3djk

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'''Unreleased structure'''
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{{Seed}}
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[[Image:3djk.jpg|left|200px]]
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The entry 3djk is ON HOLD until Paper Publication
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{{STRUCTURE_3djk| PDB=3djk | SCENE= }}
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Authors: Ghosh, A.K., Gemma, S., Baldridge, A., Leshchenko, S., Wang, Y.F., Kovalevsky, A.Y., Koh, Y., Weber, I.T., Mitsuya, H.
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===Wild Type HIV-1 Protease with potent Antiviral inhibitor GRL-0255A===
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Description: Wild Type HIV-1 Protease with potent Antiviral inhibitor GRL-0255A
 
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Jul 23 12:14:11 2008''
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The line below this paragraph, {{ABSTRACT_PUBMED_18783203}}, adds the Publication Abstract to the page
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(as it appears on PubMed at http://www.pubmed.gov), where 18783203 is the PubMed ID number.
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{{ABSTRACT_PUBMED_18783203}}
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==About this Structure==
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3DJK is a [[Single protein]] structure of sequence from [http://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=3DJK OCA].
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==Reference==
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Flexible Cyclic Ethers/Polyethers as Novel P2-Ligands for HIV-1 Protease Inhibitors: Design, Synthesis, Biological Evaluation, and Protein-Ligand X-ray Studies., Ghosh AK, Gemma S, Baldridge A, Wang YF, Kovalevsky AY, Koh Y, Weber IT, Mitsuya H, J Med Chem. 2008 Sep 11. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/18783203 18783203]
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[[Category: HIV-1 retropepsin]]
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[[Category: Human immunodeficiency virus 1]]
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[[Category: Single protein]]
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[[Category: Wang, Y F.]]
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[[Category: Weber, I T.]]
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[[Category: Aid]]
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[[Category: Aspartyl protease]]
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[[Category: Capsid maturation]]
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[[Category: Capsid protein]]
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[[Category: Cytoplasm]]
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[[Category: Dna integration]]
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[[Category: Dna recombination]]
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[[Category: Dna-directed dna polymerase]]
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[[Category: Endonuclease]]
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[[Category: Hiv-1]]
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[[Category: Hydrolase]]
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[[Category: Lipoprotein]]
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[[Category: Magnesium]]
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[[Category: Metal-binding]]
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[[Category: Multifunctional enzyme]]
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[[Category: Myristate]]
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[[Category: Nuclease]]
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[[Category: Nucleotidyltransferase]]
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[[Category: Nucleus]]
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[[Category: Phosphoprotein]]
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[[Category: Protease]]
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[[Category: Protease inhibitor]]
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[[Category: Ribosomal frameshifting]]
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[[Category: Rna-binding]]
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[[Category: Rna-directed dna polymerase]]
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[[Category: Transferase]]
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[[Category: Viral nucleoprotein]]
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[[Category: Virion]]
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[[Category: Wild type protease]]
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[[Category: Zinc]]
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[[Category: Zinc-finger]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Wed Oct 1 21:42:42 2008''

Revision as of 18:42, 1 October 2008

Image:3djk.jpg

Template:STRUCTURE 3djk

Wild Type HIV-1 Protease with potent Antiviral inhibitor GRL-0255A

Template:ABSTRACT PUBMED 18783203

About this Structure

3DJK is a Single protein structure of sequence from Human immunodeficiency virus 1. Full crystallographic information is available from OCA.

Reference

Flexible Cyclic Ethers/Polyethers as Novel P2-Ligands for HIV-1 Protease Inhibitors: Design, Synthesis, Biological Evaluation, and Protein-Ligand X-ray Studies., Ghosh AK, Gemma S, Baldridge A, Wang YF, Kovalevsky AY, Koh Y, Weber IT, Mitsuya H, J Med Chem. 2008 Sep 11. PMID:18783203

Page seeded by OCA on Wed Oct 1 21:42:42 2008

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OCA

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