Amino acids are a set of 20 different
molecules used to build proteins. Proteins consist of one or more chains of
amino acids called polypeptides. The sequence of the amino acid chain causes the
polypeptide to fold into a shape that is biologically active. The amino acid
sequences of proteins are encoded in the genes.
Amino acids |
General Structure of Amino acids
Central carbon (Cα) attached to:
- Hydrogen (H)
- Amino group (-NH2)
- Carboxyl group (-COOH)
- Side chain (R)
1. Enantiomers: The two non-super
imposable mirror images. Molecules are classified as D form (Dextrorotatory )
and L (Laevorotatory) form depending on whether they rotate the plane of plane
–polarized light clock wise or anticlockwise.
2. Naturally occurring amino acids
are L (Laevorotatory) form.
3. D-form aminoacids are rarely found
in bacterial cell walls and certain antibiotics (Gramicidin-S, Polymyxin,
Actinomycin-D and Valiomycin).
4.N-acetylmuramic acid (NAM) is a
D-aminoacid containing tetrapeptide.
5. Peptide bond: covalent bond formed
between the α -amino group of one amino acid and α -carboxylic group of other
forming a -CO-NH- linkage.
-
Example of condensation reaction
-
Exergonic
-
Rigid plannar
-
Tripeptide means: 3 aminoacids +2 peptide bond
6. All aminoacids have high melting
point more than 2000C.
7. Soluble in water and alcohol,
insoluble in non-polar solvents.
8. Aminoacids can exist as
ampholytes/Zwitter ions.
9. Essential Amino acids:
Arginine(Arg/R), Histidine(His/H),
Isoleucine (Ile/I), Leucine (Leu/L), Lysine (Lys/K), Methionine (Met/M),
Phenylalanine (Phe/F), Threonine(Thr/T), Tryptophan (Trp/W), Valine
(Val/V).
Memory tip:
Any Help In Learning These Little Molecule Proves Truly
Valuable.
This stands for Arginine, Histidine,
Isoleucine, Leucine, Threonine, Lysine, Methionine, Phenylalanine, Tryptophan,
Valine.
10. Non Essential Amino acids:
Alanine(Ala/A),Asparagine(Asn/N),Aspartate(Asp/D),Cysteine(Cys/C),Glutamate(Glu/E),Glutamine(Gln/Q),Glycine(Gly/G),Proline(Pro/P),Serine(Ser/S),Tyrosine(Tyr/Y).
11. Histidine and Arginine are
essential amino acids for infants but not healthy adults.
12. Cysteine and Tyrosine are
considered to be semi-essential amino acids. They are required by premature
infants and adults who are ill.
13.Simplest amino acid:
Glycine- An aminoacid without asymmetrical
carbon atom.
14.Acidic aminoacids: Glutamic acid
and Aspartic acid
- Glutamic acid -Most common amino acid undergo oxidative deamination.
15.Basic aminoacids: Lysine and
Arginine
- Arginine contain guanidium group
- Histones are rich in basic aminoacids
16. Neutral aminoacids: Glycine,
Valine and Phenylalanine.
17. Alcoholic aminoacid: Serine and
Threonine.
18. Aromatic aminoacids:
Tryptophan, Tryrosine, Phenylalanine
- Aromatic aminoacids absorb UV –light .This account for the characterization strong absorbance of light by most proteins at wavelength of 280 nm
- Tryrosine forms skin pigment melanin and two hormones Adrenaline and Thyroxine
19.Heterocyclic aminoacids:
Tryptophan and Histidine
- Tryptophan (Bulkiest amino acid) has indole ring
- Tryptophan: precursor of IAA (Indole 3-acetic acid- plant hormone) and nicotinamide (a β vitamin )
- Amino acids with buffering activity-Histidine
- Histidine :only aminoacid having an ionisable side chain with a pka near neutrality (pk value=6.1)
- Buffering capacity of plasma proteins and haemoglobin is mainly due to Histidine residues
- Histidine :more present in active site of an enzymes
- Histidine contain imidazole group
- Histidine found in intracellular and extracellular fluids of most animals and plants.
20. Sulphur containing aminoacid
–Cysteine, Methionine
21. Aminoacids with amide group:
Asparagine, Glutamine
22. Proline (Secondary imino amino
acid) is rarely found within alpha helix segments.
23 Selenocysteine:
21st aminoacid present in human protein.
24. Un common
aminoacids:
· Collagen (A fibrous protein of
connective tissue): 4 hydroxyproline, 5-hydroxyglycine.
· Myosin (A contractile protein of
muscle):6-N Methyllysine
· Prothrombin (Blood clotting
protein):γ-carboxyglutamate
25.Non-PROTEIN AMIINO
ACIDS:
Ornithine and Citrulline are involved
in the biosynthesis of Arginine and in the Urea cycle.
26. Glutathione is a co enzyme of oxidation –reduction reactions which consist of glutamic acid, glycine and cysteine. This chemical is important in preventing oxidative damage to erythrocytes.
27.Aspartame(Nutrasweet) is
artificial sweetner, synthetic dipeptide, chemically it is
-L-aspartyl-L-phenylalanine
28. Neurotransmitters:
- GABA (Gamma Amino Butryic Acid)-a derivative of glutamic acid
- Dopamine-derivative of tyrosine
29. Histamine- histidine derivative,
allergic reaction mediator
30. Amino acids as helix breakers-
Proline-Glycine-Tyrosine-Asparagine
31.Bend producing amino acid
:Glycine-Proline -serine -Threonine
32.Sickle cell haemoglobin differs
from normal haemoglobin by a single amino acid. In the β chain of sickle cell
haemoglobin ,a valine (a hydrophobic acid) has replaced a glutamic acid( a
negatively charged amino acid)
33. pI denotes isoelectric
point/pH
pI=1/2(pk1+pk2)
Learn more: Functions of Amino acids List
Tags:
amino acids
Biochemistry Notes
essential amino acids
isoelectric point
Non-protein amino acids
peptide bonds
pI
proline
Un common aminoacids
simply superb easy to grasp
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