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4G71

Structure of Recombinant Cytochrome ba3 Oxidase mutant V236N from Thermus thermophilus

Functional Information from GO Data
ChainGOidnamespacecontents
A0004129molecular_functioncytochrome-c oxidase activity
A0005886cellular_componentplasma membrane
A0006119biological_processoxidative phosphorylation
A0006811biological_processmonoatomic ion transport
A0009060biological_processaerobic respiration
A0016020cellular_componentmembrane
A0020037molecular_functionheme binding
A0022904biological_processrespiratory electron transport chain
A0046872molecular_functionmetal ion binding
A1902600biological_processproton transmembrane transport
B0004129molecular_functioncytochrome-c oxidase activity
B0005507molecular_functioncopper ion binding
B0005886cellular_componentplasma membrane
B0016020cellular_componentmembrane
B0022904biological_processrespiratory electron transport chain
B0046872molecular_functionmetal ion binding
B1902600biological_processproton transmembrane transport
C0004129molecular_functioncytochrome-c oxidase activity
C0005886cellular_componentplasma membrane
C0006811biological_processmonoatomic ion transport
C0022904biological_processrespiratory electron transport chain
C1902600biological_processproton transmembrane transport
Functional Information from PDB Data
site_idAC1
Number of Residues4
DetailsBINDING SITE FOR RESIDUE CUB A 601
ChainResidue
AHIS233
AHIS282
AHIS283
APER604

site_idAC2
Number of Residues24
DetailsBINDING SITE FOR RESIDUE HEM A 602
ChainResidue
AHIS72
AASN76
AALA77
ALEU132
ATYR133
APHE385
AHIS386
AVAL389
AALA390
ATHR394
ATRP428
AMET432
AMET435
AARG449
AARG450
AALA451
ALEU477
AHOH711
AHOH715
ALEU32
AGLY39
AGLN42
ATYR46
ATYR65

site_idAC3
Number of Residues29
DetailsBINDING SITE FOR RESIDUE HAS A 603
ChainResidue
ATYR133
ATRP229
AASN236
ATYR237
AHIS282
AHIS283
ASER309
ALEU310
AALA313
AALA317
ATRP335
AVAL350
ALEU353
APHE356
AGLY363
AASN366
AALA367
AASP372
AHIS376
AVAL381
AHIS384
APHE385
AGLN388
AARG449
APER604
AHOH701
AHOH737
AHOH738
CVAL11

site_idAC4
Number of Residues4
DetailsBINDING SITE FOR RESIDUE PER A 604
ChainResidue
AHIS233
AASN236
ACUB601
AHAS603

site_idAC5
Number of Residues6
DetailsBINDING SITE FOR RESIDUE OLC A 605
ChainResidue
AVAL158
ATYR161
AILE475
AVAL476
AVAL479
AOLC613

site_idAC6
Number of Residues8
DetailsBINDING SITE FOR RESIDUE OLC A 606
ChainResidue
APHE213
ALEU215
ATRP341
ATRP426
ALEU430
AOLC608
AOLC612
AOLC613

site_idAC7
Number of Residues8
DetailsBINDING SITE FOR RESIDUE OLC A 607
ChainResidue
APRO292
ATHR293
AMET296
AILE297
AVAL300
APHE304
AHOH703
BALA42

site_idAC8
Number of Residues7
DetailsBINDING SITE FOR RESIDUE OLC A 608
ChainResidue
ALYS140
ASER212
APHE213
AGLY214
ALEU430
AOLC606
AOLC615

site_idAC9
Number of Residues2
DetailsBINDING SITE FOR RESIDUE OLC A 609
ChainResidue
ATRP111
AOLC612

site_idBC1
Number of Residues4
DetailsBINDING SITE FOR RESIDUE OLC A 610
ChainResidue
ATYR161
ALEU164
AASP165
AARG168

site_idBC2
Number of Residues6
DetailsBINDING SITE FOR RESIDUE OLC A 611
ChainResidue
ALYS171
AGLY528
APHE531
ALEU164
ATRP167
AARG168

site_idBC3
Number of Residues7
DetailsBINDING SITE FOR RESIDUE OLC A 612
ChainResidue
AMET103
AGLY104
ATRP111
AVAL468
AOLC606
AOLC609
AOLC613

site_idBC4
Number of Residues10
DetailsBINDING SITE FOR RESIDUE OLC A 613
ChainResidue
AASN102
AGLY104
ALEU105
ALEU108
AMET112
AVAL151
AVAL471
AOLC605
AOLC606
AOLC612

site_idBC5
Number of Residues3
DetailsBINDING SITE FOR RESIDUE OLC A 614
ChainResidue
AASP415
AALA416
AARG419

site_idBC6
Number of Residues7
DetailsBINDING SITE FOR RESIDUE OLC A 615
ChainResidue
AARG337
ATRP341
ALEU354
ATRP426
APHE429
ALEU430
AOLC608

site_idBC7
Number of Residues6
DetailsBINDING SITE FOR RESIDUE CUA B 201
ChainResidue
BHIS114
BCYS149
BGLN151
BCYS153
BHIS157
BMET160

site_idBC8
Number of Residues4
DetailsBINDING SITE FOR RESIDUE OLC B 202
ChainResidue
BMET25
BTYR35
BOLC204
CPHE31

site_idBC9
Number of Residues9
DetailsBINDING SITE FOR RESIDUE OLC B 203
ChainResidue
ATRP441
BARG141
BPRO142
BGLU144
BTYR145
CVAL29
CARG33
COLC101
COLC102

site_idCC1
Number of Residues7
DetailsBINDING SITE FOR RESIDUE OLC B 204
ChainResidue
BALA13
BGLY17
BTRP18
BPHE21
BTYR35
BOLC202
CILE12

site_idCC2
Number of Residues6
DetailsBINDING SITE FOR RESIDUE OLC C 101
ChainResidue
BOLC203
CPHE22
CGLY25
CALA28
CVAL29
COLC102

site_idCC3
Number of Residues5
DetailsBINDING SITE FOR RESIDUE OLC C 102
ChainResidue
APRO358
BOLC203
CTHR18
CVAL21
COLC101

Functional Information from PROSITE/UniProt
site_idPS00078
Number of Residues49
DetailsCOX2 CO II and nitrous oxide reductase dinuclear copper centers signature. ViHgfhvegtninvevlpgevstvrytfkrpgeyrii......CnqyCglgHqnM
ChainResidueDetails
BVAL112-MET160

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues260
DetailsTransmembrane: {"description":"Helical","evidences":[{"evidenceCode":"ECO:0000255"}]}
ChainResidueDetails

site_idSWS_FT_FI2
Number of Residues3
DetailsBinding site: {"description":"axial binding residue","evidences":[{"evidenceCode":"ECO:0000305"}]}
ChainResidueDetails

site_idSWS_FT_FI3
Number of Residues6
DetailsBinding site: {}
ChainResidueDetails

site_idSWS_FT_FI4
Number of Residues2
DetailsBinding site: {"evidences":[{"evidenceCode":"ECO:0000305"}]}
ChainResidueDetails

site_idSWS_FT_FI5
Number of Residues2
DetailsCross-link: {"description":"1'-histidyl-3'-tyrosine (His-Tyr)"}
ChainResidueDetails

site_idSWS_FT_FI6
Number of Residues64
DetailsTransmembrane: {"description":"Helical"}
ChainResidueDetails

site_idSWS_FT_FI7
Number of Residues129
DetailsTopological domain: {"description":"Periplasmic"}
ChainResidueDetails

Catalytic Information from CSA
site_idMCSA1
Number of Residues2
DetailsM-CSA 735
ChainResidueDetails
BPHE86electron shuttle
BPHE88electron shuttle
AHIS384electron shuttle
APHE385electron shuttle
AHIS386electron shuttle
AARG449electron shuttle
AARG450electron shuttle

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PDB entries from 2025-12-24

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