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Q9H3Y0 (CRSPL_HUMAN) Reviewed, UniProtKB/Swiss-Prot

Last modified January 25, 2012. Version 70. Feed History...

Clusters with 100%, 90%, 50% identity | Documents (4) | 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:
Peptidase inhibitor R3HDML
Alternative name(s):
Cysteine-rich secretory protein R3HDML
Gene names
Name:R3HDML
OrganismHomo sapiens (Human)
Taxonomic identifier9606 [NCBI]
Taxonomic lineageEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresPrimatesHaplorrhiniCatarrhiniHominidaeHomo

Protein attributes

Sequence length253 AA.
Sequence statusComplete.
Sequence processingThe displayed sequence is further processed into a mature form.
Protein existenceEvidence at protein level

General annotation (Comments)

Function

Putative serine protease inhibitor By similarity.

Subcellular location

Secreted Potential.

Sequence similarities

Belongs to the CRISP family.

Caution

Despite its name, it does not contain a R3H domain.

Ontologies

Keywords
   Cellular componentSecreted
   Coding sequence diversityPolymorphism
   DomainSignal
   Molecular functionProtease inhibitor
   PTMGlycoprotein
   Technical termComplete proteome
Reference proteome
Gene Ontology (GO)
   Cellular componentextracellular region

Inferred from electronic annotation. Source: UniProtKB-SubCell

   Molecular functionpeptidase inhibitor activity

Inferred from electronic annotation. Source: UniProtKB-KW

Complete GO annotation...

Sequence annotation (Features)

Feature keyPosition(s)LengthDescriptionGraphical viewFeature identifier

Molecule processing

Signal peptide1 – 2424 Potential
Propeptide25 – 5632 By similarity
PRO_0000287635
Chain57 – 253197Peptidase inhibitor R3HDML
PRO_0000287636

Amino acid modifications

Glycosylation1201N-linked (GlcNAc...) Potential

Natural variations

Natural variant151F → C.
Corresponds to variant rs11699901 [ dbSNP | Ensembl ].
VAR_032339
Natural variant681D → N.
Corresponds to variant rs36117710 [ dbSNP | Ensembl ].
VAR_048834

Sequences

Sequence LengthMass (Da)Tools
Q9H3Y0 [UniParc].

Last modified March 1, 2001. Version 1.
Checksum: 28976C6F32E3887E

FASTA25328,605
        10         20         30         40         50         60 
MPLLPSTVGL AGLLFWAGQA VNALIMPNAT PAPAQPESTA MRLLSGLEVP RYRRKRHISV 

        70         80         90        100        110        120 
RDMNALLDYH NHIRASVYPP AANMEYMVWD KRLARAAEAW ATQCIWAHGP SQLMRYVGQN 

       130        140        150        160        170        180 
LSIHSGQYRS VVDLMKSWSE EKWHYLFPAP RDCNPHCPWR CDGPTCSHYT QMVWASSNRL 

       190        200        210        220        230        240 
GCAIHTCSSI SVWGNTWHRA AYLVCNYAIK GNWIGESPYK MGKPCSSCPP SYQGSCNSNM 

       250 
CFKGLKSNKF TWF 

« Hide

References

[1]"The DNA sequence and comparative analysis of human chromosome 20."
Deloukas P., Matthews L.H., Ashurst J.L., Burton J., Gilbert J.G.R., Jones M., Stavrides G., Almeida J.P., Babbage A.K., Bagguley C.L., Bailey J., Barlow K.F., Bates K.N., Beard L.M., Beare D.M., Beasley O.P., Bird C.P., Blakey S.E. expand/collapse author list , Bridgeman A.M., Brown A.J., Buck D., Burrill W.D., Butler A.P., Carder C., Carter N.P., Chapman J.C., Clamp M., Clark G., Clark L.N., Clark S.Y., Clee C.M., Clegg S., Cobley V.E., Collier R.E., Connor R.E., Corby N.R., Coulson A., Coville G.J., Deadman R., Dhami P.D., Dunn M., Ellington A.G., Frankland J.A., Fraser A., French L., Garner P., Grafham D.V., Griffiths C., Griffiths M.N.D., Gwilliam R., Hall R.E., Hammond S., Harley J.L., Heath P.D., Ho S., Holden J.L., Howden P.J., Huckle E., Hunt A.R., Hunt S.E., Jekosch K., Johnson C.M., Johnson D., Kay M.P., Kimberley A.M., King A., Knights A., Laird G.K., Lawlor S., Lehvaeslaiho M.H., Leversha M.A., Lloyd C., Lloyd D.M., Lovell J.D., Marsh V.L., Martin S.L., McConnachie L.J., McLay K., McMurray A.A., Milne S.A., Mistry D., Moore M.J.F., Mullikin J.C., Nickerson T., Oliver K., Parker A., Patel R., Pearce T.A.V., Peck A.I., Phillimore B.J.C.T., Prathalingam S.R., Plumb R.W., Ramsay H., Rice C.M., Ross M.T., Scott C.E., Sehra H.K., Shownkeen R., Sims S., Skuce C.D., Smith M.L., Soderlund C., Steward C.A., Sulston J.E., Swann R.M., Sycamore N., Taylor R., Tee L., Thomas D.W., Thorpe A., Tracey A., Tromans A.C., Vaudin M., Wall M., Wallis J.M., Whitehead S.L., Whittaker P., Willey D.L., Williams L., Williams S.A., Wilming L., Wray P.W., Hubbard T., Durbin R.M., Bentley D.R., Beck S., Rogers J.
Nature 414:865-871(2001) [PubMed: 11780052] [Abstract]
Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA].
[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].
+Additional computationally mapped references.

Cross-references

Sequence databases

EMBL
GenBank
DDBJ
AL117382 Genomic DNA. Translation: CAC04190.1.
BC107048 mRNA. Translation: AAI07049.1.
IPIIPI00024338.
RefSeqNP_848586.1. NM_178491.2.
UniGeneHs.580807.

3D structure databases

HSSPHSSP built from PDB template 1RC9 based on UniProtKB P60623.
ProteinModelPortalQ9H3Y0.
SMRQ9H3Y0. Positions 58-247.
ModBaseSearch...

Polymorphism databases

DMDM74752628.

Proteomic databases

PeptideAtlasQ9H3Y0.
PRIDEQ9H3Y0.

Protocols and materials databases

StructuralBiologyKnowledgebaseSearch...

Genome annotation databases

EnsemblENST00000217043; ENSP00000217043; ENSG00000101074.
GeneID140902.
KEGGhsa:140902.
UCSCuc002xls.1. human.

Organism-specific databases

CTD140902.
GeneCardsGC20P042965.
HGNCHGNC:16249. R3HDML.
neXtProtNX_Q9H3Y0.
PharmGKBPA34099.
GenAtlasSearch...

Phylogenomic databases

eggNOGprNOG17840.
GeneTreeENSGT00560000077066.
HOGENOMHBG445512.
HOVERGENHBG079090.
InParanoidQ9H3Y0.
OMALFWAGQT.
OrthoDBEOG4X6C8W.
PhylomeDBQ9H3Y0.

Gene expression databases

ArrayExpressQ9H3Y0.
CleanExHS_R3HDML.
GenevestigatorQ9H3Y0.

Family and domain databases

InterProIPR001283. Allrgn_V5/Tpx1.
IPR014044. CAP_domain.
[Graphical view]
Gene3DG3DSA:3.40.33.10. CAP_domain. 1 hit.
PANTHERPTHR10334. Allrgn_V5/Tpx1. 1 hit.
PfamPF00188. CAP. 1 hit.
[Graphical view]
PRINTSPR00837. V5TPXLIKE.
SMARTSM00198. SCP. 1 hit.
[Graphical view]
SUPFAMSSF55797. SCP-like_extracellular. 1 hit.
PROSITEPS01009. CRISP_1. False negative.
PS01010. CRISP_2. False negative.
[Graphical view]
ProtoNetSearch...

Other

NextBio84571.

Entry information

Entry nameCRSPL_HUMAN
AccessionPrimary (citable) accession number: Q9H3Y0
Entry history
Integrated into UniProtKB/Swiss-Prot: May 15, 2007
Last sequence update: March 1, 2001
Last modified: January 25, 2012
This is version 70 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 20

Human chromosome 20: 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

SIMILARITY comments

Index of protein domains and families