Structure of PDB 2qd1 Chain B Binding Site BS01
Receptor Information
>2qd1 Chain B (length=359) Species:
9606
(Homo sapiens) [
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RKPKTGILMLNMGGPETLGDVHDFLLRLFLDRDLMTLPIQNKLAPFIAKR
RTPKIQEQYRRIGGGSPIKIWTSKQGEGMVKLLDELSPNTAPHKYYIGFR
YVHPLTEEAIEEMERDGLERAIAFTQYPQYSCSTTGSSLNAIYRYYNQVG
RKPTMKWSTIDRWPTHHLLIQCFADHILKELDHFPLEKRSEVVILFSAHS
LPMSVVNRGDPYPQEVSATVQKVMERLEYCNPYRLVWQSKVGPMPWLGPQ
TDESIKGLCERGRKNILLVPIAFTSDHIKTLYELDIEYSQVLAKECGVEN
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
2qd1 Chain B Residue 1002 [
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Receptor-Ligand Complex Structure
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PDB
2qd1
A pi-Helix Switch Selective for Porphyrin Deprotonation and Product Release in Human Ferrochelatase.
Resolution
2.2 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 K343 E347
Catalytic site (residue number reindexed from 1)
M12 L28 L34 R100 Y101 H199 D276 K279 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:2qd1
,
PDBe:2qd1
,
PDBj:2qd1
PDBsum
2qd1
PubMed
17884090
UniProt
P22830
|HEMH_HUMAN Ferrochelatase, mitochondrial (Gene Name=FECH)
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