No deep-research provider was available; literature collected by PubMed search
and cached abstracts or full texts. PMID:16030218 (Kosono et al. 2005) is
abstract-only here (PMC1196046 is a scanned PDF). Verdicts kept consistent
with the completed PA1055 (ShaC) and PA1057 (ShaE) reviews.
PTN001865541 = Eubacteria node of PTHR42703 (root PTN000511965, LUCA, 28
leaves), 16 leaves/13 taxa, 16 GO_Central IBAs per term. GO:0015385 seeds:
B. subtilis MrpD O05229 (IMP, PMID:20509166) and PA1056. GO:0035725 seed:
PA1056 only. The archaeal MBH/MBX subunit-H proteins (TK2087, TK1220,
TK1219) are in the Archaea-Eukaryota branch, outside the node. Possible
non-antiporter leaves: Leptospira LA_4273 ("Formate hydrogenase subunit B"),
Thermotoga TM_1105/TM_1211, Rhodopirellula RB1430/RB1431.
| PTN node | node term | n_seeds | leaf IBAs | seed annotation (term, evidence, PMID) | verdict | rationale |
|---|---|---|---|---|---|---|
| PTN001865541 | GO:0015385 sodium:proton antiporter activity | 2 | 16 | GO:0015385, IMP, PMID:16030218 | INDIRECT-PHENOTYPE | The abstract describes no PA1056 mutant; the evidence is a PA1054 disruption plus whole-cluster complementation of E. coli TO114. Right only as contributes_to (subunit of the antiporter complex). The IBD itself survives: an independent B. subtilis MrpD IMP seed supports it, and the bacterial node excludes the archaeal MBH subunits. The IBD qualifier should still be contributes_to. |
| PTN001865541 | GO:0035725 sodium ion transmembrane transport | 1 (sole) | 16 | GO:0035725, IMP, PMID:16030218 | SOUND | As a subunit of the complex responsible for Na+ extrusion, PA1056 takes part in Na+ transmembrane transport; structural models couple MrpD protonation to Na+ transfer. The process fits the bacterial MrpD clade. Caveat: IMP looks like the wrong code for PA1056 (no mutant in the abstract); filed as a CHECK. |
PMID:16030218 is still abstract-only here: the PubMed MCP returns no body
text (the PMC copy, PMC1196046, is a scanned PDF the publisher does not
release as XML), and the PMC, Europe PMC and ASM pages were not retrievable.
The WRONG_EVIDENCE_CODE (IMP) defects on this gene rest on the abstract not
describing a mutant of this gene, so they are lowered from PROBABLE to
SUSPECTED. The WRONG_QUALIFIER defects (enables vs contributes_to) rest on
positive statements in other Mrp papers and stay PROBABLE. The reference
correctness for PMID:16030218 is changed from MISCITED to UNVERIFIED.
Annotation actions are unchanged.
The full text of Kosono et al. 2005 was supplied by the user and read. It
supersedes the earlier notes above that describe this paper as abstract-only.
The only sha mutant the paper constructs is the PA1054 insertion; the
cluster-level evidence comes from expressing the whole PA1054-PA1059 cluster,
or the cluster with PA1054 disrupted, in an antiporter-deficient E. coli
strain. There is no PA1056 mutant, so the IMP evidence-code defects on PA1056 are CONFIRMED.