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1ZOA

Crystal Structure Of A328V Mutant Of The Heme Domain Of P450Bm-3 With N-Palmitoylglycine

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 Residues26
DetailsBINDING SITE FOR RESIDUE HEM A 471
ChainResidue
ALYS69
ALEU272
ATHR327
AVAL328
APHE331
APRO392
APHE393
AGLY394
AARG398
AALA399
ACYS400
ALEU86
AILE401
AHOH1471
AHOH1474
AHOH1476
AHOH1478
AHOH1488
AHOH1510
APHE87
ATRP96
APHE107
APHE261
AALA264
AGLY265
ATHR268

site_idAC2
Number of Residues26
DetailsBINDING SITE FOR RESIDUE HEM B 471
ChainResidue
BLYS69
BLEU86
BPHE87
BTRP96
BPHE107
BPHE261
BALA264
BGLY265
BTHR268
BTHR269
BLEU272
BVAL328
BPHE331
BPRO392
BPHE393
BGLY394
BARG398
BALA399
BCYS400
BILE401
BHOH1492
BHOH1494
BHOH1495
BHOH1516
BHOH1527
BHOH1549

site_idAC3
Number of Residues8
DetailsBINDING SITE FOR RESIDUE 140 A 1470
ChainResidue
ALEU29
ATYR51
ASER72
AGLN73
AALA74
AALA82
ALEU188
AALA330

site_idAC4
Number of Residues8
DetailsBINDING SITE FOR RESIDUE 140 B 1471
ChainResidue
BLEU29
BTYR51
BSER72
BGLN73
BALA74
BALA82
BPHE87
BLEU188

site_idAC5
Number of Residues9
DetailsBINDING SITE FOR RESIDUE MES B 1490
ChainResidue
BILE366
BTRP367
BARG375
BARG378
BALA384
BILE385
BPRO386
BMES1491
BHOH1847

site_idAC6
Number of Residues6
DetailsBINDING SITE FOR RESIDUE MES B 1491
ChainResidue
BTHR365
BILE366
BGLY368
BPRO386
BGOL1480
BMES1490

site_idAC7
Number of Residues5
DetailsBINDING SITE FOR RESIDUE GOL B 1480
ChainResidue
AHOH1737
AHOH1825
BILE366
BMES1491
BHOH1524

site_idAC8
Number of Residues3
DetailsBINDING SITE FOR RESIDUE GOL B 1481
ChainResidue
BARG79
BGLY83
BTYR256

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
ALEU52
BLEU52

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
AILE401
BILE401

site_idSWS_FT_FI3
Number of Residues2
DetailsSITE: Important for catalytic activity => ECO:0000305|PubMed:16403573, ECO:0000305|PubMed:7578081
ChainResidueDetails
ATHR269
BTHR269

Catalytic Information from CSA
site_idCSA1
Number of Residues2
DetailsAnnotated By Reference To The Literature 1akd
ChainResidueDetails
ATHR268
AGLU267

site_idCSA2
Number of Residues2
DetailsAnnotated By Reference To The Literature 1akd
ChainResidueDetails
BTHR268
BGLU267

site_idMCSA1
Number of Residues3
DetailsM-CSA 699
ChainResidueDetails
ATHR269electrostatic stabiliser, steric role
AGLY394electrostatic stabiliser, steric role
AILE401electrostatic stabiliser

site_idMCSA2
Number of Residues3
DetailsM-CSA 699
ChainResidueDetails
BTHR269electrostatic stabiliser, steric role
BGLY394electrostatic stabiliser, steric role
BILE401electrostatic stabiliser

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PDB entries from 2024-07-31

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