Browse result page of PRRDB 2.0

ST_IDName of ReceptorPDBIDOrganismDescription
ST_3646RECEPTOR LIKE KINASE5JFKArabidopsis thalianaCrystal structure of a TDR receptor
ST_3647RECEPTOR LIKE KINASE5JR2Homo sapiensCrystal structure of the EphA4 LBD in complex with APYd3 peptide inhibitor
ST_3648RECEPTOR LIKE KINASE5K5XHomo sapiensCrystal structure of human PDGFRA
ST_3649RECEPTOR LIKE KINASE5L04Homo sapiensSTRUCTURE OF INTERFERON LAMBDA 1 RECEPTOR WITH HUMAN KINASE JAK1
ST_3650RECEPTOR LIKE KINASE5L6OHomo sapiensEphB3 kinase domain covalently bound to an irreversible inhibitor (compound 3)
ST_3651RECEPTOR LIKE KINASE5L6PHomo sapiensEphB3 kinase domain covalently bound to an irreversible inhibitor (compound 6)
ST_3652RECEPTOR LIKE KINASE5LKSHomo sapiensStructure-function insights reveal the human ribosome as a cancer target for antibiotics
ST_3653RECEPTOR LIKE KINASE5LSPHomo sapiens107_A07 Fab in complex with fragment of the Met receptor
ST_3654RECEPTOR LIKE KINASE5LYBSaccharomyces cerevisiaeCrystal structure of the S.cerevisiae 80S ribosome in complex with the A-site bound aminoacyl-tRNA analog ACCPmn
ST_3655RECEPTOR LIKE KINASE5M1JSaccharomyces cerevisiae (strain ATCC 204508 / S288c)Nonstop ribosomal complex bound with Dom34 and Hbs1
ST_3656RECEPTOR LIKE KINASE5MC6Saccharomyces cerevisiae (strain ATCC 204508 / S288c)Cryo-EM structure of a native ribosome-Ski2-Ski3-Ski8 complex from S. cerevisiae
ST_3657RECEPTOR LIKE KINASE5MEISaccharomyces cerevisiae (strain ATCC 204508 / S288c)Crystal structure of Agelastatin A bound to the 80S ribosome
ST_3658RECEPTOR LIKE KINASE5MJAHomo sapiensKinase domain of human EphB1 bound to a quinazoline-based inhibitor
ST_3659RECEPTOR LIKE KINASE5MJBHomo sapiensKinase domain of human EphB1, G703C mutant, covalently bound to a quinazoline-based inhibitor
ST_3660RECEPTOR LIKE KINASE5MYAHomo sapiensHomodimerization of Tie2 Fibronectin-like domains 1-3 in space group C2
ST_3661RECEPTOR LIKE KINASE5MYBHomo sapiensHomodimerization of Tie2 Fibronectin-like domains 2 and 3 in space group P21
ST_3662RECEPTOR LIKE KINASE5N06Homo sapiensCrystal structure of Tie1 Fibronectin-like domain 3
ST_3663RECEPTOR LIKE KINASE5NDGSaccharomyces cerevisiae (strain ATCC 204508 / S288c)Crystal structure of geneticin (G418) bound to the yeast 80S ribosome
ST_3664RECEPTOR LIKE KINASE5NDVSaccharomyces cerevisiae (strain ATCC 204508 / S288c)Crystal structure of Paromomycin bound to the yeast 80S ribosome
ST_3665RECEPTOR LIKE KINASE5NDWSaccharomyces cerevisiae (strain ATCC 204508 / S288c)Crystal structure of aminoglycoside TC007 bound to the yeast 80S ribosome
ST_3666RECEPTOR LIKE KINASE5NG0Homo sapiensStructure of RIP2K(L294F) with bound AMPPCP
ST_3667RECEPTOR LIKE KINASE5NG2Homo sapiensStructure of RIP2K(D146N) with bound Staurosporine
ST_3668RECEPTOR LIKE KINASE5NG3Homo sapiensStructure of inactive kinase RIP2K(K47R)
ST_3669RECEPTOR LIKE KINASE5O49Homo sapiensHuman FGF in complex with a covalent inhibitor
ST_3670RECEPTOR LIKE KINASE5O4AHomo sapiensHuman FGF in complex with a covalent inhibitor
ST_3671RECEPTOR LIKE KINASE5O4OHomo sapiensHER3 in complex with Fab MF3178
ST_3672RECEPTOR LIKE KINASE5O7PHomo sapiensHER3 in complex with Fab MF3178
ST_3673RECEPTOR LIKE KINASE5OA3Homo sapiens, Hepacivirus CHuman 40S-eIF2D-re-initiation complex
ST_3674RECEPTOR LIKE KINASE5OBMSaccharomyces cerevisiae (strain ATCC 204508 / S288c)Crystal structure of Gentamicin bound to the yeast 80S ribosome
ST_3675RECEPTOR LIKE KINASE5ON6Saccharomyces cerevisiae (strain ATCC 204508 / S288c)Crystal structure of haemanthamine bound to the 80S ribosome
ST_3676RECEPTOR LIKE KINASE5OXGHomo sapiensCrystal structure of the ACVR1 (ALK2) kinase in complex with LDN-212854
ST_3677RECEPTOR LIKE KINASE5OY6Homo sapiensCrystal structure of the ACVR1 (ALK2) kinase in complex with cyclical inhibitor OD36.
ST_3678RECEPTOR LIKE KINASE5T2CHomo sapiensCryoEM structure of the human ribosome at 3.6 Angstrom resolution
ST_3679RECEPTOR LIKE KINASE5T89Homo sapiensCrystal structure of VEGF-A in complex with VEGFR-1 domains D1-6
ST_3680RECEPTOR LIKE KINASE5TBWSaccharomyces cerevisiae (strain ATCC 204508 / S288c)Crystal structure of chlorolissoclimide bound to the yeast 80S ribosome
ST_3681RECEPTOR LIKE KINASE5TGASaccharomyces cerevisiae (strain ATCC 204508 / S288c)Crystal structure of the S.cerevisiae 80S ribosome in complex with the A-site bound aminoacyl-tRNA analog ACCA-Pro
ST_3682RECEPTOR LIKE KINASE5TGMSaccharomyces cerevisiaeCrystal structure of the S.cerevisiae 80S ribosome in complex with the A-site bound aminoacyl-tRNA analog ACCA-Pro
ST_3683RECEPTOR LIKE KINASE5U8QHomo sapiensStructure of the ectodomain of the human Type 1 insulin-like growth factor receptor in complex with IGF-I
ST_3684RECEPTOR LIKE KINASE5U8RHomo sapiensStructure of the ectodomain of the human Type 1 insulin-like growth factor receptor
ST_3685RECEPTOR LIKE KINASE5UQ0Homo sapiensFGFR1 kinase domain complex with fragment 2,2-dimethyl-2,3-dihydrobenzofuran-7-carboxamide
ST_3686RECEPTOR LIKE KINASE5UR1Homo sapiensFGFR1 kinase domain complex with SN37333 in reversible binding mode
ST_3687RECEPTOR LIKE KINASE5USQHomo sapiensALK-5 kinase inhibitor complex
ST_3688RECEPTOR LIKE KINASE5UV4Zea maysCrystal Structure of Maize SIRK1 (sucrose-induced receptor kinase 1) kinase domain bound to AMP-PNP
ST_3689RECEPTOR LIKE KINASE5UWQHomo sapiensCrystal Structure of CDC7 NES Peptide in complex with CRM1-Ran-RanBP1
ST_3690RECEPTOR LIKE KINASE5UWRSaccharomyces cerevisiae (strain ATCC 204508 / S288c), Homo sapiensCrystal Structure of CDC7 NES Peptide (extended) in complex with CRM1-Ran-RanBP1
ST_3691RECEPTOR LIKE KINASE5VNDHomo sapiensCrystal structure of FGFR1-Y563C (FGFR4 surrogate) covalently bound to H3B-6527
ST_3692RECEPTOR LIKE KINASE5VYCHomo sapiensCrystal structure of the human 40S ribosomal subunit in complex with DENR-MCT-1.
ST_3693RECEPTOR LIKE KINASE5W21Homo sapiensCrystal Structure of a 1:1:1 FGF23-FGFR1c-aKlotho Ternary Complex
ST_3694RECEPTOR LIKE KINASE5W59Homo sapiensCrystal structure of a monomeric human FGF9 in complex with the ectodomain of human FGFR1c
ST_3695RECEPTOR LIKE KINASE5W5JHomo sapiensIdentification of potent and selective RIPK2 inhibitors for the treatment of inflammatory diseases