Reactome: A Curated Pathway Database
THIS SITE IS USED FOR CURATION AND TESTING
IT IS NOT STABLE, IS LINKED TO AN INCOMPLETE DATA SET, AND IS NOT MONITORED FOR PERFORMANCE. WE STRONGLY RECOMMEND THE USE OF OUR PUBLIC SITE

Query author contributions in Reactome

Reactome depends on collaboration between our curation team and outside experts to assemble and peer-review its pathway modules. The integration of ORCID within Reactome enables us to meet a key challenge with authoring, curating and reviewing biological information by incentivizing and crediting the external experts that contribute their expertise and time to the Reactome curation process. More information is available at ORCID and Reactome.

If you have an ORCID ID that is not listed on this page, please forward this information to us and we will update your Reactome pathway records.

Name Email address

Details on Person Binz, Thomas

Class:IdPerson:181748
_displayNameBinz, Thomas
_timestamp2014-01-14 14:08:00
created[InstanceEdit:181756] Gopinathrao, G, 2006-06-16 17:36:48
firstnameThomas
initialT
modified[InstanceEdit:5228577] D'Eustachio, Peter, 2014-01-14
surnameBinz
(author)[LiteratureReference:181699] A molecular basis underlying differences in the toxicity of botulinum serotypes A and E
[LiteratureReference:181730] Proteolysis of SNAP-25 by types E and A botulinal neurotoxins
[LiteratureReference:181747] Minimal essential domains specifying toxicity of the light chains of tetanus toxin and botulinum neurotoxin type A
[LiteratureReference:181774] Proteolysis of SNAP-25 isoforms by botulinum neurotoxin types A, C, and E: domains and amino acid residues controlling the formation of enzyme-substrate complexes and cleavage
[LiteratureReference:181778] Cleavage of members of the synaptobrevin/VAMP family by types D and F botulinal neurotoxins and tetanus toxin
[LiteratureReference:5228582] Tetanus toxin action: inhibition of neurotransmitter release linked to synaptobrevin proteolysis
[LiteratureReference:5228676] Structural analysis of botulinum neurotoxin type E catalytic domain and its mutant Glu212-->Gln reveals the pivotal role of the Glu212 carboxylate in the catalytic pathway
[LiteratureReference:5244438] 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
[LiteratureReference:5246522] Botulinum neurotoxin C1 blocks neurotransmitter release by means of cleaving HPC-1/syntaxin
[LiteratureReference:5250887] Botulinum neurotoxin A selectively cleaves the synaptic protein SNAP-25
List all 12 refering instances
[Change default viewing format]
No pathways have been reviewed or authored by Binz, Thomas (181748)