PMID-sentid	Pub_year	Sent_text		comp_official_name	comp_offsetprotein_name	organism	prot_offset
19500310-1	2009	Human leukocyte antigen (HLA)-DRB1*1611 has one nucleotide change at codon 14 (GAG-->AAG) from DRB1*160201, resulting in a coding change from Glu to Lys.	Lysine	152-155	N-methylpurine DNA glycosylase	Homo sapiens	88-91	
18764811-2	2008	The novel allele differs from B*44020101 by a single nucleotide change in exon 3 at nucleotide 453 (C-->G), which changes codon 127 from asparagine (AAC) to lysine (AAG) explaining some aberrant B44 serology results in 2003.	Lysine	160-166	N-methylpurine DNA glycosylase	Homo sapiens	168-171	
17555508-8	2007	RESULTS: Sequence analysis revealed a novel de novo heterozygous mutation at codon 551 (AGG-->AAG), predicting a change of arginine to lysine (R551K) and a known heterozygous polymorphism (A986S) on the same allele, which was inherited from the father.	Lysine	138-144	N-methylpurine DNA glycosylase	Homo sapiens	97-100	
15921168-0	2005	Hb Kurosaki [alpha7(A5)Lys -->Glu (AAG --> GAG)]: an alpha2-globin gene mutation found in Thailand.	Lysine	23-26	N-methylpurine DNA glycosylase	Homo sapiens	35-38	
17545071-4	2007	RESULTS: In CDS of the new cloned sequence, the 658 base A in the AF172993 sequence was replaced by C, and the corresponding genetic code was also converted from AAG to CAG, leading to the alteration of the amino acid Gln to Lys.	Lysine	225-228	N-methylpurine DNA glycosylase	Homo sapiens	162-165	
15921168-1	2005	Hb Kurosaki [alpha 7(A5)Lys --> Glu (AAG --> GAG)], has been found for the first time in Thailand.	Lysine	24-27	N-methylpurine DNA glycosylase	Homo sapiens	37-40	
15921168-4	2005	Direct DNA sequence analysis of selectively amplified segments of the alpha1 and alpha2 genes showed that codon 7 of the alpha2-globin gene was heterozygous for AAG (Lys) and GAG (Glu).	Lysine	166-169	N-methylpurine DNA glycosylase	Homo sapiens	161-164	
12629650-6	2003	A heterozygous SNP, Lys 29 (AAG) --> Met (ATG), was found in the intracellular adhesion molecule-1 (ICAM-1) (receptor for rhinoviruses and some coxsackie A viruses) in one individual in both groups.	Lysine	20-23	N-methylpurine DNA glycosylase	Homo sapiens	28-31	
15558052-3	2004	Moreover, it can only bind both AAA and AAG lysine codons when doubly modified with t(6)A37 and either 5-methylaminomethyluridine or 2-thiouridine at the wobble position (mnm(5)U34 or s(2)U34).	Lysine	44-50	N-methylpurine DNA glycosylase	Homo sapiens	40-43	
15558052-5	2004	These structures allow the rationalization of how modifications in the anticodon loop enable decoding of both lysine codons AAA and AAG.	Lysine	110-116	N-methylpurine DNA glycosylase	Homo sapiens	132-135	
15140540-4	2004	In the present study, we established a convenient and reliable genotyping method for the MGMT codon 178 polymorphism, a Lys (AAG) to Arg (AGG) substitution, using restriction fragment length polymorphism (RFLP), and studied differences in the distribution of this polymorphism in 92 Caucasian lung cancer patients and 85 controls.	Lysine	120-123	N-methylpurine DNA glycosylase	Homo sapiens	125-128	
12603087-2	2003	We here report a mutation new to the Lebanese population: the insertion of a G nucleotide at codons 8/9 [(+G) AAG-TCT (Lys-Ser) --> AAG-G-TCT (beta0)] of the beta-globin gene in a thalassemic patient with a mild phenotype.	Lysine	119-122	N-methylpurine DNA glycosylase	Homo sapiens	110-113	
12653715-5	2003	In the Russian family, we found a G to A transition at the first base of codon 402, resulting in a lysine substitution (GAG to AAG), designated E402K.	Lysine	99-105	N-methylpurine DNA glycosylase	Homo sapiens	127-130	
12653715-6	2003	In the Colombian family, affected patients carried a missense mutation of codon 413, involving a transition from G to A causing a lysine substitution (GAG to AAG), designated E413K.	Lysine	130-136	N-methylpurine DNA glycosylase	Homo sapiens	158-161	
12603087-2	2003	We here report a mutation new to the Lebanese population: the insertion of a G nucleotide at codons 8/9 [(+G) AAG-TCT (Lys-Ser) --> AAG-G-TCT (beta0)] of the beta-globin gene in a thalassemic patient with a mild phenotype.	Lysine	119-122	N-methylpurine DNA glycosylase	Homo sapiens	135-138	
10632938-6	1999	In the other, we observed a novel mutation at nucleotide position 571, which changes codon 169 lysine (AAG) into the amber stop codon (TAG) (K169X).	Lysine	95-101	N-methylpurine DNA glycosylase	Homo sapiens	103-106	
10208646-7	1999	The codon 143 polymorphism appears to be linked to another new polymorphic alteration at codon 178, which converts lysine (AAG) to arginine (AGG).	Lysine	115-121	N-methylpurine DNA glycosylase	Homo sapiens	123-126	
10571960-12	1999	From this mutation followed the change of lysine (codon AAG) at 624 position of the polypeptide chain for glutamine (codon CAG) followed as a consequence.	Lysine	42-48	N-methylpurine DNA glycosylase	Homo sapiens	56-59	
10221692-4	1999	Genetic analysis revealed a single nucleotide substitution on exon 4 in the hormone-binding domain of the androgen receptor (AR) gene, resulting in a change of codon 681 GAG (glutamic acid) to AAG (lysine).	Lysine	198-204	N-methylpurine DNA glycosylase	Homo sapiens	193-196	
9615731-5	1998	Another was located on codon 174 and replaced AGG (Arg) with AAG (Lys).	Lysine	66-69	N-methylpurine DNA glycosylase	Homo sapiens	61-64	
9398839-3	1997	Two mutations, a C-->T substitution that changes the Arg 257 (CGA) to a stop codon (TGA) and an A-->G substitution that changes the Lys 83 (AAG) to a Glu codon (GAG), were found in this novel gene in Swiss and Finnish APECED patients.	Lysine	138-141	N-methylpurine DNA glycosylase	Homo sapiens	146-149	
9401066-6	1997	Amplification of this region by PCR and subsequent DNA sequencing demonstrated a single base substitution altering the normal 380 Lys (AAG) codon to Asn (AAT), producing a new Asn-Lys-Thr glycosylation site.	Lysine	130-133	N-methylpurine DNA glycosylase	Homo sapiens	135-138	
9225234-3	1996	Sequence analysis of PCR-amplified DNA from the proband of apo A-I Nanakuma2 revealed a three-base (AAG or AGA) deletion between bases 186 and 193 from the 5" end of exon 4 that leads to deletion of Lys 106 or 107.	Lysine	199-202	N-methylpurine DNA glycosylase	Homo sapiens	100-103	
10325639-6	1997	144 codon was mutated from CAG to AAG, so Gln was substituted by Lys.	Lysine	65-68	N-methylpurine DNA glycosylase	Homo sapiens	34-37	
8790154-0	1996	Fibrinogen Matsumoto II: gamma 308 Asn-->Lys (AAT-->AAG) mutation associated with bleeding tendency.	Lysine	44-47	N-methylpurine DNA glycosylase	Homo sapiens	58-61	
7635945-4	1995	DNA sequence analysis of the mutant apoE gene revealed a single-point mutation that resulted in the substitution of glutamic acid (GAG) for lysine (AAG) at residue 146 in the proposed receptor-binding domain of apoE.	Lysine	140-146	N-methylpurine DNA glycosylase	Homo sapiens	148-151	
7912945-11	1994	The results showed a point mutation in the PrP gene at codon 200; GAG to AAG (Glu-->Lys).	Lysine	87-90	N-methylpurine DNA glycosylase	Homo sapiens	73-76	
34957905-6	2021	Direct DNA sequencing of the beta-globin gene revealed heterozygosity for a missense mutation at codon 59 (AAG>ATG), causing a lysine to methionine substitution (beta59(E3)Lys Met; HBB: c.179A>T).	Lysine	127-133	N-methylpurine DNA glycosylase	Homo sapiens	107-110	
1356443-2	1992	Sequence analysis of the DNA of the proband that was amplified by PCR and subcloned, revealed a single substitution of one lysine (AAG) for one glutamic acid (GAG) at position 146, thereby adding two negatively charged units to apo E3.	Lysine	123-129	N-methylpurine DNA glycosylase	Homo sapiens	131-134	
1520883-3	1992	In all individuals, we found a single-base substitution in codon 56 of one band 3 allele changing lysine to glutamic acid (AAG----GAG) which, in some of them, was linked with an additional mutation in cdb3.	Lysine	98-104	N-methylpurine DNA glycosylase	Homo sapiens	123-126	
1364220-4	1992	Sequence analysis of the amplified product revealed a GAG > AAG transversion at codon 26, which resulted in an amino acid substitution of lysine for glutamic acid.	Lysine	141-147	N-methylpurine DNA glycosylase	Homo sapiens	63-66	
1685643-3	1991	This mutation at codon 200 changes glutamic acid coded by GAG to lysine coded by AAG.	Lysine	65-71	N-methylpurine DNA glycosylase	Homo sapiens	81-84	
1677358-6	1991	In one out of the five subjects with the apoA-IV-1/0 phenotype we identified two point mutations: 1) replacing the positively charged lysine (AAG), amino acid 167, with a negatively charged glutamic acid (GAG), and 2) converting the neutral residue 360, glutamine (CAG), to a positively charged histidine (CAT).	Lysine	134-140	N-methylpurine DNA glycosylase	Homo sapiens	142-145	
1674745-7	1991	A second G to A substitution at amino acid 13 led to the exchange of lysine (AAG) for glutamic acid (GAG), thereby adding 2 positive charge units to the protein and producing the apoE-5 variant.	Lysine	69-75	N-methylpurine DNA glycosylase	Homo sapiens	77-80	
1973689-8	1990	In the apoA-IV-3 allele we identified a single G to A substitution that converts the glutamic acid (GAG) at position 230 of the mature protein to a lysine (AAG), thus adding 2 positive charge units to the apoA-IV-1 isoprotein (pI 4.97) and forming the more basic apoA-IV-3 isoprotein (pI 5.08).	Lysine	148-154	N-methylpurine DNA glycosylase	Homo sapiens	156-159	
1973167-4	1990	Using molecular techniques, two point mutations were detected in the coding sequence of the FX Vorarlberg gene: a G----A at base pair 160 in exon II resulting in a change of Gla14 (GAA) to Lys (AAA); a G----A at base pair 424 in exon V resulting in a change from Glu102 (GAG) to Lys (AAG).	Lysine	189-192	N-methylpurine DNA glycosylase	Homo sapiens	284-287	
34957905-6	2021	Direct DNA sequencing of the beta-globin gene revealed heterozygosity for a missense mutation at codon 59 (AAG>ATG), causing a lysine to methionine substitution (beta59(E3)Lys Met; HBB: c.179A>T).	Lysine	172-175	N-methylpurine DNA glycosylase	Homo sapiens	107-110	
25897479-2	2015	The mutation results in substitution of a termination codon (TAA) for lysine (AAG) at amino acid position 56.	Lysine	70-76	N-methylpurine DNA glycosylase	Homo sapiens	78-81	
31450984-4	2019	Identification of abnormal hemoglobin (Hb) using direct DNA sequencing showed a genetic defect causing a delta-globin gene missense mutation at codon 43 (GAG>AAG) causing a glutamic acid to lysine substitution corresponding to Hb A2-Melbourne.	Lysine	193-199	N-methylpurine DNA glycosylase	Homo sapiens	161-164	
27250824-9	2016	Molecular analysis of the beta-globin gene showed heterozygosity for an AAG > ACG substitution at codon 144, resulting in a Lys Thr amino acid replacement.	Lysine	127-130	N-methylpurine DNA glycosylase	Homo sapiens	72-75	
26864977-1	2016	Hb Agenogi [beta90(F6)Glu Lys (GAG>AAG) HBB: c.271G>A)] is a very rare beta-globin chain variant.	Lysine	26-29	N-methylpurine DNA glycosylase	Homo sapiens	38-41	
3783686-6	1986	The overall incorporation of lysine into globin from a fully modified tRNALys that decodes AAG is faster by 25 to 30% than from the corresponding hypomodified tRNALys.	Lysine	29-35	N-methylpurine DNA glycosylase	Homo sapiens	91-94	
88735-3	1979	At the position corresponding to amino acid 17, replacement of an adenine by a uracil changes the triplet AAG, which codes for lysine in the normal beta chain, to an amber termination codon, UAG.	Lysine	127-133	N-methylpurine DNA glycosylase	Homo sapiens	106-109	
836035-0	1977	Lysine transfer RNA from liver: a sulfur-containing species that codes for AAG.	Lysine	0-6	N-methylpurine DNA glycosylase	Homo sapiens	75-78	
28395541-5	2017	The C to G exchange (AAC>AAG) at codon 108 of the beta-globin gene results in the substitution of asparagine by lysine.	Lysine	115-121	N-methylpurine DNA glycosylase	Homo sapiens	28-31	
26719496-5	2016	The guanine-to-adenine change causes substitution of the normal glutamic acid codon (GAG) with a mutant lysine codon (AAG) at position 312 (E312 K mutation).	Lysine	104-110	N-methylpurine DNA glycosylase	Homo sapiens	118-121	
21985917-11	2012	Although the lysine encoded by AAG was identical to the lysine encoded by AAA, it is not clear if they have functional differences due to the changing environmental conditions.	Lysine	13-19	N-methylpurine DNA glycosylase	Homo sapiens	31-34	
21985917-11	2012	Although the lysine encoded by AAG was identical to the lysine encoded by AAA, it is not clear if they have functional differences due to the changing environmental conditions.	Lysine	56-62	N-methylpurine DNA glycosylase	Homo sapiens	31-34	
22227389-1	2012	Human tRNA(Lys3)(UUU) (htRNA(Lys3)(UUU)) decodes the lysine codons AAA and AAG during translation and also plays a crucial role as the primer for HIV-1 (human immunodeficiency virus type 1) reverse transcription.	Lysine	53-59	N-methylpurine DNA glycosylase	Homo sapiens	75-78	
26889411-4	2012	DNA sequence analysis of the PROS1 gene identified a novel heterozygous nonsense mutation in exon 10 by transition of AAG (lysine) to TAG (stop codon) at codon 473 (c.1417A>T, p.K473X).	Lysine	123-129	N-methylpurine DNA glycosylase	Homo sapiens	118-121