W371S

Category 2 — Moderately DestabilizingUncertain significanceTransmembrane · predictedSource card

Tryptophan → Serine at position 371 · Transmembrane helix 3 · WFS1 (Wolframin)

Interactive 3D Structure

Wild-type reference

Wild-type W371 — hydrogen bond to R375

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DynaMut2 mutant · W371S

Mutant S371 — polar contact to N373 lost (9 contacts lost)

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Bond changes · DynaMut2 interaction analysis

9 lost3 gained9 preserved

Interaction type	Wild-type partner	Mutant partner	Status
Hydrogen bond	D367	D367	Preserved
Hydrogen bond	S368	S368	Preserved
Hydrogen bond	F374	F374	Preserved
Hydrogen bond	R375	R375	Preserved
Polar contact	D367	D367	Preserved
Polar contact	S368	S368	Preserved
Polar contact	N373	—	Lost
Polar contact	F374	F374	Preserved
Polar contact	R375	R375	Preserved
Polar contact	—	F397	Gained
Aromatic / π	F374	—	Lost
Aromatic / π	F397	—	Lost
Van der Waals	—	D367	Gained
Van der Waals	—	S368	Gained
Van der Waals	K369	K369	Preserved
Van der Waals	N373	—	Lost
Van der Waals	E394	—	Lost
Van der Waals	F397	—	Lost
Hydrophobic	F374	—	Lost
Hydrophobic	E394	—	Lost
Hydrophobic	F397	—	Lost

Lost / gained / preserved interatomic contacts at the variant residue, from the DynaMut2 (Arpeggio) interaction analysis of the wild-type and energy-minimized mutant structures.

Computational Predictions

DynaMut2 ΔΔG

-2.54kcal/mol

Destabilising — large

AlphaMissense

0.947

likely pathogenic

AlphaFold pLDDT

model confidence

Schema

Cat 2

Category 2 — Moderately Destabilizing

Clinical Evidence

ClinVar classificationUncertain significance

Review statuscriteria provided, single submitter

Associated conditions—

Population frequency (gnomAD v4)Absent from gnomAD v4

cDNA changec.1112G>C

ClinVar accessionVCV003692844

Last evaluated2024/04/15 00:00

Not observed in ~730k individuals — consistent with a rare allele (ACMG PM2_supporting).

Full Variant Card

WFS1 Wolframin — W371S Variant Card

Molecular Atlas Pilot · RareResearch.AI · Generated by wolfram-variant-card skill

Tryptophan → Serine at position 371. Transmembrane helix 3. ClinVar Uncertain significance, AlphaMissense 0.947, DynaMut2 ΔΔG -2.54 kcal/mol (destabilising).

Identity

Field	Value
Variant	W371S (p.Tryptophan371Serine)
DNA change	c.1112G>C
Gene · Protein	WFS1 · Wolframin (890 aa)
UniProt	O76024 · WFS1_HUMAN
ClinVar accession	VCV003692844
Amino acid change	Tryptophan (W) → Serine (S)

Structural Context

Field	Value
AlphaFold model	AF-O76024-F1, v6
pLDDT at residue 371	80.25 — well-folded
Domain	Transmembrane helix 3
Position context	Inside Transmembrane helix 3 · position 371 is bilayer-embedded
IDR flag	No — pLDDT above 50 threshold

UniProt features at this position:

(none catalogued)

Position 371 sits in a transmembrane helix (Transmembrane helix 3). Wolframin has eleven such helices anchoring it in the ER membrane; substitutions inside the bilayer-embedded segments can disrupt helix packing, lipid contacts, and the overall ER topology of the protein. The wild-type residue is bulky aromatic (tryptophan — indole ring); the mutant is small polar (serine — hydroxyl). The chemistry shift implies altered local packing, hydrogen-bonding, and/or electrostatics at this site.

Computational Predictions

AlphaMissense

Field	Value
am_pathogenicity	0.9472
am_class	likely pathogenic
Interpretation	Likely pathogenic (threshold 0.564)

DynaMut2

Field	Value
ΔΔG (kcal/mol)	-2.54 (Destabilising)
Job ID	178092140675
Result URL	https://biosig.lab.uq.edu.au/dynamut2/results_prediction/178092140675

Clinical Evidence

Field	Value
Classification	Uncertain significance
Review status	criteria provided, single submitter
Last evaluated	2024/04/15 00:00
Inheritance	Inheritance pattern not specified in ClinVar entry; WFS1 has both AD and AR presentations.
WFS1 variant landscape	W371S is 1 of ~326 pathogenic-spectrum variants in WFS1 (out of 2,243 catalogued in ClinVar)

(no conditions catalogued)

Research Path Decision Tree

ΔΔG < 2  + binding site affected   →  CATEGORY 3 — docking experiments
ΔΔG 2–4                            →  CATEGORY 2 — pharmacological chaperones
ΔΔG > 4                            →  CATEGORY 1 — gene therapy
pLDDT < 50                         →  CATEGORY 5 — IDR, experimental only
Stable fold + functional site hit  →  CATEGORY 4 — site-specific docking

Final Schema Categorization

Category 2 — Moderately Destabilizing

<strong>Category 2 — Moderately Destabilizing</strong><br/><br/>|ΔΔG|=2.54 in the 2–4 range. Pharmacological chaperone candidate.

Files in this folder

AF-O76024-F1-model_v6.pdb — AlphaFold structure
W371S_molstar_viewer.html — interactive 3D viewer (auto-highlights position 371 with ball-and-stick + neighbors within 5Å)
W371S_variant_card.md — this card (source of truth)
W371S_variant_card.html — styled printable card
W371S_dynamut2_summary.html — clean offline DynaMut2 result card
dynamut2_result.json — structured result data
dynamut2_result_page.html — local snapshot of the Biosig result page (asset URLs absolutized)
W371S_wildtype_interactions.pse / W371S_mutant_interactions.pse — PyMOL sessions

Generated by wolfram-variant-card skill · RareResearch.AI Molecular Atlas Every assumption documented. Every score sourced.

Therapeutic Strategy Handoff · prediction

Feed this card to Wolfram Intelligence

Download the W371S PDF below and upload it to Wolfram Intelligence to generate therapeutic-strategy proposals — guanidinium mimetics, sigma-1 agonist docking, NAC thiol-capping. NAC is already on the bench-testing list.

Download W371S PDF card ↓Strategies are AI-generated predictions, not validated therapeutics.