{
    "uniprot_canonical_ac": "P09938-1",
    "uniprot_ac": "P09938",
    "uniprot_id": "RIR2_YEAST",
    "mass": {
        "chemical_mass": 46147.0,
        "monoisotopic_mass": 46147.0
    },
    "refseq": {
        "ac": "NP_012508",
        "name": "ribonucleotide-diphosphate reductase subunit RNR2",
        "summary": "",
        "url": "https://www.ncbi.nlm.nih.gov/protein/NP_012508"
    },
    "gene_names": [
        {
            "name": "RNR2",
            "resource": "UniProtKB",
            "type": "recommended",
            "url": "https://www.uniprot.org/uniprot/P09938",
            "id": "P09938"
        },
        {
            "name": "CRT6",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_012508",
            "id": "NP_012508"
        },
        {
            "name": "CRT6",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/P09938",
            "id": "P09938"
        },
        {
            "name": "J1271",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "https://www.uniprot.org/uniprot/P09938",
            "id": "P09938"
        },
        {
            "name": "RNR2",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_012508",
            "id": "NP_012508"
        }
    ],
    "protein_names": [
        {
            "name": "Ribonucleoside-diphosphate reductase small chain 1",
            "resource": "UniProtKB",
            "type": "recommended",
            "url": "",
            "id": "P09938"
        },
        {
            "name": "1.17.4.1",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "",
            "id": "P09938"
        },
        {
            "name": "Ribonucleotide reductase R2 subunit 1",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "",
            "id": "P09938"
        },
        {
            "name": "Ribonucleotide reductase small subunit 1",
            "resource": "UniProtKB",
            "type": "synonym",
            "url": "",
            "id": "P09938"
        },
        {
            "name": "ribonucleotide-diphosphate reductase subunit RNR2",
            "resource": "RefSeq",
            "type": "synonym",
            "url": "https://www.ncbi.nlm.nih.gov/protein/NP_012508",
            "id": "NP_012508"
        }
    ],
    "function": [
        {
            "annotation": "Provides the precursors necessary for DNA synthesis. Catalyzes the biosynthesis of deoxyribonucleotides from the corresponding ribonucleotides. RNR2 provides the diiron-tyrosyl radical center.",
            "evidence": [
                {
                    "database": "UniProtKB",
                    "id": "P09938",
                    "url": "https://www.uniprot.org/uniprot/P09938#function"
                },
                {
                    "database": "PubMed",
                    "id": "10535923",
                    "url": "https://glygen.org/publication/PubMed/10535923"
                }
            ]
        }
    ],
    "disease": [
        {
            "disease_id": "DOID:0070331",
            "recommended_name": {
                "id": "DOID:0070331",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:0070331",
                "name": "mitochondrial DNA depletion syndrome 8b",
                "description": "A mitochondrial DNA depletion syndrome that is characterized by ophthalmoplegia, ptosis, gastrointestinal dysmotility, cachexia, peripheral neuropathy, and brain MRI changes, known as the MNGIE phenotype, and has_material_basis_in autosomal recessive homozygous or compound heterozygous mutation in the ribonucleotide reductase M2 B gene on chromosome 8q22."
            },
            "synonyms": [
                {
                    "id": "DOID:0070331",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0070331",
                    "name": "mitochondrial neurogastrointestinal encephalopathy syndrome, RRM2B-related",
                    "description": ""
                }
            ],
            "evidence": [
                {
                    "id": "0070331",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:0070331"
                }
            ]
        },
        {
            "disease_id": "DOID:0080127",
            "recommended_name": {
                "id": "DOID:0080127",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:0080127",
                "name": "mitochondrial DNA depletion syndrome 8a",
                "description": "A mitochondrial DNA depletion syndrome that is characterized by neonatal hypotonia, lactic acidosis, and neurologic deterioration, and has_material_basis_in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the ribonucleotide reductase regulatory TP53 inducible subunit M2B gene on chromosome 8q22."
            },
            "synonyms": [
                {
                    "id": "DOID:0080127",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0080127",
                    "name": "RRM2B-related mitochondrial DNA depletion syndrome, encephalomyopathic form with renal tubulopathy",
                    "description": ""
                },
                {
                    "id": "MONDO:0012792",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012792",
                    "name": "mitochondrial DNA depletion syndrome 8a",
                    "description": "Any mitochondrial DNA depletion syndrome in which the cause of the disease is a mutation in the RRM2B gene."
                },
                {
                    "id": "MONDO:0012792",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012792",
                    "name": "RRM2B mitochondrial DNA depletion syndrome",
                    "description": ""
                },
                {
                    "id": "MONDO:0012792",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012792",
                    "name": "mitochondrial DNA depletion syndrome caused by mutation in RRM2B",
                    "description": ""
                },
                {
                    "id": "MONDO:0012792",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012792",
                    "name": "mitochondrial DNA depletion syndrome type 8a",
                    "description": ""
                },
                {
                    "id": "MONDO:0012792",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012792",
                    "name": "mtDNA depletion syndrome, encephalomyopathic form with renal tubulopathy",
                    "description": ""
                },
                {
                    "id": "MONDO:0012792",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012792",
                    "name": "MTDPS8A",
                    "description": ""
                },
                {
                    "id": "MONDO:0012792",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012792",
                    "name": "Mngie, Rrm2B-related",
                    "description": ""
                },
                {
                    "id": "MONDO:0012792",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012792",
                    "name": "RRM2B-related mitochondrial DNA depletion syndrome",
                    "description": ""
                },
                {
                    "id": "MONDO:0012792",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012792",
                    "name": "encephalomyopathic type with renal tubulopathy",
                    "description": ""
                },
                {
                    "id": "MONDO:0012792",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012792",
                    "name": "mitochondrial DNA depletion syndrome 8A (encephalomyopathic type with renal tubulopathy)",
                    "description": ""
                },
                {
                    "id": "MONDO:0012792",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012792",
                    "name": "mitochondrial DNA depletion syndrome 8B (Mngie type)",
                    "description": ""
                },
                {
                    "id": "MONDO:0012792",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012792",
                    "name": "mitochondrial DNA depletion syndrome, encephalomyopathic form with renal tubulopathy",
                    "description": ""
                },
                {
                    "id": "MONDO:0012792",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012792",
                    "name": "mitochondrial DNA depletion syndrome, encephalomyopathic, with renal tubulopathy, autosomal recessive",
                    "description": ""
                },
                {
                    "id": "MONDO:0012792",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0012792",
                    "name": "mitochondrial neurogastrointestinal encephalopathy syndrome, Rrm2B-related",
                    "description": ""
                },
                {
                    "id": "MIM:612075",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/612075",
                    "name": "Mitochondrial DNA depletion syndrome 8A",
                    "description": "Mitochondrial DNA depletion syndrome 8A"
                }
            ],
            "evidence": [
                {
                    "id": "0080127",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:0080127"
                }
            ]
        },
        {
            "disease_id": "DOID:0111518",
            "recommended_name": {
                "id": "DOID:0111518",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:0111518",
                "name": "autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 5",
                "description": "A chronic progressive external ophthalmoplegia that has_material_basis_in heterozygous mutation in the RRM2B gene on chromosome 8q22.3."
            },
            "synonyms": [
                {
                    "id": "DOID:0111518",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0111518",
                    "name": "autosomal dominant progressive external ophthalmoplegia 5",
                    "description": ""
                },
                {
                    "id": "DOID:0111518",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:0111518",
                    "name": "PEOA5",
                    "description": ""
                },
                {
                    "id": "MONDO:0013117",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013117",
                    "name": "progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 5",
                    "description": "Any progressive external ophthalmoplegia with mitochondrial DNA deletions in which the cause of the disease is a mutation in the RRM2B gene."
                },
                {
                    "id": "MONDO:0013117",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013117",
                    "name": "RRM2B progressive external ophthalmoplegia with mitochondrial DNA deletions",
                    "description": ""
                },
                {
                    "id": "MONDO:0013117",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013117",
                    "name": "progressive external ophthalmoplegia with mitochondrial DNA deletions caused by mutation in RRM2B",
                    "description": ""
                },
                {
                    "id": "MONDO:0013117",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013117",
                    "name": "progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant 5",
                    "description": ""
                },
                {
                    "id": "MONDO:0013117",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013117",
                    "name": "progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant type 5",
                    "description": ""
                },
                {
                    "id": "MONDO:0013117",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013117",
                    "name": "PEOA5",
                    "description": ""
                },
                {
                    "id": "MONDO:0013117",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0013117",
                    "name": "progressive external ophthalmoplegia, autosomal dominant 5",
                    "description": ""
                },
                {
                    "id": "MIM:613077",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/613077",
                    "name": "Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant, 5",
                    "description": "Progressive external ophthalmoplegia with mitochondrial DNA deletions, autosomal dominant, 5"
                }
            ],
            "evidence": [
                {
                    "id": "0111518",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:0111518"
                }
            ]
        },
        {
            "disease_id": "DOID:11054",
            "recommended_name": {
                "id": "DOID:11054",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:11054",
                "name": "urinary bladder cancer",
                "description": "An urinary system cancer that results_in malignant growth located_in the urinary bladder."
            },
            "synonyms": [
                {
                    "id": "DOID:11054",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:11054",
                    "name": "bladder cancer",
                    "description": ""
                },
                {
                    "id": "DOID:11054",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:11054",
                    "name": "tumor of the bladder",
                    "description": ""
                },
                {
                    "id": "MONDO:0001187",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                    "name": "urinary bladder cancer",
                    "description": "A primary or metastatic malignant neoplasm involving the bladder."
                },
                {
                    "id": "MONDO:0001187",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                    "name": "tumor of the bladder",
                    "description": ""
                },
                {
                    "id": "MONDO:0001187",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                    "name": "tumour of the bladder",
                    "description": ""
                },
                {
                    "id": "MONDO:0001187",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                    "name": "bladder cancer, somatic",
                    "description": ""
                },
                {
                    "id": "MONDO:0001187",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                    "name": "cancer of urinary bladder",
                    "description": ""
                },
                {
                    "id": "MONDO:0001187",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                    "name": "malignant bladder neoplasm",
                    "description": ""
                },
                {
                    "id": "MONDO:0001187",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                    "name": "malignant bladder tumor",
                    "description": ""
                },
                {
                    "id": "MONDO:0001187",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                    "name": "malignant bladder tumour",
                    "description": ""
                },
                {
                    "id": "MONDO:0001187",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                    "name": "malignant neoplasm of bladder",
                    "description": ""
                },
                {
                    "id": "MONDO:0001187",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                    "name": "malignant neoplasm of the bladder",
                    "description": ""
                },
                {
                    "id": "MONDO:0001187",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                    "name": "malignant neoplasm of the urinary bladder",
                    "description": ""
                },
                {
                    "id": "MONDO:0001187",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                    "name": "malignant neoplasm of urinary bladder",
                    "description": ""
                },
                {
                    "id": "MONDO:0001187",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                    "name": "malignant neoplasm, bladder",
                    "description": ""
                },
                {
                    "id": "MONDO:0001187",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                    "name": "malignant neoplasm, urinary bladder",
                    "description": ""
                },
                {
                    "id": "MONDO:0001187",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                    "name": "malignant tumor of bladder",
                    "description": ""
                },
                {
                    "id": "MONDO:0001187",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                    "name": "malignant tumor of the bladder",
                    "description": ""
                },
                {
                    "id": "MONDO:0001187",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                    "name": "malignant tumor of the urinary bladder",
                    "description": ""
                },
                {
                    "id": "MONDO:0001187",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                    "name": "malignant tumor of urinary bladder",
                    "description": ""
                },
                {
                    "id": "MONDO:0001187",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                    "name": "malignant tumor, urinary bladder",
                    "description": ""
                },
                {
                    "id": "MONDO:0001187",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                    "name": "malignant tumour of bladder",
                    "description": ""
                },
                {
                    "id": "MONDO:0001187",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                    "name": "malignant tumour of the bladder",
                    "description": ""
                },
                {
                    "id": "MONDO:0001187",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                    "name": "malignant tumour of the urinary bladder",
                    "description": ""
                },
                {
                    "id": "MONDO:0001187",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                    "name": "malignant tumour of urinary bladder",
                    "description": ""
                },
                {
                    "id": "MONDO:0001187",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                    "name": "malignant urinary bladder neoplasm",
                    "description": ""
                },
                {
                    "id": "MONDO:0001187",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                    "name": "malignant urinary bladder tumor",
                    "description": ""
                },
                {
                    "id": "MONDO:0001187",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                    "name": "malignant urinary bladder tumour",
                    "description": ""
                },
                {
                    "id": "MONDO:0001187",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                    "name": "urinary bladder cancer",
                    "description": ""
                },
                {
                    "id": "MONDO:0001187",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                    "name": "urinary bladder malignant neoplasm",
                    "description": ""
                },
                {
                    "id": "MONDO:0001187",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                    "name": "urinary bladder malignant tumor",
                    "description": ""
                },
                {
                    "id": "MONDO:0001187",
                    "resource": "MONDO",
                    "url": "https://monarchinitiative.org/disease/MONDO:0001187",
                    "name": "urinary bladder malignant tumour",
                    "description": ""
                },
                {
                    "id": "MIM:109800",
                    "resource": "MIM",
                    "url": "https://www.omim.org/entry/109800",
                    "name": "Bladder cancer",
                    "description": "Bladder cancer"
                }
            ],
            "evidence": [
                {
                    "id": "11054",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:11054"
                }
            ]
        },
        {
            "disease_id": "DOID:1793",
            "recommended_name": {
                "id": "DOID:1793",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:1793",
                "name": "pancreatic cancer",
                "description": "An endocrine gland cancer located_in the pancreas."
            },
            "synonyms": [
                {
                    "id": "DOID:1793",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:1793",
                    "name": "Ca body of pancreas",
                    "description": ""
                },
                {
                    "id": "DOID:1793",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:1793",
                    "name": "Ca head of pancreas",
                    "description": ""
                },
                {
                    "id": "DOID:1793",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:1793",
                    "name": "Ca tail of pancreas",
                    "description": ""
                },
                {
                    "id": "DOID:1793",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:1793",
                    "name": "malignant neoplasm of body of pancreas",
                    "description": ""
                },
                {
                    "id": "DOID:1793",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:1793",
                    "name": "malignant neoplasm of head of pancreas",
                    "description": ""
                },
                {
                    "id": "DOID:1793",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:1793",
                    "name": "malignant neoplasm of tail of pancreas",
                    "description": ""
                },
                {
                    "id": "DOID:1793",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:1793",
                    "name": "pancreas neoplasm",
                    "description": ""
                },
                {
                    "id": "DOID:1793",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:1793",
                    "name": "pancreatic neoplasm",
                    "description": ""
                },
                {
                    "id": "DOID:1793",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:1793",
                    "name": "pancreatic tumor",
                    "description": ""
                }
            ],
            "evidence": [
                {
                    "id": "1793",
                    "database": "Alliance of Genome Resources",
                    "url": "https://www.alliancegenome.org/disease/DOID:1793"
                }
            ]
        },
        {
            "disease_id": "DOID:2870",
            "recommended_name": {
                "id": "DOID:2870",
                "resource": "Disease Ontology",
                "url": "http://disease-ontology.org/term/DOID:2870",
                "name": "endometrial adenocarcinoma",
                "description": "An endometrial carcinoma that derives_from epithelial cells of glandular origin."
            },
            "synonyms": [
                {
                    "id": "DOID:2870",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:2870",
                    "name": "endometrial endometrioid adenocarcinoma with squamous differentiation",
                    "description": ""
                },
                {
                    "id": "DOID:2870",
                    "resource": "Disease Ontology",
                    "url": "http://disease-ontology.org/term/DOID:2870",
                    "name": "adenocarcinoma of endometrium",
                    "description": ""
                },
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        "length": 399,
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    },
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                "length": 399,
                "header": "sp|P09938-1|RIR2_YEAST Isoform 1 of Ribonucleoside-diphosphate reductase small chain 1  OS=Saccharomyces cerevisiae S288C OX=559292 GN=RNR2 PE=1 SV=2 CANONICAL=P09938-1"
            },
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                {
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                {
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                },
                {
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                {
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                },
                {
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                {
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                {
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                    "id": "23749301",
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                }
            ],
            "site_lbl": "Ser15"
        },
        {
            "start_pos": 22,
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            "kinase_uniprot_canonical_ac": "",
            "kinase_gene_name": "",
            "residue": "Ser",
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                {
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                {
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                {
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                {
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                },
                {
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                },
                {
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                {
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            ],
            "site_lbl": "Ser22"
        },
        {
            "start_pos": 24,
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            "kinase_uniprot_canonical_ac": "",
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                {
                    "database": "PubMed",
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                },
                {
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                    "url": "http://research.bioinformatics.udel.edu/iptmnet/entry/P09938"
                },
                {
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                    "url": "https://glygen.org/publication/PubMed/18407956"
                },
                {
                    "database": "SGD",
                    "id": "P09938",
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                }
            ],
            "site_lbl": "Ser24"
        },
        {
            "start_pos": 374,
            "end_pos": 374,
            "kinase_uniprot_canonical_ac": "",
            "kinase_gene_name": "",
            "residue": "Ser",
            "comment": "",
            "evidence": [
                {
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                    "id": "P09938",
                    "url": "http://research.bioinformatics.udel.edu/iptmnet/entry/P09938"
                },
                {
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                {
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                {
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            ],
            "site_lbl": "Ser374"
        },
        {
            "start_pos": 41,
            "end_pos": 41,
            "kinase_uniprot_canonical_ac": "",
            "kinase_gene_name": "",
            "residue": "Ser",
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                    "url": "https://www.uniprot.org/uniprot/P09938"
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                {
                    "database": "PubMed",
                    "id": "17287358",
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                },
                {
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                    "id": "P09938",
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                },
                {
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                },
                {
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                    "id": "18851834",
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                }
            ],
            "site_lbl": "Ser41"
        },
        {
            "start_pos": 7,
            "end_pos": 7,
            "kinase_uniprot_canonical_ac": "",
            "kinase_gene_name": "",
            "residue": "Ser",
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                {
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                },
                {
                    "database": "PubMed",
                    "id": "18407956",
                    "url": "https://glygen.org/publication/PubMed/18407956"
                }
            ],
            "site_lbl": "Ser7"
        }
    ],
    "glycation": [],
    "keywords": [
        "enzyme"
    ],
    "publication": [
        {
            "title": "Purification of ribonucleotide reductase subunits Y1, Y2, Y3, and Y4 from yeast: Y4 plays a key role in diiron cluster assembly.",
            "journal": "Proc. Natl. Acad. Sci. U.S.A.",
            "date": "1999",
            "authors": "Ge J., Nguyen H.-H.T., Perlstein D.L., Stubbe J.",
            "evidence": [
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                    "url": "https://www.uniprot.org/uniprot/P09938"
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            ],
            "reference": [
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                    "type": "PubMed",
                    "id": "10535923",
                    "url": "https://glygen.org/publication/PubMed/10535923"
                }
            ]
        },
        {
            "title": "Yeast ribonucleotide reductase has a heterodimeric iron-radical-containing subunit.",
            "journal": "Proc. Natl. Acad. Sci. U.S.A.",
            "date": "2000",
            "authors": "Graeslund A., Liu A., Thelander L., Larsson G., Chabes A., Wijmenga S., Domkin V.",
            "evidence": [
                {
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                    "url": "https://www.uniprot.org/uniprot/P09938"
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            ],
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                    "type": "PubMed",
                    "id": "10716984",
                    "url": "https://glygen.org/publication/PubMed/10716984"
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            ]
        },
        {
            "title": "Structure of the yeast ribonucleotide reductase Y2Y4 heterodimer.",
            "journal": "Proc. Natl. Acad. Sci. U.S.A.",
            "date": "2001",
            "authors": "Ge J., Voegtli W.C., Rosenzweig A.C., Perlstein D.L., Stubbe J.",
            "evidence": [
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                    "id": "P09938",
                    "url": "https://www.uniprot.org/uniprot/P09938"
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            ],
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                {
                    "type": "PubMed",
                    "id": "11526233",
                    "url": "https://glygen.org/publication/PubMed/11526233"
                }
            ]
        },
        {
            "title": "Subcellular localization of yeast ribonucleotide reductase regulated by the DNA replication and damage checkpoint pathways.",
            "journal": "Proc. Natl. Acad. Sci. U.S.A.",
            "date": "2003",
            "authors": "Huang M., Zhang Z., An X., Yao R., Perlstein D.L., Stubbe J., Bucci B.",
            "evidence": [
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                    "id": "P09938",
                    "url": "https://www.uniprot.org/uniprot/P09938"
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            "reference": [
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                    "type": "PubMed",
                    "id": "12732713",
                    "url": "https://glygen.org/publication/PubMed/12732713"
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            ]
        },
        {
            "title": "Global analysis of protein expression in yeast.",
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            "end_pos": 361,
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            "cellular_location": "",
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                }
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                }
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            "name": "homologset.oma",
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}
