Structure of PDB 6zgp Chain E Binding Site BS02
Receptor Information
>6zgp Chain E (length=360) Species:
470
(Acinetobacter baumannii) [
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AVEKLPEDFCANPDVAWTFPKVFYTSSQVFEHEKEAIFAKSWICVAHGSE
LAQPNDYITRKVIGENIVIIRGKDSVLRAFYNVCPHRGHELLSGSGKAKN
VITCPYHAWTFKLDGSLALARNCDHVESFDKENSSMVPLKVEEYAGFVFI
NMDENATCVEDQLPGFAERLNQACGVIKDLKLAARFVTETPANWKVIVDN
YMECYHCGPAHPGFADSVQVDKYWHTTHQNWTLQYGFARSSVTDPEFHGF
WTWPCTMFNVPPGSNFMTVIYEFPVDAETTLQHYDIYFTNEELTQDQKDL
IEWYRNVFRPEDLNLVESVQRGLKSRGYRGQGRIMTDKQRSGISEHGIAY
FQHLVAQYHQ
Ligand information
Ligand ID
FES
InChI
InChI=1S/2Fe.2S
InChIKey
NIXDOXVAJZFRNF-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
[Fe]1S[Fe]S1
CACTVS 3.341
OpenEye OEToolkits 1.5.0
S1[Fe]S[Fe]1
Formula
Fe2 S2
Name
FE2/S2 (INORGANIC) CLUSTER
ChEMBL
DrugBank
ZINC
PDB chain
6zgp Chain E Residue 402 [
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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)
C86 H88 C106 Y108 H109 W111
Binding residue
(residue number reindexed from 1)
C84 H86 C104 Y106 H107 W109
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
View graph for
Biological Process
External links
PDB
RCSB:6zgp
,
PDBe:6zgp
,
PDBj:6zgp
PDBsum
6zgp
PubMed
33158989
UniProt
A0A059ZPP5
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