Structure of PDB 5klq Chain B Binding Site BS02
Receptor Information
>5klq Chain B (length=320) Species:
321
(Pseudomonas syringae pv. syringae) [
Search protein sequence
] [
Download receptor structure
] [
Download structure with residue number starting from 1
] [
View receptor structure
]
QSMRLQQKINDLKPYVRHARGPIKAYGQAALDRASGAATSVSFAELDATH
LDAMVYIENQRNPGLNLKHFRDHYYLIQALQSDGPSAFRAIFPQTCPETG
QTLKHHVMADVRLHAPTIIITEPAVIVGARYQQLQRHNLTLEDLSESGVP
LSQVAIIETQAQKTSDDCVMYSLNYAIKAHKNAAQFDDIHHGLQHGTLST
ESESRARTTLGALEASSSYSVMHEGAHAAFGADVLPVDFYKHGASLTQAY
YLMKRPDGRMAGRVNSEGHSEAENLVQRNQAFRVKRRELLDDETPSNTQF
SASIDGFRLQEIKRVLAAAQ
Ligand information
Ligand ID
COA
InChI
InChI=1S/C21H36N7O16P3S/c1-21(2,16(31)19(32)24-4-3-12(29)23-5-6-48)8-41-47(38,39)44-46(36,37)40-7-11-15(43-45(33,34)35)14(30)20(42-11)28-10-27-13-17(22)25-9-26-18(13)28/h9-11,14-16,20,30-31,48H,3-8H2,1-2H3,(H,23,29)(H,24,32)(H,36,37)(H,38,39)(H2,22,25,26)(H2,33,34,35)/t11-,14-,15-,16+,20-/m1/s1
InChIKey
RGJOEKWQDUBAIZ-IBOSZNHHSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
CC(C)(COP(=O)(O)OP(=O)(O)OCC1C(C(C(O1)n2cnc3c2ncnc3N)O)OP(=O)(O)O)C(C(=O)NCCC(=O)NCCS)O
CACTVS 3.341
CC(C)(CO[P@@](O)(=O)O[P@](O)(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1O[P](O)(O)=O)n2cnc3c(N)ncnc23)[C@@H](O)C(=O)NCCC(=O)NCCS
OpenEye OEToolkits 1.5.0
CC(C)(CO[P@](=O)(O)O[P@@](=O)(O)OC[C@@H]1[C@H]([C@H]([C@@H](O1)n2cnc3c2ncnc3N)O)OP(=O)(O)O)[C@H](C(=O)NCCC(=O)NCCS)O
CACTVS 3.341
CC(C)(CO[P](O)(=O)O[P](O)(=O)OC[CH]1O[CH]([CH](O)[CH]1O[P](O)(O)=O)n2cnc3c(N)ncnc23)[CH](O)C(=O)NCCC(=O)NCCS
ACDLabs 10.04
O=C(NCCS)CCNC(=O)C(O)C(C)(C)COP(=O)(O)OP(=O)(O)OCC3OC(n2cnc1c(ncnc12)N)C(O)C3OP(=O)(O)O
Formula
C21 H36 N7 O16 P3 S
Name
COENZYME A
ChEMBL
CHEMBL1213327
DrugBank
DB01992
ZINC
ZINC000008551087
PDB chain
5klq Chain B Residue 402 [
Download ligand structure
] [
Download structure with residue number starting from 1
] [
View ligand structure
]
Receptor-Ligand Complex Structure
Global view
Local view
Structure summary
[
Spin on
] [
Spin off
] [
Reset
]
[
High quality
] [
Low quality
]
[
White background
] [
Black background
]
[
Spin on
] [
Spin off
] [
Reset
]
[
High quality
] [
Low quality
]
[
White background
] [
Black background
]
PDB
5klq
Structure of a pathogen effector reveals the enzymatic mechanism of a novel acetyltransferase family.
Resolution
3.4 Å
Binding residue
(original residue number in PDB)
K211 T212 S293 L294 T295 R334 R335 S344 F348
Binding residue
(residue number reindexed from 1)
K163 T164 S245 L246 T247 R286 R287 S296 F300
Annotation score
3
Enzymatic activity
Enzyme Commision number
2.3.1.-
Gene Ontology
Molecular Function
GO:0000822
inositol hexakisphosphate binding
GO:0005515
protein binding
GO:0016413
O-acetyltransferase activity
GO:0016746
acyltransferase activity
GO:0090729
toxin activity
Biological Process
GO:0035821
modulation of process of another organism
Cellular Component
GO:0005576
extracellular region
GO:0016020
membrane
GO:0020002
host cell plasma membrane
GO:0030430
host cell cytoplasm
GO:0042025
host cell nucleus
GO:0044163
host cytoskeleton
View graph for
Molecular Function
View graph for
Biological Process
View graph for
Cellular Component
External links
PDB
RCSB:5klq
,
PDBe:5klq
,
PDBj:5klq
PDBsum
5klq
PubMed
27525589
UniProt
Q6VE93
|HOZ1A_PSESY Serine/threonine-protein acetyltransferase HopZ1a (Gene Name=hopZ1a)
[
Back to BioLiP
]