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Bovine heart cytochrome C oxidase in a catalytic intermediate of O at 1.84 ångström resolution

Analyse Bovine heart cytochrome C oxidase in a catalytic intermediate of O at 1.84… in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
7D5W
Type
protein
Length
3,550 residues
Chains
26
Method
x-ray diffraction
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
Cytochrome C oxidase subunit 1; Cytochrome C oxidase subunit 2; Cytochrome C oxidase…
EC
7.1.1.9
UniProt
P00396, P68530, P00415, P00423, P00426, P00428, P07471, P00429, P04038, P07470, P13183, P00430, P10175
Ligands
PGV, CHD, TGL, PEK, HEA, CDL, PSC, CUA, NA, CU, MG, ZN, PER, PO4
Pockets
20 · best druggability 0.91

Structure

x-ray diffraction · 13 distinct chains · 59% helix, 6% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
A, NCytochrome C oxidase subunit 1 (EC 7.1.1.9)protein51472% helix, 1% strandP00396
B, OCytochrome C oxidase subunit 2 (EC 7.1.1.9)protein22735% helix, 26% strandP68530
C, PCytochrome C oxidase subunit 3 (EC 7.1.1.9)protein25976% helix, 0% strandP00415
D, QCytochrome C oxidase subunit 4 isoform 1, mitochondrialprotein14452% helix, 3% strandP00423
E, RCytochrome C oxidase subunit 5A, mitochondrialprotein10564% helix, 1% strandP00426
F, SCytochrome C oxidase subunit 5B, mitochondrialprotein9416% helix, 28% strandP00428
G, TCytochrome C oxidase subunit 6A2, mitochondrialprotein8431% helix, 2% strandP07471
H, UCytochrome C oxidase subunit 6B1protein7961% helix, 1% strandP00429
I, VCytochrome C oxidase subunit 6Cprotein7370% helix, 1% strandP04038
J, WCytochrome C oxidase subunit 7A1, mitochondrialprotein5867% helix, 0% strandP07470
K, XCytochrome C oxidase subunit 7B, mitochondrialprotein4955% helix, 0% strandP13183
L, YCytochrome C oxidase subunit 7C, mitochondrialprotein4659% helix, 0% strandP00430
M, ZCytochrome C oxidase subunit 8B, mitochondrialprotein4367% helix, 2% strandP10175

Ligands and binding sites

  • PGV · (1R)-2-{[{[(2S)-2,3-dihydroxypropyl]oxy}(hydroxy) phosphoryl]oxy}-1-[(palmitoyloxy)methyl]ethyl (11E)-octadec-11-enoate · ligand · 8 copies · chains A, D, K, M, C, F, P, T, N, Q, X, Z, S, G
  • CHD · Cholic acid · ligand · 8 copies · chains A, B, T, C, P, J, G, N, O, L, M, Y, Z
  • TGL · Tristearoylglycerol · ligand · 6 copies · chains A, B, I, D, L, N, O, V, Y, Q
  • PEK · (1S)-2-{[(2-aminoethoxy)(hydroxy)phosphoryl]oxy}-1-[(stearoyloxy)methyl]ethyl (5E,8E,11E,14E)-icosa-5,8, 11,14-tetraenoate · ligand · 6 copies · chains A, C, T, G, N, P, B
  • HEA · Heme-A · ligand · 4 copies · chains A, B, N, O
  • CDL · Cardiolipin · ligand · 4 copies · chains C, J, G, N, O, P, W, A, B, T
  • PSC · (7R,17E,20E)-4-hydroxy-N,N,N-trimethyl-9-oxo-7-[(palmitoyloxy)methyl]-3,5,8-trioxa-4-phosphahexacosa-17,20-dien-1-aminium 4-oxide · ligand · 2 copies · chains A, B, I, N, O, V
  • CUA · Dinuclear copper ion · ligand · 2 copies · chains B, O
  • NA · Sodium ion · metal · 4 copies · chains A, C, N, P
  • CU · Copper (II) ion · metal · 2 copies · chains A, N
  • MG · Magnesium ion · metal · 2 copies · chains A, B, N, O
  • ZN · Zinc ion · metal · 2 copies · chains F, S
  • PER · Peroxide ion · ion · 2 copies · chains A, N
  • PO4 · Phosphate ion · ion · 2 copies · chains H, U
  • EDO · 1,2-ethanediol · additive · 80 copies · chains A, D, M, B, F, C, G, H, J, K, E, S, L, N, Q, P, Z, O, T, U, W, Y
  • DMU · Decyl-beta-D-maltopyranoside · additive · 23 copies · chains A, C, J, G, D, K, B, L, M, O, N, P, W, T, Q, X, Y, Z

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
111530.910.93132HEA, PER, PSC
211980.910.93137HEA, PER, PSC
37840.860.8985PGV
410300.860.8679PGV
510280.840.8599EDO

Interfaces

80 interfaces between chains.

  • A–B · 3628 Ų buried · 38 hydrogen bonds · protein-protein
  • N–O · 3605 Ų buried · 38 hydrogen bonds · protein-protein
  • N–P · 2651 Ų buried · 18 hydrogen bonds · protein-protein
  • A–C · 2627 Ų buried · 17 hydrogen bonds · protein-protein
  • A–L · 1742 Ų buried · 19 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 6 modified, 4 disulfide (disulfide, formylation, acetylation).

Compared structures

  • 7D5W · Bovine heart cytochrome c oxidase in a catalytic intermediate of O at 1.84 angstrom… · the same entry in another collection · chain J against J, TM-score 1.00

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