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4B7S

PikC D50N mutant bound to the 10-DML analog with the 3-(N,N- dimethylamino)propanoate anchoring group

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 Residues25
DetailsBINDING SITE FOR RESIDUE HEM A 1407
ChainResidue
ALYS72
ATHR248
ALEU251
APRO289
AALA293
ATHR294
AARG296
AALA346
APHE347
AGLY348
AILE351
AMET92
AHIS352
ACYS354
AILE355
AGLY356
AALA360
AHOH2373
ALEU93
AHIS100
AARG104
APHE111
AILE157
AGLY244
ATHR247

site_idAC2
Number of Residues12
DetailsBINDING SITE FOR RESIDUE QLE A 1408
ChainResidue
AGLU85
AGLU94
APHE178
AVAL179
AHIS238
AILE239
AVAL242
AALA243
ATHR294
AMET394
AILE395
AGOL1415

site_idAC3
Number of Residues23
DetailsBINDING SITE FOR RESIDUE HEM B 1407
ChainResidue
BMET92
BLEU93
BHIS100
BARG104
BPHE111
BALA243
BGLY244
BTHR247
BTHR248
BLEU251
BPRO289
BALA293
BTHR294
BARG296
BALA346
BPHE347
BGLY348
BILE351
BHIS352
BCYS354
BILE355
BALA360
BHOH2307

site_idAC4
Number of Residues17
DetailsBINDING SITE FOR RESIDUE QLE B 1408
ChainResidue
BGLU85
BASN89
BLEU93
BGLU94
BPHE178
BVAL179
BHIS238
BILE239
BVAL242
BALA243
BGLU246
BTHR247
BTHR294
BMET394
BILE395
BGOL1411
BHOH2194

site_idAC5
Number of Residues3
DetailsBINDING SITE FOR RESIDUE SO4 A 1409
ChainResidue
ALEU106
ATHR220
AARG227

site_idAC6
Number of Residues3
DetailsBINDING SITE FOR RESIDUE SO4 A 1410
ChainResidue
AARG114
AARG115
AHOH2186

site_idAC7
Number of Residues6
DetailsBINDING SITE FOR RESIDUE SO4 A 1411
ChainResidue
AVAL173
AGLU193
AHOH2396
AHOH2397
AHOH2398
BARG75

site_idAC8
Number of Residues3
DetailsBINDING SITE FOR RESIDUE SO4 B 1409
ChainResidue
BTHR112
BARG114
BHOH2143

site_idAC9
Number of Residues5
DetailsBINDING SITE FOR RESIDUE SO4 B 1410
ChainResidue
BHIS262
BPRO263
BASP264
BGLN265
BARG334

site_idBC1
Number of Residues3
DetailsBINDING SITE FOR RESIDUE SO4 A 1412
ChainResidue
AHOH2044
AARG36
APRO326

site_idBC2
Number of Residues5
DetailsBINDING SITE FOR RESIDUE SO4 A 1413
ChainResidue
AARG75
AHIS90
AARG99
AHOH2117
AHOH2157

site_idBC3
Number of Residues3
DetailsBINDING SITE FOR RESIDUE SO4 A 1414
ChainResidue
AGLU223
AASP224
AHOH2304

site_idBC4
Number of Residues4
DetailsBINDING SITE FOR RESIDUE GOL A 1415
ChainResidue
ATHR294
ATYR295
AQLE1408
AHOH2122

site_idBC5
Number of Residues5
DetailsBINDING SITE FOR RESIDUE GOL B 1411
ChainResidue
BTHR294
BTYR295
BMET394
BQLE1408
BHOH2115

site_idBC6
Number of Residues5
DetailsBINDING SITE FOR RESIDUE GOL A 1416
ChainResidue
APRO98
AARG99
AARG102
AHOH2167
AHOH2399

site_idBC7
Number of Residues9
DetailsBINDING SITE FOR RESIDUE GOL A 1417
ChainResidue
ATYR29
AASN254
ATYR257
ATYR286
AGLU287
AARG324
ATRP389
AARG396
AHOH2339

site_idBC8
Number of Residues3
DetailsBINDING SITE FOR RESIDUE GOL A 1418
ChainResidue
AARG361
AARG365
AHOH2382

site_idBC9
Number of Residues4
DetailsBINDING SITE FOR RESIDUE GOL A 1419
ChainResidue
AARG62
AHIS349
AHOH2401
AHOH2402

site_idCC1
Number of Residues5
DetailsBINDING SITE FOR RESIDUE GOL A 1420
ChainResidue
AVAL14
ALEU15
AARG34
AGLU38
AHOH2048

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

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PDB entries from 2024-08-07

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