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'''Unreleased structure'''


The entry 9dam is ON HOLD
==A DARPin fused to the 1TEL crystallization chaperone via a direct helical fusion==
 
<StructureSection load='9dam' size='340' side='right'caption='[[9dam]], [[Resolution|resolution]] 1.78&Aring;' scene=''>
Authors: Pedroza Romo, M.J., Averett, J.C., Keliiliki, A., Wilson, E.W., Smith, C., Hansen, D., Averett, B., Gonzalez, J., Noakes, E.W., Nickles, R., Doukov, T., Moody, J.D.
== Structural highlights ==
 
<table><tr><td colspan='2'>[[9dam]] is a 1 chain structure with sequence from [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens] and [https://en.wikipedia.org/wiki/Synthetic_construct Synthetic construct]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=9DAM OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=9DAM FirstGlance]. <br>
Description: A DARPin fused to the 1TEL crystallization chaperone via a direct helical fusion
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 1.78&#8491;</td></tr>
[[Category: Unreleased Structures]]
<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=ACY:ACETIC+ACID'>ACY</scene>, <scene name='pdbligand=CL:CHLORIDE+ION'>CL</scene>, <scene name='pdbligand=MG:MAGNESIUM+ION'>MG</scene>, <scene name='pdbligand=NA:SODIUM+ION'>NA</scene></td></tr>
[[Category: Keliiliki, A]]
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=9dam FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=9dam OCA], [https://pdbe.org/9dam PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=9dam RCSB], [https://www.ebi.ac.uk/pdbsum/9dam PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=9dam ProSAT]</span></td></tr>
[[Category: Gonzalez, J]]
</table>
[[Category: Smith, C]]
== Disease ==
[[Category: Averett, B]]
[https://www.uniprot.org/uniprot/ETV6_HUMAN ETV6_HUMAN] Note=A chromosomal aberration involving ETV6 is found in a form of chronic myelomonocytic leukemia (CMML). Translocation t(5;12)(q33;p13) with PDGFRB. It is characterized by abnormal clonal myeloid proliferation and by progression to acute myelogenous leukemia (AML).<ref>PMID:12203785</ref>  Note=Chromosomal aberrations involving ETV6 are found in a form of acute myeloid leukemia (AML). Translocation t(12;22)(p13;q11) with MN1; translocation t(4;12)(q12;p13) with CHIC2.<ref>PMID:7761424</ref> <ref>PMID:7780150</ref> <ref>PMID:15806161</ref>  Note=Chromosomal aberrations involving ETV6 are found in childhood acute lymphoblastic leukemia (ALL). Translocations t(12;21)(p12;q22) and t(12;21)(p13;q22) with RUNX1/AML1.  Note=A chromosomal aberration involving ETV6 is found in a form of pre-B acute myeloid leukemia. Translocation t(9;12)(p24;p13) with JAK2.  Note=A chromosomal aberration involving ETV6 is found in myelodysplastic syndrome (MDS) with basophilia. Translocation t(5;12)(q31;p13) with ACSL6.  Note=A chromosomal aberration involving ETV6 is found in acute eosinophilic leukemia (AEL). Translocation t(5;12)(q31;p13) with ACSL6.  Note=A chromosomal aberration involving ETV6 is found in myelodysplastic syndrome (MDS). Translocation t(1;12)(p36.1;p13) with MDS2.  Defects in ETV6 are a cause of myeloproliferative disorder chronic with eosinophilia (MPE) [MIM:[https://omim.org/entry/131440 131440]. A hematologic disorder characterized by malignant eosinophils proliferation. Note=A chromosomal aberration involving ETV6 is found in many instances of myeloproliferative disorder chronic with eosinophilia. Translocation t(5;12) with PDGFRB on chromosome 5 creating an ETV6-PDGFRB fusion protein.  Defects in ETV6 are a cause of acute myelogenous leukemia (AML) [MIM:[https://omim.org/entry/601626 601626]. AML is a malignant disease in which hematopoietic precursors are arrested in an early stage of development.<ref>PMID:7761424</ref> <ref>PMID:7780150</ref> <ref>PMID:15806161</ref>  Note=A chromosomal aberration involving ETV6 is found in acute lymphoblastic leukemia. Translocation t(9;12)(p13;p13) with PAX5.
[[Category: Doukov, T]]
== Function ==
[[Category: Nickles, R]]
[https://www.uniprot.org/uniprot/ETV6_HUMAN ETV6_HUMAN] Transcriptional repressor; binds to the DNA sequence 5'-CCGGAAGT-3'.
[[Category: Wilson, E.W]]
== References ==
[[Category: Hansen, D]]
<references/>
[[Category: Moody, J.D]]
__TOC__
[[Category: Noakes, E.W]]
</StructureSection>
[[Category: Averett, J.C]]
[[Category: Homo sapiens]]
[[Category: Pedroza Romo, M.J]]
[[Category: Large Structures]]
[[Category: Synthetic construct]]
[[Category: Averett B]]
[[Category: Averett JC]]
[[Category: Doukov T]]
[[Category: Gonzalez J]]
[[Category: Hansen D]]
[[Category: Keliiliki A]]
[[Category: Moody JD]]
[[Category: Nickles R]]
[[Category: Noakes EW]]
[[Category: Pedroza Romo MJ]]
[[Category: Smith C]]
[[Category: Wilson EW]]
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