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Protein - Coggle Diagram
Protein
10-35% Energy
4 kcal/g
Functions
Structural
Contractile proteins
actin, myosin in cardiac, skeletal, smooth muscle
Fibrous proteins
collagen, elastin, keratin: found in bone, teeth, skin, tendons, blood vessels, hair, nails
Globular proteins
spherical shape: myoblobin
Regulatory
Enzymes / Catalysts
proteins catalyzing reactions, some require cofactors
Hormones / Messengers
-act as chemical messengers : eg. insulin, glucagon, catecholamines
synthesized & secreted by endocrine glands
Transporters
In cell membrane - regulation of nutrient entry
Uniporter
Symporter - SGLT 1
Antiporter - exchange molecules
In blood
Hemoglobin
albumin ( FA)
prealbumin ( thyroxin & RBP)
trasnferrin (iron)
ceruloplasmin ( copper)
lipoproteins
Fluid balance
Intra & extracellularly: help attract water = contributes to osmotic pressure
Ascites : abnormal accumulation of fluid in abdominal cavity --> anemia
Others
acute phase reactant proteins
formed in liver, in response to infection, inflammation
-stimulate immune system, promote wound healing, chelate & remove free iron ( anti-bacterial)
C- reactive protein
indicator for inflammatory status
Storage protein
Glucose storage: glycogenin
conjugated protein
glycoprotein
Structures
Primary
AA joined by peptide bonds --> form polypeptide backbone
Seconddary
stable ; provide strength & rigidity
α - helix ( cylindric shape)
β - pleated sheet
Tertiary
Interactions among AA residues / side chains
eg. linear, globular, spherical
eg. α - lactalbumin ( part of milk, impact lactose production in milk)
Quaternary structure
Oligomers = 2/ 4 polypeptide chains held together by H bonds & electrostatic attractions
eg. Hemoglobin
Essential AA
Phenylalanine, valine, threonine, methionine, tryptophan, histidine, isoleucine, leucine, lysine
Conditionally Indispensable AA
PKU ( phenylketonuria)
Inborn error in metabolism: **missing phenylalanine hydroxylase ( cant convert to tryosine - become essential AA)
cysteine & proline in preterm neonates