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 TEFM:POLRMT:mitochondrial genome:H,L strand transcript contacts MTERF1

Class:IdReaction:9986199
_displayNameTEFM:POLRMT:mitochondrial genome:H,L strand transcript contacts MTERF1
_timestamp2026-03-30 16:40:32
authored[InstanceEdit:9985775] May, Bruce, 2026-03-26
compartment[Compartment:5460] mitochondrial matrix
created[InstanceEdit:9986192] May, Bruce, 2026-03-27
edited[InstanceEdit:9985775] May, Bruce, 2026-03-26
input[Complex:9985683] POLRMT:TEFM:mitochondrial genome:H,L strand transcript [mitochondrial matrix] [Homo sapiens]
[Complex:163321] MTERF1:mitochondrial transcription termination sequence [mitochondrial matrix] [Homo sapiens]
isChimericFALSE
literatureReference[LiteratureReference:163255] Termination of transcription in human mitochondria: identification and purification of a DNA binding protein factor that promotes termination
[LiteratureReference:164553] The human mitochondrial transcription termination factor (mTERF) is a multizipper protein but binds to DNA as a monomer, with evidence pointing to intramolecular leucine zipper interactions
[LiteratureReference:9985736] Helix unwinding and base flipping enable human MTERF1 to terminate mitochondrial transcription
[LiteratureReference:163265] Molecular characterization of the transcription termination factor from human mitochondria
[LiteratureReference:9986200] In vivo methylation of mtDNA reveals the dynamics of protein-mtDNA interactions
[LiteratureReference:164547] Human mitochondrial transcription termination exhibits RNA polymerase independence and biased bipolarity in vitro
[LiteratureReference:9986195] The human mitochondrial transcription termination factor (mTERF) is fully active in vitro in the non-phosphorylated form
modified[InstanceEdit:9986239] May, Bruce, 2026-03-27
[InstanceEdit:9986361] May, Bruce, 2026-03-30
nameTEFM:POLRMT:mitochondrial genome:H,L strand transcript contacts MTERF1
output[Complex:9986203] POLRMT:TEFM:mitochondrial genome:H,L strand transcript:MTERF1 [mitochondrial matrix] [Homo sapiens]
precedingEvent
species[Species:48887] Homo sapiens
stableIdentifier[StableIdentifier:9986208] R-HSA-9986199.1
summation[Summation:9986345] Elongation complexes (POLRMT:TEFM) that are polymerizing the...
(hasEvent)[Pathway:9985686] Mitochondrial transcription [Homo sapiens]
(precedingEvent)[BlackBoxEvent:9986204] POLRMT:TEFM:mitochondrial genome:H,L strand transcript:MTERF1 dissociates [Homo sapiens]
[Change default viewing format]
No pathways have been reviewed or authored by TEFM:POLRMT:mitochondrial genome:H,L strand transcript contacts MTERF1 (9986199)