Reactome: A Curated Pathway Database
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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.

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Details on Person The COOH termini of all ERM proteins have sequence motifs th...

Class:IdSummation:443566
_displayNameThe COOH termini of all ERM proteins have sequence motifs th...
_timestamp2009-11-19 21:03:38
created[InstanceEdit:443547] Garapati, P V, 2009-10-09
literatureReference[LiteratureReference:374416] ERM proteins and merlin: integrators at the cell cortex
[LiteratureReference:444913] The mechanism of axon growth: what we have learned from the cell adhesion molecule L1
modified[InstanceEdit:444909] Garapati, P V, 2009-10-27
[InstanceEdit:447049] Garapati, P V, 2009-11-19
textThe COOH termini of all ERM proteins have sequence motifs that bind directly to F-actin. The L1 molecules on the cell surface are translocated to the C-domain by coupling with the retrograde F-actin. The force generated by linking L1 clusters with retrograde F-actin flow leads to the migration of the growth cone.
(summation)[Reaction:443779] Linkage of L1 with treadmilling F-actin [Homo sapiens]
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No pathways have been reviewed or authored by The COOH termini of all ERM proteins have sequence motifs th... (443566)