Input sequence : format
Please input the nucleotide sequence only, or use the Fasta format.
Examples:
- ATATGTGAT...
- atgatccgt...
- > Gene name...
ATGCCGTGAAATCGTCGATCG...
Description of the table
Binding factor |
The binding factor refers to the transcription factor regulating the gene. |
Regulated gene |
The first gene in the operon regulated by the transcription factor. |
Promoter name |
Some genes have more than two transcription start sites. To distiguish those promtoers, we show promoter names when they have. |
Regulation |
This column describes how the transcription factor regulates the gene. Options are positive, negative, both, promoter (in case of a sigma factor), and unknown. |
Absolute position |
We recalculated the absolute position of each cis-element using the NCBI sequence file (accession number AL645882). |
Location |
Location of the binding site with respect to the transcription start site. |
Binding sequence (cis-element) |
We show the cis-element as well as nearby sequences.
Red characters correspond to the exact binding sequence, as shown in the reference.
Bold face shows the transcription start site. |
ND |
No Data. |
Abbreviations of Experimental Techniques Used
|
AR | DNA microarray and macroarray |
CH | Chromatin immunoprecipitation microarray (ChIP-on-chip) |
DB | Disruption of Binding Factor gene |
DP | Deletion assay |
FT | Footprinting assay (DNase I, DMS, etc.) |
FP | Fluorecent protein |
GS | Gel retardation assay |
HB | Slot blot analysis |
HM | Homology search |
OV | Overexpression of Binding Factor gene |
PE | Primer extension analysis |
RG | Reporter gene (e.g., lacZ assay) |
RO | Run-off transcription assay |
ROMA | Run-off transcription followed by macroarray analysis |
S1 | S1 mapping analysis (S1 nuclease transcript mapping) |
RACE | 5'-RACE(Rapid Amplification of cDNA Ends) method |
SDM | Site-directed mutagenesis (Oligonucleotide-directed mutagenesis) |
ND | No Data |
Weight Matrix Search (by weight matrix)
This program returns the top 10 similar weight matrices against your input weight matrix.
Use a tab (or space) deliminated format.
The first line, if starting with ">", is ignored.
Both absolute numbers and relative frequencies are acceptable.
Input nucleotides should be in the order A->C->G->T.
Example:
A | 0 0 7 7 7 7 1 6 7 2 0 0 0 0 1 |
C | 0 7 0 0 0 0 0 1 0 0 0 1 0 0 6 |
G | 7 0 0 0 0 0 2 0 0 0 0 0 0 7 0 |
T | 0 0 0 0 0 0 4 0 0 5 7 6 7 0 0 |
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Example format 1:
>RocR
0 0 7 7 7 7 1 6 7 2 0 0 0 0 1
0 7 0 0 0 0 0 1 0 0 0 1 0 0 6
7 0 0 0 0 0 2 0 0 0 0 0 0 7 0
0 0 0 0 0 0 4 0 0 5 7 6 7 0 0
Example format 2:
0 0 1 1 1 1 0.143 0.857 1 0.286 0 0 0 0 0.143
0 1 0 0 0 0 0 0.143 0 0 0 0.143 0 0 0.857
1 0 0 0 0 0 0.286 0 0 0 0 0 0 1 0
0 0 0 0 0 0 0.571 0 0 0.714 1 0.857 1 0 0
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