Current Protein Identity:Q9Y6C9 New Search
Main Difference Dimensions in This Set
Different mutation/modification Different structure-quality metrics

Difference tags compare only the current result set; every original PDB and assembly record remains separate.

Related-Structure Differences

Each row represents one biological assembly in one PDB entry; multiple monomers of the same protein are listed separately.

PDB Entry Assembly / Oligomeric State Construct Mutations and Modifications Ligands, Ions and Non-polymers Experimental Method Experimental Conditions Structure Quality
12OY Single particle cryo-EM structure of human MTCH2 Deposited 2026-04-14 Assembly 1 Insufficient information Heteromer;Protein × 2 PDB declaration: dimeric(2) Consistent with protein count
Chain A 1–202(202 aa)
Chain A 222–303(82 aa)
Mutation:L199V, A200Y, T226A Mutation:L199V, A200Y, T226A No recorded non-water small molecule ELECTRON MICROSCOPY
cryo-EM buffer pH 7.5;50 mM HEPES/KOH pH 7.5, 200 mM NaCl, 2 mM Mg Acetate, and 0.07% UDM
cryo-EM vitrification conditions Cryogen ETHANE
Resolution 3.60 Å
12OZ Single particle cryo-EM structure of human MTCH2 (hyperactive mutant F285N F286N) Deposited 2026-04-14 Assembly 1 Insufficient information Heteromer;Protein × 2 PDB declaration: dimeric(2) Consistent with protein count
Chain A 1–202(202 aa)
Chain A 222–303(82 aa)
Mutation:F285N,F286N,L199V,A200Y,T226A Mutation:F285N,F286N,L199V,A200Y,T226A No recorded non-water small molecule ELECTRON MICROSCOPY
cryo-EM buffer pH 7.5;50 mM HEPES/KOH pH 7.5, 200 mM NaCl, 2 mM Mg Acetate, and 0.07% UDM
cryo-EM vitrification conditions Cryogen ETHANE
Resolution 3.30 Å
12PB Single particle cryo-EM structure of human MTCH2 (hyperactive mutant K25E Y235A V238D) Deposited 2026-04-14 Assembly 1 Insufficient information Heteromer;Protein × 2 PDB declaration: dimeric(2) Consistent with protein count
Chain A 1–202(202 aa)
Chain A 222–303(82 aa)
Mutation:K25E,Y235A,V238D,L199V,A200Y,T226A Mutation:K25E,Y235A,V238D,L199V,A200Y,T226A No recorded non-water small molecule ELECTRON MICROSCOPY
cryo-EM buffer pH 7.5;50 mM HEPES/KOH pH 7.5, 200 mM NaCl, 2 mM Mg Acetate, and 0.07% UDM
cryo-EM vitrification conditions Cryogen ETHANE
Resolution 3.10 Å