Structure of PDB 8ixa Chain I Binding Site BS01
Receptor Information
>8ixa Chain I (length=427) Species:
10090
(Mus musculus) [
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RECISIHVGQAGVQIGNACWELYCLEHGIQPDGQMDDSFNTFFSETGAGK
HVPRAVFVDLEPTVIDEVRTGTYRQLFHPEQLITGKEDAANNYARGHYTI
GKEIIDLVLDRIRKLADQCTGLQGFLVFHSFGGGTGSGFTSLLMERLSVD
YGKKSKLEFSIYPAPQVSTAVVEPYNSILTTHTTLEHSDCAFMVDNEAIY
DICRRNLDIERPTYTNLNRLIGQIVSSITASLRFDGALNVDLTEFQTNLV
PYPRIHFPLATYAPVISAEKAYHEQLSVAEITNACFEPANQMVKCDPRHG
KYMACCLLYRGDVVPKDVNAAIATIKTKRTIQFVDWCPTGFKVGINYQPP
TVVPGGDLAKVQRAVCMLSNTTAIAEAWARLDHKFDLMYAKRAFVHWYVG
EGMEEGEFSEAREDMAALEKDYEEVGV
Ligand information
Ligand ID
GTP
InChI
InChI=1S/C10H16N5O14P3/c11-10-13-7-4(8(18)14-10)12-2-15(7)9-6(17)5(16)3(27-9)1-26-31(22,23)29-32(24,25)28-30(19,20)21/h2-3,5-6,9,16-17H,1H2,(H,22,23)(H,24,25)(H2,19,20,21)(H3,11,13,14,18)/t3-,5-,6-,9-/m1/s1
InChIKey
XKMLYUALXHKNFT-UUOKFMHZSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.7.6
c1nc2c(n1[C@H]3[C@@H]([C@@H]([C@H](O3)CO[P@](=O)(O)O[P@](=O)(O)OP(=O)(O)O)O)O)N=C(NC2=O)N
CACTVS 3.370
NC1=Nc2n(cnc2C(=O)N1)[C@@H]3O[C@H](CO[P](O)(=O)O[P](O)(=O)O[P](O)(O)=O)[C@@H](O)[C@H]3O
CACTVS 3.370
NC1=Nc2n(cnc2C(=O)N1)[CH]3O[CH](CO[P](O)(=O)O[P](O)(=O)O[P](O)(O)=O)[CH](O)[CH]3O
OpenEye OEToolkits 1.7.6
c1nc2c(n1C3C(C(C(O3)COP(=O)(O)OP(=O)(O)OP(=O)(O)O)O)O)N=C(NC2=O)N
ACDLabs 12.01
O=P(O)(O)OP(=O)(O)OP(=O)(O)OCC3OC(n2cnc1c2N=C(N)NC1=O)C(O)C3O
Formula
C10 H16 N5 O14 P3
Name
GUANOSINE-5'-TRIPHOSPHATE
ChEMBL
CHEMBL1233147
DrugBank
DB04137
ZINC
ZINC000060094177
PDB chain
8ixa Chain Q Residue 501 [
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Receptor-Ligand Complex Structure
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PDB
8ixa
Cryo-EM of alpha-tubulin isotype-containing microtubules revealed a contracted structure of alpha 4A/ beta 2A microtubules.
Resolution
4.2 Å
Binding residue
(original residue number in PDB)
G10 Q11 A12 Q15 E77 D104 A106 N107 S146 G148 G149 T151 T185 Y230 N234
Binding residue
(residue number reindexed from 1)
G9 Q10 A11 Q14 E61 D88 A90 N91 S130 G132 G133 T135 T169 Y214 N218
Annotation score
4
Enzymatic activity
Enzyme Commision number
3.6.5.-
Gene Ontology
Molecular Function
GO:0005200
structural constituent of cytoskeleton
GO:0005515
protein binding
GO:0005525
GTP binding
GO:0016787
hydrolase activity
GO:0042802
identical protein binding
GO:0044877
protein-containing complex binding
GO:0046872
metal ion binding
GO:0046982
protein heterodimerization activity
Biological Process
GO:0000226
microtubule cytoskeleton organization
GO:0001764
neuron migration
GO:0001964
startle response
GO:0006886
intracellular protein transport
GO:0007017
microtubule-based process
GO:0007098
centrosome cycle
GO:0007224
smoothened signaling pathway
GO:0007613
memory
GO:0007626
locomotory behavior
GO:0008344
adult locomotory behavior
GO:0008542
visual learning
GO:0009612
response to mechanical stimulus
GO:0010001
glial cell differentiation
GO:0010467
gene expression
GO:0021542
dentate gyrus development
GO:0021696
cerebellar cortex morphogenesis
GO:0021766
hippocampus development
GO:0021859
pyramidal neuron differentiation
GO:0021987
cerebral cortex development
GO:0022008
neurogenesis
GO:0030182
neuron differentiation
GO:0030317
flagellated sperm motility
GO:0030534
adult behavior
GO:0034612
response to tumor necrosis factor
GO:0035641
locomotory exploration behavior
GO:0046785
microtubule polymerization
GO:0048853
forebrain morphogenesis
GO:0048873
homeostasis of number of cells within a tissue
GO:0050807
regulation of synapse organization
GO:0050808
synapse organization
GO:0051402
neuron apoptotic process
GO:0061744
motor behavior
GO:0071277
cellular response to calcium ion
GO:0072384
organelle transport along microtubule
GO:0140058
neuron projection arborization
GO:1902065
response to L-glutamate
Cellular Component
GO:0000793
condensed chromosome
GO:0005737
cytoplasm
GO:0005829
cytosol
GO:0005856
cytoskeleton
GO:0005874
microtubule
GO:0005879
axonemal microtubule
GO:0005881
cytoplasmic microtubule
GO:0005886
plasma membrane
GO:0015630
microtubule cytoskeleton
GO:0031514
motile cilium
GO:0031594
neuromuscular junction
GO:0036126
sperm flagellum
GO:0036464
cytoplasmic ribonucleoprotein granule
GO:0043209
myelin sheath
GO:0045202
synapse
GO:0055037
recycling endosome
View graph for
Molecular Function
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Biological Process
View graph for
Cellular Component
External links
PDB
RCSB:8ixa
,
PDBe:8ixa
,
PDBj:8ixa
PDBsum
8ixa
PubMed
37439022
UniProt
P68369
|TBA1A_MOUSE Tubulin alpha-1A chain (Gene Name=Tuba1a)
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