GL1X · GenesisL1 explorer

Research workbench

Cryo- EM structure of the thermosynechococcus elongatus photosystem I in the presence of cytochrome C6

Analyse Cryo- EM structure of the thermosynechococcus elongatus photosystem I in the… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6TRC
Type
protein
Length
6,849 residues
Chains
36
Method
electron microscopy
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Photosystem I P700 chlorophyll a apoprotein A1; Photosystem I P700 chlorophyll a…
EC
1.97.1.12
UniProt
P0A405, P0A407, P0A415, P0A420, P0A423, P0A401, P0A427, P0A429, P0A425, Q8DGB4, P0A403, Q8DKP6
Ligands
CLA, BCR, LHG, SF4, PQN, CL0, LMG, CA
Pockets
20 · best druggability 0.86

Structure

electron microscopy · 12 distinct chains · 53% helix, 7% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, a, 1Photosystem I P700 chlorophyll a apoprotein A1 (EC 1.97.1.12)protein74658% helix, 6% strandP0A405
B, b, 2Photosystem I P700 chlorophyll a apoprotein A2 (EC 1.97.1.12)protein74060% helix, 3% strandP0A407
C, c, 3Photosystem I iron-sulfur center (EC 1.97.1.12)protein8011% helix, 21% strandP0A415
D, d, 4Photosystem I reaction center subunit IIprotein13817% helix, 28% strandP0A420
E, e, 5Photosystem I reaction center subunit IVprotein704% helix, 34% strandP0A423
F, f, 6Photosystem I reaction center subunit IIIprotein14145% helix, 6% strandP0A401
I, i, 7Photosystem I reaction center subunit VIIIprotein3866% helix, 3% strandP0A427
J, j, 8Photosystem I reaction center subunit IXprotein4171% helix, 2% strandP0A429
K, k, 9Photosystem I reaction center subunit psakprotein7958% helix, 0% strandP0A425
L, l, 0Photosystem I reaction center subunit XIprotein15266% helix, 4% strandQ8DGB4
M, m, yPhotosystem I reaction center subunit XIIprotein3181% helix, 0% strandP0A403
X, x, zPhotosystem I 4.8K proteinprotein2770% helix, 0% strandQ8DKP6

Ligands and binding sites

  • CLA · Chlorophyll A · ligand · 288 copies · chains A, B, F, J, K, L, I, 2, y, M, k, X, l, 7, 0, a, b, j, i, f, m, 9, x, 1, 6, 8, z
  • BCR · Beta-carotene · ligand · 72 copies · chains A, K, B, I, L, F, J, 0, M, a, k, b, f, j, i, l, m, 1, 2, 6, 8, 7, 9, y
  • LHG · 1,2-dipalmitoyl-phosphatidyl-glycerole · ligand · 15 copies · chains A, E, B, X, L, 7, y, 2, 0, a, e, b, x, I, M, l, 1, 5, z, i, m
  • SF4 · Iron/sulfur cluster · ligand · 9 copies · chains A, B, C, a, b, c, 1, 2, 3
  • PQN · Phylloquinone · ligand · 6 copies · chains A, J, B, a, j, b, 1, 8, 2
  • CL0 · Chlorophyll A isomer · ligand · 3 copies · chains A, B, a, b, 1, 2
  • LMG · 1,2-distearoyl-monogalactosyl-diglyceride · ligand · 3 copies · chains B, b, 2
  • CA · Calcium ion · metal · 6 copies · chains B, L, l, b, 0, 2

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
110030.860.8699CL0, CLA
28400.840.8686CL0, CLA
37380.830.8564BCR
47320.830.8680CL0, CLA
57750.790.8368LMG

Interfaces

99 interfaces between chains.

  • 1–2 · 3539 Ų buried · 40 hydrogen bonds · protein-protein
  • A–B · 3534 Ų buried · 36 hydrogen bonds · protein-protein
  • a–b · 3526 Ų buried · 38 hydrogen bonds · protein-protein
  • C–D · 1522 Ų buried · 24 hydrogen bonds · protein-protein
  • 3–4 · 1520 Ų buried · 22 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 6 modified, 3 disulfide (formylation, disulfide).

Compared structures

  • 6TRC · Cryo- EM structure of the Thermosynechococcus elongatus photosystem I in the presence of… · the same entry in another collection · chain M against M, TM-score 1.00

Analyse

GL1X is a live explorer of the GenesisL1 blockchain. Turn on JavaScript for search, charts and interactive views.