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MolNFT v1 · #119109 · protein

Double-heterohexameric rings of full-length RVB1(ADP)RVB2(APO)

5FM6: “Double-heterohexameric rings of full-length RVB1(ADP)RVB2(APO)”. X-ray diffraction, 2 ligands (ADP, PO4), 13 pockets (best druggability 0.71). MolNFT v1 #119109 on GenesisL1: 3D structure, binding sites and pockets in GL1X.

PDB
5FM6
Type
protein
Length
845 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
RVB1; RVB2
UniProt
G0RYI5, G0RYC2
Ligands
ADP, PO4
Pockets
13 · best druggability 0.71

Structure

x-ray diffraction · 2 distinct chains · 37% helix, 22% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ARVB1protein42636% helix, 21% strandG0RYI5
BRVB2protein41937% helix, 22% strandG0RYC2

Ligands and binding sites

  • ADP · Adenosine-5'-diphosphate · ligand · chains A
  • PO4 · Phosphate ion · ion · 2 copies · chains B, A

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

Pockets

13 pockets found on a 1 Å grid, 7 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
14700.710.8158PO4
25500.680.7863empty
33100.680.8346empty
41640.680.8724ADP
51590.580.8228empty

Interfaces

1 interface between chains.

  • A–B · 2360 Ų buried · 13 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 21 modified (engineered).

Compared structures

  • 5FM6 · Double-heterohexameric rings of full-length Rvb1(ADP)Rvb2(apo) · the same entry in another collection · chain A against A, TM-score 1.00

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