Structure of PDB 1fc4 Chain A Binding Site BS02
Receptor Information
>1fc4 Chain A (length=401) Species:
562
(Escherichia coli) [
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GSHMRGEFYQQLTNDLETARAEGLFKEERIITSAQQADITVADGSHVINF
CANNYLGLANHPDLIAAAKAGMDSHGFGMASVRFICGTQDSHKELEQKLA
AFLGMEDAILYSSCFDANGGLFETLLGAEDAIISDALNHASIIDGVRLCK
AKRYRYANNDMQELEARLKEAREAGARHVLIATDGVFSMDGVIANLKGVC
DLADKYDALVMVDDSHAVGFVGENGRGSHEYCDVMGRVDIITGTLGKALG
GASGGYTAARKEVVEWLRQRSRPYLFSNSLAPAIVAASIKVLEMVEAGSE
LRDRLWANARQFREQMSAAGFTLAGADHAIIPVMLGDAVVAQKFARELQK
EGIYVTGFFYPVVPKGQARIRTQMSAAHTPEQITRAVEAFTRIGKQLGVI
A
Ligand information
Ligand ID
PLP
InChI
InChI=1S/C8H10NO6P/c1-5-8(11)7(3-10)6(2-9-5)4-15-16(12,13)14/h2-3,11H,4H2,1H3,(H2,12,13,14)
InChIKey
NGVDGCNFYWLIFO-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
Cc1ncc(CO[P](O)(O)=O)c(C=O)c1O
OpenEye OEToolkits 1.5.0
Cc1c(c(c(cn1)COP(=O)(O)O)C=O)O
ACDLabs 10.04
O=P(O)(O)OCc1cnc(c(O)c1C=O)C
Formula
C8 H10 N O6 P
Name
PYRIDOXAL-5'-PHOSPHATE;
VITAMIN B6 Phosphate
ChEMBL
CHEMBL82202
DrugBank
DB00114
ZINC
ZINC000001532514
PDB chain
1fc4 Chain A Residue 1201 [
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Receptor-Ligand Complex Structure
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PDB
1fc4
Three-dimensional structure of 2-amino-3-ketobutyrate CoA ligase from Escherichia coli complexed with a PLP-substrate intermediate: inferred reaction mechanism.
Resolution
2.0 Å
Binding residue
(original residue number in PDB)
S110 C111 F112 H136 S185 D210 S212 H213 T241 K244
Binding residue
(residue number reindexed from 1)
S113 C114 F115 H139 S188 D213 S215 H216 T244 K247
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
N50 H136 D181 S185 D210 H213 K244
Catalytic site (residue number reindexed from 1)
N53 H139 D184 S188 D213 H216 K247
Enzyme Commision number
2.3.1.29
: glycine C-acetyltransferase.
Gene Ontology
Molecular Function
GO:0003824
catalytic activity
GO:0008890
glycine C-acetyltransferase activity
GO:0016740
transferase activity
GO:0016746
acyltransferase activity
GO:0016874
ligase activity
GO:0030170
pyridoxal phosphate binding
GO:0046872
metal ion binding
Biological Process
GO:0006567
threonine catabolic process
GO:0009058
biosynthetic process
GO:0019518
L-threonine catabolic process to glycine
Cellular Component
GO:0005737
cytoplasm
GO:0005829
cytosol
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Molecular Function
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Cellular Component
External links
PDB
RCSB:1fc4
,
PDBe:1fc4
,
PDBj:1fc4
PDBsum
1fc4
PubMed
11318637
UniProt
P0AB77
|KBL_ECOLI 2-amino-3-ketobutyrate coenzyme A ligase (Gene Name=kbl)
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