{"context":{"query":">>uniprot>>pdb","source_dataset":"uniprot","target_dataset":"pdb"},"stats":{"queried":4,"total":118,"mapped":4},"pagination":{"has_next":true,"next_token":"-1[]P27986,1,P27986,183,0]["},"schema":"id|title|method|resolution|source_organism|chain_count|header","mappings":[{"input":"P27986","source":"P27986|Phosphatidylinositol 3-kinase regulatory subunit alpha","targets":["1A0N|NMR STUDY OF THE SH3 DOMAIN FROM FYN PROTO-ONCOGENE TYROSINE KINASE COMPLEXED WITH THE SYNTHETIC PEPTIDE P2L CORRESPONDING TO RESIDUES 91-104 OF THE P85 SUBUNIT OF PI3-KINASE, FAMILY OF 25 STRUCTURES|SOLUTION NMR||Homo sapiens|0|COMPLEX (PHOSPHOTRANSFERASE/PEPTIDE)","1AZG|NMR STUDY OF THE SH3 DOMAIN FROM FYN PROTO-ONCOGENE TYROSINE KINASE KINASE COMPLEXED WITH THE SYNTHETIC PEPTIDE P2L CORRESPONDING TO RESIDUES 91-104 OF THE P85 SUBUNIT OF PI3-KINASE, MINIMIZED AVERAGE (PROBMAP) STRUCTURE|SOLUTION NMR||Homo sapiens|0|COMPLEX (PHOSPHOTRANSFERASE/PEPTIDE)","1H9O|PHOSPHATIDYLINOSITOL 3-KINASE, P85-ALPHA SUBUNIT: C-TERMINAL SH2 DOMAIN COMPLEXED WITH A TYR751 PHOSPHOPEPTIDE FROM THE PDGF RECEPTOR, CRYSTAL STRUCTURE AT 1.79 A|X-RAY DIFFRACTION|1.79|HOMO SAPIENS; SYNTHETIC CONSTRUCT|0|TRANSFERASE/RECEPTOR","1PBW|STRUCTURE OF BCR-HOMOLOGY (BH) DOMAIN|X-RAY DIFFRACTION|2|Homo sapiens|0|PHOSPHOTRANSFERASE","1PHT|PHOSPHATIDYLINOSITOL 3-KINASE P85-ALPHA SUBUNIT SH3 DOMAIN, RESIDUES 1-85|X-RAY DIFFRACTION|2|Homo sapiens|0|PHOSPHOTRANSFERASE","1PIC|PHOSPHATIDYLINOSITOL 3-KINASE, P85-ALPHA SUBUNIT: C-TERMINAL SH2 DOMAIN COMPLEXED WITH A TYR751 PHOSPHOPEPTIDE FROM THE PDGF RECEPTOR, NMR, MINIMIZED MEAN STRUCTURE|SOLUTION NMR||Homo sapiens|0|COMPLEX (PHOSPHOTRANSFERASE/RECEPTOR)","1PKS|STRUCTURE OF THE PI3K SH3 DOMAIN AND ANALYSIS OF THE SH3 FAMILY|SOLUTION NMR||Homo sapiens|0|PHOSPHOTRANSFERASE","1PKT|STRUCTURE OF THE PI3K SH3 DOMAIN AND ANALYSIS OF THE SH3 FAMILY|SOLUTION NMR||Homo sapiens|0|PHOSPHOTRANSFERASE","2IUG|Crystal structure of the PI3-kinase p85 N-terminal SH2 domain|X-RAY DIFFRACTION|1.89|HOMO SAPIENS|0|TRANSFERASE","2IUH|Crystal structure of the PI3-kinase p85 N-terminal SH2 domain in complex with c-Kit phosphotyrosyl peptide|X-RAY DIFFRACTION|2|HOMO SAPIENS|0|TRANSFERASE","2IUI|Crystal structure of the PI3-kinase p85 N-terminal SH2 domain in complex with PDGFR phosphotyrosyl peptide|X-RAY DIFFRACTION|2.4|Homo sapiens; SYNTHETIC CONSTRUCT|0|TRANSFERASE","2RD0|Structure of a human p110alpha/p85alpha complex|X-RAY DIFFRACTION|3.05|Homo sapiens|0|Transferase/Oncoprotein","2V1Y|Structure of a phosphoinositide 3-kinase alpha adaptor-binding domain (ABD) in a complex with the iSH2 domain from p85 alpha|X-RAY DIFFRACTION|2.4|BOS TAURUS; HOMO SAPIENS|0|TRANSFERASE","3HHM|Crystal structure of p110alpha H1047R mutant in complex with niSH2 of p85alpha and the drug wortmannin|X-RAY DIFFRACTION|2.8|Homo sapiens|0|TRANSFERASE/ONCOPROTEIN","3HIZ|Crystal structure of p110alpha H1047R mutant in complex with niSH2 of p85alpha|X-RAY DIFFRACTION|3.3|Homo sapiens|0|TRANSFERASE/ONCOPROTEIN","3I5R|PI3K SH3 domain in complex with a peptide ligand|X-RAY DIFFRACTION|1.7|Homo sapiens; SYNTHETIC CONSTRUCT|0|PROTEIN BINDING","3I5S|Crystal structure of PI3K SH3|X-RAY DIFFRACTION|3|Homo sapiens|0|PROTEIN BINDING","4A55|Crystal structure of p110alpha in complex with iSH2 of p85alpha and the inhibitor PIK-108|X-RAY DIFFRACTION|3.5|HOMO SAPIENS; MUS MUSCULUS|0|TRANSFERASE","4JPS|Co-crystal Structures of the Lipid Kinase PI3K alpha with Pan and Isoform Selective Inhibitors|X-RAY DIFFRACTION|2.2|Homo sapiens|0|TRANSFERASE/TRANSFERASE INHIBITOR","4L1B|Crystal Structure of p110alpha complexed with niSH2 of p85alpha|X-RAY DIFFRACTION|2.586|Homo sapiens|0|signaling Protein/transferase/Inhibitor","4L23|Crystal Structure of p110alpha complexed with niSH2 of p85alpha and PI-103|X-RAY DIFFRACTION|2.501|Homo sapiens|0|signaling Protein/transferase/Inhibitor","4L2Y|Crystal Structure of p110alpha complexed with niSH2 of p85alpha and compound 9d|X-RAY DIFFRACTION|2.8|Homo sapiens|0|signaling Protein/transferase/Inhibitor","4OVU|Crystal Structure of p110alpha in complex with niSH2 of p85alpha|X-RAY DIFFRACTION|2.96|Homo sapiens|0|TRANSFERASE/TRANSFERASE REGULATOR","4OVV|Crystal Structure of PI3Kalpha in complex with diC4-PIP2|X-RAY DIFFRACTION|3.5|Homo sapiens|0|TRANSFERASE/TRANSFERASE REGULATOR","4WAF|Crystal Structure of a novel tetrahydropyrazolo[1,5-a]pyrazine in an engineered PI3K alpha|X-RAY DIFFRACTION|2.39|Homo sapiens|0|transferase/transferase inhibitor","4YKN|Pi3K alpha lipid kinase with Active Site Inhibitor|X-RAY DIFFRACTION|2.9|Homo sapiens|0|Transferase/Transferase Inhibitor","4ZOP|Co-crystal Structure of Lipid Kinase PI3K alpha with a selective phosphatidylinositol-3 kinase alpha inhibitor|X-RAY DIFFRACTION|2.62|Homo sapiens|0|transferase/transferase inhibitor","5AUL|PI3K p85 C-terminal SH2 domain/CD28-derived peptide complex|X-RAY DIFFRACTION|1.1|Homo sapiens; SYNTHETIC CONSTRUCT|0|SIGNALING PROTEIN","5FI4|Discovery of imidazo[1,2-a]-pyridine inhibitors of pan-PI3 kinases that are efficacious in a mouse xenograft model|X-RAY DIFFRACTION|2.5|Homo sapiens|0|TRANSFERASE/TRANSFERASE INHIBITOR","5GJI|PI3K p85 N-terminal SH2 domain/CD28-derived peptide complex|X-RAY DIFFRACTION|0.9|Homo sapiens; SYNTHETIC CONSTRUCT|0|SIGNALING PROTEIN","5ITD|Crystal structure of PI3K alpha with PI3K delta inhibitor|X-RAY DIFFRACTION|3.02|Homo sapiens|0|Transferase/Protein Transport/Inhibitor","5M6U|HUMAN PI3KDELTA IN COMPLEX WITH LASW1579|X-RAY DIFFRACTION|2.85|Homo sapiens|0|TRANSFERASE","5SW8|Crystal structure of PI3Kalpha in complex with fragments 7 and 11|X-RAY DIFFRACTION|3.3|Homo sapiens|0|TRANSFERASE/TRANSFERASE INHIBITOR","5SWG|Crystal Structure of PI3Kalpha in complex with fragments 5 and 21|X-RAY DIFFRACTION|3.11|Homo sapiens|0|TRANSFERASE/TRANSFERASE INHIBITOR","5SWO|Crystal Structure of PI3Kalpha in complex with fragments 4 and 19|X-RAY DIFFRACTION|3.5|Homo sapiens|0|TRANSFERASE/TRANSFERASE INHIBITOR","5SWP|Crystal Structure of PI3Kalpha in complex with fragments 6 and 24|X-RAY DIFFRACTION|3.41|Homo sapiens|0|TRANSFERASE/TRANSFERASE INHIBITOR","5SWR|Crystal Structure of PI3Kalpha in complex with fragments 20 and 26|X-RAY DIFFRACTION|3.31|Homo sapiens|0|TRANSFERASE/TRANSFERASE INHIBITOR","5SWT|Crystal Structure of PI3Kalpha in complex with fragments 17 and 27|X-RAY DIFFRACTION|3.49|Homo sapiens|0|TRANSFERASE/TRANSFERASE INHIBITOR","5SX8|Crystal Structure of PI3Kalpha in complex with fragments 12 and 15|X-RAY DIFFRACTION|3.47|Homo sapiens|0|TRANSFERASE/TRANSFERASE INHIBITOR","5SX9|Crystal Structure of PI3Kalpha in complex with fragment 14|X-RAY DIFFRACTION|3.52|Homo sapiens|0|TRANSFERASE/TRANSFERASE INHIBITOR","5SXA|Crystal Structure of PI3Kalpha in complex with fragment 10|X-RAY DIFFRACTION|3.35|Homo sapiens|0|TRANSFERASE/TRANSFERASE INHIBITOR","5SXB|Crystal Structure of PI3Kalpha in complex with fragment 23|X-RAY DIFFRACTION|3.3|Homo sapiens|0|TRANSFERASE/TRANSFERASE INHIBITOR","5SXC|Crystal Structure of PI3Kalpha in complex with fragment 8|X-RAY DIFFRACTION|3.55|Homo sapiens|0|TRANSFERASE/TRANSFERASE INHIBITOR","5SXD|Crystal Structure of PI3Kalpha in complex with fragment 22|X-RAY DIFFRACTION|3.5|Homo sapiens|0|TRANSFERASE/TRANSFERASE INHIBITOR","5SXE|Crystal Structure of PI3Kalpha in complex with fragments 19 and 28|X-RAY DIFFRACTION|3.51|Homo sapiens|0|TRANSFERASE/TRANSFERASE INHIBITOR","5SXF|Crystal Structure of PI3Kalpha in complex with fragment 9|X-RAY DIFFRACTION|3.46|Homo sapiens|0|TRANSFERASE/TRANSFERASE INHIBITOR","5SXI|Crystal Structure of PI3Kalpha in complex with fragment 13|X-RAY DIFFRACTION|3.4|Homo sapiens|0|TRANSFERASE/TRANSFERASE INHIBITOR","5SXJ|Crystal Structure of PI3Kalpha in complex with fragment 29|X-RAY DIFFRACTION|3.42|Homo sapiens|0|TRANSFERASE/TRANSFERASE INHIBITOR","5SXK|Crystal Structure of PI3Kalpha in complex with fragment 18|X-RAY DIFFRACTION|3.55|Homo sapiens|0|TRANSFERASE/TRANSFERASE INHIBITOR","5UBT|CRYSTAL STRUCTURE OF PI3K DELTA IN COMPLEX WITH A 7-(3-(PIPERAZIN-1-YL)PHENYL)PYRROLO[2,1-F][1,2,4] TRIAZIN-4-AMINE DERIVIATINE|X-RAY DIFFRACTION|2.83|Homo sapiens|0|TRANSFERASE/TRANSFERASE REGULATOR","5UK8|The co-structure of (R)-4-(6-(1-(cyclopropylsulfonyl)cyclopropyl)-2-(1H-indol-4-yl)pyrimidin-4-yl)-3-methylmorpholine and a rationally designed PI3K-alpha mutant that mimics ATR|X-RAY DIFFRACTION|2.5|Homo sapiens|0|TRANSFERASE/SIGNALING PROTEIN/INHIBITOR","5UKJ|The co-structure of N,N-dimethyl-4-[(6R)-6-methyl-5-(1H-pyrrolo[2,3- b]pyridin-4-yl)-4,5,6,7-tetrahydropyrazolo[1,5- a]pyrazin-3-yl]benzenesulfonamide and a rationally designed PI3K-alpha mutant that mimics ATR|X-RAY DIFFRACTION|2.8|Homo sapiens|0|TRANSFERASE/SIGNALING PROTEIN/INHIBITOR","5UL1|The co-structure of 3-amino-6-(4-((1-(dimethylamino)propan-2-yl)sulfonyl)phenyl)-N-phenylpyrazine-2-carboxamide and a rationally designed PI3K-alpha mutant that mimics ATR|X-RAY DIFFRACTION|3|Homo sapiens|0|TRANSFERASE/SIGNALING PROTEIN/INHIBITOR","5VLR|CRYSTAL STRUCTURE OF PI3K DELTA IN COMPLEX WITH A TRIFLUORO-ETHYL-PYRAZOL-PYROLOTRIAZINE INHIBITOR|X-RAY DIFFRACTION|2.8|Homo sapiens|0|TRANSFERASE/TRANSFERASE REGULATOR","5XGH|Crystal structure of PI3K complex with an inhibitor|X-RAY DIFFRACTION|2.97|Homo sapiens|0|TRANSFERASE/INHIBITOR","5XGI|Crystal structure of PI3K complex with an inhibitor|X-RAY DIFFRACTION|2.56|Homo sapiens|0|TRANSFERASE/INHIBITOR","5XGJ|Crystal structure of PI3K complex with an inhibitor|X-RAY DIFFRACTION|2.97|Homo sapiens|0|TRANSFERASE/INHIBITOR","6NCT|Structure of p110alpha/niSH2 - vector data collection|X-RAY DIFFRACTION|3.35|Homo sapiens|0|TRANSFERASE","6PYR|Human PI3Kdelta in complex with Compound 2-10 ((3S)-3-benzyl-3-methyl-5-[5-(2-methylpyrimidin-5-yl)pyrazolo[1,5-a]pyrimidin-3-yl]-1,3-dihydro-2H-indol-2-one)|X-RAY DIFFRACTION|2.21|Homo sapiens|0|TRANSFERASE/TRANSFERASE INHIBITOR","6PYU|Human PI3Kdelta in complex with Compound 4-2 ((3S)-1'-(cyclopropanecarbonyl)-5-(quinoxalin-6-yl)spiro[indole-3,2'-pyrrolidin]-2(1H)-one)|X-RAY DIFFRACTION|2.54|Homo sapiens|0|TRANSFERASE/TRANSFERASE INHIBITOR","7CIO|Molecular interactions of cytoplasmic region of CTLA-4 with SH2 domains of PI3-kinase|X-RAY DIFFRACTION|1.1|Homo sapiens; SYNTHETIC CONSTRUCT|0|SIGNALING PROTEIN","7LM2|HUMAN PI3KDELTA IN COMPLEX WITH COMPOUND 3C|X-RAY DIFFRACTION|2.79|Homo sapiens|0|TRANSFERASE/TRANSFERASE INHIBITOR","7LQ1|HUMAN PI3KDELTA IN COMPLEX WITH COMPOUND 28|X-RAY DIFFRACTION|2.96|Homo sapiens|0|TRANSFERASE","7MYN|Cryo-EM Structure of p110alpha in complex with p85alpha|ELECTRON MICROSCOPY|2.79|Homo sapiens|0|TRANSFERASE","7MYO|Cryo-EM structure of p110alpha in complex with p85alpha inhibited by BYL-719|ELECTRON MICROSCOPY|2.92|Homo sapiens|0|TRANSFERASE","7PG5|Crystal Structure of PI3Kalpha|X-RAY DIFFRACTION|2.20029|Homo sapiens|0|TRANSFERASE","7PG6|Crystal Structure of PI3Kalpha in complex with the inhibitor NVP-BYL719|X-RAY DIFFRACTION|2.49944|Homo sapiens|0|TRANSFERASE","7RNS|nSH2 domain of p85-alpha subunit of phosphatidylinositol 3-kinase in complex with an actin peptide with phosphorylated tyrosine 53|X-RAY DIFFRACTION|1.14|Homo sapiens; SYNTHETIC CONSTRUCT|0|PEPTIDE BINDING PROTEIN","7TZ7|PI3K alpha in complex with an inhibitor|X-RAY DIFFRACTION|2.41|Homo sapiens|0|transferase/inhibitor","8AM0|Crystal structure of human T1061E PI3Kalpha in complex with its regulatory subunit and the inhibitor GDC-0077 (Inavolisib)|X-RAY DIFFRACTION|2.818|Homo sapiens|0|TRANSFERASE","8DCP|PI 3-kinase alpha with nanobody 3-126|ELECTRON MICROSCOPY|2.41|Homo sapiens|0|TRANSFERASE","8DCX|PI 3-kinase alpha with nanobody 3-159|ELECTRON MICROSCOPY|2.8|Homo sapiens|0|TRANSFERASE","8DD4|PI 3-kinase alpha with nanobody 3-142|ELECTRON MICROSCOPY|3.1|Homo sapiens|0|TRANSFERASE","8DD8|PI 3-kinase alpha with nanobody 3-142, crosslinked with DSG|ELECTRON MICROSCOPY|3.4|Homo sapiens|0|TRANSFERASE","8GUB|Cryo-EM structure of cancer-specific PI3Kalpha mutant H1047R in complex with BYL-719|ELECTRON MICROSCOPY|2.73|Homo sapiens|0|STRUCTURAL PROTEIN","8H36|Cryo-EM Structure of the KBTBD2-CUL3-Rbx1-p85a dimeric complex|ELECTRON MICROSCOPY|4.6|Homo sapiens|0|LIGASE","8H37|Cryo-EM Structure of the KBTBD2-CUL3-Rbx1-p85a tetrameric complex|ELECTRON MICROSCOPY|7.52|Homo sapiens|0|LIGASE","8ILR|Cryo-EM structure of PI3Kalpha in complex with compound 16|ELECTRON MICROSCOPY|3.05|Homo sapiens|0|STRUCTURAL PROTEIN","8ILS|Cryo-EM structure of PI3Kalpha in complex with compound 17|ELECTRON MICROSCOPY|3.1|Homo sapiens|0|STRUCTURAL PROTEIN","8ILV|Cryo-EM structure of PI3Kalpha in complex with compound 18|ELECTRON MICROSCOPY|3.19|Homo sapiens|0|STRUCTURAL PROTEIN","8SBC|Co-structure of Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform and brain penetrant inhibitors|X-RAY DIFFRACTION|2.3|Homo sapiens|0|TRANSFERASE","8SBJ|Co-structure Phosphatidylinositol 4,5-bisphosphate 3-kinase catalytic subunit alpha isoform complexed with brain penetrant inhibitors|X-RAY DIFFRACTION|3.1|Homo sapiens|0|TRANSFERASE","8TDU|STX-478, a Mutant-Selective, Allosteric Inhibitor bound to PI3Kalpha|X-RAY DIFFRACTION|3.11|Homo sapiens|0|TRANSFERASE/TRANSFERASE INHIBITOR","8TGD|STX-478, a Mutant-Selective, Allosteric Inhibitor bound to H1047R PI3Kalpha|X-RAY DIFFRACTION|2.928|Homo sapiens|0|TRANSFERASE/TRANSFERSE INHIBITOR","8TS7|Human PI3K p85alpha/p110alpha|X-RAY DIFFRACTION|2.71|Homo sapiens|0|SIGNALING PROTEIN","8TS8|p85alpha/p110alpha heterodimer H1047R mutant|X-RAY DIFFRACTION|2.72|Homo sapiens|0|SIGNALING PROTEIN","8TS9|Human PI3K p85alpha/p110alpha H1047R bound to compound 1|X-RAY DIFFRACTION|2.83|Homo sapiens|0|SIGNALING PROTEIN/INHIBITOR","8TSA|Human PI3K p85alpha/p110alpha H1047R bound to compound 2|X-RAY DIFFRACTION|2.51|Homo sapiens|0|SIGNALING PROTEIN/INHIBITOR","8TSB|Human PI3K p85alpha/p110alpha bound to compound 2|X-RAY DIFFRACTION|3.53|Homo sapiens|0|SIGNALING PROTEIN/INHIBITOR","8TSC|Human PI3K p85alpha/p110alpha H1047R bound to compound 3|X-RAY DIFFRACTION|3.62|Homo sapiens|0|SIGNALING PROTEIN/INHIBITOR","8TSD|Human PI3K p85alpha/p110alpha bound to RLY-2608|X-RAY DIFFRACTION|2.7|Homo sapiens|0|SIGNALING PROTEIN,TRANSFERASE/INHIBITOR","8TU6|CryoEM structure of PI3Kalpha|ELECTRON MICROSCOPY|3.12|Homo sapiens|0|CYTOSOLIC PROTEIN","8V8H|PI3Ka H1047R co-crystal structure with inhibitor in cryptic pocket near H1047R (compound 4).|X-RAY DIFFRACTION|3.58|Homo sapiens|0|SIGNALING PROTEIN","8V8I|PI3Ka H1047R co-crystal structure with inhibitor in cryptic pocket (compound 5).|X-RAY DIFFRACTION|3.2|Homo sapiens|0|SIGNALING PROTEIN","8V8J|PI3Ka H1047R co-crystal structure with inhibitors in two cryptic pockets (compounds 4 and 5).|X-RAY DIFFRACTION|3.35|Homo sapiens|0|SIGNALING PROTEIN","8V8U|PI3Ka H1047R co-crystal structure with inhibitor in cryptic pocket near H1047R (compound 12).|X-RAY DIFFRACTION|2.93|Homo sapiens|0|SIGNALING PROTEIN","8V8V|PI3Ka H1047R co-crystal structure with inhibitor in cryptic pocket near H1047R (compound 7).|X-RAY DIFFRACTION|2.61|Homo sapiens|0|SIGNALING PROTEIN","8W9A|CryoEM structure of human PI3K-alpha (P85/P110-H1047R) with QR-7909 binding at an allosteric site|ELECTRON MICROSCOPY|2.7|Homo sapiens|0|ONCOPROTEIN","8W9B|CryoEM structure of human PI3K-alpha (P85/P110-H1047R) with QR-8557 binding at an allosteric site|ELECTRON MICROSCOPY|3.0|Homo sapiens|0|ONCOPROTEIN","9LWQ|Cryo-EM structure of PI3Kalpha in complex with compound UCL-TRO-1938|ELECTRON MICROSCOPY|3.17|Homo sapiens|0|CYTOSOLIC PROTEIN"]},{"input":"Q9Y243","source":"Q9Y243|RAC-gamma serine/threonine-protein kinase","targets":["2X18|The crystal structure of the PH domain of human AKT3 protein kinase|X-RAY DIFFRACTION|1.46|HOMO SAPIENS|0|TRANSFERASE","8ZXW|Crystal structure of the anti-phosphorylated peptide C7 Fab antibody with peptide bound|X-RAY DIFFRACTION|1.33|Oryctolagus cuniculus; SYNTHETIC CONSTRUCT|0|IMMUNE SYSTEM"]},{"input":"Q13315","source":"Q13315|Serine-protein kinase ATM","targets":["5NP0|Closed dimer of human ATM (Ataxia telangiectasia mutated)|ELECTRON MICROSCOPY|5.7|Homo sapiens|0|SIGNALING PROTEIN","5NP1|Open protomer of human ATM (Ataxia telangiectasia mutated)|ELECTRON MICROSCOPY|5.7|Homo sapiens|0|TRANSFERASE","6HKA|The solution structure of the micelle-associated FATC domain of the human protein kinase ataxia telangiectasia mutated (ATM)|SOLUTION NMR||Homo sapiens; Streptococcus sp. group G|0|TRANSFERASE","6K9K|Monomeric human ATM (Ataxia telangiectasia mutated) kinase|ELECTRON MICROSCOPY|7.82|Homo sapiens|0|CELL CYCLE","6K9L|4.27 Angstrom resolution cryo-EM structure of human dimeric ATM kinase|ELECTRON MICROSCOPY|4.27|Homo sapiens|0|CELL CYCLE","7NI4|Human ATM kinase domain with bound M4076 inhibitor|ELECTRON MICROSCOPY|3.0|Homo sapiens|0|SIGNALING PROTEIN","7NI5|Human ATM kinase with bound inhibitor KU-55933|ELECTRON MICROSCOPY|2.78|Homo sapiens|0|SIGNALING PROTEIN","7NI6|Human ATM kinase with bound ATPyS|ELECTRON MICROSCOPY|2.8|Homo sapiens|0|SIGNALING PROTEIN","7SIC|Human ATM Dimer|ELECTRON MICROSCOPY|2.51|Homo sapiens|0|SIGNALING PROTEIN","7SID|Human ATM Dimer Bound to Nbs1|ELECTRON MICROSCOPY|2.53|Homo sapiens; SYNTHETIC CONSTRUCT|0|SIGNALING PROTEIN","8OXM|ATM(Q2971A) activated by oxidative stress in complex with Mg AMP-PNP and p53 peptide|ELECTRON MICROSCOPY|3.3|Homo sapiens; SYNTHETIC CONSTRUCT|0|SIGNALING PROTEIN","8OXO|ATM(Q2971A) dimeric C-terminal region activated by oxidative stress in complex with Mg AMP-PNP and p53 peptide|ELECTRON MICROSCOPY|3.0|Homo sapiens; SYNTHETIC CONSTRUCT|0|SIGNALING PROTEIN","8OXP|ATM(Q2971A) in complex with Mg AMP-PNP|ELECTRON MICROSCOPY|2.6|Homo sapiens|0|SIGNALING PROTEIN","8OXQ|ATM(Q2971A) dimeric C-terminal region in complex with Mg AMP-PNP|ELECTRON MICROSCOPY|2.5|Homo sapiens|0|SIGNALING PROTEIN"]},{"input":"Q02156","source":"Q02156|Protein kinase C epsilon type","targets":["2WH0|Recognition of an intrachain tandem 14-3-3 binding site within protein kinase C epsilon|X-RAY DIFFRACTION|2.25|HOMO SAPIENS; SYNTHETIC CONSTRUCT|0|SIGNALING PROTEIN","5LIH|Structure of a peptide-substrate bound to PKCiota core kinase domain|X-RAY DIFFRACTION|3.25|Homo sapiens|0|TRANSFERASE"]}]}