Aging proteomics repository / PXD045821

Intracellular Iron Accumulation Facilitates Mycobacterial Infection in Old Mouse Macrophages

PXD045821 · PRIDE record

Generated summary PXD045821 is a DDA label-free dataset (Mus musculus) with 12 runs, 12 samples and no enrichment step (whole proteome). It was reanalysed with MetaMorpheus 1.1.12. At 1% FDR the search reports 230,387 PSMs, 15,385 peptidoforms and 3,089 protein groups, and the repository holds 8,220 PTM sites for it. 6 open warnings about it are recorded.
Written from catalog fields only (D17), with no model involved. It says nothing the tables below do not.

Open findings

Recorded against this dataset: 0 errors, 6 warnings and 1 for information

count_mismatch warning
The bundle holds 230387 where the producer reported 230428 (results.txt: All target PSMs with q-value <= 0.01 (pxreprise:DEF-PSM-1PCT v1)). Both numbers are kept; treat the producer's as canonical until the difference is explained.
high_contamination warning
19.59% of protein intensity in the worst file, 18.10% median across 12 files (DEF-QC-9 v3.5)
low_core_use warning
10.91 avg cores of 32 allowed (S5)
no_sdrf warning
No SDRF was found for this dataset, so each run was given a synthetic sample of its own. There is no sample metadata: treat every sample as unannotated.
occupancy_not_stored warning
Of 9386 occupancy entries MetaMorpheus wrote, some are not in ptm_stoichiometry: 3921 site not in ptm_sites. 'site not in ptm_sites' means the entry's site has no ptm_sites row to key on; 'not determinable' means a cell's segments could not be assigned to its accessions from the sequences (QuantProject DEF-OCC-ACCESSION), which is never guessed. Absence of a row for these sites is therefore not NA. A 'duplicate' is a second entry for a (site, run) that already has a row: one with identical values loses nothing; one with DIFFERENT values means MetaMorpheus wrote two answers and the first in file order was stored (examples in bundle.json occupancy.differing_duplicates; which one should be stored is QuantProject's to define).
unplaced_ptm_sites warning
Some modifications on peptides shared between proteins were not written to ptm_sites for one or more of those proteins, because the peptide could not be located in that protein's sequence and the producer's residue spans cannot be paired with its accessions. Of the (PSM, protein) pairs affected: 242 named a protein that does not contain the stored peptide -- typically a PSM ambiguous between peptide sequences (level 4 or 5), where this protein carries a different candidate than the first, which is the one stored. Sites on the other proteins of the same PSMs are written. Counts are in bundle.json under protein_databases.
occupancy_decoy_groups info
124 occupancy entries on decoy protein groups were not stored: MetaMorpheus computes them, and they are FDR machinery, not biology.

What was found

PSMs at 1% FDR230,387
Peptidoforms at 1% FDR15,385
Protein groups at 1% FDR3,089
PTM sites8,220
Quantitative values268,893
PSMs, all (including decoys and sub-threshold)1,069,661
MS2 identification rate (pxreprise:DEF-ID-RATE)32.1%
Contaminant share of PSMs (pxreprise:DEF-CONTAM-PSM)9.9%

How it was measured

Organism searched
Mus musculus (the protein database's organism, not a statement about the samples)
Acquisition
DDA
Quantification
label_free
Labelling
none
Enrichment
none
Instrument vendor
not recorded
Runs / samples
12 / 12
Sample metadata
absent
Search engine
MetaMorpheus 1.1.12
Protein database
UP000000589_all_genecentric_2026_03_agingPTM-v3.xml
Pipeline commit
852cea5e1cd7

Modifications

Search engine's nameUNIMODSites
Carbamidomethyl on CUNIMOD:45,771
Oxidation on MUNIMOD:35831
Phosphoserine on SUNIMOD:21163
N-acetylalanine on AUNIMOD:1161
Hydroxylation on PUNIMOD:35111
N-acetylmethionine on MUNIMOD:188
Acetylation on XUNIMOD:177
N-acetylserine on SUNIMOD:167
Phosphorylation on SUNIMOD:2167
N6-acetyllysine on KUNIMOD:155
Phosphorylation on TUNIMOD:2146
GG (Ubiquitination Site) on KUNIMOD:12137
Phosphothreonine on TUNIMOD:2129
4-hydroxyproline on PUNIMOD:3526
Omega-N-methylarginine on RUNIMOD:3421
Acetylation on KUNIMOD:119
Methylation on KUNIMOD:3418
Dimethylation on KUNIMOD:3617
HexNAc on TUNIMOD:4317
Hydroxylation on KUNIMOD:3517
Asymmetric dimethylarginine on RUNIMOD:3612
N-acetylthreonine on TUNIMOD:112
Phosphotyrosine on YUNIMOD:2112
Deamidated asparagine on NUNIMOD:711
HexNAc on SUNIMOD:4311
Methylation on RUNIMOD:349
N6,N6,N6-trimethyllysine on KUNIMOD:378
N6-methyllysine on KUNIMOD:348
Phosphorylation on YUNIMOD:218
N6,N6-dimethyllysine on KUNIMOD:366
Dimethylation on RUNIMOD:365
N6-succinyllysine on K—5
Malonylation on KUNIMOD:7474
N-acetylcysteine on CUNIMOD:14
Tele-methylhistidine on HUNIMOD:343
Trimethylation on KUNIMOD:373
5-glutamyl glycerylphosphorylethanolamine on EUNIMOD:3962
Citrulline on RUNIMOD:72
Hydroxyproline on PUNIMOD:352
N-acetylglycine on GUNIMOD:12
N-acetylvaline on VUNIMOD:12
N6-propionyllysine on KUNIMOD:582
(3S)-3-hydroxyhistidine on H—1
3-hydroxyproline on PUNIMOD:351
Butyrylation on KUNIMOD:12891
Crotonylation on KUNIMOD:13631
Dimethylated arginine on RUNIMOD:361
Diphthamide on HUNIMOD:3751
Glutarylation on KUNIMOD:18481
N-acetylaspartate on DUNIMOD:11
N-acetylglutamate on EUNIMOD:11
N-myristoyl glycine on GUNIMOD:451
N5-methylglutamine on QUNIMOD:341
N6-(2-hydroxyisobutyryl)lysine on KUNIMOD:18491
N6-butyryllysine on KUNIMOD:12891
N6-glutaryllysine on K—1
N6-isonicotinyllysine on KUNIMOD:6971
N6-methacryllysine on K—1
Pros-methylhistidine on HUNIMOD:341

Every modification with a site on a target protein, most frequent first. A dash in the UNIMOD column means the modification has no UNIMOD term in the registry that searched it, not that it is unknown. One chemistry can appear under two names (UniProt's and MetaMorpheus's); the catalog's ptm_sites_by_chemistry view merges them.

Data

The Parquet files for this dataset are not published yet.

Bundle
43cc92093e51092c, written 2026-10-29T09:44:52+00:00 by ingester 1.4.0
Reconciliation
failed: psms_target_1pct (the bundle disagrees with the producer's own count here)
Licence
CC-BY-4.0
Credit
NCEMS Aging Proteome Working Group