Hypothetical protein Discussion

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The hypothetical putative sugar binding protein 2ob5 is part of the RbsD/FucU superfamily. It appears to be a FucU protein that catalyses the anomeric change of alpha-purine-fucose into beta-purine-fucose. This was found through combination of evolutionary, structural and functional analysis, and was then compared with existing literature.

The MSA and tree diagrams showed a significantly divergent group of sequences that was completely separate from the remainder of the groups (green, bootstrap 100). This divergence was attributed to their being ribose transporters (RbsD). We therefore hypothesized that the gene encoding the RbsD transporter had undergone duplication in a common ancestor, as indicated by the presence of both RbsD and FucU(which are highly divergent) in the bacterium E. coli.. It is believed that this duplication resulted the FucU paralog. In addition, Our query protein was found to have higher similarity to the FucU group of proteins than the RbsD. We did not encounter any RbsD transporter proteins in eukaryotes.

The query protein was found in several alpha-proteobacteria (high similarity), supported by a bootstrap value of 100 (tree, blue). The chordate group was monophyletic (red, bootstrap value of 99), but sister group to several bacteria (yellow, bootstrap value of 75). We could not find any significant differences distinguishing these bacteria from the bacteria that were not sister group to chordates (purple).This raises a question about the evolution of our query: why do some bacteria have transporters that are more similar to eukaryotic proteins than to other bacterial ones?

Structural alignments presented that the query protein matched well against RbsD transporters, however there were no FucU proteins to compare it to. This caused a limit to the structural comparisons that were made. From the structural alignments it can be assumed that the query forms a decamerichal oligomer possibly containing a putative chloride binding motif involved in polymerisation. These theories are based on the assumption that there is no significant difference between tertiary structures of FucU and RbsD. This aassumption was made because the secondary structures are similar. The 1ogd binding pocket (RsbD protein found in B.Subtillius) consists of, D-28, Y-120, N-122, H-98 and K-102. It also contained a H-20 from a neighboring monomer. The 2ob5A binding pocket is similarin that it has a corosponding H-22 from the other protein as well as matching D-30 and Y-136. There was no corresponding N-122, possibly due to a deletion. The H-98 and the K-102 on the other hand were substituted with R-114 and Y-118 respectively. The R and Y substitutions has been shown to be highly conserved in all FucU proteins as seen in the MSA (see figure).

Figure 1. This MSA shows the binding redidues that have been substituted in RbsD and FucU

This further suports the fact that the query protein is a member of the FucU group of transporters. Previous studies have reiterated this point, this change in the binding pocket possibly accounts for the difference in functions between the paralogs.

The crystallographic structure of 1ogD contains a metal-ion coordinating pocket formed by the interface between subunits adjacent between upper and lower sections of the ring. This ion – potentially a Cl- - is cocrystallised in the structure of 1ogD, and appears to be coordinated by the Lys2 residue. This metal ion would have a potential stabilising effect on the oligomer. Visual characteristics of the corresponding 2ob5 region suggest that 2ob5 also exists as a decamer. However, the chloride-coordinating Lysine is replaced by an aliphatic leucine in 2ob5 and all other fucose-binding proteins analysed (complete alignment). From this, we hypothesise that the chloride ion is absent in fucose-binding proteins, but the proteins are still able to assume a stable decameric ring oligomer.

The functional analyses performed failed to give any major insight on the function of the target protein. The string analsyis only showed three possible interacting proteins, all of the interactions were inconclusive and failed to provide information about the protein. The Profunc results confirmed the fact that the target protein belongs to the FucU and RbsD superfamily. Unfortunally there were only two other members of this group that have had their structures crystallized and both are members of the RbsD group of transporters. This lack of homologs caused the profunc results to be inconclusive in all aspects. Another reason for this may be the fact that the crystal structure of our protein was monomeric, but according to structural analysis it was found to be oligomeric.

We then further investigated the role of RbsdD (ribose transporter) in comparison to our query. it was found that RbsD acts as a mutarotase to convert beta purine to beta furine. A proposed mode of action for this role of RbsD mutarotase can be seen in figure 2.

Figure 2. Proposed Mode of action for RbsD

The His20 residue protonates the O5 and the His106 deprotonates the OH attached to the C1. This causes ring-breakage allowing the formation of an equilibrium between the furan and pyran forms. The FucU is fundamentally different, changing the beta to alpha pyranse. The altered FucU residues in the binding site are thought to be the reason for the different functions. The two residues may cause the conversion of L-fucose by associating with the OH group at C-1 position of the sugar.

Figure 3. This shows the importance of the H-106 and the H-20 residues

The importance of the H-20 and H-106 residues in the function of RsbD has been shown in an expereiment where these residues have been substituted for alanene. The Bacteria without H-20 residue had no pyrenase activity, and the residues without the H-106 lost appoximitly half of their activity. This was shown by growing them in a ribose substrate where the pressence of RsbD is necessary for the cell to survive (see figure 3)

Previous research has shown that although RbsD did not show any activity for L-fucose as a substrate FucU exhibited a limited pyranase activity for D-ribose. This is expected as the FucU protein still contains the functionaly important H-20 redsidue.










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