Histone recognition by human malignant brain tumor domains. Read more about Histone recognition by human malignant brain tumor domains.
Structure of the bone morphogenetic protein receptor ALK2 and implications for fibrodysplasia ossificans progressiva. Read more about Structure of the bone morphogenetic protein receptor ALK2 and implications for fibrodysplasia ossificans progressiva.
Small-molecule inhibition of MLL activity by disruption of its interaction with WDR5. Read more about Small-molecule inhibition of MLL activity by disruption of its interaction with WDR5.
Certhrax Toxin, an Anthrax-related ADP-ribosyltransferase from Bacillus cereus. Read more about Certhrax Toxin, an Anthrax-related ADP-ribosyltransferase from Bacillus cereus.
Selectivity, cocrystal structures, and neuroprotective properties of leucettines, a family of protein kinase inhibitors derived from the marine sponge alkaloid leucettamine B. Read more about Selectivity, cocrystal structures, and neuroprotective properties of leucettines, a family of protein kinase inhibitors derived from the marine sponge alkaloid leucettamine B.
Association of UHRF1 with methylated H3K9 directs the maintenance of DNA methylation. Read more about Association of UHRF1 with methylated H3K9 directs the maintenance of DNA methylation.
C-terminal processing of the teneurin proteins: Independent actions of a teneurin C-terminal associated peptide in hippocampal cells. Read more about C-terminal processing of the teneurin proteins: Independent actions of a teneurin C-terminal associated peptide in hippocampal cells.
Structural basis for the recognition and cleavage of abasic DNA in Neisseria meningitidis. Read more about Structural basis for the recognition and cleavage of abasic DNA in Neisseria meningitidis.
Crystal structure of human multiple copies in T-cell lymphoma-1 oncoprotein. Read more about Crystal structure of human multiple copies in T-cell lymphoma-1 oncoprotein.
Sinefungin derivatives as inhibitors and structure probes of protein lysine methyltransferase SETD2. Read more about Sinefungin derivatives as inhibitors and structure probes of protein lysine methyltransferase SETD2.
