hu.MAP 3.0: Complex View
Human Protein Complex Map
Search for a protein
Complex: huMAP3_13006.1
Confidence: Medium
Proteins| Genename | Protein Name | Uniprot Annotation Score | Links |
|---|---|---|---|
| PEPD | Xaa-Pro dipeptidase (X-Pro dipeptidase) (EC 3.4.13.9) (Imidodipeptidase) (Peptidase D) (Proline dipeptidase) (Prolidase) | 5 | UniProt NCBI |
| CASP3 | Caspase-3 (CASP-3) (EC 3.4.22.56) (Apopain) (Cysteine protease CPP32) (CPP-32) (Protein Yama) (SREBP cleavage activity 1) (SCA-1) [Cleaved into: Caspase-3 subunit p17; Caspase-3 subunit p12] | 5 | UniProt NCBI |
| KCNA10 | Potassium voltage-gated channel subfamily A member 10 (Voltage-gated potassium channel subunit Kv1.8) | 5 | UniProt NCBI |
| SLC35A1 | CMP-sialic acid transporter (CMP-SA-Tr) (CMP-Sia-Tr) (CST) (Solute carrier family 35 member A1) | 5 | UniProt NCBI |
Enrichments
| Term ID | Corrected Pval | Fraction Complex Coverage | Proteins | Term Name |
|---|---|---|---|---|
| WP:WP4873 | 0.0496447587094 | 0.333333333333 | CASP3 | Peroxiredoxin 2 induced ovarian failure |
| REAC:R-HSA-5619037 | 0.0498224659464 | 0.333333333333 | SLC35A1 | Defective SLC35A1 causes congenital disorder of glycosylation 2F (CDG2F) |
| REAC:R-HSA-5663020 | 0.0498224659464 | 0.333333333333 | SLC35A1 | Defective SLC35A1 causes congenital disorder of glycosylation 2F (CDG2F) |
Edges
| Protein 1 | Protein 2 | Score | ProteomeHD | Evidence |
|---|---|---|---|---|
| SLC35A1 | PEPD | 0.891 | 0.05 | bioplex3_HEK293 bioplex () bioplex_WMM bioplex3_WMM |
| CASP3 | KCNA10 | 0.883 | bioplex3_HEK293 bioplex () bioplex_WMM bioplex3_WMM | |
| SLC35A1 | CASP3 | 0.883 | 0.05 | bioplex3_HEK293 bioplex () bioplex_WMM bioplex3_WMM |
| CASP3 | PEPD | 0.009 | 0.112 | bioplex_WMM bioplex3_WMM fraction |
Related Complexes