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Showing 1251 - 1278 of 1278 result(s)
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Public
iGEM 2019 Cell Tat secretion cassette with constitutive promoter.
iGEM_2019_Cell17 Version 1 (Collection)

Public
BBa_K415005
BBa_K415005 Version 1 (Component)
pLux/cI-OR : RBS-mCherry : Term : p(tetR) : RBS-luxR : Term
Public
BBa_K223033
BBa_K223033 Version 1 (Component)
trp-operon + RBS + IL-6 + HlyA + TT Trp-sensitive IL-6 synthesizer
Public
BBa_J119408
BBa_J119408 Version 1 (Component)
Pupp promoter mutant - Substitution of C and G to A at 28 and 30
Public
BBa_K202004
BBa_K202004 Version 1 (Component)
Hybrid promoter having multiple operator sites. Promoter has tetO2 with mutation at position 3
Public
BBa_K199194
BBa_K199194 Version 1 (Component)
TT-pLux-RBS-LuxI 2 sites-RBS-GFP-RBS-RFP-pLacI-RBS-LuxR
Public
BBa_K1022125
BBa_K1022125 Version 1 (Component)
pT7: RBS: His6- SUMO: Signiferin: RBS: TetR:TT : pTet: cI: TT : pcI: Ulp : Lysis
Public
BBa_K199193
BBa_K199193 Version 1 (Component)
TT-pLux-RBS-LuxI 2 sites-RBS-RFP-RBS-GFP-pBAD-RBS-LuxR
Public
BBa_K1088059
BBa_K1088059 Version 1 (Component)
GFP reporter with flexible linker at N-terminus for creation of GFP fusions
Public
BBa_K1088052
BBa_K1088052 Version 1 (Component)
GFP reporter with flexible linker at N-terminus for creation of GFP fusions
Public
BBa_K1178000
BBa_K1178000 Version 1 (Component)
tRNA and synthetase for 3,4-dihydroxy-L-phenylalanine (L-DOPA) incorporation at UAG codon
Public
BBa_J100017
BBa_J100017 Version 1 (Component)
TT+pLux+RBS+LuxI(2-SAT 2 clause)+RBS+GFP+pLac+RBS+LuxR+tRNAs
Public
BBa_K1022126
BBa_K1022126 Version 1 (Component)
pT7: RBS: His6- SUMO: Magainin II: RBS: TetR:TT : pTet: cI: TT : pcI: Ulp : Lysis
Public
IodoY RS
BBa_K1416001 Version 1 (Component)
The tRNA synthetase/tRNA needed for incorporating 3-iodo-L-tyrosine (IodoY) at a UAG codon
Public
BBa_K1361005
BBa_K1361005 Version 1 (Component)
CsgE, CsgF, CsgG, the outer membrane secrete device for curli fiber, at relatively low constitutive
Public
BBa_J107021
BBa_J107021 Version 1 (Component)
aTc sensor (J23106 promoter) with GFP
Public
BBa_K820014
BBa_K820014 Version 1 (Component)
mazF-TT
Public
BBa_K368020
BBa_K368020 Version 1 (Component)
attB (bacterial attachment site, recombined by PhiC31 Integrase)
Public
BBa_J31016
BBa_J31016 Version 1 (Component)
part produces the RNA construct crRNA-RBS-GFPLVA-tt that can only be translated in the presence of t
Public
BBa_K199112
BBa_K199112 Version 1 (Component)
RFP-TT intermediate
Public
BBa_K660605
BBa_K660605 Version 1 (Component)
OmpF + wYFP + TT
Public
BBa_M36556
BBa_M36556 Version 1 (Component)
5' Bicistronic UTR (medium), does not include ATG start
Public
BBa_K1361007
BBa_K1361007 Version 1 (Component)
Curli Fiber generator under the control of Pbad promoter with CsgA modified by His tag at a relative
Public
BBa_K318501
BBa_K318501 Version 1 (Component)
lacI pL + RBS + RcsB + TT
Public
BBa_K199165
BBa_K199165 Version 1 (Component)
pT7 + RBS + GFP + TT in pSB3T5
Public
BBa_J107055
BBa_J107055 Version 1 (Component)
pSB3K3 with RBS-RFP-TT between SpeI-PstI
Public
BBa_S03737
BBa_S03737 Version 1 (Component)
pLac-lox-RFP(reverse)-TT-lox-RBS-Tet (psB1A2)
Public
Intein_assisted_Bisection_Mapping
Intein_assisted_Bisection_Mapping_collection Version 1 (Collection)
Split inteins are powerful tools for seamless ligation of synthetic split proteins. Yet, their use remains limited because the already intricate split site identification problem is often complicated by the requirement of extein junction sequences. To address this, we augmented a mini-Mu transposon-based screening approach and devised the intein-assisted bisection mapping (IBM) method. IBM robustly revealed clusters of split sites on five proteins, converting them into AND or NAND logic gates. We further showed that the use of inteins expands functional sequence space for splitting a protein. We also demonstrated the utility of our approach over rational inference of split sites from secondary structure alignment of homologous proteins. Furthermore, the intein inserted at an identified site could be engineered by the transposon again to become partially chemically inducible, and to some extent enabled post-translational tuning on host protein function. Our work offers a generalizable and systematic route towards creating split protein-intein fusions and conditional inteins for protein activity control.
Showing 1251 - 1278 of 1278 result(s)
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