7tx8
From Proteopedia
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| - | '''Unreleased structure''' | ||
| - | + | ==Long form D7 protein from Anopheles darlingi with U46619 and serotonin bound== | |
| + | <StructureSection load='7tx8' size='340' side='right'caption='[[7tx8]], [[Resolution|resolution]] 2.51Å' scene=''> | ||
| + | == Structural highlights == | ||
| + | <table><tr><td colspan='2'>[[7tx8]] is a 4 chain structure with sequence from [https://en.wikipedia.org/wiki/Anopheles_darlingi Anopheles darlingi]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=7TX8 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=7TX8 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]] 2.51Å</td></tr> | ||
| + | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=PUC:(5Z)-7-{(1R,4S,5S,6R)-6-[(1E,3S)-3-HYDROXYOCT-1-EN-1-YL]-2-OXABICYCLO[2.2.1]HEPT-5-YL}HEPT-5-ENOIC+ACID'>PUC</scene>, <scene name='pdbligand=SRO:SEROTONIN'>SRO</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=7tx8 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=7tx8 OCA], [https://pdbe.org/7tx8 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=7tx8 RCSB], [https://www.ebi.ac.uk/pdbsum/7tx8 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=7tx8 ProSAT]</span></td></tr> | ||
| + | </table> | ||
| + | == Function == | ||
| + | [https://www.uniprot.org/uniprot/D7L2_ANODA D7L2_ANODA] Modulates blood feeding of female mosquitoes on vertebrate species by binding and sequestering different mediators involved in the host response, such as biogenic amines and eicosanoids (By similarity). Binds serotonin with high affinity (PubMed:35568118). Binds tryptamine, octopamine, dopamine and noradrenaline with low affinity (PubMed:35568118). Binds leukotriene C4, leukotriene D4, leukotriene E4 and U-46619, a stable analog of thromboxane A2 (PubMed:35568118). Does not bind leukotriene B4, adrenaline, histamine and ADP (PubMed:35568118). Inhibits platelet aggregation induced by low concentrations of collagen and arachidonic acid but not by ADP or adrenaline (PubMed:35568118).[UniProtKB:Q0IF93]<ref>PMID:35568118</ref> | ||
| + | <div style="background-color:#fffaf0;"> | ||
| + | == Publication Abstract from PubMed == | ||
| + | The D7 proteins are highly expressed in the saliva of hematophagous Nematocera and bind biogenic amines and eicosanoid compounds produced by the host during blood feeding. These proteins are encoded by gene clusters expressing forms having one or two odorant-binding protein-like domains. Here we examine functional diversity within the D7 group in the genus Anopheles and make structural comparisons with D7 proteins from culicine mosquitoes in order to understand aspects of D7 functional evolution. Two domain long form (D7L) and one domain short form (D7S) proteins from anopheline and culicine mosquitoes were characterized to determine their ligand selectivity and binding pocket structures. We previously showed that a D7L protein from Anopheles stephensi, of the subgenus Cellia, could bind eicosanoids at a site in its N-terminal domain but could not bind biogenic amines in its C-terminal domain as does a D7L1 ortholog from the culicine species Aedes aegypti, raising the question of whether anopheline D7L proteins had lost their ability to bind biogenic amines. Here we find that D7L from anopheline species belonging to two other subgenera, Nyssorhynchus and Anopheles, can bind biogenic amines and have a structure much like the Ae. aegypti ortholog. The unusual D7L, D7L3, can also bind serotonin in the Cellia species An. gambiae. We also show through structural comparisons with culicine forms that the biogenic amine binding function of single domain D7S proteins in the genus Anopheles may have evolved through gene conversion of structurally similar proteins, which did not have biogenic amine binding capability. Collectively, the data indicate that D7L proteins had a biogenic amine and eicosanoid binding function in the common ancestor of anopheline and culicine mosquitoes, and that the D7S proteins may have acquired a biogenic amine binding function in anophelines through a gene conversion process. | ||
| - | + | Functional aspects of evolution in a cluster of salivary protein genes from mosquitoes.,Alvarenga PH, Dias DR, Xu X, Francischetti IMB, Gittis AG, Arp G, Garboczi DN, Ribeiro JMC, Andersen JF Insect Biochem Mol Biol. 2022 May 12;146:103785. doi: 10.1016/j.ibmb.2022.103785. PMID:35568118<ref>PMID:35568118</ref> | |
| - | + | From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.<br> | |
| - | [[Category: | + | </div> |
| - | [[Category: | + | <div class="pdbe-citations 7tx8" style="background-color:#fffaf0;"></div> |
| - | [[Category: | + | == References == |
| + | <references/> | ||
| + | __TOC__ | ||
| + | </StructureSection> | ||
| + | [[Category: Anopheles darlingi]] | ||
| + | [[Category: Large Structures]] | ||
| + | [[Category: Alvarenga PH]] | ||
| + | [[Category: Andersen JF]] | ||
Current revision
Long form D7 protein from Anopheles darlingi with U46619 and serotonin bound
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