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Since it’s early access, it is full of bugs and glitches. This is a huge game if you like hack-n-slash games. It’s not exactly the type of game you want to play on your notebook, but if you’re looking for something different to sink your teeth into, give it a try.
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I love science fiction and comic book movies but I have no interest in or knowledge of videogames.
And while I know the sci-fi/comic book genre of movies is hot right now, a similar trend didn’t seem to happen when Star Wars exploded back in the 70’s.
Dude, Tron is great, but the way it was presented in the 80’s was insane. It was gimmicky, obnoxious and well, just not that great. The new sequel did a better job and has a better story. The first was about Flynn being a cool guy, then he became annoying (even though he makes sense and is awesome in the sequel), and Disney failed to capitalize on his popularity. They pretty much just rehashed the story of the first movie.
I bought a copy of the third movie when it first came out and went to see it. I think it was very good, but not Tron Legacy good. It’s ok but it was just a cop-out to re-tell the story of the first movie without much new content.
But anyway, I think the next step is probably to work with videogames. Nintendo has already got a foothold in this market with the GBA and DS, and now the Wii has started gaining momentum, but it’s all Nintendo. I think the Playstation and Microsoft have a much harder time getting into the market. Now, I’m sure they will, but it’s going to be a tough sell.
But this is just a personal opinion, but like I said, I just don’t like games at all. I just can’t get into
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We have developed a new protein-ligand docking algorithm, Molegro Virtual Docker (MVD). The docking algorithm is based on a classical scoring function, the Molegro Virtual Machine (MVM), for both protein-ligand and ligand-ligand docking, and the search is performed in the two-dimensional (2D) space defined by the ligand binding site of the protein. The algorithm is designed to dock native ligands to the protein as an alternative to the one ligand/one site docking. The energy function of the Molegro Virtual Machine is the sum of two parts: (i) the protein-ligand electrostatic and (ii) the protein-ligand van der Waals (vdW) energy. The MVD re-ranker is used to select the best protein-ligand/ligand-ligand pose and rank the remaining poses. We first optimized the MVM parameters (i.e., the ligand and protein templates) and the protein-ligand binding site. In our docking experiments, the best result of docking of the native ligand to its binding site obtained using the MVD is better than that of other popular docking programs, such as the Dock, FlexX, and AutoDock. We then adopted MVD as a ligand-re-ranker to calculate ligand-re-rankings of the decoy set and found that the ligand-re-ranker retains the good ligand-re-rankings of the native ligand, which is very useful to characterize the potential ligand-binding site of the protein. We have used the MVD web server to search and evaluate a set of virtual ligands using the cocrystallized ligand sets of 57 different proteins. The docking protocol and the web server are freely available.
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