BBa_I13998
BBa_I13998 Version 1 (Component)
temporary (DE -- delete at some future point as needed)

BBa_K1065309
BBa_K1065309 Version 1 (Component)
light regulated circuit producing amilGFP+EFE at dark

BBa_K137101
BBa_K137101 Version 1 (Component)
Strong promoter + strong RBS + tetA with (AGTC)10 repeat after start codon + double terminator

BBa_K137107
BBa_K137107 Version 1 (Component)
Strong promoter + strong RBS + LacZ with (AGTC)10 repeat after start codon + double terminator

BBa_K137102
BBa_K137102 Version 1 (Component)
Strong promoter + strong RBS + tetA with (AGTC)9 repeat after start codon + double terminator

BBa_K137108
BBa_K137108 Version 1 (Component)
Strong promoter + strong RBS + LacZ with (AGTC)9 repeat after start codon + double terminator

BBa_K861169
BBa_K861169 Version 1 (Component)
Indirect regulatory device, activated at high glucose concentration

BBa_J58120
BBa_J58120 Version 1 (Component)
OmpR-P detector with a RFP pulse generator at intermediate concentrations

BBa_I744202
BBa_I744202 Version 1 (Component)
Tc sensor and cl lambda generator (medium promoter)

BBa_I744203
BBa_I744203 Version 1 (Component)
Tc sensor and cl lambda generator (strong promoter)

BBa_I744201
BBa_I744201 Version 1 (Component)
Tc sensor and cl lambda generator (weak promoter)

BBa_K1641004
BBa_K1641004 Version 1 (Component)
Fusion protein of Cre::EGFP::ssra-tag, with RBS at beginning

BBa_J04606
BBa_J04606 Version 1 (Component)
Antiswitch repressing Biobrick coding sequence at the RBS ("Off" switch)

BBa_M36080
BBa_M36080 Version 1 (Component)
Wild-type miraculin protein with His-tag at C-terminus

BBa_K1641006
BBa_K1641006 Version 1 (Component)
Fusion protein of Vcre::EGFP::ssra-tag, with RBS at beginning

BBa_K1641007
BBa_K1641007 Version 1 (Component)
Fusion protein of Scre::EGFP::ssra-tag, with RBS at beginning

BBa_K1641009
BBa_K1641009 Version 1 (Component)
Fusion protein of Vika-EGFP-ssra, with RBS at beginning

BBa_K648101
BBa_K648101 Version 1 (Component)
RecA (mutated from RecA1 at amino acid 160 G-->A

(L-C)3
BBa_K365014 Version 1 (Component)
ClpX trimer with built-in linker at N-ter end

BBa_M45689
BBa_M45689 Version 1 (Component)
Constitutive promoter with a retinoic acid response element at the end

BBa_K137035
BBa_K137035 Version 1 (Component)
Device with GFP with (AC)22 repeat after start codon

BBa_K137034
BBa_K137034 Version 1 (Component)
Device with GFP with (AC)20 repeat after start codon

BBa_I716015
BBa_I716015 Version 1 (Component)
RFP without start ATG

BBa_K806003
BBa_K806003 Version 1 (Component)
SeqA regulation of chromosome replication by preventing re-initiation at newly replicated origins

BBa_K1015015
BBa_K1015015 Version 1 (Component)
araC-pBAD-hbiF-Tc(genome insertion parts between araC and araA)

BBa_K323075
BBa_K323075 Version 1 (Component)
ATG cYFP link HIVC

BBa_K590044
BBa_K590044 Version 1 (Component)
ADC-PSB1A3-High constitutive

BBa_K590036
BBa_K590036 Version 1 (Component)
ADC-PSB3K3-High consititutive

BBa_K1088053
BBa_K1088053 Version 1 (Component)
GFP reporter with flexible linker at N-terminus for creation of GFP fusions

BBa_J24822
BBa_J24822 Version 1 (Component)
Same as J24819 but with the error at the luc-terminator junction fixed

BBa_K855006
BBa_K855006 Version 1 (Component)
pvdQ gene with a silent mutation at 1494 bp to remove the internal PstI site

BBa_K855005
BBa_K855005 Version 1 (Component)
pvdQ gene with a silent mutation at 1491 bp to remove the internal PstI site

BBa_J119408
BBa_J119408 Version 1 (Component)
Pupp promoter mutant - Substitution of C and G to A at 28 and 30

BBa_K202004
BBa_K202004 Version 1 (Component)
Hybrid promoter having multiple operator sites. Promoter has tetO2 with mutation at position 3

BBa_K1088059
BBa_K1088059 Version 1 (Component)
GFP reporter with flexible linker at N-terminus for creation of GFP fusions

BBa_K1088052
BBa_K1088052 Version 1 (Component)
GFP reporter with flexible linker at N-terminus for creation of GFP fusions

BBa_K1178000
BBa_K1178000 Version 1 (Component)
tRNA and synthetase for 3,4-dihydroxy-L-phenylalanine (L-DOPA) incorporation at UAG codon

IodoY RS
BBa_K1416001 Version 1 (Component)
The tRNA synthetase/tRNA needed for incorporating 3-iodo-L-tyrosine (IodoY) at a UAG codon

BBa_K1361005
BBa_K1361005 Version 1 (Component)
CsgE, CsgF, CsgG, the outer membrane secrete device for curli fiber, at relatively low constitutive

RFC 37
BBa_K245088 Version 1 (Component)
TC-P5

BBa_K2172009
BBa_K2172009 Version 1 (Component)
Tac Promoter-RBS-GST-Thrombin Protease-GFP-Terminator

BBa_M36556
BBa_M36556 Version 1 (Component)
5' Bicistronic UTR (medium), does not include ATG start

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

BBa_K137021
BBa_K137021 Version 1 (Component)
GFP with (AC)20 repeat after start codon

BBa_K2123112
BBa_K2123112 Version 1 (Component)
Tac promoter in tandem (3 repetition) with downstream mer operator + RFP (K081014)

BBa_K2123115
BBa_K2123115 Version 1 (Component)
Universal promoter (Tac + JK26) for both growth phase with downstream mer operator + K081014

PrtDEF
BBa_K258007 Version 1 (Component)
Export of recombinant proteins in Escherichia coli using ABC transporter of Erwinia chrysanthemi

BBa_K137033
BBa_K137033 Version 1 (Component)
Device with GFP with (AC)21 repeat after start codon

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.