SSRP1
FACT complex subunit SSRP1
Also known as: FACT80, SSRP1_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q08945
- Gene
- SSRP1
- Ensembl
- ENSG00000149136
- Chromosome
- 11
- Canonical length
- 709 aa
- Protein class
- Plasma proteins, Predicted intracellular proteins, Transcription factors
- Subcellular location
- Nucleoplasm,Cytosol
OverviewNCBI Gene
The protein encoded by this gene is a subunit of a heterodimer that, along with SUPT16H, forms chromatin transcriptional elongation factor FACT. FACT interacts specifically with histones H2A/H2B to effect nucleosome disassembly and transcription elongation. FACT and cisplatin-damaged DNA may be crucial to the anticancer mechanism of cisplatin. This encoded protein contains a high mobility group box which most likely constitutes the structure recognition element for cisplatin-modified DNA. This protein also functions as a co-activator of the transcriptional activator p63. An alternatively spliced transcript variant of this gene has been described, but its full-length nature is not known. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
709 residues, UniProt reviewed canonical sequence.
>Q08945|SSRP1
1 MAETLEFNDV YQEVKGSMND GRLRLSRQGI IFKNSKTGKV DNIQAGELTE GIWRRVALGH
61 GLKLLTKNGH VYKYDGFRES EFEKLSDFFK THYRLELMEK DLCVKGWNWG TVKFGGQLLS
121 FDIGDQPVFE IPLSNVSQCT TGKNEVTLEF HQNDDAEVSL MEVRFYVPPT QEDGVDPVEA
181 FAQNVLSKAD VIQATGDAIC IFRELQCLTP RGRYDIRIYP TFLHLHGKTF DYKIPYTTVL
241 RLFLLPHKDQ RQMFFVISLD PPIKQGQTRY HFLILLFSKD EDISLTLNMN EEEVEKRFEG
301 RLTKNMSGSL YEMVSRVMKA LVNRKITVPG NFQGHSGAQC ITCSYKASSG LLYPLERGFI
361 YVHKPPVHIR FDEISFVNFA RGTTTTRSFD FEIETKQGTQ YTFSSIEREE YGKLFDFVNA
421 KKLNIKNRGL KEGMNPSYDE YADSDEDQHD AYLERMKEEG KIREENANDS SDDSGEETDE
481 SFNPGEEEED VAEEFDSNAS ASSSSNEGDS DRDEKKRKQL KKAKMAKDRK SRKKPVEVKK
541 GKDPNAPKRP MSAYMLWLNA SREKIKSDHP GISITDLSKK AGEIWKGMSK EKKEEWDRKA
601 EDARRDYEKA MKEYEGGRGE SSKRDKSKKK KKVKVKMEKK STPSRGSSSK SSSRQLSESF
661 KSKEFVSSDE SSSGENKSKK KRRRSEDSEE EELASTPPSS EDSASGSDELocalizationUniProt · AlphaFold · HPA
Whether an antibody against SSRP1 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.
- Antibody reachability
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.42
- Highest tissue expression
- 134 nTPM
Expression across tissuesHPA
Tissue
- skeletal muscle: 134 nTPM
- tonsil: 86 nTPM
- thymus: 82 nTPM
- bone marrow: 74 nTPM
- lymph node: 71 nTPM
- pancreas: 70 nTPM
Single-cell type
- late spermatids: 212 nCPM
- esophageal basal cells: 187 nCPM
- migrating cytotrophoblasts: 162 nCPM
- erythrocyte progenitors: 160 nCPM
- oocytes: 157 nCPM
- cytotrophoblasts: 132 nCPM
Immune cell
- naive CD8 T-cell: 11 nTPM
- naive B-cell: 11 nTPM
- plasmacytoid DC: 10 nTPM
- T-reg: 9.9 nTPM
- memory CD8 T-cell: 9.5 nTPM
- gdT-cell: 8.6 nTPM
Brain region
- hypothalamus: 45 nTPM
- thalamus: 41 nTPM
- white matter: 39 nTPM
- cerebral cortex: 39 nTPM
- midbrain: 38 nTPM
- hippocampal formation: 38 nTPM
ReferencesPubMed · IEDB
Publications for SSRP1 from three distinct lines of evidence, kept separate because they answer different questions: whether antibodies are directed at the protein, whether a B-cell epitope has been mapped on it, and whether a T-cell epitope has. Each is labelled with its source.
Reference: AutoantibodyPubMed
2 publications
- High prevalence of autoantibodies against the nuclear high mobility group (HMG) protein SSRP1 in sera from patients with systemic lupus erythematosus, but not other rheumatic diseases.
2002 · J Rheumatol · RCR 0.3 · 13 citations - Prevalence of autoantibodies against structure specific recognition protein 1 in systemic lupus erythematosus.
2004 · Lupus · RCR 0.1 · 5 citations
Sources: PubMed — antigen-level antibody evidence from a custom retrieval. Records matching a controlled set of autoantibody terms (the MeSH descriptors Autoantibodies and Autoantigens, with title and abstract term variants) were obtained through NCBI E-utilities, and their titles and abstracts parsed for constructions that direct an antibody at a named protein rather than for co-occurrence. Captured names were resolved against UniProt nomenclature and each antigen adjudicated individually against the source text. Bibliographic records from PubMed and MeSH, U.S. National Library of Medicine; citation metrics from NIH iCite (Hutchins et al., PLoS Biology 2016). Titles link to PubMed; abstracts are not reproduced here. The NLM does not endorse this analysis.
Genetic constraint and essentialitygnomAD · DepMap
Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.
- gnomAD LOEUF (loss-of-function intolerance)
- 0.28
- gnomAD pLI
- 1
- gnomAD missense Z
- 4.04
- DepMap mean gene effect
- -1.31
- DepMap dependency class
- pan
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 6% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- DNA repair
- DNA replication
- nucleosome assembly
- nucleosome disassembly
- regulation of chromatin organization
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- High mobility group box domain
- PH-like domain superfamily
- Histone chaperone RTT106/FACT complex subunit SPT16-like, middle domain
- High mobility group box domain superfamily
- HMG (high mobility group) box
- Histone chaperone Rttp106-like, middle domain
- FACT complex subunit SSRP1/POB3
- SSRP1, dimerization domain
- FACT complex subunit SSRP1/POB3, N-terminal PH domain
- SSRP1 domain superfamily
- FACT complex subunit SSRP1, C-terminal domain
- FACT complex subunit SSRP1-like, first PH domain
- RTT106/SSRP1 Histone Chaperone/FACT Complex
- Structure-specific recognition protein (SSRP1)
- POB3-like N-terminal PH domain
- FACT complex subunit SSRP1, C-terminal domain
- SSRP1 PH domain
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of SSRP1 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads SSRP1 as an antibody target. Whether an autoantibody or antibody against SSRP1 could matter depends on whether native SSRP1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
SSRP1 is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label SSRP1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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