PMID-sentid	Pub_year	Sent_text	comp_official_name	comp_offset	protein_name	organism	prot_offset
12922177-3	2003	XIP-I completely inhibited the activity of AMY1 and AMY2 towards insoluble Blue Starch and a soluble hepta-oligosaccharide derivative.	Starch	80-86	xylanase inhibitor protein 1	Triticum aestivum	0-5
27405320-11	2016	Sequence analysis revealed two GH11 xylanases of F. virguliforme, FvXyn11A and FvXyn11B, have conserved residues that allow xylanase inhibitor protein I (XIP-I) binding.	gh11	31-35	xylanase inhibitor protein 1	Triticum aestivum	154-159
22233686-7	2012	The xylanase activity and XIP-I inhibitory activity was quantified by the 3,5-dinitrosalicylic (DNS).	3,5-dinitrosalicylic	74-94	xylanase inhibitor protein 1	Triticum aestivum	26-31
22233686-7	2012	The xylanase activity and XIP-I inhibitory activity was quantified by the 3,5-dinitrosalicylic (DNS).	3,5-dinitrosalicylic acid	96-99	xylanase inhibitor protein 1	Triticum aestivum	26-31
22233686-11	2012	The recombinant xylanase showed maximal activity at pH 5.5 and 37 C. XIP-I expressed as a recombinant protein inhibited HhXyl activity in vitro and caused individual H. hampei mortality in bioassays when included as a supplement in artificial diets.	hhxyl	120-125	xylanase inhibitor protein 1	Triticum aestivum	69-74
18092758-1	2008	This study is an in-depth investigation of the interaction between polysaccharides and the proteinaceous xylanase inhibitors, Triticum aestivum xylanase inhibitor (TAXI), xylanase inhibitor protein (XIP), and thaumatin-like xylanase inhibitor (TLXI).	Polysaccharides	67-82	xylanase inhibitor protein 1	Triticum aestivum	199-202
20391529-7	2010	Furthermore, it was shown that most identified TAXI- and XIP-type XI (iso)forms significantly increased in abundance from the milky (15 DPA) to the soft dough stages (25 DPA) on a per kernel basis, although the extent of increase differed greatly.	dpa	136-139	xylanase inhibitor protein 1	Triticum aestivum	57-60
20391529-7	2010	Furthermore, it was shown that most identified TAXI- and XIP-type XI (iso)forms significantly increased in abundance from the milky (15 DPA) to the soft dough stages (25 DPA) on a per kernel basis, although the extent of increase differed greatly.	dpa	170-173	xylanase inhibitor protein 1	Triticum aestivum	57-60
19118652-4	2009	We produced variants displaying increased catalytic efficiency towards wheat arabinoxylan and xylo-oligosaccharides and identified specific determinants in PgXynB "thumb" region responsible for resistance to the wheat xylanase inhibitor XIP-I.	arabinoxylan	77-89	xylanase inhibitor protein 1	Triticum aestivum	237-242
19118652-4	2009	We produced variants displaying increased catalytic efficiency towards wheat arabinoxylan and xylo-oligosaccharides and identified specific determinants in PgXynB "thumb" region responsible for resistance to the wheat xylanase inhibitor XIP-I.	xylooligosaccharide	94-115	xylanase inhibitor protein 1	Triticum aestivum	237-242
19118652-4	2009	We produced variants displaying increased catalytic efficiency towards wheat arabinoxylan and xylo-oligosaccharides and identified specific determinants in PgXynB "thumb" region responsible for resistance to the wheat xylanase inhibitor XIP-I.	pgxynb	156-162	xylanase inhibitor protein 1	Triticum aestivum	237-242
15914935-6	2005	Xip-I was expressed when the leaves were wounded, and its expression was significantly elevated by treatment with methyl jasmonate (MeJA).	methyl jasmonate	114-130	xylanase inhibitor protein 1	Triticum aestivum	0-5
15181003-6	2004	The structural determinants of XIP-I specificity demonstrate that the inhibitor is able to interact with GH10 and GH11 xylanases of both fungal and bacterial origin.	gh10	105-109	xylanase inhibitor protein 1	Triticum aestivum	31-36
12922177-3	2003	XIP-I completely inhibited the activity of AMY1 and AMY2 towards insoluble Blue Starch and a soluble hepta-oligosaccharide derivative.	hepta-oligosaccharide	101-122	xylanase inhibitor protein 1	Triticum aestivum	0-5
12922177-4	2003	A ternary complex was formed between insoluble starch, a catalytically inactive mutant of AMY1 (D180A), and XIP-I, suggesting that the substrate-XIP-I interaction is necessary for inhibition of barley alpha-amylases.	Starch	47-53	xylanase inhibitor protein 1	Triticum aestivum	108-113
12922177-4	2003	A ternary complex was formed between insoluble starch, a catalytically inactive mutant of AMY1 (D180A), and XIP-I, suggesting that the substrate-XIP-I interaction is necessary for inhibition of barley alpha-amylases.	Starch	47-53	xylanase inhibitor protein 1	Triticum aestivum	145-150
12617724-8	2003	Gly(81), located in subsite -1 of hevamine, where the reaction intermediate is formed, is replaced by Tyr(80) in XIP-I.	Glycine	0-3	xylanase inhibitor protein 1	Triticum aestivum	113-118
12617724-8	2003	Gly(81), located in subsite -1 of hevamine, where the reaction intermediate is formed, is replaced by Tyr(80) in XIP-I.	Tyrosine	102-105	xylanase inhibitor protein 1	Triticum aestivum	113-118