1fmb

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[[Image:1fmb.gif|left|200px]]
[[Image:1fmb.gif|left|200px]]
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{{Structure
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|PDB= 1fmb |SIZE=350|CAPTION= <scene name='initialview01'>1fmb</scene>, resolution 1.8&Aring;
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The line below this paragraph, containing "STRUCTURE_1fmb", creates the "Structure Box" on the page.
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|SITE=
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You may change the PDB parameter (which sets the PDB file loaded into the applet)
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|LIGAND= <scene name='pdbligand=HYB:[2-(2-METHYL-PROPANE-2-SULFONYLMETHYL)-3-NAPHTHALEN-1-YL-PROPIONYL-VALINYL]-PHENYLALANINOL'>HYB</scene>
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or the SCENE parameter (which sets the initial scene displayed when the page is loaded),
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|ACTIVITY= <span class='plainlinks'>[http://en.wikipedia.org/wiki/HIV-1_retropepsin HIV-1 retropepsin], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.4.23.16 3.4.23.16] </span>
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or leave the SCENE parameter empty for the default display.
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|GENE=
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|DOMAIN=
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{{STRUCTURE_1fmb| PDB=1fmb | SCENE= }}
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|RELATEDENTRY=
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|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1fmb FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1fmb OCA], [http://www.ebi.ac.uk/pdbsum/1fmb PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=1fmb RCSB]</span>
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}}
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'''EIAV PROTEASE COMPLEXED WITH THE INHIBITOR HBY-793'''
'''EIAV PROTEASE COMPLEXED WITH THE INHIBITOR HBY-793'''
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[[Category: Wlodawer, A.]]
[[Category: Wlodawer, A.]]
[[Category: Zdanov, A.]]
[[Category: Zdanov, A.]]
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[[Category: aspartyl protease]]
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[[Category: Aspartyl protease]]
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[[Category: endonuclease]]
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[[Category: Endonuclease]]
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[[Category: hydrolase (acid proteinase)]]
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[[Category: Polyprotein]]
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[[Category: polyprotein]]
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[[Category: Rna-directed dna polymerase]]
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[[Category: rna-directed dna polymerase]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Mar 30 20:25:42 2008''
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Revision as of 13:29, 2 May 2008

Template:STRUCTURE 1fmb

EIAV PROTEASE COMPLEXED WITH THE INHIBITOR HBY-793


Overview

Equine infectious anemia virus (EIAV), the causative agent of infectious anemia in horses, is a member of the lentiviral family. The virus-encoded proteinase (PR) processes viral polyproteins into functional molecules during replication and it also cleaves viral nucleocapsid protein during infection. The X-ray structure of a complex of the 154G mutant of EIAV PR with the inhibitor HBY-793 was solved at 1.8 A resolution and refined to a crystallographic R-factor of 0.136. The molecule is a dimer in which the monomers are related by a crystallographic twofold axis. Although both the enzyme and the inhibitor are symmetric, the interactions between the central part of the inhibitor and the active site aspartates are asymmetric, and the inhibitor and the two flaps are partially disordered. The overall fold of EIAV PR is very similar to that of other retroviral proteinases. However, a novel feature of the EIAV PR structure is the appearance of the second alpha-helix in the monomer in a position predicted by the structural template for the family of aspartic proteinases. The parts of the EIAV PR with the highest resemblance to human immunodeficiency virus type 1 PR include the substrate-binding sites; thus, the differences in the specificity of both enzymes have to be explained by enzyme-ligand interactions at the periphery of the active site as well.

About this Structure

1FMB is a Single protein structure of sequence from Equine infectious anemia virus. Full crystallographic information is available from OCA.

Reference

Structure of equine infectious anemia virus proteinase complexed with an inhibitor., Gustchina A, Kervinen J, Powell DJ, Zdanov A, Kay J, Wlodawer A, Protein Sci. 1996 Aug;5(8):1453-65. PMID:8844837 Page seeded by OCA on Fri May 2 16:29:57 2008

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