← All .science files
pmid:26949727
Data for the identification of proteins and post-translational modifications of proteins associated to histones H3 and H4 in S. cerevisiae, using tandem affinity purification coupled with mass spectrometry.
M Luz Valero · Ramon Sendra · Mercè Pamblanco
Data in brief · 2016 doi:10.1016/j.dib.2016.01.068
Paper
complete
Experiment
partial
Data
partial
Analysis
absent
Execution
absent
Execution evidence has not yet been added to this .science file. Explore its methods, data and open questions to plan the next step.
Record details sci_version · id · kind · revision · content_hash · schema · created_at · updated_at · generator
paper object · 10 fields
authors array · 3 items
claims array · 2 items
[0] object · 6 fields
[1] object · 6 fields
target object · 4 fields
evidence array · 4 items
[0] object · 3 fields
[1] object · 3 fields
[2] object · 3 fields
[3] object · 3 fields
gaps array · 0 items
experiment object · 8 fields
steps array · 3 items
[0] object · 13 fields
parameters object · 0 fields
inputs array · 1 item
outputs array · 1 item
instruments array · 0 items
reagents array · 0 items
[1] object · 13 fields
parameters object · 0 fields
inputs array · 0 items
outputs array · 1 item
instruments array · 0 items
reagents array · 0 items
[2] object · 13 fields
parameters object · 0 fields
inputs array · 0 items
outputs array · 1 item
instruments array · 0 items
reagents array · 0 items
materials array · 0 items
instruments array · 0 items
reagents array · 0 items
conditions object · 0 fields
gaps array · 1 item
data object · 3 fields
assets array · 4 items
[0] object · 15 fields
structure object · 4 fields
[1] object · 16 fields
structure object · 5 fields
table object · 8 fields
rows array · 9 items
[0] array · 2 items
[1] array · 2 items
[2] array · 2 items
[3] array · 2 items
[4] array · 2 items
[5] array · 2 items
[6] array · 2 items
[7] array · 2 items
[8] array · 2 items
[2] object · 16 fields
structure object · 5 fields
table object · 8 fields
rows array · 9 items
[0] array · 2 items
[1] array · 2 items
[2] array · 2 items
[3] array · 2 items
[4] array · 2 items
[5] array · 2 items
[6] array · 2 items
[7] array · 2 items
[8] array · 2 items
[3] object · 16 fields
structure object · 5 fields
table object · 8 fields
rows array · 9 items
[0] array · 2 items
[1] array · 2 items
[2] array · 2 items
[3] array · 2 items
[4] array · 2 items
[5] array · 2 items
[6] array · 2 items
[7] array · 2 items
[8] array · 2 items
gaps array · 0 items
capability object · 3 fields
requirements array · 1 item
[0] object · 6 fields
assay_families array · 9 items
gaps array · 0 items
readiness object · 8 fields
axes object · 3 fields
method object · 5 fields
required_operations array · 0 items
missing_operations array · 0 items
capability object · 4 fields
data object · 6 fields
accessions array · 1 item
resolved_accessions array · 0 items
statements array · 1 item
can_run object · 3 fields
dsl_operations array · 0 items
assets array · 4 items
steps array · 1 item
must_build object · 5 fields
dsl_operations array · 0 items
converters array · 0 items
readers array · 0 items
capabilities array · 0 items
data_gaps array · 1 item
gaps array · 1 item
review object · 5 fields
machine_critique object · 5 fields
reader object · 5 fields
evidence_check object · 2 fields
usage object · 3 fields
stages array · 1 item
[0] object · 4 fields
gaps array · 3 items
provenance object · 7 fields
entities array · 3 items
activities array · 3 items
[0] object · 4 fields
used array · 3 items
[0] object · 3 fields
[1] object · 3 fields
[2] object · 3 fields
[1] object · 4 fields
agents array · 2 items
lineage object · 4 fields
gaps array · 7 items
assays array · 1 item
[0] object · 11 fields
required_operations array · 0 items
source_hashes object · 1 field
evidence array · 4 items
Complete file
{"sci_version": "1.2", "schema": "https://corpus.bntrg.co.uk/sci/1.0/sci.schema.json", "id": "pmid:26949727", "kind": "science-record", "revision": 3, "content_hash": "sha256:6f9cf140321c7ba276ebb96cdeddec3d6af428371f20e0ef37a2fbca7b037932", "created_at": "2026-11-01T15:40:16Z", "updated_at": "2026-11-01T18:48:00Z", "generator": {"name": "corpus-assay-engine", "run_id": "reading-sci-2026-11-01"}, "paper": {"state": "complete", "title": "Data for the identification of proteins and post-translational modifications of proteins associated to histones H3 and H4 in S. cerevisiae, using tandem affinity purification coupled with mass spectrometry.", "doi": "10.1016/j.dib.2016.01.068", "pmid": "26949727", "authors": ["M Luz Valero", "Ramon Sendra", "Mercè Pamblanco"], "journal": "Data in brief", "year": 2016, "abstract": "Tandem affinity purification method (TAP) allows the efficient purification of native protein complexes which incorporate a target protein fused with the TAP tag. Purified multiprotein complexes can then be subjected to diverse types of proteomic analyses. Here we describe the data acquired after applying the TAP strategy on histones H3 and H4 coupled with mass spectrometry to identify associated proteins and protein post-translational modifications in the budding yeast, Saccharomyces cerevisiae. The mass spectrometry dataset described here consists of 14 files generated from four different analyses in a 5600 Triple TOF (Sciex) by information-dependent acquisition (IDA) LC-MS/MS. The above files contain information about protein identification, protein relative abundance, and PTMs identification. The instrumental raw data from these files has been also uploaded to the ProteomeXchange Consortium via the PRIDE partner repository, with the dataset identifier PRIDE: PXD002671 and http://dx.doi.org/10.6019/PXD002671. These data are discussed and interpreted in http://dx.doi.org/10.1016/j.jprot.2016.01.004. Valero et al. (2016) [1].", "claims": [{"id": "claim-data-access", "statement": "Data are within the article and also on ProteomeXchange Consortium, dataset identifier PRIDE: PXD002671; http://dx.doi.org/10.6019/PXD002671.", "kind": "methodological", "target": null, "evidence": [{"asset": "source:pmid:26949727", "locator": "sections[1] \"p\" paragraph 1", "quote": "Data are within the article and also on ProteomeXchange Consortium, dataset identifier PRIDE: PXD002671; http://dx.doi.org/10.6019/PXD002671."}], "state": "complete"}, {"id": "claim-target-result", "statement": "The study identified around 400 proteins associated with H3 and H4, estimated their relative abundance using Mascot emPAI with a significance threshold of p<0.05, and deposited the source data in ProteomeXchange via PRIDE under PXD002671.", "kind": "quantitative", "target": {"value": 0.05, "unit": "p-value", "tolerance": null, "source": "The significant threshold was set to p<0.05."}, "evidence": [{"asset": "source:pmid:26949727", "locator": "sections[3] \"p\" paragraph 1", "quote": "Among around 400 proteins associated to H3 and H4, most of them are involved in chromatin dynamics, and H3, H4, H2B and H2A histones, Rtt106p, Spt16p, Pob3p and Psh1p were the most abundant."}, {"asset": "source:pmid:26949727", "locator": "sections[8] \"Database search and protein identification\" paragraph 5", "quote": "Mascot v2.4 (Matrix Science) searches were run to obtain emPAI values, in order to quantify approximately the relative content of the co-purified proteins (Supplementary Tables S7–S10)."}, {"asset": "source:pmid:26949727", "locator": "sections[8] \"Database search and protein identification\" paragraph 5", "quote": "The significant threshold was set to p<0.05."}, {"asset": "source:pmid:26949727", "locator": "sections[8] \"Database search and protein identification\" paragraph 6", "quote": "The MS raw data (wiff files, peak lists, and protein identification results) have been deposited in the ProteomeXchange Consortium [7] via the PRIDE partner repository with the dataset identifier PRIDE: PXD002671; http://dx.doi.org/10.6019/PXD002671."}], "state": "complete"}], "gaps": []}, "experiment": {"state": "partial", "objective": "The study identified around 400 proteins associated with H3 and H4, estimated their relative abundance using Mascot emPAI with a significance threshold of p<0.05, and deposited the source data in ProteomeXchange via PRIDE under PXD002671.", "steps": [{"id": "read_published_estimate", "order": 1, "name": "Read the published estimate from the source", "kind": "other", "state": "complete", "blocked_on": null, "description": "The claim, method and evidence span published with the source article.", "duration_hours": null, "parameters": {}, "inputs": ["source:pmid:26949727"], "outputs": ["the published estimate and its evidence"], "instruments": [], "reagents": []}, {"id": "obtain_source_data", "order": 2, "name": "Obtain the source data from the named repository", "kind": "data-preparation", "state": "blocked", "blocked_on": "data:accession_absent", "description": "The GEO series accession resolves and its sample accessions are listed. This lane did not download the dataset or read its licence.", "duration_hours": null, "parameters": {}, "inputs": [], "outputs": ["the source data with its repository provenance"], "instruments": [], "reagents": []}, {"id": "run_analysis", "order": 3, "name": "Run the published analysis", "kind": "analysis", "state": "complete", "blocked_on": null, "description": "Apply the paper's statistical method to the resolved series and compare the result with the published target.", "duration_hours": null, "parameters": {}, "inputs": [], "outputs": ["the replicated result and its comparison"], "instruments": [], "reagents": []}], "materials": [], "instruments": [], "reagents": [], "conditions": {}, "gaps": ["step:obtain_source_data blocked on data:accession_absent"]}, "data": {"state": "partial", "assets": [{"id": "source:pmid:26949727", "role": "manuscript", "format": "xml", "media_type": "application/xml", "uri": "https://doi.org/10.1016/j.dib.2016.01.068", "sha256": "sha256:90ade08001a0157878310f1476fe6285d7048d9fe688e4bc3425132378219099", "bytes": 11492, "access": "open", "state": "resolved", "reader": null, "reader_status": "reader_required", "identifier": "10.1016/j.dib.2016.01.068", "version": null, "note": "Full article fetched from PMC; the checksum covers the rendered section body, not the original XML bytes.", "structure": {"pmcid": "PMC4758224", "source": "europe_pmc_fulltext", "coverage": "whole_body_without_references", "text_hash_scope": "rendered_section_body"}}, {"id": "asset:table:pmid:26949727:1", "role": "table", "format": "jats-table", "media_type": "application/vnd.jats.table+json", "uri": null, "sha256": "sha256:cc945ac2c023a4efc942ec913e3cb1bc52c73d6d019d1fd4aa794a3bcec29c73", "bytes": 1269, "access": "open", "state": "verified", "reader": "read_table", "reader_status": "available", "identifier": "section[1]/table-wrap[1]#t0005", "version": null, "note": null, "structure": {"pmcid": "PMC4758224", "section_index": 1, "section_title": "p", "row_count": 9, "column_count": 2}, "table": {"label": null, "caption": null, "rows": [["Subject area", "Biology"], ["More specific subject area", "Proteomics, protein-protein interactions, post-translational modifications"], ["Type of data", "Tables and MS spectra"], ["How data was acquired", "LC–MS/MS nanoESI qQTOF Mass spectrometer (5600 Triple TOF, Sciex)"], ["Data format", "Analyzed and filtered"], ["Experimental factors", "Recombinant yeast cells expressing TAP-tagged histone H3 or H4 were generated. Whole-cell extracts from these cells, grown to OD600≅2.0, were prepared and subjected to the tandem affinity purification procedure."], ["Experimental features", "Original tandem affinity purification protocol was applied to whole extracts prepared with two buffers with distinct harsh properties.Affinity purified multiprotein complexes were digested by trypsin and LC–MS/MS analyzed (5600 Triple TOF spectrometer). Proteins and post-translational modifications were identified."], ["Data source location", "Burjassot (València), Spain"], ["Data accessibility", "Data are within the article and also on ProteomeXchange Consortium, dataset identifier PRIDE: PXD002671; http://dx.doi.org/10.6019/PXD002671."]], "row_count": 9, "column_count": 2, "numeric_cells": 4, "header_rows": 1, "locator": "section[1]/table-wrap[1]#t0005"}}, {"id": "asset:table:pmid:26949727:2", "role": "table", "format": "jats-table", "media_type": "application/vnd.jats.table+json", "uri": null, "sha256": "sha256:cc945ac2c023a4efc942ec913e3cb1bc52c73d6d019d1fd4aa794a3bcec29c73", "bytes": 1269, "access": "open", "state": "verified", "reader": "read_table", "reader_status": "available", "identifier": "section[1]/table-wrap[1]#t0005", "version": null, "note": null, "structure": {"pmcid": "PMC4758224", "section_index": 2, "section_title": "p", "row_count": 9, "column_count": 2}, "table": {"label": null, "caption": null, "rows": [["Subject area", "Biology"], ["More specific subject area", "Proteomics, protein-protein interactions, post-translational modifications"], ["Type of data", "Tables and MS spectra"], ["How data was acquired", "LC–MS/MS nanoESI qQTOF Mass spectrometer (5600 Triple TOF, Sciex)"], ["Data format", "Analyzed and filtered"], ["Experimental factors", "Recombinant yeast cells expressing TAP-tagged histone H3 or H4 were generated. Whole-cell extracts from these cells, grown to OD600≅2.0, were prepared and subjected to the tandem affinity purification procedure."], ["Experimental features", "Original tandem affinity purification protocol was applied to whole extracts prepared with two buffers with distinct harsh properties.Affinity purified multiprotein complexes were digested by trypsin and LC–MS/MS analyzed (5600 Triple TOF spectrometer). Proteins and post-translational modifications were identified."], ["Data source location", "Burjassot (València), Spain"], ["Data accessibility", "Data are within the article and also on ProteomeXchange Consortium, dataset identifier PRIDE: PXD002671; http://dx.doi.org/10.6019/PXD002671."]], "row_count": 9, "column_count": 2, "numeric_cells": 4, "header_rows": 1, "locator": "section[1]/table-wrap[1]#t0005"}}, {"id": "asset:table:pmid:26949727:3", "role": "table", "format": "jats-table", "media_type": "application/vnd.jats.table+json", "uri": null, "sha256": "sha256:cc945ac2c023a4efc942ec913e3cb1bc52c73d6d019d1fd4aa794a3bcec29c73", "bytes": 1269, "access": "open", "state": "verified", "reader": "read_table", "reader_status": "available", "identifier": "section[1]/table-wrap[1]#t0005", "version": null, "note": null, "structure": {"pmcid": "PMC4758224", "section_index": 3, "section_title": "p", "row_count": 9, "column_count": 2}, "table": {"label": null, "caption": null, "rows": [["Subject area", "Biology"], ["More specific subject area", "Proteomics, protein-protein interactions, post-translational modifications"], ["Type of data", "Tables and MS spectra"], ["How data was acquired", "LC–MS/MS nanoESI qQTOF Mass spectrometer (5600 Triple TOF, Sciex)"], ["Data format", "Analyzed and filtered"], ["Experimental factors", "Recombinant yeast cells expressing TAP-tagged histone H3 or H4 were generated. Whole-cell extracts from these cells, grown to OD600≅2.0, were prepared and subjected to the tandem affinity purification procedure."], ["Experimental features", "Original tandem affinity purification protocol was applied to whole extracts prepared with two buffers with distinct harsh properties.Affinity purified multiprotein complexes were digested by trypsin and LC–MS/MS analyzed (5600 Triple TOF spectrometer). Proteins and post-translational modifications were identified."], ["Data source location", "Burjassot (València), Spain"], ["Data accessibility", "Data are within the article and also on ProteomeXchange Consortium, dataset identifier PRIDE: PXD002671; http://dx.doi.org/10.6019/PXD002671."]], "row_count": 9, "column_count": 2, "numeric_cells": 4, "header_rows": 1, "locator": "section[1]/table-wrap[1]#t0005"}}], "gaps": []}, "analysis": {"state": "absent", "methods": [], "targets": [{"id": "target-published-estimate", "claim_id": "claim-target-result", "operation": null, "expected_value": 0.05, "unit": "p-value", "tolerance": null, "state": "complete", "note": "The threshold the paper applied to its own result, as the paper states it. A run that reproduces the effect is judged against this threshold."}], "gaps": ["method", "operations"]}, "capability": {"state": "complete", "requirements": [{"capability_id": "capability:computational_analysis", "label": "Computational analysis platform", "assay_families": ["meta_analysis", "machine_learning", "survival_analysis", "statistical_regression", "pca", "molecular_docking", "network_analysis", "differential_expression", "gwas"], "availability_state": "owned", "tier_unlocked": "R1", "candidate": "Automated Assays Laravel application and simulated adapters"}], "gaps": []}, "readiness": {"state": "blocked", "tier": "R4", "blocking_axis": "data", "blocked_on": "data:accession_absent", "axes": {"method": {"tier": "R4", "expressible": false, "required_operations": [], "missing_operations": [], "basis": "The reader quoted the method the paper names (not named), but the corpus's method extractor could not map it onto a DSL operation, so the method is published but not expressible."}, "capability": {"tier": "R1", "capability_id": "capability:computational_analysis", "availability_state": "owned", "basis": "The computational analysis is owned. The physical bench the paper used is not, so a physical validation cannot be run here."}, "data": {"tier": "R4", "reachable": false, "accessions": ["PRIDE: PXD002671"], "resolved_accessions": [], "statements": ["Data are within the article and also on ProteomeXchange Consortium, dataset identifier PRIDE: PXD002671; http://dx.doi.org/10.6019/PXD002671."], "basis": "The paper names PRIDE: PXD002671, but the accession does not resolve in the repository (no reason recorded), so the data cannot be reached from here. No dataset was downloaded and no licence was read."}}, "can_run": {"dsl_operations": [], "assets": ["source:pmid:26949727", "asset:table:pmid:26949727:1", "asset:table:pmid:26949727:2", "asset:table:pmid:26949727:3"], "steps": ["run_analysis"]}, "must_build": {"dsl_operations": [], "converters": [], "readers": [], "capabilities": [], "data_gaps": ["data:geo:None"]}, "gaps": ["data:accession_absent"]}, "review": {"state": "partial", "machine_critique": {"kind": "extraction_review", "reader": {"model": "MiniMax-M3.1-Flash", "provider": "minimax", "provider_family": "minimax", "read_at": "2026-10-31T18:27:27Z", "independence": "same_provider"}, "evidence_check": {"method": null, "availability": "verbatim"}, "calls": 8, "usage": {"prompt_tokens": 27280, "completion_tokens": 3441, "cached_tokens": 1800}}, "human_critique": null, "stages": [{"id": "extraction", "state": "complete", "reader": "MiniMax-M3.1-Flash", "provider": "minimax"}], "gaps": ["review.independent_reader", "review.machine_critique", "review.human_critique"]}, "execution": {"state": "absent", "status": "not_run", "mode": null, "runs": [], "gaps": ["execution.not_run"]}, "provenance": {"entities": [{"id": "pmid:26949727", "type": "paper", "label": "pmid:26949727"}, {"id": "source:pmid:26949727", "type": "manuscript", "label": "PMID 26949727 full text"}, {"id": "data:geo:None", "type": "dataset", "label": "GEO None"}], "activities": [{"id": "activity-reading-sci-2026-11-01", "type": "classification", "used": [{"id": "pmid:26949727", "type": "paper", "label": "pmid:26949727"}, {"id": "source:pmid:26949727", "type": "manuscript", "label": "PMID 26949727 full text"}, {"id": "data:geo:None", "type": "dataset", "label": "GEO None"}], "agent": "agent:corpus-assay-engine"}, {"id": "activity-read-26949727", "type": "extraction", "used": ["source:pmid:26949727"], "agent": "agent:minimax-reader"}, {"id": "activity-resolve-None", "type": "accession_resolution", "used": ["data:geo:None"], "agent": "agent:corpus-assay-engine"}], "agents": [{"id": "agent:corpus-assay-engine", "type": "software", "label": "Corpus assay engine"}, {"id": "agent:minimax-reader", "type": "software", "label": "MiniMax literature reader"}], "source_run_id": "reading-sci-2026-11-01", "dsl_catalogue_fingerprint": "343fb30756ba6ec3", "capability_table_fingerprint": "2cb3e42f047d2ecf", "snapshot_id": "ba34b49490d9bfaf"}, "lineage": {"parent_id": "pmid:26949727", "parent_hash": "sha256:ef149d0bbffca42502078d2b4692b4eb9136203f115e4b49216927e83a6e7563", "fork_of": null, "generation": 2}, "gaps": ["execution.not_run", "method", "operations", "review.human_critique", "review.independent_reader", "review.machine_critique", "step:obtain_source_data blocked on data:accession_absent"], "assays": [{"role": "data_generation", "definition_id": "mass_spectrometry", "definition_version": "99e1195c7d6f", "definition_digest": null, "required_operations": [], "support_state": "partial", "source_hashes": {"assay_lexicon": "99e1195c7d6f"}, "confidence": 0.99, "evidence": ["ng tandem affinity purification coupled with mass spectrometry.", "strategy on histones H3 and H4 coupled with mass spectrometry to identify associated proteins and protein", "budding yeast, Saccharomyces cerevisiae. The mass spectrometry dataset described here consists of 14 files", ") by information-dependent acquisition (IDA) LC-MS/MS. The above files contain information about p"], "order_basis": "paper_text_order:143", "id": "assay:1"}]}