KEGG   Homo sapiens (human): 29935
Entry
29935             CDS       T01001                                 
Symbol
RPA4, HSU24186
Name
(RefSeq) replication protein A4
  KO
K10741  replication factor A4
Organism
hsa  Homo sapiens (human)
Pathway
hsa03030  DNA replication
hsa03420  Nucleotide excision repair
hsa03430  Mismatch repair
hsa03440  Homologous recombination
hsa03460  Fanconi anemia pathway
Network
nt06502  Nucleotide excision repair
nt06506  Double-strand break repair
nt06508  Interstrand crosslink repair
  Element
N01431  Core NER reaction
N01446  DNA end resection and RPA loading
N01451  ATR signaling
N01452  Homologous recombination
N01466  Homologous recombination in ICLR
N01539  RAD51 -dsDNA destabilization
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09120 Genetic Information Processing
  09124 Replication and repair
   03030 DNA replication
    29935 (RPA4)
   03420 Nucleotide excision repair
    29935 (RPA4)
   03430 Mismatch repair
    29935 (RPA4)
   03440 Homologous recombination
    29935 (RPA4)
   03460 Fanconi anemia pathway
    29935 (RPA4)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03032 DNA replication proteins [BR:hsa03032]
    29935 (RPA4)
   03400 DNA repair and recombination proteins [BR:hsa03400]
    29935 (RPA4)
DNA replication proteins [BR:hsa03032]
 Eukaryotic type
  DNA Replication Elongation Factors
   RPA (replication protein A)
    29935 (RPA4)
DNA repair and recombination proteins [BR:hsa03400]
 Eukaryotic type
  SSBR (single strand breaks repair)
   NER (nucleotide excision repair)
    RPA (replication factor A)
     29935 (RPA4)
   MMR (mismatch excision repair)
     29935 (RPA4)
  DSBR (double strand breaks repair)
   HR (homologous recombination)
     29935 (RPA4)
SSDB
Motif
Pfam: RPA_C tRNA_anti-codon RMI2 PolyA_pol
Other DBs
NCBI-GeneID: 29935
NCBI-ProteinID: NP_037479
OMIM: 300767
HGNC: 30305
Ensembl: ENSG00000204086
UniProt: Q13156
Position
X:96883908..96885467
AA seq 261 aa
MSKSGFGSYGSISAADGASGGSDQLCERDATPAIKTQRPKVRIQDVVPCNVNQLLSSTVF
DPVFKVRGIIVSQVSIVGVIRGAEKASNHICYKIDDMTAKPIEARQWFGREKVKQVTPLS
VGVYVKVFGILKCPTGTKSLEVLKIHVLEDMNEFTVHILETVNAHMMLDKARRDTTVESV
PVSPSEVNDAGDNDESHRNFIQDEVLRLIHECPHQEGKSIHELRAQLCDLSVKAIKEAID
YLTVEGHIYPTVDREHFKSAD
NT seq 786 nt   +upstreamnt  +downstreamnt
atgagtaagagtgggtttgggagctatggcagcatttctgctgctgatggagcgagtgga
ggcagtgaccaactgtgtgagagagatgcaactcctgctattaagacccaaagacctaag
gtccgaattcaggacgttgtaccgtgtaatgtgaaccagcttctcagctctactgtgttt
gaccctgtgttcaaggttaggggaattatagtttcccaggtctccatcgtgggggtaatc
agaggggcagagaaggcttcaaatcacatttgttacaaaattgatgatatgaccgcgaaa
ccaatcgaggcccgacagtggtttggtagagagaaagtcaagcaggtgactccattgtca
gtcggagtatatgtcaaagtgtttggtatcctcaaatgtcccacgggaacaaagagcctt
gaggtattgaaaattcatgtcctagaggacatgaacgagttcaccgtgcatattctggaa
acggtcaatgcacacatgatgctggataaagcccgtcgtgataccactgtagaaagtgtg
cctgtgtctccatcagaagtgaatgatgctggggataacgatgagagtcaccgcaatttc
atccaggacgaagtgctgcgtttgattcatgagtgtcctcatcaggaagggaagagcatc
catgagctccgggctcagctctgcgaccttagcgtcaaggccatcaaggaagcgattgat
tatctgaccgttgagggccacatctatcccactgtggatcgggagcattttaagtctgct
gattga

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