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MolNFT v1 · #148321 · protein

Cryo-EM structure of a single dynein tail domain bound to dynactin and BICD2N

6F3A · ARP1 actin related protein 1 homolog a: “Cryo-EM structure of a single dynein tail domain bound to dynactin and BICD2N”. Electron microscopy, 2 ligands (ADP, ATP), 20 pockets (best druggability 0.86). MolNFT v1 #148321 on GenesisL1…

PDB
6F3A
Type
protein
Length
9,810 residues
Chains
36
Method
electron microscopy
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
ARP1 actin related protein 1 homolog a; Actin, cytoplasmic 1; Actin related protein 10…
UniProt
F2Z5G5, Q6QAQ1, I3LHK5, A0PFK5, A9XFX6, D0G6S1, A0A286ZK88, F1SKF9, Q14204, Q13409, O43237, Q9NP97
Ligands
ADP, ATP
Pockets
20 · best druggability 0.86

Structure

electron microscopy · 25 distinct chains · 52% helix, 10% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, D, E, F, G, IARP1 actin related protein 1 homolog aprotein37040% helix, 14% strandF2Z5G5
HActin, cytoplasmic 1protein37042% helix, 13% strandQ6QAQ1
JActin related protein 10 homologprotein36941% helix, 15% strandI3LHK5
KCapping protein (actin filament) muscle Z-line, alpha 1protein27839% helix, 26% strandA0PFK5
LF-actin capping protein beta subunitprotein26942% helix, 24% strandA9XFX6
MDynactin subunit 2protein58794% helix, 0% strand—
NDynactin subunit 2protein61689% helix, 0% strand—
O, PDynactin subunit 3protein6542% helix, 25% strand—
Q, RDynactin subunit 2protein8790% helix, 0% strand—
UDynactin 6protein17113% helix, 14% strandD0G6S1
VDynactin subunit 5protein16511% helix, 10% strandA0A286ZK88
YDynactin subunit 4protein26413% helix, 6% strand—
ZDynactin subunit 1protein5262% helix, 0% strand—
aDynactin subunit 2protein5227% helix, 8% strandF1SKF9
bDynactin subunit 2protein7519% helix, 5% strandF1SKF9
cDynactin subunit 2protein3511% helix, 6% strandF1SKF9
dDynactin subunit 2protein2421% helix, 13% strandF1SKF9
eCytoplasmic dynein 1 heavy chain 1protein78566% helix, 3% strandQ14204
fCytoplasmic dynein 1 heavy chain 1protein83263% helix, 3% strandQ14204
gCytoplasmic dynein 1 intermediate chain 2protein3979% helix, 32% strandQ13409
hCytoplasmic dynein 1 intermediate chain 2protein4017% helix, 26% strandQ13409
jCytoplasmic dynein 1 light intermediate chain 2protein1533% helix, 0% strandO43237
k, lDynein light chain roadblock-type 1protein9334% helix, 26% strandQ9NP97
zDynactin subunit 1protein5374% helix, 0% strand—
5, 6BICD2Nprotein27599% helix, 0% strand—

Ligands and binding sites

  • ADP · Adenosine-5'-diphosphate · ligand · 9 copies · chains A, B, C, D, E, F, G, I, J
  • ATP · Adenosine-5'-triphosphate · ligand · chains H

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

Pockets

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

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
111290.860.87176empty
26010.840.8995empty
310320.840.85147empty
411940.830.84163ADP
510620.820.84152empty

Interfaces

74 interfaces between chains.

  • 5–6 · 2423 Ų buried · 0 hydrogen bonds · protein-protein
  • e–f · 1466 Ų buried · 9 hydrogen bonds · protein-protein
  • e–g · 1279 Ų buried · 6 hydrogen bonds · protein-protein
  • K–L · 1183 Ų buried · 7 hydrogen bonds · protein-protein
  • J–Y · 841 Ų buried · 3 hydrogen bonds · protein-protein

Compared structures

  • Q6QAQ1 · AlphaFold monomer V2.0 prediction for actin, cytoplasmic 1 (Q6QAQ1) · a predicted model of the same protein · chain H against A, TM-score 0.94
  • Q13409 · AlphaFold monomer V2.0 prediction for cytoplasmic dynein 1 intermediate chain 2 (Q13409) · a predicted model of the same protein · chain g against A, TM-score 0.93
  • Q9NP97 · AlphaFold monomer V2.0 prediction for dynein light chain roadblock- type 1 (Q9NP97) · a predicted model of the same protein · chain l against A, TM-score 0.91
  • O43237 · AlphaFold monomer V2.0 prediction for cytoplasmic dynein 1 light intermediate chain 2… · a predicted model of the same protein · chain j against A, TM-score 0.41

Analyse

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