Final Flashcards
Titin is present in telomeres
False
VAST stands for Vector Alignment Search Tool
True
You need a PDB ID or MMBD ID to search VAST+
True
“VAST neighbors” are non-similar structures
False
VAST+ uses protein sequence similarities to compare the 3D structures
False
VAST+ stands for Vector Alignment Sequence Tool
False
Botulinum Toxin comes from a gram-positive bacteria
True
VAST relates proteins based on geometric and sequence criteria
False
You can filter VAST+ results based on taxonomy
True
RMSD stands for Root Mean Square Deviation
True
Malate Dehydrogenase is an enzyme that catalyzes an irreversible reaction
False
Malate Dehydrogenase is a part of the Krebs Cycle
True
The Rossman fold is not a common super secondary structure
False
Prokaryotic and Eukaryotic cells alike have malate dehydrogenase
True
CD in “CD Search” on the NCBI website stands for Conserved Daltons
False
SASA stands for solvent accessible surface area
True
The primary function of katanin is to cut intermediate filaments
False
iCn3D cannot export models for 3-D printing
False
When identifying amino acids by charge using iCn3D, red is a negative amino acids and blue is a positive amino acid
True
An example of a developmental disorder caused by katanin dysfunction is microcephaly
True
Cytoglobin was discovered in 2001 within hemoglobin cells
False (within hepatic stellate cells)
A protein does not have to fall into one of the specific symmetry operations (cyclic, dihedral, helical, or cubic)
True (a protein can be listed as asymmetric)
There are more local symmetries than global symmetries in the Protein Data Bank
False (there are more global symmetries)
A protein of cyclic symmetry has one axis of rotation
True
A homomer consists of two different subunit
False
Sonic Hedgehog was named after the video game character Sonic The Hedgehog
True
IBIS shows only observed interaction
False
Sonic Hedgehog plays a role in embryogenesis of mammals
True
The Hedgehog protein was first discovered in Mice
False
IBIS does not require a number from the PDB to do a search
False
The HMMR database focuses on the structure of the protein
False
BLAST is a better tool to identify homologs than HMMER
False
Glycine oxidase is a dioxidase
True
Hydrogen peroxidase interacts with amplex red to form a pink colored complex.
True
Glycine oxidase has two differential subunits
False
IBIS stands for Inferred Biomolecular Interactions Server
True
IBIS categorizes protein binding sites into five categories
True
One of erythropoietin’s functions is to make red blood cells
True
According to IBIS, erythropoietin only binds with proteins and peptides
True
“Singleton” means a cluster which has only one non-redundant member
True
The terms polypeptide and protein are synonymous in all situations
False
Van der Wals forces help stabilize alpha helices
True
Parallel beta-sheets are stronger than anti-parallel beta-sheets because their atoms, which form hydrogen bonds, are directly opposite each other rather than at an angle
False
Phosphatases add phosphate groups on the hydroxyl group of the R chains of serine, tyrosine, or threonine residues during the post translation process of phosphorylation
False, kinases add phosphates and phosphatases remove them
Intrinsically disordered proteins have no function and are distant evolutionary remnants
False
The mammal and bird sequences above are 90% homologous
False, there cannot be a percent homology
High throughput methods are amenable to proteomic investigations
True
A domain is a separately folded part of a polypeptide chain that often has unique functions such as binding DNA
True
Protein folding is driven by hydrogen bond formation
False, hydrophobic interactions
It makes no difference when purifying a protein whether it is being purified for industrial or analytical purposes
False
Fusion tags can be put onto recombinant proteins to help prevent inclusion body formation
True
Freezing and thawing are good for both cell disruption and to maintain proper protein folding
False, disrupts protein folding
Filter is commonly used in industrial protein processing to rid cell lysates of cell debris and non lysed cells because it is very cheap and efficient
True
In industrial settings for many therapeutic molecules reading absorbance at 280nm is a good way to check for protein contamination
True
Chromatography separates complex combinations proteins based upon their chromatographic fingerprints
True
An element of chromatographic fingerprints is hydrophobicity of the protein
True
Proteins are relatively unstable compared to DNA and RNA
False, they are more stable
Protein functionality activity can be lost at any state of protein purification
True
Proteins can be destabilized so they are non functional by sheer force
True
Proteins prefer to be in a buffer and not with other proteins
False
Reducing agents are added to break disulfide bonds between two serines
False, cysteines
Dried proteins go bad very quickly except when they are frozen
False, lyophilization is fine
To isolate a recombinant protein more steps are typically needed then for a natively produced protein
False, native proteins require more
Size exclusion chromatography is a good last step in a protein purification chromatographic scheme
False, it dilutes the protein
Most biomarkers are able to be directly assayed by one biochemical reaction
False, most will require an assay (multiple reactions)
Analytical proteins are rarely used for medical diagnostics techniques, only in the lab
False
Industry uses analytical proteins for quality control
True
Beers law is applicable to optical spectrophotometry
True
Light scattering spectrophotometry is also known as turbidimetric photometry
True
Raman photometry measures visible light absorbance
False, measures fluorescent light scattering
Analytical reactions measuring biomarkers by enzyme kinetics rename substrates as analytes
True
Potentiometric analysis is also known as electrochemical analysis
True
End point assays are quicker than kinetic assays
False, you have to wait for the reaction to reach its end point while the kinetic can be meausred quickly
Kinetic analytical techniques need a standard curve
True
Oxidation reactions in analytical assays make peroxidases that convert non-colored reactant to a colored precipitant
True
There are three parts to biosensors: biological, transducer, and detector
True