KEGG   Homo sapiens (human): 9232
Entry
9232              CDS       T01001                                 
Symbol
PTTG1, EAP1, ECRAR, HPTTG, PTTG, TUTR1
Name
(RefSeq) securin
  KO
K06635  securin
Organism
hsa  Homo sapiens (human)
Pathway
hsa04110  Cell cycle
hsa04114  Oocyte meiosis
hsa05166  Human T-cell leukemia virus 1 infection
Network
nt06160  Human T-cell leukemia virus 1 (HTLV-1)
nt06230  Cell cycle (cancer)
nt06512  Chromosome cohesion and segregation
  Element
N00221  HTLV-1 Tax to spindle assembly checkpoint signaling
N00493  Spindle assembly checkpoint signaling
N01486  Cohesin dissociation in anaphase
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09140 Cellular Processes
  09143 Cell growth and death
   04110 Cell cycle
    9232 (PTTG1)
   04114 Oocyte meiosis
    9232 (PTTG1)
 09160 Human Diseases
  09172 Infectious disease: viral
   05166 Human T-cell leukemia virus 1 infection
    9232 (PTTG1)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03036 Chromosome and associated proteins [BR:hsa03036]
    9232 (PTTG1)
Chromosome and associated proteins [BR:hsa03036]
 Eukaryotic type
  Sister chromatid separation proteins
   Securin and associated proteins
    9232 (PTTG1)
SSDB
Motif
Pfam: Securin
Other DBs
NCBI-GeneID: 9232
NCBI-ProteinID: NP_001269311
OMIM: 604147
HGNC: 9690
UniProt: O95997 Q6IAL9
Structure
LinkDB
Position
5:160421855..160428744
AA seq 202 aa
MATLIYVDKENGEPGTRVVAKDGLKLGSGPSIKALDGRSQVSTPRFGKTFDAPPALPKAT
RKALGTVNRATEKSVKTKGPLKQKQPSFSAKKMTEKTVKAKSSVPASDDAYPEIEKFFPF
NPLDFESFDLPEEHQIAHLPLSGVPLMILDEERELEKLFQLGPPSPVKMPSPPWESNLLQ
SPSSILSTLDVELPPVCCDIDI
NT seq 609 nt   +upstreamnt  +downstreamnt
atggctactctgatctatgttgataaggaaaatggagaaccaggcacccgtgtggttgct
aaggatgggctgaagctggggtctggaccttcaatcaaagccttagatgggagatctcaa
gtttcaacaccacgttttggcaaaacgttcgatgccccaccagccttacctaaagctact
agaaaggctttgggaactgtcaacagagctacagaaaagtctgtaaagaccaagggaccc
ctcaaacaaaaacagccaagcttttctgccaaaaagatgactgagaagactgttaaagca
aaaagctctgttcctgcctcagatgatgcctatccagaaatagaaaaattctttcccttc
aatcctctagactttgagagttttgacctgcctgaagagcaccagattgcgcacctcccc
ttgagtggagtgcctctcatgatccttgacgaggagagagagcttgaaaagctgtttcag
ctgggccccccttcacctgtgaagatgccctctccaccatgggaatccaatctgttgcag
tctccttcaagcattctgtcgaccctggatgttgaattgccacctgtttgctgtgacata
gatatttaa

KEGG   Homo sapiens (human): 10744
Entry
10744             CDS       T01001                                 
Symbol
PTTG2
Name
(RefSeq) securin-2
  KO
K06635  securin
Organism
hsa  Homo sapiens (human)
Pathway
hsa04110  Cell cycle
hsa04114  Oocyte meiosis
hsa05166  Human T-cell leukemia virus 1 infection
Network
nt06160  Human T-cell leukemia virus 1 (HTLV-1)
nt06230  Cell cycle (cancer)
  Element
N00221  HTLV-1 Tax to spindle assembly checkpoint signaling
N00493  Spindle assembly checkpoint signaling
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09140 Cellular Processes
  09143 Cell growth and death
   04110 Cell cycle
    10744 (PTTG2)
   04114 Oocyte meiosis
    10744 (PTTG2)
 09160 Human Diseases
  09172 Infectious disease: viral
   05166 Human T-cell leukemia virus 1 infection
    10744 (PTTG2)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03036 Chromosome and associated proteins [BR:hsa03036]
    10744 (PTTG2)
Chromosome and associated proteins [BR:hsa03036]
 Eukaryotic type
  Sister chromatid separation proteins
   Securin and associated proteins
    10744 (PTTG2)
SSDB
Motif
Pfam: Securin
Other DBs
NCBI-GeneID: 10744
NCBI-ProteinID: NP_006598
OMIM: 604231
HGNC: 9691
Ensembl: ENSP00000424261.1
UniProt: Q9NZH5
LinkDB
Position
4:37960398..37961128
AA seq 191 aa
MATLIYVDKEIGEPGTRVAAKDVLKLESRPSIKALDGISQVLTRRFGKTYDAPSALPKAT
RKALGTVNRATEKSVKTNGPRKQKQPSFSAKKMTEKTVKTKSSVPASDDAYPEIEKFFPF
NLLDFESFDLPEERQIAHLPLSGVPLMILDEEGELEKLFQLGPPSPVKMPSPPWECNLFA
VSFKHSVDPGC
NT seq 576 nt   +upstreamnt  +downstreamnt
atggctactctgatctacgttgataaggaaattggagaaccaggcacccgtgtggctgcc
aaggatgtgctgaagctggagtctagaccttcaatcaaagcattagatgggatatctcaa
gttttaacacgacgttttggcaaaacatacgatgctccatcagccttacctaaagctacc
agaaaggctttgggcactgtcaacagagctacagaaaagtcagtaaagaccaatggaccc
agaaaacaaaaacagccaagcttttctgccaaaaagatgaccgagaagactgttaaaaca
aaaagttctgttcctgcctcagatgacgcctatccagaaatagaaaaattctttcccttc
aatcttctagactttgagagttttgacctgcctgaagagcgccagattgcacacctcccc
ttgagtggagtgcctctcatgatccttgatgaggagggagagcttgaaaagctgtttcag
ctgggccccccttcacctgtgaaaatgccctctccaccatgggaatgcaatctgtttgca
gtctccttcaagcattctgtcgaccctggatgttga

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