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MolNFT v1 · #148270 · protein

Cryo-EM structure of two dynein tail domains bound to dynactin and BICDR1

6F1T · ARP1 actin related protein 1 homolog a: “Cryo-EM structure of two dynein tail domains bound to dynactin and BICDR1”. Electron microscopy, 2 ligands (ADP, ATP), 20 pockets (best druggability 0.87). MolNFT v1 #148270 on GenesisL1: 3D…

PDB
6F1T
Type
protein
Length
13,986 residues
Chains
45
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, A0JNT9, F1SKF9, Q14204, Q13409, O43237, Q9NP97
Ligands
ADP, ATP
Pockets
20 · best druggability 0.87

Structure

electron microscopy · 29 distinct chains · 52% helix, 10% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, B, C, D, E, F, G, IARP1 actin related protein 1 homolog aprotein37035% helix, 20% strandF2Z5G5
HActin, cytoplasmic 1protein37041% helix, 18% strandQ6QAQ1
JActin related protein 10 homologprotein36940% helix, 13% strandI3LHK5
KCapping protein (actin filament) muscle Z-line, alpha 1protein27840% helix, 25% strandA0PFK5
LF-actin capping protein beta subunitprotein26938% helix, 26% strandA9XFX6
MDynactin subunit 2protein58793% helix, 0% strand—
NDynactin subunit 2protein61690% helix, 0% strand—
O, PDynactin subunit 3protein6543% helix, 28% strand—
Q, RDynactin subunit 2protein8789% helix, 0% strand—
UDynactin 6protein17113% helix, 14% strandD0G6S1
VDynactin subunit 5protein1658% helix, 16% strandA0A286ZK88
XBicd family-like cargo adapter 1,BICD family-like cargo adapter 1,BICD family-like cargo adapter 1,BICDR-1protein28599% helix, 0% strandA0JNT9
YDynactin subunit 4protein26311% helix, 6% strand—
ZDynactin subunit 1protein5267% helix, 0% strand—
aDynactin subunit 2protein5221% helix, 12% strandF1SKF9
bDynactin subunit 2protein759% helix, 5% strandF1SKF9
cDynactin subunit 2protein3716% helix, 16% strandF1SKF9
dDynactin subunit 2protein2413% helix, 13% strandF1SKF9
e, mCytoplasmic dynein 1 heavy chain 1,CYTOPLASMIC dynein 1 heavy chain 1,CYTOPLASMIC dynein 1 heavy chain 1,DYNEIN heavy chain, cytoplasmic dynein 1 heavy chain 1,CYTOPLASMIC dynein 1 heavy chain 1,CYTOPLASMIC dynein 1 heavy chain 1,CYTOPLASMIC dynein 1 heavy chain 1,DYNEIN heavy CHAIN,CYTOPLASMIC dynein 1 heavy chain 1,CYTOPLASMIC dynein 1 heavy chain 1protein92667% helix, 2% strandQ14204
fCytoplasmic dynein 1 heavy chain 1,CYTOPLASMIC dynein 1 heavy chain 1,CYTOPLASMIC dynein 1 heavy chain 1,DYNEIN heavy chain, cytoplasmic dynein 1 heavy chain 1,CYTOPLASMIC dynein 1 heavy chain 1,CYTOPLASMIC dynein 1 heavy chain 1,CYTOPLASMIC dynein 1 heavy chain 1,DYNEIN heavy CHAIN,CYTOPLASMIC dynein 1 heavy chain 1,CYTOPLASMIC dynein 1 heavy chain 1protein92966% helix, 4% strandQ14204
g, oCytoplasmic dynein 1 intermediate chain 2protein39710% helix, 28% strandQ13409
hCytoplasmic dynein 1 intermediate chain 2protein4008% helix, 27% strandQ13409
i, q, rCytoplasmic dynein 1 light intermediate chain 2protein26841% helix, 11% strandO43237
jCytoplasmic dynein 1 light intermediate chain 2protein28835% helix, 11% strandO43237
k, l, s, tDynein light chain roadblock-type 1protein9335% helix, 16% strandQ9NP97
nCytoplasmic dynein 1 heavy chain 1,CYTOPLASMIC dynein 1 heavy chain 1,CYTOPLASMIC dynein 1 heavy chain 1,DYNEIN heavy chain, cytoplasmic dynein 1 heavy chain 1,CYTOPLASMIC dynein 1 heavy chain 1,CYTOPLASMIC dynein 1 heavy chain 1,CYTOPLASMIC dynein 1 heavy chain 1,DYNEIN heavy CHAIN,CYTOPLASMIC dynein 1 heavy chain 1,CYTOPLASMIC dynein 1 heavy chain 1protein92867% helix, 4% strandQ14204
pCytoplasmic dynein 1 intermediate chain 2protein4019% helix, 25% strandQ13409
xBicd family-like cargo adapter 1,BICD family-like cargo adapter 1,BICD family-like cargo adapter 1protein28899% helix, 0% strandA0JNT9
zDynactin subunit 1protein5372% helix, 0% strand—

Ligands and binding sites

  • ADP · Adenosine-5'-diphosphate · ligand · 9 copies · chains A, B, C, a, 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
19920.870.88105empty
29280.850.86107ADP
38910.850.8790empty
420740.850.86248empty
521110.840.85198empty

Interfaces

105 interfaces between chains.

  • K–L · 3802 Ų buried · 53 hydrogen bonds · protein-protein
  • X–x · 3557 Ų buried · 16 hydrogen bonds · protein-protein
  • f–h · 1841 Ų buried · 23 hydrogen bonds · protein-protein
  • G–b · 1614 Ų buried · 11 hydrogen bonds · protein-protein
  • m–o · 1557 Ų buried · 16 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 6 covalent (covalent ligand).

Compared structures

  • 6F1T · Cryo-EM structure of two dynein tail domains bound to dynactin and BICDR1 · the same entry in another collection · chain K against K, TM-score 1.00

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