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3FYI

Catalytic core subunits (I and II) of cytochrome C oxidase from Rhodobacter sphaeroides in the reduced state bound with cyanide

Functional Information from GO Data
ChainGOidnamespacecontents
A0004129molecular_functioncytochrome-c oxidase activity
A0005515molecular_functionprotein binding
A0005886cellular_componentplasma membrane
A0006119biological_processoxidative phosphorylation
A0009060biological_processaerobic respiration
A0015990biological_processelectron transport coupled proton transport
A0016020cellular_componentmembrane
A0020037molecular_functionheme binding
A0022904biological_processrespiratory electron transport chain
A0045277cellular_componentrespiratory chain complex IV
A0046872molecular_functionmetal ion binding
A1902600biological_processproton transmembrane transport
B0004129molecular_functioncytochrome-c oxidase activity
B0005507molecular_functioncopper ion binding
B0005515molecular_functionprotein binding
B0005886cellular_componentplasma membrane
B0016020cellular_componentmembrane
B0016491molecular_functionoxidoreductase activity
B0022900biological_processelectron transport chain
B0042773biological_processATP synthesis coupled electron transport
B0046872molecular_functionmetal ion binding
B1902600biological_processproton transmembrane transport
C0004129molecular_functioncytochrome-c oxidase activity
C0005515molecular_functionprotein binding
C0005886cellular_componentplasma membrane
C0006119biological_processoxidative phosphorylation
C0009060biological_processaerobic respiration
C0015990biological_processelectron transport coupled proton transport
C0016020cellular_componentmembrane
C0020037molecular_functionheme binding
C0022904biological_processrespiratory electron transport chain
C0045277cellular_componentrespiratory chain complex IV
C0046872molecular_functionmetal ion binding
C1902600biological_processproton transmembrane transport
D0004129molecular_functioncytochrome-c oxidase activity
D0005507molecular_functioncopper ion binding
D0005515molecular_functionprotein binding
D0005886cellular_componentplasma membrane
D0016020cellular_componentmembrane
D0016491molecular_functionoxidoreductase activity
D0022900biological_processelectron transport chain
D0042773biological_processATP synthesis coupled electron transport
D0046872molecular_functionmetal ion binding
D1902600biological_processproton transmembrane transport
Functional Information from PDB Data
site_idAC1
Number of Residues26
DetailsBINDING SITE FOR RESIDUE HEA A 567
ChainResidue
ALEU34
AMET106
AMET107
AGLY171
ATRP172
ATYR414
APHE420
AHIS421
ASER425
AMET460
APHE468
AGLY38
AGLN471
AARG481
AARG482
ASER504
AHOH583
AHOH584
AHOH650
AVAL45
ATHR48
AMET51
AARG52
ATRP95
AILE99
AHIS102

site_idAC2
Number of Residues31
DetailsBINDING SITE FOR RESIDUE HEA A 568
ChainResidue
ATRP172
AVAL287
AVAL291
AHIS333
AHIS334
ATHR352
AALA356
AGLY360
APHE364
APHE391
AGLY395
AVAL396
AGLY398
AILE399
ALEU401
ASER402
AASP407
AHIS411
AVAL416
AHIS419
APHE420
AVAL423
AMET424
AARG481
ACYN572
AHOH595
AHOH605
AHOH634
AHOH656
AHOH661
BPRO108

site_idAC3
Number of Residues4
DetailsBINDING SITE FOR RESIDUE CU1 A 569
ChainResidue
AHIS284
AHIS333
AHIS334
ACYN572

site_idAC4
Number of Residues6
DetailsBINDING SITE FOR RESIDUE MG A 570
ChainResidue
AHIS411
AASP412
BGLU254
BHOH318
BHOH327
BHOH334

site_idAC5
Number of Residues6
DetailsBINDING SITE FOR RESIDUE CA A 571
ChainResidue
AGLU54
AALA57
AGLY59
AGLN61
AHOH628
AHOH639

site_idAC6
Number of Residues5
DetailsBINDING SITE FOR RESIDUE CYN A 572
ChainResidue
AHIS284
AHIS333
AHIS334
AHEA568
ACU1569

site_idAC7
Number of Residues10
DetailsBINDING SITE FOR RESIDUE DMU A 573
ChainResidue
ATRP451
ATYR517
ADMU574
BGLN142
BTRP143
BPRO164
BHOH289
BHOH303
BHOH308
BHOH316

site_idAC8
Number of Residues5
DetailsBINDING SITE FOR RESIDUE DMU A 574
ChainResidue
ATRP451
AALA506
ADMU573
ATRD582
AHOH681

site_idAC9
Number of Residues4
DetailsBINDING SITE FOR RESIDUE DMU A 575
ChainResidue
ATRP20
AVAL31
AMET443
ASER444

site_idBC1
Number of Residues10
DetailsBINDING SITE FOR RESIDUE DMU A 576
ChainResidue
AGLN61
ASER83
AALA84
AVAL85
APHE505
ATRD577
AHOH639
AHOH687
AMET56
AALA57

site_idBC2
Number of Residues3
DetailsBINDING SITE FOR RESIDUE TRD A 577
ChainResidue
ALEU80
ATRP81
ADMU576

site_idBC3
Number of Residues2
DetailsBINDING SITE FOR RESIDUE TRD A 578
ChainResidue
AARG476
BTHR41

site_idBC4
Number of Residues1
DetailsBINDING SITE FOR RESIDUE TRD A 579
ChainResidue
AMET350

site_idBC5
Number of Residues1
DetailsBINDING SITE FOR RESIDUE TRD A 582
ChainResidue
ADMU574

site_idBC6
Number of Residues9
DetailsBINDING SITE FOR RESIDUE HTO B 1
ChainResidue
BGLU152
BALA276
BGLU280
BHOH291
DALA276
DGLU280
DHIS283
DHOH1327
DHOH1328

site_idBC7
Number of Residues5
DetailsBINDING SITE FOR RESIDUE CU1 B 3
ChainResidue
BCU14
BCYS252
BGLU254
BCYS256
BHIS260

site_idBC8
Number of Residues5
DetailsBINDING SITE FOR RESIDUE CU1 B 4
ChainResidue
BCU13
BHIS217
BCYS252
BCYS256
BMET263

site_idBC9
Number of Residues4
DetailsBINDING SITE FOR RESIDUE CD B 8
ChainResidue
BGLU280
BHIS283
BHIS285
DGLU152

site_idCC1
Number of Residues3
DetailsBINDING SITE FOR RESIDUE CD B 9
ChainResidue
BHIS96
BGLU101
BHOH386

site_idCC2
Number of Residues13
DetailsBINDING SITE FOR RESIDUE DMU B 288
ChainResidue
APHE364
ATRP371
BLEU75
BPHE94
BHIS96
BASN97
BLEU100
BTRP104
CGLU86
DSER173
DPRO174
DGLU177
DHOH1151

site_idCC3
Number of Residues29
DetailsBINDING SITE FOR RESIDUE HEA C 567
ChainResidue
CLEU34
CGLY38
CVAL45
CTHR48
CMET51
CARG52
CTRP95
CILE99
CHIS102
CMET106
CMET107
CVAL111
CGLY171
CTRP172
CTYR414
CPHE420
CHIS421
CMET424
CSER425
CVAL429
CMET460
CPHE468
CGLN471
CARG482
CSER504
CPHE508
CHOH1003
CHOH1011
CHOH1130

site_idCC4
Number of Residues4
DetailsBINDING SITE FOR RESIDUE DMU B 11
ChainResidue
BLEU120
BPRO121
BPHE124
BGLU128

site_idCC5
Number of Residues30
DetailsBINDING SITE FOR RESIDUE HEA C 568
ChainResidue
CTRP172
CVAL287
CVAL291
CHIS333
CTHR352
CALA356
CGLY360
CPHE364
CPHE391
CGLY395
CVAL396
CGLY398
CILE399
CLEU401
CSER402
CASP407
CHIS411
CVAL416
CHIS419
CPHE420
CVAL423
CMET424
CARG481
CCYN572
CHOH1015
CHOH1030
CHOH1096
CHOH1142
CHOH1157
DPRO108

site_idCC6
Number of Residues4
DetailsBINDING SITE FOR RESIDUE CU1 C 569
ChainResidue
CHIS284
CHIS333
CHIS334
CCYN572

site_idCC7
Number of Residues6
DetailsBINDING SITE FOR RESIDUE MG C 570
ChainResidue
CHIS411
CASP412
DGLU254
DHOH1071
DHOH1082
DHOH1094

site_idCC8
Number of Residues6
DetailsBINDING SITE FOR RESIDUE CA C 571
ChainResidue
CGLU54
CALA57
CGLY59
CGLN61
CHOH1085
CHOH1107

site_idCC9
Number of Residues5
DetailsBINDING SITE FOR RESIDUE CYN C 572
ChainResidue
CHIS284
CHIS333
CHIS334
CHEA568
CCU1569

site_idDC1
Number of Residues2
DetailsBINDING SITE FOR RESIDUE TRD C 1001
ChainResidue
CTRP451
CGLY513

site_idDC2
Number of Residues2
DetailsBINDING SITE FOR RESIDUE DMU C 1002
ChainResidue
CTRP451
CHOH1102

site_idDC3
Number of Residues10
DetailsBINDING SITE FOR RESIDUE DMU C 1005
ChainResidue
CMET56
CALA57
CGLN61
CSER83
CPHE502
CPHE505
CTRD1006
CHOH1107
CHOH1364
CHOH1612

site_idDC4
Number of Residues4
DetailsBINDING SITE FOR RESIDUE TRD C 1006
ChainResidue
CLEU80
CTRP81
CPRO82
CDMU1005

site_idDC5
Number of Residues1
DetailsBINDING SITE FOR RESIDUE TRD C 1009
ChainResidue
CPHE473

site_idDC6
Number of Residues5
DetailsBINDING SITE FOR RESIDUE CU1 D 3
ChainResidue
DCU14
DCYS252
DGLU254
DCYS256
DHIS260

site_idDC7
Number of Residues5
DetailsBINDING SITE FOR RESIDUE CU1 D 4
ChainResidue
DCU13
DHIS217
DCYS252
DCYS256
DMET263

site_idDC8
Number of Residues4
DetailsBINDING SITE FOR RESIDUE CD D 8
ChainResidue
BGLU152
DGLU280
DHIS283
DHIS285

site_idDC9
Number of Residues2
DetailsBINDING SITE FOR RESIDUE CD D 9
ChainResidue
DHIS96
DGLU101

site_idEC1
Number of Residues7
DetailsBINDING SITE FOR RESIDUE DMU D 1003
ChainResidue
CTRP371
DPHE71
DLEU75
DPHE94
DHIS96
DASN97
DTRP104

site_idEC2
Number of Residues2
DetailsBINDING SITE FOR RESIDUE TRD D 1007
ChainResidue
CARG476
DTHR41

site_idEC3
Number of Residues2
DetailsBINDING SITE FOR RESIDUE DMU D 1011
ChainResidue
DPRO121
DGLU128

Functional Information from PROSITE/UniProt
site_idPS00077
Number of Residues55
DetailsCOX1_CUB Heme-copper oxidase catalytic subunit, copper B binding region signature. WFFGHPeVyiivlpafgivshviatfakkpifgylpmvyamvaigvlgfvvwa..HH
ChainResidueDetails
ATRP280-HIS334

site_idPS00078
Number of Residues49
DetailsCOX2 CO II and nitrous oxide reductase dinuclear copper centers signature. ViHswtvpafgvkqdavpgrlaqlwfraeregiffgq......CselCgisHayM
ChainResidueDetails
BVAL215-MET263

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues80
DetailsTRANSMEM: Helical => ECO:0000255
ChainResidueDetails
BPHE60-VAL80
APHE420-ILE440
ALEU455-GLY475
ALEU499-LEU519
CILE29-VAL49
CVAL97-GLY117
CLEU141-GLY161
CLEU189-ILE209
CLEU227-ALA247
CILE278-VAL298
CILE310-VAL330
BTRP104-PHE124
CPHE348-ALA368
CMET381-LEU401
CPHE420-ILE440
CLEU455-GLY475
CLEU499-LEU519
DPHE60-VAL80
DTRP104-PHE124
ALEU227-ALA247
AILE278-VAL298
AILE310-VAL330
APHE348-ALA368
AMET381-LEU401

site_idSWS_FT_FI2
Number of Residues8
DetailsBINDING: BINDING => ECO:0000305
ChainResidueDetails
BHIS217
BCYS252
BCYS256
BHIS260
DHIS217
DCYS252
DCYS256
DHIS260

site_idSWS_FT_FI3
Number of Residues8
DetailsBINDING: BINDING => ECO:0000305
ChainResidueDetails
AHIS284
ATYR288
AHIS333
AHIS334
CHIS284
CTYR288
CHIS333
CHIS334

site_idSWS_FT_FI4
Number of Residues4
DetailsCROSSLNK: 1'-histidyl-3'-tyrosine (His-Tyr) => ECO:0000250
ChainResidueDetails
AHIS284
ATYR288
CHIS284
CTYR288

Catalytic Information from CSA
site_idCSA1
Number of Residues2
DetailsAnnotated By Reference To The Literature 1ar1
ChainResidueDetails
AGLU286
ALYS362

site_idCSA2
Number of Residues2
DetailsAnnotated By Reference To The Literature 1ar1
ChainResidueDetails
CGLU286
CLYS362

site_idCSA3
Number of Residues7
DetailsAnnotated By Reference To The Literature 1ar1
ChainResidueDetails
AHIS419
AHIS421
AARG482
AARG481
APHE420
ATYR288
AHIS284

site_idCSA4
Number of Residues7
DetailsAnnotated By Reference To The Literature 1ar1
ChainResidueDetails
CHIS419
CHIS421
CARG482
CARG481
CPHE420
CTYR288
CHIS284

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PDB entries from 2024-10-30

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