Table 3. Clustered k-mers from S1 Fig used for validation of their biological function and reported riboswitch motifs.
Nucleotide location designated refers to match with their position reported in reference.
Rfam ID | K-mers | Position | Riboswitch function and motifs | Ref |
---|---|---|---|---|
RF00168 | UCAU | U57-U60 | Motifs predicted to interact with the Nova-1 protein | [40] |
RF01051 | CAAAG | C22-G26 | Secondary structure representation of the crystallized c-di-GMP aptamer, necessary for c-di-GMP binding pocket formation | [41] |
GGUC | G8-C11 | Found in Helices P1 area beginning of 5′UTR | [41] | |
RF00522 | AAAAAA AAAC |
A27-A31 A30-C33 |
Overlaying K-mers in the 3′ aptamer domain, rich in A, which has unique folding pseudoknot that compresses PreQ1 | [42] |
UCCCA | U24-A18 | Found in P2 of preQ1 riboswitch aptamer structure | [42] | |
RF00504 | CCGAAG | C168-G173 | The glycine-mediated changes in spontaneous cleavage (GAA) | [43] |
CUCU | C204-U207 | In glycine riboswitch, secondary structure and in-line decreasing cleavage pattern | [43] | |
RF00059 | UGAGA | U39-A43 | The pyrimidine part of TPP is bound by bulge J3-2 located in the pyrimidine-sensor helix P2-P3 | [44] |
RF00162 | GAGGGA | G19-A24 | It is a kink-turn motif that allows pseudoknot interaction. It interacts with SAM which helps to make stable formation, can cause the downstream expression platform to form a rho-independent TT (transcriptional terminator), turning off gene expression | [45] |
RF00634 | CAACC CCCUC |
C54-C58 C57-C61 |
Overlapping k-mers in SAM-IV RNA binds SAM, last C in cleavage increased by SAM | [46] |
RF01057 | AGGCUC | A61-C66 | In P1 SAH riboswitch control reporter gene Expression, ahcY 5'UTR | [47] |
CGCU | C28-U31 | In SAH riboswitch hairpin loops of P4 | [47] | |
RF00521 | GCUAAA | G42-A47 | Secondary structure of the Env12 metX SAM-II riboswitch its base-pairing reflecting the tertiary structure of the SAM-bound RNA | [48] |
RF00050 | AGUC | A126-C129 | In the secondary structure of FMN, the first three AGU make hairpin loops and identified from B. cleavage. | [49] |
ACAGU GGCGGU | A137-U141 G56-U61 |
Form Secondary-structure model of the 165 ribD RNA and side hairpin between P2 and 165 ribD RNA and side hairpin | [49] | |
RF00174 | CCCGC AGUCAG |
C70-C74 | Predicted secondary structure of the cobalamin riboswitch in the btuB leader region of Synechococcus sp. Strain. The boxed bases represent the B12 box-P1 helix interface, where a CC-to-TT (UU in the RNA structure | [50] |
RF01055 | GAAAGG | G120-G125 | Containing AGG at the site of Ribosomal Binding Site (RBS) located at multiple junction site. Region of the central multi-stem junction in Sequence of the 138 moaA Moco RNA. | [51] |
GCCU | G18-U21 | Found in a Moco RNA at left multiple junction site | [51] | |
GCCUCC | G106-C111 | In Moco RNA, the last UCC makes parts of multiple junctions in P4. | [51] | |
RF00380 | UGAGG | U28-G32 | k-mers that found in part of a conserved bulge-stem region of Secondary structure of the 5`M-box portion | [52] |
RF01054 | AAAGG | A83-G87 | Structural modulation and nucleotides comprise a conserved Shine–Dalgarno (SD) | [53] |
AGCAU | A58-U62 | Unpaired Structural modulation containing constant cleavage | [53] | |
AGAAAA | A88-A93 | Structural modulation, AGAA in decreasing cleavage and AA in constant cleavage | [53] | |
RF00234 | AGCGC | A12-C16 | Downstream of the ribozyme cleavage site Ribozyme core site P2a | [54] |
ACGAGG | A53-G56 | Ribozyme core region (Unpaired) | ||
RF00167 | CUAC | C50-C53 | structural features of the guanine aptamer domain and critical for metabolite binding | [55] |