MolNFT v1 · #73865 · protein

Crystal structure of INHA_T266E:NADH complex

3OEY · Enoyl-[acyl-carrier-protein] reductase [NADH]: “Crystal structure of INHA_T266E:NADH complex”. X-ray diffraction, 1 ligand (NAD), 2 pockets (best druggability 0.78). MolNFT v1 #73865 on GenesisL1: 3D structure, binding sites and…

PDB: 3OEY
Type: protein
Length: 267 residues
Chains: 1
Method: x-ray diffraction
Collection: MolNFT v1 / PDB
Contract: 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner: 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule: Enoyl-[acyl-carrier-protein] reductase [NADH]
EC: 1.3.1.9
UniProt: P0A5Y6
Ligands: NAD
Pockets: 2 · best druggability 0.78

Structure

x-ray diffraction · 1 distinct chain · 47% helix, 16% strand (DSSP).

Chain	Molecule	Type	Residues	Secondary structure	UniProt
A	Enoyl-[acyl-carrier-protein] reductase [NADH] (EC 1.3.1.9)	protein	267	47% helix, 16% strand	P0A5Y6

Ligands and binding sites

NAD · Nicotinamide-adenine-dinucleotide · ligand · chains A
MPD · (4S)-2-methyl-2,4-pentanediol · additive · chains A

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

Pockets

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

Pocket	Volume (Å³)	Druggability	Buriedness	Lining residues	Inside
1	662	0.78	0.83	51	NAD, MPD
2	79	0.39	0.78	14	empty

Compared structures

3OEY · Crystal structure of InhA_T266E:NADH complex · the same entry in another collection · chain A against A, TM-score 1.00

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 P0A5Y6
Elsewhere: RCSB PDB 3OEY · PDBe 3OEY · UniProt P0A5Y6

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