- Research article
- Open Access
Structural insights into the mechanism defining substrate affinity in Arabidopsis thaliana dUTPase: the role of tryptophan 93 in ligand orientation
© Inoguchi et al. 2015
- Received: 2 September 2015
- Accepted: 26 November 2015
- Published: 15 December 2015
Deoxyuridine triphosphate nucleotidohydrolase (dUTPase) hydrolyzes dUTP to dUMP and pyrophosphate to maintain the cellular thymine-uracil ratio. dUTPase is also a target for cancer chemotherapy. However, the mechanism defining its substrate affinity remains unclear. Sequence comparisons of various dUTPases revealed that Arabidopsis thaliana dUTPase has a unique tryptophan at position 93, which potentially contributes to its degree of substrate affinity. To better understand the roles of tryptophan 93, A. thaliana dUTPase was studied.
Enzyme assays showed that A. thaliana dUTPase belongs to a high-affinity group of isozymes, which also includes the enzymes from Escherichia coli and Mycobacterium tuberculosis. Enzymes from Homo sapiens and Saccharomyces cerevisiae are grouped as low-affinity dUTPases. The structure of the homo-trimeric A. thaliana dUTPase showed three active sites, each with a different set of ligand interactions between the amino acids and water molecules. On an α-helix, tryptophan 93 appears to keep serine 89 in place via a water molecule and to specifically direct the ligand. Upon being oriented in the active site, the C-terminal residues close the active site to promote the reaction.
In the high-affinity group, the prefixed direction of the serine residues was oriented by a positively charged residue located four amino acids away, while low-affinity enzymes possess small hydrophobic residues at the corresponding sites.
- Deoxyuridine triphosphate nucleotidohydrolase
- Substrate affinity
- Drug targets
- Arabidopsis thaliana
Deoxyuridine triphosphate nucleotidohydrolase (dUTPase; EC 22.214.171.124) is an important enzyme that prevents uracil misincorporation during de novo DNA synthesis . It catalyzes the hydrolysis of dUTP to deoxyuridine monophosphate (dUMP) and inorganic pyrophosphate [2, 3], thereby maintaining an appropriate level of dUTP with respect to deoxythymidine triphosphate (dTTP) levels . Compromising dUTPase activity in fast-growing cells causes an imbalance in the dUTP–dTTP ratio that can cause uracil misincorporation into DNA . Due to its role in fast-growth-specific cell death, dUTPase has been a target for cancer chemotherapy [5, 6].
Comparison of secondary structures and interactions at the ligand-binding site
0.4 ± 0.1 μM
13.2 ± 0.6 μM
3.6 ± 1.9 μM
(SE 17 %)
0.46 ± 0.2 μM
α helix 1st res
α helix 5th res
Tchigvintsev et al. 
Toth et al. 
Barabas et al. 
Pecsi et al. 
We found that Arabidopsis dUTPase contains a unique tryptophan at the 93rd position, which is located between motifs 2 and 3 (Fig. 1c; Table 1). To identify the role of the 93rd tryptophan, we solved the structure of Arabidopsis dUTPase in its holo form. This homo-trimeric enzyme shows a unique set of interactions with ligands, amino acids, and water molecules at each active site. A comparison of the active sites reveals that tryptophan 93 seems to play a key role in guiding serine reorientation via a water molecule to orient the incoming ligand. In high-affinity dUTPases, the serine residue can be held in place in similar manner by a positively charged residue located four amino acids away. In contrast, low-affinity enzymes lack charges at the corresponding sites.
Arabidopsis dUTPase was prepared as described previously [18, 20, 21]. Briefly, His-tagged Arabidopsis dUTPase was purified via Ni–NTA chromatography from the cleared lysate of E. coli JM103 (DE3) cells. The tag was removed by thrombin cleavage. The resulting dUTPase includes three extra amino acids, Gly–Ser–His, at the amino-terminus (Fig. 1c).
dUTPase activity assay
The enzymatic activity assay was performed using cresol red, and the Km values were calculated using the integrated Michaelis–Menten method [22, 23] with a stopped-flow instrument (Hi-Tech SF-61DX2, TgK Scientific, Bradford-on-Avon, UK) equipped with a photodiode array detector. The assay solution contained 100 mM KCl, 5 mM MgCl2, and 0.25 mM bicine at pH 7.6. dUTPase, to a final concentration of 50 nM, was rapidly mixed with 1–5 μM dUTP solutions in the stopped-flow system, and absorbance was monitored at 573 nm (Fig. 1d).
Data collection and structural refinements of Arabidopsis dUTPase
Unit cell dimensions (Å)
Resolution (scaling) range (Å)
No. of observed reflections
No. of unique reflections used
Resolution range (Å)
No. of non-hydrogen atoms
No. of water molecules
RMS deviations from ideal values
Bond lengths (Å)
Bond angles (°)
Mean B value (Å2)
Interpretable residues (out of 166)
X-ray diffraction data collection, structural analysis, and structural mining
Diffraction data were collected from a single holo dUTPase crystal at the Advanced Photon Source (Argonne, IL, USA) sector 14-BM-C. The data collection and refinement statistics are shown in Table 2. While the holo crystal diffracted beyond 1.2 Å resolution, we only used reflections up to 1.5 Å resolution to keep the redundancy more than five and the linear R factor less than 0.6. To increase the resolution of the structure in apo formats, we further refined the apo structure (PDB ID, 2P9O) with previously collected data by PHENIX ; the updated apo structure was used as the starting model for the structure in the holo format. The structure of the holo enzyme was also refined by PHENIX using the same Rfree flag assignment used in apo structure refinement. We deposited the apo and holo structures in PDB with the IDs 4OOQ and 4OOP, respectively. The COOT , PISA , and PyMOL (Schrödinger, San Diego, CA) software packages were used for structural mining and graphical presentation.
Enzymatic activity and crystallization
The Arabidopsis dUTPase showed enzymatic activity, with estimated Km and Vmax values of 0.4 ± 0.1 μM and 1.2 ± 0.05 µM s−1, respectively, at pH 7.6 and 25 ℃ (Fig. 1d). Therefore, the enzyme belongs to the high-substrate-affinity group, which also includes the E. coli and M. tuberculosis proteins (Table 1).
Crystallization of the holo Arabidopsis dUTPase was performed using the non-hydrolysable dUTP analog dUpNHpp and ammonium sulfate as the precipitant. In the apo Arabidopsis dUTPase, taurine was an indispensable additive for the growth of single crystals . In the holo format, the growth of single crystals was not dependent on the presence of taurine. The protein formed needle clusters in the absence of dUpNHpp and taurine.
Arabidopsis dUTPase structure
Three apo–holo common waters accommodate the substrate
Because the C-terminal residues are involved in ligand interactions, the environment of the ligand-binding site was analyzed (Additional file 2: Table S1 and Additional file 3: Figure S2). Aside from the three ordered water molecules that interact with the magnesium ion, there were three additional ordered water molecules (Fig. 2c) that interact with the ligand at the nitrogenous base oxygen atom O4, the α-phosphate oxygen atom, and the β-phosphate oxygen atom. When the active sites of both the apo and holo forms are superimposed, all of the apo active sites have three water molecules at similar locations as those commonly found in the holo form. These data suggest that the coordination of these water molecules is necessary for initial ligand binding at the active site.
Replacement of ligand-associated water with C-terminal residues reorients the ligand
Ligand 1 bound to active site 1 involves the shortest interpretable C-terminus (Fig. 2d, active site 1) and has the most interactions with water molecules. Ligand 2 in active site 2 involves a medium-length interpretable C-terminus, and has the fewest interactions with water molecules and amino acid residues. Ligand 2 has the highest average B-factor among the 3 ligands, namely 42.8 Å2 as calculated by COOT. A likely explanation for this result is that the C-terminal residues involved in this active site have the most interactions with neighboring subunits due to crystal packing, as discussed above (Additional file 1: Figure S1). Superimposition of the ligand 1 and 2 binding sites (Fig. 2d, active sites 1 and 2) shows that the ligand 1-interacting water molecule (indicated by a green arrow in Fig. 2d) is located at a coordinate similar to that of the Arg156 amino group in the ligand 2 binding site. The electron density map does not support the presence of the corresponding Arg156 coordinate in the ligand 1 binding site. We interpret these data as ligand 1 being in a pre-ordered state, such that the bound ligand is reoriented by the replacement of the ligand–water interaction with the ligand–Arg156 interaction.
This “interaction–replacement” phenomenon is also observed in the ligand 3 binding site (red and black arrows in Fig. 2d, active sites 2 and 3). This binding site involves the completed C-terminus and has the largest number of ligand-amino acid interactions. A superimposition of all of the ligand-binding sites shows that Arg156 undergoes a structural change to interact with the water molecule ordered by the magnesium ion in the holo form. Some ligand–water molecule interactions found in both the ligand 1 and 2 binding sites are replaced by ligand–Ser163 or ligand–Thr164 interactions in the ligand 3 binding site.
We compared ligand coordinates focusing between ligand 1 and 3 binding sites. It was because the C-terminal residues involved in the ligand 2 binding site (chain A residues from 145 to 152) had interactions with four neighboring residues, and resulted the structural difference in the C-termini residues comparing from other subunits, chain B and C (Additional file 1: Figure S1). It appears that the ligand coordinate in the ligand 3 binding site appears to be engaged in the more stable orientation in terms of increased ligand–amino acid interactions. Additionally, the ligand coordinate is in the most favorable position for nucleophilic attack. The γ-phosphate group of ligand 3 occupies a position that is different from those of the other two ligands. A comparison of the ligand 3 and 1 coordinates relative to the catalytic water shows that the ligand 3 α-phosphate is closer to the catalytic water by approximately 0.3 Å (Wcat in Fig. 1a, inhibitor-bound active site).
Roles of Trp93 in Arabidopsis dUTPase ligand binding
Tryptophan 93 of Arabidopsis dUTPase may play an important role in orienting serine 89 in the holo form (Fig. 2c). In the apo form, all of the tryptophan 93 side-chain coordinates were oriented upwards; thus, all of the tryptophan 93 Nε1 atoms were located away from the serine 89 Oγ. These are likely due to crystal-packing induced hydrophobic interactions with proline 46 in neighboring subunits. In contrast, the tryptophan 93 side chain in the holo-form chain B had different coordinates compared with those in other two subunits. It is located such that the tryptophan 93 Nε1 was closer to the serine 89 Oγ. Although tryptophan 93 in the holo form may make the same hydrophobic interactions with proline 46 in neighboring subunit, this particular orientation was likely due to the presence of a nearby water molecule, which bridges its interaction with serine 89. This serine 89–water–tryptophan 93 interaction was only found in chain B. This is part of the ligand 1 binding site, which involves the shortest interpretable C-terminus.
Together with the finding that ligand 1 is likely in a pre-ordered state for the reaction, we assume that tryptophan 93 acts as a key residue for initial ligand orientation at the active site by promoting serine 89 side-chain coordinate changes by interacting with the ordered water molecule.
Molecular mechanism for the differences in ligand affinity
Arabidopsis dUTPase belongs to the high-affinity group, along with the E. coli and Mycobacterium dUTPases (Table 1; Fig. 2c). Tryptophan 93 of Arabidopsis dUTPase holds serine 89 in place via a water molecule and forms a favorable conformation for substrate binding. It appears that the high-affinity dUTPases from species such as E. coli and Mycobacterium have charged or polar amino-acid substitutions corresponding to tryptophan 93 in Arabidopsis dUTPase. In contrast, the low-affinity dUTPases from humans and yeast have non-polar amino-acid substitutions. Additionally, chain C of the yeast dUTPase has the motif 2 serine residue whose side-chain oxygen atom is located away from the nitrogen atom between α,β-phosphate, and yeast dUTPase has the highest Km value among the five dUTPases compared in this study. These data suggest that the amino-acid substitution affects the hydration state at the active site and may influence ligand-binding affinity.
The structure of Arabidopsis dUTPase has been analyzed. Interestingly, this homotrimeric enzyme shows varying binding site environments with respect to their types of ligand interactions. Additionally, the tryptophan 93 substitution seems to use ordered water molecules to aid in coordinating Ser89 for initial ligand binding.
NI and MB carried out the protein crystallography. NI, KC, and MY carried out the kinetic analysis. NI and YJ carried out the molecular dynamics and structural mining. HM, DB, CPC, MKK conceived the study, designed the experiments, analyzed the data and wrote the manuscript. All authors read and approved the final manuscript.
We thank the Arabidopsis Biological Resource Center at the Ohio State University for providing us with the dUTPase clone. We also thank Dr. Javier Seravalli in the Dept. of Biochemistry at UNL for his contributions to the stopped-flow activity assays. This research used resources from the Advanced Photon Source, a US Department of Energy (DOE) Office of Science User Facility operated for the DOE Office of Science by Argonne National Laboratory under Contract No. DE-AC02-06CH11357.
The authors declare that they have no competing interests.
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