Malt is modified, it has to do with germination cycle. Kolbach or the SNR number found on a malt data sheet will indicate level of modification. The term protein rest is a misnomer and it beat to death within the home brew world. During the low temperature rest, proteinase reduces beta glucan to glucose. Mash viscosity is reduced during the rest. The rest is only applied to a small portion of the mash, usually in the first decoction. Glucose is the native sugar in starch. When Alpha liquefies the simple starch chain, amylose, at a 1-4 link, two chains are created. The name changes and one chain is called the reducing end and the other chain is the non-reducing end. The non-reducing end is glucose and it is rocket fuel for yeast. Non-fermentable sugar is left after Alpha liquefies the 1-4 links of the reducing end and once in a while A-Limit dextrin pops out. Conversion takes place during the maltose rest. Beta converts glucose which is released during saccharification into maltose and maltriose during the Beta rest. Starch does not convert to sugar, one type of sugar converts into another type of sugar. Starch is only the container that holds the sugar, the fuel. Saccharification and conversion are two different things. Unless the malt is slack, saccharification takes place in 20 minutes. It is a Mother Nature, science thing. Amylo-pectin which is complex starch bursts when the decoction is boiled. Amylo-pectin is responsible for body. A-Limit and B-Limit dextrin are part of gelatinization and dextrinization. A-Limit and B-Limit dextrin forms body.The temperature at which dextrinization occurs is 149F. Kudos on attempting the decoction method. Be sure to reduce mash pH before boiling the decoctions. Dough in at 95F and pull the first decoction and raise the decoction temperature to 122 to 125F and rest the decoction for 20 minutes. Then increase the decoction temperature to 155F and rest the decoction for 20 minutes, an iodine test can be used after the rest. The iodine should be a reddish/mahogany shade. If it isn't allow the decoction to rest for 10 more minutes. If iodine is blue/black after 30 minutes, not to worry. After saccharification, boil the decoction for at least 20 minutes. Better to boil it past hot break, protein gum will be reduced. The main mash will be resting at low temperature and enzymatic activity will be slow. Any glucose formed will be converted during the maltose rest. Use the first decoction to raise the main mash to 130F, saccharification will continue, but slowly. As soon as the main mash hits 130F, remove the second decoction and raise the decoction to 145F and rest it for 10 minutes and then bring it to a boil and boil it for at least 20 minutes. Use the second decoction to raise the main mash temperature to 149F and no higher than 153F. When the main mash stabilizes at 149F remove the third decoction and take it to boiling and boil it for 10 minutes. The decoction is used to raise the main mash to 155F, Alpha II temperature. Rest the main mash for 10 minutes and use boiling water to raise the mash to 162F, Alpha I temperature and rest it for 10 Minutes. Use more boiling water to raise the mash to mash out temperature if mash out is desired. It probably won't be necessary. Do not batch sparge. The wort produced will be pristine due to the method and batch sparging will only introduce protein mud into the wort. There will be a layer of tan mud on top of the grain bed, do not screw with it. If the mud is gray, sparging will take longer. Boil the wort past hot break before adding hops. Skim off any hot break that forms. There shouldn't be a lot of hot break. You will need a secondary fermentation vessel. After two weeks in the primary and two weeks in the secondary, keg the beer. It will take at least four months for the beer to age. There will be no need to prime the beer when it is kegged, maltriose will do that for you.