Type | Description |
---|---|
Definition | peroxisomal biogenesis factor 13 |
Date | Results | Publications |
---|---|---|
2020-12-12 13:22:00 | Hepatocyte-specific deletion of peroxisomal protein PEX13 results in disrupted iron homeostasis. | 32565019 |
2017-09-30 13:36:00 | Data suggest that soluble/cytosolic PEX5 interacts with PEX14/PEX13 complex, a model for the docking/translocation module (DTM) of the peroxisomal matrix protein translocon; PEX14/PEX13 complex appears to function in peroxisomal membrane as large cavity into which cytosolic PEX5 can enter to release its cargo. (PEX = peroxisomal biogenesis factor) | 28765278 |
2017-08-19 12:04:00 | our results demonstrate that PEX13 is required for selective autophagy, and suggest that dysregulation of PEX13-mediated mitophagy may contribute to ZSS pathogenesis. | 27827795 |
2014-03-22 11:40:00 | Results show PEX13 interacts with itself in peroxisomes in living cells and the import of PTS1 (peroxisomal targeting signal 1) proteins is specifically disrupted when homooligomerization of PEX13 is interrupted. | 23716570 |
2010-01-21 00:00:00 | Zellweger syndrome caused by PEX13 deficiency: report of two novel mutations. | 19449432 |
Type | IDs |
---|---|
Synonymous | NALD, PBD11A, PBD11B, ZWS |
Gene |
UniProtKB-ID:
PEX13_HUMAN
UniprotKB:
Q92968
UniParc:
UPI0000131707
EMBL:
U71374,
AK315244,
CH471053,
AF048755,
AB022192,
BC067090
Ensembl:
ENSG00000162928
KO:
hsa:5194
|
Nucleutide sequences |
EMBL-CDS:
BAA88907.1,
EAX00018.1,
AAD05572.1,
AAH67090.1,
AAC39844.1,
BAG37668.1
Ensembl_TRS:
ENST00000295030
|
Protein sequencees |
Ensembl_PRO:
ENSP00000295030
RefSeq:
NP_002609.1
|
Others |
UniRef100:
UniRef100_Q92968
UniRef90:
UniRef90_Q92968
UniRef50:
UniRef50_Q92968
UniGene:
Hs.161377
CCDS:
CCDS1866.1
|
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