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Q96HA9 (PX11C_HUMAN) Reviewed, UniProtKB/Swiss-Prot

Last modified May 1, 2013. Version 81. Feed History...

Clusters with 100%, 90%, 50% identity | Documents (5) | Third-party data text xml rdf/xml gff fasta
to top of pageNames·Attributes·General annotation·Ontologies·Alt products·Sequence annotation·Sequences·References·Cross-refs·Entry info·DocumentsCustomize order

Names and origin

Protein namesRecommended name:
Peroxisomal membrane protein 11C
Alternative name(s):
Peroxin-11C
Peroxisomal biogenesis factor 11C
Protein PEX11 homolog gamma
Short name=PEX11-gamma
Gene names
Name:PEX11G
Synonyms:PEX11C
OrganismHomo sapiens (Human) [Reference proteome]
Taxonomic identifier9606 [NCBI]
Taxonomic lineageEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresPrimatesHaplorrhiniCatarrhiniHominidaeHomo

Protein attributes

Sequence length241 AA.
Sequence statusComplete.
Protein existenceEvidence at protein level

General annotation (Comments)

Subcellular location

Peroxisome membrane; Multi-pass membrane protein Ref.1 Ref.4.

Sequence similarities

Belongs to the peroxin-11 family.

Alternative products

This entry describes 2 isoforms produced by alternative splicing. [Align] [Select]
Isoform 1 (identifier: Q96HA9-1)

This isoform has been chosen as the 'canonical' sequence. All positional information in this entry refers to it. This is also the sequence that appears in the downloadable versions of the entry.
Isoform 2 (identifier: Q96HA9-2)

The sequence of this isoform differs from the canonical sequence as follows:
     1-70: Missing.
Note: No experimental confirmation available.

Sequence annotation (Features)

Feature keyPosition(s)LengthDescriptionGraphical viewFeature identifier

Molecule processing

Chain1 – 241241Peroxisomal membrane protein 11C
PRO_0000105970

Regions

Topological domain1 – 124124Cytoplasmic Potential
Transmembrane125 – 14925Helical; Potential
Topological domain150 – 21162Lumenal Potential
Transmembrane212 – 22716Helical; Potential
Topological domain228 – 24114Cytoplasmic Potential

Natural variations

Alternative sequence1 – 7070Missing in isoform 2.
VSP_013539
Natural variant911C → W.
Corresponds to variant rs2303146 [ dbSNP | Ensembl ].
VAR_024560

Sequences

Sequence LengthMass (Da)Tools
Isoform 1 [UniParc].

Last modified December 1, 2001. Version 1.
Checksum: E8B64A196C105913

FASTA24126,636
        10         20         30         40         50         60 
MASLSGLASA LESYRGRDRL IRVLGYCCQL VGGVLVEQCP ARSEVGTRLL VVSTQLSHCR 

        70         80         90        100        110        120 
TILRLFDDLA MFVYTKQYGL GAQEEDAFVR CVSVLGNLAD QLYYPCEHVA WAADARVLHV 

       130        140        150        160        170        180 
DSSRWWTLST TLWALSLLLG VARSLWMLLK LRQRLRSPTA PFTSPLPRGK RRAMEAQMQS 

       190        200        210        220        230        240 
EALSLLSNLA DLANAVHWLP RGVLWAGRFP PWLVGLMGTI SSILSMYQAA RAGGQAEATT 


P 

« Hide

Isoform 2 [UniParc].

Checksum: 306ED7CB510BC9C1
Show »

FASTA17119,016

References

« Hide 'large scale' references
[1]"cDNA cloning and characterization of the third isoform of human peroxin Pex11p."
Tanaka A., Okumoto K., Fujiki Y.
Biochem. Biophys. Res. Commun. 300:819-823(2003) [PubMed] [Europe PMC] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [MRNA] (ISOFORM 1), SUBCELLULAR LOCATION, TOPOLOGY.
[2]"The full-ORF clone resource of the German cDNA consortium."
Bechtel S., Rosenfelder H., Duda A., Schmidt C.P., Ernst U., Wellenreuther R., Mehrle A., Schuster C., Bahr A., Bloecker H., Heubner D., Hoerlein A., Michel G., Wedler H., Koehrer K., Ottenwaelder B., Poustka A., Wiemann S., Schupp I.
BMC Genomics 8:399-399(2007) [PubMed] [Europe PMC] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORM 2).
Tissue: Testis.
[3]"The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)."
The MGC Project Team
Genome Res. 14:2121-2127(2004) [PubMed] [Europe PMC] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORM 1).
Tissue: Pancreas.
[4]"PEX11alpha is required for peroxisome proliferation in response to 4-phenylbutyrate but is dispensable for peroxisome proliferator-activated receptor alpha-mediated peroxisome proliferation."
Li X., Baumgart E., Dong G.-X., Morrell J.C., Jimenez-Sanchez G., Valle D., Smith K.D., Gould S.J.
Mol. Cell. Biol. 22:8226-8240(2002) [PubMed] [Europe PMC] [Abstract]
Cited for: SUBCELLULAR LOCATION, TOPOLOGY.
+Additional computationally mapped references.

Cross-references

Sequence databases

EMBL
GenBank
DDBJ
AB095921 mRNA. Translation: BAD01558.1.
AL833945 mRNA. Translation: CAD38800.1.
BC008780 mRNA. Translation: AAH08780.1.
IPIIPI00062958.
IPI00556568.
RefSeqNP_001257468.1. NM_001270539.1.
NP_542393.1. NM_080662.3.
UniGeneHs.515100.

3D structure databases

ProteinModelPortalQ96HA9.
ModBaseSearch...

Protein-protein interaction databases

STRING9606.ENSP00000221480.

PTM databases

PhosphoSiteQ96HA9.

Polymorphism databases

DMDM62901102.

Proteomic databases

PaxDbQ96HA9.
PRIDEQ96HA9.

Protocols and materials databases

DNASU92960.
StructuralBiologyKnowledgebaseSearch...

Genome annotation databases

EnsemblENST00000221480; ENSP00000221480; ENSG00000104883.
ENST00000593942; ENSP00000472216; ENSG00000104883.
GeneID92960.
KEGGhsa:92960.
UCSCuc002mgk.1. human.

Organism-specific databases

CTD92960.
GeneCardsGC19M007541.
H-InvDBHIX0020270.
HGNCHGNC:20208. PEX11G.
MIM607583. gene.
neXtProtNX_Q96HA9.
PharmGKBPA134987796.
GenAtlasSearch...

Phylogenomic databases

eggNOGNOG302274.
HOGENOMHOG000230635.
HOVERGENHBG053772.
InParanoidQ96HA9.
KOK13353.
OMAVLVEQCP.
OrthoDBEOG4VX266.
PhylomeDBQ96HA9.

Gene expression databases

BgeeQ96HA9.
CleanExHS_PEX11G.
GenevestigatorQ96HA9.
GermOnlineENSG00000104883. Homo sapiens.

Family and domain databases

InterProIPR008733. PEX11.
IPR026510. PEX11C_met.
[Graphical view]
PANTHERPTHR20990. PTHR20990. 1 hit.
PfamPF05648. PEX11. 1 hit.
[Graphical view]
ProtoNetSearch...

Other

GenomeRNAi92960.
NextBio77930.
SOURCESearch...

Entry information

Entry namePX11C_HUMAN
AccessionPrimary (citable) accession number: Q96HA9
Secondary accession number(s): Q8NDM0
Entry history
Integrated into UniProtKB/Swiss-Prot: April 26, 2005
Last sequence update: December 1, 2001
Last modified: May 1, 2013
This is version 81 of the entry and version 1 of the sequence. [Complete history]
Entry statusReviewed (UniProtKB/Swiss-Prot)
Annotation programChordata Protein Annotation Program
DisclaimerAny medical or genetic information present in this entry is provided for research, educational and informational purposes only. It is not in any way intended to be used as a substitute for professional medical advice, diagnosis, treatment or care.

Relevant documents

Human chromosome 19

Human chromosome 19: entries, gene names and cross-references to MIM

Human entries with polymorphisms or disease mutations

List of human entries with polymorphisms or disease mutations

Human polymorphisms and disease mutations

Index of human polymorphisms and disease mutations

MIM cross-references

Online Mendelian Inheritance in Man (MIM) cross-references in UniProtKB/Swiss-Prot

SIMILARITY comments

Index of protein domains and families