Structure of PDB 1o9t Chain B Binding Site BS02
Receptor Information
>1o9t Chain B (length=368) Species:
10116
(Rattus norvegicus) [
Search protein sequence
] [
Download receptor structure
] [
Download structure with residue number starting from 1
] [
View receptor structure
]
GAFMFTSESVGEGHPDKICDQISDAVLDAHLKQDPNAKVACETVCKTGMV
LLCGEITSMAMIDYQRVVRDTIKHIGYDDSAKGFDFKTCNVLVALEQQSP
EDVGAGDQGLMFGYATDETEECMPLTIVLAHKLNTRMADLRRSGVLPWLR
PDSKTQVTVQYVQDNGAVIPVRVHTIVISVQHNEDITLEAMREALKEQVI
KAVVPAKYLDEDTIYHLQPSGRFVIGGPQGDAGVTGRKIIVDTYGGWGAH
GGGAFSGKDYTKVDRSAAYAARWVAKSLVKAGLCRRVLVQVSYAIGVAEP
LSISIFTYGTSKKTERELLEVVNKNFDLRPGVIVRDLDLKKPIYQKTACY
GHFGRSEFPWEVPKKLVF
Ligand information
Ligand ID
PO4
InChI
InChI=1S/H3O4P/c1-5(2,3)4/h(H3,1,2,3,4)/p-3
InChIKey
NBIIXXVUZAFLBC-UHFFFAOYSA-K
SMILES
Software
SMILES
CACTVS 3.341
[O-][P]([O-])([O-])=O
ACDLabs 10.04
[O-]P([O-])([O-])=O
OpenEye OEToolkits 1.5.0
[O-]P(=O)([O-])[O-]
Formula
O4 P
Name
PHOSPHATE ION
ChEMBL
DrugBank
DB14523
ZINC
PDB chain
1o9t Chain B Residue 1398 [
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
1o9t
Crystal Structures of Methionine Adenosyltransferase Complexed with Substrates and Products Reveal the Methionine-ATP Recognition and Give Insights Into the Catalytic Mechanism
Resolution
2.9 Å
Binding residue
(original residue number in PDB)
G280 G281 A282 K286
Binding residue
(residue number reindexed from 1)
G252 G253 A254 K258
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
H30 D32 K33 E58 E71 K182 F251 D259 A260 R265 K266 K286 K290 D292
Catalytic site (residue number reindexed from 1)
H14 D16 K17 E42 E55 K154 F223 D231 A232 R237 K238 K258 K262 D264
Enzyme Commision number
2.5.1.6
: methionine adenosyltransferase.
Gene Ontology
Molecular Function
GO:0000287
magnesium ion binding
GO:0004478
methionine adenosyltransferase activity
GO:0005524
ATP binding
GO:0016597
amino acid binding
GO:0016740
transferase activity
GO:0042802
identical protein binding
GO:0043531
ADP binding
GO:0046872
metal ion binding
Biological Process
GO:0006556
S-adenosylmethionine biosynthetic process
GO:0006730
one-carbon metabolic process
GO:0009087
methionine catabolic process
GO:0051289
protein homotetramerization
GO:0065003
protein-containing complex assembly
Cellular Component
GO:0005829
cytosol
GO:0016363
nuclear matrix
GO:0048269
methionine adenosyltransferase complex
View graph for
Molecular Function
View graph for
Biological Process
View graph for
Cellular Component
External links
PDB
RCSB:1o9t
,
PDBe:1o9t
,
PDBj:1o9t
PDBsum
1o9t
PubMed
12888348
UniProt
P13444
|METK1_RAT S-adenosylmethionine synthase isoform type-1 (Gene Name=Mat1a)
[
Back to BioLiP
]