VPS26A: Difference between revisions

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<!-- The PBB_Controls template provides controls for Protein Box Bot, please see Template:PBB_Controls for details. -->
{{Infobox_gene}}
{{PBB_Controls
'''Vacuolar protein sorting-associated protein 26A''' is a [[protein]] that in humans is encoded by the ''VPS26A'' [[gene]].<ref name="pmid1638986">{{cite journal | vauthors = Lee JJ, Radice G, Perkins CP, Costantini F | title = Identification and characterization of a novel, evolutionarily conserved gene disrupted by the murine H beta 58 embryonic lethal transgene insertion | journal = Development | volume = 115 | issue = 1 | pages = 277–88 |date=Aug 1992 | pmid = 1638986 | pmc =  | doi =  }}</ref><ref name="pmid9653160">{{cite journal | vauthors = Mao M, Fu G, Wu JS, Zhang QH, Zhou J, Kan LX, Huang QH, He KL, Gu BW, Han ZG, Shen Y, Gu J, Yu YP, Xu SH, Wang YX, Chen SJ, Chen Z | title = Identification of genes expressed in human CD34+ hematopoietic stem/progenitor cells by expressed sequence tags and efficient full-length cDNA cloning | journal = Proc Natl Acad Sci U S A | volume = 95 | issue = 14 | pages = 8175–80 |date=Aug 1998 | pmid = 9653160 | pmc = 20949 | doi =10.1073/pnas.95.14.8175  }}</ref><ref name="entrez">{{cite web | title = Entrez Gene: VPS26A vacuolar protein sorting 26 homolog A (S. pombe)| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=9559| accessdate = }}</ref>
| update_page = yes
| require_manual_inspection = no
| update_protein_box = yes
| update_summary = yes
| update_citations = yes
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<!-- The GNF_Protein_box is automatically maintained by Protein Box Bot.  See Template:PBB_Controls to Stop updates. -->
This gene belongs to a group of vacuolar protein sorting (VPS) genes. The encoded protein is a component of a large multimeric complex, termed the [[retromer]] complex, involved in retrograde transport of proteins from [[endosome]]s to the [[Golgi apparatus|trans-Golgi network]]. The close structural similarity between the yeast and human proteins that make up this complex suggests a similarity in function. Expression studies in yeast and mammalian cells indicate that this protein interacts directly with [[VPS35]], which serves as the core of the retromer complex. Alternative splicing results in multiple transcript variants encoding different isoforms.<ref name="entrez" />
{{GNF_Protein_box
| image = PBB_Protein_VPS26A_image.jpg
| image_source = [[Protein_Data_Bank|PDB]] rendering based on 2fau.
| PDB = {{PDB2|2fau}}
| Name = Vacuolar protein sorting 26 homolog A (S. pombe)
| HGNCid = 12711
| Symbol = VPS26A
| AltSymbols =; FLJ12930; HB58; Hbeta58; PEP8A; VPS26
| OMIM = 605506
| ECnumber = 
| Homologene = 68420
| MGIid = 1353654
| GeneAtlas_image1 = PBB_GE_VPS26A_201807_at_tn.png
| Function = {{GNF_GO|id=GO:0005515 |text = protein binding}} {{GNF_GO|id=GO:0008565 |text = protein transporter activity}}
| Component = {{GNF_GO|id=GO:0005768 |text = endosome}} {{GNF_GO|id=GO:0005829 |text = cytosol}} {{GNF_GO|id=GO:0016020 |text = membrane}} {{GNF_GO|id=GO:0030904 |text = retromer complex}}
| Process = {{GNF_GO|id=GO:0007034 |text = vacuolar transport}} {{GNF_GO|id=GO:0015031 |text = protein transport}} {{GNF_GO|id=GO:0042147 |text = retrograde transport, endosome to Golgi}}
| Orthologs = {{GNF_Ortholog_box
    | Hs_EntrezGene = 9559
    | Hs_Ensembl = ENSG00000122958
    | Hs_RefseqProtein = NP_001030337
    | Hs_RefseqmRNA = NM_001035260
    | Hs_GenLoc_db = 
    | Hs_GenLoc_chr = 10
    | Hs_GenLoc_start = 70553274
    | Hs_GenLoc_end = 70602623
    | Hs_Uniprot = O75436
    | Mm_EntrezGene = 30930
    | Mm_Ensembl = ENSMUSG00000020078
    | Mm_RefseqmRNA = NM_133672
    | Mm_RefseqProtein = NP_598433
    | Mm_GenLoc_db = 
    | Mm_GenLoc_chr = 10
    | Mm_GenLoc_start = 61850592
    | Mm_GenLoc_end = 61882109
    | Mm_Uniprot = P40336
  }}
}}
'''Vacuolar protein sorting 26 homolog A (S. pombe)''', also known as '''VPS26A''', is a human [[gene]].<ref name="entrez">{{cite web | title = Entrez Gene: VPS26A vacuolar protein sorting 26 homolog A (S. pombe)| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=9559| accessdate = }}</ref>


<!-- The PBB_Summary template is automatically maintained by Protein Box Bot. See Template:PBB_Controls to Stop updates. -->
== Structure ==
{{PBB_Summary
[[File:Structural comparison of Vps26 with Arrestins.png|thumb|left|300x300px|Structural comparison of Vps26 with [[arrestin]]s]]
| section_title =  
Vps26 is a 38-kDa subunit that has a two-lobed structure with a polar core that resembles the [[arrestin]] family of trafficking adaptor.<ref name="pmid18088321">{{cite journal | vauthors = Collins BM, Norwood SJ, Kerr MC, Mahony D, Seaman MN, Teasdale RD, Owen DJ | title = Structure of Vps26B and mapping of its interaction with the retromer protein complex | journal = Traffic | volume = 9 | issue = 3 | pages = 366–79 |date=March 2008 | pmid = 18088321 | doi = 10.1111/j.1600-0854.2007.00688.x  }}</ref><ref name="pmid16732284">{{cite journal | vauthors = Shi H, Rojas R, Bonifacino JS, Hurley JH | title = The retromer subunit Vps26 has an arrestin fold and binds Vps35 through its C-terminal domain | journal = Nat. Struct. Mol. Biol. | volume = 13 | issue = 6 | pages = 540–8 |date=June 2006 | pmid = 16732284 | pmc = 1584284 | doi = 10.1038/nsmb1103 }}</ref> This fold consist of two related [[beta barrel|β-sandwich]] subdomains with a [[fibronectin type III domain]] topology. The two domains are joined together by a flexible linker and are closely associated by an unusual polar core.  Arrestins are regulatory proteins known for connecting [[G-protein coupled receptor]]s (GPCRs) to [[clathrin]] during endocytosis. They play many critical roles in cell signalling and membrane trafficking.<ref name="pmid16460808">{{cite journal | vauthors = Gurevich VV, Gurevich EV | title = The structural basis of arrestin-mediated regulation of G-protein-coupled receptors | journal = Pharmacol. Ther. | volume = 110 | issue = 3 | pages = 465–502 |date=June 2006 | pmid = 16460808 | pmc = 2562282 | doi = 10.1016/j.pharmthera.2005.09.008 }}</ref> Both Vps26 and arrestins are composed of two structurally related β-sheet domains forming extensive interfaces with each other, using polar and electrostatic contacts to create interdomain interactions for ligand binding. However, there are significant structural differences between both Vps26 and arrestins. Vps26 protein has extended [[C-terminal]] tails that do not contain identifiable clathrin- or [[AP2 adaptor complex|AP2]]-binding sequences, and therefore cannot form stable intramolecular contacts with clathrin and AP2, which has been observed for arrestins. Moreover, Vps26 does not have similar sequences as arrestins for GPCR and [[phospholipid]] interactions.<ref name="pmid18541005">{{cite journal | author = Collins BM | title = The structure and function of the retromer protein complex | journal = Traffic | volume = 9 | issue = 11 | pages = 1811–22 |date=November 2008 | pmid = 18541005 | doi = 10.1111/j.1600-0854.2008.00777.x }}</ref>
| summary_text = This gene belongs to a group of vacuolar protein sorting (VPS) genes. The encoded protein is a component of a large multimeric complex, termed the retromer complex, involved in retrograde transport of proteins from endosomes to the trans-Golgi network. The close structural similarity between the yeast and human proteins that make up this complex suggests a similarity in function. Expression studies in yeast and mammalian cells indicate that this protein interacts directly with VPS35, which serves as the core of the retromer complex. Alternative splicing results in multiple transcript variants encoding different isoforms.<ref name="entrez">{{cite web | title = Entrez Gene: VPS26A vacuolar protein sorting 26 homolog A (S. pombe)| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=9559| accessdate = }}</ref>
 
}}
== Vps26B paralogue ==
 
[[File:Structural differences between Vps26A and Vps26B.png|thumb|left|Structural differences between Vps26A and Vps26B]]
In yeast, there is only one Vps26 species, whereas there are two Vps26 paralogues (Vps26A and Vps26B) in mammals.<ref name="pmid16190980">{{cite journal | vauthors = Kerr MC, Bennetts JS, Simpson F, Thomas EC, Flegg C, Gleeson PA, Wicking C, Teasdale RD | title = A novel mammalian retromer component, Vps26B | journal = Traffic | volume = 6 | issue = 11 | pages = 991–1001 |date=November 2005 | pmid = 16190980 | doi = 10.1111/j.1600-0854.2005.00328.x }}</ref>
 
X-ray crystallography revealed that the structures of both Vps26A and Vps26B share a similar bilobal β-sandwich structure and possess 70% sequence homology.<ref name="pmid18088321" /> However, these two paralogues distinctly differ on the surface patch within the [[N-terminal]] domain, the apex region where the N-terminal and [[C-terminal]] domains meet and the disordered C-terminal tail. Vps26B contains several putative serine [[phosphorylation]] residues within this disordered tail, which may represent a potential mechanism to modulate the difference between Vps26A and Vps26B. A recent study conducted by Bugarcic et al. pinpointed that this disordered tail on C-terminal region of Vps26B is one of the underlying factors that contributes to the failure for Vps26B-containing Retromer to associate with CI-[[cation-dependent mannose-6-phosphate receptor|M6PR]], ultimately leading to CI-M6PR degradation, accompanied with increased [[cathepsin D]] secretion.<ref name="pmid21920005">{{cite journal | vauthors = Bugarcic A, Zhe Y, Kerr MC, Griffin J, Collins BM, Teasdale RD | title = Vps26A and Vps26B subunits define distinct retromer complexes | journal = Traffic | volume = 12 | issue = 12 | pages = 1759–73 |date=December 2011 | pmid = 21920005 | doi = 10.1111/j.1600-0854.2011.01284.x }}</ref>
{{Clear}}


==References==
==References==
{{reflist|2}}
{{reflist|colwidth=35em}}
 
==Further reading==
==Further reading==
{{refbegin | 2}}
{{refbegin|colwidth=35em}}
{{PBB_Further_reading
*{{cite journal   |vauthors=Zhang QH, Ye M, Wu XY, etal |title=Cloning and Functional Analysis of cDNAs with Open Reading Frames for 300 Previously Undefined Genes Expressed in CD34+ Hematopoietic Stem/Progenitor Cells |journal=Genome Res. |volume=10 |issue= 10 |pages= 1546–60 |year= 2001 |pmid= 11042152 |doi=10.1101/gr.140200  | pmc=310934 }}
| citations =
*{{cite journal   |vauthors=Haft CR, de la Luz Sierra M, Bafford R, etal |title=Human Orthologs of Yeast Vacuolar Protein Sorting Proteins Vps26, 29, and 35: Assembly into Multimeric Complexes |journal=Mol. Biol. Cell |volume=11 |issue= 12 |pages= 4105–16 |year= 2001 |pmid= 11102511 |doi= 10.1091/mbc.11.12.4105| pmc=15060 }}
*{{cite journal  | author=Lee JJ, Radice G, Perkins CP, Costantini F |title=Identification and characterization of a novel, evolutionarily conserved gene disrupted by the murine H beta 58 embryonic lethal transgene insertion. |journal=Development |volume=115 |issue= 1 |pages= 277-88 |year= 1992 |pmid= 1638986 |doi=  }}
*{{cite journal  | vauthors=Reddy JV, Seaman MN |title=Vps26p, a Component of Retromer, Directs the Interactions of Vps35p in Endosome-to-Golgi Retrieval |journal=Mol. Biol. Cell |volume=12 |issue= 10 |pages= 3242–56 |year= 2002 |pmid= 11598206 |doi= 10.1091/mbc.12.10.3242| pmc=60170 }}
*{{cite journal  | author=Mao M, Fu G, Wu JS, ''et al.'' |title=Identification of genes expressed in human CD34(+) hematopoietic stem/progenitor cells by expressed sequence tags and efficient full-length cDNA cloning. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=95 |issue= 14 |pages= 8175-80 |year= 1998 |pmid= 9653160 |doi= }}
*{{cite journal   |vauthors=Strausberg RL, Feingold EA, Grouse LH, etal |title=Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=99 |issue= 26 |pages= 16899–903 |year= 2003 |pmid= 12477932 |doi= 10.1073/pnas.242603899 | pmc=139241 }}
*{{cite journal | author=Zhang QH, Ye M, Wu XY, ''et al.'' |title=Cloning and functional analysis of cDNAs with open reading frames for 300 previously undefined genes expressed in CD34+ hematopoietic stem/progenitor cells. |journal=Genome Res. |volume=10 |issue= 10 |pages= 1546-60 |year= 2001 |pmid= 11042152 |doi=  }}
*{{cite journal   |vauthors=Ota T, Suzuki Y, Nishikawa T, etal |title=Complete sequencing and characterization of 21,243 full-length human cDNAs |journal=Nat. Genet. |volume=36 |issue= 1 |pages= 40–5 |year= 2004 |pmid= 14702039 |doi= 10.1038/ng1285 }}
*{{cite journal | author=Haft CR, de la Luz Sierra M, Bafford R, ''et al.'' |title=Human orthologs of yeast vacuolar protein sorting proteins Vps26, 29, and 35: assembly into multimeric complexes. |journal=Mol. Biol. Cell |volume=11 |issue= 12 |pages= 4105-16 |year= 2001 |pmid= 11102511 |doi=  }}
*{{cite journal   |vauthors=Deloukas P, Earthrowl ME, Grafham DV, etal |title=The DNA sequence and comparative analysis of human chromosome 10 |journal=Nature |volume=429 |issue= 6990 |pages= 375–81 |year= 2004 |pmid= 15164054 |doi= 10.1038/nature02462 }}
*{{cite journal  | author=Reddy JV, Seaman MN |title=Vps26p, a component of retromer, directs the interactions of Vps35p in endosome-to-Golgi retrieval. |journal=Mol. Biol. Cell |volume=12 |issue= 10 |pages= 3242-56 |year= 2002 |pmid= 11598206 |doi=  }}
*{{cite journal   |vauthors=Vergés M, Luton F, Gruber C, etal |title=The mammalian retromer regulates transcytosis of the polymeric immunoglobulin receptor |journal=Nat. Cell Biol. |volume=6 |issue= 8 |pages= 763–9 |year= 2004 |pmid= 15247922 |doi= 10.1038/ncb1153 }}
*{{cite journal | author=Strausberg RL, Feingold EA, Grouse LH, ''et al.'' |title=Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=99 |issue= 26 |pages= 16899-903 |year= 2003 |pmid= 12477932 |doi= 10.1073/pnas.242603899 }}
*{{cite journal  | vauthors=Mingot JM, Bohnsack MT, Jäkle U, Görlich D |title=Exportin 7 defines a novel general nuclear export pathway |journal=EMBO J. |volume=23 |issue= 16 |pages= 3227–36 |year= 2005 |pmid= 15282546 |doi= 10.1038/sj.emboj.7600338 | pmc=514512 }}
*{{cite journal | author=Ota T, Suzuki Y, Nishikawa T, ''et al.'' |title=Complete sequencing and characterization of 21,243 full-length human cDNAs. |journal=Nat. Genet. |volume=36 |issue= 1 |pages= 40-5 |year= 2004 |pmid= 14702039 |doi= 10.1038/ng1285 }}
*{{cite journal   |vauthors=Gerhard DS, Wagner L, Feingold EA, etal |title=The Status, Quality, and Expansion of the NIH Full-Length cDNA Project: The Mammalian Gene Collection (MGC) |journal=Genome Res. |volume=14 |issue= 10B |pages= 2121–7 |year= 2004 |pmid= 15489334 |doi= 10.1101/gr.2596504 | pmc=528928 }}
*{{cite journal | author=Deloukas P, Earthrowl ME, Grafham DV, ''et al.'' |title=The DNA sequence and comparative analysis of human chromosome 10. |journal=Nature |volume=429 |issue= 6990 |pages= 375-81 |year= 2004 |pmid= 15164054 |doi= 10.1038/nature02462 }}
*{{cite journal   |vauthors=Kerr MC, Bennetts JS, Simpson F, etal |title=A novel mammalian retromer component, Vps26B |journal=Traffic |volume=6 |issue= 11 |pages= 991–1001 |year= 2006 |pmid= 16190980 |doi= 10.1111/j.1600-0854.2005.00328.x }}
*{{cite journal | author=Vergés M, Luton F, Gruber C, ''et al.'' |title=The mammalian retromer regulates transcytosis of the polymeric immunoglobulin receptor. |journal=Nat. Cell Biol. |volume=6 |issue= 8 |pages= 763-9 |year= 2004 |pmid= 15247922 |doi= 10.1038/ncb1153 }}
*{{cite journal   |vauthors=Small SA, Kent K, Pierce A, etal |title=Model-guided microarray implicates the retromer complex in Alzheimer's disease |journal=Ann. Neurol. |volume=58 |issue= 6 |pages= 909–19 |year= 2006 |pmid= 16315276 |doi= 10.1002/ana.20667 }}
*{{cite journal  | author=Mingot JM, Bohnsack MT, Jäkle U, Görlich D |title=Exportin 7 defines a novel general nuclear export pathway. |journal=EMBO J. |volume=23 |issue= 16 |pages= 3227-36 |year= 2005 |pmid= 15282546 |doi= 10.1038/sj.emboj.7600338 }}
*{{cite journal   |vauthors=Gullapalli A, Wolfe BL, Griffin CT, etal |title=An Essential Role for SNX1 in Lysosomal Sorting of Protease-activated Receptor-1: Evidence for Retromer-, Hrs-, and Tsg101-independent Functions of Sorting Nexins |journal=Mol. Biol. Cell |volume=17 |issue= 3 |pages= 1228–38 |year= 2006 |pmid= 16407403 |doi= 10.1091/mbc.E05-09-0899 | pmc=1382312 }}
*{{cite journal | author=Gerhard DS, Wagner L, Feingold EA, ''et al.'' |title=The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). |journal=Genome Res. |volume=14 |issue= 10B |pages= 2121-7 |year= 2004 |pmid= 15489334 |doi= 10.1101/gr.2596504 }}
*{{cite journal  | vauthors=Shi H, Rojas R, Bonifacino JS, Hurley JH |title=The retromer subunit Vps26 has an arrestin fold and binds Vps35 through its C-terminal domain |journal=Nat. Struct. Mol. Biol. |volume=13 |issue= 6 |pages= 540–8 |year= 2006 |pmid= 16732284 |doi= 10.1038/nsmb1103 | pmc=1584284 }}
*{{cite journal | author=Kerr MC, Bennetts JS, Simpson F, ''et al.'' |title=A novel mammalian retromer component, Vps26B. |journal=Traffic |volume=6 |issue= 11 |pages= 991-1001 |year= 2006 |pmid= 16190980 |doi= 10.1111/j.1600-0854.2005.00328.x }}
*{{cite journal   |vauthors=Riemenschneider M, Schoepfer-Wendels A, Friedrich P, etal |title=No association of vacuolar protein sorting 26 polymorphisms with Alzheimer's disease |journal=Neurobiol. Aging |volume=28 |issue= 6 |pages= 883–4 |year= 2007 |pmid= 16784798 |doi= 10.1016/j.neurobiolaging.2006.05.009 }}
*{{cite journal | author=Small SA, Kent K, Pierce A, ''et al.'' |title=Model-guided microarray implicates the retromer complex in Alzheimer's disease. |journal=Ann. Neurol. |volume=58 |issue= 6 |pages= 909-19 |year= 2006 |pmid= 16315276 |doi= 10.1002/ana.20667 }}
*{{cite journal  | vauthors=Rojas R, Kametaka S, Haft CR, Bonifacino JS |title=Interchangeable but Essential Functions of SNX1 and SNX2 in the Association of Retromer with Endosomes and the Trafficking of Mannose 6-Phosphate Receptors |journal=Mol. Cell. Biol. |volume=27 |issue= 3 |pages= 1112–24 |year= 2007 |pmid= 17101778 |doi= 10.1128/MCB.00156-06 | pmc=1800681 }}
*{{cite journal | author=Gullapalli A, Wolfe BL, Griffin CT, ''et al.'' |title=An essential role for SNX1 in lysosomal sorting of protease-activated receptor-1: evidence for retromer-, Hrs-, and Tsg101-independent functions of sorting nexins. |journal=Mol. Biol. Cell |volume=17 |issue= 3 |pages= 1228-38 |year= 2006 |pmid= 16407403 |doi= 10.1091/mbc.E05-09-0899 }}
*{{cite journal  | author=Shi H, Rojas R, Bonifacino JS, Hurley JH |title=The retromer subunit Vps26 has an arrestin fold and binds Vps35 through its C-terminal domain. |journal=Nat. Struct. Mol. Biol. |volume=13 |issue= 6 |pages= 540-8 |year= 2006 |pmid= 16732284 |doi= 10.1038/nsmb1103 }}
*{{cite journal | author=Riemenschneider M, Schoepfer-Wendels A, Friedrich P, ''et al.'' |title=No association of vacuolar protein sorting 26 polymorphisms with Alzheimer's disease. |journal=Neurobiol. Aging |volume=28 |issue= 6 |pages= 883-4 |year= 2007 |pmid= 16784798 |doi= 10.1016/j.neurobiolaging.2006.05.009 }}
*{{cite journal  | author=Rojas R, Kametaka S, Haft CR, Bonifacino JS |title=Interchangeable but essential functions of SNX1 and SNX2 in the association of retromer with endosomes and the trafficking of mannose 6-phosphate receptors. |journal=Mol. Cell. Biol. |volume=27 |issue= 3 |pages= 1112-24 |year= 2007 |pmid= 17101778 |doi= 10.1128/MCB.00156-06 }}
}}
{{refend}}
{{refend}}
 
{{PDB Gallery|geneid=9559}}
{{protein-stub}}
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Latest revision as of 12:15, 5 August 2018

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Identifiers
Aliases
External IDsGeneCards: [1]
Orthologs
SpeciesHumanMouse
Entrez

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Ensembl

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UniProt

n/a

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RefSeq (mRNA)

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RefSeq (protein)

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Location (UCSC)n/an/a
PubMed searchn/an/a
Wikidata
View/Edit Human

Vacuolar protein sorting-associated protein 26A is a protein that in humans is encoded by the VPS26A gene.[1][2][3]

This gene belongs to a group of vacuolar protein sorting (VPS) genes. The encoded protein is a component of a large multimeric complex, termed the retromer complex, involved in retrograde transport of proteins from endosomes to the trans-Golgi network. The close structural similarity between the yeast and human proteins that make up this complex suggests a similarity in function. Expression studies in yeast and mammalian cells indicate that this protein interacts directly with VPS35, which serves as the core of the retromer complex. Alternative splicing results in multiple transcript variants encoding different isoforms.[3]

Structure

File:Structural comparison of Vps26 with Arrestins.png
Structural comparison of Vps26 with arrestins

Vps26 is a 38-kDa subunit that has a two-lobed structure with a polar core that resembles the arrestin family of trafficking adaptor.[4][5] This fold consist of two related β-sandwich subdomains with a fibronectin type III domain topology. The two domains are joined together by a flexible linker and are closely associated by an unusual polar core. Arrestins are regulatory proteins known for connecting G-protein coupled receptors (GPCRs) to clathrin during endocytosis. They play many critical roles in cell signalling and membrane trafficking.[6] Both Vps26 and arrestins are composed of two structurally related β-sheet domains forming extensive interfaces with each other, using polar and electrostatic contacts to create interdomain interactions for ligand binding. However, there are significant structural differences between both Vps26 and arrestins. Vps26 protein has extended C-terminal tails that do not contain identifiable clathrin- or AP2-binding sequences, and therefore cannot form stable intramolecular contacts with clathrin and AP2, which has been observed for arrestins. Moreover, Vps26 does not have similar sequences as arrestins for GPCR and phospholipid interactions.[7]

Vps26B paralogue

File:Structural differences between Vps26A and Vps26B.png
Structural differences between Vps26A and Vps26B

In yeast, there is only one Vps26 species, whereas there are two Vps26 paralogues (Vps26A and Vps26B) in mammals.[8]

X-ray crystallography revealed that the structures of both Vps26A and Vps26B share a similar bilobal β-sandwich structure and possess 70% sequence homology.[4] However, these two paralogues distinctly differ on the surface patch within the N-terminal domain, the apex region where the N-terminal and C-terminal domains meet and the disordered C-terminal tail. Vps26B contains several putative serine phosphorylation residues within this disordered tail, which may represent a potential mechanism to modulate the difference between Vps26A and Vps26B. A recent study conducted by Bugarcic et al. pinpointed that this disordered tail on C-terminal region of Vps26B is one of the underlying factors that contributes to the failure for Vps26B-containing Retromer to associate with CI-M6PR, ultimately leading to CI-M6PR degradation, accompanied with increased cathepsin D secretion.[9]

References

  1. ↑ Lee JJ, Radice G, Perkins CP, Costantini F (Aug 1992). "Identification and characterization of a novel, evolutionarily conserved gene disrupted by the murine H beta 58 embryonic lethal transgene insertion". Development. 115 (1): 277–88. PMID 1638986.
  2. ↑ Mao M, Fu G, Wu JS, Zhang QH, Zhou J, Kan LX, Huang QH, He KL, Gu BW, Han ZG, Shen Y, Gu J, Yu YP, Xu SH, Wang YX, Chen SJ, Chen Z (Aug 1998). "Identification of genes expressed in human CD34+ hematopoietic stem/progenitor cells by expressed sequence tags and efficient full-length cDNA cloning". Proc Natl Acad Sci U S A. 95 (14): 8175–80. doi:10.1073/pnas.95.14.8175. PMC 20949. PMID 9653160.
  3. ↑ 3.0 3.1 "Entrez Gene: VPS26A vacuolar protein sorting 26 homolog A (S. pombe)".
  4. ↑ 4.0 4.1 Collins BM, Norwood SJ, Kerr MC, Mahony D, Seaman MN, Teasdale RD, Owen DJ (March 2008). "Structure of Vps26B and mapping of its interaction with the retromer protein complex". Traffic. 9 (3): 366–79. doi:10.1111/j.1600-0854.2007.00688.x. PMID 18088321.
  5. ↑ Shi H, Rojas R, Bonifacino JS, Hurley JH (June 2006). "The retromer subunit Vps26 has an arrestin fold and binds Vps35 through its C-terminal domain". Nat. Struct. Mol. Biol. 13 (6): 540–8. doi:10.1038/nsmb1103. PMC 1584284. PMID 16732284.
  6. ↑ Gurevich VV, Gurevich EV (June 2006). "The structural basis of arrestin-mediated regulation of G-protein-coupled receptors". Pharmacol. Ther. 110 (3): 465–502. doi:10.1016/j.pharmthera.2005.09.008. PMC 2562282. PMID 16460808.
  7. ↑ Collins BM (November 2008). "The structure and function of the retromer protein complex". Traffic. 9 (11): 1811–22. doi:10.1111/j.1600-0854.2008.00777.x. PMID 18541005.
  8. ↑ Kerr MC, Bennetts JS, Simpson F, Thomas EC, Flegg C, Gleeson PA, Wicking C, Teasdale RD (November 2005). "A novel mammalian retromer component, Vps26B". Traffic. 6 (11): 991–1001. doi:10.1111/j.1600-0854.2005.00328.x. PMID 16190980.
  9. ↑ Bugarcic A, Zhe Y, Kerr MC, Griffin J, Collins BM, Teasdale RD (December 2011). "Vps26A and Vps26B subunits define distinct retromer complexes". Traffic. 12 (12): 1759–73. doi:10.1111/j.1600-0854.2011.01284.x. PMID 21920005.

Further reading

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