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MolNFT v1 · #114074 · protein

Bovine heart cytochrome C oxidase in the fully oxidized state at 1.5 ångström resolution

5B1A · Cytochrome C oxidase subunit 1: “Bovine heart cytochrome C oxidase in the fully oxidized state at 1.5 ångström resolution”. X-ray diffraction, 14 ligands (PGV, CHD, TGL), 20 pockets (best druggability 0.91). MolNFT v1 #114074 on…

PDB
5B1A
Type
protein
Length
3,558 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
1.9.3.1
UniProt
P00396, P68530, P00415, P00423, P00426, P00428, P07471, P00429, P04038, P07470, P13183, P00430, P10175
Ligands
PGV, CHD, TGL, PEK, HEA, CDL, CUA, PSC, CU, MG, NA, ZN, PER, UNX
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 1.9.3.1)protein51472% helix, 1% strandP00396
B, OCytochrome C oxidase subunit 2protein22735% helix, 27% strandP68530
C, PCytochrome C oxidase subunit 3protein25976% helix, 0% strandP00415
D, QCytochrome C oxidase subunit 4 isoform 1, mitochondrialprotein14452% helix, 3% strandP00423
E, RCytochrome C oxidase subunit 5A, mitochondrialprotein10567% helix, 1% strandP00426
F, SCytochrome C oxidase subunit 5B, mitochondrialprotein9815% helix, 27% strandP00428
G, TCytochrome C oxidase subunit 6A2, mitochondrialprotein8427% helix, 2% strandP07471
H, UCytochrome C oxidase subunit 6B1protein7959% 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, mitochondrialprotein4663% 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, C, D, K, M, F, H, P, T, N, G, U, S, Q, X, Z
  • CHD · Cholic acid · ligand · 8 copies · chains A, B, S, T, C, J, P, F, G, N, O, W
  • TGL · Tristearoylglycerol · ligand · 6 copies · chains A, B, I, D, L, N, O, V, Q, Y
  • 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 C, F, G, N, O, A, P, B, S, T
  • 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
  • CUA · Dinuclear copper ion · ligand · 2 copies · chains B, O
  • 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, E, I, N, O, R, V
  • CU · Copper (II) ion · metal · 2 copies · chains A, N
  • MG · Magnesium ion · metal · 2 copies · chains A, B, N, O
  • NA · Sodium ion · metal · 2 copies · chains A, N
  • ZN · Zinc ion · metal · 2 copies · chains F, S
  • PER · Peroxide ion · ion · 2 copies · chains A, N
  • UNX · Unknown atom or ion · ion · 2 copies · chains C, P
  • DMU · Decyl-beta-D-maltopyranoside · additive · 4 copies · chains A, C, J, D, L, M, N, P, W, Q, 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
110540.910.93119HEA, PER
211440.910.93134HEA, PER
311060.860.8685PGV
411880.860.86102PGV, PEK
510090.830.8497empty

Interfaces

80 interfaces between chains.

  • N–O · 3622 Ų buried · 40 hydrogen bonds · protein-protein
  • A–B · 3615 Ų buried · 39 hydrogen bonds · protein-protein
  • N–P · 2642 Ų buried · 18 hydrogen bonds · protein-protein
  • A–C · 2627 Ų buried · 18 hydrogen bonds · protein-protein
  • N–Y · 1778 Ų buried · 18 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 8 modified, 4 disulfide (disulfide, formylation, acetylation, phosphorylation).

Compared structures

  • 5B1A · Bovine heart cytochrome c oxidase in the fully oxidized state at 1.5 angstrom resolution · the same entry in another collection · chain K against K, TM-score 1.00

Analyse

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