Structure of PDB 2vd6 Chain C Binding Site BS03
Receptor Information
>2vd6 Chain C (length=457) Species:
9606
(Homo sapiens) [
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GDHGSPDSYRSPLASRYASPEMCFVFSDRYKFRTWRQLWLWLAEAEQTLG
LPITDEQIQEMKSNLENIDFKMAAEEEKRLRHDVMAHVHTFGHCCPKAAG
IIHLGATSCYVGDNTDLIILRNALDLLLPKLARVISRLADFAKERASLPT
LGFTHFQPAQLTTVGKRCCLWIQDLCMDLQNLKRVRDDLRFRGVKGTTGT
QASFLQLFEGDDHKVEQLDKMVTEKAGFKRAFIITGQTYTRKVDIEVLSV
LASLGASVHKICTDIRLLANLKEMEEPFYKRNPMRSERCCSLARHLMTLV
MDPLQTASVQWFERTLDDSANRRICLAEAFLTADTILNTLQNISEGLVVY
PKVIERRIRQELPFMATENIIMAMVKAGGSRQDCHEKIRVLSQQAASVVK
QEGGDNDLIERIQVDAYFSPIHSQLDHLLDPSSFTGRASQQVQRFLEEEV
YPLLKPY
Ligand information
Ligand ID
FUM
InChI
InChI=1S/C4H4O4/c5-3(6)1-2-4(7)8/h1-2H,(H,5,6)(H,7,8)/b2-1+
InChIKey
VZCYOOQTPOCHFL-OWOJBTEDSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.7.6
C(=CC(=O)O)C(=O)O
OpenEye OEToolkits 1.7.6
C(=C/C(=O)O)\C(=O)O
CACTVS 3.370
OC(=O)\C=C\C(O)=O
ACDLabs 12.01
O=C(O)\C=C\C(=O)O
CACTVS 3.370
OC(=O)C=CC(O)=O
Formula
C4 H4 O4
Name
FUMARIC ACID
ChEMBL
CHEMBL503160
DrugBank
DB01677
ZINC
ZINC000003860193
PDB chain
2vd6 Chain C Residue 1001 [
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Receptor-Ligand Complex Structure
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PDB
2vd6
Human Adenylosuccinate Lyase in Complex with its Substrate N6-(1,2-Dicarboxyethyl)-AMP, and its Products AMP and Fumarate.
Resolution
2.0 Å
Binding residue
(original residue number in PDB)
H86 S112
Binding residue
(residue number reindexed from 1)
H82 S108
Annotation score
5
Enzymatic activity
Catalytic site (original residue number in PDB)
H86 T158 H159 K295 E302
Catalytic site (residue number reindexed from 1)
H82 T154 H155 K280 E287
Enzyme Commision number
4.3.2.2
: adenylosuccinate lyase.
Gene Ontology
Molecular Function
GO:0003824
catalytic activity
GO:0004018
N6-(1,2-dicarboxyethyl)AMP AMP-lyase (fumarate-forming) activity
GO:0016829
lyase activity
GO:0042802
identical protein binding
GO:0070626
(S)-2-(5-amino-1-(5-phospho-D-ribosyl)imidazole-4-carboxamido) succinate lyase (fumarate-forming) activity
Biological Process
GO:0001666
response to hypoxia
GO:0006164
purine nucleotide biosynthetic process
GO:0006167
AMP biosynthetic process
GO:0006177
GMP biosynthetic process
GO:0006189
'de novo' IMP biosynthetic process
GO:0007584
response to nutrient
GO:0009060
aerobic respiration
GO:0009152
purine ribonucleotide biosynthetic process
GO:0009168
purine ribonucleoside monophosphate biosynthetic process
GO:0014850
response to muscle activity
GO:0042594
response to starvation
GO:0044208
'de novo' AMP biosynthetic process
GO:0044209
AMP salvage
GO:0097294
'de novo' XMP biosynthetic process
Cellular Component
GO:0005829
cytosol
GO:0032991
protein-containing complex
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:2vd6
,
PDBe:2vd6
,
PDBj:2vd6
PDBsum
2vd6
PubMed
UniProt
P30566
|PUR8_HUMAN Adenylosuccinate lyase (Gene Name=ADSL)
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