Structure of PDB 3hco Chain B Binding Site BS01
Receptor Information
>3hco Chain B (length=359) Species:
9606
(Homo sapiens) [
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RKPKTGILMLNMGGPETLGDVHDFLLRLFLDRDLMTLPIQNKLAPFIAKR
RTPKIQEQYRRIGGGSPIKIWTSKQGEGMVKLLDELSPNTAPHKYYIGFR
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
3hco Chain B Residue 501 [
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Receptor-Ligand Complex Structure
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PDB
3hco
Product release rather than chelation determines metal specificity for ferrochelatase.
Resolution
1.8 Å
Binding residue
(original residue number in PDB)
C696 R772 S902 C903 C906 C911
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)
M576 L592 L598 R664 Y665 H763 D840 E843 E847
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:3hco
,
PDBe:3hco
,
PDBj:3hco
PDBsum
3hco
PubMed
19703464
UniProt
P22830
|HEMH_HUMAN Ferrochelatase, mitochondrial (Gene Name=FECH)
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