GL1X · GenesisL1 explorer

Research workbench

Rt fs X-ray diffraction of photosystem II, first illuminated state

Analyse Rt fs X-ray diffraction of photosystem II, first illuminated state in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
4IXR
Type
protein
Length
5,270 residues
Chains
40
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Photosystem Q(B) protein 1; Photosystem II core light harvesting protein; Photosystem II…
EC
1.10.3.9
UniProt
P0A444, Q8DIQ1, Q8DIF8, Q8CM25, Q8DIP0, Q8DIN9, Q8DJ43, Q8DJZ6, P59087, Q9F1K9, Q8DIN8, Q8DHA7, P0A431, Q8DIQ0, Q9F1L5, P0A386, Q8DJI1, Q9F1R6, Q8DHJ2
Ligands
CLA, BCR, LMG, DGD, SQD, PL9, PHO, LHG, HEM, BCT, OEC, CA, FE2, CL
Pockets
20 · best druggability 0.87

Structure

x-ray diffraction · 20 distinct chains · 52% helix, 9% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, aPhotosystem Q(B) protein 1 (EC 1.10.3.9)protein33560% helix, 4% strandP0A444
B, bPhotosystem II core light harvesting proteinprotein49048% helix, 11% strandQ8DIQ1
C, cPhotosystem II CP43 proteinprotein44756% helix, 5% strandQ8DIF8
D, dPhotosystem II D2 protein (EC 1.10.3.9)protein34064% helix, 3% strandQ8CM25
E, eCytochrome B559 subunit alphaprotein8254% helix, 0% strandQ8DIP0
F, fCytochrome B559 subunit betaprotein3566% helix, 0% strandQ8DIN9
H, hPhotosystem II reaction center protein Hprotein6543% helix, 5% strandQ8DJ43
I, iPhotosystem II reaction center protein Iprotein3566% helix, 0% strandQ8DJZ6
J, jPhotosystem II reaction center protein Jprotein3465% helix, 0% strandP59087
K, kPhotosystem II reaction center protein Kprotein3770% helix, 0% strandQ9F1K9
L, lPhotosystem II reaction center protein Lprotein3762% helix, 3% strandQ8DIN8
M, mPhotosystem II reaction center protein Mprotein3471% helix, 0% strandQ8DHA7
O, oPhotosystem II manganese-stabilizing polypeptideprotein2433% helix, 46% strandP0A431
T, tPhotosystem II reaction center protein Tprotein3266% helix, 0% strandQ8DIQ0
U, uPhotosystem II 12 kda extrinsic proteinprotein9748% helix, 6% strandQ9F1L5
V, vCytochrome C-550protein13747% helix, 6% strandP0A386
y, gPhotosystem II reaction center protein YCF12protein2871% helix, 0% strandQ8DJI1
X, xPhotosystem II reaction center X proteinprotein3776% helix, 0% strandQ9F1R6
Z, zPhotosystem II reaction center protein Zprotein6285% helix, 0% strandQ8DHJ2
G, YPhotosystem II reaction center protein Yprotein2875% helix, 0% strand—

Ligands and binding sites

  • CLA · Chlorophyll A · ligand · 70 copies · chains A, D, T, L, F, I, B, H, M, m, t, C, K, y, Z, X, a, d, l, f, i, b, h, c, k, g, z, x
  • BCR · Beta-carotene · ligand · 24 copies · chains A, I, b, B, M, t, a, C, K, Z, D, F, J, H, X, T, m, y, i, c, k, z, d, f, j, h, x, g
  • LMG · 1,2-distearoyl-monogalactosyl-diglyceride · ligand · 22 copies · chains A, B, D, L, M, O, b, C, J, K, y, Z, F, T, E, I, l, m, a, d, o, c, z, f, j, t, e, i, k, g
  • DGD · Digalactosyl diacyl glycerol (dgdg) · ligand · 14 copies · chains A, C, I, O, B, D, H, a, J, V, E, F, c, i, o, b, d, h, j, v, e, f
  • SQD · 1,2-di-O-acyl-3-O-[6-deoxy-6-sulfo-alpha-D-glucopyranosyl]-sn-glycerol · ligand · 10 copies · chains A, C, D, K, I, T, b, B, L, l, m, t, H, X, E, F, a, i, c, d, k, M, h, x, e, f
  • PL9 · 2,3-dimethyl-5-(3,7,11,15,19,23,27,31,35-nonamethyl-2, 6,10,14,18,22,26,30,34-hexatriacontanonaenyl-2,5-cyclohexadiene-1,4-dione-2,3-dimethyl-5-solanesyl-1,4-benzoquinone · ligand · 6 copies · chains A, D, F, L, T, E, J, a, d, f, l, t, e, j
  • PHO · Pheophytin A · ligand · 4 copies · chains A, D, a, d
  • LHG · 1,2-dipalmitoyl-phosphatidyl-glycerole · ligand · 4 copies · chains A, C, D, K, a, c, d, k
  • HEM · Protoporphyrin IX containing Fe · ligand · 4 copies · chains E, F, Y, C, V, G, e, f, c, v
  • BCT · Bicarbonate ion · ligand · 2 copies · chains A, D, a, d
  • OEC · Oxygen evolving system · ligand · 2 copies · chains A, C, a, c
  • CA · Calcium ion · metal · 4 copies · chains K, O, k, o
  • FE2 · Fe (II) ion · metal · 2 copies · chains A, D, a, d
  • CL · Chloride ion · ion · 2 copies · chains A, D, a, d
  • LMT · Dodecyl-beta-D-maltoside · additive · 14 copies · chains B, D, H, a, t, i, o, X, I, M, m, A, T, b, O, d, h, x

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
19680.870.8777CLA, BCR
29570.870.8882HEM
39300.870.8872CLA, BCR
411060.840.8599HEM
58640.840.8585LMG

Interfaces

135 interfaces between chains.

  • a–d · 5541 Ų buried · 63 hydrogen bonds · protein-protein
  • A–D · 5521 Ų buried · 61 hydrogen bonds · protein-protein
  • a–c · 3299 Ų buried · 38 hydrogen bonds · protein-protein
  • A–C · 3275 Ų buried · 38 hydrogen bonds · protein-protein
  • B–D · 2667 Ų buried · 35 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 2 disulfide (disulfide).

Compared structures

  • 4IXR · RT fs X-ray diffraction of Photosystem II, first illuminated state · the same entry in another collection · chain K against K, TM-score 1.00

Analyse

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