20 Amino Acids Structures/Properties Flashcards
Name this Amino Acid, 3 letter abbreviation, pKa, and Category

Glycine; Gly; n/a; hydrophobic Gly is sly & slips by with nothing but an H
smallest side chain
nonpolar but not very hydrophobic either
Adds to the FLEXIBILITY of plypeptides
Name this Amino Acid, 3 letter abbreviation, pKa, and Category

Alanine, Ala, n/a, Hydrophobic Al has a simple structure
Name this Amino Acid, 3 letter abbreviation, pKa, and Category

Valine; Val; n/a; Hydrophobic R group looks like a V
Name this Amino Acid, 3 letter abbreviation, pKa, and Category

Leucine; Leu; n/a; Hydrophobic LONG Valine
Name this Amino Acid, 3 letter abbreviation, pKa, and Category

Isoleucine; Ile, n/a, Hydrophobic Isolated/lopsided Leucine
Name this Amino Acid, 3 letter abbreviation, pKa, and Category

Phenylalanine; Phe; n/a; Aromatic
Phenyl + alanine
Name this Amino Acid, 3 letter abbreviation, pKa, and Category

Tryptophan; Trp; n/a; Aromatic (W)
TWYPtophan - chubby bunnies
big fat ring structure looks like a turkey
complicated & tryps you up
Name this Amino Acid, 3 letter abbreviation, pKa, and Category

Tyrosine; Tyr; 10.46; Aromatic
My eyes (phenyl ring) ar -OH so tired
Name this Amino Acid, 3 letter abbreviation, pKa, and Category

Histidine; His; 6.04; Basic
can be + OR neutral
2 double bonds & 2 NH’s
I’m a double sneezer -> need antihistamine
can serve as proton donor & proton acceptor - has innate buffering ability
can coordinate with metals
Name this Amino Acid, 3 letter abbreviation, pKa, and Category

Serine; Ser; n/a; Hydrophilic
“Sir”
“-OH AL, stop that”
Hydroxyl + Alanine
(pKA too high for OH to dissociate in the body)
Name this Amino Acid, 3 letter abbreviation, pKa, and Category

Threonine; Thr; n/a; Hydrophilic
1 C with THRE 3 side chains (OH, CH3, H)
only T without a Y so NOT Ar
(pKA too high for OH to dissociate in the body)
Name this Amino Acid, 3 letter abbreviation, pKa, and Category

Methionine; Met; n/a; Hydrophobic
thi = sulfur
C-C-S-C
*starts every protein
Name this Amino Acid, 3 letter abbreviation, pKa, and Category

Cysteine; Cys; 8.37; Hydrophilic (keep in mind disulfide bridges)
Sistine Chapel -> burning sulfer in Hell/strucure looks like a cross
can form Disulfide bonds like “God touching Adam”
involved in apoptotic cell death
good metal ion coordinator
Name this Amino Acid, 3 letter abbreviation, pKa, and Category

Aspartate/Aspartic Acid; Asp; 3.90; Acidic
only 2 C’s = spartan -> fewer luxuries
Name this Amino Acid, 3 letter abbreviation, pKa, and Category

Glutamate/Glutamic Acid; Glu; 4.07; Acidic
gluttonout take 3 C’s
the C=O need a mate -> O-
Eh? -> (E)
*long aspartate, Extra Tail
Name this Amino Acid, 3 letter abbreviation, pKa, and Category

Asparagine; Asp; n/a; Hydrophilic
(N) because of NH2
only 2 C’s becaue spartan = fewer luxuries
Asparate with Amide on the end
add a G - so fly like a G6, no charge because famous
Name this Amino Acid, 3 letter abbreviation, pKa, and Category

Glutamine; Gln; n/a; Hydrophilic
gluttonous taking 3 c’s
amine = NH2 group
amie derivative of glutamate
(Q)tamine rhymes with Glutamine
Name this Amino Acid, 3 letter abbreviation, pKa, and Category

Lysine; Lys; 10.54; Basic
long 4 C sword with sharp NH3+ tip for lysing everything
Name this Amino Acid, 3 letter abbreviation, pKa, and Category

Arginine; Arg; 12.48; Basic
surrounded by N’s
Arg - like a pirate -> 3 C’s & 3 N’s
Name this Amino Acid, 3 letter abbreviation, pKa, and Category

Proline; Pro; n/a; Hydrophobic
3 C chain in closed loop with N
found in turns
*weird, just memorize*
Name the 6 nonpolar/hydrophobic aliphatic Amino Acids
Glycine
Alanine
Valine
Proline
Leucine
Isoleucine
Methionine???
Nonpolar/hydrophobic
tend to cluster within proteins - think a micelle
Stabilize structure through their hydrophobic interactions
Name the 6 polar/hydrophillic uncharged Amino Acids
Serine (pKA too high to dissociate in the body)
Thereonine (pKA too high to dissociate in the body)
Cystine
Proline
Asparagine
Glutamine
Name the 3 Aromatic Amino Acids
Phenylalanine
Tyrosine
Tryptophan
**All have Y’s
Try Trypping on Phentoin
**Nonpolar/hydrophobic
phenyl ring allows for stacking interaction with STRONG hydrophobic interaction
Name the 3 positively charged Amino Acids (Hydrophillic & Basic)
“HAL”
Histidine
Arginine
Lysine
very hydrophilic
all can Hydrogen bond
+ charge enables to form IONIC bonds with negative AA
Name the 2 negatively charged Amino Acids (Hydrophilic & Acidic)
Aspartate/Aspartic Acid
Glutamate/Glutamic Acid
very low pKa -> dissociate & become negative in the body’s pH
Special Amino Acids
Glycine = simplest
Cystein = creates disulfide bonds
Proline = allows for turns in protein due to structure; reduces structural flexibility b/c of rigid ring side chain
Methionine = useful for radioactive labeling with S(35)
What are the Acidic/negative side chain Amino Acids
Aspartate/Aspartic Acid (D)
Glutamate/Glutamic Acid
What are the basic/positive side chained Amino Acids
HAL
Histadine (R)
Arginine (H)
Lysine (K)