Absorption
Allergenic properties
Alternative products
Biotechnological use
Catalytic activity
Caution
Cofactor
Developmental stage
Disruption phenotype
Domain
Enzyme regulation
Erroneous gene model prediction
Erroneous initiation
Erroneous termination
Erroneous translation
Frameshift
Function
Induction
Involvement in disease
Kinetics
Mass spectrometry
Miscellaneous
Pathway
Pharmaceutical use
Polymorphism
Post-translational modification
RNA editing
Redox potential
Sequence caution
Sequence similarities
Subcellular location
Subunit structure
Temperature dependence
Tissue specificity
Toxic dose
pH dependence
Sequence annotation (Features)
Active site Alternative sequence Beta strand Binding site Calcium binding Chain Coiled coil Compositional bias Cross-link DNA binding Disulfide bond Domain Glycosylation Helix Initiator methionine Intramembrane Lipidation Metal binding Modified residue Motif Mutagenesis Natural variant Non-adjacent residues Non-standard residue Non-terminal residue Nucleotide binding Peptide Propeptide Region Repeat Sequence conflict Sequence uncertainty Signal peptide Site Topological domain Transit peptide Transmembrane Turn Zinc finger
Taxon ID
any
Superkingdom
Kingdom
Subkingdom
Superphylum
Phylum
Subphylum
Superclass
Class
Subclass
Infraclass
Superorder
Order
Suborder
Infraorder
Parvorder
Superfamily
Family
Subfamily
Tribe
Subtribe
Genus
Subgenus
Species group
Species subgroup
Species
Subspecies
Varietas
Forma
Ribonucleotide reductase M2 B (TP53 inducible), isoform CRA_c (cDNA FLJ52060, highly similar to Ribonucleoside-diphosphate reductase M2 subunit B (EC 1.17.4.1))
