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Re-refinement of crystal structure of photosystem II complex

Analyse Re-refinement of crystal structure of photosystem II complex in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
5V2C
Type
protein
Length
5,280 residues
Chains
38
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Photosystem II protein D1; Photosystem II CP47 reaction center protein; Photosystem II…
EC
1.10.3.9
UniProt
P51765, D0VWR1, D0VWR7, D0VWR8, P12238, P12239, P19052, P12240, Q7DGD4, P19054, P12241, P12312, D0VWR2, P12313, P56152, P0A387, D0VWR3, D0VWR4, D0VWR5
Ligands
CLA, BCR, LMG, LHG, SQD, DGD, PHO, PL9, BCT, OEX, HEM, HEC, CA, MG, FE2, CL
Pockets
20 · best druggability 0.87

Structure

x-ray diffraction · 23 distinct chains · 54% helix, 9% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, aPhotosystem II protein D1 (EC 1.10.3.9)protein33460% helix, 4% strandP51765
BPhotosystem II CP47 reaction center proteinprotein50450% helix, 11% strandD0VWR1
CPhotosystem II CP43 reaction center proteinprotein45158% helix, 6% strandD0VWR7
D, dPhotosystem II D2 protein (EC 1.10.3.9)protein34265% helix, 4% strandD0VWR8
E, eCytochrome B559 subunit alphaprotein8157% helix, 0% strandP12238
FCytochrome B559 subunit betaprotein3468% helix, 0% strandP12239
H, hPhotosystem II reaction center protein Hprotein6551% helix, 3% strandP19052
I, iPhotosystem II reaction center protein Iprotein3861% helix, 0% strandP12240
J, jPhotosystem II reaction center protein Jprotein3956% helix, 0% strandQ7DGD4
K, kPhotosystem II reaction center protein Kprotein3781% helix, 0% strandP19054
L, lPhotosystem II reaction center protein Lprotein3762% helix, 5% strandP12241
MPhotosystem II reaction center protein Mprotein3471% helix, 0% strandP12312
O, oPhotosystem II manganese-stabilizing polypeptideprotein2456% helix, 46% strandD0VWR2
T, tPhotosystem II reaction center protein Tprotein3070% helix, 0% strandP12313
U, uPhotosystem II 12 kda extrinsic proteinprotein9751% helix, 4% strandP56152
V, vCytochrome C-550protein13746% helix, 6% strandP0A387
Y, yPhotosystem II reaction center protein YCF12protein2979% helix, 0% strandD0VWR3
X, xPhotosystem II reaction center protein Xprotein4075% helix, 0% strandD0VWR4
Z, zPhotosystem II reaction center protein Zprotein6289% helix, 0% strandD0VWR5
bPhotosystem II CP47 reaction center proteinprotein50650% helix, 11% strandD0VWR1
cPhotosystem II CP43 reaction center proteinprotein45857% helix, 6% strandD0VWR7
fCytochrome B559 subunit betaprotein3272% helix, 0% strandP12239
mPhotosystem II reaction center protein Mprotein3569% helix, 0% strandP12312

Ligands and binding sites

  • CLA · Chlorophyll A · ligand · 70 copies · chains A, D, T, I, B, H, L, M, C, K, Y, Z, X, a, d, t, i, b, h, l, m, c, k, y, z, x
  • BCR · Beta-carotene · ligand · 22 copies · chains A, I, b, B, M, t, C, K, Z, D, F, J, H, X, Y, T, a, i, m, c, k, z, d, f, j, h, x, y
  • LMG · 1,2-distearoyl-monogalactosyl-diglyceride · ligand · 14 copies · chains A, C, I, B, D, L, M, H, X, J, K, Y, Z, F, a, c, i, b, d, l, m, j, k, y, z, h, x, f
  • LHG · 1,2-dipalmitoyl-phosphatidyl-glycerole · ligand · 12 copies · chains A, C, K, B, D, L, M, T, E, F, a, c, k, b, d, l, m, t, e, f
  • SQD · 1,2-di-O-acyl-3-O-[6-deoxy-6-sulfo-alpha-D-glucopyranosyl]-sn-glycerol · ligand · 11 copies · chains A, C, D, J, K, T, b, I, E, F, X, a, c, d, j, k, B, t, i, L, M, l, h, m, e, f, x
  • DGD · Digalactosyl diacyl glycerol (dgdg) · ligand · 10 copies · chains A, C, J, D, V, E, F, B, H, a, c, j, d, v, e, f, b, h
  • PHO · Pheophytin A · ligand · 4 copies · chains A, D, a, d
  • 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 · 4 copies · chains A, D, F, X, L, T, a, d, f, x, l, t
  • BCT · Bicarbonate ion · ligand · 3 copies · chains A, D, a, d, M, m
  • OEX · Ca-MN4-O5 cluster · ligand · 2 copies · chains A, C, a, c
  • HEM · Protoporphyrin IX containing Fe · ligand · 2 copies · chains E, F, e, f
  • HEC · Heme C · ligand · 2 copies · chains C, V, c, v
  • CA · Calcium ion · metal · 6 copies · chains B, O, b, c, h, o
  • MG · Magnesium ion · metal · 4 copies · chains F, V, J, f, v, j
  • FE2 · Fe (II) ion · metal · 2 copies · chains A, D, a, d
  • CL · Chloride ion · ion · 6 copies · chains A, D, C, U, V, a, d, c, u, v
  • PGE · Triethylene glycol · additive · 65 copies · chains A, b, J, B, D, V, C, X, E, H, I, O, T, U, Y, Z, a, i, c, L, t, d, h, x, j, o, u, M
  • GOL · Glycerol · additive · 60 copies · chains A, O, b, D, E, V, B, U, H, M, t, C, L, T, X, F, a, o, d, e, v, u, h, m, c, y, l, f, j
  • PG4 · Tetraethylene glycol · additive · 57 copies · chains A, B, H, C, D, X, E, J, I, Y, K, U, V, a, t, b, h, c, j, k, d, x, e, i, M, l
  • HTG · heptyl 1-thio-beta-D-glucopyranoside · additive · 24 copies · chains B, O, a, C, D, H, A, b, V, c, t, o, d, h
  • EDO · 1,2-ethanediol · additive · 22 copies · chains A, B, L, H, C, D, E, J, I, O, V, X, a, c, b, d, o, e, i
  • LMT · Dodecyl-beta-D-maltoside · additive · 18 copies · chains A, D, O, b, B, H, X, C, I, E, F, J, M, l, m, T, Y, a, d, o, h, x, c, i, e, f, j, y, t, L, u
  • P6G · Hexaethylene glycol · additive · 17 copies · chains A, I, T, B, C, D, H, X, F, E, b, c, d, h, x, j
  • 1PE · Pentaethylene glycol · additive · 7 copies · chains B, L, m, V, e, f, j, x
  • 2PE · Nonaethylene glycol · additive · chains V
  • PE8 · 3,6,9,12,15,18,21-heptaoxatricosane-1,23-diol · additive · chains a, i

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
110370.870.8878CLA, BCR
29930.870.8777CLA, BCR
39290.850.8696GOL, HEC
410070.850.8595GOL, HEC
510240.830.84139DGD, GOL, BCR, LMG, MG

Interfaces

132 interfaces between chains.

  • A–D · 5478 Ų buried · 69 hydrogen bonds · protein-protein
  • a–d · 5462 Ų buried · 66 hydrogen bonds · protein-protein
  • A–C · 3261 Ų buried · 37 hydrogen bonds · protein-protein
  • a–c · 3258 Ų buried · 38 hydrogen bonds · protein-protein
  • B–D · 3040 Ų buried · 48 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 8 modified, 4 cofactor, 2 disulfide (formylation, heme c attachment, disulfide, methylation).

Compared structures

  • 5V2C · Re-refinement of crystal structure of photosystem II complex · the same entry in another collection · chain L against L, TM-score 1.00

Analyse

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