Structure of PDB 5bsu Chain A Binding Site BS01
Receptor Information
>5bsu Chain A (length=529) Species:
4097
(Nicotiana tabacum) [
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VDIIFRSKLPDIYIPNHLPLHSYCFENISEFSSRPCLINGANKQIYTYAD
VELNSRKVAAGLHKQGIQPKDTIMILLPNSPEFVFAFIGASYLGAISTMA
NPLFTPAEVVKQAKASSAKIIVTQACHVNKVKDYAFENDVKIICIDSAPE
GCLHFSVLTQANEHDIPEVEIQPDDVVALPYSSGTTGLPKGVMLTHKGLV
TSVAQQVDGENPNLYIHSEDVMLCVLPLFHIYSLNSVLLCGLRVGAAILI
MQKFDIVSFLELIQRYKVTIGPFVPPIVLAIAKSPMVDDYDLSSVRTVMS
GAAPLGKELEDTVRAKFPNAKLGQGYGMTEAGPVLAMCLAFAKEPFEIKS
GACGTVVRNAEMKIVDPKTGNSLPRNQSGEICIRGDQIMKGYLNDPEATA
RTIDKEGWLYTGDIGYIDDDDELFIVDRLKELIKYKGFQVAPAELEALLL
NHPNISDAAVVPMKDEQAGEVPVAFVVRSNGSTITEDEVKDFISKQVIFY
KRIKRVFFVDAIPKSPSGKILRKDLRAKL
Ligand information
Ligand ID
4UV
InChI
InChI=1S/C19H18N5O10P/c20-17-14-18(22-7-21-17)24(8-23-14)19-16(29)15(28)12(33-19)6-32-35(30,31)34-13(27)4-2-9-1-3-10(25)11(26)5-9/h1-5,7-8,12,15-16,19,28-29H,6H2,(H,30,31)(H2,20,21,22)/b4-2+/t12-,15-,16-,19-/m1/s1
InChIKey
SRUDBSRTEMWJHC-LNTBVICDSA-N
SMILES
Software
SMILES
CACTVS 3.385
Nc1ncnc2n(cnc12)[C@@H]3O[C@H](CO[P](O)(=O)OC(=O)/C=C/C4=CC(=O)C(=O)C=C4)[C@@H](O)[C@H]3O
OpenEye OEToolkits 1.9.2
c1nc(c2c(n1)n(cn2)[C@H]3[C@@H]([C@@H]([C@H](O3)COP(=O)(O)OC(=O)/C=C/C4=CC(=O)C(=O)C=C4)O)O)N
CACTVS 3.385
Nc1ncnc2n(cnc12)[CH]3O[CH](CO[P](O)(=O)OC(=O)C=CC4=CC(=O)C(=O)C=C4)[CH](O)[CH]3O
ACDLabs 12.01
OP(OC([C@H]=CC=1C=CC(=O)C(C=1)=O)=O)(OCC2C(C(C(O2)n3cnc4c3ncnc4N)O)O)=O
OpenEye OEToolkits 1.9.2
c1nc(c2c(n1)n(cn2)C3C(C(C(O3)COP(=O)(O)OC(=O)C=CC4=CC(=O)C(=O)C=C4)O)O)N
Formula
C19 H18 N5 O10 P
Name
5'-O-[(R)-{[(2E)-3-(3,4-dioxocyclohexa-1,5-dien-1-yl)prop-2-enoyl]oxy}(hydroxy)phosphoryl]adenosine
ChEMBL
DrugBank
ZINC
ZINC000584905159
PDB chain
5bsu Chain A Residue 601 [
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Receptor-Ligand Complex Structure
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PDB
5bsu
Structural Basis for Specificity and Flexibility in a Plant 4-Coumarate:CoA Ligase.
Resolution
1.75 Å
Binding residue
(original residue number in PDB)
H237 Y239 S243 M306 A309 A310 P311 G332 G334 M335 T336 P340 D420 K437 K441 Q446
Binding residue
(residue number reindexed from 1)
H230 Y232 S236 M299 A302 A303 P304 G325 G327 M328 T329 P333 D413 K430 K434 Q439
Annotation score
3
Enzymatic activity
Catalytic site (original residue number in PDB)
S189 S209 H237 T336 E337 K441 Q446 K526
Catalytic site (residue number reindexed from 1)
S182 S202 H230 T329 E330 K434 Q439 K519
Enzyme Commision number
6.2.1.-
6.2.1.12
: 4-coumarate--CoA ligase.
6.2.1.34
: trans-feruloyl-CoA synthase.
Gene Ontology
Molecular Function
GO:0003824
catalytic activity
GO:0005524
ATP binding
GO:0016207
4-coumarate-CoA ligase activity
GO:0016405
CoA-ligase activity
GO:0016874
ligase activity
GO:0050563
trans-feruloyl-CoA synthase activity
GO:0106286
(E)-caffeate-CoA ligase activity
GO:0106290
trans-cinnamate-CoA ligase activity
Biological Process
GO:0009611
response to wounding
GO:0009698
phenylpropanoid metabolic process
GO:0009753
response to jasmonic acid
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:5bsu
,
PDBe:5bsu
,
PDBj:5bsu
PDBsum
5bsu
PubMed
26412334
UniProt
O24146
|4CL2_TOBAC 4-coumarate--CoA ligase 2 (Gene Name=4CL2)
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