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MolNFT v1 · #114508 · protein

Structural basis for MOB1-dependent activation of the core mst-lats kinase cascade in hippo signaling

5BRM · Mob kinase activator 1A: “Structural basis for MOB1-dependent activation of the core mst-lats kinase cascade in hippo signaling”. X-ray diffraction, 1 ligand (ZN), 18 pockets (best druggability 0.72). MolNFT v1 #114508 on GenesisL1…

PDB
5BRM
Type
protein
Length
1,060 residues
Chains
15
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Mob kinase activator 1A; SERINE/THREONINE-protein kinase 3
EC
2.7.11.1
UniProt
Q9H8S9, Q13188
Ligands
ZN
Pockets
18 · best druggability 0.72

Structure

x-ray diffraction · 13 distinct chains · 54% helix, 5% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
AMob kinase activator 1Aprotein15462% helix, 5% strandQ9H8S9
BMob kinase activator 1Aprotein15860% helix, 4% strandQ9H8S9
C, E, FMob kinase activator 1Aprotein16059% helix, 3% strandQ9H8S9
DMob kinase activator 1Aprotein14465% helix, 2% strandQ9H8S9
GSERINE/THREONINE-protein kinase 3 (EC 2.7.11.1)protein2214% helix, 14% strandQ13188
HSERINE/THREONINE-protein kinase 3 (EC 2.7.11.1)protein1724% helix, 18% strandQ13188
ISERINE/THREONINE-protein kinase 3 (EC 2.7.11.1)protein1242% helix, 17% strandQ13188
JSERINE/THREONINE-protein kinase 3 (EC 2.7.11.1)protein1331% helix, 15% strandQ13188
KSERINE/THREONINE-protein kinase 3 (EC 2.7.11.1)protein1136% helix, 9% strandQ13188
LSERINE/THREONINE-protein kinase 3 (EC 2.7.11.1)protein1225% helix, 17% strandQ13188
MSERINE/THREONINE-protein kinase 3 (EC 2.7.11.1)protein170% helix, 0% strandQ13188
NSERINE/THREONINE-protein kinase 3 (EC 2.7.11.1)protein120% helix, 0% strandQ13188
OSERINE/THREONINE-protein kinase 3 (EC 2.7.11.1)protein80% helix, 0% strandQ13188

Ligands and binding sites

  • ZN · Zinc ion · metal · 6 copies · chains A, B, C, D, E, F

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
16120.720.7961empty
24150.680.8046empty
3530.670.9616empty
41090.620.8729empty
54470.610.7545empty

Interfaces

23 interfaces between chains.

  • A–G · 999 Ų buried · 18 hydrogen bonds · protein-protein
  • B–H · 972 Ų buried · 17 hydrogen bonds · protein-protein
  • B–C · 876 Ų buried · 8 hydrogen bonds · protein-protein
  • F–L · 869 Ų buried · 10 hydrogen bonds · protein-protein
  • D–J · 855 Ų buried · 13 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 6 modified (phosphorylation).

Compared structures

  • 5BRM · Structural basis for Mob1-dependent activation of the core Mst-Lats kinase cascade in… · the same entry in another collection · chain K against K, TM-score 1.00

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