Amino Acid - Structure And Function Flashcards
Amino acid with non-polar side chains
No acid/base chemistry (R-group does not bind or give protons )
Do not form hydrogen bonds
Have hydrophobic interactions
When does Cys and Tyr donate protons
When at alkaline pH
Can Ser,Thr,Tyr form hydrogen bonds and how ?
Yes they can ,they contains OH or SH
What do you need to form a disulfide bridge or a cystine dimer
2-SH groups
What can we consider about -CONH2 of Asn
May serve as the sight of attachment of oligosaccharide chains in glycoproteins (N-link gylcosyation )
True or false , Asp and Glu are proton acceptors
False , they are proton donors .
What is the state of Asp and Glu at a neutral PH
The side chains are almost fully ionized or dissociated (COO-) and carry a negative charge
Finish the statement : Lys and Arg are (a)_______ ionized and carry a (b)_________ charge
(a) fully | partially
(b) positive/ negative
Fully
Positive
Why is a histidine a good buffer ?
Histidine is weakly basic and partially positively charged at a physiological pH .In proteins histidine can be positive or uncharged .
3 letter abbreviation for Asparagine
Asn
What is Gln and how is different to Glu
Glutamine , it’s different to glutamate because it’s the major carrier of NH3
Difference between phenylalanine and Tyrosine in terms of structure
Tyrosine : has an OH
Phenylalanine: has no OH
Why do we say the alpha c is a choice, or optically active
It has four different groups attached (except Gly)
Which of the following acids will have the highest pKa? A.Nitric acid B.Sulfuric acid C.Hydrocholoric acid D.Pyruvic acid
Pyruvic acid is the only acid on this list which is not strong.
•The higher the pKa the weaker the acid
•The lower the Ka, the weaker the acid: because pKa = -log(Ka)
What is the Kw(ion-product ) of water (the value)
10^14
The water dissociation equation
pH =[H+][OH-]
Which of the following amino acids will be most close to its zwitterionic form at neutral pH? A.Alanine B.Glutamate C.Aspartate D.Lysine E.Argnine
Answer is alanine
•The charges available to alanine come from its amino functional group, and its carboxylic acid functional group. Its zwitterionic form occurs when both of these functional groups are charged, resulting in a net zero charge on the entire molecule (+1 – 1 = 0)
•The other amino acids listed have additional ionizable functional groups on the R-group, so the pH where they are zwitterions will be either higher or lower than for alanine.
•Identify other amino acids that also form there zwitter ion at near neutral pH
Explain the difference between D and L isomers (amino acids )
L amino acids are those with the alpha amino group on the left and the D amino acids have alpha amino group on the right