Structure of PDB 4xyj Chain H Binding Site BS01
Receptor Information
>4xyj Chain H (length=739) Species:
9606
(Homo sapiens) [
Search protein sequence
] [
Download receptor structure
] [
Download structure with residue number starting from 1
] [
View receptor structure
]
SGAGKAIGVLTSGGDAQGMNAAVRAVVRMGIYVGAKVYFIYEGYQGMVDG
GSNIAEADWESVSSILQVGGTIIGSARCQAFRTREGRLKAACNLLQRGIT
NLCVIGGDGSLTGANLFRKEWSGLLEELARNGQIDKEAVQKYAYLNVVGM
VGSIDNDFCGTDMTIGTDSALHRIIEVVDAIMTTAQSHQRTFVLEVMGRH
CGYLALVSALACGADWVFLPESPPEEGWEEQMCVKLSENRARKKRLNIII
VAEGAIDTQNKPITSEKIKELVVTQLGYDTRVTILGHVQRGGTPSAFDRI
LASRMGVEAVIALLEATPDTPACVVSLNGNHAVRLPLMECVQMTQDVQKA
MDERRFQDAVRLRGRSFAGNLNTYKRLAIKLPDDQIPKTNCNVAVINVGA
PAAGMNAAVRSAVRVGIADGHRMLAIYDGFDGFAKGQIKEIGWTDVGGWT
GQGGSILGTKRVLPGKYLEEIATQMRTHSINALLIIGGFEAYLGLLELSA
AREKHEEFCVPMVMVPATVSNNVPGSDFSIGADTALNTITDTCDRIKQSA
SGTKRRVFIIETMGGYCGYLANMGGLAAGADAAYIFEEPFDIRDLQSNVE
HLTEKMKTTIQRGLVLRNESCSENYTTDFIYQLYSEEGKGVFDCRKNVLG
HMQQGGAPSPFDRNFGTKISARAMEWITAKLKEARKFTTDDSICVLGISK
RNVIFQPVAELKKQTDFEHRIPKEQWWLKLRPLMKILAK
Ligand information
Ligand ID
ATP
InChI
InChI=1S/C10H16N5O13P3/c11-8-5-9(13-2-12-8)15(3-14-5)10-7(17)6(16)4(26-10)1-25-30(21,22)28-31(23,24)27-29(18,19)20/h2-4,6-7,10,16-17H,1H2,(H,21,22)(H,23,24)(H2,11,12,13)(H2,18,19,20)/t4-,6-,7-,10-/m1/s1
InChIKey
ZKHQWZAMYRWXGA-KQYNXXCUSA-N
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
c1nc(c2c(n1)n(cn2)C3C(C(C(O3)COP(=O)(O)OP(=O)(O)OP(=O)(O)O)O)O)N
CACTVS 3.341
Nc1ncnc2n(cnc12)[CH]3O[CH](CO[P](O)(=O)O[P](O)(=O)O[P](O)(O)=O)[CH](O)[CH]3O
ACDLabs 10.04
O=P(O)(O)OP(=O)(O)OP(=O)(O)OCC3OC(n2cnc1c(ncnc12)N)C(O)C3O
OpenEye OEToolkits 1.5.0
c1nc(c2c(n1)n(cn2)[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
CACTVS 3.341
Nc1ncnc2n(cnc12)[C@@H]3O[C@H](CO[P@](O)(=O)O[P@@](O)(=O)O[P](O)(O)=O)[C@@H](O)[C@H]3O
Formula
C10 H16 N5 O13 P3
Name
ADENOSINE-5'-TRIPHOSPHATE
ChEMBL
CHEMBL14249
DrugBank
DB00171
ZINC
ZINC000004261765
PDB chain
4xyj Chain H Residue 801 [
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
4xyj
Structures of human phosphofructokinase-1 and atomic basis of cancer-associated mutations.
Resolution
3.1 Å
Binding residue
(original residue number in PDB)
G33 G34 Y64 R97 C98 F101 R102 G127 D128 G129 S130 G133 S173 R219
Binding residue
(residue number reindexed from 1)
G13 G14 Y44 R77 C78 F81 R82 G107 D108 G109 S110 G113 S153 R199
Annotation score
5
Enzymatic activity
Catalytic site (original residue number in PDB)
G34 R97 C98 D128 G172 S173 D175 D177 R219
Catalytic site (residue number reindexed from 1)
G14 R77 C78 D108 G152 S153 D155 D157 R199
Enzyme Commision number
2.7.1.11
: 6-phosphofructokinase.
Gene Ontology
Molecular Function
GO:0003872
6-phosphofructokinase activity
GO:0005515
protein binding
GO:0005524
ATP binding
GO:0016208
AMP binding
GO:0016301
kinase activity
GO:0042802
identical protein binding
GO:0044877
protein-containing complex binding
GO:0045296
cadherin binding
GO:0046872
metal ion binding
GO:0048029
monosaccharide binding
GO:0070095
fructose-6-phosphate binding
Biological Process
GO:0006002
fructose 6-phosphate metabolic process
GO:0006096
glycolytic process
GO:0016310
phosphorylation
GO:0030388
fructose 1,6-bisphosphate metabolic process
GO:0061621
canonical glycolysis
GO:1990830
cellular response to leukemia inhibitory factor
Cellular Component
GO:0005634
nucleus
GO:0005737
cytoplasm
GO:0005829
cytosol
GO:0005945
6-phosphofructokinase complex
GO:0016020
membrane
GO:0070062
extracellular exosome
View graph for
Molecular Function
View graph for
Biological Process
View graph for
Cellular Component
External links
PDB
RCSB:4xyj
,
PDBe:4xyj
,
PDBj:4xyj
PDBsum
4xyj
PubMed
25985179
UniProt
Q01813
|PFKAP_HUMAN ATP-dependent 6-phosphofructokinase, platelet type (Gene Name=PFKP)
[
Back to BioLiP
]