Gelatin is a biopolymer ,prepared by thermal denaturalization of collagen, which is available in animal skin and bones in the presence of dilute acids. Gelatin consists of a large number of glycine, proline, and 4-hydroxy proline residues. It is translucent, colorless, and nearly tasteless powder.
Hill constant for hemoglobin is 4, For Myoglobin is 1.. When this constant is greater than 1 means there is positive co-operativity.. And when 1(as in case of Myoglobin),it means hyperbola,no co operativity..
2019 paper ans. 1. vitamin B6 is cofactor for gylcogen phosphorylase 2. phi angle form netween C alpha and N, psi angle form between C alpha and C 3. feedforward inhibition occur when the excitory neurons activate inhibitory cells that inhibit postsynaptic excitory cells outside the initiating excitory cells area 4. Alkeptoneurea is autosomal recessive disorder 5. in pku ketone bodies get excreted with urine and in albinism the tyrosine get accumulated 6. vitD Cholcalciferol, VitB12 cobalamine, vitK quinone 7. not all closed structures are aromatic
Q2) Feedforward inhibition - mediated by interneurons IN1 located in aff layer (Ia),
Gelatin is a biopolymer ,prepared by thermal denaturalization of collagen, which is available in animal skin and bones in the presence of dilute acids. Gelatin consists of a large number of glycine, proline, and 4-hydroxy proline residues. It is translucent, colorless, and nearly tasteless powder.
DBT me aya tha yeh
Q3) Glycogen phosphorylase -B6 cofactor - pyridoxal phosphate.
Thanks sir do continue this series of all imp units.
salting in refers to the process where the solubility of a protein or other molecule increases with the addition of low concentrations of salt.
Q14) Linus Pauling American biochemist/
chemist
Discovery - cause of sickle anemia,
developed - oxygen meter
determined- structure of proteins.
PKU ( phenylketonuria ) - phenylalanine hydroxylase
Albinism - tyrosinase
T form is tensed state haveing low O2 affinity
R relaxed form is having High o2 affinity .
SDS- anionic detergent, unfolds and denatures proteins, coating proteins in negative charge.
Hill constant for hemoglobin is 4,
For Myoglobin is 1..
When this constant is greater than 1 means there is positive co-operativity..
And when 1(as in case of Myoglobin),it means hyperbola,no co operativity..
Q6) Alkaptonuria - Autosomal recessive disorder
PKU - Defective enzyme - phenylalanine hydroxylase.
Albinism - Tyrosinase
Vit.k-phylloquinone, vit.D -calciferol ,vit.b12 -cobalamine
Pkn is due to lack of phenylalanine htdroxylase , Albinism due to lack of transaminase
Q1) Φ angle between N-Cα and
Ψ angle between Cα-C
2019 paper ans.
1. vitamin B6 is cofactor for gylcogen phosphorylase
2. phi angle form netween C alpha and N, psi angle form between C alpha and C
3. feedforward inhibition occur when the excitory neurons activate inhibitory cells that inhibit postsynaptic excitory cells outside the initiating excitory cells area
4. Alkeptoneurea is autosomal recessive disorder
5. in pku ketone bodies get excreted with urine and in albinism the tyrosine get accumulated
6. vitD Cholcalciferol, VitB12 cobalamine, vitK quinone
7. not all closed structures are aromatic
Gelatin is a protein obtained by thermal denaturation of collagen, the main constituent of connective tissue.
Q .6 alkaptonuria - Autosomal recessive disorder
PKU - defective enzyme - phenylalanine hydroxylase
And Albinism - tyrosinase
Co factor of glycogen phosphorylase is B6 ( pyridoxal phosphate)
Thank you sir for awesome session
q3: pyridoxal 5'-phosphate (PLP), an active form of Vit. B6, is the cofactor of Glycogen phosphorylase
Q3. Glucose transferase (1-6 to 1-4)
Glycogen phosphorylase cofactor -B6(pyridoxal phosphate)
Thank you sir
Branch chain amino acid - leucine , isoleucine and valine
Q10) Vitamin B12 - Cynocobalamin
K- Phylloquinone
D- Cholecalciferol
Q.6 alkaptonuria -autosomal recessive disorder
Histone rich in basic amino acid -arginine and lysine
K = menaquinone, D= calciferol , b12= cobalamine
Q.3 vitamin B6 ,pyodoxine phosphate
Albinism tyrosinase enzyme defective
Pku ( phenylketonuria) phenylalanin hydroxylas enzyme is defective
q1: phi is between -NH3 and C alpha, while psi is in between -COOH and C alpha
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Psi b/w alpha c and c ,phi b /w alpha c and n
Histone rich amino acid - arginine and lysine
Thankyou sir.
Alkaptonuria is autosomal recessive disorder
Linus Pauling - nature of chemical bond
he also discovered the cause of sickle cell anemia.
And also Alpha helical structure was proposed by Linus Pauling and Robert korey ,1950
Thank you sir 🙏macular bio layiye
Vitamin D cholecalciferol
Vitamin K phylloquinone
Vitamin B12 cynocobalamin
B6 pyridoxal phosphate
Thankyou sir❤❤
Non competitive inhibition km unaffected vm decrease
Waiting for this ✨️
Alkaptonuria is autosomal recessive disorder h
DEME - dulbecco's modified eagles medium
Linus Pauling give model of alpha helix
Km remains unchanged in Non Competitive Inhibition
SDS separate the protein molecules
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Go through the link in description
HOW CAN I ENROLL IN YOUR COURSE SIR?
Beta there is link in description
plz impove ur voice .....not clr
Thanks for the input, started the work on it.
1) N-Cα --> φ angle 2) Cα-C' --> ψ angle
2) Feed forward activation -> Accumulation substrate causes its binding to the allosteric site of enz
3) Alkaptonuria - Autosomal recessive disorder
4) Vitamin B12 - Cobalamine
Vitamin D - Cholecalciferol
Vitamin K - Phylloquinone (plants), Menoquinone (Animals)
Thank you sir