{"context":{"query":">>uniprot>>pdb","source_dataset":"uniprot","target_dataset":"pdb"},"stats":{"queried":1,"total":100,"mapped":1},"pagination":{"has_next":true,"next_token":"-1[]P01116,1,P01116,190,0]["},"schema":"id|title|method|resolution|source_organism|chain_count|header","mappings":[{"input":"P01116","source":"P01116|GTPase KRas","targets":["1D8D|CO-CRYSTAL STRUCTURE OF RAT PROTEIN FARNESYLTRANSFERASE COMPLEXED WITH A K-RAS4B PEPTIDE SUBSTRATE AND FPP ANALOG AT 2.0A RESOLUTION|X-RAY DIFFRACTION|2|Rattus norvegicus; SYNTHETIC CONSTRUCT|0|TRANSFERASE","1D8E|Zinc-depleted FTase complexed with K-RAS4B peptide substrate and FPP analog.|X-RAY DIFFRACTION|3|Rattus norvegicus; SYNTHETIC CONSTRUCT|0|TRANSFERASE","1KZO|PROTEIN FARNESYLTRANSFERASE COMPLEXED WITH FARNESYLATED K-RAS4B PEPTIDE PRODUCT AND FARNESYL DIPHOSPHATE SUBSTRATE BOUND SIMULTANEOUSLY|X-RAY DIFFRACTION|2.2|Rattus norvegicus; SYNTHETIC CONSTRUCT|0|TRANSFERASE/TRANSFERASE SUBSTRATE","1KZP|PROTEIN FARNESYLTRANSFERASE COMPLEXED WITH A FARNESYLATED K-RAS4B PEPTIDE PRODUCT|X-RAY DIFFRACTION|2.1|Rattus norvegicus; SYNTHETIC CONSTRUCT|0|TRANSFERASE/TRANSFERASE SUBSTRATE","2MSC|NMR data-driven model of GTPase KRas-GDP tethered to a lipid-bilayer nanodisc|SOLUTION NMR||Homo sapiens|0|LIPID BINDING PROTEIN","2MSD|NMR data-driven model of GTPase KRas-GNP tethered to a lipid-bilayer nanodisc|SOLUTION NMR||Homo sapiens|0|LIPID BINDING PROTEIN","2MSE|NMR data-driven model of GTPase KRas-GNP:ARafRBD complex tethered to a lipid-bilayer nanodisc|SOLUTION NMR||Homo sapiens|0|LIPID BINDING PROTEIN","3GFT|Human K-Ras (Q61H) in complex with a GTP analogue|X-RAY DIFFRACTION|2.27|Homo sapiens|0|SIGNALING PROTEIN","4DSN|Small-molecule ligands bind to a distinct pocket in Ras and inhibit SOS-mediated nucleotide exchange activity|X-RAY DIFFRACTION|2.03|Homo sapiens|0|HYDROLASE","4DSO|Small-molecule ligands bind to a distinct pocket in Ras and inhibit SOS-mediated nucleotide exchange activity|X-RAY DIFFRACTION|1.85|Homo sapiens|0|HYDROLASE","4DST|Small-molecule ligands bind to a distinct pocket in Ras and inhibit SOS-mediated nucleotide exchange activity|X-RAY DIFFRACTION|2.3|Homo sapiens|0|HYDROLASE","4DSU|Small-molecule ligands bind to a distinct pocket in Ras and inhibit SOS-mediated nucleotide exchange activity|X-RAY DIFFRACTION|1.7|Homo sapiens|0|HYDROLASE","4EPR|Discovery of Small Molecules that Bind to K-Ras and Inhibit Sos-Mediated Activation.|X-RAY DIFFRACTION|2|Homo sapiens|0|HYDROLASE","4EPT|Discovery of Small Molecules that Bind to K-Ras and Inhibit Sos-mediated Activation|X-RAY DIFFRACTION|2|Homo sapiens|0|HYDROLASE","4EPV|Discovery of Small Molecules that Bind to K-Ras and Inhibit Sos-mediated Activation|X-RAY DIFFRACTION|1.35|Homo sapiens|0|HYDROLASE","4EPW|Discovery of Small Molecules that Bind to K-Ras and Inhibit Sos-mediated Activation|X-RAY DIFFRACTION|1.7|Homo sapiens|0|PROTEIN BINDING","4EPX|Discovery of Small Molecules that Bind to K-Ras and Inhibit Sos-mediated Activation|X-RAY DIFFRACTION|1.76|Homo sapiens|0|HYDROLASE","4EPY|Discovery of Small Molecules that Bind to K-Ras and Inhibit Sos-mediated Activation|X-RAY DIFFRACTION|1.801|Homo sapiens|0|HYDROLASE","4L8G|Crystal Structure of K-Ras G12C, GDP-bound|X-RAY DIFFRACTION|1.521|Homo sapiens|0|SIGNALING PROTEIN","4LDJ|Crystal Structure of a GDP-bound G12C Oncogenic Mutant of Human GTPase KRas|X-RAY DIFFRACTION|1.15|Homo sapiens|0|HYDROLASE","4LPK|Crystal Structure of K-Ras WT, GDP-bound|X-RAY DIFFRACTION|1.5|Homo sapiens|0|SIGNALING PROTEIN","4LRW|Crystal Structure of K-Ras G12C (cysteine-light), GDP-bound|X-RAY DIFFRACTION|2.151|Homo sapiens|0|SIGNALING PROTEIN","4LUC|Crystal Structure of small molecule disulfide 6 bound to K-Ras G12C|X-RAY DIFFRACTION|1.29|Homo sapiens|0|SIGNALING PROTEIN/INHIBITOR","4LV6|Crystal Structure of small molecule disulfide 4 covalently bound to K-Ras G12C|X-RAY DIFFRACTION|1.5|Homo sapiens|0|SIGNALING PROTEIN/INHIBITOR","4LYF|Crystal Structure of small molecule vinylsulfonamide 8 covalently bound to K-Ras G12C|X-RAY DIFFRACTION|1.568|Homo sapiens|0|SIGNALING PROTEIN/INHIBITOR","4LYH|Crystal Structure of small molecule vinylsulfonamide 9 covalently bound to K-Ras G12C|X-RAY DIFFRACTION|1.371|Homo sapiens|0|SIGNALING PROTEIN/INHIBITOR","4LYJ|Crystal Structure of small molecule vinylsulfonamide 9 covalently bound to K-Ras G12C, alternative space group|X-RAY DIFFRACTION|1.927|Homo sapiens|0|SIGNALING PROTEIN/INHIBITOR","4M1O|Crystal Structure of small molecule vinylsulfonamide 7 covalently bound to K-Ras G12C|X-RAY DIFFRACTION|1.571|Homo sapiens|0|SIGNALING PROTEIN/INHIBITOR","4M1S|Crystal Structure of small molecule vinylsulfonamide 13 covalently bound to K-Ras G12C|X-RAY DIFFRACTION|1.552|Homo sapiens|0|SIGNALING PROTEIN/INHIBITOR","4M1T|Crystal Structure of small molecule vinylsulfonamide 14 covalently bound to K-Ras G12C|X-RAY DIFFRACTION|1.703|Homo sapiens|0|SIGNALING PROTEIN/INHIBITOR","4M1W|Crystal Structure of small molecule vinylsulfonamide covalently bound to K-Ras G12C|X-RAY DIFFRACTION|1.58|Homo sapiens|0|SIGNALING PROTEIN/INHIBITOR","4M1Y|Crystal Structure of small molecule vinylsulfonamide 15 covalently bound to K-Ras G12C|X-RAY DIFFRACTION|1.491|Homo sapiens|0|SIGNALING PROTEIN/INHIBITOR","4M21|Crystal Structure of small molecule acrylamide 11 covalently bound to K-Ras G12C|X-RAY DIFFRACTION|1.94|Homo sapiens|0|SIGNALING PROTEIN/INHIBITOR","4M22|Crystal Structure of small molecule acrylamide 16 covalently bound to K-Ras G12C|X-RAY DIFFRACTION|2.09|Homo sapiens|0|SIGNALING PROTEIN/INHIBITOR","4NMM|Crystal Structure of a G12C Oncogenic Variant of Human KRas Bound to a Novel GDP Competitive Covalent Inhibitor|X-RAY DIFFRACTION|1.89|Homo sapiens|0|HYDROLASE/HYDROLASE INHIBITOR","4OBE|Crystal Structure of GDP-bound Human KRas|X-RAY DIFFRACTION|1.24|Homo sapiens|0|HYDROLASE","4PZY|Second-site screening of K-Ras in the presence of covalently attached first-site ligands|X-RAY DIFFRACTION|1.88|Homo sapiens|0|HYDROLASE","4PZZ|Second-site screening of K-Ras in the presence of covalently attached first-site ligands|X-RAY DIFFRACTION|1.403|Homo sapiens|0|HYDROLASE","4Q01|Second-site screening of K-Ras in the presence of covalently attached first-site ligands|X-RAY DIFFRACTION|1.291|Homo sapiens|0|HYDROLASE","4Q02|Second-site screening of K-Ras in the presence of covalently attached first-site ligands|X-RAY DIFFRACTION|1.702|Homo sapiens|0|HYDROLASE","4Q03|Second-site screening of K-Ras in the presence of covalently attached first-site ligands|X-RAY DIFFRACTION|1.201|Homo sapiens|0|HYDROLASE","4QL3|Crystal Structure of a GDP-bound G12R Oncogenic Mutant of Human GTPase KRas|X-RAY DIFFRACTION|1.041|Homo sapiens|0|HYDROLASE","4TQ9|Crystal Structure of a GDP-bound G12V Oncogenic Mutant of Human GTPase KRas|X-RAY DIFFRACTION|1.491|Homo sapiens|0|HYDROLASE","4TQA|Crystal Structure of a GDP-bound G13D Oncogenic Mutant of Human GTPase KRas|X-RAY DIFFRACTION|1.13|Homo sapiens|0|HYDROLASE","4WA7|Crystal Structure of a GDP-bound Q61L Oncogenic Mutant of Human GT- Pase KRas|X-RAY DIFFRACTION|1.986|Homo sapiens|0|signaling protein, hydrolase","5F2E|Crystal Structure of small molecule ARS-853 covalently bound to K-Ras G12C|X-RAY DIFFRACTION|1.4|Homo sapiens|0|HYDROLASE","5KYK|Covalent GTP-competitive inhibitors of KRAS G12C: Guanosine bisphosphonate Analogs|X-RAY DIFFRACTION|2.702|Homo sapiens|0|HYDROLASE/HYDROLASE inhibitor","5MLA|Crystal structure of human RAS in complex with darpin K55|X-RAY DIFFRACTION|2.19|Homo sapiens; Synthetic construct|0|HYDROLASE","5MLB|Crystal structure of human RAS in complex with darpin K27|X-RAY DIFFRACTION|3.22|Homo sapiens; synthetic construct|0|HYDROLASE","5O2S|Human KRAS in complex with darpin K27|X-RAY DIFFRACTION|3.22|Homo sapiens|0|SIGNALING PROTEIN","5O2T|Human KRAS in complex with darpin K27|X-RAY DIFFRACTION|2.19|Homo sapiens|0|SIGNALING PROTEIN","5OCG|Discovery of small molecules binding to KRAS via high affinity antibody fragment competition method.|X-RAY DIFFRACTION|1.48|Homo sapiens|0|HYDROLASE","5OCO|Discovery of small molecules binding to KRAS via high affinity antibody fragment competition method.|X-RAY DIFFRACTION|1.66|Homo sapiens|0|HYDROLASE","5OCT|Discovery of small molecules binding to KRAS via high affinity antibody fragment competition method.|X-RAY DIFFRACTION|2.07|Homo sapiens|0|HYDROLASE","5TAR|Crystal structure of farnesylated and methylated kras4b in complex with PDE-delta (crystal form II - with ordered hypervariable region)|X-RAY DIFFRACTION|1.9|Homo sapiens|0|ONCOPROTEIN","5TB5|Crystal structure of full-length farnesylated and methylated KRAS4b in complex with PDE-delta (crystal form I - with partially disordered hypervariable region)|X-RAY DIFFRACTION|2|Homo sapiens|0|ONCOPROTEIN","5UFE|Wild-type K-Ras(GNP)/R11.1.6 complex|X-RAY DIFFRACTION|2.302|Homo sapiens; Sulfolobus solfataricus|0|Hydrolase/DE NOVO PROTEIN","5UFQ|K-RasG12D(GNP)/R11.1.6 complex|X-RAY DIFFRACTION|2.199|Homo sapiens; Sulfolobus solfataricus|0|Hydrolase/DE NOVO PROTEIN","5UK9|Wild-type K-Ras(GCP) pH 6.5|X-RAY DIFFRACTION|1.887|Homo sapiens|0|HYDROLASE","5UQW|Crystal structure of human KRAS G12V mutant in complex with GDP|X-RAY DIFFRACTION|1.5|Homo sapiens|0|HYDROLASE","5US4|Crystal structure of human KRAS G12D mutant in complex with GDP|X-RAY DIFFRACTION|1.83|Homo sapiens|0|HYDROLASE","5USJ|Crystal Structure of human KRAS G12D mutant in complex with GDPNP|X-RAY DIFFRACTION|1.94|Homo sapiens|0|HYDROLASE","5V6S|Crystal structure of small molecule acrylamide 1 covalently bound to K-Ras G12C|X-RAY DIFFRACTION|1.7|Homo sapiens|0|HYDROLASE/HYDROLASE INHIBITOR","5V6V|Crystal structure of small molecule aziridine 3 covalently bound to K-Ras G12C|X-RAY DIFFRACTION|1.72|Homo sapiens|0|HYDROLASE/HYDROLASE INHIBITOR","5V71|KRAS G12C in bound to quinazoline based switch II pocket (SWIIP) binder|X-RAY DIFFRACTION|2.228|Homo sapiens|0|HYDROLASE/HYDROLASE inhibitor","5V9L|KRAS G12C in bound to quinazoline based switch II pocket (SWIIP) binder|X-RAY DIFFRACTION|1.981|Homo sapiens|0|HYDROLASE/HYDROLASE inhibitor","5V9O|KRAS G12C inhibitor|X-RAY DIFFRACTION|1.56|Homo sapiens|0|HYDROLASE/HYDROLASE inhibitor","5V9U|Crystal Structure of small molecule ARS-1620 covalently bound to K-Ras G12C|X-RAY DIFFRACTION|1.38|Homo sapiens|0|HYDROLASE/HYDROLASE INHIBITOR","5VBM|Crystal Structure of Small Molecule Disulfide 2C07 Bound to K-Ras Cys Light M72C GDP|X-RAY DIFFRACTION|1.49|Homo sapiens|0|HYDROLASE","5VP7|Crystal structure of human KRAS G12A mutant in complex with GDP|X-RAY DIFFRACTION|1.7|Homo sapiens|0|HYDROLASE","5VPI|Crystal structure of human KRAS G12A mutant in complex with GTP|X-RAY DIFFRACTION|1.62|Homo sapiens|0|HYDROLASE","5VPY|Crystal structure of human KRAS G12A mutant in complex with GppNHp|X-RAY DIFFRACTION|2|Homo sapiens|0|HYDROLASE","5VPZ|Crystal structure of human KRAS G12A mutant in complex with GTP-gamma-S|X-RAY DIFFRACTION|1.85|Homo sapiens|0|HYDROLASE","5VQ0|Crystal structure of human KRAS G12A mutant in complex with GDP (EDTA soaked)|X-RAY DIFFRACTION|2.3|Homo sapiens|0|HYDROLASE","5VQ1|Crystal structure of human KRAS Q61A mutant in complex with GDP|X-RAY DIFFRACTION|1.78|Homo sapiens|0|HYDROLASE","5VQ2|Crystal structure of human WT-KRAS in complex with GTP|X-RAY DIFFRACTION|1.96|Homo sapiens|0|HYDROLASE","5VQ6|Crystal structure of human WT-KRAS in complex with GTP-gamma-S|X-RAY DIFFRACTION|1.99|Homo sapiens|0|HYDROLASE","5VQ8|Crystal structure of human WT-KRAS in complex with GDP (EDTA soaked)|X-RAY DIFFRACTION|2.3|Homo sapiens|0|HYDROLASE","5W22|Crystal structure of human WT-KRAS in complex with GDP|X-RAY DIFFRACTION|1.762|Homo sapiens|0|HYDROLASE","5WHA|KRas G12V, bound to GDP and miniprotein 225-11|X-RAY DIFFRACTION|2.04|Homo sapiens; synthetic construct|0|PROTEIN BINDING","5WHB|KRas G12V, bound to GDP and miniprotein 225-11(A30R)|X-RAY DIFFRACTION|2.18|Homo sapiens; SYNTHETIC CONSTRUCT|0|PROTEIN BINDING","5WHD|Crystal structure of KRas G12V/D38P, bound to GDP|X-RAY DIFFRACTION|1.641|Homo sapiens|0|PROTEIN BINDING","5WHE|KRas G12V/D38P, bound to GppNHp and miniprotein 225-11|X-RAY DIFFRACTION|1.91|Homo sapiens; synthetic construct|0|PROTEIN BINDING","5WLB|KRas G12V, bound to GppNHp and miniprotein 225-15a/b|X-RAY DIFFRACTION|1.72|Homo sapiens; synthetic construct|0|PROTEIN BINDING","5WPM|KRas G12V, bound to GppNHp and miniprotein 225-11(A30R)|X-RAY DIFFRACTION|1.72|Homo sapiens; SYNTHETIC CONSTRUCT|0|SIGNALING PROTEIN","5XCO|Crystal structure of human K-Ras G12D Mutant in complex with GDP and Cyclic Inhibitory Peptide|X-RAY DIFFRACTION|1.25|Homo sapiens; SYNTHETIC CONSTRUCT|0|HYDROLASE/HYDROLASE INHIBITOR","5YXZ|Co-crystal Structure of KRAS (G12C) covalently bound with Quinazoline based inhibitor JBI484|X-RAY DIFFRACTION|1.7|Homo sapiens|0|TRANSFERASE","5YY1|Co-crystal Structure of KRAS (G12C) covalently bound with Quinazoline based inhibitor JBI739|X-RAY DIFFRACTION|1.69|Homo sapiens|0|TRANSFERASE","6ARK|Crystal Structure of compound 10 covalently bound to K-Ras G12C|X-RAY DIFFRACTION|1.75|Homo sapiens|0|signaling protein/inhibitor","6ASA|KRAS mutant-D33E in GDP-bound|X-RAY DIFFRACTION|2.545|Homo sapiens|0|HYDROLASE","6ASE|KRAS mutant-A59G in GDP-bound|X-RAY DIFFRACTION|1.554|Homo sapiens|0|HYDROLASE","6B0V|Crystal Structure of small molecule ARS-107 covalently bound to K-Ras G12C|X-RAY DIFFRACTION|1.29|Homo sapiens|0|SIGNALING PROTEIN","6B0Y|Crystal Structure of small molecule ARS-917 covalently bound to K-Ras G12C|X-RAY DIFFRACTION|1.43|Homo sapiens|0|SIGNALING PROTEIN","6BOF|Crystal structure of KRAS A146T-GDP demonstrating open switch 1 conformation|X-RAY DIFFRACTION|1.401|Homo sapiens|0|HYDROLASE","6BP1|Crystal structure of human KRAS A59G mutant in complex with GCP|X-RAY DIFFRACTION|2.001|Homo sapiens|0|HYDROLASE","6CC9|NMR data-driven model of GTPase KRas-GMPPNP:Cmpd2 complex tethered to a nanodisc|SOLUTION NMR||Homo sapiens|0|MEMBRANE PROTEIN/ONCOPROTEIN","6CCH|NMR data-driven model of GTPase KRas-GMPPNP tethered to a nanodisc (E3 state)|SOLUTION NMR||Homo sapiens|0|MEMBRANE PROTEIN/ONCOPROTEIN","6CCX|NMR data-driven model of GTPase KRas-GMPPNP:Cmpd2 complex tethered to a nanodisc|SOLUTION NMR||Homo sapiens|0|MEMBRANE PROTEIN/ONCOPROTEIN","6CU6|Crystal structure of GMPPNP-bound G12R mutant of human KRAS4b|X-RAY DIFFRACTION|1.5|Homo sapiens|0|ONCOPROTEIN","6E6F|KRAS G13D bound to GppNHp (K13GNP)|X-RAY DIFFRACTION|3.401|Homo sapiens|0|SIGNALING PROTEIN"]}]}