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Q9NNZ3 (DNJC4_HUMAN) Reviewed, UniProtKB/Swiss-Prot

Last modified January 25, 2012. Version 92. Feed History...

Clusters with 100%, 90%, 50% identity | Documents (3) | Third-party data text xml rdf/xml gff fasta
to top of pageNames·Attributes·General annotation·Ontologies·Sequence annotation·Sequences·References·Cross-refs·Entry info·DocumentsCustomize order

Names and origin

Protein namesRecommended name:
DnaJ homolog subfamily C member 4
Alternative name(s):
DnaJ-like protein HSPF2
Multiple endocrine neoplasia type 1 candidate protein number 18
Gene names
Name:DNAJC4
Synonyms:HSPF2, MCG18
OrganismHomo sapiens (Human)
Taxonomic identifier9606 [NCBI]
Taxonomic lineageEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresPrimatesHaplorrhiniCatarrhiniHominidaeHomo

Protein attributes

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

General annotation (Comments)

Subcellular location

Membrane; Single-pass membrane protein Potential.

Sequence similarities

Contains 1 J domain.

Sequence caution

The sequence AAB82426.1 differs from that shown. Reason: Several sequence rearrangements.

Ontologies

Keywords
   Cellular componentMembrane
   DomainTransmembrane
Transmembrane helix
   Molecular functionChaperone
   Technical termComplete proteome
Reference proteome
Gene Ontology (GO)
   Biological processprotein folding

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

response to unfolded protein

Traceable author statement. Source: ProtInc

   Cellular componentintegral to membrane

Inferred from electronic annotation. Source: UniProtKB-KW

membrane fraction

Traceable author statement. Source: ProtInc

   Molecular functionheat shock protein binding

Inferred from electronic annotation. Source: InterPro

unfolded protein binding

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

Complete GO annotation...

Sequence annotation (Features)

Feature keyPosition(s)LengthDescriptionGraphical viewFeature identifier

Molecule processing

Chain1 – 241241DnaJ homolog subfamily C member 4
PRO_0000071049

Regions

Transmembrane156 – 17520Helical; Potential
Domain34 – 9966J

Sequences

Sequence LengthMass (Da)Tools
Q9NNZ3 [UniParc].

Last modified October 1, 2000. Version 1.
Checksum: EA186D2FA6C2E179

FASTA24127,593
        10         20         30         40         50         60 
MPPLLPLRLC RLWPRNPPSR LLGAAAGQRS RPSTYYELLG VHPGASTEEV KRAFFSKSKE 

        70         80         90        100        110        120 
LHPDRDPGNP SLHSRFVELS EAYRVLSREQ SRRSYDDQLR SGSPPKSPRT TVHDKSAHQT 

       130        140        150        160        170        180 
HSSWTPPNAQ YWSQFHSVRP QGPQLRQQQH KQNKQVLGYC LLLMLAGMGL HYIAFRKVKQ 

       190        200        210        220        230        240 
MHLNFMDEKD RIITAFYNEA RARARANRGI LQQERQRLGQ RQPPPSEPTQ GPEIVPRGAG 


P 

« Hide

References

« Hide 'large scale' references
[1]"Characterisation of a new human and murine member of the DnaJ family of proteins."
Silins G., Grimmond S., Hayward N.
Biochem. Biophys. Res. Commun. 243:273-276(1998) [PubMed: 9473517] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [MRNA].
[2]"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: 15489334] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA].
Tissue: Brain and Placenta.
[3]"Identification and characterisation of a novel human Dnaj gene, HSPF2, mapping to chromosome 11q13."
Lloyd S.E., Thakker R.V.
Submitted (JUL-1997) to the EMBL/GenBank/DDBJ databases
Cited for: PARTIAL NUCLEOTIDE SEQUENCE [MRNA].
Tissue: Placenta.
+Additional computationally mapped references.

Cross-references

Sequence databases

EMBL
GenBank
DDBJ
AF036874 mRNA. Translation: AAF97845.1.
BC044584 mRNA. Translation: AAH44584.1.
BC057849 mRNA. Translation: AAH57849.1.
AF012106 mRNA. Translation: AAB82426.1. Sequence problems.
IPIIPI00328890.
PIRJE0169.
RefSeqNP_005519.2. NM_005528.3.
UniGeneHs.172847.

3D structure databases

ProteinModelPortalQ9NNZ3.
SMRQ9NNZ3. Positions 33-99.
ModBaseSearch...

Protein-protein interaction databases

IntActQ9NNZ3. 1 interaction.
STRINGQ9NNZ3.

PTM databases

PhosphoSiteQ9NNZ3.

Polymorphism databases

DMDM18203312.

Proteomic databases

PRIDEQ9NNZ3.

Protocols and materials databases

StructuralBiologyKnowledgebaseSearch...

Genome annotation databases

EnsemblENST00000321460; ENSP00000320548; ENSG00000110011.
ENST00000321685; ENSP00000396896; ENSG00000110011.
GeneID3338.
KEGGhsa:3338.
UCSCuc001nys.1. human.

Organism-specific databases

CTD3338.
GeneCardsGC11P063997.
H-InvDBHIX0201666.
HGNCHGNC:5271. DNAJC4.
HPAHPA011947.
MIM604189. gene.
neXtProtNX_Q9NNZ3.
PharmGKBPA27421.
GenAtlasSearch...

Phylogenomic databases

eggNOGprNOG16256.
GeneTreeENSGT00510000048574.
HOGENOMHBG714808.
HOVERGENHBG051375.
InParanoidQ9NNZ3.
OMARRSYDDQ.
OrthoDBEOG432109.
PhylomeDBQ9NNZ3.

Gene expression databases

ArrayExpressQ9NNZ3.
BgeeQ9NNZ3.
CleanExHS_DNAJC4.
GenevestigatorQ9NNZ3.
GermOnlineENSG00000110011. Homo sapiens.

Family and domain databases

InterProIPR001623. DnaJ_N.
IPR003095. Hsp_DnaJ.
[Graphical view]
Gene3DG3DSA:1.10.287.110. DnaJ_N. 1 hit.
KOK09524.
PfamPF00226. DnaJ. 1 hit.
[Graphical view]
PRINTSPR00625. JDOMAIN.
SMARTSM00271. DnaJ. 1 hit.
[Graphical view]
SUPFAMSSF46565. DnaJ_N. 1 hit.
PROSITEPS00636. DNAJ_1. False negative.
PS50076. DNAJ_2. 1 hit.
[Graphical view]
ProtoNetSearch...

Other

NextBio13212.
SOURCESearch...

Entry information

Entry nameDNJC4_HUMAN
AccessionPrimary (citable) accession number: Q9NNZ3
Secondary accession number(s): O14716
Entry history
Integrated into UniProtKB/Swiss-Prot: October 18, 2001
Last sequence update: October 1, 2000
Last modified: January 25, 2012
This is version 92 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 11

Human chromosome 11: entries, gene names and cross-references to MIM

MIM cross-references

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

SIMILARITY comments

Index of protein domains and families