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CYP11A1 V415E [mitochondrial matrix]
Stable Identifier
R-HSA-5580238
Type
Protein [EntityWithAccessionedSequence]
Species
Homo sapiens
Compartment
mitochondrial matrix
Synonyms
Cytochrome P450 11A1
Locations in the PathwayBrowser
Expand all
Disease (Homo sapiens)
Diseases of metabolism (Homo sapiens)
Metabolic disorders of biological oxidation enzymes (Homo sapiens)
Defective CYP11A1 causes AICSR (Homo sapiens)
Defective CYP11A1 does not cleave 20a,22b-DHCHOL (Homo sapiens)
CYP11A1 mutants:FDXR:FDX1,FDX1L (red.) [mitochondrial matrix] (Homo sapiens)
CYP11A1 mutants [mitochondrial matrix] (Homo sapiens)
CYP11A1 V415E [mitochondrial matrix] (Homo sapiens)
External Reference Information
External Reference
UniProt:P05108 CYP11A1
Gene Names
CYP11A1, CYP11A
Chain
transit peptide:1-39, chain:40-521
Reference Genes
BioGPS Gene:1583 CYP11A1
COSMIC (genes):CYP11A1 CYP11A1
CTD Gene:1583 CYP11A1
dbSNP Gene:1583 CYP11A1
ENSEMBL:ENSG00000140459 CYP11A1
ENSEMBL:ENSG00000140459.18 CYP11A1
ENSEMBL:ENSG00000288362.1 CYP11A1
HGNC:2590 CYP11A1
KEGG Gene (Homo sapiens):1583 CYP11A1
Monarch:1583 CYP11A1
NCBI Gene:1583 CYP11A1
OMIM:118485 CYP11A1
UCSC:P05108 CYP11A1
Reference Transcript
RefSeq:NM_001099773.1 CYP11A1
RefSeq:NM_000781.2 CYP11A1
Other Identifiers
11729652_a_at
11750526_a_at
1583
16811617
204309_PM_at
204309_at
3632863
3632864
3632867
3632870
3632872
3632873
3632874
3632875
3632876
3632877
3632878
3632879
3632887
3632888
3632889
3632893
3632894
37195_at
7990333
A_23_P129169
GE57831
GO:0003824
GO:0004497
GO:0005506
GO:0005515
GO:0005739
GO:0005743
GO:0005759
GO:0006629
GO:0006694
GO:0006700
GO:0006704
GO:0006766
GO:0008202
GO:0008203
GO:0008207
GO:0008386
GO:0016020
GO:0016125
GO:0016491
GO:0016705
GO:0020037
GO:0034650
GO:0042359
GO:0043226
GO:0046872
GO:0071375
HMNXSV003007473
ILMN_1768820
M14565_at
PH_hs_0004396
TC15001642.hg
TC15002624.hg
g4503188_3p_at
Participates
as a member of
CYP11A1 mutants [mitochondrial matrix] (Homo sapiens)
Other forms of this molecule
CYP11A1 I279Yfs*10 [mitochondrial matrix]
CYP11A1 [mitochondrial matrix]
CYP11A1 D271_V272insGD [mitochondrial matrix]
Modified Residues
Name
L-valine 415 replaced with L-glutamic acid
Coordinate
415
PsiMod
L-valine removal [MOD:01650]
A protein modification that effectively removes or replaces an L-valine.
L-glutamic acid residue [MOD:00015]
A protein modification that effectively converts a source amino acid residue to an L-glutamic acid.
Disease
Name
Identifier
Synonyms
congenital adrenal insufficiency
DOID:0050546
ADRENAL INSUFFICIENCY, CONGENITAL, WITH 46,XY SEX REVERSAL, PARTIAL OR COMPLETE, P450scc DEFICIENCY
Cross References
RefSeq
NP_001093243.1
,
NP_000772.2
Guide to Pharmacology - Targets
1358
OpenTargets
ENSG00000140459
ZINC target
P05108
PRO
P05108
PDB
3N9Z
,
3NA0
,
3N9Y
,
3NA1
IntEnz
1.14.15.6
GeneCards
P05108
HPA
ENSG00000140459-CYP11A1
Ensembl
ENSP00000268053
,
ENSP00000351455
,
ENSP00000500767
,
ENST00000358632
,
ENST00000268053
,
ENST00000672913
,
ENST00000672385
,
ENSG00000288362
,
ENSP00000499849
,
ENSG00000140459
Pharos - Targets
P05108
ZINC - Predictions - Purchasable
CP11A_HUMAN
Orphanet
15833
HMDB Protein
HMDBP00724
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