PDBsum entry 2ice

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protein ligands metals Protein-protein interface(s) links
Immune system PDB id
Protein chains
642 a.a. *
183 a.a. *
296 a.a. *
119 a.a. *
_CA ×2
* Residue conservation analysis
PDB id:
Name: Immune system
Title: Crig bound to c3c
Structure: Complement c3 beta chain. Chain: a, d. Complement c3 alpha chain. Chain: b, e. Complement c3 alpha chain. Chain: c, f. V-set and immunoglobulin domain-containing protei chain: s, t. Synonym: protein z39ig.
Source: Homo sapiens. Human. Organism_taxid: 9606. Gene: vsig4. Expressed in: escherichia coli. Expression_system_taxid: 562
Biol. unit: Tetramer (from PQS)
3.10Å     R-factor:   0.239     R-free:   0.295
Authors: C.Wiesmann
Key ref:
C.Wiesmann et al. (2006). Structure of C3b in complex with CRIg gives insights into regulation of complement activation. Nature, 444, 217-220. PubMed id: 17051150 DOI: 10.1038/nature05263
12-Sep-06     Release date:   07-Nov-06    
Go to PROCHECK summary

Protein chains
Pfam   ArchSchema ?
P01024  (CO3_HUMAN) -  Complement C3
1663 a.a.
642 a.a.*
Protein chains
Pfam   ArchSchema ?
P01024  (CO3_HUMAN) -  Complement C3
1663 a.a.
183 a.a.
Protein chains
Pfam   ArchSchema ?
P01024  (CO3_HUMAN) -  Complement C3
1663 a.a.
296 a.a.
Protein chains
Pfam   ArchSchema ?
Q9Y279  (VSIG4_HUMAN) -  V-set and immunoglobulin domain-containing protein 4
399 a.a.
119 a.a.
Key:    PfamA domain  PfamB domain  Secondary structure  CATH domain
* PDB and UniProt seqs differ at 1 residue position (black cross)

 Gene Ontology (GO) functional annotation 
  GO annot!
  Cellular component     extracellular region   1 term 
  Biochemical function     endopeptidase inhibitor activity     1 term  


DOI no: 10.1038/nature05263 Nature 444:217-220 (2006)
PubMed id: 17051150  
Structure of C3b in complex with CRIg gives insights into regulation of complement activation.
C.Wiesmann, K.J.Katschke, J.Yin, K.Y.Helmy, M.Steffek, W.J.Fairbrother, S.A.McCallum, L.Embuscado, L.DeForge, P.E.Hass, M.van Lookeren Campagne.
The complement system is a key part of the innate immune system, and is required for clearance of pathogens from the bloodstream. After exposure to pathogens, the third component of the complement system, C3, is cleaved to C3b which, after recruitment of factor B, initiates formation of the alternative pathway convertases. CRIg, a complement receptor expressed on macrophages, binds to C3b and iC3b mediating phagocytosis of the particles, but it is unknown how CRIg selectively recognizes proteolytic C3-fragments and whether binding of CRIg to C3b inhibits convertase activation. Here we present the crystal structure of C3b in complex with CRIg and, using CRIg mutants, provide evidence that CRIg acts as an inhibitor of the alternative pathway of complement. The structure shows that activation of C3 induces major structural rearrangements, including a dramatic movement (>80 A) of the thioester-bond-containing domain through which C3b attaches to pathogen surfaces. We show that CRIg is not only a phagocytic receptor, but also a potent inhibitor of the alternative pathway convertases. The structure provides insights into the complex macromolecular structural rearrangements that occur during complement activation and inhibition. Moreover, our structure-function studies relating the structural basis of complement activation and the means by which CRIg inhibits the convertases provide important clues to the development of therapeutics that target complement.
  Selected figure(s)  
Figure 1.
Figure 1: Domain architecture and structure of C3 and the C3b/C3c:CRIg complexes. a, Domain organization of C3; the -chain is depicted in green, the -chain in cyan (ANA domain), orange, (CUB), blue (TED) and violet. The red sphere indicates the thioester. b, Ribbon diagrams of native C3; (left; ref. 8), C3b in complex with CRIg (centre) and C3c in complex with CRIg (right). The surface of CRIg is shown in yellow. Note the movement of the CUB and TED domain when comparing C3 and C3b:CRIg. c, Schematic depiction of b from a slightly different orientation; the hexagon and triangle represent His 1104 and the residues that form the thioesterbond in C3, respectively.
Figure 2.
Figure 2: CRIg binds to the beta--chain of C3b and C3c and inhibits the AP C3 and C5 convertases. a, Complex between C3c (surface representation) and CRIg (ribbon diagram). b, Surface representation of CRIg, rotated 180° from a. All atoms that are close to C3c/C3b are coloured like the residues they are contacting in a. c, CRIg (filled symbols) but not control protein (open symbols) reduces formation of C3a des Arg formed on cleavage of C3 to C3a and C3b. d, CRIg (filled symbols) but not control protein (open symbols) inhibits generation of C5b, 6 formed on cleavage of C5 to C5a nd C5b. Data are representative of three independent experiments.
  The above figures are reprinted by permission from Macmillan Publishers Ltd: Nature (2006, 444, 217-220) copyright 2006.  
  Figures were selected by an automated process.  

Literature references that cite this PDB file's key reference

  PubMed id Reference
21317894 H.P.Morgan, C.Q.Schmidt, M.Guariento, B.S.Blaum, D.Gillespie, A.P.Herbert, D.Kavanagh, H.D.Mertens, D.I.Svergun, C.M.Johansson, D.Uhrín, P.N.Barlow, and J.P.Hannan (2011).
Structural basis for engagement by complement factor H of C3b on a self surface.
  Nat Struct Mol Biol, 18, 463-470.
PDB code: 3oxu
19691988 J.Chen, J.C.Crispín, J.Dalle Lucca, and G.C.Tsokos (2011).
A novel inhibitor of the alternative pathway of complement attenuates intestinal ischemia/reperfusion-induced injury.
  J Surg Res, 167, e131-e136.  
21217642 N.S.Laursen, K.R.Andersen, I.Braren, E.Spillner, L.Sottrup-Jensen, and G.R.Andersen (2011).
Substrate recognition by complement convertases revealed in the C5-cobra venom factor complex.
  EMBO J, 30, 606-616.
PDB codes: 3prx 3pvm
20467445 D.Serruto, R.Rappuoli, M.Scarselli, P.Gros, and J.A.van Strijp (2010).
Molecular mechanisms of complement evasion: learning from staphylococci and meningococci.
  Nat Rev Microbiol, 8, 393-399.  
19960015 E.Wagner, and M.M.Frank (2010).
Therapeutic potential of complement modulation.
  Nat Rev Drug Discov, 9, 43-56.  
21205667 F.Forneris, D.Ricklin, J.Wu, A.Tzekou, R.S.Wallace, J.D.Lambris, and P.Gros (2010).
Structures of C3b in complex with factors B and D give insight into complement convertase formation.
  Science, 330, 1816-1820.
PDB codes: 2xw9 2xwa 2xwb 2xwj
20876141 H.Chen, D.Ricklin, M.Hammel, B.L.Garcia, W.J.McWhorter, G.Sfyroera, Y.Q.Wu, A.Tzekou, S.Li, B.V.Geisbrecht, V.L.Woods, and J.D.Lambris (2010).
Allosteric inhibition of complement function by a staphylococcal immune evasion protein.
  Proc Natl Acad Sci U S A, 107, 17621-17626.  
20545943 J.Bestebroer, P.C.Aerts, S.H.Rooijakkers, M.K.Pandey, J.Köhl, J.A.van Strijp, and Haas (2010).
Functional basis for complement evasion by staphylococcal superantigen-like 7.
  Cell Microbiol, 12, 1506-1516.  
20666732 K.Li, J.Gor, and S.J.Perkins (2010).
Self-association and domain rearrangements between complement C3 and C3u provide insight into the activation mechanism of C3.
  Biochem J, 431, 63-72.  
20133685 N.S.Laursen, N.Gordon, S.Hermans, N.Lorenz, N.Jackson, B.Wines, E.Spillner, J.B.Christensen, M.Jensen, F.Fredslund, M.Bjerre, L.Sottrup-Jensen, J.D.Fraser, and G.R.Andersen (2010).
Structural basis for inhibition of complement C5 by the SSL7 protein from Staphylococcus aureus.
  Proc Natl Acad Sci U S A, 107, 3681-3686.
PDB codes: 3kls 3km9
20053731 P.K.Mallik, K.Nishikawa, A.J.Millis, and H.Shi (2010).
Commandeering a biological pathway using aptamer-derived molecular adaptors.
  Nucleic Acids Res, 38, e93.  
20826443 R.H.Baxter, S.Steinert, Y.Chelliah, G.Volohonsky, E.A.Levashina, and J.Deisenhofer (2010).
A heterodimeric complex of the LRR proteins LRIM1 and APL1C regulates complement-like immunity in Anopheles gambiae.
  Proc Natl Acad Sci U S A, 107, 16817-16822.
PDB codes: 3o53 3o6n 3oja
20852386 R.Martínez-Barricarte, M.Heurich, F.Valdes-Cañedo, E.Vazquez-Martul, E.Torreira, T.Montes, A.Tortajada, S.Pinto, M.Lopez-Trascasa, B.P.Morgan, O.Llorca, C.L.Harris, and S.Rodríguez de Córdoba (2010).
Human C3 mutation reveals a mechanism of dense deposit disease pathogenesis and provides insights into complement activation and regulation.
  J Clin Invest, 120, 3702-3712.  
20033014 B.Borrell (2009).
Fraud rocks protein community.
  Nature, 462, 970.  
19574954 B.J.Janssen, L.Gomes, R.I.Koning, D.I.Svergun, A.J.Koster, D.C.Fritzinger, C.W.Vogel, and P.Gros (2009).
Insights into complement convertase formation based on the structure of the factor B-cobra venom factor complex.
  EMBO J, 28, 2469-2478.
PDB codes: 3hrz 3hs0
19833734 B.Li, H.Xi, L.Diehl, W.P.Lee, L.Sturgeon, J.Chinn, L.Deforge, R.F.Kelley, C.Wiesmann, M.van Lookeren Campagne, and S.S.Sidhu (2009).
Improving therapeutic efficacy of a complement receptor by structure-based affinity maturation.
  J Biol Chem, 284, 35605-35611.  
19136636 E.Torreira, A.Tortajada, T.Montes, Córdoba, and O.Llorca (2009).
3D structure of the C3bB complex provides insights into the activation and regulation of the complement alternative pathway convertase.
  Proc Natl Acad Sci U S A, 106, 882-887.  
19800693 H.Qu, D.Ricklin, and J.D.Lambris (2009).
Recent developments in low molecular weight complement inhibitors.
  Mol Immunol, 47, 185-195.  
19503104 J.Wu, Y.Q.Wu, D.Ricklin, B.J.Janssen, J.D.Lambris, and P.Gros (2009).
Structure of complement fragment C3b-factor H and implications for host protection by complement regulators.
  Nat Immunol, 10, 728-733.
PDB code: 2wii
19196712 K.J.Katschke, S.Stawicki, J.Yin, M.Steffek, H.Xi, L.Sturgeon, P.E.Hass, K.M.Loyet, L.Deforge, Y.Wu, M.van Lookeren Campagne, and C.Wiesmann (2009).
Structural and Functional Analysis of a C3b-specific Antibody That Selectively Inhibits the Alternative Pathway of Complement.
  J Biol Chem, 284, 10473-10479.
PDB code: 3g6j
19362461 K.Murata, and W.M.Baldwin (2009).
Mechanisms of complement activation, C4d deposition, and their contribution to the pathogenesis of antibody-mediated rejection.
  Transplant Rev (Orlando), 23, 139-150.  
19503103 S.H.Rooijakkers, J.Wu, M.Ruyken, R.van Domselaar, K.L.Planken, A.Tzekou, D.Ricklin, J.D.Lambris, B.J.Janssen, J.A.van Strijp, and P.Gros (2009).
Structural and functional implications of the alternative complement pathway C3 convertase stabilized by a staphylococcal inhibitor.
  Nat Immunol, 10, 721-727.
PDB code: 2win
19368894 V.Krishnan, K.Ponnuraj, Y.Xu, K.Macon, J.E.Volanakis, and S.V.Narayana (2009).
The crystal structure of cobra venom factor, a cofactor for C3- and C5-convertase CVFBb.
  Structure, 17, 611-619.
PDB code: 3frp
18657508 D.Hatherley, S.C.Graham, J.Turner, K.Harlos, D.I.Stuart, and A.N.Barclay (2008).
Paired receptor specificity explained by structures of signal regulatory proteins alone and complexed with CD47.
  Mol Cell, 31, 266-277.
PDB codes: 2jjs 2jjt 2jju 2jjv 2jjw 2vsc
18615115 D.M.Appledorn, A.McBride, S.Seregin, J.M.Scott, N.Schuldt, A.Kiang, S.Godbehere, and A.Amalfitano (2008).
Complex interactions with several arms of the complement system dictate innate and humoral immunity to adenoviral vectors.
  Gene Ther, 15, 1606-1617.  
  19025129 D.Ricklin, and J.D.Lambris (2008).
Compstatin: a complement inhibitor on its way to clinical application.
  Adv Exp Med Biol, 632, 273-292.  
18536718 F.Fredslund, N.S.Laursen, P.Roversi, L.Jenner, C.L.Oliveira, J.S.Pedersen, M.A.Nunn, S.M.Lea, R.Discipio, L.Sottrup-Jensen, and G.R.Andersen (2008).
Structure of and influence of a tick complement inhibitor on human complement component 5.
  Nat Immunol, 9, 753-760.
PDB code: 3cu7
18252712 H.G.Hocking, A.P.Herbert, D.Kavanagh, D.C.Soares, V.P.Ferreira, M.K.Pangburn, D.Uhrín, and P.N.Barlow (2008).
Structure of the N-terminal region of complement factor H and conformational implications of disease-linked sequence variations.
  J Biol Chem, 283, 9475-9487.
PDB codes: 2rlp 2rlq
18250627 K.U.Wendt, M.S.Weiss, P.Cramer, and D.W.Heinz (2008).
Structures and diseases.
  Nat Struct Mol Biol, 15, 117-120.  
18456336 M.C.Schuster, D.Ricklin, K.Papp, K.S.Molnar, S.J.Coales, Y.Hamuro, G.Sfyroera, H.Chen, M.S.Winters, and J.D.Lambris (2008).
Dynamic structural changes during complement C3 activation analyzed by hydrogen/deuterium exchange mass spectrometry.
  Mol Immunol, 45, 3142-3151.  
19388159 M.K.Pangburn, V.P.Ferreira, and C.Cortes (2008).
Discrimination between host and pathogens by the complement system.
  Vaccine, 26, I15-I21.  
18727628 M.Tanaka, T.Nagai, Y.Tsuneyoshi, N.Sunahara, T.Matsuda, T.Nakamura, S.Tsuyama, K.Hasui, O.FitzGerald, and T.Matsuyama (2008).
Expansion of a unique macrophage subset in rheumatoid arthritis synovial lining layer.
  Clin Exp Immunol, 154, 38-47.  
18064050 P.Gros, F.J.Milder, and B.J.Janssen (2008).
Complement driven by conformational changes.
  Nat Rev Immunol, 8, 48-58.  
17467263 A.DeWan, M.B.Bracken, and J.Hoh (2007).
Two genetic pathways for age-related macular degeneration.
  Curr Opin Genet Dev, 17, 228-233.  
17684013 B.J.Janssen, E.F.Halff, J.D.Lambris, and P.Gros (2007).
Structure of compstatin in complex with complement component C3c reveals a new mechanism of complement inhibition.
  J Biol Chem, 282, 29241-29247.
PDB code: 2qki
17687277 B.J.Janssen, R.J.Read, A.T.Brünger, and P.Gros (2007).
Crystallography: crystallographic evidence for deviating C3b structure.
  Nature, 448, E1.  
  17675493 C.Q.Nguyen, H.Kim, J.G.Cornelius, and A.B.Peck (2007).
Development of Sjogren's syndrome in nonobese diabetic-derived autoimmune-prone C57BL/6.NOD-Aec1Aec2 mice is dependent on complement component-3.
  J Immunol, 179, 2318-2329.  
17989689 D.Ricklin, and J.D.Lambris (2007).
Complement-targeted therapeutics.
  Nat Biotechnol, 25, 1265-1275.  
17310251 F.J.Milder, L.Gomes, A.Schouten, B.J.Janssen, E.G.Huizinga, R.A.Romijn, W.Hemrika, A.Roos, M.R.Daha, and P.Gros (2007).
Factor B structure provides insights into activation of the central protease of the complement system.
  Nat Struct Mol Biol, 14, 224-228.
PDB code: 2ok5
17548523 K.J.Katschke, K.Y.Helmy, M.Steffek, H.Xi, J.Yin, W.P.Lee, P.Gribling, K.H.Barck, R.A.Carano, R.E.Taylor, L.Rangell, L.Diehl, P.E.Hass, C.Wiesmann, and M.van Lookeren Campagne (2007).
A novel inhibitor of the alternative pathway of complement reverses inflammation and bone destruction in experimental arthritis.
  J Exp Med, 204, 1319-1325.
PDB code: 2pnd
17590164 M.van Lookeren Campagne, C.Wiesmann, and E.J.Brown (2007).
Macrophage complement receptors and pathogen clearance.
  Cell Microbiol, 9, 2095-2102.  
17445829 P.Roversi, O.Lissina, S.Johnson, N.Ahmat, G.C.Paesen, K.Ploss, W.Boland, M.A.Nunn, and S.M.Lea (2007).
The structure of OMCI, a novel lipocalin inhibitor of the complement system.
  J Mol Biol, 369, 784-793.
PDB codes: 2cm4 2cm9
17606907 R.H.Baxter, C.I.Chang, Y.Chelliah, S.Blandin, E.A.Levashina, and J.Deisenhofer (2007).
Structural basis for conserved complement factor-like function in the antimalarial protein TEP1.
  Proc Natl Acad Sci U S A, 104, 11615-11620.
PDB code: 2pn5
17989688 R.P.Rother, S.A.Rollins, C.F.Mojcik, R.A.Brodsky, and L.Bell (2007).
Discovery and development of the complement inhibitor eculizumab for the treatment of paroxysmal nocturnal hemoglobinuria.
  Nat Biotechnol, 25, 1256-1264.  
17051146 M.Carroll (2006).
Immunology: exposure of an executioner.
  Nature, 444, 159-160.  
17172439 N.Nishida, T.Walz, and T.A.Springer (2006).
Structural transitions of complement component C3 and its activation products.
  Proc Natl Acad Sci U S A, 103, 19737-19742.  
17687278 , (0).
  , (), 0.  
The most recent references are shown first. Citation data come partly from CiteXplore and partly from an automated harvesting procedure. Note that this is likely to be only a partial list as not all journals are covered by either method. However, we are continually building up the citation data so more and more references will be included with time. Where a reference describes a PDB structure, the PDB code is shown on the right.