The alphabets for the modifications used in this package are based on the compilation of RNA modifications by http://modomics.genesilico.pl by the Bujnicki lab (Boccaletto et al. 2018). The alphabet was modified to remove some incompatible characters.

If modifications are missing, let us know.

Table 1: List of supported RNA modifications by ModRNAString objects
modification short name nomenclature orig. base abbreviation
1,2’-O-dimethyladenosine m1Am 01A A œ
1,2’-O-dimethylguanosine m1Gm 01G G ε
1,2’-O-dimethylinosine m1Im 019A A ξ
1-methyl-3-(3-amino-3-carboxypropyl)pseudouridine m1acp3Y 1309U U α
1-methyladenosine m1A 1A A
1-methylguanosine m1G 1G G K
1-methylinosine m1I 19A A O
1-methylpseudouridine m1Y 19U U ]
2,8-dimethyladenosine m2,8A 28A A ±
2-geranylthiouridine ges2U 21U U Γ
2-lysidine k2C 21C C }
2-methyladenosine m2A 2A A /
2-methylthiomethylenethio-N6-isopentenyl-adenosine msms2i6A 2361A A £
2-methylthio-cyclic-N6-threonylcarbamoyladenosine ms2ct6A 2164A A ÿ
2-methylthio-N6-(cis-hydroxyisopentenyl)-adenosine ms2io6A 2160A A
2-methylthio-N6-hydroxynorvalylcarbamoyladenosine ms2hn6A 2163A A
2-methylthio-N6-isopentenyladenosine ms2i6A 2161A A *
2-methylthio-N6-methyladenosine ms2m6A 621A A
2-methylthio-N6-threonylcarbamoyladenosine ms2t6A 2162A A [
2-selenouridine se2U 20U U ω
2-thio-2’-O-methyluridine s2Um 02U U
2-thiocytidine s2C 2C C %
2-thiouridine s2U 2U U 2
2’-O-methyladenosine Am 0A A :
2’-O-methylcytidine Cm 0C C B
2’-O-methylguanosine Gm 0G G #
2’-O-methylinosine Im 09A A
2’-O-methylpseudouridine Ym 09U U Z
2’-O-methyluridine Um 0U U J
2’-O-methyluridine 5-oxyacetic acid methyl ester mcmo5Um 0503U U Ä
2’-O-ribosyladenosine (phosphate) Ar(p) 00A A ^
2’-O-ribosylguanosine (phosphate) Gr(p) 00G G
3,2’-O-dimethyluridine m3Um 03U U σ
3-(3-amino-3-carboxypropyl)-5,6-dihydrouridine acp3D 308U U Ð
3-(3-amino-3-carboxypropyl)pseudouridine acp3Y 309U U Þ
3-(3-amino-3-carboxypropyl)uridine acp3U 30U U X
3-methylcytidine m3C 3C C
3-methylpseudouridine m3Y 39U U κ
3-methyluridine m3U 3U U δ
4-demethylwyosine imG-14 4G G
4-thiouridine s4U 74U U 4
5,2’-O-dimethylcytidine m5Cm 05C C τ
5,2’-O-dimethyluridine m5Um 05U U ¤
5-(carboxyhydroxymethyl)-2’-O-methyluridine methyl ester mchm5Um 0522U U b
5-(carboxyhydroxymethyl)uridine methyl ester mchm5U 522U U ,
5-(isopentenylaminomethyl)-2-thiouridine inm5s2U 2583U U ½
5-(isopentenylaminomethyl)-2’-O-methyluridine inm5Um 0583U U ¼
5-(isopentenylaminomethyl)uridine inm5U 583U U ¾
5-aminomethyl-2-geranylthiouridine nm5ges2U 21510U U Δ
5-aminomethyl-2-selenouridine nm5se2U 20510U U π
5-aminomethyl-2-thiouridine nm5s2U 2510U U
5-aminomethyluridine nm5U 510U U
5-carbamoylhydroxymethyluridine nchm5U 531U U r
5-carbamoylmethyl-2-thiouridine ncm5s2U 253U U l
5-carbamoylmethyl-2’-O-methyluridine ncm5Um 053U U ~
5-carbamoylmethyluridine ncm5U 53U U &
5-carboxyhydroxymethyluridine chm5U 520U U
5-carboxymethyl-2-thiouridine cm5s2U 2540U U
5-carboxymethylaminomethyl-2-geranylthiouridine cmnm5ges2U 2151U U f
5-carboxymethylaminomethyl-2-selenouridine cmnm5se2U 2051U U
5-carboxymethylaminomethyl-2-thiouridine cmnm5s2U 251U U $
5-carboxymethylaminomethyl-2’-O-methyluridine cmnm5Um 051U U )
5-carboxymethylaminomethyluridine cmnm5U 51U U !
5-carboxymethyluridine cm5U 52U U
5-cyanomethyluridine cnm5U 55U U Ѷ
5-formyl-2’-O-methylcytidine f5Cm 071C C °
5-formylcytidine f5C 71C C ×
5-hydroxycytidine ho5C 50C C Ç
5-hydroxymethylcytidine hm5C 51C C
5-hydroxyuridine ho5U 50U U
5-methoxycarbonylmethyl-2-thiouridine mcm5s2U 2521U U 3
5-methoxycarbonylmethyl-2’-O-methyluridine mcm5Um 0521U U
5-methoxycarbonylmethyluridine mcm5U 521U U 1
5-methoxyuridine mo5U 501U U 5
5-methyl-2-thiouridine m5s2U 25U U F
5-methylaminomethyl-2-geranylthiouridine mnm5ges2U 21511U U h
5-methylaminomethyl-2-selenouridine mnm5se2U 20511U U
5-methylaminomethyl-2-thiouridine mnm5s2U 2511U U S
5-methylaminomethyluridine mnm5U 511U U {
5-methylcytidine m5C 5C C ?
5-methyldihydrouridine m5D 58U U ρ
5-methyluridine m5U 5U U T
5-taurinomethyl-2-thiouridine tm5s2U 254U U
5-taurinomethyluridine tm5U 54U U Ê
7-aminocarboxypropyl-demethylwyosine yW-86 47G G ¥
7-aminocarboxypropylwyosine yW-72 347G G Ω
7-aminocarboxypropylwyosine methyl ester yW-58 348G G
7-aminomethyl-7-deazaguanosine preQ1tRNA 101G G
7-cyano-7-deazaguanosine preQ0tRNA 100G G φ
7-methylguanosine m7G 7G G 7
8-methyladenosine m8A 8A A â
N2,2’-O-dimethylguanosine m2Gm 02G G γ
N2,7,2’-O-trimethylguanosine m2,7Gm 027G G æ
N2,7-dimethylguanosine m2,7G 27G G
N2,N2,2’-O-trimethylguanosine m2,2Gm 022G G |
N2,N2,7-trimethylguanosine m2,2,7G 227G G
N2,N2-dimethylguanosine m2,2G 22G G R
N2-methylguanosine m2G 2G G L
N4,2’-O-dimethylcytidine m4Cm 04C C λ
N4,N4,2’-O-trimethylcytidine m4,4Cm 044C C β
N4,N4-dimethylcytidine m4,4C 44C C μ
N4-acetyl-2’-O-methylcytidine ac4Cm 042C C
N4-acetylcytidine ac4C 42C C M
N4-methylcytidine m4C 4C C ν
N6,2’-O-dimethyladenosine m6Am 06A A χ
N6,N6,2’-O-trimethyladenosine m6,6Am 066A A η
N6,N6-dimethyladenosine m6,6A 66A A ζ
N6-(cis-hydroxyisopentenyl)adenosine io6A 60A A `
N6-acetyladenosine ac6A 64A A
N6-formyladenosine f6A 67A A Ϩ
N6-glycinylcarbamoyladenosine g6A 65A A
N6-hydroxymethyladenosine hm6A 68A A Ϫ
N6-hydroxynorvalylcarbamoyladenosine hn6A 63A A
N6-isopentenyladenosine i6A 61A A Θ
N6-methyl-N6-threonylcarbamoyladenosine m6t6A 662A A E
N6-methyladenosine m6A 6A A =
N6-threonylcarbamoyladenosine t6A 62A A 6
agmatidine C+ 20C C ¿
archaeosine G+ 103G G (
cyclic N6-threonylcarbamoyladenosine ct6A 69A A e
dihydrouridine D 8U U D
epoxyqueuosine oQtRNA 102G G ς
galactosyl-queuosine galQtRNA 104G G 9
glutamyl-queuosine gluQtRNA 105G G
hydroxy-N6-threonylcarbamoyladenosine ht6A 2165A A «
hydroxywybutosine OHyW 34830G G
inosine I 9A A I
isowyosine imG2 42G G
mannosyl-queuosine manQtRNA 106G G 8
methylated undermodified hydroxywybutosine OHyWy 3480G G y
methylwyosine mimG 342G G
peroxywybutosine o2yW 34832G G W
pseudouridine Y 9U U P
queuosine QtRNA 10G G Q
undermodified hydroxywybutosine OHyWx 3470G G š
unknown methylated base Xm 0X N Î
unknown modification xX X N ÷
unknown modified adenosine xA ?A A H
unknown modified cytidine xC ?C C <
unknown modified guanosine xG ?G G ;
unknown modified uridine xU ?U U Ü
uridine 5-oxyacetic acid cmo5U 502U U V
uridine 5-oxyacetic acid methyl ester mcmo5U 503U U υ
wybutosine yW 3483G G Y
wyosine imG 34G G
sessioninfo::session_info()
## ─ Session info ────────────────────────────────────────────────────────────
##  setting  value                       
##  version  R version 3.6.0 (2019-04-26)
##  os       Ubuntu 18.04.2 LTS          
##  system   x86_64, linux-gnu           
##  ui       X11                         
##  language (EN)                        
##  collate  C                           
##  ctype    en_US.UTF-8                 
##  tz       America/New_York            
##  date     2019-05-02                  
## 
## ─ Packages ────────────────────────────────────────────────────────────────
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##  assertive.data.uk      0.0-2     2018-10-21 [2] CRAN (R 3.6.0)
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##  assertive.datetimes    0.0-2     2016-05-10 [2] CRAN (R 3.6.0)
##  assertive.files        0.0-2     2016-05-10 [2] CRAN (R 3.6.0)
##  assertive.matrices     0.0-2     2018-11-20 [2] CRAN (R 3.6.0)
##  assertive.models       0.0-2     2018-10-21 [2] CRAN (R 3.6.0)
##  assertive.numbers      0.0-2     2016-05-09 [2] CRAN (R 3.6.0)
##  assertive.properties   0.0-4     2016-12-30 [2] CRAN (R 3.6.0)
##  assertive.reflection   0.0-4     2016-12-30 [2] CRAN (R 3.6.0)
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##  assertthat             0.2.1     2019-03-21 [2] CRAN (R 3.6.0)
##  BiocGenerics         * 0.30.0    2019-05-02 [2] Bioconductor  
##  BiocManager            1.30.4    2018-11-13 [2] CRAN (R 3.6.0)
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##  Biostrings           * 2.52.0    2019-05-02 [2] Bioconductor  
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##  digest                 0.6.18    2018-10-10 [2] CRAN (R 3.6.0)
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##  GenomeInfoDb           1.20.0    2019-05-02 [2] Bioconductor  
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##  Modstrings           * 1.0.0     2019-05-02 [1] Bioconductor  
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##  RCurl                  1.95-4.12 2019-03-04 [2] CRAN (R 3.6.0)
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##  S4Vectors            * 0.22.0    2019-05-02 [2] Bioconductor  
##  sessioninfo            1.1.1     2018-11-05 [2] CRAN (R 3.6.0)
##  stringi                1.4.3     2019-03-12 [2] CRAN (R 3.6.0)
##  stringr                1.4.0     2019-02-10 [2] CRAN (R 3.6.0)
##  withr                  2.1.2     2018-03-15 [2] CRAN (R 3.6.0)
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##  XVector              * 0.24.0    2019-05-02 [2] Bioconductor  
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##  zlibbioc               1.30.0    2019-05-02 [2] Bioconductor  
## 
## [1] /tmp/Rtmp3LPZGE/Rinst261282ababc
## [2] /home/biocbuild/bbs-3.9-bioc/R/library

Boccaletto, Pietro, Magdalena A. Machnicka, Elzbieta Purta, Pawel Piatkowski, Blazej Baginski, Tomasz K. Wirecki, Valérie de Crécy-Lagard, et al. 2018. “MODOMICS: A Database of Rna Modification Pathways. 2017 Update.” Nucleic Acids Research 46 (D1):D303–D307. https://doi.org/10.1093/nar/gkx1030.