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| - | {{STRUCTURE_3d87|  PDB=3d87  |  SCENE=  }}  |  | 
| - | ===Crystal structure of Interleukin-23=== |  | 
| - | {{ABSTRACT_PUBMED_18708069}} |  | 
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| - | ==Disease== | + | ==Crystal structure of Interleukin-23== | 
| - | [[http://www.uniprot.org/uniprot/IL12B_HUMAN IL12B_HUMAN]]Defects in IL12B are acause of Mendelian susceptibility to mycobacterial disease (MSMD) [MIM:[http://omim.org/entry/209950 209950]]; also known as familial disseminated atypical mycobacterial infection.This rare condition confers predisposition to illness caused by moderately virulent mycobacterial species,such as Bacillus Calmette-Guerin (BCG) vaccine and environmental non-tuberculous mycobacteria,and by the more virulent Mycobacterium tuberculosis.Other microorganisms rarely cause severe clinical disease in individuals with susceptibility to mycobacterial infections,with the exception of Salmonella which infects less than 50% of these individuals.The pathogenic mechanism underlying MSMD is the impairment of interferon-gamma mediated immunity,whose severity determines the clinical outcome.Some patients die of overwhelming mycobacterial disease withlepromatous-like lesions in early childhood, whereas others develop,later inlife, disseminated but curable infections withtuberculoid granulomas.MSMD is agenetically heterogeneous disease with autosomal recessive,autosomal dominant or X-linked inheritance.<ref>PMID:9854038</ref><ref>PMID:11753820</ref> Genetic variations in IL12B are a cause of susceptibility topsoriasis type 11 (PSORS11) [MIM:[http://omim.org/entry/612599 612599]].Psoriasis is acommon, chronic inflammatorydisease of theskin withmultifactorial etiology.It is characterized by red,scaly plaques usually found on thescalp,elbows andknees.These lesions arecaused by abnormal keratinocyte proliferation and infiltration ofinflammatory cells into thedermis andepidermis.<ref>PMID:9854038</ref><ref>PMID:11753820</ref>  | + | <StructureSection load='3d87' size='340' side='right'caption='[[3d87]], [[Resolution|resolution]] 2.90Å' scene=''> | 
|  | + | == Structural highlights == | 
|  | + | <table><tr><td colspan='2'>[[3d87]] is a 4 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=3D87 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=3D87 FirstGlance]. <br> | 
|  | + | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.9Å</td></tr> | 
|  | + | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=K:POTASSIUM+ION'>K</scene>, <scene name='pdbligand=MAN:ALPHA-D-MANNOSE'>MAN</scene>, <scene name='pdbligand=PO4:PHOSPHATE+ION'>PO4</scene></td></tr> | 
|  | + | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=3d87 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=3d87 OCA], [https://pdbe.org/3d87 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=3d87 RCSB], [https://www.ebi.ac.uk/pdbsum/3d87 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=3d87 ProSAT]</span></td></tr> | 
|  | + | </table> | 
|  | + | == Function == | 
|  | + | [https://www.uniprot.org/uniprot/IL23A_HUMAN IL23A_HUMAN] Associates with IL12B to form the IL-23 interleukin, a heterodimeric cytokine which functions in innate and adaptive immunity. IL-23 may constitute with IL-17 an acute response to infection in peripheral tissues. IL-23 binds to a heterodimeric receptor complex composed of IL12RB1 and IL23R, activates the Jak-Stat signaling cascade, stimulates memory rather than naive T-cells and promotes production of proinflammatory cytokines. IL-23 induces autoimmune inflammation and thus may be responsible for autoimmune inflammatory diseases and may be important for tumorigenesis.<ref>PMID:11114383</ref> <ref>PMID:12023369</ref> <ref>PMID:16424222</ref>  | 
|  | + | == Evolutionary Conservation == | 
|  | + | [[Image:Consurf_key_small.gif|200px|right]] | 
|  | + | Check<jmol> | 
|  | + |   <jmolCheckbox> | 
|  | + |     <scriptWhenChecked>; select protein; define ~consurf_to_do selected; consurf_initial_scene = true; script "/wiki/ConSurf/d8/3d87_consurf.spt"</scriptWhenChecked> | 
|  | + |     <scriptWhenUnchecked>script /wiki/extensions/Proteopedia/spt/initialview01.spt</scriptWhenUnchecked> | 
|  | + |     <text>to colour the structure by Evolutionary Conservation</text> | 
|  | + |   </jmolCheckbox> | 
|  | + | </jmol>, as determined by [http://consurfdb.tau.ac.il/ ConSurfDB]. You may read the [[Conservation%2C_Evolutionary|explanation]] of the method and the full data available from [http://bental.tau.ac.il/new_ConSurfDB/main_output.php?pdb_ID=3d87 ConSurf]. | 
|  | + | <div style="clear:both"></div> | 
|  | + | <div style="background-color:#fffaf0;"> | 
|  | + | == Publication Abstract from PubMed == | 
|  | + | Interleukin (IL)-23 is a pro-inflammatory cytokine playing a key role in the pathogenesis of several autoimmune and inflammatory diseases. We have determined the crystal structures of the heterodimeric p19-p40 IL-23 and its complex with the Fab (antigen-binding fragment) of a neutralizing antibody at 2.9 and 1.9 A, respectively. The IL-23 structure closely resembles that of IL-12. They share the common p40 subunit, and IL-23 p19 overlaps well with IL-12 p35. Along the hydrophilic heterodimeric interface, fewer charged residues are involved for IL-23 compared with IL-12. The binding site of the Fab is located exclusively on the p19 subunit, and comparison with published cytokine-receptor structures suggests that it overlaps with the IL-23 receptor binding site. | 
|  |  |  |  | 
| - | ==Function==
 | + | Crystal structures of the pro-inflammatory cytokine interleukin-23 and its complex with a high-affinity neutralizing antibody.,Beyer BM, Ingram R, Ramanathan L, Reichert P, Le HV, Madison V, Orth P J Mol Biol. 2008 Oct 17;382(4):942-55. Epub 2008 Aug 7. PMID:18708069<ref>PMID:18708069</ref> | 
| - | [[http://www.uniprot.org/uniprot/IL23A_HUMAN IL23A_HUMAN]] Associates with IL12B to form theIL-23 interleukin, a heterodimeric cytokine which functions in innate and adaptive immunity. IL-23may constitute withIL-17 an acute response to infection in peripheral tissues.IL-23 binds to a heterodimeric receptor complex composed of IL12RB1 and IL23R,activates the Jak-Stat signaling cascade,stimulates memory rather than naive T-cells and promotes production of proinflammatory cytokines. IL-23 induces autoimmune inflammation and thus may be responsible for autoimmune inflammatory diseases and may be important for tumorigenesis.<ref>PMID:11114383</ref><ref>PMID:12023369</ref><ref>PMID:16424222</ref> [[http://www.uniprot.org/uniprot/IL12B_HUMAN IL12B_HUMAN]] Cytokine that can act as a growth factor for activated T and NK cells,enhance the lytic activity of NK/lymphokine-activated killer cells,and stimulate the production of IFN-gamma by resting PBMC.<ref>PMID:11114383</ref>  Associates with IL23A to form the IL-23 interleukin,a heterodimeric cytokine which functions in innate and adaptive immunity. IL-23 may constitute with IL-17 an acute response to infection in peripheral tissues. IL-23 binds to a heterodimeric receptor complex composed of IL12RB1 and IL23R,activates the Jak-Stat signaling cascade,stimulates memory rather than naive T-cells and promotes production of proinflammatory cytokines.IL-23 induces autoimmune inflammation and thus may be responsible for autoimmune inflammatory diseases and may be important for tumorigenesis.<ref>PMID:11114383</ref>
 | + |  | 
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| - | ==About this Structure==
 | + | From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br> | 
| - | [[3d87]] is a4 chain structure with sequence from [http://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens].Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=3D87 OCA]. 
 | + | </div> | 
|  | + | <div class="pdbe-citations 3d87" style="background-color:#fffaf0;"></div> | 
|  |  |  |  | 
|  | ==See Also== |  | ==See Also== | 
| - | *[[Interleukin|Interleukin]] | + | *[[Interleukin 3D structures|Interleukin 3D structures]] | 
| - |   | + | == References == | 
| - | ==Reference== | + | <references/> | 
| - | <ref group="xtra">PMID:018708069</ref><referencesgroup="xtra"/><references/>
 | + | __TOC__ | 
|  | + | </StructureSection> | 
|  | [[Category: Homo sapiens]] |  | [[Category: Homo sapiens]] | 
| - | [[Category: Beyer, B M.]] | + | [[Category: Large Structures]] | 
| - | [[Category: Ingram, R.]] | + | [[Category: Beyer BM]] | 
| - | [[Category: Le, H.]] | + | [[Category: Ingram R]] | 
| - | [[Category: Madison, V.]] | + | [[Category: Le H]] | 
| - | [[Category: Ramanathan, L.]] | + | [[Category: Madison V]] | 
| - | [[Category: Reichert, P.]] | + | [[Category: Ramanathan L]] | 
| - | [[Category: Cytokine]]
 | + | [[Category: Reichert P]] | 
| - | [[Category: Fab]]
 | + |  | 
| - | [[Category: Interleukin-23]]
 | + |  | 
|  |   Structural highlights   Function IL23A_HUMAN Associates with IL12B to form the IL-23 interleukin, a heterodimeric cytokine which functions in innate and adaptive immunity. IL-23 may constitute with IL-17 an acute response to infection in peripheral tissues. IL-23 binds to a heterodimeric receptor complex composed of IL12RB1 and IL23R, activates the Jak-Stat signaling cascade, stimulates memory rather than naive T-cells and promotes production of proinflammatory cytokines. IL-23 induces autoimmune inflammation and thus may be responsible for autoimmune inflammatory diseases and may be important for tumorigenesis.[1] [2] [3] 
   Evolutionary Conservation Check, as determined by ConSurfDB. You may read the explanation of the method and the full data available from ConSurf.
 
  Publication Abstract from PubMed Interleukin (IL)-23 is a pro-inflammatory cytokine playing a key role in the pathogenesis of several autoimmune and inflammatory diseases. We have determined the crystal structures of the heterodimeric p19-p40 IL-23 and its complex with the Fab (antigen-binding fragment) of a neutralizing antibody at 2.9 and 1.9 A, respectively. The IL-23 structure closely resembles that of IL-12. They share the common p40 subunit, and IL-23 p19 overlaps well with IL-12 p35. Along the hydrophilic heterodimeric interface, fewer charged residues are involved for IL-23 compared with IL-12. The binding site of the Fab is located exclusively on the p19 subunit, and comparison with published cytokine-receptor structures suggests that it overlaps with the IL-23 receptor binding site.
 Crystal structures of the pro-inflammatory cytokine interleukin-23 and its complex with a high-affinity neutralizing antibody.,Beyer BM, Ingram R, Ramanathan L, Reichert P, Le HV, Madison V, Orth P J Mol Biol. 2008 Oct 17;382(4):942-55. Epub 2008 Aug 7. PMID:18708069[4]
 From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.
  See Also  References ↑ Oppmann B, Lesley R, Blom B, Timans JC, Xu Y, Hunte B, Vega F, Yu N, Wang J, Singh K, Zonin F, Vaisberg E, Churakova T, Liu M, Gorman D, Wagner J, Zurawski S, Liu Y, Abrams JS, Moore KW, Rennick D, de Waal-Malefyt R, Hannum C, Bazan JF, Kastelein RA. Novel p19 protein engages IL-12p40 to form a cytokine, IL-23, with biological activities similar as well as distinct from IL-12. Immunity. 2000 Nov;13(5):715-25. PMID:11114383 ↑ Parham C, Chirica M, Timans J, Vaisberg E, Travis M, Cheung J, Pflanz S, Zhang R, Singh KP, Vega F, To W, Wagner J, O'Farrell AM, McClanahan T, Zurawski S, Hannum C, Gorman D, Rennick DM, Kastelein RA, de Waal Malefyt R, Moore KW. A receptor for the heterodimeric cytokine IL-23 is composed of IL-12Rbeta1 and a  novel cytokine receptor subunit, IL-23R. J Immunol. 2002 Jun 1;168(11):5699-708. PMID:12023369 ↑ Piskin G, Sylva-Steenland RM, Bos JD, Teunissen MB. In vitro and in situ expression of IL-23 by keratinocytes in healthy skin and psoriasis lesions: enhanced expression in psoriatic skin. J Immunol. 2006 Feb 1;176(3):1908-15. PMID:16424222 ↑ Beyer BM, Ingram R, Ramanathan L, Reichert P, Le HV, Madison V, Orth P. Crystal structures of the pro-inflammatory cytokine interleukin-23 and its complex with a high-affinity neutralizing antibody. J Mol Biol. 2008 Oct 17;382(4):942-55. Epub 2008 Aug 7. PMID:18708069 doi:10.1016/j.jmb.2008.08.001
 
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