Structure of PDB 3n75 Chain D Binding Site BS02
Receptor Information
>3n75 Chain D (length=711) Species:
83333
(Escherichia coli K-12) [
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MNVIAILNHMGVYFKEEPIRELHRALERLNFQIVYPNDRDDLLKLIENNA
RLCGVIFDWDKYNLELCEEISKMNENLPLYAFANTYSTLDVSLNDLRLQI
SFFEYALGAAEDIANKIKQTTDEYINTILPPLTKALFKYVREGKYTFCTP
GHMGGTAFQKSPVGSLFYDFFGPNTMKSDISISVSELGSLLDHSGPHKEA
EQYIARVFNADRSYMVTNGTSTANKIVGMYSAPAGSTILIDRNCHKSLTH
LMMMSDVTPIYFRPTRNAYGILGGIPQSEFQHATIAKRVKETPNATWPVH
AVITNSTYDGLLYNTDFIKKTLDVKSIHFDSAWVPYTNFSPIYEGKCGMS
GGRVEGKVIYETQSTHKLLAAFSQASMIHVKGDVNEETFNEAYMMHTTTS
PHYGIVASTETAAAMMKGNAGKRLINGSIERAIKFRKEIKRLRTESDGWF
FDVWQPDHIDTTECWPLRSDSTWHGFKNIDNEHMYLDPIKVTLLTPGMEK
DGTMSDFGIPASIVAKYLDEHGIVVEKTGPYNLLFLFSIGIDKTKALSLL
RALTDFKRAFDLNLRVKNMLPSLYREDPEFYENMRIQELAQNIHKLIVHH
NLPDLMYRAFEVLPTMVMTPYAAFQKELHGMTEEVYLDEMVGRINANMIL
PYPPGVPLVMPGEMITEESRPVLEFLQMLCEIGAHYPGFETDIHGAYRQA
DGRYTVKVLKE
Ligand information
Ligand ID
G4P
InChI
InChI=1S/C10H17N5O17P4/c11-10-13-7-4(8(17)14-10)12-2-15(7)9-5(16)6(30-36(26,27)32-34(21,22)23)3(29-9)1-28-35(24,25)31-33(18,19)20/h2-3,5-6,9,16H,1H2,(H,24,25)(H,26,27)(H2,18,19,20)(H2,21,22,23)(H3,11,13,14,17)/t3-,5-,6-,9-/m1/s1
InChIKey
BUFLLCUFNHESEH-UUOKFMHZSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
c1nc2c(n1C3C(C(C(O3)COP(=O)(O)OP(=O)(O)O)OP(=O)(O)OP(=O)(O)O)O)N=C(NC2=O)N
CACTVS 3.341
NC1=Nc2n(cnc2C(=O)N1)[C@@H]3O[C@H](CO[P@@](O)(=O)O[P](O)(O)=O)[C@@H](O[P@@](O)(=O)O[P](O)(O)=O)[C@H]3O
CACTVS 3.341
NC1=Nc2n(cnc2C(=O)N1)[CH]3O[CH](CO[P](O)(=O)O[P](O)(O)=O)[CH](O[P](O)(=O)O[P](O)(O)=O)[CH]3O
ACDLabs 10.04
O=P(O)(O)OP(=O)(O)OCC3OC(n2cnc1c2N=C(N)NC1=O)C(O)C3OP(=O)(O)OP(=O)(O)O
OpenEye OEToolkits 1.5.0
c1nc2c(n1[C@H]3[C@@H]([C@@H]([C@H](O3)CO[P@](=O)(O)OP(=O)(O)O)O[P@](=O)(O)OP(=O)(O)O)O)N=C(NC2=O)N
Formula
C10 H17 N5 O17 P4
Name
GUANOSINE-5',3'-TETRAPHOSPHATE;
guanosine tetraphosphate;
ppGpp
ChEMBL
DrugBank
DB04022
ZINC
ZINC000008217069
PDB chain
3n75 Chain D Residue 716 [
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Receptor-Ligand Complex Structure
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PDB
3n75
Linkage between the bacterial acid stress and stringent responses: the structure of the inducible lysine decarboxylase.
Resolution
2.0 Å
Binding residue
(original residue number in PDB)
R97 R206 K417 G418
Binding residue
(residue number reindexed from 1)
R97 R206 K417 G418
Annotation score
1
Binding affinity
MOAD
: Kd=12.8nM
PDBbind-CN
: -logKd/Ki=7.89,Kd=12.8nM
Enzymatic activity
Catalytic site (original residue number in PDB)
H245 D330 K367
Catalytic site (residue number reindexed from 1)
H245 D330 K367
Enzyme Commision number
4.1.1.18
: lysine decarboxylase.
Gene Ontology
Molecular Function
GO:0003824
catalytic activity
GO:0005515
protein binding
GO:0008923
lysine decarboxylase activity
GO:0016831
carboxy-lyase activity
GO:0042802
identical protein binding
GO:0097216
guanosine tetraphosphate binding
Biological Process
GO:0006520
amino acid metabolic process
GO:0006554
lysine catabolic process
Cellular Component
GO:0005737
cytoplasm
View graph for
Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:3n75
,
PDBe:3n75
,
PDBj:3n75
PDBsum
3n75
PubMed
21278708
UniProt
P0A9H3
|LDCI_ECOLI Inducible lysine decarboxylase (Gene Name=cadA)
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