1qzz
From Proteopedia
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- | [[Image:1qzz.jpg|left|200px]] | + | [[Image:1qzz.jpg|left|200px]] |
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- | '''Crystal structure of aclacinomycin-10-hydroxylase (RdmB) in complex with S-adensyl-L-methionine (SAM)''' | + | {{Structure |
+ | |PDB= 1qzz |SIZE=350|CAPTION= <scene name='initialview01'>1qzz</scene>, resolution 2.1Å | ||
+ | |SITE= | ||
+ | |LIGAND= <scene name='pdbligand=ACT:ACETATE+ION'>ACT</scene> and <scene name='pdbligand=SAM:S-ADENOSYLMETHIONINE'>SAM</scene> | ||
+ | |ACTIVITY= | ||
+ | |GENE= rdmb ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=1924 Streptomyces purpurascens]) | ||
+ | }} | ||
+ | |||
+ | '''Crystal structure of aclacinomycin-10-hydroxylase (RdmB) in complex with S-adensyl-L-methionine (SAM)''' | ||
+ | |||
==Overview== | ==Overview== | ||
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==About this Structure== | ==About this Structure== | ||
- | 1QZZ is a [ | + | 1QZZ is a [[Single protein]] structure of sequence from [http://en.wikipedia.org/wiki/Streptomyces_purpurascens Streptomyces purpurascens]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1QZZ OCA]. |
==Reference== | ==Reference== | ||
- | Crystal structure of aclacinomycin-10-hydroxylase, a S-adenosyl-L-methionine-dependent methyltransferase homolog involved in anthracycline biosynthesis in Streptomyces purpurascens., Jansson A, Niemi J, Lindqvist Y, Mantsala P, Schneider G, J Mol Biol. 2003 Nov 21;334(2):269-80. PMID:[http:// | + | Crystal structure of aclacinomycin-10-hydroxylase, a S-adenosyl-L-methionine-dependent methyltransferase homolog involved in anthracycline biosynthesis in Streptomyces purpurascens., Jansson A, Niemi J, Lindqvist Y, Mantsala P, Schneider G, J Mol Biol. 2003 Nov 21;334(2):269-80. PMID:[http://www.ncbi.nlm.nih.gov/pubmed/14607118 14607118] |
[[Category: Single protein]] | [[Category: Single protein]] | ||
[[Category: Streptomyces purpurascens]] | [[Category: Streptomyces purpurascens]] | ||
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[[Category: polyketide]] | [[Category: polyketide]] | ||
[[Category: spine]] | [[Category: spine]] | ||
- | [[Category: | + | [[Category: streptomyce]] |
- | [[Category: structural | + | [[Category: structural genomic]] |
[[Category: structural proteomics in europe]] | [[Category: structural proteomics in europe]] | ||
- | [[Category: tailoring | + | [[Category: tailoring enzyme]] |
- | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu | + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Thu Mar 20 13:45:00 2008'' |
Revision as of 11:45, 20 March 2008
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, resolution 2.1Å | |||||||
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Ligands: | and | ||||||
Gene: | rdmb (Streptomyces purpurascens) | ||||||
Coordinates: | save as pdb, mmCIF, xml |
Crystal structure of aclacinomycin-10-hydroxylase (RdmB) in complex with S-adensyl-L-methionine (SAM)
Overview
Anthracyclines are aromatic polyketide antibiotics, and several of these compounds are widely used as anti-tumor drugs in chemotherapy. Aclacinomycin-10-hydroxylase (RdmB) is one of the tailoring enzymes that modify the polyketide backbone in the biosynthesis of these metabolites. RdmB, a S-adenosyl-L-methionine-dependent methyltransferase homolog, catalyses the hydroxylation of 15-demethoxy-epsilon-rhodomycin to beta-rhodomycin, one step in rhodomycin biosynthesis in Streptomyces purpurascens. The crystal structure of RdmB, determined by multiwavelength anomalous diffraction to 2.1A resolution, reveals that the enzyme subunit has a fold similar to methyltransferases and binds S-adenosyl-L-methionine. The N-terminal domain, which consists almost exclusively of alpha-helices, is involved in dimerization. The C-terminal domain contains a typical alpha/beta nucleotide-binding fold, which binds S-adenosyl-L-methionine, and several of the residues interacting with the cofactor are conserved in O-methyltransferases. Adjacent to the S-adenosyl-L-methionine molecule there is a large cleft extending to the enzyme surface of sufficient size to bind the substrate. Analysis of the putative substrate-binding pocket suggests that there is no enzymatic group in proximity of the substrate 15-demethoxy-epsilon-rhodomycin, which could assist in proton abstraction and thus facilitate methyl transfer. The lack of a suitably positioned catalytic base might thus be one of the features responsible for the inability of the enzyme to act as a methyltransferase.
About this Structure
1QZZ is a Single protein structure of sequence from Streptomyces purpurascens. Full crystallographic information is available from OCA.
Reference
Crystal structure of aclacinomycin-10-hydroxylase, a S-adenosyl-L-methionine-dependent methyltransferase homolog involved in anthracycline biosynthesis in Streptomyces purpurascens., Jansson A, Niemi J, Lindqvist Y, Mantsala P, Schneider G, J Mol Biol. 2003 Nov 21;334(2):269-80. PMID:14607118
Page seeded by OCA on Thu Mar 20 13:45:00 2008
Categories: Single protein | Streptomyces purpurascens | Jansson, A. | Lindqvist, Y. | Mantsala, P. | Niemi, J. | SPINE, Structural Proteomics in Europe. | Schneider, G. | ACT | SAM | Anthracycline | Hydroxylase | Methyltransferase | Polyketide | Spine | Streptomyce | Structural genomic | Structural proteomics in europe | Tailoring enzyme