Structure of PDB 3w1w Chain A Binding Site BS01
Receptor Information
>3w1w Chain A (length=359) Species:
9606
(Homo sapiens) [
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RKPKTGILMLNMGGPETLGDVHDFLLRLFLDRDLMTLPIQNKLAPFIAKR
LTPKIQEQYRRIGGGSPIKIWTSKQGEGMVKLLDELSPNTAPHKYYIGFR
YVHPLTEEAIEEMERDGLERAIAFTQYPQYSCSTTGSSLNAIYRYYNQVG
RKPTMKWSTIDRWPTHHLLIQCFADHILKELDHFPLEKRSEVVILFSAHS
LPMSVVNRGDPYPQEVSATVQKVMERLEYCNPYRLVWQSKVGPMPWLGPQ
TDESIKGLCERGRKNILLVPIAFTSDHIETLYELDIEYSQVLAKECGVEN
IRRAESLNGNPLFSKALADLVHSHIQSNELCSKQLTLSCPLCVNPVCRET
KSFFTSQQL
Ligand information
Ligand ID
FES
InChI
InChI=1S/2Fe.2S
InChIKey
NIXDOXVAJZFRNF-UHFFFAOYSA-N
SMILES
Software
SMILES
ACDLabs 10.04
[Fe]1S[Fe]S1
CACTVS 3.341
OpenEye OEToolkits 1.5.0
S1[Fe]S[Fe]1
Formula
Fe2 S2
Name
FE2/S2 (INORGANIC) CLUSTER
ChEMBL
DrugBank
ZINC
PDB chain
3w1w Chain A Residue 1501 [
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Receptor-Ligand Complex Structure
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PDB
3w1w
Salicylic Acid induces mitochondrial injury by inhibiting ferrochelatase heme biosynthesis activity
Resolution
2.006 Å
Binding residue
(original residue number in PDB)
C196 R272 S402 C403 C406 C411
Binding residue
(residue number reindexed from 1)
C132 R208 S338 C339 C342 C347
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
M76 L92 L98 R164 Y165 H263 D340 E343 E347
Catalytic site (residue number reindexed from 1)
M12 L28 L34 R100 Y101 H199 D276 E279 E283
Enzyme Commision number
4.98.1.1
: protoporphyrin ferrochelatase.
Gene Ontology
Molecular Function
GO:0004325
ferrochelatase activity
Biological Process
GO:0006783
heme biosynthetic process
View graph for
Molecular Function
View graph for
Biological Process
External links
PDB
RCSB:3w1w
,
PDBe:3w1w
,
PDBj:3w1w
PDBsum
3w1w
PubMed
24043703
UniProt
P22830
|HEMH_HUMAN Ferrochelatase, mitochondrial (Gene Name=FECH)
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