| human | Q5 |
| P2456 | DBLP author ID | 15/9216 |
| P6178 | Dimensions author ID | 0746326075.41 |
| P1960 | Google Scholar author ID | JObeofQAAAAJ |
| P2798 | Loop ID | 165948 |
| P1315 | NLA Trove people ID | 1709380 |
| P856 | official website | https://research.monash.edu/en/persons/4e6d638d-473b-4450-910c-8406144dc98c |
| P496 | ORCID iD | 0000-0002-0102-7884 |
| P3829 | Publons author ID | 2111586 |
| P1053 | ResearcherID | H-5925-2017 |
| P2038 | ResearchGate profile ID | Trevor-Lithgow |
| P1153 | Scopus author ID | 7004149745 |
| P10861 | Springer Nature person ID | 0746326075.41 |
| P1556 | zbMATH author ID | lithgow.trevor |
| P166 | award received | Lemberg Medal | Q56257036 |
| Fellow of the Australian Academy of Science | Q59260322 | ||
| P27 | country of citizenship | Australia | Q408 |
| P69 | educated at | La Trobe University | Q1478723 |
| P108 | employer | Monash University | Q598841 |
| P734 | family name | Lithgow | Q16872307 |
| Lithgow | Q16872307 | ||
| Lithgow | Q16872307 | ||
| P735 | given name | James | Q677191 |
| James | Q677191 | ||
| Trevor | Q19800846 | ||
| Trevor | Q19800846 | ||
| P6104 | maintained by WikiProject | WikiProject Mathematics | Q8487137 |
| P106 | occupation | researcher | Q1650915 |
| P21 | sex or gender | male | Q6581097 |
| Q55113475 | 1H, 13C and 15N Resonance Assignments of the Cytosolic Domain of Tom20 from Arabidopsis thaliana |
| Q114092923 | Neisseria gonorrhoeae-derived outer membrane vesicles package β-lactamases to promote antibiotic resistance |
| Q55113432 | A Functional Tom70 in the Human Parasite Blastocystis sp.: Implications for the Evolution of the Mitochondrial Import Apparatus |
| Q27935589 | A SNARE required for retrograde transport to the endoplasmic reticulum |
| Q55113416 | A Small Tim Homohexamer in the Relict Mitochondrion of Cryptosporidium |
| Q55113500 | A Toxic Fusion Protein Accumulating between the Mitochondrial Membranes Inhibits Protein Assemblyin Vivo |
| Q34384897 | A bioinformatic strategy for the detection, classification and analysis of bacterial autotransporters |
| Q45021739 | A biophysical analysis of the tetratricopeptide repeat-rich mitochondrial import receptor, Tom70, reveals an elongated monomer that is inherently flexible, unstable, and unfolds via a multistate pathway |
| Q34283635 | A complete set of SNAREs in yeast |
| Q30153355 | A comprehensive analysis of the Omp85/TpsB protein superfamily structural diversity, taxonomic occurrence, and evolution. |
| Q43953846 | A conserved proline residue is present in the transmembrane-spanning domain of Tom7 and other tail-anchored protein subunits of the TOM translocase |
| Q55113508 | A constitutive form of heat-shock protein 70 is located in the outer membranes of mitochondria from rat liver |
| Q33783379 | A first glimpse at the structure of the TOM translocase from the mitochondrial outer membrane |
| Q53596236 | A mitochondrial protein affects cell morphology, mitochondrial segregation and virulence in Leishmania. |
| Q36471352 | A model system for mitochondrial biogenesis reveals evolutionary rewiring of protein import and membrane assembly pathways |
| Q30156997 | A modular BAM complex in the outer membrane of the alpha-proteobacterium Caulobacter crescentus. |
| Q30153376 | A mortise-tenon joint in the transmembrane domain modulates autotransporter assembly into bacterial outer membranes |
| Q55113501 | A reply to Preiss et al |
| Q42610997 | An Escherichia coli gene showing a potential ancestral relationship to the genes for the mitochondrial import site proteins ISP42 and MOM38. |
| Q36202714 | An essential novel component of the noncanonical mitochondrial outer membrane protein import system of trypanosomatids |
| Q57786250 | An investigation into the Omp85 protein BamK in hypervirulent Klebsiella pneumoniae , and its role in outer membrane biogenesis |
| Q28740899 | Ancestral and derived protein import pathways in the mitochondrion of Reclinomonas americana |
| Q55113378 | Antibacterial poly(ethylene glycol) hydrogels from combined epoxy-amine and thiol-ene click reaction |
| Q40864225 | Antibiotic regimen based on population analysis of residing persister cells eradicates Staphylococcus epidermidis biofilms |
| Q35937989 | Assembling the mitochondrial outer membrane |
| Q27675923 | Assembly of the Type II Secretion System such as Found in Vibrio cholerae Depends on the Novel Pilotin AspS |
| Q30152931 | Assembly of the secretion pores GspD, Wza and CsgG into bacterial outer membranes does not require the Omp85 proteins BamA or TamA. |
| Q26998912 | Assembly of β-barrel proteins into bacterial outer membranes |
| Q92325639 | Atlas of group A streptococcal vaccine candidates compiled using large-scale comparative genomics |
| Q92035767 | Author Correction: Atlas of group A streptococcal vaccine candidates compiled using large-scale comparative genomics |
| Q37988280 | Back to basics: a revealing secondary reduction of the mitochondrial protein import pathway in diverse intracellular parasites |
| Q55113485 | Bacterial Proteins Predisposed for Targeting to Mitochondria |
| Q46201519 | Bacteriophage Transcytosis Provides a Mechanism To Cross Epithelial Cell Layers |
| Q52652011 | Bastion6: a bioinformatics approach for accurate prediction of type VI secreted effectors. |
| Q27939705 | Bipartite signals mediate subcellular targeting of tail-anchored membrane proteins in Saccharomyces cerevisiae |
| Q54420761 | Both the p33 and p55 subunits of the Helicobacter pylori VacA toxin are targeted to mammalian mitochondria. |
| Q27936692 | Cell wall integrity is linked to mitochondria and phospholipid homeostasis in Candida albicans through the activity of the post-transcriptional regulator Ccr4-Pop2. |
| Q38989842 | Comprehensive assessment and performance improvement of effector protein predictors for bacterial secretion systems III, IV and VI. |
| Q30152784 | Conserved Features in the Structure, Mechanism, and Biogenesis of the Inverse Autotransporter Protein Family |
| Q40659834 | Conserved features in TamA enable interaction with TamB to drive the activity of the translocation and assembly module |
| Q55043415 | Conserved motifs reveal details of ancestry and structure in the small TIM chaperones of the mitochondrial intermembrane space. |
| Q33300270 | Conserved substrate binding by chaperones in the bacterial periplasm and the mitochondrial intermembrane space |
| Q47126826 | Constraints on lateral gene transfer in promoting fimbrial usher protein diversity and function |
| Q55113469 | Convergent Evolution of Receptors for Protein Import into Mitochondria |
| Q47143550 | Correction for Nguyen et al., "Bacteriophage Transcytosis Provides a Mechanism To Cross Epithelial Cell Layers". |
| Q40151234 | Defining Membrane Protein Localization by Isopycnic Density Gradients |
| Q34793169 | Delivery of nascent polypeptides to the mitochondrial surface |
| Q64072673 | Determination of the molecular basis for coprogen import by Gram-negative bacteria |
| Q39370957 | Discovery of an archetypal protein transport system in bacterial outer membranes. |
| Q27934755 | Distinct roles for the Hsp40 and Hsp90 molecular chaperones during cystic fibrosis transmembrane conductance regulator degradation in yeast |
| Q55113510 | Do cytosolic factors prevent promiscuity at the membrane surface? |
| Q55113466 | Domain Stealing by Receptors in a Protein Transport Complex |
| Q42617365 | Domain organization of the monomeric form of the Tom70 mitochondrial import receptor |
| Q30155295 | Dynamic association of BAM complex modules includes surface exposure of the lipoprotein BamC. |
| Q30152737 | Effective assembly of fimbriae in Escherichia coli depends on the translocation assembly module nanomachine. |
| Q51720956 | Efficient construction of unmarked recombinant mycobacteria using an improved system. |
| Q40559486 | Eliminating Legionella by inhibiting BCL-XL to induce macrophage apoptosis. |
| Q38157200 | Emerging rules for effective antimicrobial coatings |
| Q39514389 | Environmental stresses inhibit and stimulate different protein import pathways in plant mitochondria |
| Q55113455 | Erratum to “Domain Organization of the Monomeric Form of the Tom70 Mitochondrial Import Receptor” [J. Mol. Biol. 388 (2009) 1043–1058] |
| Q30152835 | Evidence of Distinct Channel Conformations and Substrate Binding Affinities for the Mitochondrial Outer Membrane Protein Translocase Pore Tom40. |
| Q37051180 | Evidence of a reduced and modified mitochondrial protein import apparatus in microsporidian mitosomes |
| Q33632844 | Evolution of macromolecular import pathways in mitochondria, hydrogenosomes and mitosomes |
| Q30152925 | Evolution of the Translocation and Assembly Module (TAM) |
| Q36542525 | Evolution of the molecular machines for protein import into mitochondria |
| Q30155236 | Evolution of the β-barrel assembly machinery |
| Q33857498 | Extensively Drug-Resistant Klebsiella pneumoniae Causing Nosocomial Bloodstream Infections in China: Molecular Investigation of Antibiotic Resistance Determinants, Informing Therapy, and Clinical Outcomes. |
| Q92884810 | Filamentous phages: masters of a microbial sharing economy |
| Q97867240 | Formation and function of bacterial organelles |
| Q27932446 | Functional cooperation of mitochondrial protein import receptors in yeast. |
| Q57751848 | FusC, a member of the M16 protease family acquired by bacteria for iron piracy against plants |
| Q52311187 | Genome-scale metabolic modeling of responses to polymyxins in Pseudomonas aeruginosa. |
| Q24534322 | Giardia mitosomes and trichomonad hydrogenosomes share a common mode of protein targeting |
| Q37314730 | GlycoMine(struct): a new bioinformatics tool for highly accurate mapping of the human N-linked and O-linked glycoproteomes by incorporating structural features |
| Q41675643 | High-level expression of a mitochondrial enzyme, ornithine transcarbamylase from rat liver, in a baculovirus expression system |
| Q41468893 | Highways for protein delivery to the mitochondria |
| Q33964166 | How do plant mitochondria avoid importing chloroplast proteins? Components of the import apparatus Tom20 and Tom22 from Arabidopsis differ from their fungal counterparts |
| Q55113471 | Human Bcl-2 cannot directly inhibit the Caenorhabditis elegans Apaf-1 homologue CED-4, but can interact with EGL-1 |
| Q53507748 | Identification of BamC on the Surface of E. coli. |
| Q55113513 | Identification of a GTP-binding protein in the contact sites between inner and outer mitochondrial membranes |
| Q41125221 | Import and folding of proteins by mitochondria |
| Q57786448 | Import of the Cytochrome Oxidase Subunit Va Precursor into Yeast Mitochondria Is Mediated by the Outer Membrane Receptor Mas20p |
| Q29616477 | Importing mitochondrial proteins: machineries and mechanisms |
| Q27934124 | Integral membrane proteins in the mitochondrial outer membrane of Saccharomyces cerevisiae |
| Q55113457 | Jid1 is a J-protein functioning in the mitochondrial matrix, unable to directly participate in endoplasmic reticulum associated protein degradation |
| Q33915991 | Knowledge-transfer learning for prediction of matrix metalloprotease substrate-cleavage sites |
| Q34126309 | Legionella pneumophila secretes a mitochondrial carrier protein during infection |
| Q55113388 | Light-triggered release of ciprofloxacin from an in situ forming click hydrogel for antibacterial wound dressings |
| Q42138104 | Mas37p, a novel receptor subunit for protein import into mitochondria. |
| Q24299687 | Mature DIABLO/Smac is produced by the IMP protease complex on the mitochondrial inner membrane |
| Q112747914 | Mechanistic Insights into the Capsule-Targeting Depolymerase from a Klebsiella pneumoniae Bacteriophage |
| Q55448576 | Methionine biosynthesis and transport are functionally redundant for the growth and virulence of Salmonella Typhimurium. |
| Q57233113 | Mft52, an Acid-bristle Protein in the Cytosol That Delivers Precursor Proteins to Yeast Mitochondria |
| Q35127548 | Microsporidian mitosomes retain elements of the general mitochondrial targeting system |
| Q37775723 | Minor modifications and major adaptations: the evolution of molecular machines driving mitochondrial protein import |
| Q55113450 | Mitochondrial Biogenesis: Sorting Mechanisms Cooperate in ABC Transporter Assembly |
| Q30839877 | Mitochondrial FtsZ in a chromophyte alga. |
| Q55113430 | Mitochondrial Preprotein Translocase of Trypanosomatids Has a Bacterial Origin |
| Q55113477 | Mitochondrial Release of Pro-apoptotic Proteins |
| Q52974417 | Mitochondrial biogenesis: cell-cycle-dependent investment in making mitochondria. |
| Q35867270 | Mitochondrial sorting and assembly machinery subunit Sam37 in Candida albicans: insight into the roles of mitochondria in fitness, cell wall integrity, and virulence |
| Q55113398 | Modifications and Innovations in the Evolution of Mitochondrial Protein Import Pathways |
| Q30160041 | Molecular architecture and function of the Omp85 family of proteins |
| Q40503781 | Molecular architecture of the active mitochondrial protein gate |
| Q28476704 | MrkH, a novel c-di-GMP-dependent transcriptional activator, controls Klebsiella pneumoniae biofilm formation by regulating type 3 fimbriae expression |
| Q55113409 | Nanomechanics measurements of live bacteria reveal a mechanism for bacterial cell protection: the polysaccharide capsule in Klebsiella is a responsive polymer hydrogel that adapts to osmotic stress |
| Q27011231 | Of linkers and autochaperones: an unambiguous nomenclature to identify common and uncommon themes for autotransporter secretion |
| Q54245006 | Outer membrane vesicles from Neisseria gonorrhoeae target PorB to mitochondria and induce apoptosis. |
| Q45945702 | POSSUM: a bioinformatics toolkit for generating numerical sequence feature descriptors based on PSSM profiles. |
| Q37813258 | PUF proteins: repression, activation and mRNA localization |
| Q28236926 | Patterns that define the four domains conserved in known and novel isoforms of the protein import receptor Tom20 |
| Q42650257 | Phylogenetic Analysis of Klebsiella pneumoniae from Hospitalized Children, Pakistan |
| Q91436075 | Porin Associates with Tom22 to Regulate the Mitochondrial Protein Gate Assembly |
| Q35490858 | Positive autoregulation of mrkHI by the cyclic di-GMP-dependent MrkH protein in the biofilm regulatory circuit of Klebsiella pneumoniae |
| Q55113380 | Prebiotic-chemistry inspired polymer coatings for biomedical and material science applications |
| Q52542869 | Prechaperonin 60 and preornithine transcarbamylase share components of the import apparatus but have distinct maturation pathways in rat liver mitochondria. |
| Q55113514 | Primary structure of mammalian ribosomal protein S6 |
| Q24675444 | Proapoptotic BH3-only proteins trigger membrane integration of prosurvival Bcl-w and neutralize its activity |
| Q90716777 | Protease-associated import systems are widespread in Gram-negative bacteria |
| Q35681300 | Protein hijacking: key proteins held captive against their will |
| Q36224510 | Protein import into mitochondria: origins and functions today (review). |
| Q30157537 | Protein secretion and outer membrane assembly in Alphaproteobacteria |
| Q24791451 | Protein structure and function by the sea |
| Q36151937 | Protein targeting: entropy, energetics and modular machines |
| Q57786254 | Quokka: a comprehensive tool for rapid and accurate prediction of kinase family-specific phosphorylation sites in the human proteome |
| Q27938678 | RAC, a stable ribosome-associated complex in yeast formed by the DnaK-DnaJ homologs Ssz1p and zuotin. |
| Q27973642 | Re-assessing the locations of components of the classical vesicle-mediated trafficking machinery in transfected Plasmodium falciparum |
| Q46034472 | Recognition of mitochondrial targeting sequences by the import receptors Tom20 and Tom22. |
| Q36248731 | Reconstitution of a nanomachine driving the assembly of proteins into bacterial outer membranes |
| Q27027278 | Reconstitution of membrane proteins into model membranes: seeking better ways to retain protein activities |
| Q55113506 | Reconstitution of the initial steps of mitochondrial protein import |
| Q47119414 | Reductive evolution in outer membrane protein biogenesis has not compromised cell surface complexity in Helicobacter pylori |
| Q55113427 | Response to Zarsky et al |
| Q35617768 | Role for yeast inhibitor of apoptosis (IAP)-like proteins in cell division |
| Q43106437 | Seaside transportation--from structure to function of translocation machines |
| Q39005954 | SecretEPDB: a comprehensive web-based resource for secreted effector proteins of the bacterial types III, IV and VI secretion systems |
| Q50494902 | Self-assembly of ciprofloxacin and a tripeptide into an antimicrobial nanostructured hydrogel. |
| Q33654525 | Structural Basis for Linezolid Binding Site Rearrangement in the Staphylococcus aureus Ribosome |
| Q42379907 | Structural Basis of Type 2 Secretion System Engagement between the Inner and Outer Bacterial Membranes |
| Q40115920 | Structural basis for substrate selection by the translocation and assembly module of the β-barrel assembly machinery |
| Q27679844 | Structural insight into the biogenesis of β-barrel membrane proteins |
| Q37083864 | Structure, topology and function of the translocase of the outer membrane of mitochondria |
| Q39371081 | Super-Resolution Imaging of Protein Secretion Systems and the Cell Surface of Gram-Negative Bacteria |
| Q45943465 | Systematic analysis and prediction of type IV secreted effector proteins by machine learning approaches. |
| Q34571547 | Systems biology: the next frontier for bioinformatics |
| Q55113468 | TOM and SAM Machineries in Mitochondrial Protein Import and Outer Membrane Biogenesis |
| Q55113495 | Targeting of C-Terminal (Tail)-Anchored Proteins: Understanding how Cytoplasmic Activities are Anchored to Intracellular Membranes |
| Q30155444 | Targeting of Neisserial PorB to the mitochondrial outer membrane: an insight on the evolution of β-barrel protein assembly machines |
| Q33908037 | Targeting of proteins to mitochondria |
| Q33865072 | Targeting of tail-anchored proteins to yeast mitochondria in vivo |
| Q55113473 | The C-terminal TPR Domain of Tom70 Defines a Family of Mitochondrial Protein Import Receptors Found only in Animals and Fungi |
| Q27936317 | The J-protein family: modulating protein assembly, disassembly and translocation |
| Q27931934 | The Omp85 family of proteins is essential for outer membrane biogenesis in mitochondria and bacteria. |
| Q47148365 | The Structure of a Conserved Domain of TamB Reveals a Hydrophobic β Taco Fold |
| Q47727168 | The TPR domain of BepA is required for productive interaction with substrate proteins and the β-barrel assembly machinery complex |
| Q34795107 | The Tom channel in the mitochondrial outer membrane: alive and kicking |
| Q55113465 | The Transmembrane Segment of Tom20 Is Recognized by Mim1 for Docking to the Mitochondrial TOM Complex |
| Q57751900 | The WD40 Protein BamB Mediates Coupling of BAM Complexes into Assembly Precincts in the Bacterial Outer Membrane |
| Q56973269 | The Yeast Mitochondrial Protein Import Receptor Mas20p Binds Precursor Proteins through Electrostatic Interaction with the Positively Charged Presequence |
| Q97904772 | The architecture and stabilisation of flagellotropic tailed bacteriophages |
| Q30155470 | The core components of organelle biogenesis and membrane transport in the hydrogenosomes of Trichomonas vaginalis |
| Q94473743 | The crystal structure of the TonB-dependent transporter YncD reveals a positively charged substrate-binding site |
| Q37027998 | The direct route: a simplified pathway for protein import into the mitochondrion of trypanosomes |
| Q28473253 | The essentials of protein import in the degenerate mitochondrion of Entamoeba histolytica |
| Q30155332 | The evolution of new lipoprotein subunits of the bacterial outer membrane BAM complex. |
| Q41380869 | The first steps of protein import into mitochondria |
| Q90297778 | The flagellotropic bacteriophage YSD1 targets Salmonella Typhi with a Chi-like protein tail fibre |
| Q33388227 | The major surface-associated saccharides of Klebsiella pneumoniae contribute to host cell association |
| Q33842273 | The minimal proteome in the reduced mitochondrion of the parasitic protist Giardia intestinalis |
| Q27934752 | The mitochondrial import protein Mim1 promotes biogenesis of multispanning outer membrane proteins |
| Q35951305 | The mitochondrial outer membrane protein Mas22p is essential for protein import and viability of yeast |
| Q55113498 | The mitochondrial protein targeting suppressor (mts1) mutation maps to the mRNA-binding domain of Npl3p and affects translation on cytoplasmic polysomes |
| Q30152728 | The modular nature of the β-barrel assembly machinery, illustrated in Borrelia burgdorferi |
| Q55113493 | The nascent polypeptide-associated complex (NAC) promotes interaction of ribosomes with the mitochondrial surface in vivo |
| Q33304765 | The peripheral membrane subunits of the SAM complex function codependently in mitochondrial outer membrane biogenesis |
| Q55113504 | The protein encoded by theMFT1gene is a targeting factor for mitochondrial precursor proteins, and not a core ribosomal protein |
| Q37324390 | The protein import channel in the outer mitosomal membrane of Giardia intestinalis |
| Q55113507 | The protein import receptor of mitochondria |
| Q41477528 | The protein product of the oncogene bcl-2 is a component of the nuclear envelope, the endoplasmic reticulum, and the outer mitochondrial membrane. |
| Q22066280 | The reducible complexity of a mitochondrial molecular machine |
| Q30157442 | The single mitochondrial porin of Trypanosoma brucei is the main metabolite transporter in the outer mitochondrial membrane |
| Q47586784 | The structure and membrane topography of the Vibrio-type secretin complex from the T2SS of enteropathogenic Escherichia coli (EPEC). |
| Q51735882 | The three domains of the mitochondrial outer membrane protein Mim1 have discrete functions in assembly of the TOM complex. |
| Q37035344 | The twists and turns of Maurer's cleft trafficking in P. falciparum-infected erythrocytes |
| Q36018127 | The type II secretion system and its ubiquitous lipoprotein substrate, SslE, are required for biofilm formation and virulence of enteropathogenic Escherichia coli |
| Q27939702 | The yeast PUF protein Puf5 has Pop2-independent roles in response to DNA replication stress |
| Q27931088 | The yeast nascent polypeptide-associated complex initiates protein targeting to mitochondria in vivo. |
| Q38596996 | The β-Barrel Assembly Machinery Complex |
| Q55113448 | Tinkering Inside the Organelle |
| Q47447819 | Tom22', an 8-kDa trans-site receptor in plants and protozoans, is a conserved feature of the TOM complex that appeared early in the evolution of eukaryotes |
| Q24677698 | Tom40, the import channel of the mitochondrial outer membrane, plays an active role in sorting imported proteins |
| Q37309122 | Transcriptional activation of the mrkA promoter of the Klebsiella pneumoniae type 3 fimbrial operon by the c-di-GMP-dependent MrkH protein |
| Q30156890 | Using hidden markov models to discover new protein transport machines |
| Q57786457 | Yeast mitochondria lacking the two import receptors Mas20p and Mas70p can efficiently and specifically import precursor proteins |
| Q27935898 | Zim17, a novel zinc finger protein essential for protein import into mitochondria |
| Q91153166 | cryoEM-Guided Development of Antibiotics for Drug-Resistant Bacteria |
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