Structure of PDB 5a2x Chain A Binding Site BS01
Receptor Information
>5a2x Chain A (length=468) Species:
9031
(Gallus gallus) [
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KKTFTEVQTERLEQADRSVLIKCPSKLNEKKLLQYLSSHGKIDNYFFFEN
RGIHALIEFSEKSSVASLQAVTGIPKAAEHHVVPYKSRLFTFTLKNPGSQ
AAEERPVKISPQSHIPVNELIPKLCHADSISSQMYILLNEYQLTEENIKL
RYLACSLVRDFARAYFPDSTVKPFGSSVNTFGKLGCDVDMFLDFHDKGPF
EMEYQMKRLPSERLATQKILSIIGDCLDNFGPGYSSVQKILNARCPLVKF
SHQPTGFQCDLSVSNSIAIRCSELLYIYGCLDPRVRALVFSLRCWARVHG
LTNSVPGTWITNFSLTMMIMFFLQKRSPPIIPTLDQLKELADEKDKHVIG
GYDCSFVSDLSKIKPTKNTETLDELLCDFFQYFGNFDFRKNSLNLRKGKE
VNKPESSPLYIWNPFEQDLNISKNVNQPQLEKFVAMARESAWILQKEDKT
QQMINKEPWGLAAVLIPF
Ligand information
Ligand ID
CTP
InChI
InChI=1S/C9H16N3O14P3/c10-5-1-2-12(9(15)11-5)8-7(14)6(13)4(24-8)3-23-28(19,20)26-29(21,22)25-27(16,17)18/h1-2,4,6-8,13-14H,3H2,(H,19,20)(H,21,22)(H2,10,11,15)(H2,16,17,18)/t4-,6-,7-,8-/m1/s1
InChIKey
PCDQPRRSZKQHHS-XVFCMESISA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
C1=CN(C(=O)N=C1N)C2C(C(C(O2)COP(=O)(O)OP(=O)(O)OP(=O)(O)O)O)O
OpenEye OEToolkits 1.5.0
C1=CN(C(=O)N=C1N)[C@H]2[C@@H]([C@@H]([C@H](O2)CO[P@](=O)(O)O[P@](=O)(O)OP(=O)(O)O)O)O
CACTVS 3.341
NC1=NC(=O)N(C=C1)[CH]2O[CH](CO[P](O)(=O)O[P](O)(=O)O[P](O)(O)=O)[CH](O)[CH]2O
ACDLabs 10.04
O=P(O)(O)OP(=O)(O)OP(=O)(O)OCC2OC(N1C(=O)N=C(N)C=C1)C(O)C2O
CACTVS 3.341
NC1=NC(=O)N(C=C1)[C@@H]2O[C@H](CO[P@@](O)(=O)O[P@@](O)(=O)O[P](O)(O)=O)[C@@H](O)[C@H]2O
Formula
C9 H16 N3 O14 P3
Name
CYTIDINE-5'-TRIPHOSPHATE
ChEMBL
CHEMBL223533
DrugBank
DB02431
ZINC
ZINC000003861746
PDB chain
5a2x Chain A Residue 1528 [
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Receptor-Ligand Complex Structure
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PDB
5a2x
Structure of Mitochondrial Poly(A) RNA Polymerase Reveals the Structural Basis for Dimerization, ATP Selectivity and the Spax4 Disease Phenotype.
Resolution
3.1 Å
Binding residue
(original residue number in PDB)
F224 G225 S226 D239 A327 N371 F372
Binding residue
(residue number reindexed from 1)
F174 G175 S176 D189 A268 N312 F313
Annotation score
2
Enzymatic activity
Catalytic site (original residue number in PDB)
G283 G290 K298 I408 S465
Catalytic site (residue number reindexed from 1)
G224 G231 K239 I349 S406
Enzyme Commision number
?
Gene Ontology
Molecular Function
GO:0000287
magnesium ion binding
GO:0002134
UTP binding
GO:0005524
ATP binding
GO:0005525
GTP binding
GO:0016740
transferase activity
GO:0030145
manganese ion binding
GO:0042802
identical protein binding
GO:0042803
protein homodimerization activity
GO:0046872
metal ion binding
GO:1990817
poly(A) RNA polymerase activity
Biological Process
GO:0000965
mitochondrial RNA 3'-end processing
GO:0016070
RNA metabolic process
GO:0071044
histone mRNA catabolic process
Cellular Component
GO:0005654
nucleoplasm
GO:0005739
mitochondrion
GO:0043231
intracellular membrane-bounded organelle
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:5a2x
,
PDBe:5a2x
,
PDBj:5a2x
PDBsum
5a2x
PubMed
26319014
UniProt
F1NBW0
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