PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
16971948-7	2006	The CTE interacts directly with the Tap protein (also known as nuclear RNA export factor 1, encoded by NXF1), which is thought to be a principal export receptor for cellular mRNA, leading to the hypothesis that cellular mRNAs with retained introns use cellular CTE equivalents to overcome restrictions to their expression.	1,1,1-trifluoro-2-chloroethane	4-7	nuclear RNA export factor 1	Homo sapiens	36-39	
16971948-7	2006	The CTE interacts directly with the Tap protein (also known as nuclear RNA export factor 1, encoded by NXF1), which is thought to be a principal export receptor for cellular mRNA, leading to the hypothesis that cellular mRNAs with retained introns use cellular CTE equivalents to overcome restrictions to their expression.	1,1,1-trifluoro-2-chloroethane	4-7	nuclear RNA export factor 1	Homo sapiens	103-107	
11358864-4	2001	However, changing a single residue in quail Tap, glutamine 246, to arginine, the residue found in human Tap, rescues both CTE function and CTE binding.	1,1,1-trifluoro-2-chloroethane	122-125	nuclear RNA export factor 1	Homo sapiens	44-47	
11358864-4	2001	However, changing a single residue in quail Tap, glutamine 246, to arginine, the residue found in human Tap, rescues both CTE function and CTE binding.	1,1,1-trifluoro-2-chloroethane	122-125	nuclear RNA export factor 1	Homo sapiens	104-107	
11358864-4	2001	However, changing a single residue in quail Tap, glutamine 246, to arginine, the residue found in human Tap, rescues both CTE function and CTE binding.	1,1,1-trifluoro-2-chloroethane	139-142	nuclear RNA export factor 1	Homo sapiens	44-47	
11358864-4	2001	However, changing a single residue in quail Tap, glutamine 246, to arginine, the residue found in human Tap, rescues both CTE function and CTE binding.	1,1,1-trifluoro-2-chloroethane	139-142	nuclear RNA export factor 1	Homo sapiens	104-107	
11358864-5	2001	This residue, which is located on the exterior of a recently reported molecular structure of Tap, defines a surface on Tap that is critical for CTE binding.	1,1,1-trifluoro-2-chloroethane	144-147	nuclear RNA export factor 1	Homo sapiens	93-96	
11358864-5	2001	This residue, which is located on the exterior of a recently reported molecular structure of Tap, defines a surface on Tap that is critical for CTE binding.	1,1,1-trifluoro-2-chloroethane	144-147	nuclear RNA export factor 1	Homo sapiens	119-122	
10489353-5	1999	Analysis of the RNA export activity of the recovered CTE variants revealed that Tap affinity was highly predictive of CTE biological activity.	1,1,1-trifluoro-2-chloroethane	53-56	nuclear RNA export factor 1	Homo sapiens	80-83	
10489353-5	1999	Analysis of the RNA export activity of the recovered CTE variants revealed that Tap affinity was highly predictive of CTE biological activity.	1,1,1-trifluoro-2-chloroethane	118-121	nuclear RNA export factor 1	Homo sapiens	80-83	
11854490-4	2002	To identify residues that interact with the CTE, we have introduced 38 alanine substitutions for surface residues in the Tap CTE-binding domain and tested these mutants for their ability to support CTE-dependent nuclear RNA export and CTE binding.	1,1,1-trifluoro-2-chloroethane	44-47	nuclear RNA export factor 1	Homo sapiens	121-124	
11854490-4	2002	To identify residues that interact with the CTE, we have introduced 38 alanine substitutions for surface residues in the Tap CTE-binding domain and tested these mutants for their ability to support CTE-dependent nuclear RNA export and CTE binding.	1,1,1-trifluoro-2-chloroethane	125-128	nuclear RNA export factor 1	Homo sapiens	121-124	
11854490-6	2002	The second critical CTE-interacting surface on Tap is defined by three previously identified residues on the surface of the ribonucleoprotein domain.	1,1,1-trifluoro-2-chloroethane	20-23	nuclear RNA export factor 1	Homo sapiens	47-50	
10951562-5	2000	Here we report evidence that Sam68, RHA and Tap cooperate in the nuclear export of both CTE- and RRE-containing RNA.	1,1,1-trifluoro-2-chloroethane	88-91	nuclear RNA export factor 1	Homo sapiens	44-47	
10454577-1	1999	The nuclear export of the unspliced type D retrovirus mRNA depends on the cis-acting constitutive transport RNA element (CTE) that has been shown to interact with the human TAP (hTAP) protein promoting the export of the CTE-containing mRNAs.	1,1,1-trifluoro-2-chloroethane	121-124	nuclear RNA export factor 1	Homo sapiens	173-176	
10454577-1	1999	The nuclear export of the unspliced type D retrovirus mRNA depends on the cis-acting constitutive transport RNA element (CTE) that has been shown to interact with the human TAP (hTAP) protein promoting the export of the CTE-containing mRNAs.	1,1,1-trifluoro-2-chloroethane	121-124	nuclear RNA export factor 1	Homo sapiens	178-182	
10323864-6	1999	Whereas replacement of the Tap NES with the well-defined Rev NES rescues the ability of Tap to support CTE function, this substitution also confers sensitivity to agents that block the activity of Crm1, the Rev NES cofactor.	1,1,1-trifluoro-2-chloroethane	103-106	nuclear RNA export factor 1	Homo sapiens	27-30	
10323864-6	1999	Whereas replacement of the Tap NES with the well-defined Rev NES rescues the ability of Tap to support CTE function, this substitution also confers sensitivity to agents that block the activity of Crm1, the Rev NES cofactor.	1,1,1-trifluoro-2-chloroethane	103-106	nuclear RNA export factor 1	Homo sapiens	88-91	
9660949-2	1998	Here, we report the identification of TAP as the cellular factor that specifically binds to wild-type CTE but not to export-deficient CTE mutants.	1,1,1-trifluoro-2-chloroethane	102-105	nuclear RNA export factor 1	Homo sapiens	38-41	
9660949-2	1998	Here, we report the identification of TAP as the cellular factor that specifically binds to wild-type CTE but not to export-deficient CTE mutants.	1,1,1-trifluoro-2-chloroethane	134-137	nuclear RNA export factor 1	Homo sapiens	38-41