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Q9UNU2 (Q9UNU2_HUMAN) Unreviewed, UniProtKB/TrEMBL

Last modified April 16, 2014. Version 49. Feed History...

Clusters with 100%, 90%, 50% identity | Third-party data text xml rdf/xml gff fasta
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Names and origin

Protein names
Gene names
Name:C4B EMBL AAC98380.1
OrganismHomo sapiens (Human) EMBL AAC98380.1
Taxonomic identifier9606 [NCBI]
Taxonomic lineageEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresPrimatesHaplorrhiniCatarrhiniHominidaeHomo

Protein attributes

Sequence length354 AA.
Sequence statusFragment.
Protein existencePredicted

Ontologies

Gene Ontology (GO)
   Cellular_componentextracellular space

Inferred from electronic annotation. Source: InterPro

Complete GO annotation...

Sequence annotation (Features)

Feature keyPosition(s)LengthDescriptionGraphical viewFeature identifier

Experimental info

Non-terminal residue11 EMBL AAC98380.1

Sequences

Sequence LengthMass (Da)Tools
Q9UNU2 [UniParc].

Last modified May 1, 2000. Version 1.
Checksum: DA3AAC7D85708237

FASTA35438,138
        10         20         30         40         50         60 
HRGRTLDIPG NSDPNMIPDG DFNSYVRVTA SDPLDTLGSE GALSPGGVAS LLRLPRGCGE 

        70         80         90        100        110        120 
QTMIYLAPTL AASRYLDKTE QWSTLPPETK DHAVDLIQKG YMRIQQFRKA DGSYAAWLSR 

       130        140        150        160        170        180 
DSSTWLTAFV LKVLSLAQEQ VGGSPEKLQE TSNWLLSQQQ ADGSFQDLSP VIHRSMQGGL 

       190        200        210        220        230        240 
VGNDETVALT AFVTIALHHG LAVFQDEGAE PLKQRVEASI SKASSFLGEK ASAGLLGAHA 

       250        260        270        280        290        300 
AAITAYALTL TKAPADLRGV AHNNLMAMAQ ETGDNLYWGS QSLVLRAMPC RPPRLLATHP 

       310        320        330        340        350 
TPCPRPQPCG LKPQPTPCCT SCFTRAKQRW QTRLRPGSPV RAASKGDSAV PKTR 

« Hide

References

[1]"Genetic basis of human complement C4A deficiency. Detection of a point mutation leading to nonexpression."
Barba G., Rittner C., Schneider P.M.
J. Clin. Invest. 91:1681-1686(1993) [PubMed] [Europe PMC] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE.
[2]"Deficiency of Complement Protein C4 Due to Identical Frameshift Mutations in the C4A and C4B Genes."
Lokki M.-L., Circolo A., Ahokas P., Rupert K.L., Yu C.Y., Colten H.R.
Submitted (SEP-1998) to the EMBL/GenBank/DDBJ databases
Cited for: NUCLEOTIDE SEQUENCE.
+Additional computationally mapped references.

Cross-references

Sequence databases

EMBL
GenBank
DDBJ
AF092085 Genomic DNA. Translation: AAC98380.1.
PIRI55584.
UniGeneHs.534847.
Hs.720022.

3D structure databases

ProteinModelPortalQ9UNU2.
ModBaseSearch...
MobiDBSearch...

Proteomic databases

PRIDEQ9UNU2.

Protocols and materials databases

StructuralBiologyKnowledgebaseSearch...

Family and domain databases

Gene3D1.50.10.20. 1 hit.
InterProIPR011626. A2M_comp.
IPR019742. MacrogloblnA2_CS.
IPR019565. MacrogloblnA2_thiol-ester-bond.
IPR008930. Terpenoid_cyclase/PrenylTrfase.
[Graphical view]
PfamPF07678. A2M_comp. 1 hit.
PF10569. Thiol-ester_cl. 1 hit.
[Graphical view]
SUPFAMSSF48239. SSF48239. 1 hit.
PROSITEPS00477. ALPHA_2_MACROGLOBULIN. 1 hit.
[Graphical view]
ProtoNetSearch...

Entry information

Entry nameQ9UNU2_HUMAN
AccessionPrimary (citable) accession number: Q9UNU2
Entry history
Integrated into UniProtKB/TrEMBL: May 1, 2000
Last sequence update: May 1, 2000
Last modified: April 16, 2014
This is version 49 of the entry and version 1 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.