of mean force for hydrolysis reaction.
Figure 5.
Snapshot of reactant state from QM/MM molecular dynamics free energy trajectories.
Only the active site residues, glucosyl units −1 and +1, acid catalyst Glu87, base catalyst Asp255, nucleophilic water, and a second water molecule shown in gold (omitted Hydrogen atoms for clarity), are shown here. All backbone atoms of Glu87 and Asp255 are omitted for clarity. Important distances are shown by black lines.
Figure 6.
Snapshot of transition state from QM/MM molecular dynamics free energy trajectories.
Other figure specifications are similar to Fig 5.
Figure 7.
Snapshot of product state from QM/MM molecular dynamics free energy trajectories.
Other figure specifications are similar to Fig 5.
Figure 8.
Upper panel: Puckering coordinates (Q,,
) for six membered ring.
Lower panel: Projection of puckering coordinates (q, and q
) sampled by molecular dynamics trajectories along the reaction coordinate rc2. q
and q
values are shown in gray and black, respectively. Regions corresponding to reactant (R), around transition state (TS), and product (R) are highlighted by boxes.
Figure 9.
Stoddart diagram showing ring conformations at subsite −1 with respect to q and q
.
Conformations for reactant (brown circle), transition (red triangle), and product (blue sqare) states are shown. Different regions are separated by dashed black lines. The central region represents undistorted and stable C
conformation.
Figure 10.
Setup for enzyme reaction in CelS with QM/MM method.
QM region (VDW representation) consists of catalytic residues (Asp255 and Glu87), nucleophilic water (W1), and active part of substrate (subsites −1, and +1), while rest of enzyme (green), substrate (orange), and water (cyan) are in MM region. Inset shows only QM region and hydrogen link atoms (pink) used as boundary between MM and QM.