Step 9 is carried out by enolase and again, this has a ΔG close to 0, meaning we've got our forward and reverse arrows present. Additionally, let's put in our carbon numbers because again this is important. Your professor likes to test it. So we have carbons 3 or 4, 2 or 5, and 1 or 6. This reaction is going to take 2-phosphoglycerate and turn it into phosphoenolpyruvate (PEP), and I just love calling it PEP. Actually, in the process, we will be releasing an H2O. So, we're oxidizing this molecule right now and let's put our carbon numbers on the product here. So 2, 5, and 1 or 6. Let's go ahead and take a look at step 10. Step 10 is carried out by pyruvate kinase. This is another enzyme, a really important one that you should know. And you can see that this has a very negative ΔG, meaning it's a super favorable reaction. We're going to talk more about that later. It takes PEP and ADP and converts PEP into pyruvate and generates an ATP through substrate level phosphorylation. And actually, pyruvate comes out of this reaction in its enol form and is quickly converted, by itself, it converts to the keto form. So here, we're showing the keto form but you know, it actually does immediately come out in the enol form. Anyhow, just to be super thorough, let's number our carbons again: 3, 4, 2, 5, and 1 or 6.
You may have noticed that a lot of the glycolytic reactions are readily reversible. This is because, remember that reaction 7, it had a super negative ΔG but in cellular conditions, it's actually much closer to 0. That's why it has the forward and reverse arrows. But reactions 1, 3, and 10 are not readily reversible. Those are, reactions 1 and 3 are what I call the commitment steps, and 10, this last step that converts PEP by pyruvate kinase, also has a very negative ΔG. These three reactions ensure that the whole pathway moves forward in that one direction because they have a negative ΔG and are very favorable reactions.
It's important to note that other molecules can also feed into glycolysis, but it's always going to cost 2 ATP. So, there's no cheating the system really. You know, you're going to have to "pay the piper" no matter what you do, but you don't necessarily have to start with glucose, which is a good thing because your body is not always going to have glucose available to it. So, obviously, if you do start with glucose, you turn it into glucose 6-phosphate, and that's what feeds into glycolysis, right? That is the substrate for step 2 of glycolysis. If you have lactose, lactose is a disaccharide and it gets broken up into glucose and galactose. Well, we know what's going to happen to glucose, right? Glucose is going to get converted to glucose 6-phosphate and enter glycolysis that way. Galactose, on the other hand, needs a few reactions before it's actually ready to enter the glycolytic pathway. Mannose gets converted to mannose-6-phosphate, which gets converted into fructose-6-phosphate and that's what enters the glycolytic pathway, and fructose gets converted into fructose 1-phosphate, and then that is actually broken into glyceraldehyde and DHAP, both of which will get converted into G3P. So we can see this here is fructose. This molecule right here. I'll even write it in. Fructose. Here, we have fructose 1-phosphate. This is fructose 1-phosphate. And let me just jump out of the image here. Right next to that, we have DHAP and G3P. So, here's our DHAP. This is our G3P. And the molecule glyceraldehyde, well, that's basically just G3P without that phosphate group, right? G3P is glyceraldehyde 3-phosphate. So basically, what's going to happen is you're just going to add a phosphate on to glyceraldehyde and then you have glyceraldehyde 3-phosphate. And DHAP, well, we already