[Recalls] Prelim exams - Avengers Flashcards
Alternative glucose transport
Glut 4
Thyroid hormone with iodine residues at 3,3’ and 5’ of the aromatic rings
T3
Fetal hemoglobin subunits
2 Alpha
2 Gamma
Arginosuccinate formed by aspartate and ________.
Citrulline
Amino acid with 4 nitrogen radicals
Arginine
Amino acid composed of tripeptide GCE
Glutathione
Unusual of glutathione
Presence of sulfur in Cys
A derivative of tryptophan
Serotonin
Defect in the branched chain a-keto acidic dehydrogenase
Maple syrup urine disease
Deficiency of this vitamin will lead to increase excretion of formimino glutamate in the urine
Folic acid
Intestinal lipase hydrolizes this to glycerol and fatty acids
1-monoacyl glycerol
Biosynthetic catabolic intermediate of cystein needed to form taurin
Cystein sulfinate
Atypical phenoketonuria type 3
Defect in dihydroxybiopterin reductase
True of P50 except:
It is the partial pressure of O2 that half saturates myoglobin for good storage
True of P50 except:
It is the partial pressure of O2 that half saturates myoglobin for good storage
Serine can be converted back to its intermediate:
3-phosphoglycerate
Glucosidic 4 carbon amino acid
Threonine
Rate limiting step in the synthesis of LC-PUFA
Desaturase
Methemoglobinemia
- Intake of excess antioxidants
- Genetic deficienct in NADH-dependent methemoglobin reductase system
- Inheritance of HbM
Removal of a-amino nitrogen by transmanination catalyzed by an aminotransferase is the first catabolic reaction of most of the protein amino acids. The exceptions are:
- Proline
- Hydroxyproline
- Threonine
- Lysine
Arachidonic acid
20:4w63
Completes digestion of proteins
Dipeptidase
ORESOL
SGLT
Found in the mitochondria
Carbamoyl phosphate synthase
Ketogenic
Leucine and lysine
Point in Redinger RN triangle
Bile 80%
Chole 5%
Phosphatidylcholine 15%
Carbohydrate with a-1,6 glycosidic bond
a-limit dextrin
If methionine is scarce:
Homocysteine is remethylated to methionine
PKU Type III
Defect in dihydrobiopterin reductase
Rate limiting enzyme activator in urea cycle
N acetyl glutamate
Substrate that connects urea cycle to krebs cycle
Fumarate
Valine after transamination
a-ketosiovalerate
Addition of second hydroxyl group needs what cofactor:
Tetrahydrobiopterin
Tryptophan
Indole ring
Cofactor needed for the formation of L-dopa
BH4 (Tetrahydrobiopterin)
Four nitrogen group/amino group
Arginine
Deficiency of this vitamin causes increase in FIGLU
Folic acid
Derived from G-C-E
Glutathione
Amino acid aside from tyrosine that is converted to fumarate and acetoacetyl CoA
Phenylalanine (F)
Formed from arginine via nitric oxide synthase pathway
Citrulline
Methemoglobin
Iron is ferric instead of ferrous
Last to digest CHON
Dipeptidase
Urea cycle precursor
Ornithine
Hemoglobin M
His F8 is rpelaced by tyrosine
Low oxygen will increase
2,3 -BPG
Decreased or absent in the synthesis of globin chain
Thalassemia
Name this structure NH2-CO-NH2
Urea
Common precursor of carnosine and arsenine
Histidine
Tyrosine replaces glutamine
Hemoglobin M
Formed from glycine, arginine and SAM
Creatinine phosphate
Catabolism of arginine forms
1 urea and 5 glutamate
These amino acids have the same enzymatic pathway for the first three parts:
Branched AA
All amino acid that undergo transamination except:
- Lysine
- Threonine
- Proline
- Hydroxyproline
If methionine is scarce:
Homcysteine is remethylated back to methionine
Pentose sugars are absrobed through:
Simple diffusion
Catabolic fate of carbon skeletonof arginine:
Nitrogen:
2 appear directly as urea
1 appear as glutamate
Carbon:
2 appear directly as urea
5 appear as glutamate