PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
18502798-7	2008	Asp(1653), Glu(1655), Glu(1660), Asp(1663), together with the hydrophilic side chain of Thr(1656) were shown to form a "hot spot" in the VWF A2 sequence, which drives the molecular recognition and allosteric regulation of binding to ADAMTS13.	Threonine	88-91	von Willebrand factor	Homo sapiens	137-140	
15606553-5	2005	Utilizing a neuronal network for prediction of O-linked glycosylation of mammalian proteins, threonine (T) and serine (S) residues located in the VWF-A1-loop flanking regions - not in the loop itself - were determined to be glycosylated n-terminal at amino acids T485, S490, T492 and T493 and c-terminal at T705.	Threonine	93-102	von Willebrand factor	Homo sapiens	146-149	
17261793-5	2006	The first, a C/T transition at nucleotide 1018 results in an amino acid dimorphism (Thr/Met) at residue 145 of GPIb-alpha, which is located within the vWF-binding domain of the receptor.	Threonine	84-87	von Willebrand factor	Homo sapiens	151-154	
9569179-2	1998	A six nucleotide insert, AATCCC, was found in exon 11 of the vWF gene, predicting the insertion of the amino acids asparagine and proline between phenylalanine 404 and threonine 405 of the vWF propeptide.	Threonine	168-177	von Willebrand factor	Homo sapiens	61-64	
11159522-3	2001	In the heterozygous state, a cysteine-to-threonine (C --> T) transversion was detected at nucleotide 4193 of the VWF gene of all patients and lead to the arginine (R)522C substitution in the A1 loop of vWF mature subunit (R1315C in the preprovWF).	Threonine	41-50	von Willebrand factor	Homo sapiens	116-119	
11159522-3	2001	In the heterozygous state, a cysteine-to-threonine (C --> T) transversion was detected at nucleotide 4193 of the VWF gene of all patients and lead to the arginine (R)522C substitution in the A1 loop of vWF mature subunit (R1315C in the preprovWF).	Threonine	41-50	von Willebrand factor	Homo sapiens	205-208	
10607704-0	2000	Threonine-145/methionine-145 variants of baculovirus produced recombinant ligand binding domain of GPIbalpha express HPA-2 epitopes and show equal binding of von Willebrand factor.	Threonine	0-9	von Willebrand factor	Homo sapiens	158-179	
11418460-3	2001	Three polymorphisms have been described in GP Ibalpha (Kozak T/C polymorphism, variable number of tandem repeats [VNTR], and the human platelet antigen 2a [HPA-2a] [Thr] or HPA-2b [Met] at position 145), each of which may enhance the vWf and GP Ibalpha interaction.	Threonine	0-3	von Willebrand factor	Homo sapiens	234-237	
9569179-2	1998	A six nucleotide insert, AATCCC, was found in exon 11 of the vWF gene, predicting the insertion of the amino acids asparagine and proline between phenylalanine 404 and threonine 405 of the vWF propeptide.	Threonine	168-177	von Willebrand factor	Homo sapiens	189-192	
8500791-5	1993	The patient was found to be homozygous for a single point mutation causing a Thr-->Met substitution at amino acid position 28 in the mature vWF subunit.	Threonine	77-80	von Willebrand factor	Homo sapiens	143-146	
9455905-2	1997	Previously, we demonstrated that the in vivo O-glycosylation of a sequence derived from a known glycosylation site of human von Willebrand factor (PHMAQVTVGPGL) was markedly reduced when charged residues were substituted at position -1 and +3 relative to the single threonine.	Threonine	266-275	von Willebrand factor	Homo sapiens	124-145	
23358615-12	2013	Those with the SNP in vWF gene causing homozygous threonine at codon 1381 had lower plasma vWF level than those with homozygous alanine or heterozygous alanine/threonine.	Threonine	50-59	von Willebrand factor	Homo sapiens	22-25	
23358615-12	2013	Those with the SNP in vWF gene causing homozygous threonine at codon 1381 had lower plasma vWF level than those with homozygous alanine or heterozygous alanine/threonine.	Threonine	50-59	von Willebrand factor	Homo sapiens	91-94	
23358615-12	2013	Those with the SNP in vWF gene causing homozygous threonine at codon 1381 had lower plasma vWF level than those with homozygous alanine or heterozygous alanine/threonine.	Threonine	160-169	von Willebrand factor	Homo sapiens	22-25	
2018834-10	1991	We conclude that Threonine at position 28 in plasma vWF may be crucial for the conformation and FVIII-binding capacity of its cystine-rich N-terminal domain.	Threonine	17-26	von Willebrand factor	Homo sapiens	52-55