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3FPU

The crystallographic structure of the Complex between Evasin-1 and CCL3

Summary for 3FPU
Entry DOI10.2210/pdb3fpu/pdb
Related3fpr 3fpt
DescriptorEvasin-1, C-C motif chemokine 3, NICKEL (II) ION, ... (4 entities in total)
Functional Keywordsprotein:protein complex, chemokine, glycoprotein, secreted, chemotaxis, cytokine, inflammatory response, immune system
Biological sourceRhipicephalus sanguineus (Brown dog tick)
More
Cellular locationSecreted (Probable): P0C8E7
Secreted: P10147
Total number of polymer chains2
Total formula weight19307.64
Authors
Shaw, J.P.,Dias, J.M. (deposition date: 2009-01-06, release date: 2010-01-12, Last modification date: 2023-11-01)
Primary citationDias, J.M.,Losberger, C.,Deruaz, M.,Power, C.A.,Proudfoot, A.E.I.,Shaw, J.P.
Structural basis of chemokine sequestration by a tick chemokine binding protein: the crystal structure of the complex between Evasin-1 and CCL3
Plos One, 4:-, 2009
Cited by
PubMed Abstract: Chemokines are a subset of cytokines responsible for controlling the cellular migration of inflammatory cells through interaction with seven transmembrane G protein-coupled receptors. The blocking of a chemokine-receptor interaction results in a reduced inflammatory response, and represents a possible anti-inflammatory strategy, a strategy that is already employed by some virus and parasites. Anti-chemokine activity has been described in the extracts of tick salivary glands, and we have recently described the cloning and characterization of such chemokine binding proteins from the salivary glands, which we have named Evasins.
PubMed: 20041127
DOI: 10.1371/journal.pone.0008514
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (1.76 Å)
Structure validation

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数据于2024-10-30公开中

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