Structure of PDB 1q7b Chain B Binding Site BS02
Receptor Information
>1q7b Chain B (length=241) Species:
562
(Escherichia coli) [
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NFEGKIALVTGASRGIGRAIAETLAARGAKVIGTATSENGAQAISDYLGA
NGKGLMLNVTDPASIESVLEKIRAEFGEVDILVNNAGITRDNLLMRMKDE
EWNDIIETNLSSVFRLSKAVMRAMMKKRHGRIITIGSVVGTMGNGGQANY
AAAKAGLIGFSKSLAREVASRGITVNVVAPGFIETDMTRSDDQRAGILAQ
VPAGRLGGAQEIANAVAFLASDEAAYITGETLHVNGGMYMV
Ligand information
Ligand ID
CA
InChI
InChI=1S/Ca/q+2
InChIKey
BHPQYMZQTOCNFJ-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
[Ca++]
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Ca+2]
Formula
Ca
Name
CALCIUM ION
ChEMBL
DrugBank
DB14577
ZINC
PDB chain
1q7b Chain B Residue 9003 [
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Receptor-Ligand Complex Structure
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PDB
1q7b
Cofactor-Induced Conformational Rearrangements Establish a Catalytically Competent Active Site and a Proton Relay Conduit in FabG
Resolution
2.05 Å
Binding residue
(original residue number in PDB)
G50 G53
Binding residue
(residue number reindexed from 1)
G49 G52
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
G16 E102 S138 Q148 Y151 K155
Catalytic site (residue number reindexed from 1)
G15 E101 S137 Q147 Y150 K154
Enzyme Commision number
1.1.1.100
: 3-oxoacyl-[acyl-carrier-protein] reductase.
Gene Ontology
Molecular Function
GO:0004316
3-oxoacyl-[acyl-carrier-protein] reductase (NADPH) activity
GO:0016491
oxidoreductase activity
GO:0016616
oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor
GO:0042802
identical protein binding
GO:0046872
metal ion binding
GO:0050661
NADP binding
GO:0051287
NAD binding
Biological Process
GO:0006633
fatty acid biosynthetic process
GO:0008610
lipid biosynthetic process
GO:0009102
biotin biosynthetic process
GO:0030497
fatty acid elongation
Cellular Component
GO:0005829
cytosol
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:1q7b
,
PDBe:1q7b
,
PDBj:1q7b
PDBsum
1q7b
PubMed
15016358
UniProt
P0AEK2
|FABG_ECOLI 3-oxoacyl-[acyl-carrier-protein] reductase FabG (Gene Name=fabG)
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