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{{STRUCTURE_4njs|  PDB=4njs  |  SCENE=  }}
===Crystal structure of multidrug-resistant clinical isolate A02 HIV-1 protease in complex with non-peptidic inhibitor, GRL008===


==About this Structure==
==Crystal structure of multidrug-resistant clinical isolate A02 HIV-1 protease in complex with non-peptidic inhibitor, GRL008==
[[4njs]] is a 4 chain structure. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4NJS OCA].  
<StructureSection load='4njs' size='340' side='right'caption='[[4njs]], [[Resolution|resolution]] 1.80&Aring;' scene=''>
[[Category: Das, D.]]
== Structural highlights ==
[[Category: Garimella, H.]]
<table><tr><td colspan='2'>[[4njs]] is a 4 chain structure with sequence from [https://en.wikipedia.org/wiki/Human_immunodeficiency_virus_1 Human immunodeficiency virus 1]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=4NJS OCA]. For a <b>guided tour on the structure components</b> use [https://proteopedia.org/fgij/fg.htm?mol=4NJS FirstGlance]. <br>
[[Category: Ghosh, A K.]]
</td></tr><tr id='method'><td class="sblockLbl"><b>[[Empirical_models|Method:]]</b></td><td class="sblockDat" id="methodDat">X-ray diffraction, [[Resolution|Resolution]] 1.8&#8491;</td></tr>
[[Category: Kaufman, J D.]]
<tr id='ligand'><td class="sblockLbl"><b>[[Ligand|Ligands:]]</b></td><td class="sblockDat" id="ligandDat"><scene name='pdbligand=G08:(3R,3AS,6AR)-HEXAHYDROFURO[2,3-B]FURAN-3-YL+[(2S,3R)-4-{[(4-CARBAMOYLPHENYL)SULFONYL](2-METHYLPROPYL)AMINO}-3-HYDROXY-1-PHENYLBUTAN-2-YL]CARBAMATE'>G08</scene></td></tr>
[[Category: Mitsuya, H.]]
<tr id='resources'><td class="sblockLbl"><b>Resources:</b></td><td class="sblockDat"><span class='plainlinks'>[https://proteopedia.org/fgij/fg.htm?mol=4njs FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=4njs OCA], [https://pdbe.org/4njs PDBe], [https://www.rcsb.org/pdb/explore.do?structureId=4njs RCSB], [https://www.ebi.ac.uk/pdbsum/4njs PDBsum], [https://prosat.h-its.org/prosat/prosatexe?pdbcode=4njs ProSAT]</span></td></tr>
[[Category: Wingfield, P T.]]
</table>
[[Category: Yedidi, R S.]]
== Function ==
[[Category: Darunavir analog]]
[https://www.uniprot.org/uniprot/Q9J006_9HIV1 Q9J006_9HIV1]
[[Category: Hiv-1 protease]]
 
[[Category: Hydrolase-hydrolase inhibitor complex]]
==See Also==
[[Category: Multidrug-resistance]]
*[[Immunodeficiency virus protease 3D structures|Immunodeficiency virus protease 3D structures]]
[[Category: Non-peptidic inhibitor]]
__TOC__
[[Category: Protease inhibitor]]
</StructureSection>
[[Category: Human immunodeficiency virus 1]]
[[Category: Large Structures]]
[[Category: Das D]]
[[Category: Garimella H]]
[[Category: Ghosh AK]]
[[Category: Kaufman JD]]
[[Category: Mitsuya H]]
[[Category: Wingfield PT]]
[[Category: Yedidi RS]]

Latest revision as of 15:33, 1 March 2024

Crystal structure of multidrug-resistant clinical isolate A02 HIV-1 protease in complex with non-peptidic inhibitor, GRL008Crystal structure of multidrug-resistant clinical isolate A02 HIV-1 protease in complex with non-peptidic inhibitor, GRL008

Structural highlights

4njs is a 4 chain structure with sequence from Human immunodeficiency virus 1. Full crystallographic information is available from OCA. For a guided tour on the structure components use FirstGlance.
Method:X-ray diffraction, Resolution 1.8Å
Ligands:
Resources:FirstGlance, OCA, PDBe, RCSB, PDBsum, ProSAT

Function

Q9J006_9HIV1

See Also

4njs, resolution 1.80Å

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