6t9t: Difference between revisions

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'''Unreleased structure'''


The entry 6t9t is ON HOLD  until Paper Publication
==Matriptase in complex with the synthetic inhibitor (S)-3-(3-(4-(3-(tert-butyl)ureido)piperidin-1-yl)-2-((3'-fluoro-4'-(hydroxymethyl)-[1,1'-biphenyl])-3-sulfonamido)-3-oxopropyl)benzimidamide (MI-1904)==
<StructureSection load='6t9t' size='340' side='right'caption='[[6t9t]], [[Resolution|resolution]] 1.69&Aring;' scene=''>
== Structural highlights ==
<table><tr><td colspan='2'>[[6t9t]] is a 1 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=6T9T OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=6T9T 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]] 1.69&#8491;</td></tr>
<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=CL:CHLORIDE+ION'>CL</scene>, <scene name='pdbligand=MXH:1-~{tert}-butyl-3-[1-[(2~{S})-3-(3-carbamimidoylphenyl)-2-[[3-[3-fluoranyl-4-(hydroxymethyl)phenyl]phenyl]sulfonylamino+]propanoyl]piperidin-4-yl]urea'>MXH</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=6t9t FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=6t9t OCA], [https://pdbe.org/6t9t PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=6t9t RCSB], [https://www.ebi.ac.uk/pdbsum/6t9t PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=6t9t ProSAT]</span></td></tr>
</table>
== Disease ==
[https://www.uniprot.org/uniprot/ST14_HUMAN ST14_HUMAN] Defects in ST14 are a cause of ichthyosis autosomal recessive with hypotrichosis (ARIH) [MIM:[https://omim.org/entry/610765 610765]. ARIH is a skin disorder characterized by congenital ichthyosis associated with the presence of less than the normal amount of hair.<ref>PMID:17273967</ref>
== Function ==
[https://www.uniprot.org/uniprot/ST14_HUMAN ST14_HUMAN] Degrades extracellular matrix. Proposed to play a role in breast cancer invasion and metastasis. Exhibits trypsin-like activity as defined by cleavage of synthetic substrates with Arg or Lys as the P1 site.


Authors: Mueller, J.M., Merkl, S., Keils, A., Pilgram, O., Steinmetzer, T.
==See Also==
 
*[[Matriptase 3D structures|Matriptase 3D structures]]
Description: Matriptase in complex with the synthetic inhibitor (S)-3-(3-(4-(3-(tert-butyl)ureido)piperidin-1-yl)-2-((3'-fluoro-4'-(hydroxymethyl)-[1,1'-biphenyl])-3-sulfonamido)-3-oxopropyl)benzimidamide (MI-1904)
== References ==
[[Category: Unreleased Structures]]
<references/>
[[Category: Pilgram, O]]
__TOC__
[[Category: Steinmetzer, T]]
</StructureSection>
[[Category: Mueller, J.M]]
[[Category: Homo sapiens]]
[[Category: Merkl, S]]
[[Category: Large Structures]]
[[Category: Keils, A]]
[[Category: Keils A]]
[[Category: Merkl S]]
[[Category: Mueller JM]]
[[Category: Pilgram O]]
[[Category: Steinmetzer T]]

Latest revision as of 12:58, 24 January 2024

Matriptase in complex with the synthetic inhibitor (S)-3-(3-(4-(3-(tert-butyl)ureido)piperidin-1-yl)-2-((3'-fluoro-4'-(hydroxymethyl)-[1,1'-biphenyl])-3-sulfonamido)-3-oxopropyl)benzimidamide (MI-1904)

6t9t, resolution 1.69Å

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