Structure of PDB 5c7s Chain A Binding Site BS01
Receptor Information
>5c7s Chain A (length=344) Species:
83332
(Mycobacterium tuberculosis H37Rv) [
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VPSWPQILGRLTDNRDLARGQAAWAMDQIMTGNARPAQIAAFAVAMTMKA
PTADEVGELAGVMLSHAHPLPADTVPDDAVDVVGTGGDGVNTVNLSTMAA
IVVAAAGVPVVKHGNRAASSLSGGADTLEALGVRIDLGPDLVARSLAEVG
IGFCFAPRFHPSYRHAAAVRREIGVPTVFNLLGPLTNPARPRAGLIGCAF
ADLAEVMAGVFAARRSSVLVVHGDDGLDELTTTTTSTIWRVAAGSVDKLT
FDPAGFGFARAQLDQLAGGDAQANAAAVRAVLGGARGPVRDAVVLNAAGA
IVAHAGLSSEWLPAWEEGLRRASAAIDTGAAEQLLARWVRFGRQ
Ligand information
Ligand ID
MN
InChI
InChI=1S/Mn/q+2
InChIKey
WAEMQWOKJMHJLA-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Mn+2]
CACTVS 3.341
[Mn++]
Formula
Mn
Name
MANGANESE (II) ION
ChEMBL
DrugBank
DB06757
ZINC
PDB chain
5c7s Chain A Residue 401 [
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Receptor-Ligand Complex Structure
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PDB
5c7s
Binding and mimicking of the phosphate-rich substrate, PRPP
Resolution
2.1 Å
Binding residue
(original residue number in PDB)
G107 S119 E252
Binding residue
(residue number reindexed from 1)
G84 S96 E229
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
V106
Catalytic site (residue number reindexed from 1)
V83
Enzyme Commision number
2.4.2.18
: anthranilate phosphoribosyltransferase.
Gene Ontology
Molecular Function
GO:0000287
magnesium ion binding
GO:0004048
anthranilate phosphoribosyltransferase activity
GO:0016757
glycosyltransferase activity
GO:0016763
pentosyltransferase activity
GO:0046872
metal ion binding
Biological Process
GO:0000162
tryptophan biosynthetic process
Cellular Component
GO:0005576
extracellular region
GO:0005829
cytosol
GO:0005886
plasma membrane
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:5c7s
,
PDBe:5c7s
,
PDBj:5c7s
PDBsum
5c7s
PubMed
UniProt
P9WFX5
|TRPD_MYCTU Anthranilate phosphoribosyltransferase (Gene Name=trpD)
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