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A8MYL5 (A8MYL5_HUMAN) Unreviewed, UniProtKB/TrEMBL

Last modified June 11, 2014. Version 44. Feed History...

Clusters with 100%, 90%, 50% identity | Third-party data text xml rdf/xml gff fasta
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Protein attributes

Sequence length42 AA.
Sequence statusFragment.
Protein existencePredicted

General annotation (Comments)

Caution

The sequence shown here is derived from an Ensembl automatic analysis pipeline and should be considered as preliminary data. Ensembl ENSP00000377925 Ensembl ENSP00000391737

Sequence annotation (Features)

Feature keyPosition(s)LengthDescriptionGraphical viewFeature identifier

Experimental info

Non-terminal residue421 Ensembl ENSP00000377925 Ensembl ENSP00000391737

Sequences

Sequence LengthMass (Da)Tools
A8MYL5 [UniParc].

Last modified November 3, 2009. Version 2.
Checksum: 603D577FCE4C224B

FASTA424,747
        10         20         30         40 
MSGLHLVKQG RDRKKIDSQR DFTVASPAEF VTRFGGNKVI EK 

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Cross-references

Sequence databases

EMBL
GenBank
DDBJ
AC003103 Genomic DNA. No translation available.
AC016482 Genomic DNA. No translation available.
AC068400 Genomic DNA. No translation available.

3D structure databases

ProteinModelPortalA8MYL5.
SMRA8MYL5. Positions 17-42.
ModBaseSearch...
MobiDBSearch...

Protocols and materials databases

StructuralBiologyKnowledgebaseSearch...

Genome annotation databases

EnsemblENST00000394403; ENSP00000377925; ENSG00000132142.
ENST00000413318; ENSP00000391737; ENSG00000132142.

Organism-specific databases

HGNCHGNC:84. ACACA.
GenAtlasSearch...

Phylogenomic databases

HOGENOMHOG000213683.

Family and domain databases

ProtoNetSearch...

Other

ChiTaRSACACA. human.
NextBio35465056.

Entry information

Entry nameA8MYL5_HUMAN
AccessionPrimary (citable) accession number: A8MYL5
Entry history
Integrated into UniProtKB/TrEMBL: December 4, 2007
Last sequence update: November 3, 2009
Last modified: June 11, 2014
This is version 44 of the entry and version 2 of the sequence. [Complete history]
Entry statusUnreviewed (UniProtKB/TrEMBL)
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.