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PSMC2
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<h2 id="gene">Gene</h2> <p>The gene <i>PSMC2</i> encodes one of the ATPase subunits, a member of the triple-A family of ATPases which have a chaperone-like activity. This subunit has been shown to interact with several of the basal transcription factors so, in addition to participation in proteasome functions, this subunit may participate in the regulation of transcription. This subunit may also compete with PSMC3 for binding to the HIV tat protein to regulate the interaction between the viral protein and the transcription complex.<a class="footnote-ref" id="fnref:6" href="#fn:6"><sup>6</sup></a> The human <i>PSMC2</i> gene has 13 exons and locates at chromosome band 7q22.1-q22.3. </p> <h2 id="protein">Protein</h2> <p>The human protein 26S protease regulatory subunit 7 is 48.6kDa in size and composed of 433 amino acids. The calculated theoretical pI of this protein is 526S protease regulatory subunit 5.71. One expression isoform is generated by alternative splicing, in which 1–137 of the amino acid sequence is missing.<a class="footnote-ref" id="fnref:7" href="#fn:7"><sup>7</sup></a> </p> <h2 id="complex-assembly">Complex assembly</h2> <p>26S <a href="/facts/Proteasome/8vTtg2MI">proteasome</a> complex is usually consisted of a 20S core particle (CP, or 20S proteasome) and one or two 19S regulatory particles (RP, or 19S proteasome) on either one side or both side of the barrel-shaped 20S. The CP and RPs pertain distinct structural characteristics and biological functions. In brief, 20S sub complex presents three types proteolytic activities, including caspase-like, trypsin-like, and chymotrypsin-like activities. These proteolytic active sites located in the inner side of a chamber formed by 4 stacked rings of 20S subunits, preventing random protein-enzyme encounter and uncontrolled protein degradation. The 19S regulatory particles can recognize ubiquitin-labeled protein as degradation substrate, unfold the protein to linear, open the gate of 20S core particle, and guide the substrate into the proteolytic chamber. To meet such functional complexity, 19S regulatory particle contains at least 18 constitutive subunits. These subunits can be categorized into two classes based on the ATP dependence of subunits, ATP-dependent subunits and ATP-independent subunits. According to the protein interaction and topological characteristics of this multisubunit complex, the 19S regulatory particle is composed of a base and a lid subcomplex. The base consists of a ring of six AAA ATPases (Subunit Rpt1–6, systematic nomenclature) and four non-ATPase subunits (<a href="/facts/PSMD2/fqt7H0yA">Rpn1</a>, <a href="/facts/PSMD1/0WTnUCq0">Rpn2</a>, <a href="/facts/PSMD4/SuDo5LGH">Rpn10</a>, and <a href="/facts/ADRM1/s53qLepV">Rpn13</a>). Thus, 26S protease regulatory subunit 4 (Rpt2) is an essential component of forming the base subcomplex of 19S regulatory particle. For the assembly of 19S base sub complex, four sets of pivotal assembly chaperons (Hsm3/S5b, Nas2/P27, Nas6/P28, and Rpn14/PAAF1, nomenclature in yeast/mammals) were identified by four groups independently.<a class="footnote-ref" id="fnref:8" href="#fn:8"><sup>8</sup></a><a class="footnote-ref" id="fnref:9" href="#fn:9"><sup>9</sup></a><a class="footnote-ref" id="fnref:10" href="#fn:10"><sup>10</sup></a><a class="footnote-ref" id="fnref:11" href="#fn:11"><sup>11</sup></a><a class="footnote-ref" id="fnref:12" href="#fn:12"><sup>12</sup></a><a class="footnote-ref" id="fnref:13" href="#fn:13"><sup>13</sup></a> These 19S regulatory particle base-dedicated chaperons all binds to individual ATPase subunits through the C-terminal regions. For example, Hsm3/S5b binds to the subunit Rpt1 (this protein) and <a href="/facts/PSMC1/TCstHuPp">Rpt2</a>, Nas2/p27 to <a href="/facts/PSMC3/8RuCT3wb">Rpt5</a>, Nas6/p28 to <a href="/facts/PSMC4/aJWY1rKq">Rpt3</a>, and Rpn14/PAAAF1 to <a href="/facts/PSMC5/LoIXRf99">Rpt6</a>, respectively. Subsequently, three intermediate assembly modules are formed as following, the Nas6/p28-Rpt3-Rpt6-Rpn14/PAAF1 module, the Nas2/p27-Rpt4-Rpt5 module, and the Hsm3/S5b-Rpt1-Rpt2-Rpn2 module. Eventually, these three modules assemble together to form the heterohexameric ring of 6 Atlases with Rpn1. The final addition of <a href="/facts/ADRM1/s53qLepV">Rpn13</a> indicates the completion of 19S base sub complex assembly.<a class="footnote-ref" id="fnref:14" href="#fn:14"><sup>14</sup></a> </p> <h2 id="function">Function</h2> <p>As the degradation machinery that is responsible for ~70% of intracellular proteolysis,<a class="footnote-ref" id="fnref:15" href="#fn:15"><sup>15</sup></a> proteasome complex (26S proteasome) plays a critical roles in maintaining the homeostasis of cellular proteome. Accordingly, misfolded proteins and damaged protein need to be continuously removed to recycle amino acids for new synthesis; in parallel, some key regulatory proteins fulfill their biological functions via selective degradation; furthermore, proteins are digested into peptides for MHC class I antigen presentation. To meet such complicated demands in biological process via spatial and temporal proteolysis, protein substrates have to be recognized, recruited, and eventually hydrolyzed in a well controlled fashion. Thus, 19S regulatory particle pertains a series of important capabilities to address these functional challenges. To recognize protein as designated substrate, 19S complex has subunits that are capable to recognize proteins with a special degradative tag, the ubiquitinylation. It also have subunits that can bind with nucleotides (e.g., ATPs) in order to facilitate the association between 19S and 20S particles, as well as to cause confirmation changes of alpha subunit C-terminals that form the substrate entrance of 20S complex. The ATPases subunits assemble into a six-membered ring with a sequence of Rpt1–Rpt5–Rpt4–Rpt3–Rpt6–Rpt2, which interacts with the seven-membered alpha ring of 20S core particle and establishes an asymmetric interface between the 19S RP and the 20S CP.<a class="footnote-ref" id="fnref:16" href="#fn:16"><sup>16</sup></a><a class="footnote-ref" id="fnref:17" href="#fn:17"><sup>17</sup></a> Three C-terminal tails with <a href="/facts/HbYX_motifs/YKzzSBvT">HbYX motifs</a> of distinct Rpt ATPases insert into pockets between two defined alpha subunits of the CP and regulate the gate opening of the central channels in the CP alpha ring.<a class="footnote-ref" id="fnref:18" href="#fn:18"><sup>18</sup></a><a class="footnote-ref" id="fnref:19" href="#fn:19"><sup>19</sup></a> </p> <h2 id="interactions">Interactions</h2> <p>PSMC2 has been shown to <a href="/facts/Protein-protein_interaction/etvm9Wmg">interact</a> with: </p> <ul><li><a href="/facts/NDC80/KrA0YBwv">NDC80</a>,<a class="footnote-ref" id="fnref:20" href="#fn:20"><sup>20</sup></a></li> <li><a href="/facts/PSMC1/TCstHuPp">PSMC1</a>,<a class="footnote-ref" id="fnref:21" href="#fn:21"><sup>21</sup></a><a class="footnote-ref" id="fnref:22" href="#fn:22"><sup>22</sup></a></li> <li><a href="/facts/PSMC4/aJWY1rKq">PSMC4</a>,<a class="footnote-ref" id="fnref:23" href="#fn:23"><sup>23</sup></a><a class="footnote-ref" id="fnref:24" href="#fn:24"><sup>24</sup></a> and</li> <li><a href="/facts/PSMD5/Pm9dGyEj">PSMD5</a>.<a class="footnote-ref" id="fnref:25" href="#fn:25"><sup>25</sup></a><a class="footnote-ref" id="fnref:26" href="#fn:26"><sup>26</sup></a></li></ul> <h2 id="further-reading">Further reading</h2> <ul><li>Coux O, Tanaka K, Goldberg AL (1996). "Structure and functions of the 20S and 26S proteasomes". <i>Annu. Rev. Biochem</i>. 65: 801–47. <a href="/facts/Doi_(identifier)/muM9Etpq">doi</a>:<a href="https://doi.org/10.1146%2Fannurev.bi.65.070196.004101">10.1146/annurev.bi.65.070196.004101</a>. <a href="/facts/PMID_(identifier)/JlHAvMHt">PMID</a> <a href="https://pubmed.ncbi.nlm.nih.gov/8811196">8811196</a>.</li> <li>Goff SP (2003). <a href="https://doi.org/10.1016%2FS0092-8674%2803%2900602-0">"Death by deamination: a novel host restriction system for HIV-1"</a>. <i>Cell</i>. 114 (3): 281–3. <a href="/facts/Doi_(identifier)/muM9Etpq">doi</a>:<a href="https://doi.org/10.1016%2FS0092-8674%2803%2900602-0">10.1016/S0092-8674(03)00602-0</a>. <a href="/facts/PMID_(identifier)/JlHAvMHt">PMID</a> <a href="https://pubmed.ncbi.nlm.nih.gov/12914693">12914693</a>. <a href="/facts/S2CID_(identifier)/ldJsHa2Y">S2CID</a> <a href="https://api.semanticscholar.org/CorpusID:16340355">16340355</a>.</li> <li>Dawson SJ, White LA (1992). "Treatment of Haemophilus aphrophilus endocarditis with ciprofloxacin". <i>J. Infect</i>. 24 (3): 317–20. <a href="/facts/Doi_(identifier)/muM9Etpq">doi</a>:<a href="https://doi.org/10.1016%2FS0163-4453%2805%2980037-4">10.1016/S0163-4453(05)80037-4</a>. <a href="/facts/PMID_(identifier)/JlHAvMHt">PMID</a> <a href="https://pubmed.ncbi.nlm.nih.gov/1602151">1602151</a>.</li> <li>Nacken W, Kingsman AJ, Kingsman SM, Sablitzky F, Sorg C (1995). "A homologue of the human MSS1 gene, a positive modulator of HIV-1 gene expression, is massively expressed in Xenopus oocytes". <i>Biochim. Biophys. Acta</i>. 1261 (2): 293–5. <a href="/facts/Doi_(identifier)/muM9Etpq">doi</a>:<a href="https://doi.org/10.1016%2F0167-4781%2895%2900022-9">10.1016/0167-4781(95)00022-9</a>. <a href="/facts/PMID_(identifier)/JlHAvMHt">PMID</a> <a href="https://pubmed.ncbi.nlm.nih.gov/7711076">7711076</a>.</li> <li>Ghislain M, Udvardy A, Mann C (1993). "S. cerevisiae 26S protease mutants arrest cell division in G2/metaphase". <i>Nature</i>. 366 (6453): 358–62. <a href="/facts/Bibcode_(identifier)/9HtdQSGB">Bibcode</a>:<a href="https://ui.adsabs.harvard.edu/abs/1993Natur.366..358G">1993Natur.366..358G</a>. <a href="/facts/Doi_(identifier)/muM9Etpq">doi</a>:<a href="https://doi.org/10.1038%2F366358a0">10.1038/366358a0</a>. <a href="/facts/PMID_(identifier)/JlHAvMHt">PMID</a> <a href="https://pubmed.ncbi.nlm.nih.gov/8247132">8247132</a>. <a href="/facts/S2CID_(identifier)/ldJsHa2Y">S2CID</a> <a href="https://api.semanticscholar.org/CorpusID:2168133">2168133</a>.</li> <li>Dubiel W, Ferrell K, Rechsteiner M (1993). "Peptide sequencing identifies MSS1, a modulator of HIV Tat-mediated transactivation, as subunit 7 of the 26 S protease". <i>FEBS Lett</i>. 323 (3): 276–8. <a href="/facts/Bibcode_(identifier)/9HtdQSGB">Bibcode</a>:<a href="https://ui.adsabs.harvard.edu/abs/1993FEBSL.323..276D">1993FEBSL.323..276D</a>. <a href="/facts/Doi_(identifier)/muM9Etpq">doi</a>:<a href="https://doi.org/10.1016%2F0014-5793%2893%2981356-5">10.1016/0014-5793(93)81356-5</a>. <a href="/facts/PMID_(identifier)/JlHAvMHt">PMID</a> <a href="https://pubmed.ncbi.nlm.nih.gov/8500623">8500623</a>. <a href="/facts/S2CID_(identifier)/ldJsHa2Y">S2CID</a> <a href="https://api.semanticscholar.org/CorpusID:26726988">26726988</a>.</li> <li>Seeger M, Ferrell K, Frank R, Dubiel W (1997). <a href="https://doi.org/10.1074%2Fjbc.272.13.8145">"HIV-1 tat inhibits the 20 S proteasome and its 11 S regulator-mediated activation"</a>. <i>J. Biol. Chem</i>. 272 (13): 8145–8. <a href="/facts/Doi_(identifier)/muM9Etpq">doi</a>:<a href="https://doi.org/10.1074%2Fjbc.272.13.8145">10.1074/jbc.272.13.8145</a>. <a href="/facts/PMID_(identifier)/JlHAvMHt">PMID</a> <a href="https://pubmed.ncbi.nlm.nih.gov/9079628">9079628</a>.</li> <li>Chen Y, Sharp ZD, Lee WH (1997). <a href="https://doi.org/10.1074%2Fjbc.272.38.24081">"HEC binds to the seventh regulatory subunit of the 26 S proteasome and modulates the proteolysis of mitotic cyclins"</a>. <i>J. Biol. Chem</i>. 272 (38): 24081–7. <a href="/facts/Doi_(identifier)/muM9Etpq">doi</a>:<a href="https://doi.org/10.1074%2Fjbc.272.38.24081">10.1074/jbc.272.38.24081</a>. <a href="/facts/PMID_(identifier)/JlHAvMHt">PMID</a> <a href="https://pubmed.ncbi.nlm.nih.gov/9295362">9295362</a>.</li> <li>Madani N, Kabat D (1998). <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC110608">"An Endogenous Inhibitor of Human Immunodeficiency Virus in Human Lymphocytes Is Overcome by the Viral Vif Protein"</a>. <i>J. Virol</i>. 72 (12): 10251–5. <a href="/facts/Doi_(identifier)/muM9Etpq">doi</a>:<a href="https://doi.org/10.1128%2FJVI.72.12.10251-10255.1998">10.1128/JVI.72.12.10251-10255.1998</a>. <a href="/facts/PMC_(identifier)/dX1zMt71">PMC</a> <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC110608">110608</a>. <a href="/facts/PMID_(identifier)/JlHAvMHt">PMID</a> <a href="https://pubmed.ncbi.nlm.nih.gov/9811770">9811770</a>.</li> <li>Simon JH, Gaddis NC, Fouchier RA, Malim MH (1998). "Evidence for a newly discovered cellular anti-HIV-1 phenotype". <i>Nat. Med</i>. 4 (12): 1397–400. <a href="/facts/Doi_(identifier)/muM9Etpq">doi</a>:<a href="https://doi.org/10.1038%2F3987">10.1038/3987</a>. <a href="/facts/PMID_(identifier)/JlHAvMHt">PMID</a> <a href="https://pubmed.ncbi.nlm.nih.gov/9846577">9846577</a>. <a href="/facts/S2CID_(identifier)/ldJsHa2Y">S2CID</a> <a href="https://api.semanticscholar.org/CorpusID:25235070">25235070</a>.</li> <li>Zheng L, Chen Y, Lee WH (1999). <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC84384">"Hec1p, an Evolutionarily Conserved Coiled-Coil Protein, Modulates Chromosome Segregation through Interaction with SMC Proteins"</a>. <i>Mol. Cell. Biol</i>. 19 (8): 5417–28. <a href="/facts/Doi_(identifier)/muM9Etpq">doi</a>:<a href="https://doi.org/10.1128%2Fmcb.19.8.5417">10.1128/mcb.19.8.5417</a>. <a href="/facts/PMC_(identifier)/dX1zMt71">PMC</a> <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC84384">84384</a>. <a href="/facts/PMID_(identifier)/JlHAvMHt">PMID</a> <a href="https://pubmed.ncbi.nlm.nih.gov/10409732">10409732</a>.</li> <li>Gorbea C, Taillandier D, Rechsteiner M (2000). <a href="https://doi.org/10.1074%2Fjbc.275.2.875">"Mapping subunit contacts in the regulatory complex of the 26 S proteasome. S2 and S5b form a tetramer with ATPase subunits S4 and S7"</a>. <i>J. Biol. Chem</i>. 275 (2): 875–82. <a href="/facts/Doi_(identifier)/muM9Etpq">doi</a>:<a href="https://doi.org/10.1074%2Fjbc.275.2.875">10.1074/jbc.275.2.875</a>. <a href="/facts/PMID_(identifier)/JlHAvMHt">PMID</a> <a href="https://pubmed.ncbi.nlm.nih.gov/10625621">10625621</a>.</li> <li>Mulder LC, Muesing MA (2000). <a href="https://doi.org/10.1074%2Fjbc.M004670200">"Degradation of HIV-1 integrase by the N-end rule pathway"</a>. <i>J. Biol. Chem</i>. 275 (38): 29749–53. <a href="/facts/Doi_(identifier)/muM9Etpq">doi</a>:<a href="https://doi.org/10.1074%2Fjbc.M004670200">10.1074/jbc.M004670200</a>. <a href="/facts/PMID_(identifier)/JlHAvMHt">PMID</a> <a href="https://pubmed.ncbi.nlm.nih.gov/10893419">10893419</a>.</li> <li>Hwang J, Fauzi H, Fukuda K, Sekiya S, Kakiuchi N, Shimotohno K, Taira K, Kusakabe I, Nishikawa S (2001). "The RNA aptamer-binding site of hepatitis C virus NS3 protease". <i>Biochem. Biophys. Res. Commun</i>. 279 (2): 557–62. <a href="/facts/Doi_(identifier)/muM9Etpq">doi</a>:<a href="https://doi.org/10.1006%2Fbbrc.2000.4007">10.1006/bbrc.2000.4007</a>. <a href="/facts/PMID_(identifier)/JlHAvMHt">PMID</a> <a href="https://pubmed.ncbi.nlm.nih.gov/11118325">11118325</a>.</li> <li>Yanagi S, Shimbara N, Tamura Ta (2001). "Tissue and cell distribution of a mammalian proteasomal ATPase, MSS1, and its complex formation with the basal transcription factors". <i>Biochem. Biophys. Res. Commun</i>. 279 (2): 568–73. <a href="/facts/Doi_(identifier)/muM9Etpq">doi</a>:<a href="https://doi.org/10.1006%2Fbbrc.2000.3969">10.1006/bbrc.2000.3969</a>. <a href="/facts/PMID_(identifier)/JlHAvMHt">PMID</a> <a href="https://pubmed.ncbi.nlm.nih.gov/11118327">11118327</a>.</li> <li>Hartmann-Petersen R, Tanaka K, Hendil KB (2001). "Quaternary structure of the ATPase complex of human 26S proteasomes determined by chemical cross-linking". <i>Arch. Biochem. Biophys</i>. 386 (1): 89–94. <a href="/facts/Doi_(identifier)/muM9Etpq">doi</a>:<a href="https://doi.org/10.1006%2Fabbi.2000.2178">10.1006/abbi.2000.2178</a>. <a href="/facts/PMID_(identifier)/JlHAvMHt">PMID</a> <a href="https://pubmed.ncbi.nlm.nih.gov/11361004">11361004</a>.</li> <li>Sheehy AM, Gaddis NC, Choi JD, Malim MH (2002). "Isolation of a human gene that inhibits HIV-1 infection and is suppressed by the viral Vif protein". <i>Nature</i>. 418 (6898): 646–50. <a href="/facts/Bibcode_(identifier)/9HtdQSGB">Bibcode</a>:<a href="https://ui.adsabs.harvard.edu/abs/2002Natur.418..646S">2002Natur.418..646S</a>. <a href="/facts/Doi_(identifier)/muM9Etpq">doi</a>:<a href="https://doi.org/10.1038%2Fnature00939">10.1038/nature00939</a>. <a href="/facts/PMID_(identifier)/JlHAvMHt">PMID</a> <a href="https://pubmed.ncbi.nlm.nih.gov/12167863">12167863</a>. <a href="/facts/S2CID_(identifier)/ldJsHa2Y">S2CID</a> <a href="https://api.semanticscholar.org/CorpusID:4403228">4403228</a>.</li></ul> <h2 id="references">References</h2> <ol> <li id="fn:1"><p>Tanahashi N, Suzuki M, Fujiwara T, Takahashi E, Shimbara N, Chung CH, Tanaka K (March 1998). "Chromosomal localization and immunological analysis of a family of human 26S proteasomal ATPases". Biochem Biophys Res Commun. 243 (1): 229–32. doi:10.1006/bbrc.1997.7892. PMID 9473509. <a href="/wiki/Doi_(identifier)" target="_blank">/wiki/Doi_(identifier)</a> <a href="#fnref:1" class="footnote-back-ref">↩</a></p></li> <li id="fn:2"><p>Shibuya H, Irie K, Ninomiya-Tsuji J, Goebl M, Taniguchi T, Matsumoto K (July 1992). "New human gene encoding a positive modulator of HIV Tat-mediated transactivation". Nature. 357 (6380): 700–2. Bibcode:1992Natur.357..700S. doi:10.1038/357700a0. PMID 1377363. S2CID 4343919. <a href="/wiki/Bibcode_(identifier)" target="_blank">/wiki/Bibcode_(identifier)</a> <a href="#fnref:2" class="footnote-back-ref">↩</a></p></li> <li id="fn:3"><p>"Entrez Gene: PSMC2 proteasome (prosome, macropain) 26S subunit, ATPase, 2". <a href="https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=5701" target="_blank">https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=5701</a> <a href="#fnref:3" class="footnote-back-ref">↩</a></p></li> <li id="fn:4"><p>Gu ZC, Enenkel C (Dec 2014). "Proteasome assembly". Cellular and Molecular Life Sciences. 71 (24): 4729–45. doi:10.1007/s00018-014-1699-8. PMC 11113775. PMID 25107634. S2CID 15661805. <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11113775" target="_blank">https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11113775</a> <a href="#fnref:4" class="footnote-back-ref">↩</a></p></li> <li id="fn:5"><p>Gu ZC, Enenkel C (Dec 2014). "Proteasome assembly". Cellular and Molecular Life Sciences. 71 (24): 4729–45. doi:10.1007/s00018-014-1699-8. PMC 11113775. PMID 25107634. S2CID 15661805. <a href="https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11113775" target="_blank">https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11113775</a> <a href="#fnref:5" class="footnote-back-ref">↩</a></p></li> <li id="fn:6"><p>"Entrez Gene: PSMC2 proteasome (prosome, macropain) 26S subunit, ATPase, 2". <a href="https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=5701" target="_blank">https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=5701</a> <a href="#fnref:6" class="footnote-back-ref">↩</a></p></li> <li id="fn:7"><p>"Uniprot: P35998 - PRS7_HUMAN". <a href="https://www.uniprot.org/uniprot/P35998" target="_blank">https://www.uniprot.org/uniprot/P35998</a> <a href="#fnref:7" class="footnote-back-ref">↩</a></p></li> <li id="fn:8"><p>Le Tallec B, Barrault MB, Guérois R, Carré T, Peyroche A (Feb 2009). "Hsm3/S5b participates in the assembly pathway of the 19S regulatory particle of the proteasome". 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