Structure of PDB 5yb0 Chain K Binding Site BS01
Receptor Information
>5yb0 Chain K (length=316) Species:
5759
(Entamoeba histolytica) [
Search protein sequence
] [
Download receptor structure
] [
Download structure with residue number starting from 1
] [
View receptor structure
]
LEISHRSKEWINVMNETKALMKEVMDIPEGYEILFFGGGASLQFLMVAMN
LLNKKACYLDTGVWASKAIKEAENIGEVKIIGTSKDKNYTYIPEYQIPSD
YDYFHITTNNTIYGTEIRKDIESPIPLVADMSSDILSKPIDISKYSLIYA
GAQKNCGAAGVTIVIIKKEILGKVQRKIPIILDYQVHILNNSMYNTPPVI
SIFTVNQTLKYIKKIGGLKKIQELNEEKARLLYAEIDRNKIFRGTVRKKD
RSIMNVCFVMEEQYKQLENEFSEYALQKGIIGIKGHRSVGGFRASIYNAV
TIESVQALIKCMHDFE
Ligand information
Ligand ID
PLP
InChI
InChI=1S/C8H10NO6P/c1-5-8(11)7(3-10)6(2-9-5)4-15-16(12,13)14/h2-3,11H,4H2,1H3,(H2,12,13,14)
InChIKey
NGVDGCNFYWLIFO-UHFFFAOYSA-N
SMILES
Software
SMILES
CACTVS 3.341
Cc1ncc(CO[P](O)(O)=O)c(C=O)c1O
OpenEye OEToolkits 1.5.0
Cc1c(c(c(cn1)COP(=O)(O)O)C=O)O
ACDLabs 10.04
O=P(O)(O)OCc1cnc(c(O)c1C=O)C
Formula
C8 H10 N O6 P
Name
PYRIDOXAL-5'-PHOSPHATE;
VITAMIN B6 Phosphate
ChEMBL
CHEMBL82202
DrugBank
DB00114
ZINC
ZINC000001532514
PDB chain
5yb0 Chain K Residue 401 [
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
5yb0
N-terminal residues are crucial for quaternary structure and active site conformation for the phosphoserine aminotransferase from enteric human parasite E. histolytica.
Resolution
2.94 Å
Binding residue
(original residue number in PDB)
G76 A77 S78 W101 T148 D167 S169
Binding residue
(residue number reindexed from 1)
G39 A40 S41 W64 T111 D130 S132
Annotation score
1
Enzymatic activity
Enzyme Commision number
2.6.1.52
: phosphoserine transaminase.
Gene Ontology
Molecular Function
GO:0004648
O-phospho-L-serine:2-oxoglutarate aminotransferase activity
GO:0008483
transaminase activity
GO:0030170
pyridoxal phosphate binding
Biological Process
GO:0006563
L-serine metabolic process
GO:0006564
L-serine biosynthetic process
Cellular Component
GO:0005737
cytoplasm
View graph for
Molecular Function
View graph for
Biological Process
View graph for
Cellular Component
External links
PDB
RCSB:5yb0
,
PDBe:5yb0
,
PDBj:5yb0
PDBsum
5yb0
PubMed
30959130
UniProt
Q60I38
[
Back to BioLiP
]