Literature DB >> 26599633

Correction: Modulation of the Surface Proteome through Multiple Ubiquitylation Pathways in African Trypanosomes.

Martin Zoltner, Ka Fai Leung, Sam Alsford, David Horn, Mark C Field.   

Abstract

Entities:  

Year:  2015        PMID: 26599633      PMCID: PMC4657948          DOI: 10.1371/journal.ppat.1005291

Source DB:  PubMed          Journal:  PLoS Pathog        ISSN: 1553-7366            Impact factor:   6.823


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There are typographical errors in Table 1. Some of the sub-rows were separated into individual rows, when they should be included in prior rows. Please see the corrected table here.
Table 1

Percentage abundance of selected protein groups upon TbUsp7 and TbVdu1 RNAi derived from normalised SILAC ratios.

AnnotationProtein groupProtein abundance upon RNAi (percent relative to non-induced)Predicted featuresPredicted Trans-membrane domainPredictedN-terminal signalNumber of lysines in cytoplasmic domainPredicted GPI-anchorSequence length(inclusive signal seq.)
TbUsp7 26hTbUsp7 48hTbVdu1 48h
USP7Tb927.9.1447028 *13 *101 (+/- 3)USP7_C2 superfamilyNoNoNANA1161
VDU1Tb927.11.12240ND105 *ND Peptidase_C19 superfamily NoNoNANA790
ISG75Tb927.5.39043 (+/- 4)40 (+/- 34)52 (+/- 5)ISG65-75 superfamily468–490Yes5NA522
Tb927.5.400468–4904522
Tb927.5.350468–4904522
Tb927.5.36042 (+/- 3)39 (+/- 26)53 (+/- 4)ISG65-75 superfamily469–491Yes5NA523
Tb927.5.370NDND64 (+/- 23) *ISG65-75 superfamily469–491Yes5NA523
ISG65Tb927.2.328096 (+/- 2)117 (+/-5)69 (+/- 8)ISG65-75 superfamily386–408Yes4NA436
Tb927.2.3290388–4104436
Tb927.2.3300388–4104436
Tb927.2.3310388–4103436
Tb927.2.332097 (+/- 2)109 (+/- 41)45 (+/- 2)ISG65-75 superfamily387–409Yes3NA437
Tb927.2.327090 (+/- 2)105 (+/- 22)62 (+/- 8)ISG65-75 superfamily388–410Yes4NA436
Tb11.v5.0231469–4915523
Tb11.v5.0731388–4102430
ISG-relatedTb927.5.63075 (+/- 3)79 (+/- 16)76 (+/- 11)ISG65-75 superfamily349–372Yes4NA401
ISG64Tb927.5.1390*92 (+/- 3)98 (+/- 2)87 (+/- 19)ISG65-75 superfamily376–398Yes4NA434
Tb927.5.1410377–3994435
Tb927.5.143097 (+/- 9)107 (+/- 5)94 (+/- 20)ISG65-75 superfamily376–398Yes4NA434
MBAP1Tb927.11.1313050 (+/- 1)29 (+/- 2)101 (+/- 11)acidic phosphatase [33]459–481Yes2No524
putative type I membrane protein 1Tb927.7.47038 (+/- 1)32 *85 (+/- 4)182–204Yes4No297
putative type I membrane protein 2Tb927.9.1148045 (+/- 4)34 (+/- 3)87 (+/- 2)512–537Yes1No561
putative type IV membrane proteinTb927.11.755051 (+/- 2)38 *97 (+/- 7)*49–71,112–134,141–163,190–212No3No221
VAMP7BTb927.5.356070 (+/- 3)62 (+/- 12)81 (+/- 21)Vesicle-associated membrane protein184–206NoNoNo796
TPR-repeat proteinTb927.11.81046 *55 (+/- 4)97 (+/- 4)Tetratrico peptide repeat [42]NoNoNoNo216
ESAG5Tb11.v5.0826142 (+/- 2)170 (+/- 26)132 (+/- 12)potential lipid or lipo-polysaccha ride binding [36,37]NoYesNANo464
Tb927.7.6860480
ESAG6Tb927.7.3250132 (+/- 17)202 (+/-56)101 (+/- 43)*Transferrin receptorNoYesNAYes397
ESAG7Tb927.7.3260NoYesNANo339
ESAG2Tb927.11.14620114 (+/- 8)115 (+/- 21)85 (+/- 3)NoYesNAYes458
VSG-related proteinTb927.7.180126 (+/- 17)139 *117 (+/- 4)*VSG-relatedNoYesNANo437

Values represent average percentage protein abundance relative to uninduced cells ± standard deviation. TbUsp7 and TbVdu1 RNAi samples were analysed at indicated time points in experimental duplicate and triplicate, respectively. Asterisks mark proteins not quantified in all replicates. Polypeptide features predicted using TMHMM2 for trans-membrane domains [39], signalP for N-terminal ER-targeting signal [40], PredGPI for GPI-anchor addition C-terminal signal sequence [41] and TPRpred for tetratrico peptide repeats [42]. Predictions are given as Yes, No responses or sequence positions (inclusive signal sequence) using default parameters. In most cases the topology of the protein is experimentally known or predictable based on close homology of experimentally derived information. All protein hits shown have been inspected for their genomic context and integrity. Protein groups consist of indistinguishable paralogs, sharing identical quantified peptides. For the complete quantification data see S1 Table. NA; not applicable, ND; not detected.

Values represent average percentage protein abundance relative to uninduced cells ± standard deviation. TbUsp7 and TbVdu1 RNAi samples were analysed at indicated time points in experimental duplicate and triplicate, respectively. Asterisks mark proteins not quantified in all replicates. Polypeptide features predicted using TMHMM2 for trans-membrane domains [39], signalP for N-terminal ER-targeting signal [40], PredGPI for GPI-anchor addition C-terminal signal sequence [41] and TPRpred for tetratrico peptide repeats [42]. Predictions are given as Yes, No responses or sequence positions (inclusive signal sequence) using default parameters. In most cases the topology of the protein is experimentally known or predictable based on close homology of experimentally derived information. All protein hits shown have been inspected for their genomic context and integrity. Protein groups consist of indistinguishable paralogs, sharing identical quantified peptides. For the complete quantification data see S1 Table. NA; not applicable, ND; not detected.
  1 in total

1.  Modulation of the Surface Proteome through Multiple Ubiquitylation Pathways in African Trypanosomes.

Authors:  Martin Zoltner; Ka Fai Leung; Sam Alsford; David Horn; Mark C Field
Journal:  PLoS Pathog       Date:  2015-10-22       Impact factor: 6.823

  1 in total
  2 in total

1.  Landscapes of Protein Posttranslational Modifications of African Trypanosoma Parasites.

Authors:  Naiwen Zhang; Ning Jiang; Kai Zhang; Lili Zheng; Di Zhang; Xiaoyu Sang; Ying Feng; Ran Chen; Na Yang; Xinyi Wang; Zhongyi Cheng; Xun Suo; Zhaorong Lun; Qijun Chen
Journal:  iScience       Date:  2020-04-18

2.  Instability of aquaglyceroporin (AQP) 2 contributes to drug resistance in Trypanosoma brucei.

Authors:  Juan F Quintana; Juan Bueren-Calabuig; Fabio Zuccotto; Harry P de Koning; David Horn; Mark C Field
Journal:  PLoS Negl Trop Dis       Date:  2020-07-09
  2 in total

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