Codon dwell-time tables (per-codon timing)¶
Per-codon timing (Synthesis in coarse-grained ribosome model) needs a codon dwell-time table — the
codon_times key of a csp.ini / cylinder.ini. It maps each codon to its mean
in-vivo per-codon translation (dwell) time in seconds (the codon’s mean
first-passage time), which is what sets each residue’s MD-segment length. There is no
bundled default: you pick a table for your organism (and, where relevant, elongation
rate). TOPO ships a small library of them.
Where they live & the format¶
The tables are under assets/csp/codon_dwell_times/<organism>/. Each is a plain
text file, one row per codon:
# codon dwell_time_seconds amino_acid
UUU 0.068164 PHE
...
UAA 0.005513 STOP
RNA alphabet (
U), tab-separated,#comments ignored; 64 rows (61 sense + 3 stop). Larger time = slower codon; stop codons carry the amino acidSTOP.The third column (amino acid) is what
mrna = fastest/slowest/medianuses to pick each residue’s synonymous codon — see Fastest / slowest / median mRNA.Every organism directory also has a
*_dwell_time_methods.mdwith the full provenance (source dataset, references, how relative data were scaled to seconds).
Shipped tables¶
Organism |
File(s) |
Basis (see the methods note for full provenance) |
|---|---|---|
E. coli |
|
Fluitt, Pienaar & Viljoen (2007) mechanistic decoding times, O’Brien-rescaled so the codon-usage-weighted mean = 0.061 s/codon (16.5 aa/s) at 310 K. Absolute; the most-validated table. |
S. cerevisiae |
|
Gardin et al. (2014) relative decoding rates (RRT), frequency-weighted → seconds (~0.108 s/codon; ~9.3 codons/s). |
|
O’Brien-lab chemical-kinetic model, absolute (~0.233 s/codon; ~4.3 codons/s) — the most pipeline-native yeast table. |
|
|
The O’Brien table rescaled to 9.3 aa/s (matches the Gardin rate). |
|
H. sapiens |
|
Gobet et al. (2020) liver ribosome-profiling dwell times (Lintner dataset) → seconds. |
|
Same, frequency-weighted to an elongation-rate anchor R = 5.6 codons/s. |
|
N. crassa |
|
Yang et al. (2019) relative codon decoding times (RCDT) → seconds at three measured elongation-rate anchors (5.35 / 6.7 / 8.02 codons/s). Least-certain table (relative values digitized from a figure). |
|
Frequency-weighted variants of the three anchors. |
Frequency-weighted (v2) variants. These rescale the per-codon times so the
codon-usage-weighted mean over the organism’s transcriptome hits the target
elongation rate, instead of an unweighted mean. Use them when you want the genome-wide
average speed to match the anchor; use the plain (v1) tables for the raw per-codon
values.
Note
References — E. coli: Fluitt, Pienaar & Viljoen, Comput. Biol. Chem. 31:335–346 (2007). Yeast: Gardin et al., eLife 3:e03735 (2014). Human: Gobet et al., PNAS 117(17):9630–9641 (2020). N. crassa: Yang et al., Nucleic Acids Res. 47(17):9243–9258 (2019).
Use one in a run¶
Point the codon_times key at a table (a path selects per-codon timing; a plain
number would instead mean a uniform time for every codon):
pdb_file = my_protein.pdb
mrna = my_protein_mrna.txt
codon_times = assets/csp/codon_dwell_times/ecoli/ecoli_codon_dwell_times_310K.txt
Keep the thermostat consistent with the table’s temperature: ref_t defaults to
310 K to match the E. coli table — set it to your table’s temperature if it
differs. See Synthesis control options for the full key reference.
Fastest / slowest / median mRNA¶
Because each table carries the codon→amino-acid mapping (column 3), you can set
mrna = fastest, slowest or median (instead of a sequence file) to auto-build a
synonymous-codon mRNA that encodes your protein with every residue’s fastest/slowest/
median-dwell-time codon for the chosen table — the extremes of the codon-optimization
axis, or a neutral middle reference. See
Fastest / slowest / median (synonymous-codon) mRNA,
or pre-generate one standalone:
topo-make-mrna --pdb my_protein.pdb \
--codon-times assets/csp/codon_dwell_times/yeast/yeast_codon_dwell_times_OBrien.txt \
--mode slowest