| P50 | author | Joshua R Burns | Q88088537 |
| P2093 | author name string | Michael R Baldwin | |
| P2860 | cites work | Botulinum neurotoxin B recognizes its protein receptor with high affinity and specificity | Q27643303 |
| | Glycosylated SV2 and Gangliosides as Dual Receptors for Botulinum Neurotoxin Serotype F | Q27655649 |
| | Gangliosides as High Affinity Receptors for Tetanus Neurotoxin | Q27656415 |
| | Unique Ganglioside Recognition Strategies for Clostridial Neurotoxins | Q27671814 |
| | Botulinum Neurotoxin Serotype C Associates with Dual Ganglioside Receptors to Facilitate Cell Entry | Q27673821 |
| | Crystal structure of the anthrax toxin protective antigen | Q27734828 |
| | Phase separation of integral membrane proteins in Triton X-114 solution | Q29547600 |
| | Botulinum neurotoxin devoid of receptor binding domain translocates active protease | Q33394567 |
| | Clostridial toxins as therapeutic agents: benefits of nature's most toxic proteins | Q33765977 |
| | Botulinum neurotoxin D-C uses synaptotagmin I and II as receptors, and human synaptotagmin II is not an effective receptor for type B, D-C and G toxins | Q33793263 |
| | Neurotoxins affecting neuroexocytosis | Q33881286 |
| | Sequence variation within botulinum neurotoxin serotypes impacts antibody binding and neutralization | Q34034156 |
| | Receptor binding enables botulinum neurotoxin B to sense low pH for translocation channel assembly. | Q35626467 |
| | Beltless translocation domain of botulinum neurotoxin A embodies a minimum ion-conductive channel | Q35693923 |
| | Botulinum neurotoxins B and E translocate at different rates and exhibit divergent responses to GT1b and low pH | Q36099792 |
| | Synaptotagmins I and II mediate entry of botulinum neurotoxin B into cells | Q36325534 |
| | Tetanus toxin fragment forms channels in lipid vesicles at low pH | Q36325692 |
| | General aspects and recent advances on bacterial protein toxins | Q36554621 |
| | Glycosylated SV2A and SV2B mediate the entry of botulinum neurotoxin E into neurons. | Q36992893 |
| | Cell entry strategy of clostridial neurotoxins | Q37490213 |
| | Entry of a recombinant, full-length, atoxic tetanus neurotoxin into Neuro-2a cells | Q37546383 |
| | Channels formed by botulinum, tetanus, and diphtheria toxins in planar lipid bilayers: relevance to translocation of proteins across membranes | Q37680475 |
| | Double anchorage to the membrane and intact inter-chain disulfide bond are required for the low pH induced entry of tetanus and botulinum neurotoxins into neurons. | Q39500669 |
| | Type F botulism due to neurotoxigenic Clostridium baratii from an unknown source in an adult | Q40214264 |
| | SV2 is the protein receptor for botulinum neurotoxin A. | Q40303506 |
| | Sequence homology and structural analysis of the clostridial neurotoxins | Q41695875 |
| | Kinetic intermediate reveals staggered pH-dependent transitions along the membrane insertion pathway of the diphtheria toxin T-domain | Q42562431 |
| | On the analysis of membrane protein circular dichroism spectra | Q43104925 |
| | Botulinum neurotoxins C, E and F bind gangliosides via a conserved binding site prior to stimulation-dependent uptake with botulinum neurotoxin F utilising the three isoforms of SV2 as second receptor | Q43299518 |
| | Arg(362) and Tyr(365) of the botulinum neurotoxin type a light chain are involved in transition state stabilization | Q43876643 |
| | Two carbohydrate binding sites in the H(CC)-domain of tetanus neurotoxin are required for toxicity | Q44312023 |
| | Synaptotagmins I and II act as nerve cell receptors for botulinum neurotoxin G. | Q44881077 |
| | A novel strain of Clostridium botulinum that produces type B and type H botulinum toxins | Q45345427 |
| | Analysis of active site residues of botulinum neurotoxin E by mutational, functional, and structural studies: Glu335Gln is an apoenzyme | Q46530120 |
| | Molecular basis for tetanus toxin coreceptor interactions | Q46547987 |
| | Sequences of the botulinal neurotoxin E derived from Clostridium botulinum type E (strain Beluga) and Clostridium butyricum (strains ATCC 43181 and ATCC 43755) | Q48184773 |
| | Micellar properties of glycosphingolipids in aqueous media | Q48604649 |
| | Insertion of Anthrax Protective Antigen into Liposomal Membranes | Q57213769 |
| | Light Chain of Botulinum Neurotoxin Serotype A: Structural Resolution of a Catalytic Intermediate†,‡ | Q61779321 |
| | Membrane interactions of tetanus and botulinum neurotoxins: a photolabelling study with photoactivatable phospholipids | Q68682703 |
| | Inhibition of vacuolar adenosine triphosphatase antagonizes the effects of clostridial neurotoxins but not phospholipase A2 neurotoxins | Q72389951 |
| | Spectroscopic analysis of low pH and lipid-induced structural changes in type A botulinum neurotoxin relevant to membrane channel formation and translocation | Q74769349 |
| | Botulinum neurotoxin light chain refolds at endosomal pH for its translocation | Q79370818 |
| P433 | issue | 32 | |
| P407 | language of work or name | English | Q1860 |
| P1104 | number of pages | 9 | |
| P304 | page(s) | 22450-22458 | |
| P577 | publication date | 2014-06-27 | |
| P1433 | published in | Journal of Biological Chemistry | Q867727 |
| P1476 | title | Tetanus neurotoxin utilizes two sequential membrane interactions for channel formation | |
| P478 | volume | 289 | |