Structure of PDB 1ld8 Chain A Binding Site BS01
Receptor Information
>1ld8 Chain A (length=313) Species:
9606
(Homo sapiens) [
Search protein sequence
] [
Download receptor structure
] [
Download structure with residue number starting from 1
] [
View receptor structure
]
FVSLDSPSYVLYRDRAEWADIDPVPQNDGPNPVVQIIYSDKFRDVYDYFR
AVLQRDERSERAFKLTRDAIELNAANYTVWHFRRVLLKSLQKDLHEEMNY
ITAIIEEQPKNYQVWHHRRVLVEWLRDPSQELEFIADILNQDAKNYHAWQ
HRQWVIQEFKLWDNELQYVDQLLKEDVRNNSVWNQRYFVISNTTGYNDRA
VLEREVQYTLEMIKLVPHNESAWNYLKGILQDRGLSKYPNLLNQLLDLQP
SHSSPYLIAFLVDIYEDMLENQCDNKEDILNKALELCEILAKEKDTIRKE
YWRYIGRSLQSKH
Ligand information
Ligand ID
GLC
InChI
InChI=1S/C6H12O6/c7-1-2-3(8)4(9)5(10)6(11)12-2/h2-11H,1H2/t2-,3-,4+,5-,6+/m1/s1
InChIKey
WQZGKKKJIJFFOK-DVKNGEFBSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
C(C1C(C(C(C(O1)O)O)O)O)O
OpenEye OEToolkits 1.5.0
C([C@@H]1[C@H]([C@@H]([C@H]([C@H](O1)O)O)O)O)O
CACTVS 3.341
OC[CH]1O[CH](O)[CH](O)[CH](O)[CH]1O
CACTVS 3.341
OC[C@H]1O[C@H](O)[C@H](O)[C@@H](O)[C@@H]1O
ACDLabs 10.04
OC1C(O)C(OC(O)C1O)CO
Formula
C6 H12 O6
Name
alpha-D-glucopyranose;
alpha-D-glucose;
D-glucose;
glucose
ChEMBL
CHEMBL423707
DrugBank
ZINC
ZINC000003861213
PDB chain
1ld8 Chain C Residue 1 [
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
1ld8
3-Aminopyrrolidinone farnesyltransferase inhibitors: design of macrocyclic compounds with improved pharmacokinetics and excellent cell potency.
Resolution
1.8 Å
Binding residue
(original residue number in PDB)
Y241 D286
Binding residue
(residue number reindexed from 1)
Y187 D232
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
K164
Catalytic site (residue number reindexed from 1)
K110
Enzyme Commision number
2.5.1.58
: protein farnesyltransferase.
2.5.1.59
: protein geranylgeranyltransferase type I.
Gene Ontology
Molecular Function
GO:0004659
prenyltransferase activity
GO:0004660
protein farnesyltransferase activity
GO:0004661
protein geranylgeranyltransferase activity
GO:0004662
CAAX-protein geranylgeranyltransferase activity
GO:0004663
Rab geranylgeranyltransferase activity
GO:0005515
protein binding
GO:0008017
microtubule binding
GO:0008318
protein prenyltransferase activity
GO:0030971
receptor tyrosine kinase binding
GO:0043014
alpha-tubulin binding
GO:0060090
molecular adaptor activity
Biological Process
GO:0007167
enzyme-linked receptor protein signaling pathway
GO:0007179
transforming growth factor beta receptor signaling pathway
GO:0007528
neuromuscular junction development
GO:0018342
protein prenylation
GO:0018343
protein farnesylation
GO:0018344
protein geranylgeranylation
GO:0035022
positive regulation of Rac protein signal transduction
GO:0071340
skeletal muscle acetylcholine-gated channel clustering
GO:0090044
positive regulation of tubulin deacetylation
GO:0090045
positive regulation of deacetylase activity
GO:1904395
positive regulation of skeletal muscle acetylcholine-gated channel clustering
Cellular Component
GO:0005737
cytoplasm
GO:0005829
cytosol
GO:0005875
microtubule associated complex
GO:0005886
plasma membrane
GO:0005953
CAAX-protein geranylgeranyltransferase complex
GO:0005965
protein farnesyltransferase complex
View graph for
Molecular Function
View graph for
Biological Process
View graph for
Cellular Component
External links
PDB
RCSB:1ld8
,
PDBe:1ld8
,
PDBj:1ld8
PDBsum
1ld8
PubMed
12036349
UniProt
P49354
|FNTA_HUMAN Protein farnesyltransferase/geranylgeranyltransferase type-1 subunit alpha (Gene Name=FNTA)
[
Back to BioLiP
]