| scholarly article | Q13442814 |
| P50 | author | Aravind L Iyer | Q4784512 |
| Dapeng Zhang | Q55136846 | ||
| Maxwell Burroughs | Q57749112 | ||
| Lakshminarayan M. Iyer | Q57749186 | ||
| A Maxwell Burroughs | Q89891231 | ||
| P2860 | cites work | Purine biosynthesis in archaea: variations on a theme | Q21203751 |
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| The crystal structure of a bacterial Sufu-like protein defines a novel group of bacterial proteins that are similar to the N-terminal domain of human Sufu | Q24625469 | ||
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| The structure of the endoribonuclease XendoU: From small nucleolar RNA processing to severe acute respiratory syndrome coronavirus replication | Q24670190 | ||
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| Identification of novel restriction endonuclease-like fold families among hypothetical proteins | Q24811792 | ||
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| Mutability of an HNH nuclease imidazole general base and exchange of a deprotonation mechanism | Q27644841 | ||
| Crystal structure of the -Me type II restriction endonuclease Hpy99I with target DNA | Q27654971 | ||
| Structure of ERA in complex with the 3' end of 16S rRNA: Implications for ribosome biogenesis | Q27657159 | ||
| The structural and energetic basis for high selectivity in a high-affinity protein-protein interaction | Q27661721 | ||
| Structural insight into the zinc finger CW domain as a histone modification reader | Q27664368 | ||
| Structural basis for 16S ribosomal RNA cleavage by the cytotoxic domain of colicin E3 | Q27664595 | ||
| Structure and Function of APH(4)-Ia, a Hygromycin B Resistance Enzyme | Q27665944 | ||
| The Structure of the CRISPR-Associated Protein Csa3 Provides Insight into the Regulation of the CRISPR/Cas System | Q27665992 | ||
| Crystal structures of antibiotic-bound complexes of aminoglycoside 2''-phosphotransferase IVa highlight the diversity in substrate binding modes among aminoglycoside kinases | Q27670461 | ||
| Characterization and crystal structure of the type IIG restriction endonuclease RM.BpuSI | Q27670651 | ||
| Activity, specificity and structure of I-Bth0305I: a representative of a new homing endonuclease family | Q27673004 | ||
| The Crystal Structure of the Intact E. coli RelBE Toxin-Antitoxin Complex Provides the Structural Basis for Conditional Cooperativity | Q27673158 | ||
| Reshaping Antibody Diversity | Q27678538 | ||
| Structures of a Bifunctional Cell Wall Hydrolase CwlT Containing a Novel Bacterial Lysozyme and an NlpC/P60 dl-Endopeptidase | Q27679991 | ||
| Evolution of CRISPR RNA recognition and processing by Cas6 endonucleases | Q27680426 | ||
| Structure of a Naegleria Tet-like dioxygenase in complex with 5-methylcytosine DNA | Q27681187 | ||
| Structures of Cas9 Endonucleases Reveal RNA-Mediated Conformational Activation | Q27681624 | ||
| Crystal structure and nucleic acid-binding activity of the CRISPR-associated protein Csx1 of Pyrococcus furiosus | Q27682287 | ||
| CdiA from Enterobacter cloacae Delivers a Toxic Ribosomal RNase into Target Bacteria | Q27682361 | ||
| The structure of SAICAR synthase: an enzyme in the de novo pathway of purine nucleotide biosynthesis | Q27749393 | ||
| Form and flexibility in phosphoinositide 3-kinases | Q28252407 | ||
| Novel predicted peptidases with a potential role in the ubiquitin signaling pathway | Q28287730 | ||
| The kinase activity of human Rio1 is required for final steps of cytoplasmic maturation of 40S subunits | Q28596592 | ||
| The RNase H-like superfamily: new members, comparative structural analysis and evolutionary classification | Q29037102 | ||
| A new generation of homology search tools based on probabilistic inference | Q29616170 | ||
| CARF and WYL domains: ligand-binding regulators of prokaryotic defense systems | Q30009424 | ||
| Protein kinases: evolution of dynamic regulatory proteins | Q30014836 | ||
| Identification of homology in protein structure classification. | Q30329161 | ||
| Diversification of catalytic activities and ligand interactions in the protein fold shared by the sugar isomerases, eIF2B, DeoR transcription factors, acyl-CoA transferases and methenyltetrahydrofolate synthetase. | Q30352344 | ||
| Structural relationships among proteins with different global topologies and their implications for function annotation strategies | Q30381353 | ||
| How far divergent evolution goes in proteins | Q30431003 | ||
| Comparative proteomics identifies the cell-associated lethality of M. tuberculosis RelBE-like toxin-antitoxin complexes | Q30549619 | ||
| SURVEY AND SUMMARY: holliday junction resolvases and related nucleases: identification of new families, phyletic distribution and evolutionary trajectories | Q30612214 | ||
| Emergence of diverse biochemical activities in evolutionarily conserved structural scaffolds of proteins | Q30883445 | ||
| Crystal structure of A. fulgidus Rio2 defines a new family of serine protein kinases | Q30955879 | ||
| A novel immunity system for bacterial nucleic acid degrading toxins and its recruitment in various eukaryotic and DNA viral systems | Q30999460 | ||
| Using a library of structural templates to recognise catalytic sites and explore their evolution in homologous families | Q31152169 | ||
| Phosphatidylinositol phosphate kinase: a link between protein kinase and glutathione synthase folds | Q31388296 | ||
| Comparative genomics of the FtsK-HerA superfamily of pumping ATPases: implications for the origins of chromosome segregation, cell division and viral capsid packaging | Q33207648 | ||
| The RAGNYA fold: a novel fold with multiple topological variants found in functionally diverse nucleic acid, nucleotide and peptide-binding proteins | Q33294961 | ||
| Amidoligases with ATP-grasp, glutamine synthetase-like and acetyltransferase-like domains: synthesis of novel metabolites and peptide modifications of proteins | Q33519914 | ||
| A highly conserved family of domains related to the DNA-glycosylase fold helps predict multiple novel pathways for RNA modifications | Q33823011 | ||
| Unification of Cas protein families and a simple scenario for the origin and evolution of CRISPR-Cas systems | Q33960829 | ||
| Evolution of the deaminase fold and multiple origins of eukaryotic editing and mutagenic nucleic acid deaminases from bacterial toxin systems | Q34010890 | ||
| Divergent evolution in enolase superfamily: strategies for assigning functions | Q34070425 | ||
| The PHD finger: a versatile epigenome reader | Q34180042 | ||
| Polymorphic toxin systems: Comprehensive characterization of trafficking modes, processing, mechanisms of action, immunity and ecology using comparative genomics | Q34283923 | ||
| Structural diversity and protein engineering of the aminoacyl-tRNA synthetases | Q34306657 | ||
| On the evolution of protein folds: are similar motifs in different protein folds the result of convergence, insertion, or relics of an ancient peptide world? | Q34364840 | ||
| Gene flow and biological conflict systems in the origin and evolution of eukaryotes | Q34392545 | ||
| A case of convergent evolution of nucleic acid binding modules | Q34411103 | ||
| Homing endonuclease structure and function | Q34473961 | ||
| Plasticity of enzyme active sites | Q34768892 | ||
| Comprehensive analysis of the HEPN superfamily: identification of novel roles in intra-genomic conflicts, defense, pathogenesis and RNA processing | Q34773696 | ||
| A model for statistical significance of local similarities in structure. | Q35069452 | ||
| Determinants of the cytotoxicity of PrrC anticodon nuclease and its amelioration by tRNA repair | Q35682185 | ||
| Immune related genes underpin the evolution of adaptive immunity in jawless vertebrates | Q35841331 | ||
| Mechanisms, biology and inhibitors of deubiquitinating enzymes | Q36975731 | ||
| The AID/APOBEC family of nucleic acid mutators. | Q37206307 | ||
| Enzyme (re)design: lessons from natural evolution and computation | Q37399741 | ||
| Nucleases: diversity of structure, function and mechanism. | Q37790458 | ||
| Toxins-antitoxins: diversity, evolution and function | Q37912155 | ||
| Recognition of methylated histones: new twists and variations | Q37953134 | ||
| Structure of an XPF endonuclease with and without DNA suggests a model for substrate recognition. | Q41376744 | ||
| The wobble nucleotide-excising anticodon nuclease RloC is governed by the zinc-hook and DNA-dependent ATPase of its Rad50-like region | Q41810652 | ||
| Editorial: NAR surveys the past, present and future of restriction endonucleases | Q42773415 | ||
| Diversity of bacterial type II toxin-antitoxin systems: a comprehensive search and functional analysis of novel families | Q42836520 | ||
| Evolution of new protein topologies through multistep gene rearrangements | Q56899286 | ||
| RNA Ligase Structures Reveal the Basis for RNA Specificity and Conformational Changes that Drive Ligation Forward | Q58050055 | ||
| Protein structure space is much more than the sum of its folds | Q80429092 | ||
| P304 | page(s) | 92-103 | |
| P577 | publication date | 2014-06-19 | |
| P1433 | published in | Current Opinion in Structural Biology | Q15758416 |
| P1476 | title | Resilience of biochemical activity in protein domains in the face of structural divergence | |
| P478 | volume | 26 |
| Q87837788 | A malaria parasite subtilisin propeptide-like protein is a potent inhibitor of the egress protease SUB1. |
| Q28492996 | An interbacterial NAD(P)(+) glycohydrolase toxin requires elongation factor Tu for delivery to target cells |
| Q64064061 | Antimicrobial Peptides, Polymorphic Toxins, and Self-Nonself Recognition Systems in Archaea: an Untapped Armory for Intermicrobial Conflicts |
| Q35847777 | Comparative genomic analyses reveal a vast, novel network of nucleotide-centric systems in biological conflicts, immunity and signaling |
| Q28083323 | Contact-Dependent Growth Inhibition (CDI) and CdiB/CdiA Two-Partner Secretion Proteins |
| Q90082260 | Convergent Evolution of the Barnase/EndoU/Colicin/RelE (BECR) Fold in Antibacterial tRNase Toxins |
| Q64236159 | Different Ways of Doing the Same: Variations in the Two Last Steps of the Purine Biosynthetic Pathway in Prokaryotes |
| Q52718444 | Evolutionary convergence and divergence in archaeal chromosomal proteins and Chromo-like domains from bacteria and eukaryotes. |
| Q89891233 | Highly-regulated, diversifying NTP-based biological conflict systems with implications for emergence of multicellularity |
| Q30945256 | New players in the toxin field: polymorphic toxin systems in bacteria |
| Q35804736 | One cannot rule them all: Are bacterial toxins-antitoxins druggable? |
| Q36385479 | Polyvalent Proteins, a Pervasive Theme in the Intergenomic Biological Conflicts of Bacteriophages and Conjugative Elements |
| Q36106467 | RNA damage in biological conflicts and the diversity of responding RNA repair systems |
| Q90437907 | Small protein folds at the root of an ancient metabolic network |
| Q50026012 | The ColM Family, Polymorphic Toxins Breaching the Bacterial Cell Wall. |
| Q30370436 | The enzymatic nature of an anonymous protein sequence cannot reliably be inferred from superfamily level structural information alone |
| Q35605573 | The eukaryotic translation initiation regulator CDC123 defines a divergent clade of ATP-grasp enzymes with a predicted role in novel protein modifications |
| Q35984251 | Transposons to toxins: the provenance, architecture and diversification of a widespread class of eukaryotic effectors |
| Q27700906 | Two independently folding units of Plasmodium profilin suggest evolution via gene fusion |
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