The lac repressor prevents the lac genes in the DNA of E. coli from being expressed most of the time. The answer to your question is A. I hope this is the answer that you are looking for and it comes to your help.
Answer:
cell
tissue
organ
system
human organism
Explanation:
unicellular organisms only have one cell since two or more cells form a tissue their level of organization is restricted to cell
cell
two or more cells form a tissue
two or more tissue forms an organ
two or more organs form a system which must work in coordination for efficiency
two or more systems make up a human organism
The correct answer is B. After filtration, the lymph from lymph node travels to the subclavian veins, through efferent lymph vessels. The whole transport process is affected by smooth muscle contraction, changes in pressure and opening/closing of valves.
Protein-protein interactions within the CARMA1-BCL10-MALT1 complex:
- The T-cell receptor and B-cell receptor-dependent NF-B induction and lymphocyte activation are mediated by the CBM complex, which is made up of the proteins CARMA1, BCL10, and MALT1.
- Each of the proto-oncoproteins CARMA1, BCL10, and MALT1 is a somatic gain-of-function mutation or chromosomal translocation, and dysregulation of CBM signaling is a characteristic of numerous lymphoid malignancies, including Activated B-cell Diffuse Large B-cell Lymphoma.
- Moreover, a number of immunological dysregulation diseases have been linked to both gain- and loss-of-function germline mutations in CBM complex proteins.
- Over the past ten years, careful examination of the interactions of CBM components has yielded a wealth of detailed structural knowledge.
- Here, we discuss important discoveries about the molecular nature of these protein-protein interactions that have helped the research develop a detailed understanding of how these proteins come together to form high-order filamentous CBM complexes.
- Approaches to therapeutic suppression of the CBM complex have thus far centered on obstructing MALT1 protease activity in order to treat lymphoid malignancy and/or autoimmunity.
- The structural effects of MALT1 protease inhibitors on significant protein-protein interactions are also reviewed in detail.
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