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MolNFT v1 · #143213 · protein

Structural consequences of effector binding to the T state of aspartate carbamoyltransferase. crystal structures of the unligated and ATP-, and CTP-complexed enzymes at 2.6-ångströms resolution

6AT1 · Aspartate carbamoyltransferase (T state), catalytic chain: “Structural consequences of effector binding to the T state of aspartate carbamoyltransferase. crystal…”. X-ray diffraction, 1 ligand (ZN), 8 pockets (best druggability…

PDB
6AT1
Type
protein
Length
912 residues
Chains
4
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Aspartate carbamoyltransferase (T state), catalytic chain; Aspartate carbamoyltransferase…
EC
2.1.3.2
UniProt
P0A786, P0A7F3
Ligands
ZN
Pockets
8 · best druggability 0.61

Structure

x-ray diffraction · 2 distinct chains · 32% helix, 22% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, CAspartate carbamoyltransferase (T state), catalytic chain (EC 2.1.3.2)protein31039% helix, 17% strandP0A786
B, DAspartate carbamoyltransferase regulatory chainprotein14616% helix, 34% strandP0A7F3

Ligands and binding sites

  • ZN · Zinc ion · metal · 2 copies · chains B, D

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

Pockets

8 pockets found on a 1 Å grid, 3 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
12710.610.8029empty
23000.600.7930empty
31970.520.7828empty
4540.480.8519empty
51440.470.7725empty

Interfaces

3 interfaces between chains.

  • B–D · 850 Ų buried · 21 hydrogen bonds · protein-protein
  • C–D · 725 Ų buried · 21 hydrogen bonds · protein-protein
  • A–B · 690 Ų buried · 16 hydrogen bonds · protein-protein

Compared structures

  • 6AT1 · Structural consequences of effector binding to the T state of aspartate… · the same entry in another collection · chain A against A, TM-score 1.00

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