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https://w3id.org/delphi/resource/assessment/levin-2019-boundary-14--claim-test
http://www.w3.org/2000/01/rdf-schema#comment
Measured: undefined undefined. Interpretation: 'The exact same ion channel mechanisms' is read as shared structural ancestry of the channel protein, the strongest sense in which a mechanism can be 'the same' across 3+ billion years; a shared biophysical principle without homology (e.g. any force-gated pore) would not count. Senses are mapped to the channels that transduce them in mammals: touch to PIEZO2; temperature to TRPV1 (heat) and TRPM8 (cold); taste to OTOP1 (sour), ENaC alpha/SCNN1A (salty) and TRPM5 (sweet, bitter and umami downstream of GPCRs); hearing to TMC1. Monomers are compared because the pore-forming fold lives in a single subunit for all of these families.
https://w3id.org/delphi/resource/assessment/levin-2019-boundary-14--claim-test
http://www.w3.org/2000/01/rdf-schema#label
Claim test of levin-2019-boundary-14: mixed, confidence 0.55
https://w3id.org/delphi/resource/assessment/levin-2019-boundary-14--claim-test
http://www.w3.org/2000/01/rdf-schema#seeAlso
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https://w3id.org/delphi/ontology/admissibleDatasets
Canonical UniProtKB sequences of channels with an established role in transducing the named sense, and of bacterial channels with experimentally confirmed channel function; structures predicted by a model that sees only the sequence (no templates from the comparison set).
https://w3id.org/delphi/resource/assessment/levin-2019-boundary-14--claim-test
https://w3id.org/delphi/ontology/assessmentType
claim-test/0.1.0
https://w3id.org/delphi/resource/assessment/levin-2019-boundary-14--claim-test
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computational
https://w3id.org/delphi/resource/assessment/levin-2019-boundary-14--claim-test
https://w3id.org/delphi/ontology/disconfirmingObservation
Transducing channels for some or all named senses (e.g. Piezo for touch, TMC for hearing, otopetrin for sour taste) align to no bacterial channel better than an unrelated membrane transporter does.
https://w3id.org/delphi/resource/assessment/levin-2019-boundary-14--claim-test
https://w3id.org/delphi/ontology/evidenceAgainst
Pre-registered rule: mixed, because two of the four senses share a bacterial channel fold (TM >= 0.50 and at least 0.10 above GLUT1 on the same bacterial chain) and two do not. Controls pass: KCNA2 versus KcsA is 0.614, myoglobin's best is 0.365, GLUT1's best is 0.496.
https://w3id.org/delphi/resource/assessment/levin-2019-boundary-14--claim-test
https://w3id.org/delphi/ontology/evidenceAgainst
Taste is shared only through TRPM5 versus NavAb (0.640). TRPM5 is the downstream transduction channel for sweet, bitter and umami, not the receptor. The sour channel OTOP1 tops out at 0.495 and the salt channel SCNN1A at 0.418, both under the 0.50 line.
https://w3id.org/delphi/resource/assessment/levin-2019-boundary-14--claim-test
https://w3id.org/delphi/ontology/evidenceAgainst
Temperature is shared by both listed channels, not only the one the summary picks: TRPV1 versus NavAb is 0.661 and TRPM8 versus NavAb is 0.621.
https://w3id.org/delphi/resource/assessment/levin-2019-boundary-14--claim-test
https://w3id.org/delphi/ontology/evidenceAgainst
These are ESMFold2 single-sequence monomers, TM-score normalised by the bacterial chain. A shared fold is not a shared gating mechanism, and a miss is not proof the proteins are unrelated.
https://w3id.org/delphi/resource/assessment/levin-2019-boundary-14--claim-test
https://w3id.org/delphi/ontology/evidenceAgainst
Touch (PIEZO2, best 0.493 versus NaK, and below GLUT1 on that chain) and hearing (TMC1, best 0.481 versus NaK) are not shared. PIEZO2 was folded as two overlapping windows after the full chain ran out of GPU memory; that deviation was recorded before any score was read.
https://w3id.org/delphi/resource/assessment/levin-2019-boundary-14--claim-test
https://w3id.org/delphi/ontology/expectedObservation
Each named sense has a transducing channel whose predicted structure aligns to a bacterial channel at TM >= 0.5 (the conventional same-fold threshold), clearly above a non-channel membrane protein's score.
https://w3id.org/delphi/resource/assessment/levin-2019-boundary-14--claim-test
https://w3id.org/delphi/ontology/failCriterion
Pre-registered. Refutes: no sense is shared. Mixed: one to three senses shared. Inconclusive (reason 'other'): the positive control scores below 0.50, either negative control reaches 0.50 against any bacterial channel, or every channel listed for a sense has mean pLDDT < 50 (that sense is then reported as undetermined and the verdict is at most mixed).
https://w3id.org/delphi/resource/assessment/levin-2019-boundary-14--claim-test
https://w3id.org/delphi/ontology/hasConfidence
0.55
https://w3id.org/delphi/resource/assessment/levin-2019-boundary-14--claim-test
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https://w3id.org/delphi/resource/assessment/levin-2019-boundary-14--claim-test
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mixed
https://w3id.org/delphi/resource/assessment/levin-2019-boundary-14--claim-test
https://w3id.org/delphi/ontology/hypothesis
For each of the four senses named (touch, taste, temperature, hearing), at least one ion channel that transduces that sense in animals has a predicted structure containing the fold of a known bacterial ion channel, as measured by TM-score, clearly above the score a non-channel membrane protein reaches against the same bacterial channel.
https://w3id.org/delphi/resource/assessment/levin-2019-boundary-14--claim-test
https://w3id.org/delphi/ontology/inferenceMethod
Pairwise TM-align on predicted monomer structures, TM-score normalised by the bacterial chain; per-sense maximum compared with a fixed threshold (0.50) and with the GLUT1 negative-control margin (0.10); verdict by count of shared senses.
https://w3id.org/delphi/resource/assessment/levin-2019-boundary-14--claim-test
https://w3id.org/delphi/ontology/passCriterion
Pre-registered. Structures for every protein are predicted with ESMFold2 on the Nebius Scientific AI Platform (single-sequence mode, seed 0) and aligned pairwise with TM-align (tmtools); the TM-score is normalised by the length of the bacterial chain. A sense is 'shared' if some channel listed for it reaches TM >= 0.50 against some bacterial channel AND that score exceeds the GLUT1 negative control's score against the same bacterial channel by >= 0.10. Supports: all four senses shared, with both controls behaving (positive control KCNA2 vs KcsA TM >= 0.50; negative controls myoglobin and GLUT1 below 0.50 against every bacterial channel).
https://w3id.org/delphi/resource/assessment/levin-2019-boundary-14--claim-test
https://w3id.org/delphi/ontology/preregistered
false
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Claim test of levin-2019-boundary-14: mixed, confidence 0.55
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