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Q9BWW9 (APOL5_HUMAN) Reviewed, UniProtKB/Swiss-Prot

Last modified January 25, 2012. Version 78. 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·Interactions·Sequence annotation·Sequences·References·Cross-refs·Entry info·DocumentsCustomize order

Names and origin

Protein namesRecommended name:
Apolipoprotein L5
Alternative name(s):
Apolipoprotein L-V
Short name=ApoL-V
Gene names
Name:APOL5
OrganismHomo sapiens (Human)
Taxonomic identifier9606 [NCBI]
Taxonomic lineageEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresPrimatesHaplorrhiniCatarrhiniHominidaeHomo

Protein attributes

Sequence length433 AA.
Sequence statusComplete.
Protein existenceEvidence at protein level

General annotation (Comments)

Function

May affect the movement of lipids in the cytoplasm or allow the binding of lipids to organelles.

Subcellular location

Cytoplasm Probable.

Tissue specificity

Low level of expression; detected in uterus, testis, skeletal muscle and stomach.

Sequence similarities

Belongs to the apolipoprotein L family.

Ontologies

Keywords
   Biological processLipid transport
Transport
   Cellular componentCytoplasm
   Coding sequence diversityPolymorphism
   Technical termComplete proteome
Reference proteome
Gene Ontology (GO)
   Biological processlipid metabolic process

Non-traceable author statement Ref.1. Source: UniProtKB

lipid transport

Inferred from electronic annotation. Source: UniProtKB-KW

lipoprotein metabolic process

Inferred from electronic annotation. Source: InterPro

   Cellular componentcytoplasm

Inferred from electronic annotation. Source: UniProtKB-SubCell

extracellular region

Inferred from electronic annotation. Source: InterPro

   Molecular functionhigh-density lipoprotein particle binding

Non-traceable author statement Ref.1. Source: UniProtKB

lipid binding

Inferred from electronic annotation. Source: InterPro

Complete GO annotation...

Sequence annotation (Features)

Feature keyPosition(s)LengthDescriptionGraphical viewFeature identifier

Molecule processing

Chain1 – 433433Apolipoprotein L5
PRO_0000137603

Natural variations

Natural variant811E → K.
Corresponds to variant rs5999985 [ dbSNP | Ensembl ].
VAR_053012
Natural variant2721T → M.
Corresponds to variant rs2076671 [ dbSNP | Ensembl ].
VAR_020355
Natural variant3231T → M.
Corresponds to variant rs2076672 [ dbSNP | Ensembl ].
VAR_020356
Natural variant4061S → C.
Corresponds to variant rs2076673 [ dbSNP | Ensembl ].
VAR_020357

Sequences

Sequence LengthMass (Da)Tools
Q9BWW9 [UniParc].

Last modified June 1, 2001. Version 1.
Checksum: F64416DE8FEB7E9E

FASTA43347,044
        10         20         30         40         50         60 
MPCGKQGNLQ VPGSKVLPGL GEGCKEMWLR KVIYGGEVWG KSPEPEFPSL VNLCQSWKIN 

        70         80         90        100        110        120 
NLMSTVHSDE AGMLSYFLFE ELMRCDKDSM PDGNLSEEEK LFLSYFPLHK FELEQNIKEL 

       130        140        150        160        170        180 
NTLADQVDTT HELLTKTSLV ASSSGAVSGV MNILGLALAP VTAGGSLMLS ATGTGLGAAA 

       190        200        210        220        230        240 
AITNIVTNVL ENRSNSAARD KASRLGPLTT SHEAFGGINW SEIEAAGFCV NKCVKAIQGI 

       250        260        270        280        290        300 
KDLHAYQMAK SNSGFMAMVK NFVAKRHIPF WTARGVQRAF EGTTLAMTNG AWVMGAAGAG 

       310        320        330        340        350        360 
FLLMKDMSSF LQSWKHLEDG ARTETAEELR ALAKKLEQEL DRLTQHHRHL PQKASQTCSS 

       370        380        390        400        410        420 
SRGRAVRGSR VVKPEGSRSP LPWPVVEHQP RLGPGVALRT PKRTVSAPRM LGHQPAPPAP 

       430 
ARKGRQAPGR HRQ 

« Hide

References

« Hide 'large scale' references
[1]"The human apolipoprotein L gene cluster: identification, classification, and sites of distribution."
Page N.M., Butlin D.J., Lomthaisong K., Lowry P.J.
Genomics 74:71-78(2001) [PubMed: 11374903] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [MRNA].
Tissue: Placenta.
[2]"The DNA sequence of human chromosome 22."
Dunham I., Hunt A.R., Collins J.E., Bruskiewich R., Beare D.M., Clamp M., Smink L.J., Ainscough R., Almeida J.P., Babbage A.K., Bagguley C., Bailey J., Barlow K.F., Bates K.N., Beasley O.P., Bird C.P., Blakey S.E., Bridgeman A.M. expand/collapse author list , Buck D., Burgess J., Burrill W.D., Burton J., Carder C., Carter N.P., Chen Y., Clark G., Clegg S.M., Cobley V.E., Cole C.G., Collier R.E., Connor R., Conroy D., Corby N.R., Coville G.J., Cox A.V., Davis J., Dawson E., Dhami P.D., Dockree C., Dodsworth S.J., Durbin R.M., Ellington A.G., Evans K.L., Fey J.M., Fleming K., French L., Garner A.A., Gilbert J.G.R., Goward M.E., Grafham D.V., Griffiths M.N.D., Hall C., Hall R.E., Hall-Tamlyn G., Heathcott R.W., Ho S., Holmes S., Hunt S.E., Jones M.C., Kershaw J., Kimberley A.M., King A., Laird G.K., Langford C.F., Leversha M.A., Lloyd C., Lloyd D.M., Martyn I.D., Mashreghi-Mohammadi M., Matthews L.H., Mccann O.T., Mcclay J., Mclaren S., McMurray A.A., Milne S.A., Mortimore B.J., Odell C.N., Pavitt R., Pearce A.V., Pearson D., Phillimore B.J.C.T., Phillips S.H., Plumb R.W., Ramsay H., Ramsey Y., Rogers L., Ross M.T., Scott C.E., Sehra H.K., Skuce C.D., Smalley S., Smith M.L., Soderlund C., Spragon L., Steward C.A., Sulston J.E., Swann R.M., Vaudin M., Wall M., Wallis J.M., Whiteley M.N., Willey D.L., Williams L., Williams S.A., Williamson H., Wilmer T.E., Wilming L., Wright C.L., Hubbard T., Bentley D.R., Beck S., Rogers J., Shimizu N., Minoshima S., Kawasaki K., Sasaki T., Asakawa S., Kudoh J., Shintani A., Shibuya K., Yoshizaki Y., Aoki N., Mitsuyama S., Roe B.A., Chen F., Chu L., Crabtree J., Deschamps S., Do A., Do T., Dorman A., Fang F., Fu Y., Hu P., Hua A., Kenton S., Lai H., Lao H.I., Lewis J., Lewis S., Lin S.-P., Loh P., Malaj E., Nguyen T., Pan H., Phan S., Qi S., Qian Y., Ray L., Ren Q., Shaull S., Sloan D., Song L., Wang Q., Wang Y., Wang Z., White J., Willingham D., Wu H., Yao Z., Zhan M., Zhang G., Chissoe S., Murray J., Miller N., Minx P., Fulton R., Johnson D., Bemis G., Bentley D., Bradshaw H., Bourne S., Cordes M., Du Z., Fulton L., Goela D., Graves T., Hawkins J., Hinds K., Kemp K., Latreille P., Layman D., Ozersky P., Rohlfing T., Scheet P., Walker C., Wamsley A., Wohldmann P., Pepin K., Nelson J., Korf I., Bedell J.A., Hillier L.W., Mardis E., Waterston R., Wilson R., Emanuel B.S., Shaikh T., Kurahashi H., Saitta S., Budarf M.L., McDermid H.E., Johnson A., Wong A.C.C., Morrow B.E., Edelmann L., Kim U.J., Shizuya H., Simon M.I., Dumanski J.P., Peyrard M., Kedra D., Seroussi E., Fransson I., Tapia I., Bruder C.E., O'Brien K.P., Wilkinson P., Bodenteich A., Hartman K., Hu X., Khan A.S., Lane L., Tilahun Y., Wright H.
Nature 402:489-495(1999) [PubMed: 10591208] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA].
+Additional computationally mapped references.

Cross-references

Sequence databases

EMBL
GenBank
DDBJ
AY014878 mRNA. Translation: AAK07723.1.
AL049748 Genomic DNA. No translation available.
IPIIPI00032680.
RefSeqNP_085145.1. NM_030642.1.
UniGeneHs.326561.

3D structure databases

ProteinModelPortalQ9BWW9.
ModBaseSearch...

Protein-protein interaction databases

IntActQ9BWW9. 7 interactions.
MINTMINT-7241622.
STRINGQ9BWW9.

Polymorphism databases

DMDM17433287.

Proteomic databases

PRIDEQ9BWW9.

Protocols and materials databases

StructuralBiologyKnowledgebaseSearch...

Genome annotation databases

EnsemblENST00000249044; ENSP00000249044; ENSG00000128313.
GeneID80831.
KEGGhsa:80831.
UCSCuc003aof.1. human.

Organism-specific databases

CTD80831.
GeneCardsGC22P036113.
H-InvDBHIX0203203.
HGNCHGNC:14869. APOL5.
HPAHPA040968.
MIM607255. gene.
neXtProtNX_Q9BWW9.
PharmGKBPA24908.
GenAtlasSearch...

Phylogenomic databases

eggNOGprNOG09003.
GeneTreeENSGT00510000046700.
InParanoidQ9BWW9.
OMANSGFMAM.
OrthoDBEOG49ZXPX.
PhylomeDBQ9BWW9.

Gene expression databases

ArrayExpressQ9BWW9.
BgeeQ9BWW9.
CleanExHS_APOL5.
GenevestigatorQ9BWW9.
GermOnlineENSG00000128313. Homo sapiens.

Family and domain databases

InterProIPR008405. ApoL.
[Graphical view]
KOK14480.
PANTHERPTHR14096. ApoL. 1 hit.
PfamPF05461. ApoL. 1 hit.
[Graphical view]
ProtoNetSearch...

Other

NextBio71244.
SOURCESearch...

Entry information

Entry nameAPOL5_HUMAN
AccessionPrimary (citable) accession number: Q9BWW9
Secondary accession number(s): Q5TFL9, Q9UGW5
Entry history
Integrated into UniProtKB/Swiss-Prot: August 29, 2001
Last sequence update: June 1, 2001
Last modified: January 25, 2012
This is version 78 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 22

Human chromosome 22: 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