GL1X · GenesisL1 explorer

Research workbench

Crystal structure of a flavin binding protein from thermotoga maritima, TM379

Analyse Crystal structure of a flavin binding protein from thermotoga maritima, TM379 in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
1MRZ
Type
protein
Length
536 residues
Chains
2
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Riboflavin KINASE/FMN adenylyltransferase
UniProt
Q9WZW1
Pockets
11 · best druggability 0.87

Structure

x-ray diffraction · 2 distinct chains · 32% helix, 28% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
ARiboflavin KINASE/FMN adenylyltransferaseprotein26633% helix, 28% strandQ9WZW1
BRiboflavin KINASE/FMN adenylyltransferaseprotein27032% helix, 28% strandQ9WZW1

Ligands and binding sites

  • CIT · Citric acid · additive · 2 copies · chains A, B

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

Pockets

11 pockets found on a 1 Å grid, 4 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
17220.870.9158CIT
23720.670.8037CIT
3850.580.8720empty
41380.550.8122empty
51890.480.7636empty

Interfaces

1 interface between chains.

  • A–B · 1028 Ų buried · 15 hydrogen bonds · protein-protein

Compared structures

  • 1MRZ · Crystal structure of a flavin binding protein from Thermotoga Maritima, TM379 · the same entry in another collection · chain A against A, TM-score 1.00

Analyse

GL1X is a live explorer of the GenesisL1 blockchain. Turn on JavaScript for search, charts and interactive views.