1q9e
From Proteopedia
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|SITE= | |SITE= | ||
|LIGAND= <scene name='pdbligand=TRS:2-AMINO-2-HYDROXYMETHYL-PROPANE-1,3-DIOL'>TRS</scene> | |LIGAND= <scene name='pdbligand=TRS:2-AMINO-2-HYDROXYMETHYL-PROPANE-1,3-DIOL'>TRS</scene> | ||
- | |ACTIVITY= [http://en.wikipedia.org/wiki/Ribonuclease_T(1) Ribonuclease T(1)], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.1.27.3 3.1.27.3] | + | |ACTIVITY= <span class='plainlinks'>[http://en.wikipedia.org/wiki/Ribonuclease_T(1) Ribonuclease T(1)], with EC number [http://www.brenda-enzymes.info/php/result_flat.php4?ecno=3.1.27.3 3.1.27.3] </span> |
|GENE= RNTA ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=5062 Aspergillus oryzae]) | |GENE= RNTA ([http://www.ncbi.nlm.nih.gov/Taxonomy/Browser/wwwtax.cgi?mode=Info&srchmode=5&id=5062 Aspergillus oryzae]) | ||
+ | |DOMAIN= | ||
+ | |RELATEDENTRY= | ||
+ | |RESOURCES=<span class='plainlinks'>[http://oca.weizmann.ac.il/oca-docs/fgij/fg.htm?mol=1q9e FirstGlance], [http://oca.weizmann.ac.il/oca-bin/ocaids?id=1q9e OCA], [http://www.ebi.ac.uk/pdbsum/1q9e PDBsum], [http://www.rcsb.org/pdb/explore.do?structureId=1q9e RCSB]</span> | ||
}} | }} | ||
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[[Category: Straeter, N.]] | [[Category: Straeter, N.]] | ||
[[Category: Struhalla, M.]] | [[Category: Struhalla, M.]] | ||
- | [[Category: TRS]] | ||
[[Category: adenine specificity]] | [[Category: adenine specificity]] | ||
[[Category: hydrolase]] | [[Category: hydrolase]] | ||
[[Category: ribonuclease]] | [[Category: ribonuclease]] | ||
- | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on | + | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Sun Mar 30 23:10:37 2008'' |
Revision as of 20:10, 30 March 2008
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, resolution 1.70Å | |||||||
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Ligands: | |||||||
Gene: | RNTA (Aspergillus oryzae) | ||||||
Activity: | Ribonuclease T(1), with EC number 3.1.27.3 | ||||||
Resources: | FirstGlance, OCA, PDBsum, RCSB | ||||||
Coordinates: | save as pdb, mmCIF, xml |
RNase T1 variant with adenine specificity
Overview
Attempts to alter the guanine specificity of ribonuclease T1 (RNase T1) by rational or random mutagenesis have failed so far. The RNase T1 variant RV (Lys41Glu, Tyr42Phe, Asn43Arg, Tyr45Trp, and Glu46Asn) designed by combination of a random and a rational mutagenesis approach, however, exhibits a stronger preference toward adenosine residues than wild-type RNase T1. Steady state kinetics of the cleavage reaction of the two dinucleoside phosphate substrates adenylyl-3',5'-cytidine and guanylyl-3',5'-cytidine revealed that the ApC/GpC ratio of the specificity coefficient (k(cat)/K(m)) was increased approximately 7250-fold compared to that of the wild-type. The crystal structure of the nucleotide-free RV variant has been refined in space group P6(1) to a crystallographic R-factor of 19.9% at 1.7 A resolution. The primary recognition site of the RV variant adopts a similar conformation as already known from crystal structures of RNase T1 not complexed to any nucleotide. Noteworthy is a high flexibility of Trp45 and Asn46 within the three individual molecules in the asymmetric unit. In addition to the kinetic studies, these data indicate the participation of Asn46 in the specific recognition of the base and therefore a specific binding of adenosine.
About this Structure
1Q9E is a Single protein structure of sequence from Aspergillus oryzae. Full crystallographic information is available from OCA.
Reference
RNase T1 variant RV cleaves single-stranded RNA after purines due to specific recognition by the Asn46 side chain amide., Czaja R, Struhalla M, Hoschler K, Saenger W, Strater N, Hahn U, Biochemistry. 2004 Mar 16;43(10):2854-62. PMID:15005620
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