| review article | Q7318358 |
| scholarly article | Q13442814 |
| P356 | DOI | 10.1007/S12275-014-4087-Z |
| P2888 | exact match | https://scigraph.springernature.com/pub.10.1007/s12275-014-4087-z |
| P932 | PMC publication ID | 4012431 |
| P698 | PubMed publication ID | 24585055 |
| P5875 | ResearchGate publication ID | 260446531 |
| P50 | author | Ry Young | Q37376402 |
| P2860 | cites work | Nucleotide sequence of bacteriophage φX174 DNA | Q22122422 |
| Holins kill without warning | Q24555812 | ||
| Bacteriophage lysis: mechanism and regulation | Q24634690 | ||
| Identification and mutational analysis of bacteriophage PRD1 holin protein P35 | Q24672200 | ||
| Phage lysis: do we have the hole story yet? | Q26864407 | ||
| Regulation of a muralytic enzyme by dynamic membrane topology | Q27658032 | ||
| Identification and functional analysis of the Rz/Rz1-like accessory lysis genes in the membrane-containing bacteriophage PRD1 | Q28273948 | ||
| SNAREs--engines for membrane fusion | Q29547230 | ||
| Lipoprotein sorting in bacteria. | Q30155534 | ||
| The spanin complex is essential for lambda lysis | Q30525303 | ||
| A signal-arrest-release sequence mediates export and control of the phage P1 endolysin | Q33694582 | ||
| Micron-scale holes terminate the phage infection cycle | Q33719960 | ||
| Characterization of the dual start motif of a class II holin gene. | Q33864293 | ||
| Dimerization between the holin and holin inhibitor of phage lambda | Q33921201 | ||
| Genetic and biochemical analysis of dimer and oligomer interactions of the lambda S holin | Q33921206 | ||
| Genetic analysis of the T4 holin: timing and topology | Q33938601 | ||
| Functional analysis of the phage T4 holin in a lambda context | Q33947544 | ||
| An ancient player unmasked: T4 rI encodes a t-specific antiholin. | Q34088865 | ||
| Holin triggering in real time | Q34156732 | ||
| How SNARE molecules mediate membrane fusion: recent insights from molecular simulations | Q34256932 | ||
| Protein determinants of phage T4 lysis inhibition. | Q34258546 | ||
| Diversity in bacterial lysis systems: bacteriophages show the way. | Q34304410 | ||
| Topological and phylogenetic analyses of bacterial holin families and superfamilies | Q34357623 | ||
| A protein linkage map of Escherichia coli bacteriophage T7. | Q34367837 | ||
| Three functions of bacteriophage P1 involved in cell lysis | Q34372837 | ||
| Periplasmic domains define holin-antiholin interactions in t4 lysis inhibition | Q34451357 | ||
| Topological dynamics of holins in programmed bacterial lysis | Q34591617 | ||
| Disulfide isomerization after membrane release of its SAR domain activates P1 lysozyme | Q34650167 | ||
| The T4 RI antiholin has an N-terminal signal anchor release domain that targets it for degradation by DegP. | Q34662182 | ||
| The pinholin of lambdoid phage 21: control of lysis by membrane depolarization. | Q34683134 | ||
| Structure of the lethal phage pinhole | Q35009796 | ||
| The N-terminal transmembrane domain of lambda S is required for holin but not antiholin function | Q35011824 | ||
| S gene expression and the timing of lysis by bacteriophage lambda | Q35587403 | ||
| Functions involved in bacteriophage P2-induced host cell lysis and identification of a new tail gene | Q35968121 | ||
| Oligomerization of the bacteriophage lambda S protein in the inner membrane of Escherichia coli | Q36158132 | ||
| Mutational analysis of bacteriophage lambda lysis gene S. | Q36306838 | ||
| S gene product: identification and membrane localization of a lysis control protein | Q36332303 | ||
| Genetic studies of coliphage P1. I. Mapping by use of prophage deletions | Q36539361 | ||
| Localization of Membrane Protein Synthesized After Infection with Bacteriophage T4 | Q36555505 | ||
| Prediction of lipoprotein signal peptides in Gram-negative bacteria | Q36572165 | ||
| Subcellular localization of lethal lysis proteins of bacteriophages lambda and phiX174. | Q36899946 | ||
| Lethal action of bacteriophage lambda S gene | Q36927668 | ||
| The disulfide bond formation (Dsb) system | Q37136271 | ||
| The 'Bayer bridges' confronted with results from improved electron microscopy methods | Q37948365 | ||
| Stable micron-scale holes are a general feature of canonical holins | Q39223065 | ||
| Spanin function requires subunit homodimerization through intermolecular disulfide bonds | Q39441542 | ||
| The N-terminal region of the Oenococcus oeni bacteriophage fOg44 lysin behaves as a bona fide signal peptide in Escherichia coli and as a cis-inhibitory element, preventing lytic activity on oenococcal cells | Q39500910 | ||
| Transposition mutagenesis of bacteriophage lambda: a new gene affecting cell lysis | Q39905012 | ||
| Dual start motif in two lambdoid S genes unrelated to lambda S. | Q39941459 | ||
| Dual translational initiation sites control function of the lambda S gene | Q40820178 | ||
| The lambda spanin components Rz and Rz1 undergo tertiary and quaternary rearrangements upon complex formation | Q41148437 | ||
| The lethal lambda S gene encodes its own inhibitor | Q41205783 | ||
| The final step in the phage infection cycle: the Rz and Rz1 lysis proteins link the inner and outer membranes | Q41776739 | ||
| Mapping the pinhole formation pathway of S21 | Q41850197 | ||
| Mutational analysis of the S21 pinholin | Q41926970 | ||
| Regulation of a phage endolysin by disulfide caging | Q42045723 | ||
| Expression of the Rz gene and the overlapping Rz1 reading frame present at the right end of the bacteriophage lambda genome | Q42613531 | ||
| Complementation and characterization of the nested Rz and Rz1 reading frames in the genome of bacteriophage lambda | Q42616873 | ||
| Lysis timing and bacteriophage fitness | Q42714601 | ||
| Murein transglycosylase from phage lambda lysate. Purification and properties | Q43644081 | ||
| Synthesis of two bacteriophage lambda S proteins in an in vivo system | Q43814049 | ||
| Endopeptidase activity of phage lamba-endolysin | Q44380760 | ||
| Binding of mammalian ribosomes to MS2 phage RNA reveals an overlapping gene encoding a lysis function | Q44938103 | ||
| Nucleotide sequence of the bacteriophage P22 gene 19 to 3 region: identification of a new gene required for lysis. | Q45168353 | ||
| The Rz1 gene product of bacteriophage lambda is a lipoprotein localized in the outer membrane of Escherichia coli | Q48066352 | ||
| Location of the Rz gene in bacteriophage lambda | Q48394574 | ||
| Conversion of murein to non-reducing fragments by enzymes from phage λ and Vi II lysates | Q50231507 | ||
| 67 Separation of the inner (cytoplasmic) and outer membranes of gram-negative bacteria | Q50232039 | ||
| Rz/Rz1 lysis gene equivalents in phages of Gram-negative hosts. | Q51701491 | ||
| Areas of adhesion between wall and membrane of Escherichia coli. | Q54313482 | ||
| Charged amino-terminal amino acids affect the lethal capacity of Lambda lysis proteins S107 and S105. | Q54658367 | ||
| On a Remarkable Bacteriolytic Element Found in Tissues and Secretions | Q55877851 | ||
| Response of Escherichia coli cell membranes to induction of lambda cl857 prophage by heat shock | Q67907493 | ||
| Dominance in lambda S mutations and evidence for translational control | Q70050092 | ||
| Cell lysis by induction of cloned lambda lysis genes | Q70557007 | ||
| The R gene product of bacteriophage lambda is the murein transglycosylase | Q70566570 | ||
| Relation between hen egg white lysozyme and bacteriophage T4 lysozyme: Evolutionary implications | Q70915193 | ||
| A dominant mutation in the bacteriophage lambda S gene causes premature lysis and an absolute defective plating phenotype | Q72898951 | ||
| Membrane fusion by proline-rich Rz1 lipoprotein, the bacteriophage lambda Rz1 gene product | Q73395534 | ||
| Molecular function of the dual-start motif in the lambda S holin | Q78032482 | ||
| Genetic details, optimization and phage life histories | Q83345188 | ||
| P433 | issue | 3 | |
| P304 | page(s) | 243-258 | |
| P577 | publication date | 2014-03-01 | |
| P1433 | published in | The Journal of Microbiology | Q15749838 |
| P1476 | title | Phage lysis: three steps, three choices, one outcome | |
| P478 | volume | 52 |
| Q47228549 | A cytoplasmic antiholin is embedded in-frame with the holin in a Lactobacillus fermentum bacteriophage |
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| Q41667348 | A two-component, multimeric endolysin encoded by a single gene |
| Q90138118 | Active S2168 and inactive S21IRS pinholin interact differently with the lipid bilayer: A 31P and 2H solid state NMR study |
| Q88984461 | Activity of a Holin-Endolysin System in the Insecticidal Pathogenicity Island of Yersinia enterocolitica |
| Q41462758 | Analysis of 58 Families of Holins Using a Novel Program, PhyST. |
| Q26781115 | Antimicrobial bacteriophage-derived proteins and therapeutic applications |
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| Q26830795 | Bacteriophage lambda: Early pioneer and still relevant |
| Q30234522 | Bacteriophages and Their Immunological Applications against Infectious Threats. |
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| Q64089670 | Complete Genome Sequence of Salmonella enterica Serovar Enteritidis Myophage Mooltan |
| Q57279763 | Complete genomic sequence of the Vibrio alginolyticus bacteriophage Vp670 and characterization of the lysis-related genes, cwlQ and holA |
| Q93069536 | Continuous Wave Electron Paramagnetic Resonance Spectroscopy Reveals the Structural Topology and Dynamic Properties of Active Pinholin S2168 in a Lipid Bilayer |
| Q61798807 | Countermeasures Defeat a Virulent Bacteriophage |
| Q38635530 | Current and future therapies for Pseudomonas aeruginosa infection in patients with cystic fibrosis. |
| Q36386119 | Different Ancestries of R Tailocins in Rhizospheric Pseudomonas Isolates |
| Q36128097 | Diversity in a Polymicrobial Community Revealed by Analysis of Viromes, Endolysins and CRISPR Spacers |
| Q34046319 | Diversity of phage infection types and associated terminology: the problem with 'Lytic or lysogenic'. |
| Q93205347 | Dominant Vibrio cholerae phage exhibits lysis inhibition sensitive to disruption by a defensive phage satellite |
| Q52642775 | Engineering of Phage-Derived Lytic Enzymes: Improving Their Potential as Antimicrobials. |
| Q59355700 | Enzymes and Mechanisms Employed by Tailed Bacteriophages to Breach the Bacterial Cell Barriers |
| Q59356725 | Evaluation of the genomic diversity of viruses infecting bacteria, archaea and eukaryotes using a common bioinformatic platform: steps towards a unified taxonomy |
| Q42047038 | Evolved Populations of Shigella flexneri Phage Sf6 Acquire Large Deletions, Altered Genomic Architecture, and Faster Life Cycles |
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| Q47212786 | Genomic and Biochemical Characterization of Acinetobacter Podophage Petty Reveals a Novel Lysis Mechanism and Tail-Associated Depolymerase Activity. |
| Q89697787 | Gram-Negative Bacterial Lysins |
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| Q41028437 | Hydrogen peroxide causes Vibrio vulnificus bacteriolysis accelerated by sulfonyl fluoride compounds |
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| Q58781379 | Larger Than Life: Isolation and Genomic Characterization of a Jumbo Phage That Infects the Bacterial Plant Pathogen, |
| Q64271021 | May the Phage be With You? Prophage-Like Elements in the Genomes of Soft Rot : spp. and spp |
| Q35566997 | Membrane fusion during phage lysis. |
| Q46289250 | Molecular analysis of the low-temperature Escherichia coli phage vB_EcoS_NBD2. |
| Q42234380 | Molecular microbiology in antibacterial research. |
| Q28601826 | Monitoring Physiological Changes in Haloarchaeal Cell during Virus Release |
| Q40689252 | More than a hole: the holin lethal function may be required to fully sensitize bacteria to the lytic action of canonical endolysins. |
| Q51145669 | Multiple mechanisms drive phage infection efficiency in nearly identical hosts. |
| Q58780325 | Mycobacteriophage Lysis Enzymes: Targeting the Mycobacterial Cell Envelope |
| Q91714335 | Nine Novel Phages from a Plateau Lake in Southwest China: Insights into Aeromonas Phage Diversity |
| Q54212660 | Novel N4-Like Bacteriophages of Pectobacterium atrosepticum. |
| Q64107269 | Novel Stenotrophomonas maltophilia temperate phage DLP4 is capable of lysogenic conversion |
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