human | Q5 |
P106 | occupation | author | Q482980 |
Q27683670 | A Ctf4 trimer couples the CMG helicase to DNA polymerase α in the eukaryotic replisome. |
Q33481004 | A multidrug ABC transporter with a taste for salt |
Q59576150 | An artificial CO-releasing metalloprotein built by histidine-selective metallation |
Q46261652 | Analysis of the natively unstructured RNA/protein-recognition core in the Escherichia coli RNA degradosome and its interactions with regulatory RNA/Hfq complexes |
Q27641685 | Crystal structure of human cytochrome P450 2C9 with bound warfarin |
Q24299505 | Crystal structures of human cytochrome P450 3A4 bound to metyrapone and progesterone |
Q42052070 | Evidence for the assembly of a bacterial tripartite multidrug pump with a stoichiometry of 3:6:3. |
Q48132061 | Fragment Screening against the EthR-DNA Interaction by Native Mass Spectrometry. |
Q46576409 | Mass Spectrometry Reveals Protein Kinase CK2 High-Order Oligomerization via the Circular and Linear Assembly |
Q41961293 | Mass spectrometry of intact V-type ATPases reveals bound lipids and the effects of nucleotide binding |
Q48235531 | Mining 2:2 Complexes from 1:1 Stoichiometry: Formation of Cucurbit[8]uril-Diarylviologen Quaternary Complexes Favored by Electron-Donating Substituents. |
Q27679000 | Multimeric Complexes among Ankyrin-Repeat and SOCS-box Protein 9 (ASB9), ElonginBC, and Cullin 5: Insights into the Structure and Assembly of ECS-type Cullin-RING E3 Ubiquitin Ligases |
Q50992581 | Nanoelectrospray ionization mass spectrometric study of Mycobacterium tuberculosis CYP121-ligand interactions. |
Q46292463 | Nanoscale click-reactive scaffolds from peptide self-assembly. |
Q27674365 | Non-homologous end-joining partners in a helical dance: structural studies of XLF-XRCC4 interactions |
Q42004967 | Opening of the outer membrane protein channel in tripartite efflux pumps is induced by interaction with the membrane fusion partner |
Q28477960 | Rv2607 from Mycobacterium tuberculosis is a pyridoxine 5'-phosphate oxidase with unusual substrate specificity |
Q47814232 | Sequential Release of Proteins from Structured Multishell Microcapsules |
Q35863628 | Spontaneous CO release from Ru(II)(CO)2-protein complexes in aqueous solution, cells, and mice |
Q38943227 | Structural characterization of CYP144A1 - a cytochrome P450 enzyme expressed from alternative transcripts in Mycobacterium tuberculosis |
Q55657250 | Structural complexity of the co-chaperone SGTA: a conserved C-terminal region is implicated in dimerization and substrate quality control. |
Q27642604 | Structural constraints on protein self-processing in L-aspartate- -decarboxylase |
Q48135782 | Structural insights into the EthR-DNA interaction using native mass spectrometry. |
Q27675055 | Structure of a Blinkin-BUBR1 Complex Reveals an Interaction Crucial for Kinetochore-Mitotic Checkpoint Regulation via an Unanticipated Binding Site |
Q57540699 | Structure of a Blinkin-BUBR1 Complex Reveals an Interaction Crucial for Kinetochore-Mitotic Checkpoint Regulation via an Unanticipated Binding Site |
Q41518158 | Structure of a single-chain Fv bound to the 17 N-terminal residues of huntingtin provides insights into pathogenic amyloid formation and suppression. |
Q33322101 | Subunit architecture of intact protein complexes from mass spectrometry and homology modeling. |
Q34649774 | Suppression of the FOXM1 transcriptional programme via novel small molecule inhibition |
Q24658416 | The crystal structure of the N-terminal region of BUB1 provides insight into the mechanism of BUB1 recruitment to kinetochores |
Q27933768 | eIF2B is a decameric guanine nucleotide exchange factor with a γ2ε2 tetrameric core |
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