Structure of PDB 6hqp Chain A

Receptor sequence
>6hqpA (length=402) Species: 385957 (Amycolatopsis sp. ATCC 39116) [Search protein sequence]
RPDLAWLDEVTMTQLERNPYEVYERLRAEAPLAFVPVLGSYVASTAEVCR
EVATSPDFEAVITPAGGRTFGHPAIIGVNGDIHADLRSMVEPALQPAEVD
RWIDDLVRPIARRYLERFENDGHAELVAQYCEPVSVRSLGDLLGLQEVDS
DKLREWFAKLNRSVTNAAVDENGEFANPEGFAEGDQAKAEIRAVVDPLID
KWIEHPDDSAISHWLHDGMPPGQTRDREYIYPTIYVYLLGAMQEPGHGMA
STLVGLFSRPEQLEEVVDDPTLIPRAIAEGLRWTSPIWSATARISTKPVT
IAGVDLPAGTPVMLSYGSANHDTGKYEAPSQYDLHRPPLPHLAFGAGNHA
CAGIYFANHVMRIALEELFEAIPNLERDTREGVEFWGWGFRGPTSLHVTW
EV
3D structure
PDB6hqp Enabling microbial syringol conversion through structure-guided protein engineering.
ChainA
Resolution1.62 Å
3D
structure
Catalytic site residues are labeled in the structure
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Enzymatic activity
Catalytic site (original residue number in PDB) R167 Q248 E249 C356 A357 G358
Catalytic site (residue number reindexed from 1) R162 Q243 E244 C351 A352 G353
Enzyme Commision number 1.14.14.-
Interaction with ligand
Site
#
Ligand Ligand
chain
Binding residues on receptor
(original residue number in PDB)
Binding residues on receptor
(residue number reindexed from 1)
Binding affinity
BS01 HEM A I81 H88 R92 Y242 A246 E249 P250 I292 T296 R298 Y321 A348 F349 G350 A351 H354 C356 A362 M366 I76 H83 R87 Y237 A241 E244 P245 I287 T291 R293 Y316 A343 F344 G345 A346 H349 C351 A357 M361
BS02 JZ3 A V241 L244 G245 A246 I292 T296 V236 L239 G240 A241 I287 T291
Gene Ontology
Molecular Function
GO:0004497 monooxygenase activity
GO:0005506 iron ion binding
GO:0016705 oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen
GO:0020037 heme binding
GO:0046872 metal ion binding
Biological Process
GO:0009056 catabolic process

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Molecular Function

View graph for
Biological Process
External links
PDB RCSB:6hqp, PDBe:6hqp, PDBj:6hqp
PDBsum6hqp
PubMed31235604
UniProtP0DPQ7|GCOA_AMYS7 Aromatic O-demethylase, cytochrome P450 subunit (Gene Name=gcoA)

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