Structure of PDB 5h81 Chain B Binding Site BS03
Receptor Information
>5h81 Chain B (length=354) Species:
4058
(Catharanthus roseus) [
Search protein sequence
] [
Download receptor structure
] [
Download structure with residue number starting from 1
] [
View receptor structure
]
PVEAYGWAAKDTSGLLSPFKFLRRTTGEHDVQFKVLYCGLCDWDVITTKN
TYGTTKYPFVPGHEIMGIVTEIGNKVKKFKVGDKVGVGNFIGSCGKCERC
NEGLEPYCPKVIYTDGTAFSDENNTVYGDVSGDGEDRIYGGYSNIMVANE
YVVFRWPENLPLAAGVPILCGGIVPYSPMRHFGLDKPGLSIGVVGFGRIG
KLAVKFAKAFGANVTVISTSISKKQEAIEKYGVDRFLISKEPEEMKAAES
TLDGIFDCVPSVHPLHPLLNLLKFEGTFVMLGVSPLLMGRRKFVGSISGT
MKETQEMLDFAAKHNIVSDIELIPMDYVNTALERIAKGNHKDAFVIDIEN
TLKS
Ligand information
Ligand ID
ZN
InChI
InChI=1S/Zn/q+2
InChIKey
PTFCDOFLOPIGGS-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
[Zn++]
ACDLabs 10.04
OpenEye OEToolkits 1.5.0
[Zn+2]
Formula
Zn
Name
ZINC ION
ChEMBL
CHEMBL1236970
DrugBank
DB14532
ZINC
PDB chain
5h81 Chain B Residue 1002 [
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
5h81
Structural investigation of heteroyohimbine alkaloid synthesis reveals active site elements that control stereoselectivity.
Resolution
2.1 Å
Binding residue
(original residue number in PDB)
C101 C104 C107 C115
Binding residue
(residue number reindexed from 1)
C94 C97 C100 C108
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
A359
Catalytic site (residue number reindexed from 1)
A343
Enzyme Commision number
?
Gene Ontology
Molecular Function
GO:0000166
nucleotide binding
GO:0008270
zinc ion binding
GO:0016491
oxidoreductase activity
GO:0016616
oxidoreductase activity, acting on the CH-OH group of donors, NAD or NADP as acceptor
GO:0045551
cinnamyl-alcohol dehydrogenase activity
GO:0046872
metal ion binding
Biological Process
GO:0009809
lignin biosynthetic process
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:5h81
,
PDBe:5h81
,
PDBj:5h81
PDBsum
5h81
PubMed
27418042
UniProt
A0A1C7D193
[
Back to BioLiP
]