BBa_J58120BBa_J58120 Version 1 (Component)OmpR-P detector with a RFP pulse generator at intermediate concentrations
BBa_K1641004BBa_K1641004 Version 1 (Component)Fusion protein of Cre::EGFP::ssra-tag, with RBS at beginning
BBa_J04606BBa_J04606 Version 1 (Component)Antiswitch repressing Biobrick coding sequence at the RBS ("Off" switch)
BBa_M36080BBa_M36080 Version 1 (Component)Wild-type miraculin protein with His-tag at C-terminus
BBa_K638401BBa_K638401 Version 1 (Component)Arabinose inducible TorA Export Tagged Reflectin A1 Poly His generator
BBa_K1641006BBa_K1641006 Version 1 (Component)Fusion protein of Vcre::EGFP::ssra-tag, with RBS at beginning
BBa_K1641007BBa_K1641007 Version 1 (Component)Fusion protein of Scre::EGFP::ssra-tag, with RBS at beginning
BBa_K1641009BBa_K1641009 Version 1 (Component)Fusion protein of Vika-EGFP-ssra, with RBS at beginning
BBa_K648101BBa_K648101 Version 1 (Component)RecA (mutated from RecA1 at amino acid 160 G-->A
(L-C)3BBa_K365014 Version 1 (Component)ClpX trimer with built-in linker at N-ter end
BBa_M45689BBa_M45689 Version 1 (Component)Constitutive promoter with a retinoic acid response element at the end
BBa_I716015BBa_I716015 Version 1 (Component)RFP without start ATG
BBa_K806003BBa_K806003 Version 1 (Component)SeqA regulation of chromosome replication by preventing re-initiation at newly replicated origins
BBa_K1228009BBa_K1228009 Version 1 (Component)38aa and 25aa fusion peptide with T1 terminator and Constitutive promoter veg
BBa_K323075BBa_K323075 Version 1 (Component)ATG cYFP link HIVC
BBa_K1088053BBa_K1088053 Version 1 (Component)GFP reporter with flexible linker at N-terminus for creation of GFP fusions
BBa_J24822BBa_J24822 Version 1 (Component)Same as J24819 but with the error at the luc-terminator junction fixed
BBa_K2146006BBa_K2146006 Version 1 (Component)pWH1266 ori-Ptac-lacOc-ampC ADC-33-T1-lacI-PT5-gusA-T2-pSB1C3
BBa_M36586BBa_M36586 Version 1 (Component)T1 Transcription Terminator
BBa_K855006BBa_K855006 Version 1 (Component)pvdQ gene with a silent mutation at 1494 bp to remove the internal PstI site
BBa_K855005BBa_K855005 Version 1 (Component)pvdQ gene with a silent mutation at 1491 bp to remove the internal PstI site
BBa_J119408BBa_J119408 Version 1 (Component)Pupp promoter mutant - Substitution of C and G to A at 28 and 30
BBa_K202004BBa_K202004 Version 1 (Component)Hybrid promoter having multiple operator sites. Promoter has tetO2 with mutation at position 3
BBa_K1088059BBa_K1088059 Version 1 (Component)GFP reporter with flexible linker at N-terminus for creation of GFP fusions
BBa_K1088052BBa_K1088052 Version 1 (Component)GFP reporter with flexible linker at N-terminus for creation of GFP fusions
BBa_K1178000BBa_K1178000 Version 1 (Component)tRNA and synthetase for 3,4-dihydroxy-L-phenylalanine (L-DOPA) incorporation at UAG codon
IodoY RSBBa_K1416001 Version 1 (Component)The tRNA synthetase/tRNA needed for incorporating 3-iodo-L-tyrosine (IodoY) at a UAG codon
BBa_J176083BBa_J176083 Version 1 (Component)Polycomb ATF neg. ctrl. 3 "
BBa_K1361005BBa_K1361005 Version 1 (Component)CsgE, CsgF, CsgG, the outer membrane secrete device for curli fiber, at relatively low constitutive
BBa_J107021BBa_J107021 Version 1 (Component)aTc sensor (J23106 promoter) with GFP
BBa_M36556BBa_M36556 Version 1 (Component)5' Bicistronic UTR (medium), does not include ATG start
BBa_K1361007BBa_K1361007 Version 1 (Component)Curli Fiber generator under the control of Pbad promoter with CsgA modified by His tag at a relative
BBa_M36918BBa_M36918 Version 1 (Component)T1 from E. coli rrnB
BBa_K1824558BBa_K1824558 Version 1 (Component)RNA Thermometer A1 (Specially designed for T7)
BBa_K638201BBa_K638201 Version 1 (Component)Arabinose inducible Poly-His Reflectin A1 generator
Intein_assisted_Bisection_MappingIntein_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.