"Volume_ID","Dataset_Version","Target_Order","Target_Code","Prediction_Handle","Parent_Prediction_ID","Prediction_Title","Target_Release","Target_Window","Prepared_Date","Primary_Terrain_Surface","Eligibility","Target_Prediction","Numerical_Target_or_Invariant","Expected_Direction","Failure_Condition","Input_Separation_Statement","Source_Paper","Source_Section","Derivation_Summary","Status_At_Publication","Citation_Handle","Row_SHA256"
"MH-PRED-V1","1.0","2","WWPDB","MH-PRED-V1-WWPDB-P1","P1","Equilateral-triad enrichment in resolved protein cores","wwPDB weekly structural release, 15 July 2026","Advance sequence opening: 2026-07-11 03:00 UTC; coordinate opening: 2026-07-15 00:00 UTC","2026-07-10","All coordinate-resolved protein structures","Cα coordinate model; Delaunay contact graph; resolved core compared with surface/mobile/unresolved controls","The distribution of Delaunay contact-triangle equilateralness Q_△ will shift toward 1 in resolved protein cores relative to surface, mobile, or unresolved structural terrain.","Q_△=4√3A/(a²+b²+c²); Q_△=1 is exactly equilateral","median(Q_△|core) > median(Q_△|surface/mobile/unresolved)","No positive core shift or a stable reversed shift.","No July 15 entry, sequence, title, coordinate model, or biological assembly was used to generate the prediction.","MH_PREDICTION_02_wwPDB_Weekly_Structural_Release_2026-07-15_Mass_Harmonics_Governed.md","Derivation 1: Equilateral-Triad Enrichment in Closed Cores","Stable cubic biological closure must preserve the successful equilateral triad locally in the folded core.","PROSPECTIVE_UNRESOLVED_IN_VOLUME_I","MH-PRED-V1-WWPDB-P1","a8066adef7fea74c75aa8e602b121973c49de2ea48a8824134c3650c5543f584"
"MH-PRED-V1","1.0","2","WWPDB","MH-PRED-V1-WWPDB-P2","P2","2/3/5 axis recovery in near-spherical cages","wwPDB weekly structural release, 15 July 2026","Advance sequence opening: 2026-07-11 03:00 UTC; coordinate opening: 2026-07-15 00:00 UTC","2026-07-10","Compact near-spherical cages, capsids, and shell-like assemblies","Topology selected from coordinate geometry before deposited symmetry labels are read","Eligible closed cages will recover coordinate-derived 2-fold, 3-fold, and 5-fold rotational axes, with the full directional structure approaching 12 vertex, 20 face-normal, and 30 edge-midpoint directions.","Axis family 2/3/5; directional structure 12/20/30","Icosahedral closure scaffold in eligible compact cages","A closed eligible cage requires an unrelated axis family.","No July 15 entry, sequence, title, coordinate model, or biological assembly was used to generate the prediction.","MH_PREDICTION_02_wwPDB_Weekly_Structural_Release_2026-07-15_Mass_Harmonics_Governed.md","Derivation 2: Icosahedral Axis Recovery in Near-Spherical Cages","S₃ closure forces the icosahedral rotational structure for the correct compact-cage topology.","PROSPECTIVE_UNRESOLVED_IN_VOLUME_I","MH-PRED-V1-WWPDB-P2","91d739f3c7a302d9efc126f3a753030c70d2e6d45981106254d4c8e8365b624a"
"MH-PRED-V1","1.0","2","WWPDB","MH-PRED-V1-WWPDB-P3","P3","Codon Z-cascade residual versus structural resolution","wwPDB weekly structural release, 15 July 2026","Advance sequence opening: 2026-07-11 03:00 UTC; coordinate opening: 2026-07-15 00:00 UTC","2026-07-10","Structures with recoverable actual coding sequence","Actual construct codons required; no amino-acid back-translation; first-shell Delaunay neighborhood","The first-shell codon residual D_i=|Δ_i+Σ_j∈N(i)Δ_j| will be lower in resolved core neighborhoods and higher in mobile or unresolved regions.","D_i=|Δ_i+Σ_j∈N(i)Δ_j|; fold closure R_Z(Σ)=0","Lower residual corresponds to greater structural resolution","No association between D_i and structural resolution, or a reversed association.","No July 15 entry, sequence, title, coordinate model, or biological assembly was used to generate the prediction.","MH_PREDICTION_02_wwPDB_Weekly_Structural_Release_2026-07-15_Mass_Harmonics_Governed.md","Derivation 3: Codon Z-Cascade Residual and Structural Resolution","Folded stability is the local cancellation of ordered codon-transport residue through the physical contact neighborhood.","PROSPECTIVE_UNRESOLVED_IN_VOLUME_I","MH-PRED-V1-WWPDB-P3","86621b976521f4b50e466d77b4338f796681875ec128ac42811ca526e41821fc"
"MH-PRED-V1","1.0","2","WWPDB","MH-PRED-V1-WWPDB-P4","P4","Synonymous-codon orientation stratification","wwPDB weekly structural release, 15 July 2026","Advance sequence opening: 2026-07-11 03:00 UTC; coordinate opening: 2026-07-15 00:00 UTC","2026-07-10","Residues matched within the same amino-acid identity but encoded by different actual synonymous codons","Actual coding sequence and structural neighborhood available; amino-acid identity held fixed","Within synonymous-codon matched residues, lower locally cancelled codon Orientation Δ will correspond to greater structural order and lower mobility or unresolved-density probability.","Same amino-acid face anchor, different ordered codon Orientation Δ","Lower residual → greater order; higher residual → greater mobility/unresolved probability","No synonymous-codon stratification or a stable reversed direction.","No July 15 entry, sequence, title, coordinate model, or biological assembly was used to generate the prediction.","MH_PREDICTION_02_wwPDB_Weekly_Structural_Release_2026-07-15_Mass_Harmonics_Governed.md","Derivation 4: Synonymous-Codon Orientation Stratification","Synonymous codons retain distinct ordered temporal trajectories even when they terminate at the same amino-acid identity.","PROSPECTIVE_UNRESOLVED_IN_VOLUME_I","MH-PRED-V1-WWPDB-P4","10aec0b7f1ece6c8db3e3412294aec321fe80d639967b7fff2c1fd977a52c9bf"
