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post-translational modification

11259 relationships annotated with this phrase. Showing first 500 of 11259.
Source entity Relationship Target entity Species
reversible acetylation of K183 regulates activity of GSK3 Homo sapiens
consensus motif of SP was reported as nonlight-induced phospho-sites Arabidopsis thaliana
exogenous sulfide could affect persulfidation of a broader number of proteins
(VUP1, AT3G21710) phosphorylation is critical for regulation of (VUP1, AT3G21710) activity Arabidopsis thaliana
RcphyB and RcOST1L accumulation in the nucleus results in almost complete phosphorylation of RcPIF4 Rosa sp.
lysine acetylation elaborately regulated GSK3 activity
β-CA1, 2, 3, and 4 are modified by persulfidation Arabidopsis thaliana
RcOST1L directly phosphorylates RcPIF4 at serine 198 Rosa sp.
suppression of photorespiration induces level of protein persulfidation in plants Arabidopsis thaliana
large number of photorespiratory enzymes were targets of persulfidation
MYBs regulating lignin synthesis and vessel development undergo regulation at posttranslational levels including protein phosphorylation
ATP-mediated NO might be involved in thioredoxin-mediated S-nitrosylation modifications of (ATNPR1, NIM1, NPR1, SAI1, AT1G64280)
p50 subunit of NF-kappaB is likely glutathionylated
main molecular mechanism of sulfide is through persulfidation of certain targets
activity of (DES1, AT5G28030) is induced by ABA-triggered persulfidation
rice RePRPs are likely heavily glycosylated Oryza sativa
methylamine used for removal of O-linked glycans from proteins Oryza sativa
six phospho-sites identified in this study show different phosphorylation regulation of (PAP3, PIF3, POC1, AT1G09530) in response to different stimuli Arabidopsis thaliana
FERONIA (FER, AT3G51550) phosphorylates (ATMYB63, MYB63, AT1G79180) Solanum lycopersicum
sulfide regulates physiological processes by increasing or decreasing persulfidation level of certain targets
Lys13 (K13) residue is SUMOylation site of (PAP3, PIF3, POC1, AT1G09530) Arabidopsis thaliana
phosphoproteomic studies revealed various phosphorylation sites among CESAs
purified RePRP1 shows hydroxylated and methylamine-linked Pro residues Oryza sativa
(AHA2, AtHA2, HA2, PMA2, AT4G30190) activity appears to be regulated by protein phosphorylation pathways Arabidopsis thaliana
plastid transcription kinase is under phosphorylation control phosphorylation
hydroxyproline (Hyp) is found in Val–Pro–Ser sequence
phosphorylation or dephosphorylation events occur on serine, threonine, and tyrosine residues
dynamics of acetylation at diverse development stages need more research protein acetylation in plant pathogenic fungi
glycine decarboxylase is also inhibited by S-glutathionylation
regulator of G-protein signaling MoRgs1 undergoes phosphorylation Magnaporthe oryzae
RcphyB enhances RcPIF4 phosphorylation mediated by RcOST1L Rosa sp.
phosphorylation sites localize to CSR domain
mitogen-activated protein kinase SlMPK8 phosphorylated SlERF.C1 at Ser 174 residue Solanum lycopersicum
several β-CA isoforms are modified by persulfidation Arabidopsis thaliana
N-terminal serine phosphorylation decrease catalytic activity of GSK3
lysine acetylation is emerging as novel post-translational modification regulating GSK3 activity
proline (Pro) hydroxylation in Asp–Pro–Ser context has never been described in plant proteins
oxohistidine has never been reported in plant proteins
(FER, AT3G51550) phosphorylates CAR proteins
RcOST1L phosphorylates RcPIF4 at serine 198 residues Rosa sp.
the ease with which these modifications were found is a testament to the power of the approach used Solanum tuberosum
direct feedback mechanisms may include S-nitrosylation, S-glutathionylation, S-sulfenylation, S-sulfinylation, and S-sulfonylation of Cys residues in diverse proteins of the translation machinery Arabidopsis thaliana
NITRATE TRANSPORTER1.1 (AtNPF6.3, ATNRT1, B-1, CHL1, CHL1-1, NPF6.3, NRT1, NRT1.1, AT1G12110) is phosphorylated on Thr-101 residue by CYSTATHIONINE BETA-LYASE-interacting protein kinase Arabidopsis thaliana
the (DDP1, PTM, AT5G35210) (posttranslational modification) sites unless the (DDP1, PTM, AT5G35210) sites are introduced in an ordered rather than a random manner Solanum tuberosum
(DDP1, PTM, AT5G35210) (posttranslational modification) such as Lys or Arg oxidation causing missed trypsin cleavage sites results in larger peptides that are more difficult to ionize and fragment Solanum tuberosum
environmental or nutritional cues trigger differential changes in phosphorylation status and abundance of cytosolic ribosomal protein (RP) paralogs
NbHIPP26 is lipid modified by S-acylation through residue C13 Nicotiana benthamiana
chemical proteomics offers insights into functional biology of post-translational modifications (PTMs)
(APRR5, PRR5, AT5G24470) is known to be modified by phosphorylation
Gly dehydrogenase had as many as 50 (DDP1, PTM, AT5G35210) (posttranslational modification) events of six different kinds Solanum tuberosum
phosphoenolpyruvate carboxylase (PPC) activity is modulated via dark-phase protein phosphorylation of N-terminal Ser
c-Jun subunit of AP-1 complex is likely glutathionylated
(GLV11, RGF1, AT5G60810) signaling peptide is tyrosine-sulfated by (AQC1, HPS7, TPST, AT1G08030)
mechanism of removing S335 phosphorylation of AvrPtoB exists in plants Arabidopsis thaliana
paralogs of cytosolic ribosomal proteins (RPs) can differentially change phosphorylation status
specific effect of thioredoxin f1 (TRX f1) could be further modulated by glutathionylation of thioredoxin f (TRX f)
2-Cys Prxs undergo acetylation
rNAD-ME1 showed complete absence of phosphoenolpyruvate carboxylase (PPC) phosphorylation in LL Kalanchoë fedtschenkoi
self-glucosylation changes protein molecular mass and properties
the coverage of modified peptides was likely underestimated due to (DDP1, PTM, AT5G35210) (posttranslational modification) such as Lys or Arg oxidation causing missed trypsin cleavage sites Solanum tuberosum
the large number of (DDP1, PTM, AT5G35210) (posttranslational modification) sites on some proteins could give rise to a very large number of differentially modified versions of the protein Solanum tuberosum
Nuclear Factor 1 is likely glutathionylated
more than half the proteins detected in the potato mitochondrial proteome were posttranslationally modified on at least one site Solanum tuberosum
CCMC active site motif is likely involved in post-translational modification of proteins by reversible disulfide reduction
Gly dehydrogenase had three Asp (aspartate) deamidations Solanum tuberosum
persulfidation and S-nitrosylation both modify cysteine-SH groups
S-thiolation involves reversible mixed disulfide
62 Pro residues detected by mass spectrometry (MS) in RePRP1 13% are glycosylated (eight methylamine-labeled Hyp) Oryza sativa
SIZ1-mediated SUMOylation of (ATMYB30, MYB30, AT3G28910) increases stability of (ATMYB30, MYB30, AT3G28910) Arabidopsis thaliana
the oxidation of a Met (methionine) residue to Met sulfoxide next to a potential phosphorylation site abolishes the phosphorylation on that site
organelle proteome is regulated at post-translational modification level
chloroplast protein fractions containing (PAS2, PEP, PEPINO, AT5G10480) and other DNA-binding proteins analyzed for phosphorylation state
metal-catalyzed oxidation of histidine (His) to oxohistidines is described in human proteins Homo sapiens
reduction of TZF9-labelled PB structures is dependent on phosphosites Arabidopsis thaliana
circadian clocks in autotrophic and heterotrophic organisms can be refined by post-translational modification (PTM) cascades
OsAKT2 is modulated by phosphorylation/dephosphorylation mechanism Oryza sativa
PSEUDO-RESPONSE REGULATOR (PRR) family is subjected to phosphorylation
persulfidation enhances Cys reactivity
multiple isoelectric forms of fatty acid synthesis proteins suggests presence of post-transcriptional modification Brassica napus
FC lyase synthesized in vitro in presence of microsomal membranes migrates at higher apparent molecular mass than FC lyase synthesized in absence of microsomal membranes Arabidopsis thaliana
(AtRIN4, RIN4, AT3G25070) is phosphorylated in response to P. syringae effectors AvrB and AvrRpm1 Arabidopsis thaliana
phosphorylation of S86 is actually important in vivo Arabidopsis thaliana
(ATFKBP12, FKBP12, FKP12, AT5G64350) overexpression showed effect on phosphorylated form of CONSTANS (CO) Arabidopsis thaliana
cPTIO inhibits protein S-nitrosylation Arabidopsis thaliana
(LecRK-IX.2, AT5G65600) phosphorylates AvrPtoB at serine site 335 (S335) Arabidopsis thaliana; Pseudomonas syringae
S-nitrosylation of (ATMYB30, MYB30, AT3G28910) represses DNA binding activity of (ATMYB30, MYB30, AT3G28910) Arabidopsis thaliana
peptides from resin-enriched nascent protein datasets contained PTMs in only 9% or 10% of proteins from AHA- or HPG-treated cells Arabidopsis thaliana
Aleuria aurantia lectin (AAL) is used to determine O-fucosylation of (APRR5, PRR5, AT5G24470) Arabidopsis thaliana
(OSCA1.3, AT1G11960) channel bears phosphosite (SerXXLeu) Arabidopsis thaliana
glycine decarboxylase P-protein 2 (AtGLDP2, GLDP2, AT2G26080) can be O-glycosylated Arabidopsis thaliana
CIPK undergoes post-translational modification
persulfidation is similar to S-nitrosylation
35S:CO fk12-1 double mutant shows reduction of phosphorylated band in CONSTANS (CO) Arabidopsis thaliana
tyrosylprotein sulfotransferase catalyzes (PSY1, AT5G58650) sulfation
previously identified proteins in fatty acid synthesis are represented by multiple isoelectric forms Brassica napus
recombinant Arabidopsis FC lyase is larger than predicted molecular mass by 11.7 kDa Arabidopsis thaliana
40S ribosomal protein S6 kinases (S6Ks) are activated by phosphorylation
interaction of Arabidopsis RAPTOR (AtRAPTOR) with Arabidopsis (TOR, AT1G50030) (AtTOR) and Arabidopsis (ATPK1, ATPK6, ATS6K1, PK1, PK6, S6K1, AT3G08730) results in phosphorylation of S6 substrate Arabidopsis thaliana
plant-specific post-translational modification of the (CCT, CRP, MED12, AT4G00450) domain is not present in yeast Saccharomyces cerevisiae
35S:FK plants show induction of phosphorylated band in CONSTANS (CO) Arabidopsis thaliana
flg22-induced protein destabilisation is dependent on phosphosites Arabidopsis thaliana
post-translational modifications are critical for maintaining protein activities and stability
phosphosite (SerXXLeu) is conserved in NADPH oxidase (ATRBOHD, DELT1, RBOHD, AT5G47910) Arabidopsis thaliana
AB-6b have ADP ribosylation activity
lysine residues could be post-translationally modified in multiple ways
persulfidation enhances activity of peptides
S-nitrosylation diminishes cysteine reactivity
proportion of spectral hits for PTM-containing peptides per protein was greater in bulk datasets compared with enriched counterparts in all cases for AHA-treated cells Arabidopsis thaliana
polyamines (PAs) enhances protein S-nitrosylation Arabidopsis thaliana
(PIF7, AT5G61270) activity is likely regulated by phosphorylation/dephosphorylation
sumoylation of (ATMYB30, MYB30, AT3G28910) is mediated by (ATSIZ1, SIZ1, AT5G60410) Arabidopsis thaliana
(ATFKBP12, FKBP12, FKP12, AT5G64350) mutant showed effect on phosphorylated form of CONSTANS (CO) Arabidopsis thaliana
MP is a target for phosphorylation
EF-TU RECEPTOR (EFR, AT5G20480) inhibits phosphorylation through phosphorylation of BRI1-ASSOCIATED RECEPTOR KINASE (ATBAK1, ATSERK3, BAK1, ELG, RKS10, SERK3, AT4G33430) at Thr-455 in the activation domain
S86 and Y104 residues in the NTE of (HY3, OOP1, PHYB, AT2G18790) have been investigated and exhibit light-dependent dephosphorylation (S86) or phosphorylation (Y104) in Arabidopsis Arabidopsis thaliana
(PGF5, AT3G16850) polygalacturonase contains proline hydroxylation in Asp–Pro–Ser context
ATP binding to SUBTILISIN-LIKE SERINE PROTEASE 1.7 (ARA12, SBT1.7, AT5G67360) is controlled by unidentified post-translational modification Arabidopsis thaliana
BnaC01.NPC4 is S-acylated S-acylation modification Brassica napus
in vitro kinase assays demonstrated presence of HopAO1 results in significant decrease in elf18-induced Tyr phosphorylation on EF-TU RECEPTOR (EFR, AT5G20480)
hydroxyproline (Hyp) is found in cell wall protein (CWP) different from HRGPs and H/PRPs
(OSCA1.3, AT1G11960) channel is phosphorylated upon PAMP treatment Arabidopsis thaliana
RNA-binding properties is dependent on phosphosites Arabidopsis thaliana
S-acylation involves reversible addition of acyl group to cysteine residue
SPINDLY (SPY) O-fucosylates PSEUDO-RESPONSE REGULATOR 5 (APRR5, PRR5, AT5G24470) Arabidopsis thaliana
O-GlcNAc transferase competes with casein kinase to post-translationally modify PER2 mammalian
prolines in valine–proline pairs were good candidates to be targeted by (ATFKBP12, FKBP12, FKP12, AT5G64350) activity in order to modify CO structure Arabidopsis thaliana
nitrate mediates dephosphorylation of Ser439 in (AGR, AGR1, ATPIN2, EIR1, MM31, PIN2, WAV6, AT5G57090) protein
two MP fractions could be differentially modified by post-translational modifications
SPK kinase activity may regulate nuclear targeting of OsNF-YB9 by phosphorylation Oryza sativa
(AtNPC4, NPC4, AT3G03530) Cys-533 is S-acylated by protein S-acyl transferase (PAT) Arabidopsis thaliana
glycosylation of proteins involved in MT nucleation and severing presents promising avenue for future research plants
root side exposed to air undergoes SUMOylation of AUXIN RESPONSE FACTOR 7 (ARF7, BIP, IAA21, IAA23, IAA25, MSG1, NPH4, TIR5, AT5G20730) Arabidopsis thaliana
(AtRIN4, RIN4, AT3G25070) might be regulated by 14-3-3 proteins Arabidopsis thaliana
charge-variant spots of SUBTILISIN-LIKE SERINE PROTEASE 1.7 (ARA12, SBT1.7, AT5G67360) indicate existence of post-translational modifications that significantly alter the charge of the protein Arabidopsis thaliana
CKII kinase phosphorylates core clock transcription factors Arabidopsis thaliana
alternative splicing potentially influences protein stability
O-GlcNAcylation physiological significance remains to be fully elucidated in plants plants
Ser residues marked with asterisks are targets of protein kinase (ATMAPK6, ATMPK6, MAPK6, MPK6, AT2G43790) phosphorylation
S-nitrosylation of cysteine residues is common structural modification of proteins by NO
phosphorylation of Fragaria × ananassa (ATWRKY1, WRKY1, ZAP1, AT2G04880) (FaWRKY1) may modulate Fragaria × ananassa (ATWRKY1, WRKY1, ZAP1, AT2G04880) (FaWRKY1) activity Fragaria × ananassa
human NMNAT-1 (human nicotinate/nicotinamide mononucleotide adenyltransferase 1) is subjected to phosphorylation by protein kinase C Homo sapiens
MP ubiquitination does not occur for MP associated with microtubules
(AtNPC4, NPC4, AT3G03530) is S-acylated protein Brassica napus
TIR-only or TNL proteins form ADP-ribosylated ATP (ADPr-ATP)
nascent and bulk proteins from AHA-treated cell cultures appeared similar in terms of (DDP1, PTM, AT5G35210) frequencies Arabidopsis thaliana
(ATNPR1, NIM1, NPR1, SAI1, AT1G64280) is regulated at (DDP1, PTM, AT5G35210) level
(HCR1, PP4-1, PPX-1, PPX1, AT4G26720) regulates phosphorylation of (HEI10, AT1G53490) Arabidopsis thaliana
mammalian NF-YA Ser292 phosphorylation has been demonstrated to decrease stability of NF-Y/CCAAT complex
high degree of modification of proteins in primary metabolism and protein biosynthesis pathways may indicate that these proteins are exposed for longer or to harsher (bio)chemical environments than other proteins in vivo Arabidopsis thaliana
fatty acid acylation modification affects subcellular localization and biological functions of (AtNPC4, NPC4, AT3G03530) Arabidopsis thaliana
(ARAC11, ATRAC11, ATROP1, ROP1, ROP1AT, AT3G51300) is prenylated
MP may be differentially phosphorylated when associated with microtubules
LaSCR1 and LaSCR2 contain cAMP-dependent protein kinase phosphorylation motif Lupinus albus
C-terminal tyrosine can be reversibly removed and religated α-tubulin
sub-cellular localization of UP9C and its ability to interact with other proteins can be regulated by additional factors, such as by redox potential and posttranslational modifications (phosphorylation, ubiquitination) Nicotiana tabacum
phosphorylation of (FHY1, FRY1, PAT3, AT2G37678) occurs at sites near NLS and NES domains
PEPC2 has conserved N-terminal phosphoserine residue
differential phosphorylation of (AtRIN4, RIN4, AT3G25070) in response to bacterial effectors or plant immune signaling directly impacts AHA activity in guard cells and other cell types Arabidopsis thaliana
AvrRpm1 (AHA1, HA1, OST2, PMA, AT2G18960) induces phosphorylation of T166 in (AtRIN4, RIN4, AT3G25070)
removal of PST domain may result in absence of post-translational modifications Pisum sativum
(AtNPC4, NPC4, AT3G03530) is S-acylated protein Arabidopsis thaliana
post-translational modifications modulate stability of transcriptional regulators
proteins are regulated by NO-mediated S-nitrosylation
593 proteins found in both nascent and total datasets using HPG had only nine (2%) containing more PTMs in enriched dataset than in bulk dataset Arabidopsis thaliana
high proportional frequency of Arg methylation in nascent proteins from AHA-treated cell cultures was not a general difference but a case of enrichment of a specific protein with a dominant (DDP1, PTM, AT5G35210) Arabidopsis thaliana
nitric oxide (NO) readily nitrosylates cysteine residues
MS analysis of intensely fluorescent spots could not confirm presence of phosphorylated or glycosylated post-translational modifications Triticale
Cys-533 is S-acylation site in (AtNPC4, NPC4, AT3G03530) Arabidopsis thaliana
(NPC5, AT3G03540) cannot be acylated S-acylation modification Arabidopsis thaliana
H2O2-mediated sulfenylation of (ATTSB1, TRP2, TRPB, TSB1, AT5G54810) likely occurs on Cys-308
Tyr5 nitration may not have physiological relevance Pisum sativum
GmFAD7 protein shows tissue-specific post-translational regulatory mechanisms affecting distribution and conformation of different GmFAD7 family members Glycine max
S-nitrosylation is important prototypic redox-based post-translational protein modification
N-terminal acetylation was found across 48 HPG-enriched proteins Arabidopsis thaliana
phosphorylation status of the remorin intrinsically disordered domain (IDD) modulates properties of remorin-containing nanodomains
SUMOylation increases stability of (ABI5, AtABI5, DPBF1, GIA1, AT2G36270) (ABA INSENSITIVE 5)
3-nitro-L-tyrosine (nitrotyrosine, NO₂Tyr) can be incorporated into detyrosinated α-tubulin
eukaryotic tubulins undergo phosphorylation
relative rate of biosynthesis and degradation of Rubisco are regulated by post-translational modification
novel phosphoproteins are present in root nodules Medicago truncatula
S/I substitution at H5 position may affect post-translation process
(ATTOC34, OEP34, TOC34, AT5G05000) G-domain undergoes phosphorylation
wounding-inducible kinase activity phosphorylates within (REM11, VAL, AT5G60140) and Ser residues found in the conserved C-terminal region Arabidopsis thaliana; Solanum lycopersicum
All Ps-ACS predicted proteins, except Ps-ACS3 have Ser residue that is phosphorylated by a calcium-dependent protein kinase, CDPK Prunus salicina
phosphorylation of least three proteins, GBSS, BEIIb, and starch phosphorylase was revealed by phospho-protein specific dye staining
PwTUA1 protein contains phosphorylated residue at K336 Picea wilsonii
partial N-acetylation is unusual post-translational modification in E. coli Escherichia coli
TIR-only or TNL proteins form ADP-ribosylated ADPR (di-ADPR)
nitric oxide (NO) readily nitrates tyrosine residues
SUMOylation regulates (ABI5, AtABI5, DPBF1, GIA1, AT2G36270) (ABA INSENSITIVE 5) activity
nascent proteins from HPG-treated cell cultures contained much lower frequency of Met oxidation Arabidopsis thaliana
(ckl4, AT4G28860) kinase phosphorylates core clock transcription factors Arabidopsis thaliana
glycosylation was previously reported in pea 7S family Pisum sativum
Type 2 (ACS, AT5G36880) isozymes contain calcium-dependent protein kinase (CDPK) phosphorylation site
CK2-mediated phosphorylation results in alteration of protein function
hormone-responsive transcription factors are subject to multiple modifications
D2 peptide only one species was identified with hydroxylation at Pro11 Medicago truncatula
LaSCR1 and LaSCR2 contain N-glycosylation motif Lupinus albus
(ACR2, ARATH;CDC25, AtACR2, CDC25, AT5G03455) removes phosphate group on conserved tyrosine 15 in catalytic cleft of CDK (cyclin-dependent kinase) Schizosaccharomyces pombe
specific phosphatases belonging to PP2 family dephosphorylate H+ -ATPase
diurnal phosphorylation of PEPC was not observed in transgenic rice expressing maize PEPC Oryza sativa
insect antimicrobial peptides undergo post-translational degradation by intracellular proteases
LaSCR1 and LaSCR2 contain cGMP-dependent protein kinase phosphorylation motif Lupinus albus
NO₂Tyr is accepted as substrate by tubulin–tyrosine ligase (TTL)
histone phosphorylation drives acetylation of histone H3 Animalia
BRASSINOSTEROID INSENSITIVE 1-ASSOCIATED RECEPTOR KINASE 1 (ATBAK1, ATSERK3, BAK1, ELG, RKS10, SERK3, AT4G33430) phosphorylates cyclic nucleotide-gated channel 20 (ATCNGC20, CNBT1, CNGC20, AT3G17700) Arabidopsis thaliana
(EFR, AT5G20480) (elongation-factor-Tu-perceiving RK) undergoes ligand-responsive S-acylation at conserved cysteine (Cys975)
SSIIa was found to be phosphorylated
Arabidopsis and tomato (ACS, AT5G36880) proteins have been shown to be post-translationally phosphorylated Arabidopsis thaliana; Solanum lycopersicum
endogenous NO production or exogenous ONOO- addition increases tyrosine nitration
many post-translational modifications are crucial for regulation of protein function
(ATTOC159, PPI2, TOC159, TOC160, TOC86, AT4G02510) G-domain undergoes phosphorylation
BEIIb and starch phosphorylase is consistent with previous finding that soluble forms in wheat amyloplasts accept transfer of a radioactive phosphate group from labelled ATP
PpFT1 protein was predicted to have seven N-glycosylation sites (N-X-S/T)
rcd1-3; sro1-1 double mutants show accumulation of excess sumoylated proteins Arabidopsis thaliana
alteration of plasma membrane proton pump under heavy metals is due to dephosphorylation of enzyme protein Cucumis sativus
degree of N-glycosylation may lead to changes in native molecular weight Vigna unguiculata
cantharidin treatment distinctly diminished inhibitory effect of metals on plasma membrane proton pump Cucumis sativus
PEPC-k catalyzes phosphorylation of phosphoenolpyruvate carboxylase (PEPC)
phosphorylation may affect binding to glucans in the granule and/or to other internal granule-associated proteins
nitric oxide (NO) can directly modify proteins
purified GSTs MS analysis showed they had undergone cleavage of the N-terminal methionine Escherichia coli
highly dynamic MTs are mostly tyrosinated
elimination of photosynthate supply to developing COS caused Class-1 PEPC's subunits to be rapidly dephosphorylated, and then subsequently monoubiquitinated in vivo Ricinus communis
NAC transcription factors can be regulated on post-translational level encompassing phosphorylation, protein degradation, and dimerization Arabidopsis thaliana; Oryza sativa
monoubiquitination of p110 subunit occurs at conserved Lys624 residue Sorghum bicolor
proline hydroxylation is described in mature GLV peptides
N-Tyr is incorporated into C-terminus of α-tubulin
short O1 transcript conceptually encoded truncated, headless O1 Zea mays
hydroxylation occurred at Pro11 Medicago truncatula
hydroxylation occurred at Pro7 and Pro11 Medicago truncatula
stoichiometry of phosphorylation remains to be addressed regarding phosphorylation of internal granule-associated proteins
enzyme activity may be regulated by post-translational modification
post-translational modifications could explain discrepancy between number of detected spots and number of genes identified Brachypodium distachyon
multiple spots from single gene mostly arises from post-translational modifications Brachypodium distachyon
four D1 peptide variants were identified as having triarabinosylation at Pro11 Medicago truncatula
tyrosine nitration in animal systems is mediated by enzymatic mechanism
proteins detected only at 0 h and 24 h after pollination may represent proteins that have changed location on the gel due to post-translational modification Petunia × hybrida
down-regulated PhADF1 and PhADF2 isoforms were acetylated at the second amino acid of the N-terminus Petunia × hybrida
eukaryotic tubulins undergo acetylation
FaPIP2;1 contains Ser280 and Ser283 amino acids Fragaria × ananassa
conserved threonine 14 and tyrosine 15 replaced with alanine and phenylalanine results in mutants not down-regulated by phosphorylation of tyrosine 15
each cysteine residue could be important for specific redox-based post-translational modification by NO Arabidopsis thaliana
(ATXTH14, XTH14, XTR9, AT4G25820) and (ATXTH26, XTH26, AT4G28850) contain N-linked sugars Arabidopsis thaliana
phosphorylation sites of (ATTOC33, PPI1, TOC33, AT1G02280) and ps (ATTOC34, OEP34, TOC34, AT5G05000) have been mapped in different areas of the protein from different sources Arabidopsis thaliana; Pisum sativum
change in important antigenic site causes loss of signal for faster migrating protein
FolSir2 regulates kinase activity of FolGsk3 by removing K271ac Fusarium oxysporum
S-nitrosylation is general mechanism implicated in broad spectrum of plant processes Arabidopsis thaliana
CTD exists in two phosphorylation states: hypophosphorylated ( (POL, AT2G46920) IIA) and hyperphosphorylated ( IIO)
phosphorylation of the C-terminus of Type 1 (ACS, AT5G36880) proteins by (ATMAPK6, ATMPK6, MAPK6, MPK6, AT2G43790) suggests involvement of the (ACS, AT5G36880) C-terminal region in post-transcriptional regulation
phosphorylation of WRKY proteins modulates WRKY protein function
GOX and glycine decarboxylase are inhibited by S-nitrosylation
NPH3-domain GTPase is modified by phosphorylation
NΔNcP1-3A mutant protein is not phosphorylated phosphorylation Nicotiana benthamiana
C1P1-4A mutant protein was weakly phosphorylated phosphorylation Nicotiana benthamiana
bTOP2 modified in property or properties of pTOP2 critical for SA binding Arabidopsis thaliana
acetylation of cohesin rings occurs at conserved lysine residues in SMC proteins
plasma membrane H+-ATPase has complex phosphorylation pattern with multiple in vivo phosphorylation sites in its terminal regulatory domains Arabidopsis thaliana
CALMODULIN-BINDING RECEPTOR-LIKE CYTOPLASMIC KINASE 3 (CRCK3, AT2G11520) phosphorylated CATALASE 2 (CAT2, AT4G35090) Arabidopsis thaliana
monoubiquitination at Lys624/Lys628 site may be universal (DDP1, PTM, AT5G35210) of Class-1 PEPC subunits throughout plant kingdom
acylated proanthocyanidins in legumes involve gallic acid, typically attached as ester at C3 of ring systems
multiple spots with different pIs and molecular masses point to existence of isoforms possibly resulting from post-translational modifications, multimeric forms, proteolytic processing, and alternative transcripts Triticale
Pgl (ATPGIP1, PGIP1, AT5G06860) has seven putative N-glycosylation sites Pennisetum glaucum
Nn and Nc regions of the N-terminal domain of (ATUPF1, LBA1, UPF1, AT5G47010) are phosphorylated phosphorylation
p110 is monoubiquitinated form of p107 Sorghum bicolor
Prolyl 4-hydroxylase (P4H) converts proline to hydroxyproline Arabidopsis thaliana
sulfonation increases peptide bioactivity
higher proportion of isoforms in triticale stigma may indicate higher degree of post-translational modification within the stigma Triticale
N-glycosylation sites have consensus sequence N-x-S/T (where x is any amino acid except P) Pennisetum glaucum
binding of glutathione through S-glutathionylation of cysteine C205 occurs in amino-terminal domain clamshell of (ATGLR3.4, GLR3.4, GLUR3, AT1G05200) Arabidopsis thaliana
other enzymes were reported to lose (XET, XTH33, AT1G10550) activity totally when glycosylation was absent
NO gas treatment of Anticaria toxicaria seeds causes S-nitrosylation of APX Anticaria toxicaria
Cys168 in Arabidopsis (APX1, ATAPX01, ATAPX1, CS1, MEE6, AT1G07890) is proposed to be target of S-nitrosylation Arabidopsis thaliana
Arabidopsis (ATMPK4, MAPK4, MPK4, AT4G01370) phosphorylates microtubule-associated protein 65-1 Arabidopsis thaliana
effectors carry acetyltransferase activities
(AtNPF6.3, ATNRT1, B-1, CHL1, CHL1-1, NPF6.3, NRT1, NRT1.1, AT1G12110) under low nitrate conditions promotes coreceptor QSK1 phosphorylation Arabidopsis thaliana
Arabidopsis and Brachypodium possess and express headless variant of (ATXIK, XI-17, XI-K, XIK, AT5G20490) Arabidopsis thaliana; Brachypodium distachyon
modifications of hormone-responsive transcription factors can affect protein stability
(ATFLS2, FLS2, AT5G63580) is S-acylated at juxta-transmembrane domain cysteines (Cys830,831)
protein phosphorylation is evolutionarily conserved module
APX is target of nitration
phosphorylation on a conserved N-terminal serine residue causes decrease in affinity for dicarboxylic acids
ATP-binding and or autophosphorylation occurs in the cells but not in vitro in the absence of ATP
monosaccharides of chains A and B are methylated and/or acetylated methylation and acetylation
(GLL23, AT1G54010) C-terminal tyrosine residues might be targeted by carboxypeptidase
Peptide sulfation in plants is mediated by unique Golgi-membrane localized tyrosylprotein sulfotransferase (AQC1, HPS7, TPST, AT1G08030)
(CP29B, SEBF, AT2G37220) is characterized by N-terminal cleavage of five amino acids Arabidopsis thaliana
prokaryotic expression system may not produce glycosylated proteins
HvDRF1 protein undergoes post-translational activation upon stress Hordeum vulgare
certain amino acid interactions in PttXTH34 are thought to be crucial for stability when the interactions between other amino acids and the N-glycan are disrupted by the removal of the N-glycan Populus trichocarpa
acetyl-CoA participates in protein acetylation
p110 in developing sorghum seeds is monoubiquitinated version of p107 Sorghum bicolor
short myosin transcript is rather headless variant of O1 Zea mays
peptides were identified with triarabinosylation at Pro11 Medicago truncatula
11S globulin proproteins undergo maturation leading to two polypeptides: acidic polypeptide of about 35–40 kDa and basic polypeptide of about 20 kDa Brachypodium distachyon
SIN-1 concentration increases degree of tyrosine nitration of APX Pisum sativum
actin S-nitrosylation causes disturbances on actin cytoskeleton structure Arabidopsis thaliana
ubiquitination is one of specific modifications of hormone-responsive transcription factors
small secreted peptides are cleaved from precursor
recombinant (AQC1, HPS7, TPST, AT1G08030) has been shown to sulfate PSKα and (PSY1, AT5G58650) precursor peptides in vitro
SSPs requiring post-translational modification were identified maize (BSK12, SSP, AT2G17090) repertoire Zea mays
mutation in putative phospho-accepting Asp residue into Asn residue ( (ARR7, AT1G19050) (D85N)) inhibits phosphorylation of Arabidopsis response regulator 7 (ARR7, AT1G19050) Arabidopsis thaliana
(CESA5, MUM3, AT5G09870) phosphorylation has been observed in light-grown cell cultures
post-translational modifications may be affected by physiological conditions
phosphorylation/dephosphorylation of proteins is reversible mechanism
(ATTPS1, TPS1, AT1G78580) is potentially phosphorylated by calcium-dependent protein kinases Arabidopsis thaliana
(AtPHR1, PHR1, AT4G28610) is small ubiquitin-like modifier (SUMO)ylation target of SAP and Miz protein (ATSIZ1, SIZ1, AT5G60410) Arabidopsis thaliana
oxidative modifications are known to occur in cell walls
persulfidation of a specific protein in the mitochondria or cytosol is regulated by endogenous sulfide
phosphorylation of LRP by (PRP4KA, AT3G25840) at Ser17 is essential for LRP protein stability Arabidopsis thaliana
AvrRps4-GFP does not acetylate (ATWRKY52, RRS1, RRS1-R, SLH1, AT5G45260) and -S proteins Nicotiana benthamiana
BTL2 autophosphorylates at T669
Mp rr-myb5 mutants show changes to protein phosphorylation Marchantia polymorpha
S-nitrosylation of (AtTIR1, TIR1, AT3G62980) protein indicates role for redox-based mechanism in control of (AtTIR1, TIR1, AT3G62980) action Arabidopsis thaliana
glutathionylation represents major form of S-thiolation
In C3 and C4 species, pyruvate orthophosphate dikinase (PPDK, AT4G15530) activity is regulated via phosphorylation/dephosphorylation
dark phosphorylation of phosphoenolpyruvate carboxylase (PPC) in mature leaves of rNAD-ME1 was reduced relative to wild type Kalanchoë fedtschenkoi
hydroxylated proline (Hyp) is found in cell wall proteins (CWPs)
proline (Pro) hydroxylation is performed by prolyl 4-hydroxylases
transient S-acylation of Arabidopsis (ARAC3, ATROP6, RAC3, RHO1PS, ROP6, AT4G35020) takes place on C21 and C156 cysteine residues Arabidopsis thaliana
post-translational modification of same gene product may result in multiple forms of a protein
ΔNΔC protein showed only background phosphorylation level phosphorylation Nicotiana benthamiana
plant NADPH oxidase (ATRBOHD, DELT1, RBOHD, AT5G47910) is target of S-nitrosylation at Cys890 Arabidopsis thaliana
peptides were identified with hydroxylation at Pro7 and triarabinosylation at Pro11 Medicago truncatula
(CESA5, MUM3, AT5G09870) is phosphorylated at Ser122, Ser126, Ser229, and Ser230
(ACK1, AtKRP6, ICK4, KRP6, AT3G19150) and (AtKRP7, ICK5, ICN6, KRP7, AT1G49620) incorporated γ32-phosphate from radiolabelled ATP Arabidopsis thaliana
N-terminal domain of (ATUPF1, LBA1, UPF1, AT5G47010) is phosphorylated phosphorylation
Nn and Nc regions of N-terminal domain of (ATUPF1, LBA1, UPF1, AT5G47010) are phosphorylated phosphorylation
ΔNU1C1 protein is strongly phosphorylated phosphorylation Nicotiana benthamiana
dolichol has indispensible role in post-translational modification of proteins
mitosis induces hyperphosphorylation of RPAP1
(CESA6, E112, IXR2, PRC1, AT5G64740) lacks evidence for phosphorylation at Ser122, Ser126, Ser229, and Ser230
PRR proteins undergo phase-dependent changes in phosphorylation state
acetylation second most pronounced peptide modification Arabidopsis thaliana
kinases and phosphatases were over-represented among proteins with oscillating phosphorylation pattern Arabidopsis thaliana
salt treatment significantly induced CATALASE 2 (CAT2, AT4G35090) phosphorylation Arabidopsis thaliana
N-terminal chloroplastic peptides some were acetylated acetylation modification Arabidopsis thaliana
SUMO substrates in Arabidopsis include RNA-related factors Arabidopsis thaliana
β–GalA residues are O–methylated at positions 3 and 4 O-methylation
hypusinated eukaryotic translation initiation factor 5A (ATELF5A-1, EIF-5A, EIF5A, ELF5A-1, AT1G13950) is thought to be active form of (ATELF5A-1, EIF-5A, EIF5A, ELF5A-1, AT1G13950)
two bands with similar molecular weights in P315 probably represent populations of GFP with and without cleaved signal peptide Zea mays
acetylation including acetylation of the protein N-terminus Arabidopsis thaliana
S-nitrosylation influences protein stability
(PRP4KB, AT1G13350) and (PRP4Kc, AT3G53640) may phosphorylate other RRM-containing proteins Arabidopsis thaliana
function of OsUGP1 might be precisely modulated by distinct post-translational modifications Oryza sativa
proteins encoding transcription factors preferentially modified by phosphorylation Oryza sativa
phenylalanine ammonia-lyase (PAL) undergoes phosphorylation following naringenin (NAR) induction Arabidopsis thaliana
native NbWRKY transcription factors acetylated by PopP2 Nicotiana benthamiana
(OPS, AT3G09070) activity could be modulated by differential phosphorylation during PPSE ontogeny Arabidopsis thaliana
receptor kinase QSK1 specifically phosphorylates plasma membrane H+-ATPase (AHA2, AtHA2, HA2, PMA2, AT4G30190) at S899 Arabidopsis thaliana
GSH (glutathione) yields reduction in recombinant APX activity Pisum sativum
cyclin-dependent kinases phosphorylate MAP3K (NPK1) Arabidopsis thaliana
(SDS, AT1G14750) in complex with CDKA;1 phosphorylates (ASY1, ATASY1, AT1G67370) Arabidopsis thaliana
(OSCA1.7, AT4G02900) is OSCA member with conserved SerXXLeu phosphosite Arabidopsis thaliana
(ATFKBP12, FKBP12, FKP12, AT5G64350) single mutant shows reduction of phosphorylated band in CONSTANS (CO) Arabidopsis thaliana
(DREB2, DREB2A, AT5G05410) undergoes post-translational modification
TRANSPORT INHIBITOR RESPONSE1 (AtTIR1, TIR1, AT3G62980) undergoes S-nitrosylation at two particular Cys residues Arabidopsis thaliana
Avirulence protein Pseudomonas phaseolicolaB (AvrPphB) is myristoylated and palmitoylated upon entry into plant cells Arabidopsis thaliana
Calmodulin (CaM)-binding proteins have physiological functions implicated in dephosphorylation
(ATCCH1, ATTPC1, FOU2, TPC1, AT4G03560) /SV channel contains putative phosphorylation sites
all ubiquitin lysines in rice, except Lys29 are modified by acetylation, malonylation, butyrylation, and/or succinylation Oryza sativa
flg22 treatment induces (BIK1, AT2G39660) phosphorylation Nicotiana benthamiana; Arabidopsis thaliana
CAMEL (Canalization-related Auxin-regulated Malectin-type (RLK, AT5G67280) ) phosphorylates five different amino acids on the cytoplasmic loop of (ATPIN1, PIN1, AT1G73590)
S/TQ sites of C1 region are phosphorylated phosphorylation
N-terminal domain of (ATUPF1, LBA1, UPF1, AT5G47010) is phosphorylated phosphorylation
cryptochrome C termini (CCT) are targets for phosphorylation
SlMPK1 and SlMPK2 phosphorylate SlBBX17 Solanum lycopersicum
less stable phosphorylation modifications occur on other residues
RNP complex formation involves RNA-methylation
SlMPK8-mediated phosphorylation of SlERF.C1 increases transcriptional activity of SlERF.C1 Solanum lycopersicum
different ROS have different activities and elicit different protein modifications
phosphorylation of proteins might affect protein function
S-nitrosylation diminishes Cys reactivity
flg22 enhances AvrPtoB S335 phosphorylation Arabidopsis thaliana; Pseudomonas syringae
ABA-triggered persulfidation drives persulfidation of the NADPH oxidase respiratory burst oxidase homolog protein D (ATRBOHD, DELT1, RBOHD, AT5G47910)
proline residue in SCOOP10#2 is often hydroxylated in Arabidopsis Arabidopsis thaliana
SUMOylation by (ATSIZ1, SIZ1, AT5G60410) modifies (ATICE1, ICE1, SCREAM, SCRM, AT3G26744) Arabidopsis thaliana
persulfidation and nitrosylation on Cys137 affect SnRK2.6 activity in competitive and opposite manners (ATOST1, OST1, P44, SNRK2-6, SNRK2.6, SRK2E, AT4G33950) activity
tyrosine phosphorylation is necessary for catalytic activity of GSK3
increased molecular mass of rice RePRP could be caused by addition of multiple glycan chains on hydroxylated Pro residues Oryza sativa
RNP complex formation involves protein phosphorylation
OPEN STOMATA 1-Like (RcOST1L) directly phosphorylates RcPIF4 on serine 198 Rosa spp.
GSK3 is constitutively phosphorylated GSK3
endoglycosidic enzyme peptide N-glycosidase F (PNGase F) employed to verify N-linked glycosylation of rice RePRPs Oryza sativa
nitrated heme is green derivative of leghemoglobin (Lb)
(ATMYB63, MYB63, AT1G79180) was cleaved R2R3-domain of (ATMYB63, MYB63, AT1G79180) Solanum lycopersicum
reversible acetylation of K183 regulates activity of GSK3 independent of inhibitory phosphorylation Homo sapiens
K189 deacetylation of (ATSK21, BIN2, DWF12, SK21, UCU1, AT4G18710) represses kinase activity of (ATSK21, BIN2, DWF12, SK21, UCU1, AT4G18710) Arabidopsis thaliana
quite a few Pro residues of RePRPs are hydroxylated Oryza sativa
hydroxylated Pro residues is important feature for glycosylation in plant hydroxyproline-rich glycoproteins (HRGPs) Oryza sativa
narrowband UV-B light does not significantly affect phosphorylation status of (BIM1, AT5G08130)
(ATOST1, OST1, P44, SNRK2-6, SNRK2.6, SRK2E, AT4G33950) phosphorylates (ATICE1, ICE1, SCREAM, SCRM, AT3G26744) Arabidopsis thaliana
glycosylation may alter hydrophilicity of signaling and defense molecules
acetylation can affect cellular localization
(BGT, GCN5, HAC3, HAG01, HAG1, HAT1, AT3G54610) acetylates (TPL, WSIP1, AT1G15750) (TOPLESS) Arabidopsis thaliana; Nicotiana benthamiana
GDP-bound and GTP-bound conformations of plant Rops were also toxin B substrates toxin B glucosylation Arabidopsis thaliana
(AT-PHH1, ATCRY2, CRY2, FHA, PHH1, AT1G04400) phosphorylation shows peak at around 15 min Arabidopsis thaliana
search parameters include variable modifications carbamidomethyl (C)
(APRR5, PRR5, AT5G24470) is known to be modified by ubiquitylation
OSCA1.3-S54A phosphoablative mutant cannot be phosphorylated at Ser54 Arabidopsis thaliana
AK-6B and AB-6B ADP-ribosylate SERRATE Arabidopsis thaliana
mammalian (TOR, AT1G50030) (mTOR) activation results in phosphorylation of eIF4E-binding proteins (4E-BPs)
glycine decarboxylase P-protein 1 (AtGLDP1, GLDP1, AT4G33010) can be O-glycosylated Arabidopsis thaliana
NΔNc protein was phosphorylated phosphorylation Nicotiana benthamiana
NMD-relevant phosphorylated sites are in the S/TQ context potential PIKK target sites
post-translational sulfation of PSK precursor proteins is required for peptide activity Arabidopsis thaliana
peptide tyrosine sulfation is mediated by (AQC1, HPS7, TPST, AT1G08030) Arabidopsis thaliana; animals
terminal segments of plant (ATUPF1, LBA1, UPF1, AT5G47010) are also phosphorylated plant (ATUPF1, LBA1, UPF1, AT5G47010)
GTPγS-loaded (ARAC5, ATGP3, ATROP4, ROP4, AT1G75840) could be glucosylated by toxin B Arabidopsis thaliana
hydroxylated prolines subsequently O-glycosylated to form hydroxyproline-rich glycoproteins
carboxypeptidase-mediated cleavage results in C-terminal truncation
regulation and impact of methylation/demethylation is barely studied current knowledge Arabidopsis thaliana
glutamate decarboxylase was found to be phosphorylated in mature Arabidopsis pollen Arabidopsis thaliana
basal AtSnRK1 activity is unable to exhaustively phosphorylate huge amounts of (ACK1, AtKRP6, ICK4, KRP6, AT3G19150) present in OE- WT plants Arabidopsis thaliana
redox-based post-translational modification of (AtTIR1, TIR1, AT3G62980) by NO reveals E3-ubiquitin-ligase Arabidopsis thaliana
(ACK1, AtKRP6, ICK4, KRP6, AT3G19150) T150D mutant exhibited phosphorylation on Thr152 Arabidopsis thaliana
(AQC1, HPS7, TPST, AT1G08030) loss-of-function mutants suffer from loss of tyrosine sulfation at all tyrosine-sulfated peptides Arabidopsis thaliana
(ATOST1, OST1, P44, SNRK2-6, SNRK2.6, SRK2E, AT4G33950) phosphorylates Thr(38) in the amino-terminal cytoplasmic domain of (ATCLC-A, ATCLCA, CLC-A, CLCA, AT5G40890) Arabidopsis thaliana
four proteins (K14 and S16 in LOC_Os04g47220; K358 and S360 in LOC_Os01g70020; S570 and K572 in LOC_Os03g40010; K81 and S83 in LOC_Os03g51470) observed closely neighboring acetylation and phosphorylation sites in closely spaced post-translational modifications Oryza sativa
(ATSNAK2, GRIK1, AT3G45240) alone was unable to phosphorylate (ACK1, AtKRP6, ICK4, KRP6, AT3G19150) /7 Arabidopsis thaliana
(AtNPF6.3, ATNRT1, B-1, CHL1, CHL1-1, NPF6.3, NRT1, NRT1.1, AT1G12110) has high- or low-affinity function depending on phosphorylation status of threonine-101 (T101) Arabidopsis thaliana
calcineurin B-like proteins ( (ATCBL2, CBL2, SCaBP1, AT5G55990) /3) and CBL-interacting protein kinases ( (CIPK3, SnRK3.17, AT2G26980) /9/26) phosphorylate Metal tolerance protein 11 (ATMTP11, MTP11, AT2G39450) Arabidopsis thaliana
N-terminal (ATUPF1, LBA1, UPF1, AT5G47010) mutants (NP1-4A, NΔNn) were also heavily phosphorylated phosphorylation Nicotiana benthamiana
TOP2–SA interaction may be dependent on plant-specific modifications of (TOP2, AT5G10540) Arabidopsis thaliana
S-nitrosoglutathione (GSNO) inhibits (ALDH3H1, ALDH4, AT1G44170) Arabidopsis thaliana
catalytic thiol of (ALDH3H1, ALDH4, AT1G44170) is converted into catalytically non-active nitrosothiol Arabidopsis thaliana
(ATIRT1, IRT1, AT4G19690) 4HA showed lack of K63 polyubiquitination
OsSMC3 (structural maintenance of chromosomes protein 3) contains acetylation sites at K105 and K106 in acetyl-peptide TVASK(ac)K(ac)DEYYLDGK Oryza sativa
114 proteins undergone dual modifications for acetylation and phosphorylation in rice vegetative tissues Oryza sativa
other WRKY proteins are also acetylated by PopP2 Arabidopsis thaliana
PopP2 acetylates lysines within canonical WRKYGQK motif of (ATWRKY52, RRS1, RRS1-R, SLH1, AT5G45260)
peptide SYPTVSPDYQK contains nitrated Tyr5 Pisum sativum
proanthocyanidins in white cotton fibres were modified by acylation
plant cytoskeletal proteins can undergo nitration
phosphorylation plays roles in TGB protein functions
several members of Arabidopsis PROPEPs are SUMOylation substrates Arabidopsis thaliana
Phosphorylated S175 and S267 residues are necessary for biochemical function of persulfidation in (ATOST1, OST1, P44, SNRK2-6, SNRK2.6, SRK2E, AT4G33950)
CH and helicase domains were weakly phosphorylated phosphorylation
UPF1-SMG7 complex formation is most probably in a phospho-dependent manner phosphorylation
zinc excess triggers (ATIRT1, IRT1, AT4G19690) phosphorylation Arabidopsis thaliana
CALMODULIN-BINDING RECEPTOR-LIKE CYTOPLASMIC KINASE 3 (CRCK3, AT2G11520) phosphorylated CAT2 at Thr209 residue Arabidopsis thaliana
tyrosylprotein sulfotransferase (AQC1, HPS7, TPST, AT1G08030) catalyzes post-translational sulfation of PSK precursor proteins Arabidopsis thaliana
toxin B was able to glucosylate (ARAC5, ATGP3, ATROP4, ROP4, AT1G75840) Arabidopsis thaliana
function of aldehyde dehydrogenases (ALDHs) may be susceptible to posttranslational regulation through S-nitrosation Arabidopsis thaliana
ethylene production enhanced phosphorylation of SlERF.C1 Solanum lycopersicum
K271 acetylation of FolGsk3 impairs catalytic activity of FolGsk3 Fusarium oxysporum
(AtCLV3, CLV3, AT2G27250) propeptide is processed and modified with L-arabinose into active 13 amino acid glycopeptide form, CLV3p Arabidopsis thaliana
acetylation including acetylation of the N-terminal α-amine of peptides Arabidopsis thaliana
auxin provides environment suitable for S-nitrosylation Arabidopsis thaliana
similar regulatory mechanism in plants possibly occurs through different effector kinases targeting Thr residues Arabidopsis thaliana
(ATNRAMP1, NRAMP1, PMIT1, AT1G80830) contains nine predicted phosphorylated residues Arabidopsis thaliana
nascent and bulk proteins from AHA-treated cell cultures showed small differences in oxidation (higher frequency in bulk dataset) and N-terminal acetylation (higher frequency in nascent dataset) Arabidopsis thaliana
potential PIKK target (S/TQ) sites were mutated N-terminal domain
continuous blue-light treatment does not result in complete phosphorylation of all (AT-PHH1, ATCRY2, CRY2, FHA, PHH1, AT1G04400) molecules Arabidopsis thaliana
(CP29A, AT3G53460) is characterized by free N-terminus Arabidopsis thaliana
this first step in Met (methionine) oxidation is reversible
mass spectrometry and site-directed mutagenesis identified phosphorylation sites fitting SP motif Arabidopsis thaliana
oxidations or hydroxylations were localized in PSHWD region
proline (Pro) hydroxylation and consecutive O-glycosylation occurs in Hyp/Pro-rich proteins (H/PRPs)
(ATTSB1, TRP2, TRPB, TSB1, AT5G54810) sulfenylation decreases (ATTSB1, TRP2, TRPB, TSB1, AT5G54810) enzymatic activity
(ATMPK4, MAPK4, MPK4, AT4G01370) phosphorylates Thr386, Ser448, and Ser486 of (AtSTOP1, STOP1, AT1G34370)
nitration in plants results in loss of function
S-nitrosation involves covalent but reversible oxidation of thiol groups
Hydroxyproline O-arabinosyltransferases (HPATs) catalyze the transfer to hydroxyl group of Hyp residues
the fact that so many proteins contained at least one, and many contained more than one, (DDP1, PTM, AT5G35210) (posttranslational modification) further suggests that approaches beyond transcriptional profiling will be not only desired, but required, if we are to better understand how mitochondria help plants respond to stress and changing environments
ATP-induced NO plays key role for S-nitrosylation of proteins
MAPKs may regulate other PIFs through different residues Arabidopsis thaliana
card1-1 mutant shows phosphorylation status change at serine5 and serine2 of the repeat Arabidopsis thaliana
Gly dehydrogenase is the most modified protein Solanum tuberosum
P peptide isotopic massifs may correspond to oxidation or hydroxylation of amino acids
Proteomic-based studies increased number of known glutathionylated protein targets photosynthetic organisms
bioinformatic tool developed to locate N-glycosylation Arabidopsis thaliana
glutathionylation was found specific for thioredoxin f (TRX f) Arabidopsis thaliana
at least in one case we know that such an interaction takes place
glutathione is involved in glutathionylation
the oxidation of a Met (methionine) residue to Met sulfoxide is likely a regulatory mechanism
S86 phosphorylation was reduced in light Arabidopsis thaliana
SSH group has stronger activity than SNO group
AK-6B have ADP ribosylation activity
S3, S13 and T29 residues are phosphorylated phosphorylation
osmtd2-2 mutant anthers show upregulation of genes involved in protein modification Oryza sativa
post-translational modifications govern protein ubiquitination in the nucleus
Arabidopsis (HEI10, AT1G53490) is modified by poly-SUMOylation Arabidopsis thaliana
hydroxyaspartate has never been reported in plant proteins
a relatively unexplored research area is the interaction between different (DDP1, PTM, AT5G35210) (posttranslational modification) types
about 100 proteins had more than 10 (DDP1, PTM, AT5G35210) (posttranslational modification) sites Solanum tuberosum
rNAD-ME1 showed reduced phosphoenolpyruvate carboxylase (PPC) phosphorylation at the dark/light transition Kalanchoë fedtschenkoi
S228A mutation of (ATSOS2, CIPK24, SNRK3.11, SOS2, AT5G35410) (Salt Overly Sensitive 2) decreases autophosphorylation rate of (ATSOS2, CIPK24, SNRK3.11, SOS2, AT5G35410) Arabidopsis thaliana
initiation of regulation at multiple levels is probably via cysteine oxidation and protein phosphatase activities Zea mays
post-translational modification (PTM) of APX mainly affects Met or Cys residues
CALCIUM-DEPENDENT PROTEIN KINASE 6 (AeCDPK6) is required for hyperoside-induced phosphorylation of AeMYB30 Abelmoschus esculentus
S-acylation is reversible lipid modification
FERONIA receptor kinase regulates AHA2 through transient phosphorylation at Ser-899 site Arabidopsis thaliana
paralogs of cytosolic ribosomal proteins (RPs) can differentially change abundance
Methods for identifying and analyzing glutathionylated proteins allowed identification of nearly 200 glutathionylated protein targets mammals
proline (Pro) hydroxylation and consecutive O-glycosylation occurs in Hyp-rich glycoproteins (HRGPs)
AVRPPHB SUSCEPTIBLE1 (PBS1, AT5G13160) is targeted to plasma membrane (PM) via S-acylation at its N terminus Arabidopsis thaliana
2-Cys Prxs undergo S-nitrosylation
HIPP proteins are modified posttranslationally by attachment of lipid moieties
(AtMYB62, BW62B, BW62C, MYB62, AT1G68320) contains conserved sumoylation target domains Arabidopsis thaliana