Structure of PDB 6zgp Chain J Binding Site BS01
Receptor Information
>6zgp Chain J (length=356) Species:
470
(Acinetobacter baumannii) [
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AVEKLPEDFCANPDVAWTFPKVFYTSSQVFEHEKEAIFAKSWICVAHGSE
LAQPNDYITRKVIGENIVIIRGKDSVLRAFYNVCPHRGHELLSGSGKAKN
VITCPYHAWTFKLDGSLALARNCDHVESFDKENSSMVPLKVEEYAGFVFI
NMDENATCVEDQLPGFAERLNQACGVIKDLKLAARFVTETPANWKVIVDN
YMECYHCGPAHPGFADSVQVDKYWHTTHQNWTLQYGFATDPEFHGFWTWP
CTMFNVPPGSNFMTVIYEFPVDAETTLQHYDIYFTNEELTQDQKDLIEWY
RNVFRPEDLNLVESVQRGLKSRGYRGQGRIMTDKQRSGISEHGIAYFQHL
VAQYHQ
Ligand information
Ligand ID
FE
InChI
InChI=1S/Fe/q+3
InChIKey
VTLYFUHAOXGGBS-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
CACTVS 3.341
OpenEye OEToolkits 1.5.0
[Fe+3]
Formula
Fe
Name
FE (III) ION
ChEMBL
DrugBank
DB13949
ZINC
PDB chain
6zgp Chain J Residue 401 [
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Receptor-Ligand Complex Structure
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PDB
6zgp
Structural basis of carnitine monooxygenase CntA substrate specificity, inhibition, and intersubunit electron transfer.
Resolution
2.01 Å
Binding residue
(original residue number in PDB)
H208 H213 D323
Binding residue
(residue number reindexed from 1)
H206 H211 D308
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
H109 E205 H208 H213
Catalytic site (residue number reindexed from 1)
H107 E203 H206 H211
Enzyme Commision number
1.14.13.239
: carnitine monooxygenase.
Gene Ontology
Molecular Function
GO:0004497
monooxygenase activity
GO:0005506
iron ion binding
GO:0016709
oxidoreductase 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
GO:0046872
metal ion binding
GO:0051213
dioxygenase activity
GO:0051537
2 iron, 2 sulfur cluster binding
Biological Process
GO:0009437
carnitine metabolic process
GO:0044237
cellular metabolic process
View graph for
Molecular Function
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Biological Process
External links
PDB
RCSB:6zgp
,
PDBe:6zgp
,
PDBj:6zgp
PDBsum
6zgp
PubMed
33158989
UniProt
A0A059ZPP5
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