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2WHW

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
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
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 Residues24
DetailsBINDING SITE FOR RESIDUE HEM A 1407
ChainResidue
ALYS72
ALEU251
APRO289
AALA293
ATHR294
AARG296
AALA346
APHE347
AGLY348
AILE351
AHIS352
AMET92
ACYS354
AILE355
AALA360
A1D41410
AHOH2355
ALEU93
AHIS100
AARG104
APHE111
AALA243
ATHR247
ATHR248

site_idAC2
Number of Residues4
DetailsBINDING SITE FOR RESIDUE 1D4 A 1410
ChainResidue
AGLU94
AALA243
AVAL290
AHEM1407

site_idAC3
Number of Residues23
DetailsBINDING SITE FOR RESIDUE HEM B 1407
ChainResidue
BLYS72
BMET92
BLEU93
BHIS100
BARG104
BLEU240
BALA243
BTHR247
BTHR248
BALA293
BTHR294
BARG296
BALA346
BPHE347
BGLY348
BILE351
BHIS352
BCYS354
BILE355
BGLY356
BALA360
B1D41410
BHOH2353

site_idAC4
Number of Residues4
DetailsBINDING SITE FOR RESIDUE SO4 B 1408
ChainResidue
BASP167
BTYR197
BARG200
BLEU201

site_idAC5
Number of Residues6
DetailsBINDING SITE FOR RESIDUE SO4 B 1409
ChainResidue
BARG62
BLEU106
BARG109
BTHR220
BARG227
BHOH2356

site_idAC6
Number of Residues8
DetailsBINDING SITE FOR RESIDUE 1D4 B 1410
ChainResidue
BLEU93
BGLU94
BILE239
BVAL242
BTHR247
BVAL290
BHEM1407
BHOH2090

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

225158

PDB entries from 2024-09-18

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