RPA1 - replication protein A1 Gene

Also Known as HSSB; RF-A; RP-A; REPA1; RPA70; MST075; PFBMFT6

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 6117

About RPA1

Cytogenetic location: 17p13.3 Genomic coordinates (GRCh38): 17:1,830,005-1,900,082 (from NCBI)

This gene has 7 transcripts (splice variants), 268 orthologues and is associated with 1 phenotype. Ubiquitous expression in lymph node (RPKM 21.6), ovary (RPKM 19.7) and 25 other tissues.

Summary

This gene encodes the largest subunit of the heterotrimeric Replication Protein A (RPA) complex, which binds to single-stranded DNA (ssDNA), forming a nucleoprotein complex that plays an important role in DNA metabolism, being involved in DNA replication, repair, recombination, telomere maintenance, and co-ordinating the cellular response to DNA damage through activation of the ataxia telangiectasia and Rad3-related protein (ATR) kinase. The nucleoprotein complex protects the single-stranded DNA from nucleases, prevents formation of secondary structures that would interfere with repair, and co-ordinates the recruitment and departure of different genome maintenance factors. This subunit contains four oligonucleotide/oligosaccharide-binding (OB) domains, though the majority of ssDNA binding occurs in two of these domains. The heterotrimeric complex has two different modes of ssDNA binding, a low-affinity and high-affinity mode, determined by which ssDNA binding domains are utilized. The different binding modes differ in the length of DNA bound and in the proteins with which it interacts, thereby playing a role in regulating different genomic maintenance pathways. [provided by RefSeq, Sep 2017]

RPA1 Products (3)

mRNA Protein Name
NM_001355120.2 NP_001342049.1 replication protein A 70 kDa DNA-binding subunit isoform 2
NM_001355121.2 NP_001342050.1 replication protein A 70 kDa DNA-binding subunit isoform 3
NM_002945.5 NP_002936.1 replication protein A 70 kDa DNA-binding subunit isoform 1
Molecular Function GO Annotation Evidence References Source
enables G-rich strand telomeric DNA binding IDA
IDA: Inferred from direct assay
16973897 GOA
enables G-rich strand telomeric DNA binding IMP
IMP: Inferred from mutant phenotype
26041456 GOA
enables chromatin-protein adaptor activity IDA
IDA: Inferred from direct assay
35597237 GOA
enables damaged DNA binding IDA
IDA: Inferred from direct assay
7700386 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
1311258 GOA
enables single-stranded DNA binding IDA
IDA: Inferred from direct assay
8990123 GOA
Biological Process GO Annotation Evidence References Source
involved in DNA damage response IMP
IMP: Inferred from mutant phenotype
27248496 GOA
involved in DNA repair IDA
IDA: Inferred from direct assay
20545304 GOA
involved in DNA repair IMP
IMP: Inferred from mutant phenotype
18469000 GOA
involved in DNA replication IMP
IMP: Inferred from mutant phenotype
9430682 GOA
involved in base-excision repair IDA
IDA: Inferred from direct assay
9765279 GOA
involved in double-strand break repair via homologous recombination IMP
IMP: Inferred from mutant phenotype
17765923 GOA
involved in mismatch repair IMP
IMP: Inferred from mutant phenotype
9430682 GOA
involved in nucleotide-excision repair IMP
IMP: Inferred from mutant phenotype
9430682 GOA
involved in protein localization to chromosome IDA
IDA: Inferred from direct assay
27723717 GOA
involved in protein localization to site of double-strand break IDA
IDA: Inferred from direct assay
35597237 GOA
involved in telomere maintenance IMP
IMP: Inferred from mutant phenotype
17959650 GOA
Cellular Component GO Annotation Evidence References Source
part of DNA replication factor A complex IDA
IDA: Inferred from direct assay
11927569 GOA
part of DNA replication factor A complex IPI
IPI: Inferred from physical interaction
7760808 GOA
colocalizes with PML body IDA
IDA: Inferred from direct assay
17959650 GOA
located in PML body IDA
IDA: Inferred from direct assay
16135809 GOA
located in nucleus IDA
IDA: Inferred from direct assay
17959650 GOA
located in site of DNA damage IMP
IMP: Inferred from mutant phenotype
27248496 GOA
is active in site of double-strand break IDA
IDA: Inferred from direct assay
35597237 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

RPA1 Protein Structure

Rep-A_N

Rep-A_N: Replication factor-A protein 1, N-terminal domain (5 - 104)

tRNA_anti-codon

tRNA_anti-codon: OB-fold nucleic acid binding domain (197 - 281)

Rep_fac-A_C

Rep_fac-A_C: Replication factor-A C terminal domain (461 - 606)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 500
  • 616 a.a.
Protein Preferred Names Protein Names

replication protein A 70 kDa DNA-binding subunit

  • MSTP075

RPA1 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
RPA1 P27694 PRIMPOL Homo sapiens Q96LW4 24126761
Intra
RPA1 P27694 PRIMPOL Homo sapiens Q96LW4
TAP
24126761
Intra
RPA1 P27694 PRIMPOL Homo sapiens Q96LW4 24126761
Intra
RPA1 P27694 MTUS2 Homo sapiens Q5JR59-3 32296183
Intra
RPA1 P27694 MTUS2 Homo sapiens Q5JR59-3 32296183
Intra
RPA1 P27694 MTUS2 Homo sapiens Q5JR59-3 32296183
Intra
RPA1 P27694 RPA4 Homo sapiens Q13156 7760808
Intra
RPA1 P27694 RPA4 Homo sapiens Q13156
Y2H
7760808
Intra
RPA1 P27694 HSPA6 Homo sapiens P17066 32296183
Intra
RPA1 P27694 HSPA6 Homo sapiens P17066 32296183
Intra
RPA1 P27694 WRN Homo sapiens Q14191 15965237
Intra
RPA1 P27694 WRN Homo sapiens Q14191
TAP
24126761
Intra
RPA1 P27694 WRN Homo sapiens Q14191 15965237
Intra
RPA1 P27694 WRN Homo sapiens Q14191 15735006
Cross
RPA1 P27694 lt_sv40 Simian virus 40 P03070 17666013
Cross
RPA1 P27694 lt_sv40 Simian virus 40 P03070 8381428
Intra
RPA1 P27694 BLM Homo sapiens P54132
TAP
24126761
Intra
RPA1 P27694 BLM Homo sapiens P54132 15965237
Intra
RPA1 P27694 RPA2 Homo sapiens P15927
TAP
24126761
Intra
RPA1 P27694 RPA2 Homo sapiens P15927
TAP
24981860
Intra
RPA1 P27694 RPA2 Homo sapiens P15927 26496610
Intra
RPA1 P27694 RPA2 Homo sapiens P15927 32296183
Intra
RPA1 P27694 RPA2 Homo sapiens P15927 20811460
Intra
RPA1 P27694 RPA2 Homo sapiens P15927 11927569
Intra
RPA1 P27694 RPA2 Homo sapiens P15927 32296183
Intra
RPA1 P27694 RPA2 Homo sapiens P15927
GMS
12527904
Intra
RPA1 P27694 RPA2 Homo sapiens P15927 7760808
Intra
RPA1 P27694 RPA2 Homo sapiens P15927 2159011
Intra
RPA1 P27694 RPA3 Homo sapiens P35244 7760808
Intra
RPA1 P27694 RPA3 Homo sapiens P35244
TAP
24981860
Intra
RPA1 P27694 RPA3 Homo sapiens P35244
Y2H
19338310
Intra
RPA1 P27694 RPA3 Homo sapiens P35244
TAP
24126761
Intra
RPA1 P27694 RPA3 Homo sapiens P35244 26496610
Intra
RPA1 P27694 RPA3 Homo sapiens P35244 11927569
Intra
RPA1 P27694 RPA3 Homo sapiens P35244 2159011
Intra
RPA1 P27694 RPA3 Homo sapiens P35244
GMS
12527904
Intra
RPA1 P27694 RPA3 Homo sapiens P35244 20811460
Intra
RPA1 P27694 MTUS2 Homo sapiens Q5JR59 25416956
Intra
RPA1 P27694 MTUS2 Homo sapiens Q5JR59 25416956
Intra
RPA1 P27694 POLA1 Homo sapiens P09884 17666013
Cross: Cross-species interaction Intra: Intraspecies interaction

RPA1 Antibodies

Cat. No. Product Name Application Reactivity
HY-P80884 RPA70 Antibody (YA678) WB, ICC/IF, IP Human, Monkey, Mouse, Rat
HY-P80884A RPA70 Antibody (YA678)(PBS only) WB, ICC/IF, IP Human, Monkey, Mouse, Rat
HY-P85588 RPA70 Antibody (YA5280) WB, ICC/IF, IP Human, Monkey, Mouse, Rat

Related Diseases

Diseases Alias
Pulmonary Fibrosis And/Or Bone Marrow Failure, Telomere-Related, 6
  • PFBMFT6

  • Pulmonary Fibrosis, And/Or Bone Marrow Failure, Telomere-Related, 6

Ataxia-Telangiectasia
  • Ataxia Telangiectasia

  • Louis-Bar Syndrome

  • AT

  • At1

  • Ataxia-Telangiectasia Syndrome

  • Ataxia - Telangiectasia Variant

  • Boder-Sedgwick Syndrome

  • Louis Bar Syndrome

  • Cerebello-Oculocutaneous Telangiectasia

  • Immunodeficiency With Ataxia Telangiectasia

  • A-T

  • Ataxia Telangiectasia Syndrome

  • Atm

  • Telangiectasia, Cerebello-Oculocutaneous

  • Ataxia-Telangiectasia Variant

Werner Syndrome
  • Werner'S Syndrome

  • WRN

  • Adult Progeria

  • Ws

  • Adult Premature Ageing Syndrome

  • Adult Premature Aging Syndrome

  • Werners Syndrome

Xeroderma Pigmentosum, Variant Type
  • Xeroderma Pigmentosum

  • XPV

  • Xeroderma Pigmentosum Variant Type

  • Xeroderma Pigmentosum With Normal Dna Repair Rates

  • Photosensitivity With Defective Dna Synthesis

  • Xp

  • De Sanctis-Cacchione Syndrome

  • Desanctis-Cacchione Syndrome

  • Xeroderma Pigmentosa

  • Xerodermic Idiocy

  • Xeroderma Pigmentosum Variant

  • Xp - [Xeroderma Pigmentosum]

  • Atrophoderma Pigmentosum

Microphthalmia, Syndromic 10
  • MCOPS10

  • Moba

  • Microphthalmia And Brain Atrophy

  • Syndromic Microphthalmia 10

  • Microphthalmia-Brain Atrophy Syndrome

  • Microphthalmia Syndromic 10

  • Moba Syndrome

  • Syndromic Microphthalmia Type 10

Bloom Syndrome
  • BLM

  • Bs

  • Bls

  • Bloom-Torre-Machacek Syndrome

  • Microcephaly, Growth Restriction, And Increased Sister Chromatid Exchange 1

  • Mgrisce1

  • Congenital Telangiectatic Erythema

  • Congenital Telangiectatic Erythema Syndrome

  • Growth Deficiency, Sun-Sensitive, Telangiectatic, Hypo And Hyperpigmented Skin, Predisposition To Malignancy And Chromosomal Instability

  • Bloom'S Syndrome

  • Bsyn

Trichothiodystrophy
  • Ttd

  • Amish Brittle Hair Syndrome

  • Bids Syndrome

  • Brittle Hair-Intellectual Impairment-Decreased Fertility-Short Stature Syndrome

  • Ibids

  • Pibids

  • Trichothiodystrophy Syndromes

Alzheimer Disease 13
  • AD13

  • Alzheimer Disease-13

  • Alzheimer'S Disease 13

  • Alzheimer'S Disease 13, Late Onset

Nijmegen Breakage Syndrome
  • Berlin Breakage Syndrome

  • NBS

  • Microcephaly, Normal Intelligence And Immunodeficiency

  • Ataxia-Telangiectasia Variant

  • Ataxia-Telangiectasia Variant V1

  • Seemanova Syndrome Ii

  • Immunodeficiency-Microcephaly-Chromosomal Instability Syndrome

  • Seemanova Syndrome Type 2

  • At-V1

  • Microcephaly With Normal Intelligence, Immunodeficiency, And Lymphoreticular Malignancies

  • Nonsyndromal Microcephaly, Autosomal Recessive, With Normal Intelligence

  • Immunodeficiency, Microcephaly, And Chromosomal Instability

  • Microcephaly-Immunodeficiency-Lymphoreticuloma Syndrome

  • Microcephaly Immunodeficiency Lymphoreticuloma

  • Microcephaly With Normal Intelligence Immunodeficiency And Lymphoreticular Malignancies

  • Nonsyndromal Microcephaly Autosomal Recessive With Normal Intelligence

  • Seemanova Syndrome 2

  • Ataxia-Telangiectasia Variant 1

  • Seemanova Syndrome

  • At V1

  • Ataxia-Telangiectasia, Variant 1

  • Microcephaly-Immunodeficiency-Lymphoid Malignancy Syndrome

  • V-At

  • Ataxia Telangiectasia Variant V1

Haverhill Fever
  • Streptobacillosis

  • Streptobacillary Rat-Bite Fever

  • Streptobacillary Fever

  • Rat-Bite Fever Due To Streptobacillus Moniliformis

  • Erythema Arthriticum Epidemicum

  • Epidemic Arthritic Erythema

Xeroderma Pigmentosum, Complementation Group A
  • Xeroderma Pigmentosum Group A

  • Xp1

  • Xeroderma Pigmentosum, Group A

  • XPA

  • Xeroderma Pigmentosum I

  • Xeroderma Pigmentosum Complementation Group A

  • Xp Group A

  • Xp, Group A

  • Xeroderma Pigmentosum 1

  • Xeroderma Pigmentosum, Type 1

  • XP-A

Seckel Syndrome
  • Microcephalic Primordial Dwarfism

  • Bird-Headed Dwarfism

  • Harper'S Syndrome

  • Virchow-Seckel Dwarfism

  • Nanocephalic Dwarfism

  • Sckl

  • Seckel-Type Dwarfism

Fanconi Anemia, Complementation Group A
  • Fanconi Anemia

  • Fanconi Pancytopenia

  • Fanconi Anemia Complementation Group A

  • FANCA

  • Fa

  • Fanconi Panmyelopathy

  • Fanconi'S Anemia

  • Fanconi Anaemia

  • Fanconi'S Anaemia

  • Fanconi Hypoplastic Anemia

  • Estren-Dameshek Variant Of Fanconi Anemia

  • Estren-Dameshek Variant Of Fanconi Pancytopenia

  • Fanconi Anemia Estren-Dameshek Variant

  • Fanconis Anemia

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Rattus norvegicus RPA1 RGD RGD:1307376
Felis catus RPA1 VGNC VGNC:64726
Canis familiaris RPA1 VGNC VGNC:45702
Bos taurus RPA1 VGNC VGNC:34094
Mus musculus RPA1 MGD MGI:1915525
Others RPA1 NCBI