MolNFT v1 · #182612 · protein

Structure of full length human ampk (A2B1G1) in complex with a small molecule activator MSG011

7MYJ · 5'-AMP-activated protein kinase catalytic subunit alpha-2: “Structure of full length human ampk (A2B1G1) in complex with a small molecule activator MSG011”. X-ray diffraction, 3 ligands (AMP, 4O7, ZQV), 20 pockets (best druggability…

PDB: 7MYJ
Type: protein
Length: 1,877 residues
Chains: 6
Method: x-ray diffraction
Collection: MolNFT v1 / PDB
Contract: 0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner: 0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule: 5'-AMP-activated protein kinase catalytic subunit alpha-2; 5'-AMP-activated protein…
EC: 2.7.11.1, 2.7.11.27, 2.7.11.31
UniProt: P54646, Q9Y478, P54619
Ligands: AMP, 4O7, ZQV
Pockets: 20 · best druggability 0.85

Structure

x-ray diffraction · 5 distinct chains · 31% helix, 24% strand (DSSP).

Chain	Molecule	Type	Residues	Secondary structure	UniProt
A	5'-AMP-activated protein kinase catalytic subunit alpha-2 (EC 2.7.11.1, 2.7.11.27, 2.7.11.31)	protein	435	34% helix, 20% strand	P54646
B	5'-AMP-activated protein kinase subunit beta-1	protein	184	14% helix, 39% strand	Q9Y478
C	5'-AMP-activated protein kinase catalytic subunit alpha-2 (EC 2.7.11.1, 2.7.11.27, 2.7.11.31)	protein	465	37% helix, 18% strand	P54646
D	5'-AMP-activated protein kinase subunit beta-1	protein	187	13% helix, 37% strand	Q9Y478
E, F	5'-AMP-activated protein kinase subunit gamma-1	protein	303	40% helix, 21% strand	P54619

Ligands and binding sites

AMP · Adenosine monophosphate · ligand · 4 copies · chains E, A, F, C
4O7 · (5s,6r,7r,9r,13cr,14r,16as)-6-methoxy-5-methyl-7-(methylamino)-6,7,8,9,14,15,16,16A-octahydro-5h,13ch-5,9-epoxy-4B,9A,1 5-triazadibenzo[b,h]cyclonona[1,2,3, 4-jkl]cyclopenta[e]-as-indacen-14-ol · ligand · 2 copies · chains A, C
ZQV · 5-({5-[(4'R)-4'-acetamido-2',3',4',5'-tetrahydro[1,1'-biphenyl]-4-yl]-6-chloro-1H-imidazo[4,5-b]pyridin-2-yl}oxy)-2-methylbenzoic acid · ligand · 2 copies · chains A, B, C, D

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

Pockets

20 pockets found on a 1 Å grid, 14 with a druggability of 0.5 or more.

Pocket	Volume (Å³)	Druggability	Buriedness	Lining residues	Inside
1	999	0.85	0.85	104	AMP
2	242	0.79	0.92	38	empty
3	732	0.76	0.81	69	AMP
4	937	0.75	0.78	73	empty
5	971	0.72	0.76	70	empty

Interfaces

7 interfaces between chains.

A–B · 4351 Å² buried · 47 hydrogen bonds · protein-protein
C–D · 4147 Å² buried · 45 hydrogen bonds · protein-protein
C–F · 1666 Å² buried · 27 hydrogen bonds · protein-protein
A–E · 1641 Å² buried · 25 hydrogen bonds · protein-protein
B–E · 1267 Å² buried · 22 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 4 modified (phosphorylation).

Compared structures

7MYJ · Structure of full length human AMPK (a2b1g1) in complex with a small molecule activator… · the same entry in another collection · chain F against F, TM-score 1.00
P54619 · AlphaFold monomer V2.0 prediction for 5'-AMP-activated protein kinase subunit gamma-1… · a predicted model of the same protein · chain E against A, TM-score 0.96
P54646 · AlphaFold monomer V2.0 prediction for 5'-AMP-activated protein kinase catalytic subunit… · a predicted model of the same protein · chain A against A, TM-score 0.95
Q9Y478 · AlphaFold monomer V2.0 prediction for 5'-AMP-activated protein kinase subunit beta-1… · a predicted model of the same protein · chain B against A, TM-score 0.86

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 P54646
Every structure of UniProt Q9Y478
Every structure of UniProt P54619
Elsewhere: RCSB PDB 7MYJ · PDBe 7MYJ · UniProt P54646 · UniProt Q9Y478 · UniProt P54619

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