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4LHT

Crystal Structure of P450cin Y81F mutant, crystallized in 3 mM 1,8-cineole

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
A0016709molecular_functionoxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, NAD(P)H as one donor, and incorporation of one atom of oxygen
A0020037molecular_functionheme binding
A0046232biological_processcarbazole catabolic 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
B0016709molecular_functionoxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, NAD(P)H as one donor, and incorporation of one atom of oxygen
B0020037molecular_functionheme binding
B0046232biological_processcarbazole catabolic 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 501
ChainResidue
AASN73
ATHR243
APHE246
APRO284
AARG289
APHE312
ASER339
ALEU340
AGLY341
AILE344
AHIS345
AVAL76
ACYS347
ALEU348
AILE353
ACNL502
AHOH628
AMET90
AALA91
AHIS98
AARG102
AILE234
AGLY238
AASN242

site_idAC2
Number of Residues3
DetailsBINDING SITE FOR RESIDUE CNL A 502
ChainResidue
AGLY238
AASN242
AHEM501

site_idAC3
Number of Residues4
DetailsBINDING SITE FOR RESIDUE PEG A 503
ChainResidue
APRO304
AGLY305
AGLN306
APGE504

site_idAC4
Number of Residues2
DetailsBINDING SITE FOR RESIDUE PGE A 504
ChainResidue
ATRP45
APEG503

site_idAC5
Number of Residues5
DetailsBINDING SITE FOR RESIDUE SO4 A 505
ChainResidue
AARG346
AALA350
AHIS351
AARG354
AHOH771

site_idAC6
Number of Residues3
DetailsBINDING SITE FOR RESIDUE CL A 506
ChainResidue
AASP323
AARG332
AHOH730

site_idAC7
Number of Residues25
DetailsBINDING SITE FOR RESIDUE HEM B 501
ChainResidue
BASN73
BVAL76
BMET90
BALA91
BHIS98
BARG102
BPHE109
BILE234
BGLY238
BASN242
BTHR243
BPHE246
BPRO284
BARG289
BPHE312
BSER339
BLEU340
BGLY341
BILE344
BHIS345
BCYS347
BLEU348
BILE353
BCNL502
BHOH675

site_idAC8
Number of Residues5
DetailsBINDING SITE FOR RESIDUE CNL B 502
ChainResidue
BGLY238
BASN242
BALA285
BVAL287
BHEM501

site_idAC9
Number of Residues4
DetailsBINDING SITE FOR RESIDUE PG4 B 503
ChainResidue
BTRP45
BGLY50
BHOH682
BHOH753

Functional Information from SwissProt/UniProt
site_idSWS_FT_FI1
Number of Residues10
DetailsBINDING: BINDING => ECO:0000269|PubMed:15260491, ECO:0000269|PubMed:18270198, ECO:0000269|PubMed:22775403
ChainResidueDetails
AASN73
BHIS345
AHIS98
AARG102
AARG289
AHIS345
BASN73
BHIS98
BARG102
BARG289

site_idSWS_FT_FI2
Number of Residues2
DetailsBINDING: BINDING => ECO:0000269|PubMed:15260491
ChainResidueDetails
AASN242
BASN242

site_idSWS_FT_FI3
Number of Residues2
DetailsBINDING: axial binding residue
ChainResidueDetails
ACYS347
BCYS347

site_idSWS_FT_FI4
Number of Residues2
DetailsSITE: Controls regioselective substrate oxidation
ChainResidueDetails
AASN242
BASN242

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PDB entries from 2025-06-18

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