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| | <StructureSection load='6pi7' size='340' side='right'caption='[[6pi7]], [[Resolution|resolution]] 2.80Å' scene=''> | | <StructureSection load='6pi7' size='340' side='right'caption='[[6pi7]], [[Resolution|resolution]] 2.80Å' scene=''> |
| | == Structural highlights == | | == Structural highlights == |
| - | <table><tr><td colspan='2'>[[6pi7]] is a 7 chain structure with sequence from [http://en.wikipedia.org/wiki/Human Human]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=6PI7 OCA]. For a <b>guided tour on the structure components</b> use [http://proteopedia.org/fgij/fg.htm?mol=6PI7 FirstGlance]. <br> | + | <table><tr><td colspan='2'>[[6pi7]] is a 7 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=6PI7 OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6PI7 FirstGlance]. <br> |
| - | </td></tr><tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=UNX:UNKNOWN+ATOM+OR+ION'>UNX</scene></td></tr> | + | </td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 2.8Å</td></tr> |
| - | <tr id='gene'><td class="sblockLbl"><b>[[Gene|Gene:]]</b></td><td class="sblockDat">TDRKH, TDRD2 ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=9606 HUMAN])</td></tr> | + | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=UNX:UNKNOWN+ATOM+OR+ION'>UNX</scene></td></tr> |
| - | <tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[http://proteopedia.org/fgij/fg.htm?mol=6pi7 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6pi7 OCA], [http://pdbe.org/6pi7 PDBe], [http://www.rcsb.org/pdb/explore.do?structureId=6pi7 RCSB], [http://www.ebi.ac.uk/pdbsum/6pi7 PDBsum], [http://prosat.h-its.org/prosat/prosatexe?pdbcode=6pi7 ProSAT]</span></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=6pi7 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6pi7 OCA], [https://pdbe.org/6pi7 PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6pi7 RCSB], [https://www.ebi.ac.uk/pdbsum/6pi7 PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6pi7 ProSAT]</span></td></tr> |
| | </table> | | </table> |
| | + | == Function == |
| | + | [https://www.uniprot.org/uniprot/TDRKH_HUMAN TDRKH_HUMAN] |
| | <div style="background-color:#fffaf0;"> | | <div style="background-color:#fffaf0;"> |
| | == Publication Abstract from PubMed == | | == Publication Abstract from PubMed == |
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| | __TOC__ | | __TOC__ |
| | </StructureSection> | | </StructureSection> |
| - | [[Category: Human]] | + | [[Category: Homo sapiens]] |
| | [[Category: Large Structures]] | | [[Category: Large Structures]] |
| - | [[Category: Liu, K]] | + | [[Category: Liu K]] |
| - | [[Category: Min, J R]] | + | [[Category: Min JR]] |
| - | [[Category: Structural genomic]]
| + | |
| - | [[Category: Fab]]
| + | |
| - | [[Category: Piwil1]]
| + | |
| - | [[Category: Protein binding]]
| + | |
| - | [[Category: Sgc]]
| + | |
| - | [[Category: Tudor domain]]
| + | |
| Structural highlights
Function
TDRKH_HUMAN
Publication Abstract from PubMed
The interaction of Tudor domain-containing proteins (TDRDs) with P-element-induced wimpy testis (PIWI) proteins plays critical roles in transposon silencing and spermatogenesis. Most human TDRDs recognize PIWI proteins in a methylarginine-dependent manner via their extended Tudor (eTudor) domains, except TDRD2, which prefers an unmethylated PIWI protein. In order to illustrate the recognition of unmethylated PIWI proteins by TDRD2, we extensively tried co-crystallization of the TDRD2 eTudor with different PIWIL1 peptides, but to no avail. Recombinant antigen-binding fragments (Fabs) have been used to crystallize some difficult proteins in the past, so we generated Fab against the TDRD2 eTudor protein using a phage-display antibody library, and one of these Fab fragments indeed facilitated the co-crystallization of TDRD2 and PIWIL1. Structural analysis of Fab, the TDRD2 eTudor domain in complex with an unmethylated PIWIL1-derived peptide revealed that the PIWIL1 residues G3 through R8 bound between the Tudor core and SN domain of TDRD2. The C-terminal residues of the PIWIL1 peptide were not resolved, presumably due to steric competition with the heavy chain of the Fab. We propose Fab-assisted crystallization as a tool not only for structural studies of single proteins, but also for analysis of interactions between proteins and their ligands in cases where co-crystallization of native protein complexes fails.
Lesson from a Fab-enabled co-crystallization study of TDRD2 and PIWIL1.,Chen S, Zhang W, Min J, Liu K Methods. 2019 Jul 6. pii: S1046-2023(19)30126-4. doi:, 10.1016/j.ymeth.2019.07.002. PMID:31288074[1]
From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.
References
- ↑ Chen S, Zhang W, Min J, Liu K. Lesson from a Fab-enabled co-crystallization study of TDRD2 and PIWIL1. Methods. 2019 Jul 6. pii: S1046-2023(19)30126-4. doi:, 10.1016/j.ymeth.2019.07.002. PMID:31288074 doi:http://dx.doi.org/10.1016/j.ymeth.2019.07.002
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