1ds7

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[[Image:1ds7.jpg|left|200px]]<br /><applet load="1ds7" size="350" color="white" frame="true" align="right" spinBox="true"
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[[Image:1ds7.jpg|left|200px]]
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caption="1ds7, resolution 2.06&Aring;" />
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'''A MINOR FMN-DEPENDENT NITROREDUCTASE FROM ESCHERICHIA COLI B'''<br />
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{{Structure
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|PDB= 1ds7 |SIZE=350|CAPTION= <scene name='initialview01'>1ds7</scene>, resolution 2.06&Aring;
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|SITE=
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|LIGAND= <scene name='pdbligand=FMN:FLAVIN MONONUCLEOTIDE'>FMN</scene>
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|ACTIVITY= [http://en.wikipedia.org/wiki/6,7-dihydropteridine_reductase 6,7-dihydropteridine reductase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=1.5.1.34 1.5.1.34]
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|GENE=
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}}
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'''A MINOR FMN-DEPENDENT NITROREDUCTASE FROM ESCHERICHIA COLI B'''
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==Overview==
==Overview==
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==About this Structure==
==About this Structure==
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1DS7 is a [http://en.wikipedia.org/wiki/Single_protein Single protein] structure of sequence from [http://en.wikipedia.org/wiki/Escherichia_coli Escherichia coli] with <scene name='pdbligand=FMN:'>FMN</scene> as [http://en.wikipedia.org/wiki/ligand ligand]. Active as [http://en.wikipedia.org/wiki/6,7-dihydropteridine_reductase 6,7-dihydropteridine reductase], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=1.5.1.34 1.5.1.34] Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1DS7 OCA].
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1DS7 is a [[Single protein]] structure of sequence from [http://en.wikipedia.org/wiki/Escherichia_coli Escherichia coli]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1DS7 OCA].
==Reference==
==Reference==
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Crystal structure of FMN-dependent nitroreductase from Escherichia coli B: a prodrug-activating enzyme., Parkinson GN, Skelly JV, Neidle S, J Med Chem. 2000 Oct 5;43(20):3624-31. PMID:[http://ispc.weizmann.ac.il//pmbin/getpm?pmid=11020276 11020276]
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Crystal structure of FMN-dependent nitroreductase from Escherichia coli B: a prodrug-activating enzyme., Parkinson GN, Skelly JV, Neidle S, J Med Chem. 2000 Oct 5;43(20):3624-31. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/11020276 11020276]
[[Category: 6,7-dihydropteridine reductase]]
[[Category: 6,7-dihydropteridine reductase]]
[[Category: Escherichia coli]]
[[Category: Escherichia coli]]
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[[Category: nitroreductase]]
[[Category: nitroreductase]]
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Feb 21 12:19:54 2008''
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''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Mar 20 10:43:31 2008''

Revision as of 08:43, 20 March 2008


PDB ID 1ds7

Drag the structure with the mouse to rotate
, resolution 2.06Å
Ligands:
Activity: 6,7-dihydropteridine reductase, with EC number 1.5.1.34
Coordinates: save as pdb, mmCIF, xml



A MINOR FMN-DEPENDENT NITROREDUCTASE FROM ESCHERICHIA COLI B


Overview

The FMN-dependent flavoprotein nitroreductase from Escherichia coli B (NTR) is used in cancer chemotherapy to activate a range of prodrugs. The crystal structure of this enzyme has been determined, using molecular replacement methods and refined at 2.06 A resolution. The recombinant 24-kDa enzyme was crystallized in the tetragonal space group P4(1)2(1)2, with unit cell dimensions of a = b = 57.74 A and c = 275.51 A and two molecules in the asymmetric unit. The structure has a final R factor of 20.3% (R(free) = 26.7%), for all data between the resolution ranges of 10-2.06 A, and includes 4453 protein atoms, 230 water molecules, and 2 flavin mononucleotide (FMN) molecules. The functional unit is a homodimer, which forms the asymmetric unit in the crystal structure. The tertiary structures of these two monomers and their subunit interactions are nearly identical. The molecular replacement search model, the crystal structure of the major NAD(P)H:FMN oxidoreductase of Vibrio fisheri (FRase 1), was selected on the basis of its high sequence identity to that of NTR. The final superposition of these two enzymes revealed a very similar overall fold, with variation in the structures focused around surface loops and helices near the FMN cofactor. Helix G is implicated in substrate specificity and is better resolved in the present NTR structure than in the previously reported FRase 1 structure. The FMN binding pocket is also well-resolved, showing the presence of two channels leading into the active site. The amino acid side chains and main chain atoms interacting with the FMN are well-ordered. The structure of the substrate binding pocket has been used to examine substrate specificity and enzyme kinetics for prodrugs used in antibody-directed enzyme prodrug therapy (ADEPT) and gene-directed enzyme prodrug therapy (GDEPT).

About this Structure

1DS7 is a Single protein structure of sequence from Escherichia coli. Full crystallographic information is available from OCA.

Reference

Crystal structure of FMN-dependent nitroreductase from Escherichia coli B: a prodrug-activating enzyme., Parkinson GN, Skelly JV, Neidle S, J Med Chem. 2000 Oct 5;43(20):3624-31. PMID:11020276

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