| scholarly article | Q13442814 |
| P2093 | author name string | Jing Li | |
| Yu Liu | |||
| Fan Zhang | |||
| Qi Zhu | |||
| Dan Li | |||
| Zhonghua Liu | |||
| Xi Zhou | |||
| Songping Liang | |||
| Meichun Deng | |||
| Weijun Hu | |||
| Jiayan Li | |||
| Tianfu Cai | |||
| P2860 | cites work | Overview of the voltage-gated sodium channel family | Q21999779 |
| Unique bell-shaped voltage-dependent modulation of Na+ channel gating by novel insect-selective toxins from the spider Agelena orientalis | Q24598512 | ||
| Mapping the receptor site for alpha-scorpion toxins on a Na+ channel voltage sensor | Q24635953 | ||
| Function and solution structure of huwentoxin-IV, a potent neuronal tetrodotoxin (TTX)-sensitive sodium channel antagonist from Chinese bird spider Selenocosmia huwena | Q27639643 | ||
| Function and solution structure of hainantoxin-I, a novel insect sodium channel inhibitor from the Chinese bird spider Selenocosmia hainana | Q27642791 | ||
| Solution structure and alanine scan of a spider toxin that affects the activation of mammalian voltage-gated sodium channels | Q27643216 | ||
| Venoms as a platform for human drugs: translating toxins into therapeutics | Q37937049 | ||
| Molecular interactions of the gating modifier toxin ProTx-II with NaV 1.5: implied existence of a novel toxin binding site coupled to activation | Q40163109 | ||
| Interaction of SNX482 with domains III and IV inhibits activation gating of alpha(1E) (Ca(V)2.3) calcium channels | Q40185471 | ||
| Disulfide structures of highly bridged peptides: a new strategy for analysis | Q42016457 | ||
| A common structural motif incorporating a cystine knot and a triple-stranded beta-sheet in toxic and inhibitory polypeptides | Q42131475 | ||
| Distinct repriming and closed-state inactivation kinetics of Nav1.6 and Nav1.7 sodium channels in mouse spinal sensory neurons | Q42169958 | ||
| Inhibition of sodium channel gating by trapping the domain II voltage sensor with protoxin II. | Q42640701 | ||
| Echistatin disulfide bridges: selective reduction and linkage assignment | Q42842315 | ||
| Structure--activity relationships of hainantoxin-IV and structure determination of active and inactive sodium channel blockers | Q44939687 | ||
| Sequence-specific 1H-NMR assignment and determination of the secondary structure of hainantoxin-III from the spider Ornithoctonus hainana | Q45138421 | ||
| Venomics as a drug discovery platform | Q47671683 | ||
| Inhibition of neuronal tetrodotoxin-sensitive Na+ channels by two spider toxins: hainantoxin-III and hainantoxin-IV | Q48949713 | ||
| Common features in the functional surface of scorpion beta-toxins and elements that confer specificity for insect and mammalian voltage-gated sodium channels. | Q51821558 | ||
| The effects of huwentoxin-I on the voltage-gated sodium channels of rat hippocampal and cockroach dorsal unpaired median neurons. | Q52730869 | ||
| Modulation by adenosine of GABA-activated current in rat dorsal root ganglion neurons | Q73397049 | ||
| A positively charged surface patch is important for hainantoxin-IV binding to voltage-gated sodium channels | Q84882964 | ||
| The Xplor-NIH NMR molecular structure determination package | Q27860805 | ||
| From ionic currents to molecular mechanisms: the structure and function of voltage-gated sodium channels | Q28143653 | ||
| Voltage-dependent inhibition of N- and P-type calcium channels by the peptide toxin omega-grammotoxin-SIA | Q28257902 | ||
| Molecular diversification of peptide toxins from the tarantula Haplopelma hainanum (Ornithoctonus hainana) venom based on transcriptomic, peptidomic, and genomic analyses | Q28274590 | ||
| The chemical shift index: a fast and simple method for the assignment of protein secondary structure through NMR spectroscopy | Q28293625 | ||
| Isolation and characterization of hainantoxin-IV, a novel antagonist of tetrodotoxin-sensitive sodium channels from the Chinese bird spider Selenocosmia hainana | Q30807017 | ||
| The cystine knot motif in toxins and implications for drug design. | Q31425913 | ||
| ATDB: a uni-database platform for animal toxins | Q33302479 | ||
| ATDB 2.0: A database integrated toxin-ion channel interaction data | Q33647219 | ||
| Targeting voltage sensors in sodium channels with spider toxins. | Q33759435 | ||
| Molecular mechanisms of neurotoxin action on voltage-gated sodium channels. | Q33925844 | ||
| Voltage-gated ion channels and gating modifier toxins. | Q34161355 | ||
| Neurotoxins and their binding areas on voltage-gated sodium channels | Q34232755 | ||
| Voltage-gated sodium channels at 60: structure, function and pathophysiology | Q34265707 | ||
| The Tarantula Toxins ProTx-II and Huwentoxin-IV Differentially Interact with Human Nav1.7 Voltage Sensors to Inhibit Channel Activation and Inactivation | Q34359543 | ||
| Voltage-sensor activation with a tarantula toxin as cargo. | Q34442179 | ||
| Four novel tarantula toxins as selective modulators of voltage-gated sodium channel subtypes | Q34464859 | ||
| Are voltage-gated sodium channels on the dorsal root ganglion involved in the development of neuropathic pain? | Q34639336 | ||
| μ-Conotoxins that differentially block sodium channels NaV1.1 through 1.8 identify those responsible for action potentials in sciatic nerve | Q35064387 | ||
| Navβ subunits modulate the inhibition of Nav1.8 by the analgesic gating modifier μO-conotoxin MrVIB | Q35122879 | ||
| Common molecular determinants of tarantula huwentoxin-IV inhibition of Na+ channel voltage sensors in domains II and IV | Q35144846 | ||
| Structure-function map of the receptor site for β-scorpion toxins in domain II of voltage-gated sodium channels | Q35312565 | ||
| Docking of mu-conotoxin GIIIA in the sodium channel outer vestibule | Q35540469 | ||
| Mapping the interaction site for a β-scorpion toxin in the pore module of domain III of voltage-gated Na(+) channels | Q36216475 | ||
| Neuronal voltage-gated sodium channel subtypes: key roles in inflammatory and neuropathic pain. | Q36571422 | ||
| ProTx-I and ProTx-II: gating modifiers of voltage-gated sodium channels | Q36646408 | ||
| Tarantula huwentoxin-IV inhibits neuronal sodium channels by binding to receptor site 4 and trapping the domain ii voltage sensor in the closed configuration | Q36914467 | ||
| Animal peptides targeting voltage-activated sodium channels. | Q37264921 | ||
| Molecular requirements for recognition of brain voltage-gated sodium channels by scorpion alpha-toxins | Q37344014 | ||
| Interaction between voltage-gated sodium channels and the neurotoxin, tetrodotoxin | Q37355526 | ||
| Synthesis, solution structure, and phylum selectivity of a spider delta-toxin that slows inactivation of specific voltage-gated sodium channel subtypes | Q37433422 | ||
| Voltage-gated sodium channels: therapeutic targets for pain | Q37612027 | ||
| Sodium channels in normal and pathological pain | Q37724336 | ||
| Nociceptors: the sensors of the pain pathway | Q37805996 | ||
| P433 | issue | 28 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | voltage | Q25428 |
| P304 | page(s) | 20392-20403 | |
| P577 | publication date | 2013-05-23 | |
| P1433 | published in | Journal of Biological Chemistry | Q867727 |
| P1476 | title | Structure and function of hainantoxin-III, a selective antagonist of neuronal tetrodotoxin-sensitive voltage-gated sodium channels isolated from the Chinese bird spider Ornithoctonus hainana | |
| P478 | volume | 288 |
| Q34778955 | Bacterial voltage-gated sodium channels (BacNa(V)s) from the soil, sea, and salt lakes enlighten molecular mechanisms of electrical signaling and pharmacology in the brain and heart |
| Q92989953 | Chemical Synthesis, Proper Folding, Nav Channel Selectivity Profile and Analgesic Properties of the Spider Peptide Phlotoxin 1 |
| Q36941125 | Development of a μO-Conotoxin Analogue with Improved Lipid Membrane Interactions and Potency for the Analgesic Sodium Channel NaV1.8. |
| Q58554174 | Discovery of a Novel Na1.7 Inhibitor From Venom With Potent Analgesic Efficacy |
| Q38282832 | Discovery of functional antibodies targeting ion channels |
| Q58764288 | Engineering Gain-of-Function Analogues of the Spider Venom Peptide HNTX-I, A Potent Blocker of the hNa1.7 Sodium Channel |
| Q92826608 | Evaluation of the Spider (Phlogiellus genus) Phlotoxin 1 and Synthetic Variants as Antinociceptive Drug Candidates |
| Q91734245 | From identification to functional characterization of cyriotoxin-1a, an antinociceptive toxin from the spider Cyriopagopus schioedtei |
| Q36036465 | Heterologous expression and purification of neurotoxic Hainantoxin-III in E. coli |
| Q50968183 | Joannsin, a novel Kunitz-type FXa inhibitor from the venom of Prospirobolus joannsi. |
| Q90089706 | Manipulation of a spider peptide toxin alters its affinity for lipid bilayers and potency and selectivity for voltage-gated sodium channel subtype 1.7. |
| Q55037976 | Pharmacological characterization of potent and selective NaV1.7 inhibitors engineered from Chilobrachys jingzhao tarantula venom peptide JzTx-V. |
| Q38778694 | Plant cystine-knot peptides: pharmacological perspectives |
| Q50111328 | Potential Uses of Isolated Toxin Peptides in Neuropathic Pain Relief: A Literature Review |
| Q57479263 | Purification and Characterization of JZTx-14, a Potent Antagonist of Mammalian and Prokaryotic Voltage-Gated Sodium Channels |
| Q94569487 | Spider venom-derived peptide induces hyperalgesia in Nav1.7 knockout mice by activating Nav1.9 channels |
| Q64054939 | Structure-Function and Therapeutic Potential of Spider Venom-Derived Cysteine Knot Peptides Targeting Sodium Channels |
| Q30629019 | Synergetic action of domain II and IV underlies persistent current generation in Nav1.3 as revealed by a tarantula toxin |
| Q58764681 | The Na1.7 Channel Subtype as an Antinociceptive Target for Spider Toxins in Adult Dorsal Root Ganglia Neurons |
| Q33681373 | The tarantula toxin β/δ-TRTX-Pre1a highlights the importance of the S1-S2 voltage-sensor region for sodium channel subtype selectivity. |
| Q64249760 | Transcriptomic Analysis of the Spider Venom Gland Reveals Venom Diversity and Species Consanguinity |
| Q58085867 | µ-TRTX-Ca1a: a novel neurotoxin from Cyriopagopus albostriatus with analgesic effects |
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