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3GKE

Crystal Structure of Dicamba Monooxygenase

Functional Information from GO Data
ChainGOidnamespacecontents
A0004497molecular_functionmonooxygenase activity
A0016491molecular_functionoxidoreductase activity
A0016705molecular_functionoxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen
A0019439biological_processobsolete aromatic compound catabolic process
A0046872molecular_functionmetal ion binding
A0051537molecular_function2 iron, 2 sulfur cluster binding
B0004497molecular_functionmonooxygenase activity
B0016491molecular_functionoxidoreductase activity
B0016705molecular_functionoxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen
B0019439biological_processobsolete aromatic compound catabolic process
B0046872molecular_functionmetal ion binding
B0051537molecular_function2 iron, 2 sulfur cluster binding
C0004497molecular_functionmonooxygenase activity
C0016491molecular_functionoxidoreductase activity
C0016705molecular_functionoxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen
C0019439biological_processobsolete aromatic compound catabolic process
C0046872molecular_functionmetal ion binding
C0051537molecular_function2 iron, 2 sulfur cluster binding
Functional Information from PDB Data
site_idAC1
Number of Residues8
DetailsBINDING SITE FOR RESIDUE FES A 500
ChainResidue
ACYS49
AHIS51
AARG52
ACYS68
ATYR70
AHIS71
AGLY72
ALEU73

site_idAC2
Number of Residues4
DetailsBINDING SITE FOR RESIDUE FE A 501
ChainResidue
AHIS165
AASP294
AACT354
AHIS160

site_idAC3
Number of Residues9
DetailsBINDING SITE FOR RESIDUE EDO A 350
ChainResidue
ATRP9
ATYR10
AVAL11
AVAL225
ASER226
AALA227
AILE252
ALEU253
ATHR254

site_idAC4
Number of Residues6
DetailsBINDING SITE FOR RESIDUE EDO A 351
ChainResidue
AGLU16
AARG130
AGLY139
AHOH464
AHOH487
AHOH516

site_idAC5
Number of Residues7
DetailsBINDING SITE FOR RESIDUE EDO A 352
ChainResidue
AASP126
AGLY128
ACYS129
ALEU229
AARG248
AHOH375
AHOH519

site_idAC6
Number of Residues6
DetailsBINDING SITE FOR RESIDUE ACT A 353
ChainResidue
AASN230
AILE232
AHIS251
ATRP285
AHOH359
AHOH428

site_idAC7
Number of Residues6
DetailsBINDING SITE FOR RESIDUE ACT A 354
ChainResidue
AHIS160
AHIS165
ALEU290
AASP294
AFE501
AHOH567

site_idAC8
Number of Residues7
DetailsBINDING SITE FOR RESIDUE FES B 500
ChainResidue
BCYS49
BHIS51
BARG52
BALA54
BCYS68
BHIS71
BLEU73

site_idAC9
Number of Residues5
DetailsBINDING SITE FOR RESIDUE FE B 501
ChainResidue
BASN154
BHIS160
BHIS165
BASP294
BOXY600

site_idBC1
Number of Residues4
DetailsBINDING SITE FOR RESIDUE OXY B 600
ChainResidue
BHIS160
BHIS165
BASP294
BFE501

site_idBC2
Number of Residues5
DetailsBINDING SITE FOR RESIDUE ACT B 700
ChainResidue
BASN230
BILE232
BHIS251
BTRP285
BHOH396

site_idBC3
Number of Residues10
DetailsBINDING SITE FOR RESIDUE EDO B 350
ChainResidue
BTRP9
BTYR10
BVAL11
BVAL225
BSER226
BALA227
BILE252
BLEU253
BTHR254
BEDO351

site_idBC4
Number of Residues7
DetailsBINDING SITE FOR RESIDUE EDO B 351
ChainResidue
BALA8
BTRP9
BPRO125
BLYS224
BVAL225
BEDO350
BHOH428

site_idBC5
Number of Residues7
DetailsBINDING SITE FOR RESIDUE EDO B 352
ChainResidue
BMET156
BASP157
BLEU158
BARG179
BALA190
BASN218
BILE220

site_idBC6
Number of Residues7
DetailsBINDING SITE FOR RESIDUE FES C 500
ChainResidue
CCYS49
CHIS51
CARG52
CCYS68
CTYR70
CHIS71
CLEU73

site_idBC7
Number of Residues12
DetailsBINDING SITE FOR RESIDUE EDO C 350
ChainResidue
CTYR10
CVAL11
CLYS224
CVAL225
CSER226
CALA227
CILE252
CLEU253
CTHR254
CHOH453
CHOH481
CTRP9

site_idBC8
Number of Residues3
DetailsBINDING SITE FOR RESIDUE EDO C 351
ChainResidue
AGLU104
AHOH730
CHOH464

site_idBC9
Number of Residues6
DetailsBINDING SITE FOR RESIDUE EDO C 352
ChainResidue
CGLU16
CARG130
CVAL138
CGLY139
CHOH407
CHOH540

site_idCC1
Number of Residues5
DetailsBINDING SITE FOR RESIDUE ACT C 353
ChainResidue
BALA117
CVAL62
CASN63
CGLU74
CHOH376

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues21
DetailsBINDING: BINDING => ECO:0000269|PubMed:19616009, ECO:0000269|PubMed:19616011, ECO:0007744|PDB:3GB4, ECO:0007744|PDB:3GKE, ECO:0007744|PDB:3GL0, ECO:0007744|PDB:3GL2, ECO:0007744|PDB:3GOB, ECO:0007744|PDB:3GTE, ECO:0007744|PDB:3GTS
ChainResidueDetails
ACYS49
AASP294
BCYS49
BHIS51
BCYS68
BHIS71
BHIS160
BHIS165
BASP294
CCYS49
CHIS51
CCYS68
CHIS71
CHIS160
CHIS165
CASP294
AHIS51
ACYS68
AHIS71
AHIS160
AHIS165

site_idSWS_FT_FI2
Number of Residues6
DetailsBINDING: BINDING => ECO:0000269|PubMed:19616009, ECO:0000269|PubMed:19616011, ECO:0007744|PDB:3GB4, ECO:0007744|PDB:3GKE, ECO:0007744|PDB:3GL0, ECO:0007744|PDB:3GL2, ECO:0007744|PDB:3GOB, ECO:0007744|PDB:3GTS
ChainResidueDetails
AASN230
AHIS251
BASN230
BHIS251
CASN230
CHIS251

site_idSWS_FT_FI3
Number of Residues3
DetailsBINDING: BINDING => ECO:0000269|PubMed:19616009, ECO:0000269|PubMed:19616011, ECO:0007744|PDB:3GB4, ECO:0007744|PDB:3GKE, ECO:0007744|PDB:3GL0, ECO:0007744|PDB:3GL2, ECO:0007744|PDB:3GTS
ChainResidueDetails
ATRP285
BTRP285
CTRP285

site_idSWS_FT_FI4
Number of Residues3
DetailsSITE: Plays a role in the stabilization of the metal coordination => ECO:0000269|PubMed:19616009
ChainResidueDetails
AASN154
BASN154
CASN154

221051

PDB entries from 2024-06-12

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