PMID-sentid	Pub_year	Sent_text	compound_name	comp_offset	prot_official_name	organism	prot_offset
8212570-5	1993	Unique features of BICP4 were two large clusters of glutamic acid residues near the end of region 3, and the displacement of a polyserine tract to region 5, which in all other ICP4 homologs residues near the end of region 1.	polyserine	127-137	transcriptional regulator ICP4	Bovine alphaherpesvirus 1	19-24
24216761-7	2014	Using comparative proteomics of wild-type (WT) and KSSR mutant CK2beta, we identified an uncharacterized cellular protein, C18orf25/ARKL1, that also binds CK2beta through the KSSR motif and show that this involves a polyserine sequence resembling the CK2beta binding sequence in EBNA1.	polyserine	216-226	EBNA-1	Human gammaherpesvirus 4	279-284
32240172-4	2020	RAN translation of the CAG sense and CUG anti-sense RNAs produces six distinct repeat peptides: polyalanine (polyAla, from both CAG and CUG repeats), polyserine (polySer), polyleucine (polyLeu), polycysteine (polyCys), and polyglutamine (polyGln).	polyserine	150-160	RAN, member RAS oncogene family	Homo sapiens	0-3
32240172-4	2020	RAN translation of the CAG sense and CUG anti-sense RNAs produces six distinct repeat peptides: polyalanine (polyAla, from both CAG and CUG repeats), polyserine (polySer), polyleucine (polyLeu), polycysteine (polyCys), and polyglutamine (polyGln).	polyserine	162-169	RAN, member RAS oncogene family	Homo sapiens	0-3
31740453-8	2020	The END-1,3 proteins share a region upstream of their zinc finger and an unusual amino-terminal poly-serine domain exhibiting high codon bias.	polyserine	96-107	GATA-type domain-containing protein	Caenorhabditis elegans	4-9
26578877-4	2015	In addition, WAG-HCN1 has a stretch of six amino acids, directly following the deletion, where the wild-type sequence (GNSVCF) is changed to a polyserine motif.	polyserine	143-153	hyperpolarization-activated cyclic nucleotide-gated potassium channel 1	Rattus norvegicus	17-21
35102230-1	2022	Repeat-associated non-AUG (RAN) translation of mRNAs/transcripts responsible for polyglutamine (polyQ) diseases may generate peptides containing different mono amino acid tracts such as polyserine (polyS) and polyleucine (polyL).	polyserine	186-196	RAN, member RAS oncogene family	Mus musculus	27-30
35102230-1	2022	Repeat-associated non-AUG (RAN) translation of mRNAs/transcripts responsible for polyglutamine (polyQ) diseases may generate peptides containing different mono amino acid tracts such as polyserine (polyS) and polyleucine (polyL).	polyserine	198-203	RAN, member RAS oncogene family	Mus musculus	27-30
35102230-3	2022	However, whether the RAN translation-related polyS and polyL have the ability to propagate remains unclear, and if they do, whether the exogenous polyS and polyL exert toxicity on the recipient cells is also not known yet.	polyserine	45-50	RAN, member RAS oncogene family	Mus musculus	21-24
35102230-9	2022	Thus, the RAN translation-related proteins containing polyS and polyL have the potential to propagate and the proteins generated by all polyQ diseases might exert universal toxicity in the recipient cells.	polyserine	54-59	RAN, member RAS oncogene family	Mus musculus	10-13
30387551-0	2018	The Golgi "casein kinase" Fam20C is a genuine "phosvitin kinase" and phosphorylates polyserine stretches devoid of the canonical consensus.	polyserine	84-94	FAM20C golgi associated secretory pathway kinase	Gallus gallus	26-32
30387551-0	2018	The Golgi "casein kinase" Fam20C is a genuine "phosvitin kinase" and phosphorylates polyserine stretches devoid of the canonical consensus.	polyserine	84-94	Casein kinase II subunit beta	Gallus gallus	47-56
28750098-10	2017	We further studied a poly-serine stretch present in the N-terminal region of MSSN and observed that the voltage-activation curves of BKCa channels either containing or lacking this poly-serine stretch were leftward shifted by beta1-subunit in a similar way.	polyserine	21-32	potassium calcium-activated channel subfamily M regulatory beta subunit 1	Homo sapiens	226-231
28750098-10	2017	We further studied a poly-serine stretch present in the N-terminal region of MSSN and observed that the voltage-activation curves of BKCa channels either containing or lacking this poly-serine stretch were leftward shifted by beta1-subunit in a similar way.	polyserine	181-192	potassium calcium-activated channel subfamily M regulatory beta subunit 1	Homo sapiens	226-231
24216761-5	2014	We show that the EBNA1-CK2beta interaction is primed by phosphorylation of EBNA1 on S393 (within a polyserine region).	polyserine	99-109	EBNA-1	Human gammaherpesvirus 4	17-22
24216761-5	2014	We show that the EBNA1-CK2beta interaction is primed by phosphorylation of EBNA1 on S393 (within a polyserine region).	polyserine	99-109	casein kinase 2 beta	Homo sapiens	23-30
24216761-5	2014	We show that the EBNA1-CK2beta interaction is primed by phosphorylation of EBNA1 on S393 (within a polyserine region).	polyserine	99-109	EBNA-1	Human gammaherpesvirus 4	75-80
23688307-6	2013	In correlation with the observed variations in the subnuclear distribution of Jmjd6, the structure of Jmjd6 oligomers in vitro changes in the absence of the polyS domain, possibly reflecting the role of the polyS domain in nuclear/nucleolar shuttling of Jmjd6.	polyserine	207-212	jumonji domain containing 6, arginine demethylase and lysine hydroxylase	Homo sapiens	102-107
24216761-7	2014	Using comparative proteomics of wild-type (WT) and KSSR mutant CK2beta, we identified an uncharacterized cellular protein, C18orf25/ARKL1, that also binds CK2beta through the KSSR motif and show that this involves a polyserine sequence resembling the CK2beta binding sequence in EBNA1.	polyserine	216-226	casein kinase 2 beta	Homo sapiens	63-70
24216761-7	2014	Using comparative proteomics of wild-type (WT) and KSSR mutant CK2beta, we identified an uncharacterized cellular protein, C18orf25/ARKL1, that also binds CK2beta through the KSSR motif and show that this involves a polyserine sequence resembling the CK2beta binding sequence in EBNA1.	polyserine	216-226	chromosome 18 open reading frame 25	Homo sapiens	123-131
24216761-7	2014	Using comparative proteomics of wild-type (WT) and KSSR mutant CK2beta, we identified an uncharacterized cellular protein, C18orf25/ARKL1, that also binds CK2beta through the KSSR motif and show that this involves a polyserine sequence resembling the CK2beta binding sequence in EBNA1.	polyserine	216-226	chromosome 18 open reading frame 25	Homo sapiens	132-137
24216761-7	2014	Using comparative proteomics of wild-type (WT) and KSSR mutant CK2beta, we identified an uncharacterized cellular protein, C18orf25/ARKL1, that also binds CK2beta through the KSSR motif and show that this involves a polyserine sequence resembling the CK2beta binding sequence in EBNA1.	polyserine	216-226	casein kinase 2 beta	Homo sapiens	155-162
24216761-7	2014	Using comparative proteomics of wild-type (WT) and KSSR mutant CK2beta, we identified an uncharacterized cellular protein, C18orf25/ARKL1, that also binds CK2beta through the KSSR motif and show that this involves a polyserine sequence resembling the CK2beta binding sequence in EBNA1.	polyserine	216-226	casein kinase 2 beta	Homo sapiens	155-162
23688307-0	2013	The polyserine domain of the lysyl-5 hydroxylase Jmjd6 mediates subnuclear localization.	polyserine	4-14	jumonji domain containing 6, arginine demethylase and lysine hydroxylase	Homo sapiens	49-54
23688307-3	2013	In the present study we show that an alternatively spliced version of Jmjd6 lacking the polyS (polyserine) domain localizes to the nucleolus, predominantly in the fibrillar centre.	polyserine	88-93	jumonji domain containing 6, arginine demethylase and lysine hydroxylase	Homo sapiens	70-75
23688307-3	2013	In the present study we show that an alternatively spliced version of Jmjd6 lacking the polyS (polyserine) domain localizes to the nucleolus, predominantly in the fibrillar centre.	polyserine	95-105	jumonji domain containing 6, arginine demethylase and lysine hydroxylase	Homo sapiens	70-75
23688307-4	2013	Jmjd6 with the polyS domain deleted also interacts with nucleolar proteins.	polyserine	15-20	jumonji domain containing 6, arginine demethylase and lysine hydroxylase	Homo sapiens	0-5
23688307-6	2013	In correlation with the observed variations in the subnuclear distribution of Jmjd6, the structure of Jmjd6 oligomers in vitro changes in the absence of the polyS domain, possibly reflecting the role of the polyS domain in nuclear/nucleolar shuttling of Jmjd6.	polyserine	207-212	jumonji domain containing 6, arginine demethylase and lysine hydroxylase	Homo sapiens	102-107
21423665-5	2011	A recent advance reveals that RNA transcripts with expanded CAG repeats can be translated in the complete absence of a starting ATG, and this Repeat Associated Non-ATG translation (RAN-translation) occurs across expanded CAG repeats in all reading frames (CAG, AGC, and GCA) to produce homopolymeric proteins of long polyglutamine, polyserine, and polyalanine tracts.	polyserine	332-342	RAN, member RAS oncogene family	Homo sapiens	181-184
22573762-0	2012	A vitellogenin polyserine cleavage site: highly disordered conformation protected from proteolysis by phosphorylation.	polyserine	15-25	vitellogenin	Apis mellifera	2-14
20346000-7	2010	A previously unidentified insertion of three bases in a region coding for a polyserine cluster in exon 1 of the HDAC2 gene was identified in 6/32 adenomas.	polyserine	76-86	histone deacetylase 2	Homo sapiens	112-117
16877497-7	2006	The polyserine tract within the phosphatidylserine receptor protein is used as an excellent example of one such case.	polyserine	4-14	jumonji domain containing 6, arginine demethylase and lysine hydroxylase	Homo sapiens	32-59
19582790-4	2009	Three distinct motifs can be discerned in the SRrp37 protein: (1) a serine-arginine (SR) dipeptide enriched domain, (2) a polyserine stretch, and (3) a potential nucleolar localization signal comprising a long array of basic amino acids.	polyserine	122-132	ADP ribosylation factor like GTPase 6 interacting protein 4	Homo sapiens	46-52
16801344-9	2006	This may be relevant to the pathogenesis of human Huntington"s disease, as we have previously shown that both polyserine and polyalanine-containing proteins are modifiers of mutant huntingtin toxicity, with low expression levels of polyalanine-containing proteins having a protective effect.	polyserine	110-120	huntingtin	Homo sapiens	181-191
11759817-5	2001	No tumor-specific mutation was detected, but polymorphisms were identified in E2F-1 exon 5 and in the polyserine tract of E2F-4.	polyserine	102-112	E2F transcription factor 4	Homo sapiens	122-127
12917402-10	2003	Our results suggest that the polyserine (S) domain is most likely the site of phosphorylation in ERD14 responsible for the activation of calcium binding.	polyserine	29-39	Dehydrin family protein	Arabidopsis thaliana	97-102
14578391-11	2003	Analysis of the Pnn motifs using two-hybrid system assays demonstrated that the polyserine/RS motif within Pnn plays a central but not exclusive role in mediating molecular interactions with identified SR-rich proteins.	polyserine	80-90	pinin, desmosome associated protein	Homo sapiens	16-19
14578391-11	2003	Analysis of the Pnn motifs using two-hybrid system assays demonstrated that the polyserine/RS motif within Pnn plays a central but not exclusive role in mediating molecular interactions with identified SR-rich proteins.	polyserine	80-90	pinin, desmosome associated protein	Homo sapiens	107-110
12213201-5	2002	A 27-bp trinucleotide repeat (CAG)(9) encoding polyserine was found in human BHLHB5, but only one CAG was found at the corresponding position in the mouse Bhlhb5 and hamster BETA3 genes.	polyserine	47-57	basic helix-loop-helix family member e22	Homo sapiens	77-83
10668804-4	2000	SRm300 also contains a novel and highly conserved N-terminal domain, several unique repeated motifs rich in S, R, and proline residues, and two very long polyserine tracts.	polyserine	154-164	serine/arginine repetitive matrix 2	Homo sapiens	0-6