Details of experiments between Q9Y3R0 and K9N5R3 Note that the results of all experiments are listed, regardless of the modification states of the fragments.
Experiment series 1 Protein A Protein: GRIP1 Fragment: 996-1086 Site: PDZ_7 Construct: his6-MBP-TEVsite-PDZ
Protein B Protein: MERS-E Fragment: 73-82 Site: PBM Sequence: KPPLPPDEWV Construct: Biotin-ado-ado-KPPLPPDEWV
Average holdup BI: 0.15
Normalized holdup BI: 0.15
Immobilized partner concentration (10-6 M): 18
Experiment method: DAPF_holdup
Details of affinity fitting: fluorescein + mCherry internal standards + normalization based on CALIP_holdup data + reverse layout
Number of measurements: 1
Measured pK d : 3.99
Experimental Details Crude peptide synthesis product. The peptide concentration in the affinity conversion step may differ from reality. Not reported internal standards of holdup layout #6
Experiment series 2 Protein A Protein: GRIP1 Fragment: 996-1086 Site: PDZ_7 Construct: his6-MBP-TEVsite-PDZ
Protein B Protein: MERS-E Fragment: 71-82 Site: PBM Sequence: KPPLPPDEWV Construct: biotin-DSKPPLPPDEWV
Average holdup BI: 0.12
Normalized holdup BI: 0.12
Immobilized partner concentration (10-6 M): 18
Experiment method: DAPF_holdup
Details of affinity fitting: fluorescein + mCherry internal standards + normalization based on CALIP_holdup data + reverse layout
Number of measurements: 1
Measured pK d : 3.88
Experiment series 3 Protein A Protein: GRIP1 Fragment: 145-239 Site: PDZ_2 Construct: his6-MBP-TEVsite-PDZ
Protein B Protein: MERS-E Fragment: 73-82 Site: PBM Sequence: KPPLPPDEWV Construct: Biotin-ado-ado-KPPLPPDEWV
Average holdup BI: 0.08
Normalized holdup BI: 0.08
Immobilized partner concentration (10-6 M): 18
Experiment method: DAPF_holdup
Details of affinity fitting: fluorescein + mCherry internal standards + normalization based on CALIP_holdup data + reverse layout
Number of measurements: 1
Measured pK d : 3.7
Experimental Details Crude peptide synthesis product. The peptide concentration in the affinity conversion step may differ from reality. Not reported internal standards of holdup layout #6
Experiment series 4 Protein A Protein: GRIP1 Fragment: 563-659 Site: PDZ_5 Construct: his6-MBP-TEVsite-PDZ
Protein B Protein: MERS-E Fragment: 71-82 Site: PBM Sequence: KPPLPPDEWV Construct: biotin-DSKPPLPPDEWV
Average holdup BI: 0.08
Normalized holdup BI: 0.08
Immobilized partner concentration (10-6 M): 18
Experiment method: DAPF_holdup
Details of affinity fitting: fluorescein + mCherry internal standards + normalization based on CALIP_holdup data + reverse layout
Number of measurements: 1
Measured pK d : 3.68
Experiment series 5 Protein A Protein: GRIP1 Fragment: 145-239 Site: PDZ_2 Construct: his6-MBP-TEVsite-PDZ
Protein B Protein: MERS-E Fragment: 71-82 Site: PBM Sequence: KPPLPPDEWV Construct: biotin-DSKPPLPPDEWV
Average holdup BI: 0.07
Normalized holdup BI: 0.07
Immobilized partner concentration (10-6 M): 18
Experiment method: DAPF_holdup
Details of affinity fitting: fluorescein + mCherry internal standards + normalization based on CALIP_holdup data + reverse layout
Number of measurements: 1
Measured pK d : 3.62
Experiment series 6 Protein A Protein: GRIP1 Fragment: 145-239 Site: PDZ_2 Construct: his6-MBP-TEVsite-PDZ
Protein B Protein: MERS-E Fragment: 71-82 Site: PBM Sequence: KPPLPPDEWV Construct: biotin-DSKPPLPPDEWV
Average holdup BI: -0.02
Holdup BI standard deviation: 0.01
Immobilized partner concentration (10-6 M): 20
Experiment method: CALIP_holdup
Details of affinity fitting: BSA and lysozyme internal standards + bacterial cell lysate + normal layout
Number of measurements: 2
The affinity was below the detection threshold of the assay.
Experiment series 7 Protein A Protein: GRIP1 Fragment: 242-344 Site: PDZ_3 Construct: his6-MBP-TEVsite-PDZ
Protein B Protein: MERS-E Fragment: 71-82 Site: PBM Sequence: KPPLPPDEWV Construct: biotin-DSKPPLPPDEWV
Average holdup BI: 0.05
Normalized holdup BI: 0.05
Immobilized partner concentration (10-6 M): 18
Experiment method: DAPF_holdup
Details of affinity fitting: fluorescein + mCherry internal standards + normalization based on CALIP_holdup data + reverse layout
Number of measurements: 1
The affinity was below the detection threshold of the assay.
Experiment series 8 Protein A Protein: GRIP1 Fragment: 242-344 Site: PDZ_3 Construct: his6-MBP-TEVsite-PDZ
Protein B Protein: MERS-E Fragment: 71-82 Site: PBM Sequence: KPPLPPDEWV Construct: biotin-DSKPPLPPDEWV
Average holdup BI: 0.03
Holdup BI standard deviation: 0.02
Immobilized partner concentration (10-6 M): 20
Experiment method: CALIP_holdup
Details of affinity fitting: BSA and lysozyme internal standards + bacterial cell lysate + normal layout
Number of measurements: 2
The affinity was below the detection threshold of the assay.
Experiment series 9 Protein A Protein: GRIP1 Fragment: 242-344 Site: PDZ_3 Construct: his6-MBP-TEVsite-PDZ
Protein B Protein: MERS-E Fragment: 73-82 Site: PBM Sequence: KPPLPPDEWV Construct: Biotin-ado-ado-KPPLPPDEWV
Average holdup BI: 0.01
Normalized holdup BI: 0.01
Immobilized partner concentration (10-6 M): 18
Experiment method: DAPF_holdup
Details of affinity fitting: fluorescein + mCherry internal standards + normalization based on CALIP_holdup data + reverse layout
Number of measurements: 1
The affinity was below the detection threshold of the assay.
Experimental Details Crude peptide synthesis product. The peptide concentration in the affinity conversion step may differ from reality. Not reported internal standards of holdup layout #6
Experiment series 10 Protein A Protein: GRIP1 Fragment: 464-567 Site: PDZ_4 Construct: his6-MBP-TEVsite-PDZ
Protein B Protein: MERS-E Fragment: 71-82 Site: PBM Sequence: KPPLPPDEWV Construct: biotin-DSKPPLPPDEWV
Average holdup BI: 0.02
Normalized holdup BI: 0.02
Immobilized partner concentration (10-6 M): 18
Experiment method: DAPF_holdup
Details of affinity fitting: fluorescein + mCherry internal standards + normalization based on CALIP_holdup data + reverse layout
Number of measurements: 1
The affinity was below the detection threshold of the assay.
Experiment series 11 Protein A Protein: GRIP1 Fragment: 464-567 Site: PDZ_4 Construct: his6-MBP-TEVsite-PDZ
Protein B Protein: MERS-E Fragment: 71-82 Site: PBM Sequence: KPPLPPDEWV Construct: biotin-DSKPPLPPDEWV
Average holdup BI: -0.05
Holdup BI standard deviation: 0.03
Immobilized partner concentration (10-6 M): 20
Experiment method: CALIP_holdup
Details of affinity fitting: BSA and lysozyme internal standards + bacterial cell lysate + normal layout
Number of measurements: 2
The affinity was below the detection threshold of the assay.
Experiment series 12 Protein A Protein: GRIP1 Fragment: 464-567 Site: PDZ_4 Construct: his6-MBP-TEVsite-PDZ
Protein B Protein: MERS-E Fragment: 73-82 Site: PBM Sequence: KPPLPPDEWV Construct: Biotin-ado-ado-KPPLPPDEWV
Average holdup BI: 0.01
Normalized holdup BI: 0.01
Immobilized partner concentration (10-6 M): 18
Experiment method: DAPF_holdup
Details of affinity fitting: fluorescein + mCherry internal standards + normalization based on CALIP_holdup data + reverse layout
Number of measurements: 1
The affinity was below the detection threshold of the assay.
Experimental Details Crude peptide synthesis product. The peptide concentration in the affinity conversion step may differ from reality. Not reported internal standards of holdup layout #6
Experiment series 13 Protein A Protein: GRIP1 Fragment: 47-137 Site: PDZ_1 Construct: his6-MBP-TEVsite-PDZ
Protein B Protein: MERS-E Fragment: 71-82 Site: PBM Sequence: KPPLPPDEWV Construct: biotin-DSKPPLPPDEWV
Average holdup BI: 0.02
Holdup BI standard deviation: 0.05
Immobilized partner concentration (10-6 M): 20
Experiment method: CALIP_holdup
Details of affinity fitting: BSA and lysozyme internal standards + bacterial cell lysate + normal layout
Number of measurements: 2
The affinity was below the detection threshold of the assay.
Experiment series 14 Protein A Protein: GRIP1 Fragment: 563-659 Site: PDZ_5 Construct: his6-MBP-TEVsite-PDZ
Protein B Protein: MERS-E Fragment: 71-82 Site: PBM Sequence: KPPLPPDEWV Construct: biotin-DSKPPLPPDEWV
Average holdup BI: -0.07
Holdup BI standard deviation: 0.01
Immobilized partner concentration (10-6 M): 20
Experiment method: CALIP_holdup
Details of affinity fitting: BSA and lysozyme internal standards + bacterial cell lysate + normal layout
Number of measurements: 2
The affinity was below the detection threshold of the assay.
Experiment series 15 Protein A Protein: GRIP1 Fragment: 563-659 Site: PDZ_5 Construct: his6-MBP-TEVsite-PDZ
Protein B Protein: MERS-E Fragment: 73-82 Site: PBM Sequence: KPPLPPDEWV Construct: Biotin-ado-ado-KPPLPPDEWV
Average holdup BI: -0.01
Normalized holdup BI: -0.01
Immobilized partner concentration (10-6 M): 18
Experiment method: DAPF_holdup
Details of affinity fitting: fluorescein + mCherry internal standards + normalization based on CALIP_holdup data + reverse layout
Number of measurements: 1
The affinity was below the detection threshold of the assay.
Experimental Details Crude peptide synthesis product. The peptide concentration in the affinity conversion step may differ from reality. Not reported internal standards of holdup layout #6
Experiment series 16 Protein A Protein: GRIP1 Fragment: 666-762 Site: PDZ_6 Construct: his6-MBP-TEVsite-PDZ
Protein B Protein: MERS-E Fragment: 71-82 Site: PBM Sequence: KPPLPPDEWV Construct: biotin-DSKPPLPPDEWV
Average holdup BI: -0.02
Holdup BI standard deviation: 0.03
Immobilized partner concentration (10-6 M): 20
Experiment method: CALIP_holdup
Details of affinity fitting: BSA and lysozyme internal standards + bacterial cell lysate + normal layout
Number of measurements: 2
The affinity was below the detection threshold of the assay.
Experiment series 17 Protein A Protein: GRIP1 Fragment: 996-1086 Site: PDZ_7 Construct: his6-MBP-TEVsite-PDZ
Protein B Protein: MERS-E Fragment: 71-82 Site: PBM Sequence: KPPLPPDEWV Construct: biotin-DSKPPLPPDEWV
Average holdup BI: 0.01
Holdup BI standard deviation: 0
Immobilized partner concentration (10-6 M): 20
Experiment method: CALIP_holdup
Details of affinity fitting: BSA and lysozyme internal standards + bacterial cell lysate + normal layout
Number of measurements: 2
The affinity was below the detection threshold of the assay.
Please cite ProfAff! (Gogl, G. et al., Nature Communications 2022)
© The ProfAff database is developped by the research team of Gergo Gogl .