CATH Classification
| Level | CATH Code | Description | 
|---|---|---|
|   | 1 | Mainly Alpha | 
|   | 1.10 | Orthogonal Bundle | 
|   | 1.10.620 | Ribonucleotide Reductase, subunit A | 
|   | 1.10.620.20 | Ribonucleotide Reductase, subunit A | 
Domain Context
CATH Clusters
| Superfamily | Ribonucleotide Reductase, subunit A | 
| Functional Family | Ribonucleotide reductase subunit | 
Enzyme Information
| 1.17.4.1 | Ribonucleoside-diphosphate reductase. based on mapping to UniProt P09938 2'-deoxyribonucleoside diphosphate + thioredoxin disulfide + H(2)O = ribonucleoside diphosphate + thioredoxin. -!- This enzyme is responsible for the de novo conversion of ribonucleoside diphosphates into deoxyribonucleoside diphosphates, which are essential for DNA synthesis and repair. -!- There are three types of this enzyme differing in their cofactors. -!- Class Ia enzymes contain a diiron(III)-tyrosyl radical, class Ib enzymes contain a dimanganese-tyrosyl radical, and class II enzymes contain adenosylcobalamin. -!- In all cases the cofactors are involved in generation of a transient thiyl (sulfanyl) radical on a cysteine residue, which attacks the substrate, forming a ribonucleotide 3'-radical, followed by water loss to form a ketyl (alpha-oxoalkyl) radical. -!- The ketyl radical is reduced to 3'-keto-deoxynucleotide concomitant with formation of a disulfide anion radical between two cysteine residues. -!- A proton-coupled electron-transfer from the disulfide radical to the substrate generates a 3'-deoxynucleotide radical, and the the final product is formed when the hydrogen atom that was initially removed from the 3'-position of the nucleotide by the thiyl radical is returned to the same position. -!- The disulfide bridge is reduced by the action of thioredoxin. -!- Cf. EC 1.1.98.6 and EC 1.17.4.2. | 
UniProtKB Entries (1)
| P09938 | RIR2_YEAST Saccharomyces cerevisiae S288C Ribonucleoside-diphosphate reductase small chain 1 | 
PDB Structure
| PDB | 1SMQ | 
| External Links | |
| Method | X-RAY DIFFRACTION | 
| Organism | Escherichia | 
| Primary Citation | Structures of the yeast ribonucleotide reductase Rnr2 and Rnr4 homodimers. Biochemistry | 
