PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
21454715-7	2011	A citrulline-mimicking Arg-NLS-Gln ING4 mutant, which has all Arg residues in the NLS mutated to Gln, loses its affinity for p53, can no longer promote p53 acetylation, and results in repression of downstream p21 expression.	Glutamine	31-34	H3 histone pseudogene 16	Homo sapiens	209-212	
6311615-2	1983	A tridecapeptide: Arg-Arg-Leu56-Asp-Thr-Thr59-Gly-Gln-Glu-Tyr-Ser-Ala66 containing residues 56-66 of p21 is phosphorylated solely on tyrosine by the epidermal growth factor (EGF)-stimulated tyrosine kinase of A431 cell membranes.	Glutamine	50-53	H3 histone pseudogene 16	Homo sapiens	101-104	
30991803-9	2019	For this reason, in the last set of calculations carried out for p21 N-ras Gln 61 mutants, only the active site structural conformations obtained through hybrid MD are considered.	Glutamine	75-78	H3 histone pseudogene 16	Homo sapiens	65-68	
22385209-1	2012	Mutations of human oncoprotein p21(Ras) (hereafter Ras) at glutamine 61 are known to slow the rate of guanosine triphosphate (GTP) hydrolysis and transform healthy cells into malignant cells.	Glutamine	59-68	H3 histone pseudogene 16	Homo sapiens	31-34	
1282032-1	1992	Point mutations in ras genes resulting in substitutions of amino acid Gly in positions 12 and 13, and Gln in position 61 of the ras gene product p21, are commonly found in human tumors.	Glutamine	102-105	H3 histone pseudogene 16	Homo sapiens	145-148	
9717256-2	1998	CNF1 covalently and specifically modifies the p21 Rho GTP-binding protein in mammalian cells by deamidation of the p21 Rho glutamine 63.	Glutamine	123-132	H3 histone pseudogene 16	Homo sapiens	46-49	
9717256-2	1998	CNF1 covalently and specifically modifies the p21 Rho GTP-binding protein in mammalian cells by deamidation of the p21 Rho glutamine 63.	Glutamine	123-132	H3 histone pseudogene 16	Homo sapiens	115-118	
8060496-1	1994	Oncogenic p21 protein, encoded by the ras-oncogene, that causes malignant transformation of normal cells and many human tumors, is almost identical in sequence to its normal protooncogene-encoded counterpart protein, except for the substitution of arbitrary amino acids for the normally occurring amino acids at critical positions such as Gly 12 and Gln 61.	Glutamine	350-353	H3 histone pseudogene 16	Homo sapiens	10-13	
8496156-9	1993	In the course of these studies, we found, in contrast to previous observations, that both GAP and NF1-GRD can weakly activate the GTPase of Leu-61 mutant p21, showing that Gln-61 is not absolutely required for the stimulation of GTPase activity by GAPs.	Glutamine	172-175	H3 histone pseudogene 16	Homo sapiens	154-157	
1282032-3	1992	Here we report that CD4+ T cells of memory type (CD45RO+) from a patient with a follicular thyroid carcinoma respond against a synthetic peptide derived from aberrant p21 ras having a Gln-->Leu substitution at position 61.	Glutamine	184-187	H3 histone pseudogene 16	Homo sapiens	167-170	
2199064-6	1990	Gln-61 in cellular p21 adopts a conformation where it is able to catalyze GTP hydrolysis.	Glutamine	0-3	H3 histone pseudogene 16	Homo sapiens	19-22	
1637501-3	1992	A complete three-dimensional structure for the ras-gene-encoded p21 protein with Gly 12 and Gln 61, bound to GDP, has been constructed in four stages using the available alpha-carbon coordinates as deposited in the Brookhaven National Laboratories Protein Data Bank.	Glutamine	92-95	H3 histone pseudogene 16	Homo sapiens	64-67	
1569940-2	1992	Mutations of residues in loop L1 (Gly-12 and Gly-13), in loop L2 (Thr-35 and Asp-38), and in loop L4 (Gln-61 and Glu-63) influence the reaction in different ways, but all of these mutant p21 proteins still form complexes with GAP.	Glutamine	102-105	H3 histone pseudogene 16	Homo sapiens	187-190	
2279848-1	1990	The GTP-binding p21 protein, encoded by the ras-oncogene, becomes transforming if amino acid substitutions are made at critical positions in the polypeptide chain, e.g., at Gly 12, Gly 13, Ala 59, Gln 61 and Glu 63.	Glutamine	197-200	H3 histone pseudogene 16	Homo sapiens	16-19	
2115641-3	1990	The Gln 227 site of alpha s corresponds to the Gln 61 site in the low Mw G protein, p21 ras, where the Leu substitution had already been shown to be oncogenic.	Glutamine	4-7	H3 histone pseudogene 16	Homo sapiens	84-87	
2115641-3	1990	The Gln 227 site of alpha s corresponds to the Gln 61 site in the low Mw G protein, p21 ras, where the Leu substitution had already been shown to be oncogenic.	Glutamine	47-50	H3 histone pseudogene 16	Homo sapiens	84-87	
2691018-5	1989	A point mutation at this location corresponds to a substitution of histidine for glutamine in the N-ras gene product, p21.	Glutamine	81-90	H3 histone pseudogene 16	Homo sapiens	118-121