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    {
        "title": "Differential interaction of the tyrosine phosphatases PTP-SL, STEP and HePTP with the mitogen-activated protein kinases ERK1/2 and p38alpha is determined by a kinase specificity sequence and influenced by reducing agents.",
        "journal": "The Biochemical journal",
        "date": "2003",
        "authors": "Munoz JJ, Tarrega C, Blanco-Aparicio C, Pulido R",
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                "uniprot_canonical_ac": "P28562-1",
                "protein_name": "Dual specificity protein phosphatase 1",
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                "uniprot_canonical_ac": "P30086-1",
                "protein_name": "Phosphatidylethanolamine-binding protein 1",
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                "uniprot_canonical_ac": "P53778-1",
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    {
        "title": "Loss-of-function mutations in FGFR1 cause autosomal dominant Kallmann syndrome.",
        "journal": "Nature genetics",
        "date": "2003",
        "authors": "Dode C, Levilliers J, Dupont JM, De Paepe A, Le Du N, Soussi-Yanicostas N, Coimbra RS, Delmaghani S, Compain-Nouaille S, Baverel F, Pecheux C, Le Tessier D, Cruaud C, Delpech M, Speleman F, Vermeulen S, Amalfitano A, Bachelot Y, Bouchard P, Cabrol S, Carel JC, Delemarre-van de Waal H, Goulet-Salmon B, Kottler ML, Richard O, Sanchez-Franco F, Saura R, Young J, Petit C, Hardelin JP",
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                            "name": "hypogonadotropic hypogonadism 7 with or without anosmia",
                            "description": "A hypogonadotropic hypogonadism that has_material_basis_in homozygous or compound heterozygous mutation in the GNRHR gene on chromosome 4q13, sometimes in association with mutation in another gene. No patients with anosmia have been reported."
                        },
                        "synonyms": [
                            {
                                "id": "MONDO:0007794",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007794",
                                "name": "hypogonadotropic hypogonadism 7 with or without anosmia",
                                "description": "A hypogonadotropic hypogonadism that has material basis in homozygous or compound heterozygous mutation in the GNRHR gene on chromosome 4q13, sometimes in association with mutation in another gene. No patients with anosmia have been reported."
                            },
                            {
                                "id": "MONDO:0007794",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007794",
                                "name": "hypogonadotropic hypogonadism 7 with or without anosmia",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007794",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007794",
                                "name": "hypogonadotropic hypogonadism 7 without anosmia",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007794",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007794",
                                "name": "HH7",
                                "description": ""
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                                "id": "MIM:146110",
                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/146110",
                                "name": "Hypogonadotropic hypogonadism 7 with or without anosmia",
                                "description": "Hypogonadotropic hypogonadism 7 with or without anosmia"
                            }
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                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:14705",
                            "name": "Pfeiffer syndrome",
                            "description": "An acrocephalosyndactylia that has_material_basis_in mutations in the FGFR1 and FGFR2 gene which results_in premature fusion located_in skull."
                        },
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                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:14705",
                                "name": "acrocephalosyndactylia type V",
                                "description": ""
                            },
                            {
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                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007043",
                                "name": "Pfeiffer syndrome",
                                "description": "Pfeiffer syndrome (PS) is a common form of acrocephalosyndactyly, a group of inherited congenital malformation disorders, characterized by variable degrees of bicoronal craniosynostosis, variable hand and foot malformations and various other associated manifestations."
                            },
                            {
                                "id": "MONDO:0007043",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007043",
                                "name": "ACS5",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007043",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007043",
                                "name": "Pfeiffer syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007043",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007043",
                                "name": "acrocephalosyndactyly type 5",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007043",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007043",
                                "name": "acrocephalosyndactyly type V",
                                "description": ""
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                            {
                                "id": "MONDO:0007043",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007043",
                                "name": "type V Acrocephalosyndactyly",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007043",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007043",
                                "name": "Noack syndrome",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007043",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007043",
                                "name": "Pfeiffer type acrocephalosyndactyly",
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                            {
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                                "resource": "MIM",
                                "url": "https://www.omim.org/entry/101600",
                                "name": "Pfeiffer syndrome",
                                "description": "Pfeiffer syndrome"
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                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0090070",
                                "name": "congenital idiopathic hypogonadotropic hypogonadism",
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                            },
                            {
                                "id": "DOID:0090070",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0090070",
                                "name": "isolated congenital gonadotropin deficiency",
                                "description": ""
                            },
                            {
                                "id": "DOID:0090070",
                                "resource": "Disease Ontology",
                                "url": "https://disease-ontology.org/term/DOID:0090070",
                                "name": "hypogonadotropism",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007844",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007844",
                                "name": "hypogonadotropic hypogonadism 2 with or without anosmia",
                                "description": "Any hypogonadotropic hypogonadism in which the cause of the disease is a mutation in the FGFR1 gene."
                            },
                            {
                                "id": "MONDO:0007844",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007844",
                                "name": "FGFR1 hypogonadotropic hypogonadism",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007844",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007844",
                                "name": "hypogonadotropic hypogonadism 2 with or without anosmia",
                                "description": ""
                            },
                            {
                                "id": "MONDO:0007844",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007844",
                                "name": "hypogonadotropic hypogonadism caused by mutation in FGFR1",
                                "description": ""
                            },
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                                "id": "MONDO:0007844",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007844",
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                            },
                            {
                                "id": "MONDO:0007844",
                                "resource": "MONDO",
                                "url": "https://monarchinitiative.org/disease/MONDO:0007844",
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                                "url": "https://www.omim.org/entry/147950",
                                "name": "Hypogonadotropic hypogonadism 2 with or without anosmia",
                                "description": "Hypogonadotropic hypogonadism 2 with or without anosmia"
                            }
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                            "resource": "Disease Ontology",
                            "url": "https://disease-ontology.org/term/DOID:0090083",
                            "name": "hypogonadotropic hypogonadism 2 with or without anosmia",
                            "description": "A hypogonadotropic hypogonadism that has_material_basis_in heterozygous mutation in the FGFR1 gene on chromosome 8p11, sometimes in association with mutation in other genes."
                        },
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                                "url": "https://monarchinitiative.org/disease/MONDO:0007844",
                                "name": "hypogonadotropic hypogonadism 2 with or without anosmia",
                                "description": "Any hypogonadotropic hypogonadism in which the cause of the disease is a mutation in the FGFR1 gene."
                            },
                            {
                                "id": "MONDO:0007844",
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                                "url": "https://monarchinitiative.org/disease/MONDO:0007844",
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                            {
                                "id": "MONDO:0007844",
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                                "url": "https://monarchinitiative.org/disease/MONDO:0007844",
                                "name": "hypogonadotropic hypogonadism 2 with or without anosmia",
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                            {
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                                "url": "https://monarchinitiative.org/disease/MONDO:0007844",
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    {
        "title": "Trk receptors: roles in neuronal signal transduction.",
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        "authors": "Huang EJ, Reichardt LF",
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        "title": "Phosphorylation of Grb10 by mitogen-activated protein kinase: identification of Ser150 and Ser476 of human Grb10zeta as major phosphorylation sites.",
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        "title": "Identification of a selective ERK inhibitor and structural determination of the inhibitor-ERK2 complex.",
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        "authors": "Ohori Makoto, Kinoshita Takayoshi, Okubo Mitsuru, Sato Kentaro, Yamazaki Akiko, Arakawa Hiroyuki, Nishimura Shintaro, Inamura Noriaki, Nakajima Hidenori, Neya Masahiro, Miyake Hiroshi, Fujii Takashi",
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            {
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        ],
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                "name": "Homo sapiens",
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                    {
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                ],
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                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
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        ],
        "record_id": "pubmed.16764984",
        "abstract": "",
        "glycosylation": [],
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    },
    {
        "title": "Regulation of the Raf-MEK-ERK pathway by protein phosphatase 5.",
        "journal": "Nature cell biology",
        "date": "2006",
        "authors": "von Kriegsheim A, Pitt A, Grindlay GJ, Kolch W, Dhillon AS",
        "reference": {
            "type": "PubMed",
            "id": "16892053",
            "url": "https://pubmed.ncbi.nlm.nih.gov/16892053"
        },
        "referenced_glycans": [],
        "referenced_proteins": [
            {
                "uniprot_canonical_ac": "P28482-1",
                "protein_name": "Mitogen-activated protein kinase 1",
                "gene_name": "MAPK1",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P01112-1",
                "protein_name": "GTPase HRas",
                "gene_name": "HRAS",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P01111-1",
                "protein_name": "GTPase NRas",
                "gene_name": "NRAS",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q6TCH7-1",
                "protein_name": "Progestin and adipoQ receptor family member 3",
                "gene_name": "PAQR3",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P62714-1",
                "protein_name": "Serine/threonine-protein phosphatase 2A catalytic subunit beta isoform",
                "gene_name": "PPP2CB",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9Y6W6-1",
                "protein_name": "Dual specificity protein phosphatase 10",
                "gene_name": "DUSP10",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q16829-1",
                "protein_name": "Dual specificity protein phosphatase 7",
                "gene_name": "DUSP7",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P28562-1",
                "protein_name": "Dual specificity protein phosphatase 1",
                "gene_name": "DUSP1",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P30086-1",
                "protein_name": "Phosphatidylethanolamine-binding protein 1",
                "gene_name": "PEBP1",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P53778-1",
                "protein_name": "Mitogen-activated protein kinase 12",
                "gene_name": "MAPK12",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q05923-1",
                "protein_name": "Dual specificity protein phosphatase 2",
                "gene_name": "DUSP2",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q16690-1",
                "protein_name": "Dual specificity protein phosphatase 5",
                "gene_name": "DUSP5",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P53042-1",
                "protein_name": "Serine/threonine-protein phosphatase 5",
                "gene_name": "Ppp5c",
                "tax_name": "Rat"
            },
            {
                "uniprot_canonical_ac": "Q16537-1",
                "protein_name": "Serine/threonine-protein phosphatase 2A 56 kDa regulatory subunit epsilon isoform",
                "gene_name": "PPP2R5E",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q15172-1",
                "protein_name": "Serine/threonine-protein phosphatase 2A 56 kDa regulatory subunit alpha isoform",
                "gene_name": "PPP2R5A",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P53041-1",
                "protein_name": "Serine/threonine-protein phosphatase 5",
                "gene_name": "PPP5C",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q7Z569-1",
                "protein_name": "BRCA1-associated protein",
                "gene_name": "BRAP",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P62979-1",
                "protein_name": "Ubiquitin-ribosomal protein eS31 fusion protein",
                "gene_name": "RPS27A",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q8IVT5-1",
                "protein_name": "Kinase suppressor of Ras 1",
                "gene_name": "KSR1",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P35236-1",
                "protein_name": "Tyrosine-protein phosphatase non-receptor type 7",
                "gene_name": "PTPN7",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P0CG47-1",
                "protein_name": "Polyubiquitin-B",
                "gene_name": "UBB",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P27361-1",
                "protein_name": "Mitogen-activated protein kinase 3",
                "gene_name": "MAPK3",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P62987-1",
                "protein_name": "Ubiquitin-ribosomal protein eL40 fusion protein",
                "gene_name": "UBA52",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q13202-1",
                "protein_name": "Dual specificity protein phosphatase 8",
                "gene_name": "DUSP8",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q9BY84-1",
                "protein_name": "Dual specificity protein phosphatase 16",
                "gene_name": "DUSP16",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q13115-1",
                "protein_name": "Dual specificity protein phosphatase 4",
                "gene_name": "DUSP4",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q16828-1",
                "protein_name": "Dual specificity protein phosphatase 6",
                "gene_name": "DUSP6",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q99956-1",
                "protein_name": "Dual specificity protein phosphatase 9",
                "gene_name": "DUSP9",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P15056-1",
                "protein_name": "Serine/threonine-protein kinase B-raf",
                "gene_name": "BRAF",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P04049-1",
                "protein_name": "RAF proto-oncogene serine/threonine-protein kinase",
                "gene_name": "RAF1",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P31946-1",
                "protein_name": "14-3-3 protein beta/alpha",
                "gene_name": "YWHAB",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P10398-1",
                "protein_name": "Serine/threonine-protein kinase A-Raf",
                "gene_name": "ARAF",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P26045-1",
                "protein_name": "Tyrosine-protein phosphatase non-receptor type 3",
                "gene_name": "PTPN3",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P27448-5",
                "protein_name": "MAP/microtubule affinity-regulating kinase 3",
                "gene_name": "MARK3",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P0CG48-1",
                "protein_name": "Polyubiquitin-C",
                "gene_name": "UBC",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P30154-1",
                "protein_name": "Serine/threonine-protein phosphatase 2A 65 kDa regulatory subunit A beta isoform",
                "gene_name": "PPP2R1B",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P30153-1",
                "protein_name": "Serine/threonine-protein phosphatase 2A 65 kDa regulatory subunit A alpha isoform",
                "gene_name": "PPP2R1A",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P67775-1",
                "protein_name": "Serine/threonine-protein phosphatase 2A catalytic subunit alpha isoform",
                "gene_name": "PPP2CA",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q14738-1",
                "protein_name": "Serine/threonine-protein phosphatase 2A 56 kDa regulatory subunit delta isoform",
                "gene_name": "PPP2R5D",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q13362-1",
                "protein_name": "Serine/threonine-protein phosphatase 2A 56 kDa regulatory subunit gamma isoform",
                "gene_name": "PPP2R5C",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "Q15173-1",
                "protein_name": "Serine/threonine-protein phosphatase 2A 56 kDa regulatory subunit beta isoform",
                "gene_name": "PPP2R5B",
                "tax_name": "Human"
            }
        ],
        "species": [
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                "name": "Homo sapiens",
                "taxid": 9606,
                "evidence": [
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                        "database": "UniProtKB",
                        "id": "P28482",
                        "url": "https://www.uniprot.org/uniprotkb/P28482"
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                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
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        ],
        "mutagenesis": [
            {
                "start_pos": 304,
                "end_pos": 304,
                "sequence_org": "H",
                "sequence_mut": "Q",
                "comment": "Catalytically inactive; no effect on interaction with CRY2 but increases the stability of the interaction with CSNK1E. No effect on RAF1 phosphorylation.",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P53041",
                        "url": "https://www.uniprot.org/uniprotkb/P53041"
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                    {
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                        "id": "16790549",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/16790549"
                    },
                    {
                        "database": "PubMed",
                        "id": "16892053",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/16892053"
                    },
                    {
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                        "id": "19948726",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/19948726"
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                ],
                "uniprot_canonical_ac": "P53041-1"
            },
            {
                "start_pos": 97,
                "end_pos": 97,
                "sequence_org": "K",
                "sequence_mut": "A",
                "comment": "Loss of interaction with HSP90AA1. No effect on interaction with S100A1, S100A2 and S100A6. Loss of interaction with RAF1.",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P53041",
                        "url": "https://www.uniprot.org/uniprotkb/P53041"
                    },
                    {
                        "database": "PubMed",
                        "id": "16892053",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/16892053"
                    },
                    {
                        "database": "PubMed",
                        "id": "22399290",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/22399290"
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                ],
                "uniprot_canonical_ac": "P53041-1"
            },
            {
                "start_pos": 338,
                "end_pos": 339,
                "sequence_org": "SS",
                "sequence_mut": "AA",
                "comment": "Reduced kinase activity; when associated with 340-D-D-341.",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P04049",
                        "url": "https://www.uniprot.org/uniprotkb/P04049"
                    },
                    {
                        "database": "PubMed",
                        "id": "16892053",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/16892053"
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                ],
                "uniprot_canonical_ac": "P04049-1"
            },
            {
                "start_pos": 338,
                "end_pos": 339,
                "sequence_org": "SS",
                "sequence_mut": "DE",
                "comment": "Non-inhibited by PPP5C. Constitutively active and non-inhibited by PPP5C; when associated with 340-D-D-341.",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P04049",
                        "url": "https://www.uniprot.org/uniprotkb/P04049"
                    },
                    {
                        "database": "PubMed",
                        "id": "16892053",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/16892053"
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                ],
                "uniprot_canonical_ac": "P04049-1"
            },
            {
                "start_pos": 340,
                "end_pos": 341,
                "sequence_org": "YY",
                "sequence_mut": "DD",
                "comment": "Constitutively active and highly phosphorylated on S-338, inhibited by PPP5C. Reduced kinase activity; when associated with 338-A-A-339. Constitutively active and non-inhibited by PPP5C; when associated with 338-D-E-339.",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P04049",
                        "url": "https://www.uniprot.org/uniprotkb/P04049"
                    },
                    {
                        "database": "PubMed",
                        "id": "16892053",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/16892053"
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                ],
                "uniprot_canonical_ac": "P04049-1"
            },
            {
                "start_pos": 491,
                "end_pos": 491,
                "sequence_org": "T",
                "sequence_mut": "D",
                "comment": "Increased kinase activity but can still be inhibited by PPP5C; when associated with D-494.",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P04049",
                        "url": "https://www.uniprot.org/uniprotkb/P04049"
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                    {
                        "database": "PubMed",
                        "id": "16892053",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/16892053"
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                ],
                "uniprot_canonical_ac": "P04049-1"
            },
            {
                "start_pos": 494,
                "end_pos": 494,
                "sequence_org": "S",
                "sequence_mut": "D",
                "comment": "Increased kinase activity but can still be inhibited by PPP5C; when associated with D-491.",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P04049",
                        "url": "https://www.uniprot.org/uniprotkb/P04049"
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                    {
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                        "id": "16892053",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/16892053"
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                ],
                "uniprot_canonical_ac": "P04049-1"
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                "start_pos": 259,
                "end_pos": 259,
                "kinase_uniprot_canonical_ac": "",
                "kinase_gene_name": "",
                "residue": "Ser",
                "comment": "Phosphoserine; by PKA, PKC and PKB/AKT1",
                "evidence": [
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                        "id": "P04049",
                        "url": "https://www.uniprot.org/uniprotkb/P04049"
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                    {
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                        "id": "P04049",
                        "url": "http://research.bioinformatics.udel.edu/iptmnet/entry/P04049"
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                    {
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                        "id": "10576742",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/10576742"
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                    {
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                        "id": "11971957",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/11971957"
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                    {
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                        "id": "11997508",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/11997508"
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                    {
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                        "id": "18669648",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/18669648"
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                    {
                        "database": "PubMed",
                        "id": "18691976",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/18691976"
                    },
                    {
                        "database": "PubMed",
                        "id": "18767875",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/18767875"
                    },
                    {
                        "database": "PubMed",
                        "id": "20068231",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/20068231"
                    },
                    {
                        "database": "PubMed",
                        "id": "20230923",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/20230923"
                    },
                    {
                        "database": "IntAct",
                        "id": "P04049",
                        "url": "https://www.ebi.ac.uk/intact/interactors/id:P04049*"
                    },
                    {
                        "database": "PubMed",
                        "id": "35044719",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/35044719"
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                    {
                        "database": "PRO",
                        "id": "P04049",
                        "url": "https://proconsortium.org/cgi-bin/entry_pro?id=P04049"
                    },
                    {
                        "database": "PubMed",
                        "id": "14688280",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/14688280"
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                    {
                        "database": "PubMed",
                        "id": "10801873",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/10801873"
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                    {
                        "database": "PubMed",
                        "id": "11041243",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/11041243"
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                    {
                        "database": "PubMed",
                        "id": "11341776",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/11341776"
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                    {
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                        "count": 0
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                        "field": "o_linked_glycan_sites",
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                        "field": "n_linked_glycans",
                        "count": 0
                    },
                    {
                        "field": "o_linked_glycans",
                        "count": 0
                    }
                ],
                "sort_fields": []
            },
            {
                "table_id": "phosphorylation",
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                    {
                        "field": "total",
                        "count": 2
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                    {
                        "field": "total_sites",
                        "count": 2
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                ],
                "sort_fields": [
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                "table_id": "glycosylation_reported",
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                        "field": "total",
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                        "field": "total_sites",
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                        "field": "n_linked_sites",
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                        "field": "o_linked_sites",
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                        "field": "n_linked_glycan_sites",
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                    },
                    {
                        "field": "o_linked_glycan_sites",
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                    },
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                        "field": "n_linked_glycans",
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                    {
                        "field": "o_linked_glycans",
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                ],
                "sort_fields": []
            },
            {
                "table_id": "glycosylation_reported_with_glycan",
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                        "field": "total",
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                        "field": "total_sites",
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                        "field": "o_linked_sites",
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                        "field": "n_linked_glycan_sites",
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                        "field": "o_linked_glycan_sites",
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                "table_id": "glycosylation_predicted",
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                        "field": "o_linked_sites",
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                        "field": "n_linked_glycan_sites",
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                        "field": "o_linked_glycan_sites",
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                        "field": "n_linked_glycans",
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                        "field": "o_linked_glycans",
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            {
                "table_id": "glycosylation_automatic_literature_mining",
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                        "field": "total",
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                        "field": "total_sites",
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                        "field": "o_linked_sites",
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                        "field": "n_linked_glycan_sites",
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                        "field": "o_linked_glycan_sites",
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                    {
                        "field": "n_linked_glycans",
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                    {
                        "field": "o_linked_glycans",
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                ],
                "sort_fields": []
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        ]
    },
    {
        "title": "Extracellular signal-regulated kinase 2 (ERK2) phosphorylation sites and docking domain on the nuclear pore complex protein Tpr cooperatively regulate ERK2-Tpr interaction.",
        "journal": "Molecular and cellular biology",
        "date": "2008",
        "authors": "Vomastek T, Iwanicki MP, Burack WR, Tiwari D, Kumar D, Parsons JT, Weber MJ, Nandicoori VK",
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            "url": "https://pubmed.ncbi.nlm.nih.gov/18794356"
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                "uniprot_canonical_ac": "P28482-1",
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                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P27361-1",
                "protein_name": "Mitogen-activated protein kinase 3",
                "gene_name": "MAPK3",
                "tax_name": "Human"
            },
            {
                "uniprot_canonical_ac": "P12270-1",
                "protein_name": "Nucleoprotein TPR",
                "gene_name": "TPR",
                "tax_name": "Human"
            }
        ],
        "species": [
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                "name": "Homo sapiens",
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                        "database": "UniProtKB",
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                ],
                "common_name": "Human",
                "glygen_name": "Human",
                "reference_species": "Homo sapiens [9606]"
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        ],
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            {
                "start_pos": 176,
                "end_pos": 179,
                "sequence_org": "PDHD",
                "sequence_mut": "",
                "comment": "Inhibits homodimerization and interaction with TPR.",
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                    {
                        "database": "UniProtKB",
                        "id": "P28482",
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                    {
                        "database": "PubMed",
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                ],
                "uniprot_canonical_ac": "P28482-1"
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            {
                "start_pos": 185,
                "end_pos": 185,
                "sequence_org": "T",
                "sequence_mut": "A",
                "comment": "Inhibits interaction with TPR; when associated with A-187.",
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                    {
                        "database": "UniProtKB",
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                    {
                        "database": "PubMed",
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                        "url": "https://pubmed.ncbi.nlm.nih.gov/18794356"
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                ],
                "uniprot_canonical_ac": "P28482-1"
            },
            {
                "start_pos": 187,
                "end_pos": 187,
                "sequence_org": "Y",
                "sequence_mut": "A",
                "comment": "Inhibits interaction with TPR; when associated with A-185.",
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                    {
                        "database": "UniProtKB",
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                    {
                        "database": "PubMed",
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                        "url": "https://pubmed.ncbi.nlm.nih.gov/18794356"
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                ],
                "uniprot_canonical_ac": "P28482-1"
            },
            {
                "start_pos": 234,
                "end_pos": 234,
                "sequence_org": "L",
                "sequence_mut": "A",
                "comment": "Inhibits interaction with TPR.",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P28482",
                        "url": "https://www.uniprot.org/uniprotkb/P28482"
                    },
                    {
                        "database": "PubMed",
                        "id": "18794356",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/18794356"
                    }
                ],
                "uniprot_canonical_ac": "P28482-1"
            },
            {
                "start_pos": 318,
                "end_pos": 318,
                "sequence_org": "D",
                "sequence_mut": "A",
                "comment": "Loss of dephosphorylation by PTPRJ.",
                "evidence": [
                    {
                        "database": "UniProtKB",
                        "id": "P28482",
                        "url": "https://www.uniprot.org/uniprotkb/P28482"
                    },
                    {
                        "database": "PubMed",
                        "id": "18794356",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/18794356"
                    },
                    {
                        "database": "PubMed",
                        "id": "19494114",
                        "url": "https://pubmed.ncbi.nlm.nih.gov/19494114"
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                ],
                "uniprot_canonical_ac": "P28482-1"
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            {
                "start_pos": 318,
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                "sequence_org": "D",
                "sequence_mut": "N",
                "comment": "Inhibits interaction with MAP2K1 but not with TPR; when associated with N-321.",
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                    {
                        "database": "UniProtKB",
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                    {
                        "database": "PubMed",
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                    {
                        "database": "PubMed",
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                        "url": "https://pubmed.ncbi.nlm.nih.gov/19494114"
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                ],
                "uniprot_canonical_ac": "P28482-1"
            },
            {
                "start_pos": 321,
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                "sequence_org": "D",
                "sequence_mut": "N",
                "comment": "Inhibits interaction with MAP2K1 but not with TPR; when associated with N-318.",
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                    {
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                    {
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                ],
                "uniprot_canonical_ac": "P28482-1"
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            {
                "start_pos": 54,
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                "sequence_org": "K",
                "sequence_mut": "R",
                "comment": "Does not inhibit interaction with MAP2K1.",
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                        "url": "https://pubmed.ncbi.nlm.nih.gov/18794356"
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                ],
                "uniprot_canonical_ac": "P28482-1"
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        ],
        "phosphorylation": [
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                "start_pos": 2116,
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                    {
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                    {
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                    {
                        "database": "PubMed",
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                ],
                "site_lbl": "Thr2116",
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                    {
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                ],
                "site_lbl": "Thr2137",
                "uniprot_canonical_ac": "P12270-1"
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            {
                "start_pos": 2155,
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                "kinase_uniprot_canonical_ac": "P28482-1",
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                ],
                "site_lbl": "Ser2155",
                "uniprot_canonical_ac": "P12270-1"
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            {
                "start_pos": 2214,
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                "kinase_uniprot_canonical_ac": "P28482-1",
                "kinase_gene_name": "MAPK1",
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                "evidence": [
                    {
                        "database": "iPTMnet",
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                    {
                        "database": "PubMed",
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                ],
                "site_lbl": "Thr2214",
                "uniprot_canonical_ac": "P12270-1"
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        "record_id": "pubmed.18794356",
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            },
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            {
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                        "field": "o_linked_glycan_sites",
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                        "field": "n_linked_glycans",
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                ],
                "sort_fields": []
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            {
                "table_id": "phosphorylation",
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                ],
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                        "field": "o_linked_glycan_sites",
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                ],
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            {
                "table_id": "glycosylation_reported_with_glycan",
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                        "field": "o_linked_sites",
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                        "field": "n_linked_glycan_sites",
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                        "field": "o_linked_glycan_sites",
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                ],
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                "table_id": "glycosylation_predicted",
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                        "field": "o_linked_sites",
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                        "field": "n_linked_glycan_sites",
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                        "field": "o_linked_glycan_sites",
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                        "field": "n_linked_glycan_sites",
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                        "field": "o_linked_glycan_sites",
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                        "field": "o_linked_glycans",
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                ],
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        ]
    },
    {
        "title": "The RSK family of kinases: emerging roles in cellular signalling.",
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        "authors": "Anjum R, Blenis J",
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            {
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            {
                "uniprot_canonical_ac": "Q15349-1",
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            {
                "uniprot_canonical_ac": "Q9UK32-1",
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            {
                "uniprot_canonical_ac": "Q15418-1",
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            {
                "uniprot_canonical_ac": "P27361-1",
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            {
                "uniprot_canonical_ac": "O15530-1",
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        ],
        "species": [
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                "name": "Homo sapiens",
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                ],
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        ],
        "record_id": "pubmed.18813292",
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