1at3: Difference between revisions

From Proteopedia
Jump to navigation Jump to search
No edit summary
No edit summary
Line 4: Line 4:
|PDB= 1at3 |SIZE=350|CAPTION= <scene name='initialview01'>1at3</scene>, resolution 2.5&Aring;
|PDB= 1at3 |SIZE=350|CAPTION= <scene name='initialview01'>1at3</scene>, resolution 2.5&Aring;
|SITE= <scene name='pdbsite=ACT:Novel+Active+Site+Triad+SER+129,+HIS+61+And+HIS+148'>ACT</scene>
|SITE= <scene name='pdbsite=ACT:Novel+Active+Site+Triad+SER+129,+HIS+61+And+HIS+148'>ACT</scene>
|LIGAND= <scene name='pdbligand=DFP:DIISOPROPYL PHOSPHONATE'>DFP</scene>
|LIGAND= <scene name='pdbligand=DFP:DIISOPROPYL+PHOSPHONATE'>DFP</scene>
|ACTIVITY=  
|ACTIVITY=  
|GENE=  
|GENE=  
|DOMAIN=
|RELATEDENTRY=
|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1at3 FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1at3 OCA], [http://www.ebi.ac.uk/pdbsum/1at3 PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=1at3 RCSB]</span>
}}
}}


Line 16: Line 19:


==About this Structure==
==About this Structure==
1AT3 is a [[Single protein]] structure of sequence from [http://en.wikipedia.org/wiki/Human_herpesvirus_1 Human herpesvirus 1]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1AT3 OCA].  
1AT3 is a [[Single protein]] structure of sequence from [http://en.wikipedia.org/wiki/Human_herpesvirus_2 Human herpesvirus 2]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1AT3 OCA].  


==Reference==
==Reference==
Active site cavity of herpesvirus proteases revealed by the crystal structure of herpes simplex virus protease/inhibitor complex., Hoog SS, Smith WW, Qiu X, Janson CA, Hellmig B, McQueney MS, O'Donnell K, O'Shannessy D, DiLella AG, Debouck C, Abdel-Meguid SS, Biochemistry. 1997 Nov 18;36(46):14023-9. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/9369473 9369473]
Active site cavity of herpesvirus proteases revealed by the crystal structure of herpes simplex virus protease/inhibitor complex., Hoog SS, Smith WW, Qiu X, Janson CA, Hellmig B, McQueney MS, O'Donnell K, O'Shannessy D, DiLella AG, Debouck C, Abdel-Meguid SS, Biochemistry. 1997 Nov 18;36(46):14023-9. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/9369473 9369473]
[[Category: Human herpesvirus 1]]
[[Category: Human herpesvirus 2]]
[[Category: Single protein]]
[[Category: Single protein]]
[[Category: Abdel-Meguid, S S.]]
[[Category: Abdel-Meguid, S S.]]
Line 26: Line 29:
[[Category: Qiu, X.]]
[[Category: Qiu, X.]]
[[Category: Smith, W W.]]
[[Category: Smith, W W.]]
[[Category: DFP]]
[[Category: hsv2 protease]]
[[Category: hsv2 protease]]
[[Category: serine protease]]
[[Category: serine protease]]
[[Category: viral protease]]
[[Category: viral protease]]


''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Mar 20 10:01:55 2008''
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Mar 30 18:46:57 2008''

Revision as of 18:47, 30 March 2008

File:1at3.gif


PDB ID 1at3

Drag the structure with the mouse to rotate
, resolution 2.5Å
Sites:
Ligands:
Resources: FirstGlance, OCA, PDBsum, RCSB
Coordinates: save as pdb, mmCIF, xml



HERPES SIMPLEX VIRUS TYPE II PROTEASE


OverviewOverview

Human herpes simplex virus type 1 (HSV-1) and type 2 (HSV-2) are responsible for herpes labialis (cold sores) and genital herpes, respectively. They encode a serine protease that is required for viral replication, and represent a viable target for therapeutic intervention. Here, we report the crystal structures of HSV-1 and HSV-2 proteases, the latter in the presence and absence of the covalently bound transition state analog inhibitor diisopropyl phosphate (DIP). The HSV-1 and HSV-2 protease structures show a fold that is neither like chymotrypsin nor like subtilisin, and has been seen only in the recently determined cytomegalovirus (CMV) and varicella-zoster virus (VZV) protease structures. HSV-1 and HSV-2 proteases share high sequence homology and have almost identical three-dimensional structures. However, structural differences are observed with the less homologous CMV protease, offering a structural basis for herpes virus protease ligand specificity. The bound inhibitor identifies the oxyanion hole of these enzymes and defines the active site cavity.

About this StructureAbout this Structure

1AT3 is a Single protein structure of sequence from Human herpesvirus 2. Full crystallographic information is available from OCA.

ReferenceReference

Active site cavity of herpesvirus proteases revealed by the crystal structure of herpes simplex virus protease/inhibitor complex., Hoog SS, Smith WW, Qiu X, Janson CA, Hellmig B, McQueney MS, O'Donnell K, O'Shannessy D, DiLella AG, Debouck C, Abdel-Meguid SS, Biochemistry. 1997 Nov 18;36(46):14023-9. PMID:9369473

Page seeded by OCA on Sun Mar 30 18:46:57 2008

Proteopedia Page Contributors and Editors (what is this?)Proteopedia Page Contributors and Editors (what is this?)

OCA