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vfrex
10-10-2006, 04:59 PM
For years now, folding@home has been the default distributive computing project that I think of, and I think that applies for most other people. Its cumulative computing power is still growing between faster processors and now the GPU client coming into existence. The competition between teams/tech sites keeps many people involved, and many others joining.

As of October 2006, more than 178,000 CPUs were actively participating in Folding@Home (active CPUs are defined as those returning work units within the last 50 days), with over 1,700,000 CPUs registered. This level of participation makes the Folding@home distributed supercomputer one of the most powerful supercomputers in the world, capable of a sustained computational level of over 190 teraFLOPS.

http://en.wikipedia.org/wiki/Folding@home

However, there are other valid projects that aren't getting enough attention. So, the majority of the rest of this post will be about other DC projects that I might consider participating in, and that I think other bjorn members might as well. If others are interested, maybe we could set up a team.

One example, rosetta@home has teams and works on windows, linux, and OSX:

Rosetta researchers are rely on a technique known as distributed computing, which pools the resources of idle computers everywhere. The project already has ~70,000 active PCs (Jun-2006) for ~38 TeraFLOPS sustained cumulative processing power, but is still actively seeking new participants to reach the 150 TeraFLOPS computing speed mark.

Rosetta also works on proteins, but here is an explanation of the difference:

I know Baker and Ranganathan and their work very well and (like the rest of the protein community) find their work very important and impressive. However, Rosetta@home and Folding@Home are addressing very different problems.

Rosetta only predicts the final folded state, not how do proteins fold (and Rosetta has nothing to do with protein misfolding). Thus, those methods are not useful for the questions we're interested in and the diseases we're tackling (Alzheimer's Disease and other aggregation related diseases).

Also, one should note that accurate computational protein structure prediction is still very challenging compared to what one can do experimentally, whereas the information obtained from Folding@home on the nature of folding and misfolding pathways matches experiment (eg with quantitative validation in rates, free energy, etc) and then goes beyond what experiment can tell us in that arena. While Rosetta has gone a long way and is a very impressive project, given the choice between a Rosetta predicted structure and a crystal structure, one would always chose the crystal structure. I bet that will be changing due to their great efforts, but that may still be a ways off for that dream to be realized.

So, both are valuable projects IMHO, but addressing very different questions. I think there are some misunderstandings out there, though. Some people think FAH is all about structure prediction (which it is not -- that's Rosetta's strength) and some think Rosetta is about misfolding related disease (which it's not, that's Folding@Home's strength). Hopefully this post helps straighten some of that out.


Then there is Grid.org, which is searching for possible cancer drugs. The downside to this project is that there is only a client for Windows. That said, most people here run Windows anyway. It features teams as well. Also, it is backed by a company, and has gone through a few projects so far, so it is quite stable and successful. Further, I like the idea that the projects here are more discrete than folding@home.


http://en.wikipedia.org/wiki/United_Devices_Cancer_Research_Project


Here is a list of other DC projects: http://en.wikipedia.org/wiki/List_of_distributed_computing_projects

Here are a few from that list that I considered noteworthy:

http://www.childhooddiseases.org/download.html - searching for drugs to treat Tuberous Sclerosis Complex

http://www.d2ol.com/ - "The Drug Design and Optimization Lab (D2OL)™ works to discover drug candidates against Anthrax, Smallpox, Ebola and SARS and other potentially devastating infectious diseases." This one also supports teams and Windows, Linux, Solaris, OSX.

http://www.stephenbrooks.org/muon1/ - The experiment is called the Neutrino Factory, scheduled for construction some time from 2015. Its primary aim is to fire beams of neutrinos (fundamental particles) through the Earth's interior to detector stations on different continents. They're doing this to measure whether they change type en route (there are 3 types of neutrino) and data from this in turn will allow them to determine the neutrino's mass more accurately.

The reason they want to do this is that the neutrino is just about the most common particle in the universe (billions pass through your body every second) and its mass will influence such things as the evolution of the universe and the exact way matter was first formed in the 'big bang'. In fact, neutrinos make up one quarter of the types of matter particles specified in the current 'standard model' of physics. In order to progress to more advanced theories of physics, it is often crucial to know the properties of particles to high precision in order to distinguish between the slightly different predictions of alternative theories.

Actually the entire Neutrino Factory complex (estimated to cost at least $1.9bn) will have several scientific aims. The neutrinos are used for fundamental physics experiments, but the proton beam that is produced at the start (this hits the target rod at the beginning of the simulation you download) is also going to be used in experiments such as neutralising radioactive waste by transmuting the radioactive elements into stable ones, and providing a high intensity source of neutrons for 3D atomic microscopy. The muon beam that will be coming from the end of the section we are optimising can also be used as the basis for a 'muon collider', a machine that could produce the highest-energy collisions between fundamental particles ever made artificially.

You are simulating the part of the process where the proton beam hits the target rod and causes pions to be emitted, which decay into muons. These would then proceed to a storage ring and decay into electrons and the neutrinos that are used for experiments. This is a fairly critical part of the apparatus, which catches the pions and confines some of them into a beam while they decay. The efficiency of this dictates that of the entire machine because it is built of a lot of acceleration stages 'in series' with each other. Whether the project eventually gets funded to be built depends on what levels of performance can be achieved with the designs generated during the present R&D. However, users of this program have already doubled the estimated efficiency of one stage and more are to be optimised in the future.

http://www.netdimes.org/ - Not so much a CPU cruncher, but this might be something a community of tech geeks should be interested in:

How does the Internet look like? How does it evolve?

DIMES is a distributed scientific research project, aimed to study the structure and topology of the Internet, with the help of a volunteer community (similar in spirit to projects such as SETI@Home).

Due to the way the Internet is engineered, distributing the Internet mapping effort is very important, and the only efficient way to measure the Internet structure is by asking you to participate. What we ask is not so much your CPU or bandwidth (which we hardly consume), but rather, your location. The more places we'll have presence in, the more accurate our maps will be. Understanding the structure and function of the Internet is an important research task, that will allow to make the Internet a better place for all of us.

The DIMES agent performs Internet measurements such as TRACEROUTE and PING at a low rate, consuming at peak 1KB/S. The agent DOES NOT send any information about its host's activity/personal data, and sends ONLY the results of its own measurements. Aside from giving a good feeling, running the DIMES agent will also provide you with maps of how the Internet looks from your home (currently) and will (in the future) provide you with a personalized 'Internet weather report' and other user-focused features.



Rosetta seems nice being cross platform, and in that it is attacking proteins from a different angle than F@H. There are a few projects that are attempting the same as Rosetta, although using different methods. Rosetta is one of the most accurate from that bunch. From the quote from Professor Vijay Pande above about the differences between F@H and Rosetta@H, While Rosetta has gone a long way and is a very impressive project, given the choice between a Rosetta predicted structure and a crystal structure, one would always chose the crystal structure. I bet that will be changing due to their great efforts, but that may still be a ways off for that dream to be realized.


I'm going to continue editing this post over the next couple of hours with more details about other projects and stuff. What I'd like to see though for now though, is discussion about the main point. That is, whether you guys feel that more emphasis should be placed on other projects. Could our idle CPU cycles be used more effectively than throwing them at what everybody else is anyway.

As if you needed more reading material, here is a nice writeup of the differences and goals of some of these projects: http://www.hyper.net/dc-howto.html#diffs

Scott
10-10-2006, 05:07 PM
We start doing another DC if we want next month, but the majority would have to agree on which client to make the switch.

vfrex
10-10-2006, 05:43 PM
Ugh, just made big edits and they didn't apply since I got logged out...

Anyway, I just question whether 5-10 teraFlops lost from F@H would hurt their research and progress as much as another project would gain from adding that computing power. I think its at least worth a thought as to which projects might stand to gain from the support of a Bjorn3D computing team, and whether they are causes that we believe in collectively.

Das Capitolin
10-10-2006, 07:36 PM
I am already working with Rosetta, and although it doesn't directly contribute to cancer research, it is still important. I think that it would be interesting to research a team for that as well.

Gray
10-11-2006, 01:27 AM
It would never hurt to run SETI ;)

Imo, I am getting annoid with the fact that some people may still actually think that we are the only living beings in the universe. Hopefully in my life time they can be proved wrong.

SETI @ HOME (http://setiathome.berkeley.edu/)

vfrex
10-11-2006, 01:36 AM
I would argue that it does hurt to run Seti, at least in comparison to running something else. For one, Seti is a few magnitudes more popular already than the next biggest project. And while other projects are actively returning results that will improve life on our planet, I don't believe that seti can say the same...

Gray
10-11-2006, 02:13 AM
Has anything @ all come from Folding @ home?
It's a good idea but only if it works, just like SETI.

Kougar
10-11-2006, 02:54 AM
If you are looking to join any of those other distributed computing groups, then I'd definitely suggest you check out the entire subforum dedicated to Dristributed Computing. Anandtech pubbers are active in almost if not every one of those projects, and more you probably have not even heard of.

Has anything @ all come from Folding @ home?
It's a good idea but only if it works, just like SETI.

Yes.

SETI@Home is looking for proof of aliens. It's a yes or no question, and that is all SETI does. So far, it's a big no.

Folding@home work is being done to better understand the internal processes within the human genome through protein folding. They specifically design each test to give them results so they can better understand what is going on, and ask more questions. Does every single WU completed help this process? Yes.

For a better understanding of Folding@home, I suggest fully reading this one page: http://www.anandtech.com/video/showdoc.aspx?i=2849&p=2 (http://www.anandtech.com/video/showdoc.aspx?i=2849&p=2) For those to much in a hurry, I quoted the major part.

The biggest hurdle in this line of research is that it's very computing intensive: a single calculation can take 1 million days (that's over 2700 years) on a fast CPU. Coupled with this is the need to run multiple calculations in order to simulate the entire folding process, which can take upwards of several seconds. Even splitting this load among processors in a supercomputer, the process is still too computing intensive to complete in any reasonable amount of time; a processor will simulate 1 nanosecond of folding per day, and even if all grant money given out by the United States government was put towards buying supercomputers, it wouldn't even come close to being enough.

This is where the "@Home" portion of Folding@Home comes in. Needing even more computing power than they could hope to buy, the Folding@Home research team decided to try to spread processing to computers all throughout the world, in a process called distributed computing. Their hopes were that average computer users would be willing to donate spare/unused processor cycles to the Folding@Home project by running the Folding@Home client, which would grab small pieces of data from their central servers and return it upon completion.

The call for help was successful, as computer owners were more than willing to donate computer cycles to help with this research, and hopefully help in coming up with a way to cure diseases like Alzheimer's. Entire teams formed in a race to see who could get more processing done, including our own Team AnandTech, and the combined power of over two-hundred thousand CPUs resulted in the Folding@Home project netting over 200 Teraflops (one trillion Floating-point Operations Per Second) of sustained performance.

While this was a good enough start to do research, it was still ultimately falling short of the kind of power the Folding@Home research group needed to do the kind of long-runs they needed along side short-run research that the Folding@Home community could do. Additionally, as processors have recently hit a cap in terms of total speed in megahertz, AMD and Intel have been moving to multiple-core designs, which introduce scaling problems for the Folding@Home design and is not as effective as increasing clockspeeds.

The human body is far, far more complex than almost anyone realizes. The first quoted paragraph should at least underscore that point... ;)

vfrex
10-11-2006, 04:14 AM
Also, here is a list of papers that have been written from analyzed folding@home research:

http://folding.stanford.edu/papers.html

GIBSON
10-11-2006, 01:04 PM
Has anything @ all come from Folding @ home?
It's a good idea but only if it works, just like SETI.

Folding @ home does a lot! Multiple progresses have been made by FAH results.
Seti on the other hand does absolutely nothing but throw away your cpu cycles which could be used for a much better project.
just my 2 cents.

Enigmachine
10-11-2006, 02:35 PM
I'm a proponent of the "fix things at home before you start looking at your neighbor". :)

It's hard to believe there is no other intelligent life in the Universe, but it is equally hard to believe that SETI@home will find it.

Considering how unlikely it seems for humanity to still be around in 50 years I think it's currently more important to get our house in order (control our environment, cure "easy" diseases like heart problems, organ transplants, find all asteroids in Near Earth Orbit, simulate the coming global warming/ice age) before we dedicate all our computing resources to talking to strangers...

There's 4 scenarios: 1) they don't exist 2) they exist but SETI@home can't find them - there's an endless list of reasons why 3) they know about us but don't care to talk to us 4) We will find them soon, but any communication would take 60 years round-trip, by which time we'll either have blown ourselves to bits or be a different kind of "humanity" thanks to our evolving technology.

I think it's more important to ensure that we're still there when it happens. :) I think SETI is important, but I think SITI should get higher priority. (Search for Improved Terrestrial Intelligence). :)

just my 2 cents :)

Scott
10-11-2006, 03:05 PM
I thought the Seti thing stopped running?

tomato
10-11-2006, 04:00 PM
I'd rather be F@H than S@H... I'd like to find & destroy cancer instead of hunting for something that may or may not be out there...

GIBSON
10-11-2006, 04:20 PM
Well my priorities would be like this:
1) FAH and the likes for fight against cancer and other diseases, and sharing the number 1 place with the global warming program as that one is at least as important (or probably even more as there are no more diseases to cure when there are no people left)
2) the neutrino program sounds really really interesting, but at the moment there are more urgent topics to be dealt with (see 1 ;))
3) well, by the time we've solved all the above and there are no other problems left (which I doubt, but hey, let's be optimistic) then we COULD run seti
:)

vfrex
10-11-2006, 04:25 PM
Heh Enig, you put that into words very well. Exactly what I was thinking!

Honestly, I don't mind the concept of using DC to crunch signal numbers to look for ETI. But that should take up a minority of our spare CPU cycles. 5-10% would make sense to me. However, SETI is hitting the 250 TFlop range. That is a problem.

From wikipedia: Seth Shostak (2004), a prominent SETI figure, has stated that he expects to get a conclusive signal and proof of alien contact between 2020 and 2025, based on the Drake equation.

That means it will take 15-20 years, presumably at the current clip, for SETI to actually find something. It will take more time after that to actually make contact with said intelligence. In the meantime, #2 Folding@Home is around 190 Tflops, and is churning out research that will help to save/improve lives in the next 5 years. The same can be said about Rosetta, United Devices, and more of these medical and drug research projects. Further, there are other science ones helping us to learn about climate change, quantum chemistry, etc. I saw a couple listed on anandtech that help with research for nanotechnology. These projects are doing research that WILL help us to better understand the body, diseases, and the world we live in.

If you took 100 Tflops off the top of SETI and gave it to other, less popular projects, we probably wouldn't find ETI any faster while improving life on earth in the meantime.

That said, I don't really want this thread to be about FOLDING vs SETI. The purpose is to discuss whether there are better medical/disease/drug projects out there to be involved in than folding, since it is so much more popular than most others.

GIBSON
10-11-2006, 04:55 PM
Well, to say one last thing about SETI... I really don't understand how they will ever be able to proof there is life in other places in the universe by doing computations on earth?

Enigmachine
10-11-2006, 05:24 PM
You know, if someone could come up with a simple explanation of the reasonable paybacks of every distributed program and what % of our considerable idle CPU time we should dedicate to each, that person would certainly gain a great degree of Internet fame.

I would love to know that by spending 50% of my spare cycles to Rosetta I have a 5% chance of not dying from prostate cancer, with 30% cycles to FAh we have a 0.1% of curing Alzheimer's and with 1% to SETI@ I have a 1 in 1000000000000000 chance of finding the Alien.

Just getting those 1 in a gazillion numbers we'd have a good tool for setting our priorities...

GIBSON, regarding SETI@h, I am not an astrophysicist (though I know plenty :) ) so my explanations might be wrong, but basically what SETI does it look through old recorded radiotelescope data for organized signals (repetitions, regular waves, etc). Which means that basically we're looking at a very specific radio band (Hydrogen band?) which, despite being a reasonably intelligent creature, I would never have tought to broadcast on. Also the signal has to be pretty much broadcast in all directions from the source so that a listener in any direction may catch it. Then we have to have been recording signals while looking in the direction of the source.

So finding something given our current technology is highly unlikely. My own fiddling around with the Drake equation led me to believe that there is less than 1 civilization in our local sphere capable of detecting signals from another civilization, and we are it.

We will probably be capable of detecting civilizations rapidly when we get the right technology (orbital or deep space radiotelescope array) but it's almost as if we aren't ready for it yet. But I'll stop there, I think my faith is showing and no one's come up with a Religion@home distributed computing software. :)

GIBSON
10-11-2006, 07:04 PM
So basically they are putting all that computational power on a wave scan. So basically, even if there would be life out there, it would require them to send out signals on this particular wave, and they would need to be doing it for a long time already.

Mirrim
10-11-2006, 07:19 PM
I am comfortable staying with F@H and/or other medical research programs. I might also be willing to run one of the climate change programs. The protein folding and related research hits close to home for me, as I've lost my mother and two aunts from lung cancer, a grandmother from Alzheimer's and my father has rampant emphysema.

Although the premise and possibilities of SETI@home are intriguing, overall I think we benefit more from the medical and climate research.

Enigmachine
10-11-2006, 10:45 PM
So basically they are putting all that computational power on a wave scan. So basically, even if there would be life out there, it would require them to send out signals on this particular wave, and they would need to be doing it for a long time already.

Well, yeah, but if you say it so succintly it doesn't count as a post for the contests. ;)

Gray
10-12-2006, 02:35 AM
SETI@Home is looking for proof of aliens. It's a yes or no question, Ahem, that would be a matter of When we are in contact.

I am glad we can do cancer research on our pc's but like someone said about seti, I don't understand how our pc's can obtain that goal... I don't understand how software could be written that could emulate the workings of protean folding could be done, non the less flawlessly. I hope that guy got that software wrtten correctally the first time around and that he was not part of the Windows Longhorn pre release team.

It's a preatty lofty goal I do hope it works.

I will just keep chugging along with my Seti I think, how unlikely it may seem I relish the chance to understand space from as many angles as I can.

And hey I started Seti early so being in the top 3% solo I enjoy it. Gl with whatever @ home project you get into.

I don't take any @ home project to seriously I just enjoy participating.

O and scott nope Seti is expanding, not kaput. It joined BOINC (http://boinc.berkeley.edu/download.php), (Berkeley Open Infrastructure for Network Computing.)

There are a few more distributed network options there.

vfrex
10-12-2006, 01:14 PM
http://www.hyper.net/dc-howto.html#diffs

^That site is very informative. It brings a lot of information about these projects to one place. Better yet, the author draws his conclusion which I will quote below:


My choices
How did I decide which of all BOINC projects to contribute to? Due to most "life science" projects having joined BOINC very recently (e.g. Rosetta@home came online out of beta Nov05) they are under-represented in terms of CPU time. Looking at late-2005 stats, about 90% of donated CPU time via BOINC goes to SETI+CPDN+Einstein+LHC. Searching for ETI is fine, but I agree with a post I saw that "it (SETI) is a lot like the lottery. If you buy one ticket a week, you're a dreamer, if you buy 100 tickets a week, you've got a problem".

SETI has plenty of crunchers already, enough to process every WU 5 times. It's not constrained by available CPU power. At this point SETI could use more funds (monetary donations), rather than CPUs.

Priority wise, Human Proteome Folding which applied the Rosetta software on the human genome seems to be among the most important (grid.org thinks HPF is the most important life science project they've ever tackled). WCG forums discussion (illuminating). Unfortunately, WCG's (IBM's) current redundancy (initial replication, quorum) settings are just too wasteful IMHO.

Rosetta is probably the most-advanced project investigating protein 3D shape prediction, as it has consistently been among the top performing methods for ab initio prediction in recent bi-annual CASP experiments and also does disease related research. Improving those algorithms has a multiplier effect for the progress of other programs (e.g. HPF).

Folding@home is a life sciences (protein-research) project (non-BOINC though), the oldest (since 2000) and biggest one. Yet, over the years I never really understood how the science done at Folding@home would eventually lead to treatments or cures. With Rosetta@home the connection to identifying drug targets and to drug design seemed much more obvious.

So, for the moment I donate my CPU time to

1. Rosetta@Home 85%
2. SIMAP 15%

Predictor@Home might be a fine project, but it's Science news was last updated 21-Dec-04. CPDN is another fine project but quite heavy and would love to add it, running on a PC on its own, at a later point. Many projects in my list are new and still have relatively few participants.

I think I am leaning towards Rosetta.

GIBSON
10-12-2006, 10:54 PM
Well, yeah, but if you say it so succintly it doesn't count as a post for the contests. ;)
I couldn't care any less, I'm not posting here for the contest. The contest is just a very nice thing on the side.

Ahem, that would be a matter of When we are in contact.

I am glad we can do cancer research on our pc's but like someone said about seti, I don't understand how our pc's can obtain that goal... I don't understand how software could be written that could emulate the workings of protean folding could be done, non the less flawlessly. I hope that guy got that software wrtten correctally the first time around and that he was not part of the Windows Longhorn pre release team.

It's a preatty lofty goal I do hope it works.

I will just keep chugging along with my Seti I think, how unlikely it may seem I relish the chance to understand space from as many angles as I can.

And hey I started Seti early so being in the top 3% solo I enjoy it. Gl with whatever @ home project you get into.

I don't take any @ home project to seriously I just enjoy participating.

O and scott nope Seti is expanding, not kaput. It joined BOINC (http://boinc.berkeley.edu/download.php), (Berkeley Open Infrastructure for Network Computing.)

There are a few more distributed network options there.
I personally believe it to be much more easier to predict how a proteïn folds by doing computer calculations (with todays science there aren't a lot of things you can't calculate with computers) anyhow, I think it's a lot harder to find proof of life in outer space. I'm not saying it isn't interesting, I just think it isn't as important as the other projects, and judging from what i've read (I think vfrex posted that, not sure) the conditions need to be just right to discover life in outer space this way, so chances are very likely SETI comes up with nothing. (which doesn't mean there isn't life in outer space)

Gray
10-13-2006, 03:04 AM
I personally believe it to be much more easier to predict how a proteïn folds by doing computer calculations (with todays science there aren't a lot of things you can't calculate with computers)

I don't agree that is it "much more easier" to wright software that folds protean molicules then it is to scan for abnormalities in radio waves.

I think it's a lot harder to find proof of life in outer space.

I am sure it is harder to find proof of life in outer space but Seti does not look for 'Life" in outer space. It looks for abnormalities in radio waves. A vary easy thing to observe but the background "noise" must be removed so that you can "hear" it. Thats all your computer is doing, that is a very easy task.

(which doesn't mean there isn't life in outer space)

Well one can argue.... But hell we are here are we not? Thats proof enough for me. ;)

DragonMaster
10-13-2006, 10:11 PM
Would be nice if there could be stats and teams for this
http://mlns.starring.se/

Llanerion
10-13-2006, 10:12 PM
Hippocritical though it may sound, I'd rather be helping out F@H than any of the other proteomics projects. Rosetta may be attempting to predict the structures of sequenced proteins, but those are still only predictions, and the modelling algorithms used in developing those models have to be tweaked each time a new protein structure is deduced in the lab in order to match those models.

Attempting to investigate the mechanisms by which proteins assemble towards their final structures seems a more robust line of research, since you can check against known structures assembled within known cell conditions.

Just a note towards how knowing folding mechanisms might help in healthcare; even if you don't consider that the mechanisms researched by F@H will go on to help projects like Rosetta, then there are a large number of diseases relating to misfolding of proteins. Prion diseases which are responsible for a large number of degenerative conditions in the elderly; but also affecting younger generations as well, Retinitis Pigmentosa (progressive loss of sight leading to blindness at an early age) is commonly due to the accumlation of misfolded proteins leading to degradation and loss of the retinal structure.

Assuming everyone skipped over the previous paragraphs ... blah blah F@H good.

Kougar
10-14-2006, 02:44 AM
Actaully, you're probably the most qualified person here to give an opinion on the topic. Thanks for the insight. :)

GIBSON
10-14-2006, 10:13 AM
Assuming everyone skipped over the previous paragraphs ... blah blah F@H good.
Nope, I don't do that :)
As kougar said, you're indeed an "authority" on the subject here. So yes, maybe we should just stick to FAH.

vfrex
10-14-2006, 01:55 PM
Let me see if I have the difference straight...

Folding is using a known, starting protein structure (found through NMR or crystallography), and using physics to determine all of the possible mistakes and paths it can take in trying to fold into another known structure? If that is the case, where is the bottleneck? Is it in the processing power that F@H holds? Or is it in the limited number of protein structures that have currently been discovered in labs? That is, will F@H run out of protein structures to study at the current rate of discovery? (maybe not with this (http://www.bio.brandeis.edu/nmr/avance800.html) puppy operation).

On another note, Llanerion, what type of lab do you work in?

Llanerion
10-14-2006, 07:41 PM
Authority is far too strong a word, maybe I just looked things up in the dictionary =p

Folding is pretty much taking the coded sequence of the gene, converting that to a linear chain, and then deducing in what manner that chain may fold or misfold based upon the interactions between the amino acid subunits, taking into account the conditions of the environment in which that protein is assembling, and the order in which the chain will emerge from the ribosomes, all the while under physiological temperatures that cause the chain to be in a state of constant flex.
By comparison, protein folding is kind of like trying to build a piece of machinery out of a piece of spaghetti in a bowl of soapy water =p

With regards to if F@H will run out of known structures to compare against; I honestly could'nt tell you the numbers of known protein structures at this time, other than that they are comparitively rare. I do believe that some of the major benefits from F@H's angle of analysis should be in the field of modelling putative protein motif's; secondary structures incorporated into the final tertiary structure of the protein which have conserved functions between proteins. Zinc fingers as an example are a telltale that whichever proteins they are found in interact with DNA directly.

Deducing the presence and functions of other conserved protein motifs would not only allow us to gain insights into the functions of related orphan proteins, but also to work on a picture of how the protein functions, and possibly a strong tool in in studying the evolution of proteins.

I study in the Cell Biophysics lab at my university, although my project really spills over across a few different disciplines; for now though my aim is in working with Codopsins with an eye in the future towards attaining a structure though X-ray crystallography, or failing that, NMR work. I'm supposed to be working with a pair of other PhD students who are working on developing 3D models of Rho- and Codopsins, and there's a running friendly rivalry between their lab and ours =p

in conclusion, never trust wordy types, they're obviously trying to hide something!

GIBSON
10-14-2006, 09:16 PM
Authority is far too strong a word, maybe I just looked things up in the dictionary =p
I knew what you're studying, so compared to most of us here on the forum, you can be seen as an authority ;-)

BTW sounds interesting work your doing llanerion. Keep us updated! :-D