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2X7Y

P450 BM3 F87A in complex with DMSO

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
A0020037molecular_functionheme binding
B0004497molecular_functionmonooxygenase activity
B0005506molecular_functioniron ion binding
B0016705molecular_functionoxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen
B0020037molecular_functionheme binding
Functional Information from PDB Data
site_idAC1
Number of Residues28
DetailsBINDING SITE FOR RESIDUE HEM A 1456
ChainResidue
ALYS69
ATHR268
ATHR269
APHE331
APRO392
APHE393
AGLY394
AARG398
ACYS400
AILE401
AGLY402
ALEU75
AALA406
ADMS1460
AHOH2272
AHOH2273
AHOH2274
AHOH2275
AHOH2276
AHOH2277
AHOH2279
ALEU86
AALA87
ATRP96
APHE107
APHE261
AALA264
AGLY265

site_idAC2
Number of Residues4
DetailsBINDING SITE FOR RESIDUE ZN A 1457
ChainResidue
AASP231
AHIS236
AHIS285
AHOH2278

site_idAC3
Number of Residues3
DetailsBINDING SITE FOR RESIDUE ZN A 1458
ChainResidue
AHIS92
ALYS336
BGLU373

site_idAC4
Number of Residues3
DetailsBINDING SITE FOR RESIDUE ZN A 1459
ChainResidue
AASP338
AGLU348
BHIS285

site_idAC5
Number of Residues3
DetailsBINDING SITE FOR RESIDUE DMS A 1460
ChainResidue
AALA264
AHEM1456
AHOH2279

site_idAC6
Number of Residues26
DetailsBINDING SITE FOR RESIDUE HEM B 1456
ChainResidue
BLYS69
BLEU86
BALA87
BTRP96
BPHE107
BPHE261
BALA264
BGLY265
BTHR268
BTHR269
BALA328
BPHE331
BPRO392
BPHE393
BGLY394
BARG398
BALA399
BCYS400
BILE401
BGLY402
BDMS1458
BHOH2194
BHOH2268
BHOH2269
BHOH2270
BHOH2272

site_idAC7
Number of Residues3
DetailsBINDING SITE FOR RESIDUE ZN B 1457
ChainResidue
BASP231
BHIS236
BGLU430

site_idAC8
Number of Residues2
DetailsBINDING SITE FOR RESIDUE DMS B 1458
ChainResidue
BHEM1456
BHOH2273

Functional Information from PROSITE/UniProt
site_idPS00086
Number of Residues10
DetailsCYTOCHROME_P450 Cytochrome P450 cysteine heme-iron ligand signature. FGnGQRACIG
ChainResidueDetails
APHE393-GLY402

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues2
DetailsBINDING: BINDING => ECO:0000269|PubMed:15020590, ECO:0007744|PDB:1SMJ
ChainResidueDetails
ATYR51
BTYR51

site_idSWS_FT_FI2
Number of Residues2
DetailsBINDING: axial binding residue => ECO:0000269|PubMed:10051560, ECO:0000269|PubMed:11695889, ECO:0000269|PubMed:11695892, ECO:0000269|PubMed:14653735, ECO:0000269|PubMed:15020590, ECO:0000269|PubMed:15299332, ECO:0000269|PubMed:16403573, ECO:0000269|PubMed:17077084, ECO:0000269|PubMed:17429965, ECO:0000269|PubMed:17868686, ECO:0000269|PubMed:18004886, ECO:0000269|PubMed:18298086, ECO:0000269|PubMed:18619466, ECO:0000269|PubMed:18721129, ECO:0000269|PubMed:19492389, ECO:0000269|PubMed:20180779, ECO:0000269|PubMed:20947800, ECO:0000269|PubMed:21110374, ECO:0000269|PubMed:21875028, ECO:0000269|PubMed:7578081, ECO:0000269|PubMed:8342039, ECO:0000269|PubMed:9033595, ECO:0007744|PDB:1BU7, ECO:0007744|PDB:1BVY, ECO:0007744|PDB:1FAG, ECO:0007744|PDB:1FAH, ECO:0007744|PDB:1JME, ECO:0007744|PDB:1JPZ, ECO:0007744|PDB:1P0V, ECO:0007744|PDB:1P0W, ECO:0007744|PDB:1P0X, ECO:0007744|PDB:1SMI, ECO:0007744|PDB:1SMJ, ECO:0007744|PDB:1YQO, ECO:0007744|PDB:1YQP, ECO:0007744|PDB:1ZO4, ECO:0007744|PDB:1ZO9, ECO:0007744|PDB:1ZOA, ECO:0007744|PDB:2BMH, ECO:0007744|PDB:2HPD, ECO:0007744|PDB:2IJ2, ECO:0007744|PDB:2IJ3, ECO:0007744|PDB:2IJ4, ECO:0007744|PDB:2J1M, ECO:0007744|PDB:2J4S, ECO:0007744|PDB:2UWH, ECO:0007744|PDB:3BEN, ECO:0007744|PDB:3CBD, ECO:0007744|PDB:3EKB, ECO:0007744|PDB:3EKD, ECO:0007744|PDB:3EKF, ECO:0007744|PDB:3HF2, ECO:0007744|PDB:3KX3, ECO:0007744|PDB:3KX4, ECO:0007744|PDB:3KX5, ECO:0007744|PDB:3M4V, ECO:0007744|PDB:3NPL
ChainResidueDetails
ACYS400
BCYS400

site_idSWS_FT_FI3
Number of Residues2
DetailsSITE: Important for catalytic activity => ECO:0000305|PubMed:16403573, ECO:0000305|PubMed:7578081
ChainResidueDetails
ATHR268
BTHR268

Catalytic Information from CSA
site_idMCSA1
Number of Residues3
DetailsM-CSA 699
ChainResidueDetails
ATHR268electrostatic stabiliser, steric role
APHE393electrostatic stabiliser, steric role
ACYS400electrostatic stabiliser

site_idMCSA2
Number of Residues3
DetailsM-CSA 699
ChainResidueDetails
BTHR268electrostatic stabiliser, steric role
BPHE393electrostatic stabiliser, steric role
BCYS400electrostatic stabiliser

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PDB entries from 2024-10-30

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