- Joined
- Dec 28, 2010
- Messages
- 5,052
- Reaction score
- 6,084
Figured I'd start this one out. I'll be registering for the MCAT first thing tomorrow. Who else is taking it on this date? How do you all plan on studying over the school year?
have you guys started practice exams yet? i'm trying to get through berkeley review books and keep getting 4-5 on each end of chapter exam and freak out mode is: on!
First you hate them. Then you get used to them. Then you start to like them. I'll tell you how I really feel after the real one, which will be #27 if I use all of what I have available 🙂
I'm using gold standard right now but their verbal is crap, so I'm doing the cbt sciences with a full ek verbal in between. I'm seeing linear improvement, with my last two tests the same at 11/10/11. I'm convinced I'm leaving points on the table with calculation and goofball errors so I'm adjusting my strategy to correct. Plan is to insert an aamc this week and see how I do on a more realistic test.
have you guys started practice exams yet? i'm trying to get through berkeley review books and keep getting 4-5 on each end of chapter exam and freak out mode is: on!
I might get the gold standard tests, just because they're so cheap.. 10 for $150 or something?
I wouldnt freak out until you take a practice exam. and according to SN2ED's schedule, if you have a month to do practice exams you are on track. I made a separate schedule that has me finishing CR by the end of the month giving me 2 months for practice exams but I'm having difficulties sticking to it. for all intents and purposes i'm a retaker, and captain cisko has been prepping for like a year now 😛
So tired. I keep trying to catch up but it's not working, I'll have to push the schedule out a few days. That's ok because i've still got a lot of time after I've completed content review.
how's everyone else doing, when do you guys plan to finish content review?
See yesterday's Fact here
Today's fact concerns DNA structure!
For today, I'll let this great picture do the talking:
![]()
Questions for the GTLO "Passage":
1) Histones are proteins that bind to DNA through ionic interactions. Histone residues responsible for bonding to the DNA are most likely to be:
a) Histamine
b) Glutamate
c) Lysine
d) Glycine
2) Core histones involve histone proteins H2a, H2b, H3 and H4. Two each of these proteins complex to form an octamer at the center of each nucleosome. The octamer is an example of:
a) Prosthetic Groups
b) Tertiary Structure
c) Quaternary Structure
d) Nucleophilic Attraction
3) Histone charges that enable binding to DNA are neutralized by the addition of an acetyl group. The enzyme and cofactor responsible for this reaction are, respectively:
a) Histone acetyl kinase, B6
b) Histone acetyl kinase, Acetyl CoA
c) Histone acetyl transferase, B6
d) Histone acetyl transferase, Acetyl CoA
4) Histones are made in the:
a) Nucleus
b) Histosome
c) Cytoplasm
d) Nucleolus
5) Transcription of rRNA takes place in:
a) Ribosomes
b) Nucleoplasm
c) Nucleolus
d) Rough Endoplasmic Reticulum
6) The core histones range between 11 and 15 kDa (1 Da = 1 g/mol). With the average amino acid size being approximately 110 Da, what is the approximate length of a post-transcriptionally modified mRNA strand used to code for H3?
a) 10,000 bases
b) 4,000 bases
c) 1,000 bases
d) 400 bases
The question asks where are HISTONES made, not the proteins like H3. So I would say the histones are made in the nucleus (since they must incorporate DNA)
Also, pretty sure all transcription occurs in the nucleus. The rRNA is then transported to the nucleolus. (Please correct me if I'm wrong)
The question asks where are HISTONES made, not the proteins like H3. So I would say the histones are made in the nucleus (since they must incorporate DNA)
Questions for the GTLO "Passage":
1) Histones are proteins that bind to DNA through ionic interactions. Histone residues responsible for bonding to the DNA are most likely to be:
a) Histamine
b) Glutamate
c) Lysine
d) Glycine
2) Core histones involve histone proteins H2a, H2b, H3 and H4. Two each of these proteins complex to form an octamer at the center of each nucleosome. The octamer is an example of:
a) Prosthetic Groups
b) Tertiary Structure
c) Quaternary Structure
d) Nucleophilic Attraction
3) Histone charges that enable binding to DNA are neutralized by the addition of an acetyl group. The enzyme and cofactor responsible for this reaction are, respectively:
a) Histone acetyl kinase, B6
b) Histone acetyl kinase, Acetyl CoA
c) Histone acetyl transferase, B6
d) Histone acetyl transferase, Acetyl CoA
4) Histones are made in the:
a) Nucleus
b) Histosome
c) Cytoplasm
d) Nucleolus
5) Transcription of rRNA takes place in:
a) Ribosomes
b) Nucleoplasm
c) Nucleolus
d) Rough Endoplasmic Reticulum
6) The core histones range between 11 and 15 kDa (1 Da = 1 g/mol). With the average amino acid size being approximately 110 Da, what is the approximate length of a post-transcriptionally modified mRNA strand used to code for H3?
a) 10,000 bases
b) 4,000 bases
c) 1,000 bases
d) 400 bases
Should I be worried I couldn't answer half of these?
Guys I could be wrong on both counts. It looks like Histone monomers like H3 combine to make Histones, which when added to DNA make Nucleosomes.
I wonder if the monomers are transported to the nucleus before or after assembly to become quaternary histones?
That's what I exactly what I was wondering.
That was awesome quick meeting.
In perusing google before posting the questions I did come across an abstract that said individual histone proteins like h2 etc undergo nuclear import so I assume they're assembled inside.
The last problem is a little tricky. Think about translation, as a hint.
For #1 you have to have the non-polar, polar, and charged groups of amino acids memorized (you should.
#2 You should be able to answer.
#3 You should be able to deduce from the enzyme names given and the typical function of acetyl CoA. I have no idea what B6 refers to if not the vitamin.
#4 Is tricky as Entadus pointed out, but you should know that nonsecretory proteins are translated by free ribosomes in the cytosol.
#5 and #6 you should be able to answer.
Someone want to explain #6 for me? 😳
11 to 15 kDa gives about 13 kDa as an average. Using 110 Da per amino acid as a conversion factor, we get a little over 100 as the number of amino acids. Since we're looking at processed mRNA, we know that introns are gone, and all remaining bases are codons for the polypeptide. 3 bases per amino acid as a conversion factor gives us about 300 bases, but we rounded down with the 110 average, so a little more. 400 is closest. Bam.
11 to 15 kDa gives about 13 kDa as an average. Using 110 Da per amino acid as a conversion factor, we get a little over 100 as the number of amino acids. Since we're looking at processed mRNA, we know that introns are gone, and all remaining bases are codons for the polypeptide. 3 bases per amino acid as a conversion factor gives us about 300 bases, but we rounded down with the 110 average, so a little more. 400 is closest. Bam.
Awwwww man missed todays discussion...:/ stupid classes lol
Sent from my T-Mobile myTouch Q using SDN Mobile
For #1 you have to have the non-polar, polar, and charged groups of amino acids memorized (you should.
#2 You should be able to answer.
#3 You should be able to deduce from the enzyme names given and the typical function of acetyl CoA. I have no idea what B6 refers to if not the vitamin.
#4 Is tricky as Entadus pointed out, but you should know that nonsecretory proteins are translated by free ribosomes in the cytosol.
#5 and #6 you should be able to answer.
Quick question: In reading the acids and bases chapter I'm a bit confused. The concentration of an acid or base does not affect the strength of the acid or base just the pH correct? So if i had 3.0 M HCl and .05 M HCl the more concentrated one would have a lower pH but the strengths would
be the same?? Thanks again!
Quick question: In reading the acids and bases chapter I'm a bit confused. The concentration of an acid or base does not affect the strength of the acid or base just the pH correct? So if i had 3.0 M HCl and .05 M HCl the more concentrated one would have a lower pH but the strengths would
be the same?? Thanks again!
The strength of an acid or base primarily depends on how well the compound dissociates in an aqueous solution at a given temperature (Ka/Kb values), and not the pH.
Precisely. Acid strength is a function of molecular structure or ionic properties, and is expressed mathematically in the acid's Ka. The Ka holds constant (given constant temperature) regardless of concentration because it is a ratio.
Just to add on to what gettheleadout said. This one like stuck with me from that chapter, "a highly concentrated weak acid may have a lower pH than a strong acid in low concentration." So while the strong acid in low concentration would may have a higher pH in this case, it is still a stronger acid because of its structure and as a result, a much higher Ka.
Ahhhhh i see...so basically the Ka is the main determinant of acid strength and regardless of the pH the acid strength is fixed. Sound about right?
Sent from my T-Mobile myTouch Q using SDN Mobile
Ka is a measure of the acid strength, the determinant is the structure of the acid. But yes, all that matters for acid strength is the Ka. pH is a function of both Ka and concentration.
Ahhhhh i see...so basically the Ka is the main determinant of acid strength and regardless of the pH the acid strength is fixed. Sound about right?
Sent from my T-Mobile myTouch Q using SDN Mobile
He ^ basically covered it. Strong acids dissociate fully in water and therefore have a higher Ka than weaker acids. And I guess from what ^ said, the Ka is based on the structure and how willing the acid is to donate a proton or accept a pair of electrons.
Hey gtlo you told me once that you had a nice trick for logs. Care to share?? Doing pH stuff lol
Sent from my T-Mobile myTouch Q using SDN Mobile
Cheaper, old sport!
Go on eBay, you can purchase a 6 month access for $100. Just search for gs mcat.
it's rough, i'm so glad i didnt take more classes as i was tempted to do a few weeks ago.. heheI'm in the same boat as you my friend. I make very little progress in terms of catching up. Hopefully some of these chapters are a little shorter and I can get through 2 a day.
i'm pretty sure there's a post with EK-TBR chapters lined up, how about htis one:For those following SN2's study schedule, I'm having trouble deciding on something. I purchased the EK set during my first go around with this test and did only a few chapters and then took a PR course. I've been following the schedule in every aspect except for the Bio Part; I've only been using BR bio for content review and passages. Are there any suggestions for how I can take the end of chapter practice exams with the EK? My biology has been very hit or miss and I feel like I'm forgetting a lot of it as I move on. Thanks and happy studying (if there was such a thing).
First day of class..ugghh...woke up at 6 to start studying...I'm pooped...
Anyone using any apps to review here and there? I have MCAT once a day , and the questions are pretty good, if I covered the topic I can get it right or at least narrow it down, if I didn't cover it I'll just guess and read the brief explanation , there is also another app for Physics And Gen Chem Via BrainScape? anyone using/used those?
Just flashcards on Anki. Haven't bought the $25 mobile app component though.
Well I have several strategies that take longer to explain than I have right now, but I'll give you this to start:
![]()
And read this post.