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{"accession":"Q14790","entry_name":"CASP8_HUMAN","gene":"CASP8","protein_name":"Caspase-8","length":479,"mass_kda":55.4,"chromosome":"2","ec_numbers":"3.4.22.61","locations":"Cytoplasm; Nucleus; Cell projection","transmembrane_helices":0,"disease_count":1,"diseases":"Caspase-8 deficiency","pdb_structures":36,"evidence_level":1,"annotation_score":5,"first_public":"1997-11-01"}
{"accession":"Q99459","entry_name":"CDC5L_HUMAN","gene":"CDC5L","protein_name":"Cell division cycle 5-like protein","length":802,"mass_kda":92.3,"chromosome":"6","ec_numbers":null,"locations":"Nucleus; Nucleus speckle; Cytoplasm","transmembrane_helices":0,"disease_count":0,"diseases":null,"pdb_structures":36,"evidence_level":1,"annotation_score":5,"first_public":"2005-08-16"}
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{"accession":"P00751","entry_name":"CFAB_HUMAN","gene":"CFB","protein_name":"Complement factor B","length":764,"mass_kda":85.5,"chromosome":"6","ec_numbers":"3.4.21.47","locations":"Secreted","transmembrane_helices":0,"disease_count":3,"diseases":"Macular degeneration, age-related, 14; Hemolytic uremic syndrome, atypical, 4; Complement factor B deficiency","pdb_structures":26,"evidence_level":1,"annotation_score":5,"first_public":"1986-07-21"}
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{"accession":"P78356","entry_name":"PI42B_HUMAN","gene":"PIP4K2B","protein_name":"Phosphatidylinositol 5-phosphate 4-kinase type-2 beta","length":416,"mass_kda":47.4,"chromosome":"17","ec_numbers":"2.7.1.149","locations":"Endoplasmic reticulum membrane; Cell membrane; Nucleus; Cytoplasm","transmembrane_helices":0,"disease_count":0,"diseases":null,"pdb_structures":26,"evidence_level":1,"annotation_score":5,"first_public":"2004-05-24"}
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{"accession":"O94804","entry_name":"STK10_HUMAN","gene":"STK10","protein_name":"Serine/threonine-protein kinase 10","length":968,"mass_kda":112.1,"chromosome":"5","ec_numbers":"2.7.11.1","locations":"Cell membrane","transmembrane_helices":0,"disease_count":1,"diseases":"Testicular germ cell tumor","pdb_structures":14,"evidence_level":1,"annotation_score":5,"first_public":"2001-01-24"}
{"accession":"P01876","entry_name":"IGHA1_HUMAN","gene":"IGHA1","protein_name":"Immunoglobulin heavy constant alpha 1","length":398,"mass_kda":42.8,"chromosome":"14","ec_numbers":null,"locations":"Secreted","transmembrane_helices":1,"disease_count":0,"diseases":null,"pdb_structures":14,"evidence_level":1,"annotation_score":5,"first_public":"1986-07-21"}
{"accession":"P07237","entry_name":"PDIA1_HUMAN","gene":"P4HB","protein_name":"Protein disulfide-isomerase","length":508,"mass_kda":57.1,"chromosome":"17","ec_numbers":"5.3.4.1","locations":"Endoplasmic reticulum; Endoplasmic reticulum lumen; Melanosome; Cell membrane","transmembrane_helices":0,"disease_count":1,"diseases":"Cole-Carpenter syndrome 1","pdb_structures":14,"evidence_level":1,"annotation_score":5,"first_public":"1988-04-01"}
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{"accession":"Q08211","entry_name":"DHX9_HUMAN","gene":"DHX9","protein_name":"ATP-dependent RNA helicase A","length":1270,"mass_kda":141,"chromosome":"1","ec_numbers":"3.6.4.13","locations":"Nucleus; Cytoplasm","transmembrane_helices":0,"disease_count":1,"diseases":"Intellectual developmental disorder, autosomal dominant 75","pdb_structures":6,"evidence_level":1,"annotation_score":5,"first_public":"1995-02-01"}
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