#	Aladdin ID	Assay Type	Description	Organism	Compounds	Reference	BAO Format	Source
1.	ALA992487	B	Inhibition of PCTK2 at 3 uM		1	ALA1142492	single protein format	Scientific Literature
2.	ALA1051349	B	Binding constant for full-length PCTK2	Homo sapiens	38	ALA1150977	single protein format	Scientific Literature
3.	ALA1057576	B	Inhibition of PCTK2 assessed as enzyme activity at 1 uM relative to untreated control		1	ALA1155237	single protein format	Scientific Literature
4.	ALA1102994	B	Inhibition of PCTK2		1	ALA1154951	single protein format	Scientific Literature
5.	ALA1166610	B	Inhibition of PCTK2 at 1 uM		6	ALA1165965	single protein format	Scientific Literature
6.	ALA1175186	B	Inhibition of PCTK2 at 10 uM		2	ALA1177794	single protein format	Scientific Literature
7.	ALA1244556	B	Binding affinity to PCTK2		7	ALA1240346	single protein format	Scientific Literature
8.	ALA1827260	B	Activity of PCTK2 kinase at 1 uM		1	ALA1821651	single protein format	Scientific Literature
9.	ALA1908473	B	Binding constant for PCTK2 kinase domain		72	ALA1908390	single protein format	Scientific Literature
10.	ALA1944429	B	Inhibition of human PCTAIRE2 in HL-60 cells lysate assessed as reduction of labeling of acyl-phosphate ATP probe at 100 nM	Homo sapiens	4	ALA1938230	cell-based format	Scientific Literature
11.	ALA2215412	B	Inhibition of PCTK2 assessed as residual activity at 10 uM relative to control		1	ALA2203081	single protein format	Scientific Literature
12.	ALA2429142	B	Competitive binding affinity to PCTK2 (unknown origin) at 10 uM in presence of ATP relative to control	Homo sapiens	3	ALA2424622	single protein format	Scientific Literature
13.	ALA3111955	B	Inhibition of PCTK2 (unknown origin) assessed as residual activity at 10 uM after 1 hr by qPCR analysis relative to control	Homo sapiens	1	ALA3108735	single protein format	Scientific Literature
14.	ALA3991655	B	Kinobeads (epsilon), multiple immobilized ATP-competitive broad spectrum kinase inhibitors, used to assess residual binding of ~300 proteins simultaneously from cell lysate in the presence of a compound. Quantitative readout performed by mass spectrometry.	Homo sapiens	218	ALA3991601	subcellular format	Kuster lab chemical proteomics drug profiling
15.	ALA4025293	B	Inhibition of wild-type human full length PCTK2 (M1 to F523 residues) expressed in bacterial expression system assessed as residual activity at 1 uM by Kinomescan method relative to control	Homo sapiens	1	ALA4024706	assay format	Scientific Literature
16.	ALA4044104	B	Inhibition of wild-type human full length PCTK2 (M1 to F523 residues) expressed in Escherichia coli BL21 assessed as residual activity at 1000 nM after 30 mins by Kinomescan method relative to control	Homo sapiens	1	ALA4043093	assay format	Scientific Literature
17.	ALA4055116	B	Inhibition of recombinant human full length PCTAIRE2 (M1 to F523 residues) assessed as residual activity at 50 nM by Kinomescan method relative to control	Homo sapiens	2	ALA4052645	single protein format	Scientific Literature
18.	ALA4118444	B	Inhibition of PCTAIRE2 in human SKCO1 cells at 1 uM after 4 hrs using biotin labeled SKLTENLVALKEIR probe by mass-spectrometric analysis relative to control	Homo sapiens	3	ALA4118021	cell-based format	Scientific Literature
19.	ALA4157183	B	Binding affinity to wild-type human full length PCTK2 (M1 to F523 residues) expressed in bacterial expression system assessed as residual binding at 1 uM by Kinomescan method relative to control	Homo sapiens	1	ALA4152344	assay format	Scientific Literature
20.	ALA4185962	B	Binding affinity to wild-type human full length PCTK2 (M1 to F523 residues) expressed in Escherichia coli BL21 at 1 uM by Kinomescan method relative to control	Homo sapiens	2	ALA4184148	assay format	Scientific Literature