Structure of PDB 1u7z Chain A Binding Site BS01
Receptor Information
>1u7z Chain A (length=216) Species:
562
(Escherichia coli) [
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VNDLKHLNIMITAGPTREPLDPVRYISDHSSGKMGFAIAAAAARRGANVT
LVSGPVSLPTPPFVKRVDVMTALEMEAAVNASVQQQNIFIGCAAVADYRA
ATVAPEKIDELTIKMVKNPDIVAGVAALKDHRPYVVGFAAETNNVEEYAR
QKRIRKNLDLICANDVSQPTQGFNSDNNALHLFWQDGDKVLPLERKELLG
QLLLDEIVTRYDEKNR
Ligand information
Ligand ID
PMT
InChI
InChI=1S/C18H30N4O15P2/c1-18(2,8-35-38(29,30)31)14(26)15(27)20-5-3-11(23)37-39(32,33)34-7-9-12(24)13(25)16(36-9)22-6-4-10(19)21-17(22)28/h4,6,9,12-14,16,24-26H,3,5,7-8H2,1-2H3,(H,20,27)(H,32,33)(H2,19,21,28)(H2,29,30,31)/t9-,12-,13-,14+,16-/m1/s1
InChIKey
JURRMAHLXBVXRF-FIEZRUJPSA-N
SMILES
Software
SMILES
CACTVS 3.341
CC(C)(CO[P](O)(O)=O)[CH](O)C(=O)NCCC(=O)O[P](O)(=O)OC[CH]1O[CH]([CH](O)[CH]1O)N2C=CC(=NC2=O)N
OpenEye OEToolkits 1.5.0
CC(C)(COP(=O)(O)O)[C@H](C(=O)NCCC(=O)O[P@@](=O)(O)OC[C@@H]1[C@H]([C@H]([C@@H](O1)N2C=CC(=NC2=O)N)O)O)O
CACTVS 3.341
CC(C)(CO[P](O)(O)=O)[C@@H](O)C(=O)NCCC(=O)O[P@](O)(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1O)N2C=CC(=NC2=O)N
ACDLabs 10.04
O=P(O)(O)OCC(C)(C)C(O)C(=O)NCCC(=O)OP(=O)(O)OCC2OC(N1C(=O)N=C(N)C=C1)C(O)C2O
OpenEye OEToolkits 1.5.0
CC(C)(COP(=O)(O)O)C(C(=O)NCCC(=O)OP(=O)(O)OCC1C(C(C(O1)N2C=CC(=NC2=O)N)O)O)O
Formula
C18 H30 N4 O15 P2
Name
PHOSPHORIC ACID MONO-[3-(3-{[5-(4-AMINO-2-OXO-2H-PYRIMIDIN-1-YL)-3,4- DIHYDROXY-TETRAHYDRO-FURAN-2- YLMETHOXY]-HYDROXY-PHOSPHORYLOXY}-3-OXO-PROPYLCARBAMOYL)-3-HYDROXY-2,2- DIMETHYL-PROPYL] ESTER;
4'-PHOSPHOPANTOTHENOYL- CYTIDINE-5'-MONOPHOSPHATE
ChEMBL
DrugBank
ZINC
ZINC000016051552
PDB chain
1u7z Chain A Residue 500 [
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Receptor-Ligand Complex Structure
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PDB
1u7z
Structural Basis of CTP-Dependent Peptide Bond Formation in Coenzyme A Biosynthesis Catalyzed by Escherichia coli PPC Synthetase
Resolution
2.3 Å
Binding residue
(original residue number in PDB)
S212 S213 G214 K215 M216 G273 C274 A275 A276 V277 D309 I310 V311 F327 A329 K341 K345 N353 F362 K385
Binding residue
(residue number reindexed from 1)
S30 S31 G32 K33 M34 G91 C92 A93 A94 V95 D120 I121 V122 F138 A140 K152 K156 N164 F173 K196
Annotation score
2
Enzymatic activity
Catalytic site (original residue number in PDB)
D210
Catalytic site (residue number reindexed from 1)
D28
Enzyme Commision number
4.1.1.36
: phosphopantothenoylcysteine decarboxylase.
6.3.2.5
: phosphopantothenate--cysteine ligase (CTP).
Gene Ontology
Molecular Function
GO:0004632
phosphopantothenate--cysteine ligase activity
GO:0004633
phosphopantothenoylcysteine decarboxylase activity
GO:0010181
FMN binding
Biological Process
GO:0015937
coenzyme A biosynthetic process
GO:0015941
pantothenate catabolic process
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:1u7z
,
PDBe:1u7z
,
PDBj:1u7z
PDBsum
1u7z
PubMed
15530362
UniProt
P0ABQ0
|COABC_ECOLI Coenzyme A biosynthesis bifunctional protein CoaBC (Gene Name=coaBC)
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