Browse result page of PRRDB 2.0

ST_IDName of ReceptorPDBIDOrganismDescription
ST_3546RECEPTOR LIKE KINASE4U4RSaccharomyces cerevisiae S288CCrystal structure of Lactimidomycin bound to the yeast 80S ribosome
ST_3547RECEPTOR LIKE KINASE4U4USaccharomyces cerevisiae (strain ATCC 204508 / S288c)Crystal structure of Lycorine bound to the yeast 80S ribosome
ST_3548RECEPTOR LIKE KINASE4U4YSaccharomyces cerevisiae (strain ATCC 204508 / S288c)Crystal structure of Pactamycin bound to the yeast 80S ribosome
ST_3549RECEPTOR LIKE KINASE4U4ZSaccharomyces cerevisiae (strain ATCC 204508 / S288c)Crystal structure of Phyllanthoside bound to the yeast 80S ribosome
ST_3550RECEPTOR LIKE KINASE4U50Saccharomyces cerevisiae (strain ATCC 204508 / S288c)Crystal structure of Verrucarin bound to the yeast 80S ribosome
ST_3551RECEPTOR LIKE KINASE4U51Saccharomyces cerevisiae S288CCrystal structure of Narciclasine bound to the yeast 80S ribosome
ST_3552RECEPTOR LIKE KINASE4U52Saccharomyces cerevisiae (strain ATCC 204508 / S288c)Crystal structure of Nagilactone C bound to the yeast 80S ribosome
ST_3553RECEPTOR LIKE KINASE4U53Saccharomyces cerevisiae (strain ATCC 204508 / S288c)Crystal structure of Deoxynivalenol bound to the yeast 80S ribosome
ST_3554RECEPTOR LIKE KINASE4U55Saccharomyces cerevisiae (strain ATCC 204508 / S288c)Crystal structure of Cryptopleurine bound to the yeast 80S ribosome
ST_3555RECEPTOR LIKE KINASE4U56Saccharomyces cerevisiae (strain ATCC 204508 / S288c)Crystal structure of Blasticidin S bound to the yeast 80S ribosome
ST_3556RECEPTOR LIKE KINASE4U6FSaccharomyces cerevisiae (strain ATCC 204508 / S288c)Crystal structure of T-2 toxin bound to the yeast 80S ribosome
ST_3557RECEPTOR LIKE KINASE4UG0Homo sapiensSTRUCTURE OF THE HUMAN 80S RIBOSOME
ST_3558RECEPTOR LIKE KINASE4UJEOryctolagus cuniculus, Bos taurus, Escherichia coliRegulation of the mammalian elongation cycle by 40S subunit rolling: a eukaryotic-specific ribosome rearrangement
ST_3559RECEPTOR LIKE KINASE4UWBHomo sapiensFibroblast growth factor receptor 1 kinase in complex with JK-P5
ST_3560RECEPTOR LIKE KINASE4UWCHomo sapiensFibroblast growth factor receptor 1 kinase in complex with JK-P3
ST_3561RECEPTOR LIKE KINASE4UWYHomo sapiensFGFR1 Apo structure
ST_3562RECEPTOR LIKE KINASE4V6WDrosophila melanogasterStructure of the D. melanogaster 80S ribosome
ST_3563RECEPTOR LIKE KINASE4V6XHomo sapiensStructure of the human 80S ribosome
ST_3564RECEPTOR LIKE KINASE4V7RSaccharomyces cerevisiae (strain ATCC 204508 / S288c)Yeast 80S ribosome.
ST_3565RECEPTOR LIKE KINASE4V88Saccharomyces cerevisiae (strain ATCC 204508 / S288c)The structure of the eukaryotic ribosome at 3.0 A resolution.
ST_3566RECEPTOR LIKE KINASE4V8YSaccharomyces cerevisiae (strain ATCC 204508 / S288c)Cryo-EM reconstruction of the 80S-eIF5B-Met-itRNAMet Eukaryotic Translation Initiation Complex
ST_3567RECEPTOR LIKE KINASE4V8ZSaccharomyces cerevisiae (strain ATCC 204508 / S288c)Cryo-EM reconstruction of the 80S-eIF5B-Met-itRNAMet Eukaryotic Translation Initiation Complex
ST_3568RECEPTOR LIKE KINASE4W4ZHomo sapiensStructure of the EphA4 LBD in complex with peptide
ST_3569RECEPTOR LIKE KINASE4W50Homo sapiensStructure of the EphA4 LBD in complex with peptide
ST_3570RECEPTOR LIKE KINASE4WUNHomo sapiensStructure of FGFR1 in complex with AZD4547 (N-{3-[2-(3,5-DIMETHOXYPHENYL)ETHYL]-1H-PYRAZOL-5-YL}-4-[(3R,5-DIMETHYLPIPERAZIN-1-YL]BENZAMIDE) at 1.65 an
ST_3571RECEPTOR LIKE KINASE4X0MHomo sapiensSelection of fragments for kinase inhibitor design: decoration is key
ST_3572RECEPTOR LIKE KINASE4X2FHomo sapiensSelection of fragments for kinase inhibitor design: decoration is key
ST_3573RECEPTOR LIKE KINASE4X2GHomo sapiensSelection of fragments for kinase inhibitor design: decoration is key
ST_3574RECEPTOR LIKE KINASE4X2JHomo sapiensSelection of fragments for kinase inhibitor design: decoration is key
ST_3575RECEPTOR LIKE KINASE4X2KHomo sapiensSelection of fragments for kinase inhibitor design: decoration is key
ST_3576RECEPTOR LIKE KINASE4X2NHomo sapiensSelection of fragments for kinase inhibitor design: decoration is key
ST_3577RECEPTOR LIKE KINASE4XUFHomo sapiensCrystal structure of the FLT3 kinase domain bound to the inhibitor quizartinib (AC220)
ST_3578RECEPTOR LIKE KINASE4YRURattus norvegicusCrystal structure of C-terminally truncated Neuronal Calcium Sensor (NCS-1) from Rattus norvegicus
ST_3579RECEPTOR LIKE KINASE4Z61Daucus carota, Arabidopsis thalianaThe plant peptide hormone receptor complex
ST_3580RECEPTOR LIKE KINASE4Z64Arabidopsis thalianathe plant peptide hormone receptor complex in arabidopsis
ST_3581RECEPTOR LIKE KINASE4ZSAHomo sapiensCrystal structure of FGFR1 kinase domain in complex with 7n
ST_3582RECEPTOR LIKE KINASE5ABDHomo sapiensCRYSTAL STRUCTURE OF VEGFR-1 DOMAIN 2 IN PRESENCE OF CU
ST_3583RECEPTOR LIKE KINASE5AEQRattus norvegicusNeuronal calcium sensor (NCS-1)from Rattus norvegicus
ST_3584RECEPTOR LIKE KINASE5AERRattus norvegicus, Homo sapiensNeuronal calcium sensor-1 (NCS-1)from Rattus norvegicus complex with D2 dopamine receptor peptide from Homo sapiens
ST_3585RECEPTOR LIKE KINASE5AFPRattus norvegicus, Homo sapiensNeuronal calcium sensor-1 (NCS-1)from Rattus norvegicus complex with rhodopsin kinase peptide from Homo sapiens
ST_3586RECEPTOR LIKE KINASE5AJ0Homo sapiensCryo electron microscopy of actively translating human polysomes (POST state).
ST_3587RECEPTOR LIKE KINASE5AM6Homo sapiensNative FGFR1 with an inhibitor
ST_3588RECEPTOR LIKE KINASE5AM7Homo sapiensFGFR1 mutant with an inhibitor
ST_3589RECEPTOR LIKE KINASE5AR2Homo sapiensRIP2 Kinase Catalytic Domain (1 - 310)
ST_3590RECEPTOR LIKE KINASE5AR3Homo sapiensRIP2 Kinase Catalytic Domain (1 - 310) complex with AMP-PCP
ST_3591RECEPTOR LIKE KINASE5AR4Homo sapiensRIP2 Kinase Catalytic Domain (1 - 310) complex with SB-203580
ST_3592RECEPTOR LIKE KINASE5AR5Homo sapiensRIP2 Kinase Catalytic Domain (1 - 310) complex with Benzimidazole
ST_3593RECEPTOR LIKE KINASE5AR7Homo sapiensRIP2 Kinase Catalytic Domain (1 - 310) complex with Biaryl Urea
ST_3594RECEPTOR LIKE KINASE5AR8Homo sapiensRIP2 Kinase Catalytic Domain (1 - 310) complex with Biphenylsulfonamide
ST_3595RECEPTOR LIKE KINASE5BVKHomo sapiensFragment-based discovery of potent and selective DDR1/2 inhibitors