Structure of PDB 4h0w Chain A Binding Site BS02
Receptor Information
>4h0w Chain A (length=679) Species:
9606
(Homo sapiens) [
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VPDKTVRWCAVSEHEATKCQSFRDHMKSVIPSDGPSVACVKKASYLDCIR
AIAANEADAVTLDAGLVYDAYLAPNNLKPVVAEFYGSKEDPQTFYYAVAV
VKKDSGFQMNQLRGKKSCHTGLGRSAGWNIPIGLLYCDLPEPRKPLEKAV
ANFFSGSCAPCADGTDFPQLCQLCPGCGCSTLNQYFGYSGAFKCLKDGAG
DVAFVKHSTIFENLANKADRDQYELLCLDNTRKPVDEYKDCHLAQVPSHT
VVARSMGGKEDLIWELLNQAQEHFGKDKSKEFQLFSSPHGKDLLFKDSAH
GFLKVPPRMDAKMYLGYEYVTAIRNLREGTCPEAPTDECKPVKWCALSHH
ERLKCDEWSVNSVGKIECVSAETTEDCIAKIMNGEADAMSLDGGFVYIAG
KCGLVPVLAENYNKSDNCEDTPEAGYFAIAVVKKSASDLTWDNLKGKKSC
HTAVGRTAGWNIPMGLLYNKINHCRFDEFFSEGCAPGSKKDSSLCKLCMG
SGLNLCEPNNKEGYYGYTGAFRCLVEKGDVAFVKHQTVPQNTGGKNPDPW
AKNLNEKDYELLCLDGTRKPVEEYANCHLARAPNHAVVTRKDKEACVHKI
LRQQQHLFGSNVTDCSGNFCLFRSETKDLLFRDDTVCLAKLHDRNTYEKY
LGEEYVKAVGNLRKCSTSSLLEACTFRRP
Ligand information
Ligand ID
CO3
InChI
InChI=1S/CH2O3/c2-1(3)4/h(H2,2,3,4)/p-2
InChIKey
BVKZGUZCCUSVTD-UHFFFAOYSA-L
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
C(=O)([O-])[O-]
ACDLabs 10.04
CACTVS 3.341
[O-]C([O-])=O
Formula
C O3
Name
CARBONATE ION
ChEMBL
DrugBank
DB14531
ZINC
PDB chain
4h0w Chain A Residue 702 [
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Receptor-Ligand Complex Structure
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PDB
4h0w
Iron and bismuth bound human serum transferrin reveals a partially-opened conformation in the N-lobe.
Resolution
2.4 Å
Binding residue
(original residue number in PDB)
D392 T452 R456 T457 A458 G459 Y517
Binding residue
(residue number reindexed from 1)
D392 T452 R456 T457 A458 G459 Y517
Annotation score
3
Enzymatic activity
Enzyme Commision number
?
Gene Ontology
Molecular Function
GO:0005515
protein binding
GO:0008198
ferrous iron binding
GO:0008199
ferric iron binding
GO:0019899
enzyme binding
GO:0034986
iron chaperone activity
GO:0044325
transmembrane transporter binding
GO:0046872
metal ion binding
GO:1990459
transferrin receptor binding
Biological Process
GO:0006826
iron ion transport
GO:0006879
intracellular iron ion homeostasis
GO:0007015
actin filament organization
GO:0009617
response to bacterium
GO:0019731
antibacterial humoral response
GO:0030316
osteoclast differentiation
GO:0031647
regulation of protein stability
GO:0032436
positive regulation of proteasomal ubiquitin-dependent protein catabolic process
GO:0034756
regulation of iron ion transport
GO:0042327
positive regulation of phosphorylation
GO:0045780
positive regulation of bone resorption
GO:0045893
positive regulation of DNA-templated transcription
GO:0048260
positive regulation of receptor-mediated endocytosis
GO:0060586
multicellular organismal-level iron ion homeostasis
GO:0070371
ERK1 and ERK2 cascade
GO:0071281
cellular response to iron ion
GO:2000147
positive regulation of cell motility
Cellular Component
GO:0005576
extracellular region
GO:0005615
extracellular space
GO:0005768
endosome
GO:0005769
early endosome
GO:0005770
late endosome
GO:0005788
endoplasmic reticulum lumen
GO:0005886
plasma membrane
GO:0005905
clathrin-coated pit
GO:0009925
basal plasma membrane
GO:0009986
cell surface
GO:0010008
endosome membrane
GO:0016020
membrane
GO:0016324
apical plasma membrane
GO:0030139
endocytic vesicle
GO:0030669
clathrin-coated endocytic vesicle membrane
GO:0031410
cytoplasmic vesicle
GO:0031982
vesicle
GO:0034774
secretory granule lumen
GO:0045178
basal part of cell
GO:0048471
perinuclear region of cytoplasm
GO:0055037
recycling endosome
GO:0070062
extracellular exosome
GO:0072562
blood microparticle
GO:1990712
HFE-transferrin receptor complex
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Molecular Function
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Biological Process
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Cellular Component
External links
PDB
RCSB:4h0w
,
PDBe:4h0w
,
PDBj:4h0w
PDBsum
4h0w
PubMed
23256035
UniProt
P02787
|TRFE_HUMAN Serotransferrin (Gene Name=TF)
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