Structure of PDB 5llx Chain A Binding Site BS01
Receptor Information
>5llx Chain A (length=667) Species:
1036674
(Idiomarina sp. A28L) [
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ISKLIAACDQEPIHIPNAIQPFGAMLIVEKDTQQIVYASANSAEYFSVAD
NTIHELSDIKQANINSLLPEHLISGLASAIRENEPIWVETDRLSFLGWRH
ENYYIIEVERYHVQTSNWFEIQFQRAFQKLRNCKTHNDLINTLTRLIQEI
SGYDRVMIYQFDPEWNGRVIAESVRQLFTSMLNHHFPASDIPAQARAMYS
INPIRIIPDVNAEPQPLHMIHKPQNTEAVNLSSGVLRAVSPLHMQYLRNF
GVSASTSIGIFNEDELWGIVACHHTKPRAIGRRIRRLLVRTVEFAAERLW
LIHSRNVERYMVTVQAAREQLSTTADDKHSSHEIVIEHAADWCKLFRCDG
IGYLRGEELTTYGETPDQTTINKLVEWLEENGKKSLFWHSHMLKEDAPGL
LPDGSRFAGLLAIPLKSYLLLFRVAQNEVRTWAGKPEKLSVETSTGTMLG
PRKSFEAWQDEVSGKSQPWRTAQLYAARDIARDLLIVADSMQLNLLNDQL
ADANENLEKLASFDDLTGIFNRRRMEDRLESEVKEAQRYKKQFGILLFDL
DKFKSVNDTYGHNIGDQILQNTCAAVSETLRDTDKFGRWGGEEFLIIAPQ
TGMPELMQLGERVRAAVEKMQHKDLPAVTISIGVAEFQNDTRWDHMIDRA
DKAMYRAKENGRNQVCS
Ligand information
Ligand ID
LBV
InChI
InChI=1S/C33H36N4O6/c1-7-20-19(6)32(42)37-27(20)14-25-18(5)23(10-12-31(40)41)29(35-25)15-28-22(9-11-30(38)39)17(4)24(34-28)13-26-16(3)21(8-2)33(43)36-26/h7-8,13-15,19,35H,2,9-12H2,1,3-6H3,(H,36,43)(H,37,42)(H,38,39)(H,40,41)/p+1/b20-7+,26-13-,27-14-,28-15-/t19-/m0/s1
InChIKey
DKMLMZVDTGOEGU-ISEYCTJISA-O
SMILES
Software
SMILES
OpenEye OEToolkits 1.7.2
CC=C1C(C(=O)NC1=Cc2c(c(c([nH]2)C=C3C(=C(C(=[NH+]3)C=C4C(=C(C(=O)N4)C=C)C)C)CCC(=O)O)CCC(=O)O)C)C
OpenEye OEToolkits 1.7.2
C/C=C/1\C(C(=O)N\C1=C/c2c(c(c([nH]2)/C=C\3/C(=C(C(=[NH+]3)/C=C\4/C(=C(C(=O)N4)C=C)C)C)CCC(=O)O)CCC(=O)O)C)C
CACTVS 3.370
CC=C1[CH](C)C(=O)NC1=Cc2[nH]c(C=C3[NH+]=C(C=C4NC(=O)C(=C4C)C=C)C(=C3CCC(O)=O)C)c(CCC(O)=O)c2C
CACTVS 3.370
C/C=C/1[C@H](C)C(=O)NC/1=C/c2[nH]c(/C=C/3[NH+]=C(/C=C/4NC(=O)C(=C/4C)C=C)C(=C/3CCC(O)=O)C)c(CCC(O)=O)c2C
Formula
C33 H37 N4 O6
Name
3-[2-[(Z)-[3-(2-carboxyethyl)-5-[(Z)-(4-ethenyl-3-methyl-5-oxidanylidene-pyrrol-2-ylidene)methyl]-4-methyl-pyrrol-1-ium -2-ylidene]methyl]-5-[(Z)-[(3E)-3-ethylidene-4-methyl-5-oxidanylidene-pyrrolidin-2-ylidene]methyl]-4-methyl-1H-pyrrol-3- yl]propanoic acid;
2(R),3(E)- PHYTOCHROMOBILIN
ChEMBL
DrugBank
ZINC
PDB chain
5llx Chain A Residue 701 [
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Receptor-Ligand Complex Structure
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PDB
5llx
Long-range allosteric signaling in red light-regulated diguanylyl cyclases.
Resolution
2.8 Å
Binding residue
(original residue number in PDB)
C17 M166 F195 S198 D199 I200 P201 A204 R214 R246 H252 S266 H282
Binding residue
(residue number reindexed from 1)
C8 M157 F186 S189 D190 I191 P192 A195 R205 R237 H243 S257 H273
Annotation score
1
Enzymatic activity
Enzyme Commision number
2.7.7.65
: diguanylate cyclase.
Gene Ontology
Molecular Function
GO:0005525
GTP binding
GO:0009881
photoreceptor activity
GO:0046872
metal ion binding
GO:0052621
diguanylate cyclase activity
Biological Process
GO:0006355
regulation of DNA-templated transcription
GO:0009584
detection of visible light
GO:0043709
cell adhesion involved in single-species biofilm formation
GO:1902201
negative regulation of bacterial-type flagellum-dependent cell motility
Cellular Component
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:5llx
,
PDBe:5llx
,
PDBj:5llx
PDBsum
5llx
PubMed
28275738
UniProt
F7RW09
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