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Accession Number: | Q9Y5Y5 |
Protein Name: | Peroxisomal membrane protein PEX16 |
Length: | 336 |
Molecular Weight: | 38643.00 |
Species: | Homo sapiens (Human) [9606] |
Number of TMSs: | 3 |
Location1 / Topology2 / Orientation3: | Peroxisome membrane1 / Multi-pass membrane protein2 |
Substrate |
Cross database links:
RefSeq: | NP_004804.1 NP_476515.1 |
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Entrez Gene ID: | 9409 |
Pfam: | PF08610 |
OMIM: |
214100 phenotype 601539 phenotype 603360 gene+phenotype |
KEGG: | hsa:9409 |
Gene Ontology
GO:0005789
C:endoplasmic reticulum membrane
GO:0005779
C:integral to peroxisomal membrane
GO:0008022
F:protein C-terminus binding
GO:0032581
P:ER-dependent peroxisome organization
GO:0016557
P:peroxisome membrane biogenesis
GO:0016558
P:protein import into peroxisome matrix
GO:0045046
P:protein import into peroxisome membrane
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References (9)[1] “Mutation in PEX16 is causal in the peroxisome-deficient Zellweger syndrome of complementation group D.” Honsho M.et.al. 9837814 [2] “Peroxisome synthesis in the absence of preexisting peroxisomes.” South S.T.et.al. 9922452 [3] “Human chromosome 11 DNA sequence and analysis including novel gene identification.” Taylor T.D.et.al. 16554811 [4] “The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).” The MGC Project Teamet.al. 15489334 [5] “PEX19 binds multiple peroxisomal membrane proteins, is predominantly cytoplasmic, and is required for peroxisome membrane synthesis.” Sacksteder K.A.et.al. 10704444 |
External Searches:
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Analyze:
Predict TMSs (Predict number of transmembrane segments) | ||||
FASTA formatted sequence |
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1: MEKLRLLGLR YQEYVTRHPA ATAQLETAVR GFSYLLAGRF ADSHELSELV YSASNLLVLL 61: NDGILRKELR KKLPVSLSQQ KLLTWLSVLE CVEVFMEMGA AKVWGEVGRW LVIALIQLAK 121: AVLRMLLLLW FKAGLQTSPP IVPLDRETQA QPPDGDHSPG NHEQSYVGKR SNRVVRTLQN 181: TPSLHSRHWG APQQREGRQQ QHHEELSATP TPLGLQETIA EFLYIARPLL HLLSLGLWGQ 241: RSWKPWLLAG VVDVTSLSLL SDRKGLTRRE RRELRRRTIL LLYYLLRSPF YDRFSEARIL 301: FLLQLLADHV PGVGLVTRPL MDYLPTWQKI YFYSWG