O14513 (NCKP5_HUMAN) Reviewed, UniProtKB/Swiss-Prot
Last modified
January 25, 2012.
Version 68.
History...
Names·Attributes·General annotation·Ontologies·Alt products·Sequence annotation·Sequences·References·Cross-refs·Entry info·DocumentsCustomize order
Names·Attributes·General annotation·Ontologies·Alt products·Sequence annotation·Sequences·References·Cross-refs·Entry info·DocumentsCustomize orderNames and origin
| Protein names | Recommended name: Nck-associated protein 5 Short name=NAP-5 Alternative name(s): Peripheral clock protein | ||||
| Gene names |
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| Organism | Homo sapiens (Human) | ||||
| Taxonomic identifier | 9606 [NCBI] | ||||
| Taxonomic lineage | Eukaryota › Metazoa › Chordata › Craniata › Vertebrata › Euteleostomi › Mammalia › Eutheria › Euarchontoglires › Primates › Haplorrhini › Catarrhini › Hominidae › Homo |
Protein attributes
| Sequence length | 1909 AA. |
| Sequence status | Complete. |
| Protein existence | Evidence at transcript level |
General annotation (Comments)
| Subunit structure | Interacts with the SH3-containing region of the adapter protein Nck. |
| Tissue specificity | Expressed in fetal and adult brain, leukocytes and fetal fibroblasts. |
| Caution | It is uncertain whether Met-1 or Met-26 is the initiator. |
| Sequence caution | The sequence BAA22433.1 differs from that shown. Reason: Frameshift at positions 856, 877, 920, 926, 957 and 967. The sequence BAC85920.1 differs from that shown. Reason: Erroneous initiation. |
Ontologies
| Keywords | |
|---|---|
| Coding sequence diversity | Alternative splicing Polymorphism |
| Domain | Coiled coil |
| Technical term | Complete proteome Reference proteome |
| Gene Ontology (GO) | |
| None. [Check GOA] | |
Alternative products
| This entry describes 4 isoforms produced by alternative splicing. [Align] [Select] | ||||||
| Isoform 1 (identifier: O14513-1) Also known as: Peripheral clock protein 2; ERIH2; This isoform has been chosen as the 'canonical' sequence. All positional information in this entry refers to it. This is also the sequence that appears in the downloadable versions of the entry. | ||||||
| Isoform 2 (identifier: O14513-2) Also known as: Peripheral clock protein 1; ERIH1; The sequence of this isoform differs from the canonical sequence as follows: 365-1683: Missing. | ||||||
| Isoform 3 (identifier: O14513-3) The sequence of this isoform differs from the canonical sequence as follows: 1-25: Missing. 194-203: AENSALALEN → KHGWNWRPLS 204-1909: Missing. | ||||||
| Isoform 4 (identifier: O14513-4) The sequence of this isoform differs from the canonical sequence as follows: 115-118: MEET → RRKM 119-1909: Missing. |
Sequence annotation (Features)
| Feature key | Position(s) | Length | Description | Graphical view | Feature identifier | ||||
Molecule processing | |||||||||
|---|---|---|---|---|---|---|---|---|---|
| Chain | 1 – 1909 | 1909 | Nck-associated protein 5 | PRO_0000096711 | |||||
Regions | |||||||||
| Coiled coil | 71 – 253 | 183 | Potential | ||||||
| Compositional bias | 331 – 386 | 56 | Ser-rich | ||||||
| Compositional bias | 927 – 933 | 7 | Poly-Pro | ||||||
| Compositional bias | 1080 – 1130 | 51 | Ser-rich | ||||||
Natural variations | |||||||||
| Alternative sequence | 1 – 25 | 25 | Missing in isoform 3. | VSP_021601 | |||||
| Alternative sequence | 115 – 118 | 4 | MEET → RRKM in isoform 4. | VSP_021602 | |||||
| Alternative sequence | 119 – 1909 | 1791 | Missing in isoform 4. | VSP_021603 | |||||
| Alternative sequence | 194 – 203 | 10 | AENSALALEN → KHGWNWRPLS in isoform 3. | VSP_021604 | |||||
| Alternative sequence | 204 – 1909 | 1706 | Missing in isoform 3. | VSP_021605 | |||||
| Alternative sequence | 365 – 1683 | 1319 | Missing in isoform 2. | VSP_021606 | |||||
| Natural variant | 250 | 1 | R → Q. Corresponds to variant rs58963837 [ dbSNP | Ensembl ]. | VAR_061686 | |||||
| Natural variant | 600 | 1 | S → T. Corresponds to variant rs17325719 [ dbSNP | Ensembl ]. | VAR_051220 | |||||
| Natural variant | 937 | 1 | V → I. Corresponds to variant rs12611515 [ dbSNP | Ensembl ]. | VAR_051221 | |||||
| Natural variant | 977 | 1 | I → T. Corresponds to variant rs12691830 [ dbSNP | Ensembl ]. | VAR_051222 | |||||
| Natural variant | 1093 | 1 | N → Y. Corresponds to variant rs16841277 [ dbSNP | Ensembl ]. | VAR_051223 | |||||
| Natural variant | 1260 | 1 | P → Q. Corresponds to variant rs13016342 [ dbSNP | Ensembl ]. | VAR_051224 | |||||
| Natural variant | 1403 | 1 | V → A. Corresponds to variant rs2278752 [ dbSNP | Ensembl ]. | VAR_051225 | |||||
Experimental info | |||||||||
| Sequence conflict | 931 – 932 | 2 | PP → QS in BAA22433. Ref.5 | ||||||
| Sequence conflict | 948 | 1 | S → P in BAA22433. Ref.5 | ||||||
| Sequence conflict | 1018 | 1 | T → S in BAA22433. Ref.5 | ||||||
Sequences
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References
| « Hide 'large scale' references | |
| [1] | "Complete sequencing and characterization of 21,243 full-length human cDNAs." Ota T., Suzuki Y., Nishikawa T., Otsuki T., Sugiyama T., Irie R., Wakamatsu A., Hayashi K., Sato H., Nagai K., Kimura K., Makita H., Sekine M., Obayashi M., Nishi T., Shibahara T., Tanaka T., Ishii S. Sugano S.Nat. Genet. 36:40-45(2004) [PubMed: 14702039] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORM 3), NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] OF 1586-1909 (ISOFORM 1). Tissue: Amygdala and Teratocarcinoma. |
| [2] | "Generation and annotation of the DNA sequences of human chromosomes 2 and 4." Hillier L.W., Graves T.A., Fulton R.S., Fulton L.A., Pepin K.H., Minx P., Wagner-McPherson C., Layman D., Wylie K., Sekhon M., Becker M.C., Fewell G.A., Delehaunty K.D., Miner T.L., Nash W.E., Kremitzki C., Oddy L., Du H. Wilson R.K.Nature 434:724-731(2005) [PubMed: 15815621] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA]. |
| [3] | "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] OF 6-1909 (ISOFORM 4). Tissue: Testis. |
| [4] | Hisa T. Submitted (FEB-2005) to the EMBL/GenBank/DDBJ databases Cited for: NUCLEOTIDE SEQUENCE [MRNA] OF 69-1909 (ISOFORMS 1 AND 2). |
| [5] | "A novel ligand for an SH3 domain of the adaptor protein Nck bears an SH2 domain and nuclear signaling motifs." Matuoka K., Miki H., Takahashi K., Takenawa T. Biochem. Biophys. Res. Commun. 239:488-492(1997) [PubMed: 9344857] [Abstract] Cited for: NUCLEOTIDE SEQUENCE [MRNA] OF 661-1077 (ISOFORM 1). Tissue: Brain. |
| + | Additional computationally mapped references. |
Cross-references
Sequence databases | |
|---|---|
| EMBL GenBank DDBJ | AK057980 mRNA. No translation available. AK092189 mRNA. Translation: BAC03824.1. AK124659 mRNA. Translation: BAC85920.1. Different initiation. AC010890 Genomic DNA. No translation available. AC010974 Genomic DNA. No translation available. AC011243 Genomic DNA. No translation available. AC011755 Genomic DNA. No translation available. AC011996 Genomic DNA. No translation available. AC012489 Genomic DNA. No translation available. AC016909 Genomic DNA. No translation available. BC110831 mRNA. Translation: AAI10832.1. AY946007 mRNA. Translation: AAY23346.1. AY946008 mRNA. Translation: AAY23347.1. AB005217 mRNA. Translation: BAA22433.1. Frameshift. |
| IPI | IPI00410416. IPI00419253. IPI00807489. IPI00807540. |
| RefSeq | NP_997246.2. NM_207363.2. NP_997364.3. NM_207481.3. |
| UniGene | Hs.537329. |
3D structure databases | |
| ProteinModelPortal | O14513. |
| ModBase | Search... |
Protein-protein interaction databases | |
| IntAct | O14513. 6 interactions. |
| MINT | MINT-7241081. |
| STRING | O14513. |
PTM databases | |
| PhosphoSite | O14513. |
Proteomic databases | |
| PRIDE | O14513. |
Protocols and materials databases | |
| StructuralBiologyKnowledgebase | Search... |
Genome annotation databases | |
| Ensembl | ENST00000409261; ENSP00000387128; ENSG00000176771. |
| GeneID | 344148. |
| KEGG | hsa:344148. |
| UCSC | uc002ttp.1. human. uc002ttq.1. human. uc002tts.1. human. uc002ttt.1. human. |
Organism-specific databases | |
| CTD | 344148. |
| GeneCards | GC02M133429. |
| HGNC | HGNC:29847. NCKAP5. |
| HPA | HPA034639. |
| MIM | 608789. gene. |
| neXtProt | NX_O14513. |
| PharmGKB | PA165696957. |
| GenAtlas | Search... |
Phylogenomic databases | |
| eggNOG | prNOG04399. |
| GeneTree | ENSGT00530000063607. |
| HOGENOM | HBG283756. |
| HOVERGEN | HBG062295. |
| InParanoid | O14513. |
| OMA | PGKHEKD. |
| OrthoDB | EOG43JC66. |
Gene expression databases | |
| ArrayExpress | O14513. |
| Bgee | O14513. |
| Genevestigator | O14513. |
Family and domain databases | |
| ProtoNet | Search... |
Other | |
| NextBio | 98641. |
| SOURCE | Search... |
Entry information
| Entry name | NCKP5_HUMAN | ||||||||
| Accession | Primary (citable) accession number: O14513 Secondary accession number(s): B8ZZL0 Q8NAS3 | ||||||||
| Entry history |
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| Entry status | Reviewed (UniProtKB/Swiss-Prot) | ||||||||
| Annotation program | Chordata Protein Annotation Program | ||||||||
| Disclaimer | Any 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 2 Human chromosome 2: 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 |

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