Structure of PDB 1bg3 Chain B
Receptor sequence
>1bg3B (length=902) Species:
10116
(Rattus norvegicus) [
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MIAAQLLAYYFTELKDDQVKKIDKYLYAMRLSDEILIDILTRFKKEMKNG
LSRDYNPTASVKMLPTFVRSIPDGSEKGDFIALDLGGSSFRILRVQVNVS
MESEIYDTPENIVHGSGTQLFDHVADCLGDFMEKKDKKLPVGFTFSFPCR
QSKIDEAVLITWTKRFKASGVEGADVVKLLNKAIKKRGDYDANIVAVVND
TVGTMMTCGYDDQQCEVGLIIGTGTNACYMEELRHIDLVEGDEGRMCINT
EWGAFGDDGSLEDIRTEFDRELDRGSLNPGKQLFEKMVSGMYMGELVRLI
LVKMAKEGLLFEGRITPELLTRGKFNTSDVSAIEKDKEGIQNAKEILTRL
GVEPSDVDCVSVQHICTIVSFRSANLVAATLGAILNRLRDNKGTPRLRTT
VGVDGSLYKMHPQYSRRFHKTLRRLVPDSDVRFLLSESGTGKGAAMVTAV
AYRLAEQHRQIEETLAHFRLSKQTLMEVKKRLRTEMEMGLRKETNSKATV
KMLPSFVRSIPDGTEHGDFLALDLGGTNFRVLLVKIRSGKKRTVEMHNKI
YSIPLEIMQGTGDELFDHIVSCISDFLDYMGIKGPRMPLGFTFSFPCHQT
NLDCGILISWTKGFKATDCEGHDVASLLRDAVKRREEFDLDVVAVVNDTV
GTMMTCAYEEPTCEIGLIVGTGTNACYMEEMKNVEMVEGNQGQMCINMEW
GAFGDNGCLDDIRTDFDKVVDEYSLNSGKQRFEKMISGMYLGEIVRNILI
DFTKKGFLFRGQISEPLKTRGIFETKFLSQIESDRLALLQVRAILQQLGL
NSTCDDSILVKTVCGVVSKRAAQLCGAGMAAVVEKIRENRGLDHLNVTVG
VDGTLYKLHPHFSRIMHQTVKELSPKCTVSFLLSEDGSGKGAALITAVGV
RL
3D structure
PDB
1bg3
The structure of mammalian hexokinase-1.
Chain
B
Resolution
2.8 Å
3D
structure
Catalytic site residues are labeled in the structure
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Enzymatic activity
Catalytic site (original residue number in PDB)
R539 S603 S618 D657
Catalytic site (residue number reindexed from 1)
R530 S594 S609 D648
Enzyme Commision number
2.7.1.1
: hexokinase.
Interaction with ligand
Site
#
Ligand
Ligand
chain
Binding residues on receptor
(original residue number in PDB)
Binding residues on receptor
(residue number reindexed from 1)
Binding affinity
BS01
BGC
B
S155 F156 T172 K173 N208 D209 N235 E260 E294
S146 F147 T163 K164 N199 D200 N226 E251 E285
BS02
G6P
B
D84 G87 S88 D209 G231 T232 D413 S415 T449
D84 G87 S88 D200 G222 T223 D404 S406 T440
BS03
BGC
B
F604 T620 K621 N656 D657 N683 E708 E742
F595 T611 K612 N647 D648 N674 E699 E733
BS04
G6P
B
D532 G535 T536 D657 G679 T680 D861 T863 S897
D523 G526 T527 D648 G670 T671 D852 T854 S888
Gene Ontology
Molecular Function
GO:0004340
glucokinase activity
GO:0004396
hexokinase activity
GO:0004672
protein kinase activity
GO:0005515
protein binding
GO:0005524
ATP binding
GO:0005536
D-glucose binding
GO:0008865
fructokinase activity
GO:0016301
kinase activity
GO:0016773
phosphotransferase activity, alcohol group as acceptor
GO:0016887
ATP hydrolysis activity
GO:0019158
mannokinase activity
GO:0042802
identical protein binding
GO:0042834
peptidoglycan binding
GO:0044877
protein-containing complex binding
GO:0047931
glucosamine kinase activity
Biological Process
GO:0001666
response to hypoxia
GO:0001678
intracellular glucose homeostasis
GO:0002720
positive regulation of cytokine production involved in immune response
GO:0002931
response to ischemia
GO:0005975
carbohydrate metabolic process
GO:0006002
fructose 6-phosphate metabolic process
GO:0006006
glucose metabolic process
GO:0006013
mannose metabolic process
GO:0006096
glycolytic process
GO:0006954
inflammatory response
GO:0009741
response to brassinosteroid
GO:0016310
phosphorylation
GO:0019318
hexose metabolic process
GO:0032731
positive regulation of interleukin-1 beta production
GO:0043066
negative regulation of apoptotic process
GO:0045087
innate immune response
GO:0046835
carbohydrate phosphorylation
GO:0051156
glucose 6-phosphate metabolic process
GO:0061621
canonical glycolysis
GO:0061728
GDP-mannose biosynthetic process from mannose
GO:0072655
establishment of protein localization to mitochondrion
GO:0072656
maintenance of protein location in mitochondrion
GO:0141199
GDP-mannose biosynthetic process from glucose
GO:1901986
response to ketamine
Cellular Component
GO:0005737
cytoplasm
GO:0005739
mitochondrion
GO:0005741
mitochondrial outer membrane
GO:0005829
cytosol
GO:0005901
caveola
GO:0032991
protein-containing complex
GO:0045121
membrane raft
View graph for
Molecular Function
View graph for
Biological Process
View graph for
Cellular Component
External links
PDB
RCSB:1bg3
,
PDBe:1bg3
,
PDBj:1bg3
PDBsum
1bg3
PubMed
9665168
UniProt
P05708
|HXK1_RAT Hexokinase-1 (Gene Name=Hk1)
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