MolNFT v1 · #6797 · protein

Structure of thermus thermophilus ef-G H573A

1FNM · Elongation factor G: “Structure of thermus thermophilus ef-G H573A”. X-ray diffraction, 2 ligands (GDP, MG), 8 pockets (best druggability 0.79). MolNFT v1 #6797 on GenesisL1: 3D structure, binding sites and pockets in GL1X.

PDB: 1FNM
Type: protein
Length: 655 residues
Chains: 1
Method: x-ray diffraction
Collection: MolNFT v1 / PDB
Contract: 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner: 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule: Elongation factor G
UniProt: P13551
Ligands: GDP, MG
Pockets: 8 · best druggability 0.79

Structure

x-ray diffraction · 1 distinct chain · 29% helix, 34% strand (DSSP).

Chain	Molecule	Type	Residues	Secondary structure	UniProt
A	Elongation factor G	protein	655	29% helix, 34% strand	P13551

Ligands and binding sites

GDP · Guanosine-5'-diphosphate · ligand · chains A
MG · Magnesium ion · metal · chains A

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

Pockets

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

Pocket	Volume (Å³)	Druggability	Buriedness	Lining residues	Inside
1	934	0.79	0.81	83	empty
2	148	0.57	0.82	22	empty
3	253	0.52	0.75	34	empty
4	54	0.52	0.87	21	empty
5	57	0.36	0.79	16	empty

Compared structures

1FNM · Structure of thermus thermophilus ef-G H573A · the same entry in another collection · chain A against A, TM-score 1.00
P13551 · AlphaFold monomer V2.0 prediction for elongation factor G (P13551) · a predicted model of the same protein · chain A against A, TM-score 0.72

Analyse

Open in the research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides and crosslinks on the 3D structure
Every structure of UniProt P13551
Elsewhere: RCSB PDB 1FNM · PDBe 1FNM · UniProt P13551

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