General Information of Target

Target ID LDTP02279
Target Name Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial (PDHA1)
Gene Name PDHA1
Gene ID 5160
Synonyms
PHE1A; Pyruvate dehydrogenase E1 component subunit alpha, somatic form, mitochondrial; EC 1.2.4.1; PDHE1-A type I
3D Structure
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2D Sequence (FASTA)
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3D Structure (PDB)
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Sequence
MRKMLAAVSRVLSGASQKPASRVLVASRNFANDATFEIKKCDLHRLEEGPPVTTVLTRED
GLKYYRMMQTVRRMELKADQLYKQKIIRGFCHLCDGQEACCVGLEAGINPTDHLITAYRA
HGFTFTRGLSVREILAELTGRKGGCAKGKGGSMHMYAKNFYGGNGIVGAQVPLGAGIALA
CKYNGKDEVCLTLYGDGAANQGQIFEAYNMAALWKLPCIFICENNRYGMGTSVERAAAST
DYYKRGDFIPGLRVDGMDILCVREATRFAAAYCRSGKGPILMELQTYRYHGHSMSDPGVS
YRTREEIQEVRSKSDPIMLLKDRMVNSNLASVEELKEIDVEVRKEIEDAAQFATADPEPP
LEELGYHIYSSDPPFEVRGANQWIKFKSVS
Target Bioclass
Enzyme
Subcellular location
Mitochondrion matrix
Function The pyruvate dehydrogenase complex catalyzes the overall conversion of pyruvate to acetyl-CoA and CO(2), and thereby links the glycolytic pathway to the tricarboxylic cycle.
Uniprot ID
P08559
Ensemble ID
ENST00000355808.10
HGNC ID
HGNC:8806

Target Site Mutations in Different Cell Lines

Cell line Mutation details Probe for labeling this protein in this cell
NB1 SNV: p.A236V DBIA    Probe Info 
YSCCC SNV: p.R22K DBIA    Probe Info 

Probe(s) Labeling This Target

ABPP Probe
Click To Hide/Show 38 Probe Related to This Target
Probe name Structure Binding Site(Ratio) Interaction ID Ref
m-APA
 Probe Info 
10.18  LDD0402  [1]
N1
 Probe Info 
100.00  LDD0242  [2]
TH211
 Probe Info 
Y118(20.00); Y227(20.00); Y301(20.00); Y156(13.01)  LDD0257  [3]
TH214
 Probe Info 
Y243(7.62)  LDD0258  [3]
TH216
 Probe Info 
Y227(20.00)  LDD0259  [3]
YN-1
 Probe Info 
100.00  LDD0444  [4]
STPyne
 Probe Info 
K18(7.14); K313(8.93); K321(9.71); K385(10.00)  LDD0277  [5]
ONAyne
 Probe Info 
N.A.  LDD0273  [5]
Probe 1
 Probe Info 
Y82(29.77); Y156(8.93); Y227(58.05); Y272(14.51)  LDD3495  [6]
BTD
 Probe Info 
C273(1.80); C41(1.57)  LDD1700  [7]
AHL-Pu-1
 Probe Info 
C273(6.24)  LDD0170  [8]
EA-probe
 Probe Info 
C181(0.88)  LDD2210  [9]
DBIA
 Probe Info 
C261(4.31)  LDD0209  [10]
HHS-482
 Probe Info 
Y156(0.59); Y227(0.71)  LDD0285  [11]
5E-2FA
 Probe Info 
N.A.  LDD2235  [12]
ATP probe
 Probe Info 
K149(0.00); K385(0.00); K83(0.00); K85(0.00)  LDD0199  [13]
4-Iodoacetamidophenylacetylene
 Probe Info 
C273(0.00); C181(0.00); C261(0.00); C218(0.00)  LDD0038  [14]
IA-alkyne
 Probe Info 
C261(0.00); C273(0.00); C218(0.00)  LDD0032  [15]
Lodoacetamide azide
 Probe Info 
C273(0.00); C181(0.00); C261(0.00); C218(0.00)  LDD0037  [14]
ATP probe
 Probe Info 
N.A.  LDD0035  [16]
IPM
 Probe Info 
N.A.  LDD0025  [17]
JW-RF-010
 Probe Info 
C41(0.00); C273(0.00)  LDD0026  [17]
NAIA_4
 Probe Info 
C181(0.00); C222(0.00)  LDD2226  [18]
TFBX
 Probe Info 
C273(0.00); C218(0.00)  LDD0027  [17]
WYneN
 Probe Info 
N.A.  LDD0021  [19]
NHS
 Probe Info 
K321(0.00); K77(0.00); K244(0.00); K277(0.00)  LDD0010  [19]
SF
 Probe Info 
Y227(0.00); Y272(0.00); Y287(0.00); Y301(0.00)  LDD0028  [20]
Phosphinate-6
 Probe Info 
C91(0.00); C145(0.00)  LDD0018  [21]
1c-yne
 Probe Info 
N.A.  LDD0228  [22]
Acrolein
 Probe Info 
C261(0.00); C181(0.00); C218(0.00); C222(0.00)  LDD0217  [23]
Cinnamaldehyde
 Probe Info 
C261(0.00); C273(0.00)  LDD0220  [23]
Crotonaldehyde
 Probe Info 
H292(0.00); H290(0.00); H121(0.00); C273(0.00)  LDD0219  [23]
Methacrolein
 Probe Info 
C261(0.00); C273(0.00); C41(0.00)  LDD0218  [23]
W1
 Probe Info 
N.A.  LDD0236  [24]
AOyne
 Probe Info 
7.40  LDD0443  [25]
NAIA_5
 Probe Info 
C41(0.00); C273(0.00); C145(0.00); C261(0.00)  LDD2223  [18]
TER-AC
 Probe Info 
N.A.  LDD0426  [26]
HHS-465
 Probe Info 
N.A.  LDD2240  [27]
PAL-AfBPP Probe
Click To Hide/Show 5 Probe Related to This Target
Probe name Structure Binding Site(Ratio) Interaction ID Ref
FFF probe13
 Probe Info 
20.00  LDD0475  [28]
FFF probe2
 Probe Info 
5.50  LDD0463  [28]
FFF probe3
 Probe Info 
5.15  LDD0465  [28]
STS-1
 Probe Info 
N.A.  LDD0136  [29]
STS-2
 Probe Info 
N.A.  LDD0138  [29]

Competitor(s) Related to This Target

Competitor ID Name Cell line Binding Site(Ratio) Interaction ID Ref
 LDCM0548  1-(4-(Benzo[d][1,3]dioxol-5-ylmethyl)piperazin-1-yl)-2-nitroethan-1-one MDA-MB-231 C41(0.78)  LDD2142  [7]
 LDCM0519  1-(6-methoxy-3,4-dihydroquinolin-1(2H)-yl)-2-nitroethan-1-one MDA-MB-231 C41(1.09); C261(0.72)  LDD2112  [7]
 LDCM0502  1-(Cyanoacetyl)piperidine MDA-MB-231 C41(0.76)  LDD2095  [7]
 LDCM0537  2-Cyano-N,N-dimethylacetamide MDA-MB-231 C41(0.97); C273(1.01)  LDD2130  [7]
 LDCM0524  2-Cyano-N-(2-morpholin-4-yl-ethyl)-acetamide MDA-MB-231 C41(1.09); C273(1.06); C261(0.93)  LDD2117  [7]
 LDCM0558  2-Cyano-N-phenylacetamide MDA-MB-231 C41(1.04); C273(1.15)  LDD2152  [7]
 LDCM0510  3-(4-(Hydroxydiphenylmethyl)piperidin-1-yl)-3-oxopropanenitrile MDA-MB-231 C41(1.39)  LDD2103  [7]
 LDCM0539  3-(4-Isopropylpiperazin-1-yl)-3-oxopropanenitrile MDA-MB-231 C41(0.59)  LDD2132  [7]
 LDCM0025  4SU-RNA DM93 C273(6.24)  LDD0170  [8]
 LDCM0545  Acetamide MDA-MB-231 C41(0.42); C273(0.81)  LDD2138  [7]
 LDCM0520  AKOS000195272 MDA-MB-231 C41(0.77); C273(0.99)  LDD2113  [7]
 LDCM0498  BS-3668 MDA-MB-231 C41(0.45); C273(0.82)  LDD2091  [7]
 LDCM0108  Chloroacetamide HeLa C181(0.00); C261(0.00); H292(0.00); C218(0.00)  LDD0222  [23]
 LDCM0213  Electrophilic fragment 2 MDA-MB-231 C273(2.17); C261(2.00); C41(1.34)  LDD1702  [7]
 LDCM0175  Ethacrynic acid HeLa C181(0.88)  LDD2210  [9]
 LDCM0625  F8 Ramos C273(0.85); C261(0.70); C181(1.10); 0.73  LDD2187  [30]
 LDCM0572  Fragment10 Ramos C273(0.64); C261(0.54); C181(0.54); 0.68  LDD2189  [30]
 LDCM0573  Fragment11 Ramos C273(0.06); C261(0.28); C181(0.12); 0.22  LDD2190  [30]
 LDCM0574  Fragment12 Ramos C273(0.70); C261(0.79); C181(0.55); 0.72  LDD2191  [30]
 LDCM0575  Fragment13 Ramos C273(1.08); C261(1.23); C181(0.98); 0.41  LDD2192  [30]
 LDCM0576  Fragment14 Ramos C273(0.68); C261(0.66); C181(0.64); 0.89  LDD2193  [30]
 LDCM0579  Fragment20 Ramos C273(0.56); C261(0.56); C181(0.56); 0.40  LDD2194  [30]
 LDCM0580  Fragment21 Ramos C273(0.88); C261(1.08); C181(0.88); 0.87  LDD2195  [30]
 LDCM0582  Fragment23 Ramos C273(0.46); C261(0.52); C181(0.74); 0.64  LDD2196  [30]
 LDCM0578  Fragment27 Ramos C273(1.00); C261(1.09); C181(1.07); 1.49  LDD2197  [30]
 LDCM0586  Fragment28 Ramos C273(0.85); C261(0.34); C181(1.30); 0.03  LDD2198  [30]
 LDCM0588  Fragment30 Ramos C273(1.13); C261(1.16); C181(0.70); 0.54  LDD2199  [30]
 LDCM0589  Fragment31 Ramos C273(0.88); C261(1.15); C181(0.78); 1.05  LDD2200  [30]
 LDCM0590  Fragment32 Ramos C273(0.47); C261(0.60); C181(0.47); 0.65  LDD2201  [30]
 LDCM0468  Fragment33 Ramos C273(0.95); C261(0.88); C181(0.65); 0.70  LDD2202  [30]
 LDCM0596  Fragment38 Ramos C273(0.97); C261(0.94); C181(0.93)  LDD2203  [30]
 LDCM0566  Fragment4 Ramos C273(0.84); C261(0.78); C181(0.66); 0.64  LDD2184  [30]
 LDCM0610  Fragment52 Ramos C273(1.28); C261(0.98); C181(0.83); 1.21  LDD2204  [30]
 LDCM0614  Fragment56 Ramos C273(1.02); C261(1.10); C181(0.89); 0.62  LDD2205  [30]
 LDCM0569  Fragment7 Ramos C273(0.64); C261(0.55); C181(0.59); 0.38  LDD2186  [30]
 LDCM0571  Fragment9 Ramos C273(0.51); C261(0.57); C181(0.45); 0.42  LDD2188  [30]
 LDCM0107  IAA HeLa C261(0.00); H292(0.00); C218(0.00); C273(0.00)  LDD0221  [23]
 LDCM0123  JWB131 DM93 Y156(0.59); Y227(0.71)  LDD0285  [11]
 LDCM0124  JWB142 DM93 Y156(0.87); Y227(0.05)  LDD0286  [11]
 LDCM0125  JWB146 DM93 Y156(0.50); Y227(0.05)  LDD0287  [11]
 LDCM0126  JWB150 DM93 Y156(1.51); Y227(4.55)  LDD0288  [11]
 LDCM0127  JWB152 DM93 Y156(1.14); Y227(3.45)  LDD0289  [11]
 LDCM0128  JWB198 DM93 Y156(0.13); Y227(0.12)  LDD0290  [11]
 LDCM0129  JWB202 DM93 Y156(0.64); Y227(0.36)  LDD0291  [11]
 LDCM0130  JWB211 DM93 Y156(0.52); Y227(0.56)  LDD0292  [11]
 LDCM0022  KB02 HEK-293T C273(1.03); C261(0.97); C218(1.15); C222(1.00)  LDD1492  [31]
 LDCM0023  KB03 Jurkat C261(4.31)  LDD0209  [10]
 LDCM0024  KB05 COLO792 C219(0.69); C299(1.28)  LDD3310  [32]
 LDCM0528  N-(4-bromophenyl)-2-cyano-N-phenylacetamide MDA-MB-231 C41(0.58); C273(0.88)  LDD2121  [7]
 LDCM0109  NEM HeLa H292(0.00); C261(0.00); H290(0.00); H121(0.00)  LDD0223  [23]
 LDCM0496  Nucleophilic fragment 11a MDA-MB-231 C41(0.52); C273(1.07)  LDD2089  [7]
 LDCM0499  Nucleophilic fragment 12b MDA-MB-231 C41(0.76)  LDD2092  [7]
 LDCM0500  Nucleophilic fragment 13a MDA-MB-231 C41(1.04); C273(1.19)  LDD2093  [7]
 LDCM0501  Nucleophilic fragment 13b MDA-MB-231 C41(1.14)  LDD2094  [7]
 LDCM0503  Nucleophilic fragment 14b MDA-MB-231 C41(0.60)  LDD2096  [7]
 LDCM0504  Nucleophilic fragment 15a MDA-MB-231 C41(1.23); C273(0.74)  LDD2097  [7]
 LDCM0505  Nucleophilic fragment 15b MDA-MB-231 C41(0.98)  LDD2098  [7]
 LDCM0506  Nucleophilic fragment 16a MDA-MB-231 C41(1.00); C273(1.11); C261(1.12)  LDD2099  [7]
 LDCM0507  Nucleophilic fragment 16b MDA-MB-231 C41(0.70)  LDD2100  [7]
 LDCM0508  Nucleophilic fragment 17a MDA-MB-231 C41(1.07); C273(0.89)  LDD2101  [7]
 LDCM0511  Nucleophilic fragment 18b MDA-MB-231 C41(0.74)  LDD2104  [7]
 LDCM0512  Nucleophilic fragment 19a MDA-MB-231 C41(1.37)  LDD2105  [7]
 LDCM0513  Nucleophilic fragment 19b MDA-MB-231 C41(0.62)  LDD2106  [7]
 LDCM0514  Nucleophilic fragment 20a MDA-MB-231 C41(0.94); C261(1.33)  LDD2107  [7]
 LDCM0515  Nucleophilic fragment 20b MDA-MB-231 C41(0.82); C222(1.06)  LDD2108  [7]
 LDCM0516  Nucleophilic fragment 21a MDA-MB-231 C41(0.83); C273(0.87); C261(0.93)  LDD2109  [7]
 LDCM0517  Nucleophilic fragment 21b MDA-MB-231 C41(1.18)  LDD2110  [7]
 LDCM0518  Nucleophilic fragment 22a MDA-MB-231 C41(0.97); C273(1.27)  LDD2111  [7]
 LDCM0522  Nucleophilic fragment 24a MDA-MB-231 C41(0.76)  LDD2115  [7]
 LDCM0523  Nucleophilic fragment 24b MDA-MB-231 C41(0.93)  LDD2116  [7]
 LDCM0525  Nucleophilic fragment 25b MDA-MB-231 C41(0.83)  LDD2118  [7]
 LDCM0526  Nucleophilic fragment 26a MDA-MB-231 C41(1.62); C273(1.84)  LDD2119  [7]
 LDCM0527  Nucleophilic fragment 26b MDA-MB-231 C41(0.63); C273(1.53)  LDD2120  [7]
 LDCM0529  Nucleophilic fragment 27b MDA-MB-231 C41(0.86)  LDD2122  [7]
 LDCM0530  Nucleophilic fragment 28a MDA-MB-231 C41(1.02); C273(1.19); C261(1.05)  LDD2123  [7]
 LDCM0531  Nucleophilic fragment 28b MDA-MB-231 C41(0.82)  LDD2124  [7]
 LDCM0532  Nucleophilic fragment 29a MDA-MB-231 C41(0.93); C273(0.95); C261(1.06)  LDD2125  [7]
 LDCM0533  Nucleophilic fragment 29b MDA-MB-231 C41(1.01)  LDD2126  [7]
 LDCM0534  Nucleophilic fragment 30a MDA-MB-231 C41(1.15); C273(1.07)  LDD2127  [7]
 LDCM0535  Nucleophilic fragment 30b MDA-MB-231 C41(0.91)  LDD2128  [7]
 LDCM0536  Nucleophilic fragment 31 MDA-MB-231 C41(1.06); C273(1.37)  LDD2129  [7]
 LDCM0540  Nucleophilic fragment 35 MDA-MB-231 C41(0.65); C273(0.81)  LDD2133  [7]
 LDCM0541  Nucleophilic fragment 36 MDA-MB-231 C41(0.62); C273(0.54)  LDD2134  [7]
 LDCM0542  Nucleophilic fragment 37 MDA-MB-231 C41(1.06); C273(1.21)  LDD2135  [7]
 LDCM0543  Nucleophilic fragment 38 MDA-MB-231 C41(1.13); C273(1.32); C261(1.40)  LDD2136  [7]
 LDCM0544  Nucleophilic fragment 39 MDA-MB-231 C41(1.01); C261(1.02); C222(0.91)  LDD2137  [7]
 LDCM0211  Nucleophilic fragment 3b MDA-MB-231 C273(1.80); C41(1.57)  LDD1700  [7]
 LDCM0546  Nucleophilic fragment 40 MDA-MB-231 C41(0.93); C273(0.94); C261(0.95)  LDD2140  [7]
 LDCM0547  Nucleophilic fragment 41 MDA-MB-231 C41(0.95); C261(0.71)  LDD2141  [7]
 LDCM0549  Nucleophilic fragment 43 MDA-MB-231 C41(0.99)  LDD2143  [7]
 LDCM0550  Nucleophilic fragment 5a MDA-MB-231 C41(2.16); C273(1.87)  LDD2144  [7]
 LDCM0551  Nucleophilic fragment 5b MDA-MB-231 C41(1.05); C261(1.01)  LDD2145  [7]
 LDCM0552  Nucleophilic fragment 6a MDA-MB-231 C41(0.85); C273(1.08)  LDD2146  [7]
 LDCM0554  Nucleophilic fragment 7a MDA-MB-231 C41(0.98); C273(0.56)  LDD2148  [7]
 LDCM0555  Nucleophilic fragment 7b MDA-MB-231 C41(1.29)  LDD2149  [7]
 LDCM0556  Nucleophilic fragment 8a MDA-MB-231 C41(0.31); C273(0.63)  LDD2150  [7]
 LDCM0557  Nucleophilic fragment 8b MDA-MB-231 C41(0.84)  LDD2151  [7]
 LDCM0628  OTUB2-COV-1 HEK-293T C181(0.70)  LDD2207  [33]
 LDCM0131  RA190 MM1.R C273(1.52); C261(1.24)  LDD0304  [34]

The Interaction Atlas With This Target

The Protein(s) Related To This Target

Enzyme
Click To Hide/Show 2 Protein(s) Interacting with This Target
Protein name Family Uniprot ID
[Pyruvate dehydrogenase (acetyl-transferring)] kinase isozyme 1, mitochondrial (PDK1) PDK/BCKDK protein kinase family Q15118
Pyruvate dehydrogenase E1 component subunit beta, mitochondrial (PDHB) . P11177
Transporter and channel
Click To Hide/Show 1 Protein(s) Interacting with This Target
Protein name Family Uniprot ID
MICOS complex subunit MIC60 (IMMT) MICOS complex subunit Mic60 family Q16891

The Drug(s) Related To This Target

Approved
Click To Hide/Show 1 Drug(s) Interacting with This Target
Drug Name Drug Type External ID
Nadh Small molecular drug DB00157

References

1 Quantitative and Site-Specific Chemoproteomic Profiling of Targets of Acrolein. Chem Res Toxicol. 2019 Mar 18;32(3):467-473. doi: 10.1021/acs.chemrestox.8b00343. Epub 2019 Jan 15.
2 Cyclopropenone, Cyclopropeniminium Ion, and Cyclopropenethione as Novel Electrophilic Warheads for Potential Target Discovery of Triple-Negative Breast Cancer. J Med Chem. 2023 Feb 23;66(4):2851-2864. doi: 10.1021/acs.jmedchem.2c01889. Epub 2023 Feb 10.
3 Chemoproteomic profiling of kinases in live cells using electrophilic sulfonyl triazole probes. Chem Sci. 2021 Jan 21;12(9):3295-3307. doi: 10.1039/d0sc06623k.
4 Ynamide Electrophile for the Profiling of Ligandable Carboxyl Residues in Live Cells and the Development of New Covalent Inhibitors. J Med Chem. 2022 Aug 11;65(15):10408-10418. doi: 10.1021/acs.jmedchem.2c00272. Epub 2022 Jul 26.
5 A Paal-Knorr agent for chemoproteomic profiling of targets of isoketals in cells. Chem Sci. 2021 Oct 15;12(43):14557-14563. doi: 10.1039/d1sc02230j. eCollection 2021 Nov 10.
Mass spectrometry data entry: PXD028270
6 An Azo Coupling-Based Chemoproteomic Approach to Systematically Profile the Tyrosine Reactivity in the Human Proteome. Anal Chem. 2021 Jul 27;93(29):10334-10342. doi: 10.1021/acs.analchem.1c01935. Epub 2021 Jul 12.
7 Nucleophilic covalent ligand discovery for the cysteine redoxome. Nat Chem Biol. 2023 Nov;19(11):1309-1319. doi: 10.1038/s41589-023-01330-5. Epub 2023 May 29.
Mass spectrometry data entry: PXD039908 , PXD029761
8 Chemoproteomic capture of RNA binding activity in living cells. Nat Commun. 2023 Oct 7;14(1):6282. doi: 10.1038/s41467-023-41844-z.
Mass spectrometry data entry: PXD044625
9 Chemoproteomic Profiling Reveals Ethacrynic Acid Targets Adenine Nucleotide Translocases to Impair Mitochondrial Function. Mol Pharm. 2018 Jun 4;15(6):2413-2422. doi: 10.1021/acs.molpharmaceut.8b00250. Epub 2018 May 15.
10 Covalent Inhibition by a Natural Product-Inspired Latent Electrophile. J Am Chem Soc. 2023 May 24;145(20):11097-11109. doi: 10.1021/jacs.3c00598. Epub 2023 May 15.
11 Chemoproteomic profiling of kinases in live cells using electrophilic sulfonyl triazole probes. Chem Sci. 2021 Jan 21;12(9):3295-3307. doi: 10.1039/d0sc06623k.
12 Global profiling of functional histidines in live cells using small-molecule photosensitizer and chemical probe relay labelling. Nat Chem. 2024 Jun 4. doi: 10.1038/s41557-024-01545-6. Online ahead of print.
Mass spectrometry data entry: PXD042377
13 Targeted Proteomic Approaches for Proteome-Wide Characterizations of the AMP-Binding Capacities of Kinases. J Proteome Res. 2022 Aug 5;21(8):2063-2070. doi: 10.1021/acs.jproteome.2c00225. Epub 2022 Jul 12.
14 Enhancing Cysteine Chemoproteomic Coverage through Systematic Assessment of Click Chemistry Product Fragmentation. Anal Chem. 2022 Mar 8;94(9):3800-3810. doi: 10.1021/acs.analchem.1c04402. Epub 2022 Feb 23.
Mass spectrometry data entry: PXD028853
15 SP3-FAIMS Chemoproteomics for High-Coverage Profiling of the Human Cysteinome*. Chembiochem. 2021 May 14;22(10):1841-1851. doi: 10.1002/cbic.202000870. Epub 2021 Feb 18.
Mass spectrometry data entry: PXD023056 , PXD023059 , PXD023058 , PXD023057 , PXD023060
16 Comparison of Quantitative Mass Spectrometry Platforms for Monitoring Kinase ATP Probe Uptake in Lung Cancer. J Proteome Res. 2018 Jan 5;17(1):63-75. doi: 10.1021/acs.jproteome.7b00329. Epub 2017 Nov 22.
Mass spectrometry data entry: PXD006095 , PXD006096
17 Chemoproteomic Profiling by Cysteine Fluoroalkylation Reveals Myrocin G as an Inhibitor of the Nonhomologous End Joining DNA Repair Pathway. J Am Chem Soc. 2021 Dec 8;143(48):20332-20342. doi: 10.1021/jacs.1c09724. Epub 2021 Nov 24.
Mass spectrometry data entry: PXD029255
18 N-Acryloylindole-alkyne (NAIA) enables imaging and profiling new ligandable cysteines and oxidized thiols by chemoproteomics. Nat Commun. 2023 Jun 15;14(1):3564. doi: 10.1038/s41467-023-39268-w.
Mass spectrometry data entry: PXD041264
19 A modification-centric assessment tool for the performance of chemoproteomic probes. Nat Chem Biol. 2022 Aug;18(8):904-912. doi: 10.1038/s41589-022-01074-8. Epub 2022 Jul 21.
Mass spectrometry data entry: PXD027758 , PXD027755 , PXD027760 , PXD027762 , PXD027756 , PXD027591 , PXD007149 , PXD030064 , PXD032392 , PXD027789 , PXD027767 , PXD027764
20 Solid Phase Synthesis of Fluorosulfate Containing Macrocycles for Chemoproteomic Workflows. bioRxiv [Preprint]. 2023 Feb 18:2023.02.17.529022. doi: 10.1101/2023.02.17.529022.
Mass spectrometry data entry: PXD039931
21 DFT-Guided Discovery of Ethynyl-Triazolyl-Phosphinates as Modular Electrophiles for Chemoselective Cysteine Bioconjugation and Profiling. Angew Chem Int Ed Engl. 2022 Oct 10;61(41):e202205348. doi: 10.1002/anie.202205348. Epub 2022 Aug 22.
Mass spectrometry data entry: PXD033004
22 Tunable Amine-Reactive Electrophiles for Selective Profiling of Lysine. Angew Chem Int Ed Engl. 2022 Jan 26;61(5):e202112107. doi: 10.1002/anie.202112107. Epub 2021 Dec 16.
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24 Oxidant-Induced Bioconjugation for Protein Labeling in Live Cells. ACS Chem Biol. 2023 Jan 20;18(1):112-122. doi: 10.1021/acschembio.2c00740. Epub 2022 Dec 21.
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27 Global profiling identifies a stress-responsive tyrosine site on EDC3 regulating biomolecular condensate formation. Cell Chem Biol. 2022 Dec 15;29(12):1709-1720.e7. doi: 10.1016/j.chembiol.2022.11.008. Epub 2022 Dec 6.
Mass spectrometry data entry: PXD038010
28 Ligand and Target Discovery by Fragment-Based Screening in Human Cells. Cell. 2017 Jan 26;168(3):527-541.e29. doi: 10.1016/j.cell.2016.12.029. Epub 2017 Jan 19.
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Mass spectrometry data entry: PXD027578
31 Accelerating multiplexed profiling of protein-ligand interactions: High-throughput plate-based reactive cysteine profiling with minimal input. Cell Chem Biol. 2024 Mar 21;31(3):565-576.e4. doi: 10.1016/j.chembiol.2023.11.015. Epub 2023 Dec 19.
Mass spectrometry data entry: PXD044402
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Mass spectrometry data entry: PXD047840
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