diff --git a/components/content/Contributors.vue b/components/content/Contributors.vue new file mode 100644 index 0000000000000000000000000000000000000000..d182bb88c0b1acf2398e009cf8b527e6873d2caa --- /dev/null +++ b/components/content/Contributors.vue @@ -0,0 +1,14 @@ +<script setup lang="ts"> + +const { page } = useContent(); +const contributorsString = computed(() => { + if (page.value?.contributors) { + return page.value.contributors.join(', ') + } else { return null } +}) + +</script> +<template> + <div v-if="contributorsString" class="mt-n6 mb-6 text-subtitle-1 text-primary">Contributors: {{ contributorsString }} + </div> +</template> \ No newline at end of file diff --git a/content/3.defense-systems/abi2.md b/content/3.defense-systems/abi2.md index 6f8549ec2378baf5dd358518c8fe643e1b09cf1e..3b1227560d1b87673a628e4d7df6695036ec1613 100644 --- a/content/3.defense-systems/abi2.md +++ b/content/3.defense-systems/abi2.md @@ -12,6 +12,8 @@ tableColumns: --- # Abi2 +:contributors + The Abi2 system is composed of one protein: Abi_2. Here is an example found in the RefSeq database: diff --git a/content/3.defense-systems/detocs.md b/content/3.defense-systems/detocs.md index c3ec3aa42ce06c172a8a4eddb67952120ccb05db..ff9c7cfcc0de71290247d32f348350b987fe399d 100644 --- a/content/3.defense-systems/detocs.md +++ b/content/3.defense-systems/detocs.md @@ -6,11 +6,13 @@ tableColumns: abstract: | During viral infection, cells can deploy immune strategies that deprive viruses of molecules essential for their replication. Here, we report a family of immune effectors in bacteria that, upon phage infection, degrade cellular adenosine triphosphate (ATP) and deoxyadenosine triphosphate (dATP) by cleaving the N-glycosidic bond between the adenine and sugar moieties. These ATP nucleosidase effectors are widely distributed within multiple bacterial defense systems, including cyclic oligonucleotide-based antiviral signaling systems (CBASS), prokaryotic argonautes, and nucleotide-binding leucine-rich repeat (NLR)-like proteins, and we show that ATP and dATP degradation during infection halts phage propagation. By analyzing homologs of the immune ATP nucleosidase domain, we discover and characterize Detocs, a family of bacterial defense systems with a two-component phosphotransfer-signaling architecture. The immune ATP nucleosidase domain is also encoded within diverse eukaryotic proteins with immune-like architectures, and we show biochemically that eukaryotic homologs preserve the ATP nucleosidase activity. Our findings suggest that ATP and dATP degradation is a cell-autonomous innate immune strategy conserved across the tree of life. PFAM: PF01048, PF18742 -contributors: François Rousset +contributors: + - François Rousset --- # Detocs +:contributors ## Description Detocs (**De**fensive **T**w**o**-**C**omponent **S**ystem) is a family of 3-gene defense systems that mediate anti-phage activity by abortive infection. diff --git a/layouts/article.vue b/layouts/article.vue index 64e4f13a0fcea8c523b2361f98226d40ad995154..f724344b203aeccdc9a32e4800c384fa08dff99b 100644 --- a/layouts/article.vue +++ b/layouts/article.vue @@ -9,7 +9,7 @@ console.log("================================") console.log(surround) console.log(prev) console.log(next) - +console.log(page) </script> <template> <VApp>