4e7r
From Proteopedia
(Difference between revisions)
(New page: '''Unreleased structure''' The entry 4e7r is ON HOLD Authors: Ruehmann, E., Heine, A., Klebe, G. Description: Thrombin in complex with 3-amidinophenylalanine inhibitor) |
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| - | '''Unreleased structure''' | ||
| - | + | ==Thrombin in complex with 3-amidinophenylalanine inhibitor== | |
| + | <StructureSection load='4e7r' size='340' side='right'caption='[[4e7r]], [[Resolution|resolution]] 2.25Å' scene=''> | ||
| + | == Structural highlights == | ||
| + | <table><tr><td colspan='2'>[[4e7r]] is a 6 chain structure with sequence from [https://en.wikipedia.org/wiki/Hirudo_medicinalis Hirudo medicinalis] and [https://en.wikipedia.org/wiki/Homo_sapiens Homo sapiens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4E7R OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=4E7R 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]] 2.25Å</td></tr> | ||
| + | <tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=0NW:3-[(2S)-3-[4-(2-AMINOETHYL)PIPERIDIN-1-YL]-2-{[(2,4-DICHLOROBIPHENYL-3-YL)SULFONYL]AMINO}-3-OXOPROPYL]BENZENECARBOXIMIDAMIDE'>0NW</scene>, <scene name='pdbligand=GOL:GLYCEROL'>GOL</scene>, <scene name='pdbligand=NA:SODIUM+ION'>NA</scene>, <scene name='pdbligand=NAG:N-ACETYL-D-GLUCOSAMINE'>NAG</scene>, <scene name='pdbligand=PO4:PHOSPHATE+ION'>PO4</scene>, <scene name='pdbligand=TYS:O-SULFO-L-TYROSINE'>TYS</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=4e7r FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4e7r OCA], [https://pdbe.org/4e7r PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4e7r RCSB], [https://www.ebi.ac.uk/pdbsum/4e7r PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4e7r ProSAT]</span></td></tr> | ||
| + | </table> | ||
| + | == Function == | ||
| + | [https://www.uniprot.org/uniprot/HIRV2_HIRME HIRV2_HIRME] Hirudin is a potent thrombin-specific protease inhibitor. It forms a stable non-covalent complex with alpha-thrombin, thereby abolishing its ability to cleave fibrinogen. | ||
| - | + | ==See Also== | |
| - | + | *[[Hirudin 3D structures|Hirudin 3D structures]] | |
| - | + | *[[Thrombin 3D Structures|Thrombin 3D Structures]] | |
| + | __TOC__ | ||
| + | </StructureSection> | ||
| + | [[Category: Hirudo medicinalis]] | ||
| + | [[Category: Homo sapiens]] | ||
| + | [[Category: Large Structures]] | ||
| + | [[Category: Heine A]] | ||
| + | [[Category: Klebe G]] | ||
| + | [[Category: Ruehmann E]] | ||
Current revision
Thrombin in complex with 3-amidinophenylalanine inhibitor
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