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2WI9

Selective oxidation of carbolide C-H bonds by engineered macrolide P450 monooxygenase

Functional Information from GO Data
ChainGOidnamespacecontents
A0004497molecular_functionmonooxygenase activity
A0005506molecular_functioniron ion binding
A0016491molecular_functionoxidoreductase activity
A0016705molecular_functionoxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen
A0017000biological_processantibiotic biosynthetic process
A0020037molecular_functionheme binding
A0033068biological_processmacrolide biosynthetic process
A0046872molecular_functionmetal ion binding
A0055114biological_processobsolete oxidation-reduction process
B0004497molecular_functionmonooxygenase activity
B0005506molecular_functioniron ion binding
B0016491molecular_functionoxidoreductase activity
B0016705molecular_functionoxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen
B0017000biological_processantibiotic biosynthetic process
B0020037molecular_functionheme binding
B0033068biological_processmacrolide biosynthetic process
B0046872molecular_functionmetal ion binding
B0055114biological_processobsolete oxidation-reduction process
Functional Information from PDB Data
site_idAC1
Number of Residues25
DetailsBINDING SITE FOR RESIDUE HEM A 1408
ChainResidue
ALYS72
ALEU251
APRO289
AALA293
ATHR294
AARG296
AALA346
APHE347
AGLY348
AILE351
AHIS352
AMET92
ACYS354
AILE355
AALA360
A1D21409
AHOH2294
AHOH2295
ALEU93
AHIS100
AARG104
APHE111
AALA243
ATHR247
ATHR248

site_idAC2
Number of Residues11
DetailsBINDING SITE FOR RESIDUE 1D2 A 1409
ChainResidue
ALEU93
AGLU94
APHE178
AVAL242
AALA243
AGLU246
AILE395
AHEM1408
AHOH2086
AHOH2294
AHOH2296

site_idAC3
Number of Residues24
DetailsBINDING SITE FOR RESIDUE HEM B 1408
ChainResidue
BLYS72
BMET92
BLEU93
BHIS100
BARG104
BPHE111
BLEU240
BALA243
BTHR247
BTHR248
BLEU251
BALA293
BTHR294
BARG296
BALA346
BPHE347
BGLY348
BILE351
BHIS352
BCYS354
BILE355
BALA360
B1D21409
BHOH2276

site_idAC4
Number of Residues18
DetailsBINDING SITE FOR RESIDUE 1D2 B 1409
ChainResidue
BGLU85
BLEU88
BASN91
BLEU93
BGLU94
BPHE178
BHIS238
BILE239
BALA243
BGLU246
BTHR247
BTHR294
BMET394
BILE395
BHEM1408
BHOH2072
BHOH2277
BHOH2278

site_idAC5
Number of Residues7
DetailsBINDING SITE FOR RESIDUE SO4 B 1410
ChainResidue
BARG62
BLEU106
BARG109
BTHR220
BARG227
BHOH2279
BHOH2280

site_idAC6
Number of Residues4
DetailsBINDING SITE FOR RESIDUE SO4 B 1411
ChainResidue
BARG60
BASP303
BLEU304
BASP305

site_idAC7
Number of Residues3
DetailsBINDING SITE FOR RESIDUE SO4 B 1412
ChainResidue
BASP167
BTYR197
BSER204

Functional Information from PROSITE/UniProt
site_idPS00086
Number of Residues10
DetailsCYTOCHROME_P450 Cytochrome P450 cysteine heme-iron ligand signature. FGhGIHFCIG
ChainResidueDetails
APHE347-GLY356

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues6
DetailsBINDING: BINDING => ECO:0000269|PubMed:16825192, ECO:0000269|PubMed:19124459
ChainResidueDetails
AGLU94
AALA187
AHIS238
BGLU94
BALA187
BHIS238

site_idSWS_FT_FI2
Number of Residues2
DetailsBINDING: axial binding residue => ECO:0000269|PubMed:16825192, ECO:0000269|PubMed:19124459, ECO:0000269|PubMed:19833867, ECO:0000269|PubMed:24627965, ECO:0000312|PDB:2C6H, ECO:0000312|PDB:2C7X, ECO:0000312|PDB:2CA0, ECO:0000312|PDB:2CD8, ECO:0000312|PDB:2VZ7, ECO:0000312|PDB:2VZM, ECO:0000312|PDB:2WHW, ECO:0000312|PDB:2WI9, ECO:0000312|PDB:3ZK5, ECO:0000312|PDB:4B7D, ECO:0000312|PDB:4B7S, ECO:0000312|PDB:4BF4
ChainResidueDetails
ACYS354
BCYS354

Catalytic Information from CSA
site_idCSA1
Number of Residues2
DetailsAnnotated By Reference To The Literature 1akd
ChainResidueDetails
AGLU246
ATHR247

site_idCSA2
Number of Residues2
DetailsAnnotated By Reference To The Literature 1akd
ChainResidueDetails
BGLU246
BTHR247

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PDB entries from 2025-06-18

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