PMID-sentid	Pub_year	Sent_text	compound_name	comp_offset	prot_official_name	organism	prot_offset
31455781-7	2019	However, an appropriate length MTS (MethaneThioSulfonate) cross-linking reagent (MTS14) restricted the activation of TREK-1_A286C channels by repeated application of FFA.	methanethiosulfonate	36-56	potassium two pore domain channel subfamily K member 2	Homo sapiens	117-123
23731861-4	2013	Internal dynamics of spin labels and their static conformational distributions have been studied mainly by electron paramagnetic resonance spectroscopy and molecular dynamics simulations, with a large body of results for the most widely applied methanethiosulfonate spin label MTSL.	methanethiosulfonate	245-265	spindlin 1	Homo sapiens	21-25
30248959-7	2018	The methane thiosulfonate (MTS) assay revealed that cell proliferation was significantly reduced after transient transfection of miR-331-3p precursor and/or NACC1 siRNA in UC cells.	methanethiosulfonate	4-25	microRNA 331	Homo sapiens	129-136
30248959-7	2018	The methane thiosulfonate (MTS) assay revealed that cell proliferation was significantly reduced after transient transfection of miR-331-3p precursor and/or NACC1 siRNA in UC cells.	methanethiosulfonate	4-25	nucleus accumbens associated 1	Homo sapiens	157-162
30248959-7	2018	The methane thiosulfonate (MTS) assay revealed that cell proliferation was significantly reduced after transient transfection of miR-331-3p precursor and/or NACC1 siRNA in UC cells.	methanethiosulfonate	27-30	microRNA 331	Homo sapiens	129-136
30248959-7	2018	The methane thiosulfonate (MTS) assay revealed that cell proliferation was significantly reduced after transient transfection of miR-331-3p precursor and/or NACC1 siRNA in UC cells.	methanethiosulfonate	27-30	nucleus accumbens associated 1	Homo sapiens	157-162
28097912-0	2017	Methanethiosulfonate derivatives as ligands of the STAT3-SH2 domain.	methanethiosulfonate	0-20	signal transducer and activator of transcription 3	Homo sapiens	51-56
28097912-1	2017	With the aim to discover new STAT3 direct inhibitors, potentially useful as anticancer agents, a set of methanethiosulfonate drug hybrids were synthesized.	methanethiosulfonate	104-124	signal transducer and activator of transcription 3	Homo sapiens	29-34
28097912-4	2017	These results suggest that methanethiosulfonate moiety can be considered a useful scaffold in the preparation of new direct STAT3 inhibitors.	methanethiosulfonate	27-47	signal transducer and activator of transcription 3	Homo sapiens	124-129
28235784-5	2017	Here, we studied the accessibility of single cysteines substituted along the pre-TM2 and TM2 helix (residues 327-357) of the P2X7R using as readouts (i) the covalent maleimide fluorescence accessibility of the surface-bound P2X7R and (ii) covalent modulation of macroscopic and single-channel currents using extracellularly and intracellularly applied methanethiosulfonate (MTS) reagents.	methanethiosulfonate	352-372	purinergic receptor P2X 7	Homo sapiens	125-130
27214582-5	2016	Here we report a new methanethiosulfonate derivative of a TAM radical that reacts rapidly and selectively with an engineered cysteine residue to generate a TAM containing side chain (TAM1) in high yield.	methanethiosulfonate	21-41	stromal interaction molecule 1	Homo sapiens	183-187
26356049-2	2016	PREs are commonly generated using paramagnetic spin labels (SLs) that contain an unpaired electron in the form of a nitroxide radical, with 1-oxyl-2,2,5,5-tetramethyl-2,5-dihydropyrrol-3-ylmethyl methane thiosulfonate (MTSL) being the most popular tag.	methanethiosulfonate	219-223	spindlin 1	Homo sapiens	47-51
26324677-2	2015	Using the Xenopus laevis oocyte expression system and two-electrode voltage clamp, we performed cysteine-scanning mutagenesis of several pore-lining residues of connexin 26 (Cx26) hemichannels, followed by chemical modification using a methanethiosulfonate (MTS) reagent, to help identify the position of the gate.	methanethiosulfonate	236-256	gap junction protein beta 2 L homeolog	Xenopus laevis	161-172
26324677-2	2015	Using the Xenopus laevis oocyte expression system and two-electrode voltage clamp, we performed cysteine-scanning mutagenesis of several pore-lining residues of connexin 26 (Cx26) hemichannels, followed by chemical modification using a methanethiosulfonate (MTS) reagent, to help identify the position of the gate.	methanethiosulfonate	236-256	gap junction protein beta 2 L homeolog	Xenopus laevis	174-178
26324677-2	2015	Using the Xenopus laevis oocyte expression system and two-electrode voltage clamp, we performed cysteine-scanning mutagenesis of several pore-lining residues of connexin 26 (Cx26) hemichannels, followed by chemical modification using a methanethiosulfonate (MTS) reagent, to help identify the position of the gate.	methanethiosulfonate	258-261	gap junction protein beta 2 L homeolog	Xenopus laevis	161-172
26324677-2	2015	Using the Xenopus laevis oocyte expression system and two-electrode voltage clamp, we performed cysteine-scanning mutagenesis of several pore-lining residues of connexin 26 (Cx26) hemichannels, followed by chemical modification using a methanethiosulfonate (MTS) reagent, to help identify the position of the gate.	methanethiosulfonate	258-261	gap junction protein beta 2 L homeolog	Xenopus laevis	174-178
25635140-3	2015	GluN1(F639C)/GluN2A receptors were less inhibited by ethanol than wild-type receptors, and inhibition was restored to wild-type levels following treatment with ethanol-like methanethiosulfonate reagents.	methanethiosulfonate	173-193	glutamate ionotropic receptor NMDA type subunit 1	Homo sapiens	0-5
25635140-3	2015	GluN1(F639C)/GluN2A receptors were less inhibited by ethanol than wild-type receptors, and inhibition was restored to wild-type levels following treatment with ethanol-like methanethiosulfonate reagents.	methanethiosulfonate	173-193	glutamate ionotropic receptor NMDA type subunit 2A	Homo sapiens	13-19
24302985-3	2013	As S4 of the human skeletal muscle voltage-gated sodium channel, hNav1.4, moves in response to depolarization from the resting to the inactivated state, two D4S4 reporters (R2C and R3C, Arg1451Cys and Arg1454Cys, respectively) move from internal to external positions as deduced by reactivity to internally or externally applied sulfhydryl group reagents, methane thiosulfonates (MTS).	methanethiosulfonate	356-378	sodium voltage-gated channel alpha subunit 4	Homo sapiens	65-72
24302985-5	2013	Scorpion alpha-toxin binding impedes D4S4 segment movement during inactivation since the modification rates of R3C in hNav1.4 with methanethiosulfonate (CH3SO2SCH2CH2R, where R = -N(CH3)3 (+) trimethylammonium, MTSET) and benzophenone-4-carboxamidocysteine methanethiosulfonate (BPMTS) were slowed ~10-fold in toxin-modified channels.	methanethiosulfonate	131-151	sodium voltage-gated channel alpha subunit 4	Homo sapiens	118-125
23731861-4	2013	Internal dynamics of spin labels and their static conformational distributions have been studied mainly by electron paramagnetic resonance spectroscopy and molecular dynamics simulations, with a large body of results for the most widely applied methanethiosulfonate spin label MTSL.	methanethiosulfonate	245-265	spindlin 1	Homo sapiens	266-270
23552283-5	2013	Modification of five of these substituted Cys residues (positions 147, 152, 157, 158, and 161) by methanethiosulfonate (MTS) reagents led to reduction of PCFT function.	methanethiosulfonate	98-118	solute carrier family 46 member 1	Homo sapiens	154-158
21746847-4	2011	We find that methanethiosulfonate (MTS) reagents irreversibly modify cysteines substituted for TM1 residues K95, Q98, P99, and L102 when applied to the cytoplasmic side of open channels.	methanethiosulfonate	13-33	protein phosphatase 1 regulatory subunit 10	Homo sapiens	118-121
23442957-5	2013	Here, we investigated CFTR"s TM1 by applying methanethiosulfonate (MTS) reagents from both cytoplasmic and extracellular sides of the membrane.	methanethiosulfonate	45-65	CF transmembrane conductance regulator	Homo sapiens	22-26
23442957-5	2013	Here, we investigated CFTR"s TM1 by applying methanethiosulfonate (MTS) reagents from both cytoplasmic and extracellular sides of the membrane.	methanethiosulfonate	67-70	CF transmembrane conductance regulator	Homo sapiens	22-26
21746847-4	2011	We find that methanethiosulfonate (MTS) reagents irreversibly modify cysteines substituted for TM1 residues K95, Q98, P99, and L102 when applied to the cytoplasmic side of open channels.	methanethiosulfonate	35-38	protein phosphatase 1 regulatory subunit 10	Homo sapiens	118-121
21306584-0	2011	Effect of verapamil on the action of methanethiosulfonate reagents on human voltage-gated K(v)1.3 channels: implications for the C-type inactivated state.	methanethiosulfonate	37-57	potassium voltage-gated channel subfamily A member 3	Homo sapiens	90-97
20109441-4	2010	We also reported Cys-targeting methanethiosulfonate molecules (AMTSn), which, under conditions that spared human AChE, caused total irreversible inhibition of aphid AChE, 95% inhibition of AChE from the malaria vector mosquito (Anopheles gambia), and >80% inhibition of activity from the yellow fever mosquito (Aedes aegypti) and northern house mosquito (Culex pipiens).	methanethiosulfonate	31-51	acetylcholinesterase (Cartwright blood group)	Homo sapiens	113-117
21525301-4	2011	We use a thiol-reactive methane thiosulfonate (MTS) reagent to modify a conformationally sensitive cysteine residue to demonstrate that hSERT spends more time in an outward facing conformation when transporting DA than when transporting 5-HT.	methanethiosulfonate	24-45	solute carrier family 6 member 4	Homo sapiens	136-141
21525301-4	2011	We use a thiol-reactive methane thiosulfonate (MTS) reagent to modify a conformationally sensitive cysteine residue to demonstrate that hSERT spends more time in an outward facing conformation when transporting DA than when transporting 5-HT.	methanethiosulfonate	47-50	solute carrier family 6 member 4	Homo sapiens	136-141
21209359-3	2011	Epitope-tagged AE1 R730C at the Xenopus laevis oocyte surface exhibited severely reduced Cl(-) transport insensitive to rescue by glycophorin A (GPA) coexpression or by methanethiosulfonate (MTS) treatment.	methanethiosulfonate	169-189	solute carrier family 4 member 1 (Diego blood group)S homeolog	Xenopus laevis	15-18
21209359-3	2011	Epitope-tagged AE1 R730C at the Xenopus laevis oocyte surface exhibited severely reduced Cl(-) transport insensitive to rescue by glycophorin A (GPA) coexpression or by methanethiosulfonate (MTS) treatment.	methanethiosulfonate	191-194	solute carrier family 4 member 1 (Diego blood group)S homeolog	Xenopus laevis	15-18
20664003-4	2010	To test this hypothesis we have begun to obtain structural information about family B GPCRs, using as a prototype the CRF(1), by determining the ability of sulfhydryl-specific methanethiosulfonate derivatives, such as the methanethiosulfonate-ethylammonium (MTSEA), to react with CRF(1) and thus irreversibly inhibit (125)I-Tyr(0)-sauvagine binding.	methanethiosulfonate	176-196	corticotropin releasing hormone receptor 1	Homo sapiens	118-124
20664003-4	2010	To test this hypothesis we have begun to obtain structural information about family B GPCRs, using as a prototype the CRF(1), by determining the ability of sulfhydryl-specific methanethiosulfonate derivatives, such as the methanethiosulfonate-ethylammonium (MTSEA), to react with CRF(1) and thus irreversibly inhibit (125)I-Tyr(0)-sauvagine binding.	methanethiosulfonate	176-196	corticotropin releasing hormone receptor 1	Homo sapiens	280-286
20109441-4	2010	We also reported Cys-targeting methanethiosulfonate molecules (AMTSn), which, under conditions that spared human AChE, caused total irreversible inhibition of aphid AChE, 95% inhibition of AChE from the malaria vector mosquito (Anopheles gambia), and >80% inhibition of activity from the yellow fever mosquito (Aedes aegypti) and northern house mosquito (Culex pipiens).	methanethiosulfonate	31-51	acetylcholinesterase (Cartwright blood group)	Homo sapiens	165-169
20109441-4	2010	We also reported Cys-targeting methanethiosulfonate molecules (AMTSn), which, under conditions that spared human AChE, caused total irreversible inhibition of aphid AChE, 95% inhibition of AChE from the malaria vector mosquito (Anopheles gambia), and >80% inhibition of activity from the yellow fever mosquito (Aedes aegypti) and northern house mosquito (Culex pipiens).	methanethiosulfonate	31-51	acetylcholinesterase (Cartwright blood group)	Homo sapiens	165-169
19714254-8	2009	Herein, we report that, under conditions that spare the human AChE, a methanethiosulfonate-containing molecule at 6 microM irreversibly inhibited 95% of the AChE activity extracted from An.	methanethiosulfonate	70-90	acetylcholinesterase (Cartwright blood group)	Homo sapiens	62-66
19714254-8	2009	Herein, we report that, under conditions that spare the human AChE, a methanethiosulfonate-containing molecule at 6 microM irreversibly inhibited 95% of the AChE activity extracted from An.	methanethiosulfonate	70-90	acetylcholinesterase (Cartwright blood group)	Homo sapiens	157-161
19714254-11	2009	This type of inhibition is fast ( approximately 30 min) and due to conjugation of the inhibitor to the active-site Cys of mosquito AP-AChE, according to our observed reactivation of the methanethiosulfonate-inhibited AChE by 2-mercaptoethanol.	methanethiosulfonate	186-206	acetylcholinesterase (Cartwright blood group)	Homo sapiens	134-138
19714254-11	2009	This type of inhibition is fast ( approximately 30 min) and due to conjugation of the inhibitor to the active-site Cys of mosquito AP-AChE, according to our observed reactivation of the methanethiosulfonate-inhibited AChE by 2-mercaptoethanol.	methanethiosulfonate	186-206	acetylcholinesterase (Cartwright blood group)	Homo sapiens	217-221
19456123-7	2009	Treatment of CP12 with a methane thiosulfonate derivative spin-label (MTSL) led to the labeling of the cysteine residues involved in the C-terminal bridge only as revealed by mass spectrometry.	methanethiosulfonate	25-46	uncharacterized protein	Chlamydomonas reinhardtii	13-17
18272676-6	2008	Moreover, M3c residues at or below A651(NR2B, A7 in SYTANLAAF) react with external methanethiosulfonate (MTS) reagents approximately 500 to 1000-fold faster in the presence than in the absence of agonists NMDA and glycine.	methanethiosulfonate	83-103	glutamate ionotropic receptor NMDA type subunit 2B	Homo sapiens	40-44
19538299-3	2009	Using stable transfected Madin Darby canine kidney type I cells, induced to express claudin-2, we show that paracellular cation transport can be blocked by sulfhydryl-specific methanethiosulfonate (MTS) and that SCAM can be used to identify residues that line paracellular pores.	methanethiosulfonate	198-201	claudin 2	Canis lupus familiaris	84-93
18628241-6	2008	Cysteine mutants at those positions confirmed the accessibility of hSERT/F556 to different methanethiosulfonate (MTS) reagents, suggesting its presence in a hydrophilic environment of the protein.	methanethiosulfonate	91-111	solute carrier family 6 member 4	Homo sapiens	67-72
18311924-1	2008	We report the involvement of transmembrane domain 4 (TM4) of hASBT in forming the putative translocation pathway, using cysteine-scanning mutagenesis in conjunction with solvent-accessibility studies using the membrane-impermeant, sulfhydryl-specific methanethiosulfonate reagents.	methanethiosulfonate	251-271	solute carrier family 10 member 2	Homo sapiens	61-66
19381710-3	2009	We have combined SCAM with investigation of the charge-dependent effects of methanethiosulfonate (MTS) reagents on the functional permeation properties of cystic fibrosis transmembrane conductance regulator (CFTR) Cl(-) channels.	methanethiosulfonate	76-96	CF transmembrane conductance regulator	Homo sapiens	155-206
19381710-3	2009	We have combined SCAM with investigation of the charge-dependent effects of methanethiosulfonate (MTS) reagents on the functional permeation properties of cystic fibrosis transmembrane conductance regulator (CFTR) Cl(-) channels.	methanethiosulfonate	76-96	CF transmembrane conductance regulator	Homo sapiens	208-212
19381710-3	2009	We have combined SCAM with investigation of the charge-dependent effects of methanethiosulfonate (MTS) reagents on the functional permeation properties of cystic fibrosis transmembrane conductance regulator (CFTR) Cl(-) channels.	methanethiosulfonate	98-101	CF transmembrane conductance regulator	Homo sapiens	155-206
19381710-3	2009	We have combined SCAM with investigation of the charge-dependent effects of methanethiosulfonate (MTS) reagents on the functional permeation properties of cystic fibrosis transmembrane conductance regulator (CFTR) Cl(-) channels.	methanethiosulfonate	98-101	CF transmembrane conductance regulator	Homo sapiens	208-212
19194505-6	2009	Herein we report the development of a methanethiosulfonate-containing small molecule that, at 6.0 microM, irreversibly inhibits 99% of all AChE activity extracted from the greenbug aphid (Schizaphis graminum) without any measurable inhibition of the human AChE.	methanethiosulfonate	38-58	acetylcholinesterase (Cartwright blood group)	Homo sapiens	139-143
19194505-6	2009	Herein we report the development of a methanethiosulfonate-containing small molecule that, at 6.0 microM, irreversibly inhibits 99% of all AChE activity extracted from the greenbug aphid (Schizaphis graminum) without any measurable inhibition of the human AChE.	methanethiosulfonate	38-58	acetylcholinesterase (Cartwright blood group)	Homo sapiens	256-260
18487206-0	2008	Cysteine substitution mutagenesis and the effects of methanethiosulfonate reagents at P2X2 and P2X4 receptors support a core common mode of ATP action at P2X receptors.	methanethiosulfonate	53-73	purinergic receptor P2X 2	Homo sapiens	86-90
18272676-6	2008	Moreover, M3c residues at or below A651(NR2B, A7 in SYTANLAAF) react with external methanethiosulfonate (MTS) reagents approximately 500 to 1000-fold faster in the presence than in the absence of agonists NMDA and glycine.	methanethiosulfonate	105-108	glutamate ionotropic receptor NMDA type subunit 2B	Homo sapiens	40-44
14522974-0	2003	Methanethiosulfonate derivatives of rhodamine and verapamil activate human P-glycoprotein at different sites.	methanethiosulfonate	0-20	ATP binding cassette subfamily B member 1	Homo sapiens	75-89
17428985-3	2007	We used cysteine-scanning mutagenesis, radiolabeled 2-azido ATP binding, and methanethiosulfonate (MTS) compounds to identify amino acid residues involved in ATP binding and gating of the human P2X1 receptor.	methanethiosulfonate	77-97	purinergic receptor P2X 1	Homo sapiens	194-207
17428985-3	2007	We used cysteine-scanning mutagenesis, radiolabeled 2-azido ATP binding, and methanethiosulfonate (MTS) compounds to identify amino acid residues involved in ATP binding and gating of the human P2X1 receptor.	methanethiosulfonate	99-102	purinergic receptor P2X 1	Homo sapiens	194-207
16092934-4	2005	hNET and the mutants were also resistant to methanethiosulfonate (MTS), ethylammonium (MTSEA) and MTStrimethylammonium (MTSET).	methanethiosulfonate	44-64	solute carrier family 6 member 2	Homo sapiens	0-4
16092934-4	2005	hNET and the mutants were also resistant to methanethiosulfonate (MTS), ethylammonium (MTSEA) and MTStrimethylammonium (MTSET).	methanethiosulfonate	66-69	solute carrier family 6 member 2	Homo sapiens	0-4
16891366-2	2006	Cytoplasmic-side methanethiosulfonate (MTS) reagents blocked K(+) permeation in native Kir1.1 channels, expressed in Xenopus oocytes.	methanethiosulfonate	17-37	potassium inwardly rectifying channel subfamily J member 1 S homeolog	Xenopus laevis	87-93
16891366-2	2006	Cytoplasmic-side methanethiosulfonate (MTS) reagents blocked K(+) permeation in native Kir1.1 channels, expressed in Xenopus oocytes.	methanethiosulfonate	39-42	potassium inwardly rectifying channel subfamily J member 1 S homeolog	Xenopus laevis	87-93
16631150-4	2006	It is shown that the spectral peaks assigned to the methyl head groups of phosphatidylcholine and sphingomyelin in the (1)H spectra of LDL exhibit line broadening when otherwise free thiol groups of apoB are covalently modified by methanethiosulfonate spin label.	methanethiosulfonate	231-251	apolipoprotein B	Homo sapiens	199-203
16584200-1	2006	Using cysteine mutagenesis and chemical modification by methanethiosulfonate derivatives, it was demonstrated that the external putative loop, joining transmembrane segments (TM"s) IV-V of rabbit Na+/glucose cotransporter, rSGLT1, forms part of a Na+ binding and voltage sensing domain.	methanethiosulfonate	56-76	solute carrier family 5 member 1	Rattus norvegicus	223-229
15840841-1	2005	In this study, the sensitivity of the CB2 receptor to methanethiosulfonate (MTS) derivatives was tested, and a native cysteine residue conferring the sensitivity was identified.	methanethiosulfonate	54-74	cannabinoid receptor 2	Homo sapiens	38-41
15840841-1	2005	In this study, the sensitivity of the CB2 receptor to methanethiosulfonate (MTS) derivatives was tested, and a native cysteine residue conferring the sensitivity was identified.	methanethiosulfonate	76-79	cannabinoid receptor 2	Homo sapiens	38-41
14609334-3	2003	To apply this approach to the C2 domain of cytosolic phospholipase A(2) (cPLA(2)), single cysteines were introduced at all 27 positions in the three Ca(2+)-binding loops and labeled with a methanethiosulfonate spin-label.	methanethiosulfonate	189-209	phospholipase A2 group IVA	Homo sapiens	43-80
12963712-0	2003	Methanethiosulfonate ethylammonium block of amine currents through the ryanodine receptor reveals single pore architecture.	methanethiosulfonate	0-20	ryanodine receptor 1	Homo sapiens	71-89
11004203-4	2000	The double-barrel model proposed for ClC-0 was recently challenged by a one-pore model partly based on experiments with ClC-1 exploiting cysteine mutagenesis followed by modification with methanethiosulfonate (MTS) reagents.	methanethiosulfonate	210-213	chloride voltage-gated channel 1	Homo sapiens	120-125
12879165-0	2003	Methanethiosulfonate-modification alters local anesthetic block in rNav1.4 cysteine-substituted mutants S1276C and L1280C.	methanethiosulfonate	0-20	neuron navigator 1	Rattus norvegicus	67-72
11395483-1	2001	The binding affinity of the cocaine analog [(3)H]2 beta-carbomethoxy-3beta-(4-fluorophenyl) tropane (WIN) for the dopamine transporter (DAT) is increased by the reaction of Cys-90, at the extracellular end of the first transmembrane segment, with methanethiosulfonate (MTS) reagents.	methanethiosulfonate	247-267	solute carrier family 6 member 3	Homo sapiens	114-134
11395483-1	2001	The binding affinity of the cocaine analog [(3)H]2 beta-carbomethoxy-3beta-(4-fluorophenyl) tropane (WIN) for the dopamine transporter (DAT) is increased by the reaction of Cys-90, at the extracellular end of the first transmembrane segment, with methanethiosulfonate (MTS) reagents.	methanethiosulfonate	247-267	solute carrier family 6 member 3	Homo sapiens	136-139
11279063-0	2001	Defining the drug-binding site in the human multidrug resistance P-glycoprotein using a methanethiosulfonate analog of verapamil, MTS-verapamil.	methanethiosulfonate	88-108	ATP binding cassette subfamily B member 1	Homo sapiens	65-79
12885876-0	2003	Probing the pore of ClC-0 by substituted cysteine accessibility method using methane thiosulfonate reagents.	methanethiosulfonate	77-98	Charcot-Leyden crystal galectin	Homo sapiens	20-23
11986364-5	2002	To investigate this mechanism, we used the membrane-impermeable methanethiosulfonates, MTSET and MTS-TEAH, to modify Kir6.2 channels.	methanethiosulfonate	64-85	potassium inwardly rectifying channel subfamily J member 11	Homo sapiens	117-123
11790775-1	2002	Intracellular application of certain charged methanethiosulfonate (MTS) reagents modified and irreversibly inhibited Kir6.2 channels when cysteine substitutions were introduced at positions Ile-210, Ile-211, or Ser-212 within the putative cytoplasmic region.	methanethiosulfonate	45-65	potassium inwardly rectifying channel subfamily J member 11	Homo sapiens	117-123
11054653-2	2000	A methanethiosulfonate spin label was used to probe the free cysteine residues of apoB with electron paramagnetic resonance (EPR) spectroscopy.	methanethiosulfonate	2-22	apolipoprotein B	Homo sapiens	82-86
9062118-8	1997	The cysteine-specific spin-label, methanethiosulfonate spin-label (MTSSL), was attached to yeast iso-1-cytochrome c at the single naturally occurring cysteine102, and the emphasis for this work was on this disulfide-attached spin-labeled prototype.	methanethiosulfonate	34-54	threonine ammonia-lyase ILV1	Saccharomyces cerevisiae S288C	97-102
10423365-2	1999	The peptide, which follows the single letter sequence, was reacted with the methanethiosulfonate spin label at the cysteine sulfur.	methanethiosulfonate	76-96	spindlin 1	Homo sapiens	97-101
10824857-1	1999	A cysteine-specific methanethiosulfonate spin label was introduced into yeast iso-1-cytochrome c at three different positions.	methanethiosulfonate	20-40	threonine ammonia-lyase ILV1	Saccharomyces cerevisiae S288C	78-83
9689064-2	1998	Binding of the cocaine analog, [3H]2-beta-carbomethoxy-3-beta-(4-fluorophenyl) tropane (CFT) to the dopamine transporter is sensitive to polar sulfhydryl-specific derivatives of methanethiosulfonate (MTS).	methanethiosulfonate	178-198	solute carrier family 6 member 3	Homo sapiens	100-120
9689064-2	1998	Binding of the cocaine analog, [3H]2-beta-carbomethoxy-3-beta-(4-fluorophenyl) tropane (CFT) to the dopamine transporter is sensitive to polar sulfhydryl-specific derivatives of methanethiosulfonate (MTS).	methanethiosulfonate	200-203	solute carrier family 6 member 3	Homo sapiens	100-120
9041453-0	1997	Methanethiosulfonate derivatives inhibit current through the ryanodine receptor/channel.	methanethiosulfonate	0-20	ryanodine receptor 1	Homo sapiens	61-79
1667623-0	1991	Improved method for measurement of rhodanese activity using methanethiosulfonate as sulfur donor substrate and its application to human serum.	methanethiosulfonate	60-80	thiosulfate sulfurtransferase	Bos taurus	35-44
1667623-1	1991	We have developed a sensitive method for the measurement of rhodanese activity in human serum which is based on the colorimetric method for the determination of thiocyanate produced from methanethiosulfonate and cyanide as substrates.	methanethiosulfonate	187-207	thiosulfate sulfurtransferase	Bos taurus	60-69
34776648-2	2021	Methanethiosulfonate spin label (MTSSL), has become ubiquitous in the SDSL of proteins, however, has limitations owing to its high number of rotamers, and reducibility.	methanethiosulfonate	0-20	spindlin 1	Homo sapiens	21-25
32472188-4	2021	We found that alpha5-containing nAChRs are irreversibly blocked by methanethiosulfonate (MTS) reagents through a covalent reaction with a cysteine present only in alpha5.	methanethiosulfonate	67-87	immunoglobulin kappa variable 2D-26	Homo sapiens	14-20
32472188-4	2021	We found that alpha5-containing nAChRs are irreversibly blocked by methanethiosulfonate (MTS) reagents through a covalent reaction with a cysteine present only in alpha5.	methanethiosulfonate	67-87	immunoglobulin kappa variable 2D-26	Homo sapiens	163-169
32472188-4	2021	We found that alpha5-containing nAChRs are irreversibly blocked by methanethiosulfonate (MTS) reagents through a covalent reaction with a cysteine present only in alpha5.	methanethiosulfonate	89-92	immunoglobulin kappa variable 2D-26	Homo sapiens	14-20
32472188-4	2021	We found that alpha5-containing nAChRs are irreversibly blocked by methanethiosulfonate (MTS) reagents through a covalent reaction with a cysteine present only in alpha5.	methanethiosulfonate	89-92	immunoglobulin kappa variable 2D-26	Homo sapiens	163-169