1w3v: Difference between revisions

From Proteopedia
Jump to navigation Jump to search
No edit summary
No edit summary
Line 4: Line 4:
|PDB= 1w3v |SIZE=350|CAPTION= <scene name='initialview01'>1w3v</scene>, resolution 1.40&Aring;
|PDB= 1w3v |SIZE=350|CAPTION= <scene name='initialview01'>1w3v</scene>, resolution 1.40&Aring;
|SITE= <scene name='pdbsite=AC1:Mdz+Binding+Site+For+Chain+A'>AC1</scene>
|SITE= <scene name='pdbsite=AC1:Mdz+Binding+Site+For+Chain+A'>AC1</scene>
|LIGAND= <scene name='pdbligand=FE2:FE+(II)+ION'>FE2</scene> and <scene name='pdbligand=MDZ:N~6~-METHYL-6-OXO-L-LYSINE - 2-[(3-MERCAPTOBUTANOYL)OXY]-3-METHYLBUTANOIC ACID'>MDZ</scene>
|LIGAND= <scene name='pdbligand=FE2:FE+(II)+ION'>FE2</scene>, <scene name='pdbligand=MDZ:N~6~-METHYL-6-OXO-L-LYSINE+-+2-[(3-MERCAPTOBUTANOYL)OXY]-3-METHYLBUTANOIC+ACID'>MDZ</scene>
|ACTIVITY= [http://en.wikipedia.org/wiki/Isopenicillin-N_synthase Isopenicillin-N synthase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=1.21.3.1 1.21.3.1]  
|ACTIVITY= <span class='plainlinks'>[http://en.wikipedia.org/wiki/Isopenicillin-N_synthase Isopenicillin-N synthase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=1.21.3.1 1.21.3.1] </span>
|GENE=  
|GENE=  
|DOMAIN=
|RELATEDENTRY=
|RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1w3v FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1w3v OCA], [http://www.ebi.ac.uk/pdbsum/1w3v PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=1w3v RCSB]</span>
}}
}}


Line 26: Line 29:
[[Category: Daruzzaman, A.]]
[[Category: Daruzzaman, A.]]
[[Category: Rutledge, P J.]]
[[Category: Rutledge, P J.]]
[[Category: FE2]]
[[Category: MDZ]]
[[Category: 3d-structure]]
[[Category: 3d-structure]]
[[Category: antibiotic biosynthesis]]
[[Category: antibiotic biosynthesis]]
Line 36: Line 37:
[[Category: penicillin biosynthesis]]
[[Category: penicillin biosynthesis]]


''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Mar 20 14:51:47 2008''
''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Mar 31 00:30:51 2008''

Revision as of 00:30, 31 March 2008

File:1w3v.gif


PDB ID 1w3v

Drag the structure with the mouse to rotate
, resolution 1.40Å
Sites:
Ligands: ,
Activity: Isopenicillin-N synthase, with EC number 1.21.3.1
Resources: FirstGlance, OCA, PDBsum, RCSB
Coordinates: save as pdb, mmCIF, xml



ISOPENICILLIN N SYNTHASE D-(L-A-AMINOADIPOYL)-(3R)-METHYL-L-CYSTEINE D-A-HYDROXYISOVALERYL ESTER COMPLEX (ANAEROBIC)


OverviewOverview

Isopenicillin N synthase (IPNS) is a non-heme iron(ii)-dependent oxidase that is central to penicillin biosynthesis. Herein, we report mechanistic studies of the IPNS reaction in the crystalline state, using the substrate analogue delta-(L-alpha-aminoadipoyl)-(3R)-methyl-L-cysteine D-alpha-hydroxyisovaleryl ester (AmCOV) to probe the early stages of the catalytic cycle. The X-ray crystal structure of the anaerobic IPNS:Fe(II):AmCOV complex was solved to 1.40 A resolution, and it reveals several subtle differences in the active site relative to the complex of the enzyme with its natural substrate. The crystalline IPNS:Fe(II):AmCOV complex was then exposed to oxygen gas at high pressure; this brought about reaction to give what appears to be a hydroxymethyl/ene-thiol product. A mechanism for this reaction is proposed. These results offer further insight into the delicate interplay of steric and electronic effects in the IPNS active site and the mechanistic intricacies of this remarkable enzyme.

About this StructureAbout this Structure

1W3V is a Single protein structure of sequence from Emericella nidulans. Full crystallographic information is available from OCA.

ReferenceReference

Unexpected oxidation of a depsipeptide substrate analogue in crystalline isopenicillin N synthase., Daruzzaman A, Clifton IJ, Adlington RM, Baldwin JE, Rutledge PJ, Chembiochem. 2006 Feb;7(2):351-8. PMID:16444759

Page seeded by OCA on Mon Mar 31 00:30:51 2008

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

OCA