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plasmodium protein kinases: from database mining to the search for
plasmodium protein kinases: from database mining to the search for

... that no malarial PK clustered with the tyrosine kinase (TK) group; and (iv) that no members of the dualspecificity protein kinase (MAPKK) family (a subgroup of the STE group) are present in the P. falciparum genome. In addition, a novel, apparently Plasmodium-specific family of 18 genes encoding pro ...
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Translation Notes 2015 - Liberty Union High School District
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... take its amino acid? A: tRNA has an anti-codon that lets it find its spot on the mRNA strand.  Anti-codon: A region of tRNA consisting of 3 bases complementary to the mRNA codon (A with U, G with C) ...
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... Genetic tests can find the presence of “diseases” recessive alleles. Testing for Alleles: (person is a carrier). The DNA code for the recessive allele is slightly different than the normal allele. Ways to test: 1. DNA Probes- used to detect special DNA sequences of disease causing alleles (sequence ...
Name Due date ______ Strive for a 5 – AP Biology Review Unit 1
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Chapter 12 Presentation-The Cell Cycle
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... nucleotide variations and copy number (CN) variations. CN variations represent genomic segments with a size range of ~100 bp to several Mbs demonstrating an altered (or non-neutral) dosage status.5 They are typically introduced in the genome by recombination-based or replication-based mechanisms. Th ...
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... 4) In the cytoplasm, ribosomes then translate all of these different mRNAs into all of the different proteins that can then go on to do their jobs in the cell. Show the details of a generic example either in your story or off to the side. [Not only does the cell have to double all of its proteins an ...
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... 1. What are activator binding sites? Where are they located? Why? These are usually upstream from the RNA pol binding site. It's upstream so that it can activate the RNA pol site...if it was downstream, the RNA pol would already have been activated. 2. What is the difference between negative and pos ...
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Point mutation



A point mutation, or single base modification, is a type of mutation that causes a single nucleotide base change, insertion, or deletion of the genetic material, DNA or RNA. The term frameshift mutation indicates the addition or deletion of a base pair. A point mutant is an individual that is affected by a point mutation.Repeat induced point mutations are recurring point mutations, discussed below.
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