Structure of PDB 3hcn Chain A Binding Site BS02
Receptor Information
>3hcn Chain A (length=359) Species:
9606
(Homo sapiens) [
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RKPKTGILMLNMGGPETLGDVHDFLLRLFLDRDLMTLPIQNKLAPFIAKR
RTPKIQEQYRRIGGGSPIKIWTSKQGEGMVKLLDELSPNTAPHKYYIGFR
YVHPLTEEAIEEMERDGLERAIAFTQYPQYSCSTTGSSLNAIYRYYNQVG
RKPTMKWSTIDRWPTHHLLIQCFADHILKELDHFPLEKRSEVVILFSAHS
LPMSVVNRGDPYPQEVSATVQKVMERLEYCNPYRLVWQSKVGPMPWLGPQ
TDESIKGLCERGRKNILLVPIAFTSDHIETLYELDIEYSQVLAKECGVEN
IRRAESLNGNPLFSKALADLVHSHIQSNELCSKQLTLSCPLCVNPVCRET
KSFFTSQQL
Ligand information
Ligand ID
BCT
InChI
InChI=1S/CH2O3/c2-1(3)4/h(H2,2,3,4)/p-1
InChIKey
BVKZGUZCCUSVTD-UHFFFAOYSA-M
SMILES
Software
SMILES
OpenEye OEToolkits 1.5.0
C(=O)(O)[O-]
CACTVS 3.341
OC([O-])=O
ACDLabs 10.04
[O-]C(=O)O
Formula
C H O3
Name
BICARBONATE ION
ChEMBL
DrugBank
ZINC
PDB chain
3hcn Chain A Residue 1 [
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Receptor-Ligand Complex Structure
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PDB
3hcn
Product release rather than chelation determines metal specificity for ferrochelatase.
Resolution
1.6 Å
Binding residue
(original residue number in PDB)
L98 Y165
Binding residue
(residue number reindexed from 1)
L34 Y101
Annotation score
1
Enzymatic activity
Catalytic site (original residue number in PDB)
M76 L92 L98
Catalytic site (residue number reindexed from 1)
M12 L28 L34
Enzyme Commision number
4.98.1.1
: protoporphyrin ferrochelatase.
Gene Ontology
Molecular Function
GO:0004325
ferrochelatase activity
Biological Process
GO:0006783
heme biosynthetic process
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Molecular Function
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Biological Process
External links
PDB
RCSB:3hcn
,
PDBe:3hcn
,
PDBj:3hcn
PDBsum
3hcn
PubMed
19703464
UniProt
P22830
|HEMH_HUMAN Ferrochelatase, mitochondrial (Gene Name=FECH)
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