User:Lois A. Fridmann/Sandbox 3

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==Background and History of HIV==
==Background and History of HIV==
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The Human Immunodefiency Virus (HIV) is the causative agent of acquired immunodefiency syndrom (AIDS) in which the immune system of a human being begins to fail, leading to life threatening infections.
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Tumor susceptibility gene 101, also known as TSG101, is a human gene that encodes for a cellular protein of the same name.TSG101 plays an important role in the pathogenesis of HIV. In infected cells, TSG101 functions in the biogenesis of the multivesicular body (MVB), which suggests that HIV may bind TSG101 in order to gain access to the downstream machinery that catalyzes MVB vesicle budding.
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Group-specific antigen is the genetic material that codes for the core structural proteins of a retrovirus. Gag proteins are encoded by the gag gene, and provide structural elements of the virus.
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The protein encoded by this gene belongs to a group of apparently inactive homologs of ubiquitin-conjugating enzymes. The gene product contains a coiled-coil domain that interacts with tathmin, a cytosolic phosphoprotein implicated in tumorigenesis. The protein may play a role in cell growth and differentiation and act as a negative growth regulator. In vitro steady-state expression of this tumor susceptibility gene appears to be important for maintenance of genomic stability and cell cycle regulation. Mutations and alternative splicing in this gene occur in high frequency in breast cancer and suggest that defects occur during breast cancer tumorigenesis and/or progression.
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TSG101 belongs to a group of apparently inactive homologs of ubiquitin-conjugating enzymes. TSG101 contains a coiled-coil domain that interacts with stathmin. a cytosolic phosphoprotein implicated in tumorigenesis. TSG101 may play a role in cell growth. TSG101 is a regulator of vesicular trafficking process. Required for the sorting of endocytic ubiquitinated cargos into ultivesicular
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bodies. May be involved in cell growth and differentiation. Acts as a negative growth regulator. Involved in the budding of many viruses. The UEV domain is required for the interaction of the complex with ubiquitin. It also mediates the interaction with PTAP/PSAP motifs of HIV-1 P6 protein and human spumaretrovirus Gag protein. TSG101 (tumor susceptibility gene 101) reacts with human. Ubiquitination inactivates TSG101, possibly by regulating its shuttling between an active membrane-bound protein and an inactive soluble form. TSG101 belongs to the ubiquitin-conjugating enzyme family. UEV subfamily.

Revision as of 13:33, 2 April 2009

Tsg101 UEV Domain - Residue Mutations in the C-Terminal End

Contents

Background and History of HIV

The Human Immunodefiency Virus (HIV) is the causative agent of acquired immunodefiency syndrom (AIDS) in which the immune system of a human being begins to fail, leading to life threatening infections.

Tumor susceptibility gene 101, also known as TSG101, is a human gene that encodes for a cellular protein of the same name.TSG101 plays an important role in the pathogenesis of HIV. In infected cells, TSG101 functions in the biogenesis of the multivesicular body (MVB), which suggests that HIV may bind TSG101 in order to gain access to the downstream machinery that catalyzes MVB vesicle budding.

Group-specific antigen is the genetic material that codes for the core structural proteins of a retrovirus. Gag proteins are encoded by the gag gene, and provide structural elements of the virus.

The protein encoded by this gene belongs to a group of apparently inactive homologs of ubiquitin-conjugating enzymes. The gene product contains a coiled-coil domain that interacts with tathmin, a cytosolic phosphoprotein implicated in tumorigenesis. The protein may play a role in cell growth and differentiation and act as a negative growth regulator. In vitro steady-state expression of this tumor susceptibility gene appears to be important for maintenance of genomic stability and cell cycle regulation. Mutations and alternative splicing in this gene occur in high frequency in breast cancer and suggest that defects occur during breast cancer tumorigenesis and/or progression.

TSG101 belongs to a group of apparently inactive homologs of ubiquitin-conjugating enzymes. TSG101 contains a coiled-coil domain that interacts with stathmin. a cytosolic phosphoprotein implicated in tumorigenesis. TSG101 may play a role in cell growth. TSG101 is a regulator of vesicular trafficking process. Required for the sorting of endocytic ubiquitinated cargos into ultivesicular bodies. May be involved in cell growth and differentiation. Acts as a negative growth regulator. Involved in the budding of many viruses. The UEV domain is required for the interaction of the complex with ubiquitin. It also mediates the interaction with PTAP/PSAP motifs of HIV-1 P6 protein and human spumaretrovirus Gag protein. TSG101 (tumor susceptibility gene 101) reacts with human. Ubiquitination inactivates TSG101, possibly by regulating its shuttling between an active membrane-bound protein and an inactive soluble form. TSG101 belongs to the ubiquitin-conjugating enzyme family. UEV subfamily.


(Generalized to other viruses: A large number of viruses in other families conserve the PTAP binding site, conserving something that is affective for other viruses)


Structural Details of C-terminal mutant Tsg101

Chemical Properties

Additional Mutations

Contributions to Future Research and Therapies

References

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4.

External Links

Proteopedia Page Contributors and Editors (what is this?)

Lois A. Fridmann

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