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BCMB 3100: EXAM 1

Water
solvent of life polar molecule (oxygen partial negative, hydrogens partial positive)
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Electrostatic interaction
ionic bonds or salt bridges between distinct electrical charges on an atomNaCl in H2O
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Hydrogen Bonds
forms between an electronegative atom (N,O,F) and a Hydrogen occur wherever H is covalently bonded with an electroneg. atomwater disrupts hydrogen bonds (competes)
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van de Waals interaction
between nonpolar and uncharged molecules transient asymmetry induces complementary asymmetry
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Hydrophobic effect
powered by the increase in the entropy of water that results when hydrophobic molecules come together powerful organizing force (ie. membrane formation, protein folding)
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pH
measure of H+ concentration of a solution greater concentration of H+ lower pH
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Acids
proton donors form conjugate base and proton when ionized
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Base
proton acceptor forms hydroxide ion and conjugate acid
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pKa
a measure of the strength of an acid pH>pKa conj. base predominates (basic)pH<pKa acid predominates (acidic)
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Buffers
resist changes in the pH most effective at a pH near its pKacrucial in biological systems (ie. buffers in blood, carbonic acid and bicarbonate)
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Amino Acids
most commonly found in the L-isomer contain an NH3+ group, COO- group, H group, and R group side chains differ size, shape, charge, H-bonding capacity, hydrophobic character, and chemical reactivity 20 AAs
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Hydrophobic Amino Acids
have mainly hydrocarbon side chains Glycine, Alanine, Valine, Leucine, Isoleucine, Methionine, Proline, Phenylalanine, TryptophanLIPPT MAG
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Polar Amino Acids
have side chains that contain and Electronegative atoms (O,S) Serine, Threonine, Tyrosine, Cysteine, Asparagine, GlutamineSACT GT
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Positively Charged Amino Acids
are hydrophilic Lysine, Arginine, HistidineHistidine can be neutral or positive HAL
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Negatively Charged Amino Acids
have acidic side chains Aspartate, Glutamate GA
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Polypeptide bond
A peptide bond is a covalent chemical bond formed between two amino acid molecules. amide bondamino terminal end is the beginning, carbonyl terminal end is the end 6 atoms in a plane, alpha carbon, NH, CO, alpha carbon of next AAin Trans configuration to reduce steric clash between R groups primary structure
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Secondary structure
alpha structure beta sheet3-D structure formed by H-bonds between NH and CO groups in the main chain
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Alpha Helix
C1 H-bonded to C5 backbone forms H-bonds to create helix shape R groups are located outside helix
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Beta sheets
formed by adjacent beta strands polypeptide in a beta strand is fully extended
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Tertiary structure
protein folding myoglobin
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Quaternary structure
multiple peptide chains form together to create subunits that display quaternary structure
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Enzymes
protein catalysts that accelerate the rate of a reaction facilitate the formation of the transition state 6 major classes:oxidoreducatse catalyze oxidation-reducation rxnstransferase move functional groups between moleculeshydrolases cleave bonds w/ addn of waterlyases remove atoms to form dbl bondsisomerases move functional groups within moleculeligases join two molecules at the expense of ATP
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Free energy (G)
enzymes do not alter delta G reaction will occur if delta G is negative (exergonic)will not occur spontaneously if delta G is positive (endergonic)at equilibrium delta G=0enzymes alter the reaction rate but not the reaction equilibrium
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Active Site of Enzymes
enzyme and substrate complex form here this interaction promotes the formation of the transition state3-D cleft created by AAInteraction at the active site involves multiple weak interactions Enzyme specificity due to active site not lock and key fit but induced fit
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Carbonic Anhydrase Case
H2O+CO2 --> H2CO3 In water: H2CO3 --> HCO3-+H+ HCO3- --> CO3-+H+Higher [CO2]: lower pH (due to more H+)With CA deficiency: reaction would take place slower, less acidicHistidine is neutral (can make 2 hydrogen bonds) while Tyrosine is negative (can only make one hydrogen bond)Osteoclasts acidify bone-resorption, CA deficiency would inhibit this process (less acidic environment)
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Enzyme kinematics
reaction begins as 1st order (linear) becomes zero order at high [S] the rate doesn't depend on [S]E+S <--> ES --> E+P k1 k2at high [S] [Etotal]=[ES]
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Michaelis-Menten equation
Vmax = k2[Etotal] fastes that the enzyme can turnover Km=Vmax/2 or Km=k-1+k2/k1indicates the stability of the [ES] complex / how much substrate will saturate Ekcat is the rate limiting step (turnover number) kcat=k2kcat/Km is a measure of catalytic efficiency
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Lineweaver-Burk equation
inverse of the MM equation 1/Vo=(Km/Vmax)(1/[S])+(1/Vmax)
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Km
Km>>[S] // Vo=(Vmax/Km)[S] [S]>>Km // Vo=VmaxKm=[S] // Vo=Vmax/2
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Kinetics Case
Varies: [S] Constants: [E], temperature, pH (use buffer), timeMeasure: Vo by the product formed at certain time and [S]Wild type has larger Vmax (generates reactants to products quicker)Mutant has larger Km (less affinity to bind)Histidine substitution would result in more H-bondingMISFOLDING
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Allosteric Enzymes
switch between functioning and non functioning conformations by: 1. binding of a regulator at a site distant from the active site2. cooperative binding of multiple substrate molecules (or both)Inducing quaternary structure change
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Hemoglobin
"honorary enzyme" 4 O2 binding subunits, 2 alpha and 2 beta (pair of alpha beta dimers)Binds O2 cooperatively; as one binds, Hb conformation changes, increasing affinity for other subunitssigmodal curve (contrast with myglobin which only has one binding site -- MM curve)
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Tense state (T)
low affinity for O2 favored until O2 has bound to one subunit of each alpha beta dimerinduces conformational change
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Relaxed state (R)
high affinity for O2 favored until O2 is released from one complete alpha beta dimer
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Molecular Basis of Hb Cooperativity
O2 binds to heme in Hb, Fe complexed with N of heme, Fe can form 2 add'nl bonds Fe forms covalent bond with proximal His in HbFe2+/3+ can be oxidizedO2 pulls Fe into plane of the heme by redistributing e-*O2 binding induces conformational changes in one Hb chain, which triggers a conformational change in other Hb chains*Cleft is lined with hydrophobic AA, bound O2 forms H-bond with distal His in Hb which helps keep O2 uncharged so it can leave the cleft
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Role of Electrostatic Interactions in Conformational Change
Binding of O2 induces conformational change between T and R state T state can be stabilized by His and Asp in the beta chain Negative Asp helps stabilize positive charge on His, increasing His pKa (~7)
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Bohr Effect
decrease in pH or increase in CO2 leads to stabilization of the T state of Hb and unloading of O2
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Hemoglobin Case
His --> Asp disrupts salt bridge reaction, due to change in charge of the AA R state favored due to substitution Increase in O2 affinity curve is instead sigmodal (as opposed to usual MM curve)results in O2 starvation
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Competitive Inhibition
binds to enzyme Vmax remains unchanged (higher [S] necessary to reach Vmax)Km increases
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Uncompetitive Inhibition
bind to ES Vmax changes (decreases)Km changes (decreases)
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Noncompetitive Inhibition
binds to E and ES Vmax changes (decreases)Km remains unchanged
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Inhibitor Case
Acetazolamide taken to inhibit CA enzyme Vmax changes, but Km doesn't resulting in a noncompetitive inhibitor Inhibitor works to slow down process of CA enzyme so AMS doesn't occur
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