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Ternary structure of hhai methyltransferase with native DNA and adohcy

Analyse Ternary structure of hhai methyltransferase with native DNA and adohcy in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4MHT
Type
protein + DNA
Length
352 residues
Chains
3
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
DNA (5'-D(*GP*AP*TP*AP*GP*(5CM) P*GP*CP*TP*AP*TP*C)-3'); DNA…
UniProt
P05102
Ligands
SAH
Pockets
6 · best druggability 0.72

Structure

x-ray diffraction · 3 distinct chains · 33% helix, 19% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
CDNA (5'-D(*GP*AP*TP*AP*GP*(5CM) P*GP*CP*TP*AP*TP*C)-3')dna12——
DDNA (5'-D(*TP*GP*AP*TP*AP*GP*(5CM) P*GP*CP*TP*AP*TP*C)-3')dna13——
AProtein (hhai methyltransferase (E.C.2.1.1.73))protein32733% helix, 19% strandP05102

Ligands and binding sites

  • SAH · S-adenosyl-L-homocysteine · ligand · chains D, A

Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.

Pockets

6 pockets found on a 1 Å grid, 3 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12700.720.8635SAH
2510.710.9921empty
31530.560.8220empty
41090.430.7813empty
5600.390.8017empty

Interfaces

3 interfaces between chains.

  • D–A · 1038 Ų buried · 31 hydrogen bonds · protein-nucleic
  • C–A · 730 Ų buried · 10 hydrogen bonds · protein-nucleic
  • C–D · 554 Ų buried · 47 hydrogen bonds · nucleic-nucleic

Modifications

Observed in the structure: 2 modified (nucleotide modification).

Compared structures

  • 4MHT · Ternary structure of hhai methyltransferase with native DNA and adohcy · the same entry in another collection · chain C against C, TM-score 1.00
  • P05102 · AlphaFold monomer V2.0 prediction for modification methylase hhai (P05102) · a predicted model of the same protein · chain A against A, TM-score 0.99

Analyse

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