diff --git a/content/3.defense-systems/rm.md b/content/3.defense-systems/rm.md
index d1b9e5c0ecb858cfc96973b214fd57da04218829..2b888439e9b89a4279a3a8a17fa043dcd8990169 100644
--- a/content/3.defense-systems/rm.md
+++ b/content/3.defense-systems/rm.md
@@ -21,15 +21,14 @@ relevantAbstracts:
 # RM
 
 ## Description
-Restriction modification systems are the most abundant antiphage systems. They already have their own wiki pages
-https://en.wikipedia.org/wiki/Restriction_modification_system
+Restriction modification systems are the most abundant antiphage systems. They already have their own [Wikipedia page](https://en.wikipedia.org/wiki/Restriction_modification_system)
 
 ## Molecular Mechanisms
-Several reviews detail the molecular mechanisms of restriction modification systems. For example in :ref{doi=10.1016/j.mib.2005.06.003} :
+Several reviews detail the molecular mechanisms of restriction modification systems. For example in :ref{doi=10.1016/j.mib.2005.06.003}:
 
 "Bacterial restriction-modification (R-M) systems function as prokaryotic immune systems that attack foreign DNA entering the cell :ref{doi=10.1128/jb.65.2.113-121.1953}. Typically, R-M systems have enzymes responsible for two opposing activities: a restriction endonuclease (REase) that recognizes a specific DNA sequence for cleavage and a cognate methyltransferase (MTase) that confers protection from cleavage by methylation of adenine or cytosine bases within the same recognition sequence. REases recognize ‘non-self’ DNA (Figure 1), such as that of phage and plasmids, by its lack of characteristic modification within specific recognition sites :ref{doi=10.1093/nar/29.18.3705}. Foreign DNA is then inactivated by endonucleolytic cleavage. Generally, methylation of a specific cytosine or adenine within the recognition sequence confers protection from restriction. Host DNA is normally methylated by the MTase following replication, whereas invading non-self DNA is not."
 
-![Figure 1](/rm/Figure_1_Tock_Dryden_2005.png){max-width=750px}
+![Figure_1](/rm/Figure_1_Tock_Dryden_2005.png){max-width=750px}
 
 Figure 1. The function of R-M systems, as illustrated by Type I R-M enzymes. From :ref{doi=10.1016/j.mib.2005.06.003}.
 
@@ -75,7 +74,7 @@ Proportion of genome encoding the RM system for the 14 phyla with more than 50 g
 
 ### Experimentaly determined structure
 
-Many structure for the different types of restriction-modification system are available on the [Protein Data Bank](https://www.rcsb.org/).
+Many structure for the different types of restriction-modification system are available on the [Protein Data Bank](https://www.rcsb.org).
 
 ### RM
 #### Restriction modification Type I Prr
@@ -83,7 +82,7 @@ Many structure for the different types of restriction-modification system are av
 ::molstar-pdbe-plugin
 ---
 height: 700
-dataUrl:
+dataUrls:
   - /rm/RM__Type_I_REases-plddts_86.33796.pdb
   - /rm/RM__Type_I_S-plddts_91.98582.pdb
   - /prrc/PrrC__EcoprrI-plddts_91.30003.pdb