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Co-crystal structure of triacetyloleandomcyin bound to the large ribosomal subunit

Analyse Co-crystal structure of triacetyloleandomcyin bound to the large ribosomal… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
3I56
Type
protein + RNA
Length
6,651 residues
Chains
31
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
50S ribosomal protein L2P; 50S ribosomal protein L3P; 50S ribosomal protein L4P; 50S…
UniProt
P20276, P20279, P12735, P14124, P14135, P12743, P15825, P60617, P14122, P29198, P22450, P12737, P60618, P14123, P12733, P14119, P12734, P10970, P12732, P10972, P14116, P10971, P14121, P18138, P12736, P60619, P32410, P22452, P32411
Ligands
TAO, SR, MG, NA, CD, K, CL
Pockets
20 · best druggability 0.90

Structure

x-ray diffraction · 31 distinct chains · 28% helix, 21% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A50S ribosomal protein L2Pprotein2379% helix, 24% strandP20276
B50S ribosomal protein L3Pprotein33712% helix, 29% strandP20279
C50S ribosomal protein L4Pprotein24629% helix, 14% strandP12735
D50S ribosomal protein L5Pprotein14026% helix, 23% strandP14124
E50S ribosomal protein L6Pprotein17222% helix, 41% strandP14135
F50S ribosomal protein L7AEprotein11944% helix, 15% strandP12743
G50S ribosomal protein L10Eprotein2983% helix, 0% strandP15825
H50S ribosomal protein L10Eprotein16024% helix, 28% strandP60617
I50S ribosomal protein L11Pprotein7043% helix, 6% strandP14122
J50S ribosomal protein L13Pprotein14239% helix, 15% strandP29198
K50S ribosomal protein L14Pprotein1328% helix, 37% strandP22450
L50S ribosomal protein L15Pprotein14519% helix, 17% strandP12737
M50S ribosomal protein L15Eprotein19432% helix, 16% strandP60618
N50S ribosomal protein L18Pprotein18636% helix, 15% strandP14123
O50S ribosomal protein L18Eprotein11546% helix, 23% strandP12733
P50S ribosomal protein L19Eprotein14358% helix, 4% strandP14119
Q50S ribosomal protein L21Eprotein9513% helix, 32% strandP12734
R50S ribosomal protein L22Pprotein15031% helix, 31% strandP10970
S50S ribosomal protein L23Pprotein8135% helix, 31% strandP12732
T50S ribosomal protein L24Pprotein11929% helix, 29% strandP10972
U50S ribosomal protein L24Eprotein5315% helix, 19% strandP14116
V50S ribosomal protein L29Pprotein6577% helix, 0% strandP10971
W50S ribosomal protein L30Pprotein15438% helix, 14% strandP14121
X50S ribosomal protein L31Eprotein8239% helix, 29% strandP18138
Y50S ribosomal protein L32Eprotein14220% helix, 12% strandP12736
Z50S ribosomal protein L37AEprotein7330% helix, 18% strandP60619
150S ribosomal protein L37Eprotein5613% helix, 16% strandP32410
250S ribosomal protein L39Eprotein4641% helix, 0% strandP22452
350S ribosomal protein L44Eprotein9214% helix, 30% strandP32411
023S ribosomal RNArna2754——
95S ribosomal RNArna122——

Ligands and binding sites

  • TAO · Troleandomycin · ligand · chains 0
  • SR · Strontium ion · metal · 108 copies · chains A, 0, B, H, R, S, T, Y, 1, 3, L, M, 2, 9, J, F
  • MG · Magnesium ion · metal · 93 copies · chains A, 0, B, C, K, T, Y, 2, R, S, 1, W, 3, P, M, 9
  • NA · Sodium ion · metal · 75 copies · chains B, 0, C, H, J, M, Q, R, S, 2, T, 9, 3, L, D
  • CD · Cadmium ion · metal · 5 copies · chains O, U, Z, 1, 3
  • K · Potassium ion · metal · 2 copies · chains 0, M
  • CL · Chloride ion · ion · 22 copies · chains A, 0, B, E, J, K, L, M, D, N, O, Q, R, Y, 3, 2, W

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
110530.900.9294MG, NA, SR
29390.880.91115CL, MG, SR
39660.870.89111MG, NA, SR
49420.860.8987empty
510430.860.8890SR

Interfaces

55 interfaces between chains.

  • B–0 · 7474 Ų buried · 232 hydrogen bonds · protein-nucleic
  • M–0 · 6597 Ų buried · 195 hydrogen bonds · protein-nucleic
  • A–0 · 6321 Ų buried · 197 hydrogen bonds · protein-nucleic
  • C–0 · 5661 Ų buried · 147 hydrogen bonds · protein-nucleic
  • P–0 · 4435 Ų buried · 134 hydrogen bonds · protein-nucleic

Modifications

Observed in the structure: 5 modified (nucleotide modification).

Compared structures

  • 3I56 · Co-crystal structure of Triacetyloleandomcyin Bound to the Large Ribosomal Subunit · the same entry in another collection · chain K against K, TM-score 1.00

Analyse

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