| human | Q5 |
| P12541 | Ludzie Nauki ID (new) | crK1WCrHFOX |
| P496 | ORCID iD | 0000-0002-7157-0014 |
| P3124 | Polish scientist ID | 254323 |
| P214 | VIAF ID | 256407012 |
| P10832 | WorldCat Entities ID | E39PBJtxbgW3gyFHVc3CwwhJXd |
| P27 | country of citizenship | Poland | Q36 |
| P184 | doctoral advisor | Irmgard Sinning | Q21262403 |
| P69 | educated at | Jagiellonian University | Q189441 |
| Heidelberg University | Q151510 | ||
| P108 | employer | Jagiellonian University | Q189441 |
| P734 | family name | Grudnik | Q118063121 |
| Grudnik | Q118063121 | ||
| Grudnik | Q118063121 | ||
| P735 | given name | Przemysław | Q4385098 |
| Przemysław | Q4385098 | ||
| Marek | Q17520946 | ||
| Marek | Q17520946 | ||
| P1412 | languages spoken, written or signed | Polish | Q809 |
| P1559 | name in native language | Przemysław Grudnik | |
| P106 | occupation | researcher | Q1650915 |
| P21 | sex or gender | male | Q6581097 |
| Q27728180 | A Unique Mdm2-Binding Mode of the 3-Pyrrolin-2-one- and 2-Furanone-Based Antagonists of the p53-Mdm2 Interaction |
| Q27697263 | Atomic resolution crystal structure of HV-BBI protease inhibitor from amphibian skin in complex with bovine trypsin |
| Q47842052 | Bioactive Macrocyclic Inhibitors of the PD-1/PD-L1 Immune Checkpoint. |
| Q97083781 | Chromosomal localization of PemIK toxin-antitoxin system results in the loss of toxicity - Characterization of pemIKSa1-Sp from Staphylococcus pseudintermedius |
| Q90381249 | Crystal Structure of Kluyveromyces lactis Glucokinase (KlGlk1) |
| Q100542459 | Crystal Structure of Mannose Specific IIA Subunit of Phosphotransferase System from Streptococcus pneumoniae |
| Q48202462 | Crystal structure of ADP-dependent glucokinase from Methanocaldococcus jannaschii in complex with 5-iodotubercidin reveals phosphoryl transfer mechanism |
| Q41094657 | Crystal structure of a low molecular weight activator Blm-pep with yeast 20S proteasome - insights into the enzyme activation mechanism |
| Q89399514 | Crystal structure of the FAS1 domain of the hyaluronic acid receptor stabilin-2 |
| Q61798851 | Development of a novel, high-affinity ssDNA trypsin inhibitor |
| Q90810250 | Half Way to Hypusine-Structural Basis for Substrate Recognition by Human Deoxyhypusine Synthase |
| Q112135149 | Human and mouse PD-L1: similar molecular structure, but different druggability profiles |
| Q27683723 | Insights into eukaryotic Rubisco assembly - crystal structures of RbcX chaperones from Arabidopsis thaliana |
| Q27701655 | Investigation of Serine-Proteinase-Catalyzed Peptide Splicing in Analogues of Sunflower Trypsin Inhibitor 1 (SFTI-1) |
| Q112155048 | Macrocyclic Peptide Inhibitor of PD‐1/PD‐L1 Immune Checkpoint |
| Q99235493 | Molecular basis for the bifunctional Uba4-Urm1 sulfur-relay system in tRNA thiolation and ubiquitin-like conjugation |
| Q34989260 | Protein targeting by the signal recognition particle. |
| Q48278713 | Small-Molecule Inhibitors of the Programmed Cell Death-1/Programmed Death-Ligand 1 (PD-1/PD-L1) Interaction via Transiently Induced Protein States and Dimerization of PD-L1. |
| Q42700822 | Small-molecule inhibitors of PD-1/PD-L1 immune checkpoint alleviate the PD-L1-induced exhaustion of T-cells. |
| Q36133953 | Structural Basis of GD2 Ganglioside and Mimetic Peptide Recognition by 14G2a Antibody. |
| Q47999524 | Structural Biology of the Immune Checkpoint Receptor PD-1 and Its Ligands PD-L1/PD-L2. |
| Q104500890 | Structural Characterization of Glycerol Kinase from the Thermophilic Fungus Chaetomium thermophilum |
| Q42684031 | Structural analysis of PIM1 kinase complexes with ATP-competitive inhibitors |
| Q88764273 | Structural basis for ADP-dependent glucokinase inhibition by 8-bromo-substituted adenosine nucleotide |
| Q28822250 | Structural basis for small molecule targeting of the programmed death ligand 1 (PD-L1) |
| Q27675406 | Structural basis for the molecular evolution of SRP-GTPase activation by protein |
| Q21262403 | Irmgard Sinning | doctoral student | P185 |
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