KEGG   Homo sapiens (human): 3836
Entry
3836              CDS       T01001                                 
Symbol
KPNA1, IPOA5, NPI-1, RCH2, SRP1
Name
(RefSeq) importin subunit alpha-5
  KO
K23940  importin subunit alpha-5
Organism
hsa  Homo sapiens (human)
Pathway
hsa03013  Nucleocytoplasmic transport
hsa05132  Salmonella infection
hsa05164  Influenza A
hsa05207  Chemical carcinogenesis - receptor activation
Network
nt06181  Salmonella
nt06516  TNF signaling
  Element
N01118  Salmonella SpvD to TNF-NFKB signaling pathway
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09120 Genetic Information Processing
  09122 Translation
   03013 Nucleocytoplasmic transport
    3836 (KPNA1)
 09160 Human Diseases
  09161 Cancer: overview
   05207 Chemical carcinogenesis - receptor activation
    3836 (KPNA1)
  09172 Infectious disease: viral
   05164 Influenza A
    3836 (KPNA1)
  09171 Infectious disease: bacterial
   05132 Salmonella infection
    3836 (KPNA1)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03036 Chromosome and associated proteins [BR:hsa03036]
    3836 (KPNA1)
Chromosome and associated proteins [BR:hsa03036]
 Eukaryotic type
  Centrosome formation proteins
   Spindle formation proteins
    3836 (KPNA1)
SSDB
Motif
Pfam: Arm IBB Arm_3 ARM_ARMC5 HEAT_EZ HEAT_2 ARM_PUB HEAT TMCO6 SIL1_FES1_HPBP1_C V-ATPase_H_C ARMC6 WRM1_C TOR1L1_N Luteo_Vpg ScaA_C TPR_TRIP12_N
Other DBs
NCBI-GeneID: 3836
NCBI-ProteinID: NP_002255
OMIM: 600686
HGNC: 6394
Ensembl: ENSP00000343701.6
UniProt: P52294
Structure
LinkDB
Position
3:complement(122421902..122514939)
AA seq 538 aa
MTTPGKENFRLKSYKNKSLNPDEMRRRREEEGLQLRKQKREEQLFKRRNVATAEEETEEE
VMSDGGFHEAQISNMEMAPGGVITSDMIEMIFSKSPEQQLSATQKFRKLLSKEPNPPIDE
VISTPGVVARFVEFLKRKENCTLQFESAWVLTNIASGNSLQTRIVIQAGAVPIFIELLSS
EFEDVQEQAVWALGNIAGDSTMCRDYVLDCNILPPLLQLFSKQNRLTMTRNAVWALSNLC
RGKSPPPEFAKVSPCLNVLSWLLFVSDTDVLADACWALSYLSDGPNDKIQAVIDAGVCRR
LVELLMHNDYKVVSPALRAVGNIVTGDDIQTQVILNCSALQSLLHLLSSPKESIKKEACW
TISNITAGNRAQIQTVIDANIFPALISILQTAEFRTRKEAAWAITNATSGGSAEQIKYLV
ELGCIKPLCDLLTVMDSKIVQVALNGLENILRLGEQEAKRNGTGINPYCALIEEAYGLDK
IEFLQSHENQEIYQKAFDLIEHYFGTEDEDSSIAPQVDLNQQQYIFQQCEAPMEGFQL
NT seq 1617 nt   +upstreamnt  +downstreamnt
atgaccaccccaggaaaagagaactttcgcctgaaaagttacaagaacaaatctctgaat
cccgatgagatgcgcaggaggagggaggaagaaggactgcagttacgaaagcagaaaaga
gaagagcagttattcaagcggagaaatgttgctacagcagaagaagaaacagaagaagaa
gttatgtcagatggaggctttcatgaggctcagattagtaacatggagatggcaccaggt
ggtgtcatcacttctgacatgattgaaatgatattttccaaaagcccagagcaacagctt
tcagcaacacagaaattcaggaagctgctttcaaaagaacctaaccctcctattgatgaa
gttatcagcacaccaggagtagtggccaggtttgtggagttcctcaaacgaaaagagaat
tgtacactgcagtttgaatcagcttgggtactgacaaatattgcttcaggaaattctctt
cagacccgaattgtgattcaggcaggagctgtgcccatcttcatagagttgctcagctca
gagtttgaagatgtccaggaacaggcagtctgggctcttggcaacattgctggagatagt
accatgtgcagggactatgtcttagactgcaatatccttccccctcttttgcagttattt
tcaaagcaaaaccgcctgaccatgacccggaatgcagtatgggctttgtctaatctctgt
agagggaaaagtccacctccagaatttgcaaaggtttctccatgtctgaatgtgctttcc
tggttgctgtttgtcagtgacactgatgtactggctgatgcctgctgggccctctcatat
ctatcagatggacccaatgataaaattcaagcggtcatcgatgcgggagtatgtaggaga
cttgtggaactgctgatgcataatgattataaagtggtttctcctgctttgcgagctgtg
ggaaacattgtcacaggggatgatattcagacacaggtaattctgaattgctcagctctg
cagagtttattgcatttgctgagtagcccaaaggaatctatcaaaaaggaagcatgttgg
acgatatctaatattacagctggaaatagggcacagatccagactgtgatagatgccaac
attttcccagccctcattagtattttacaaactgctgaatttcggacaagaaaagaagca
gcttgggccatcacaaatgcaacttctggaggatcagctgaacagatcaagtacctagta
gaactgggttgtatcaagccgctctgtgatctcctcacggtcatggactctaagattgta
caggttgccctaaatggcttggaaaatatcctgaggcttggagaacaggaagccaaaagg
aatggcactggcattaacccttactgtgctttgattgaagaagcttatggtctggataaa
attgagttcttacagagtcatgaaaaccaggagatctaccaaaaggcctttgatcttatt
gagcattacttcgggaccgaagatgaagacagcagcattgcaccccaggttgaccttaac
cagcagcagtacatcttccaacagtgtgaggctcctatggaaggtttccagctttga

KEGG   Homo sapiens (human): 3839
Entry
3839              CDS       T01001                                 
Symbol
KPNA3, IPOA4, SPG88, SRP1, SRP1gamma, SRP4, hSRP1
Name
(RefSeq) importin subunit alpha-4
  KO
K23583  importin subunit alpha-4/3
Organism
hsa  Homo sapiens (human)
Pathway
hsa03013  Nucleocytoplasmic transport
hsa05132  Salmonella infection
hsa05207  Chemical carcinogenesis - receptor activation
Network
nt06181  Salmonella
nt06516  TNF signaling
  Element
N01118  Salmonella SpvD to TNF-NFKB signaling pathway
Disease
H00266  Hereditary spastic paraplegia
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09120 Genetic Information Processing
  09122 Translation
   03013 Nucleocytoplasmic transport
    3839 (KPNA3)
 09160 Human Diseases
  09161 Cancer: overview
   05207 Chemical carcinogenesis - receptor activation
    3839 (KPNA3)
  09171 Infectious disease: bacterial
   05132 Salmonella infection
    3839 (KPNA3)
SSDB
Motif
Pfam: Arm HEAT_EZ Arm_3 IBB ARM_ARMC5 HEAT HEAT_2 TMCO6 Adaptin_N TPR_TRIP12_N TOR1L1_N HEAT_MROH2B_C ARMC6 HEAT_GCN1 Cnd1 ARM_PUB SIL1_FES1_HPBP1_C Arm_2 TPR_DNAAF5 XMAP215_CLASP_TOG PIK3R4-like_middle ScaA_C Mo25
Other DBs
NCBI-GeneID: 3839
NCBI-ProteinID: NP_002258
OMIM: 601892
HGNC: 6396
Ensembl: ENSP00000261667.3
UniProt: O00505
LinkDB
Position
13:complement(49699320..49792682)
AA seq 521 aa
MAENPSLENHRIKSFKNKGRDVETMRRHRNEVTVELRKNKRDEHLLKKRNVPQEESLEDS
DVDADFKAQNVTLEAILQNATSDNPVVQLSAVQAARKLLSSDRNPPIDDLIKSGILPILV
KCLERDDNPSLQFEAAWALTNIASGTSAQTQAVVQSNAVPLFLRLLRSPHQNVCEQAVWA
LGNIIGDGPQCRDYVISLGVVKPLLSFISPSIPITFLRNVTWVIVNLCRNKDPPPPMETV
QEILPALCVLIYHTDINILVDTVWALSYLTDGGNEQIQMVIDSGVVPFLVPLLSHQEVKV
QTAALRAVGNIVTGTDEQTQVVLNCDVLSHFPNLLSHPKEKINKEAVWFLSNITAGNQQQ
VQAVIDAGLIPMIIHQLAKGDFGTQKEAAWAISNLTISGRKDQVEYLVQQNVIPPFCNLL
SVKDSQVVQVVLDGLKNILIMAGDEASTIAEIIEECGGLEKIEVLQQHENEDIYKLAFEI
IDQYFSGDDIDEDPCLIPEATQGGTYNFDPTANLQTKEFNF
NT seq 1566 nt   +upstreamnt  +downstreamnt
atggccgagaaccccagcttggagaaccaccgcatcaagagcttcaagaacaagggccgc
gatgtggaaacaatgcgaagacatagaaatgaagtgacagtggaactgcggaagaacaaa
agagatgaacacttattgaaaaagagaaatgttccccaagaagaaagtctagaagattca
gatgttgatgctgattttaaagcacaaaatgtaaccctagaagctatattgcagaatgcc
acaagtgataacccagtggtccaattgagtgctgtccaggcagcaagaaaactgttatcc
agtgacagaaatccaccgattgatgacttaataaaatctgggattttaccaattctagtc
aaatgtctagaaagggatgataatccttcattacagtttgaagctgcttgggcattaact
aacatagcatcaggaacttctgcacagactcaagctgttgtgcagtctaatgcagtacct
ctttttctgagacttcttcgttcaccacatcagaatgtttgtgaacaagcagtatgggct
ttgggaaacattataggtgatggtcctcaatgtagagattatgtcatatcactgggagtt
gtcaaacctcttctgtccttcatcagtccctccatccccatcaccttccttcggaacgtc
acatgggtcattgtcaatctctgcaggaataaggatcccccgccgcctatggagacagtt
caggagattttgccagctttatgtgtcctcatataccatacagatataaacattcttgta
gacactgtttgggctctgtcatacttgacagatggaggtaatgaacagatacagatggtt
attgattcaggagttgtgccctttcttgtgccccttctgagccatcaggaagtcaaagtt
caaacagcagccctcagagcagttggcaacatagtgactggcaccgacgagcagacccag
gttgttctcaattgtgatgtcctgtcacacttcccaaatctcttatcacacccaaaagag
aagataaataaggaagcagtgtggttcctttccaacataacagcaggcaaccagcaacaa
gttcaagctgtaatagatgctggattaattcctatgataattcatcagcttgctaagggg
gactttggaacacaaaaagaagctgcttgggcaatcagcaacttaacaataagtggcaga
aaagatcaggttgagtaccttgtacagcagaatgtaataccaccgttctgtaatttactg
tcagtgaaagattctcaagtggttcaggtggttctagatggtctaaaaaacattctgata
atggccggtgatgaagcaagcacaatagctgaaataatagaggaatgtggaggtttggag
aaaattgaagttttacagcaacatgaaaatgaagacatatataaattagcatttgaaatc
atagatcagtatttctctggtgatgatattgatgaagatccctgcctcattcctgaagca
acacaaggaggtacctacaattttgatccaacagccaaccttcaaacaaaagaatttaat
ttttaa

KEGG   Homo sapiens (human): 3840
Entry
3840              CDS       T01001                                 
Symbol
KPNA4, IPOA3, QIP1, SRP3
Name
(RefSeq) importin subunit alpha-3
  KO
K23583  importin subunit alpha-4/3
Organism
hsa  Homo sapiens (human)
Pathway
hsa03013  Nucleocytoplasmic transport
hsa05132  Salmonella infection
hsa05207  Chemical carcinogenesis - receptor activation
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09120 Genetic Information Processing
  09122 Translation
   03013 Nucleocytoplasmic transport
    3840 (KPNA4)
 09160 Human Diseases
  09161 Cancer: overview
   05207 Chemical carcinogenesis - receptor activation
    3840 (KPNA4)
  09171 Infectious disease: bacterial
   05132 Salmonella infection
    3840 (KPNA4)
SSDB
Motif
Pfam: Arm Arm_3 HEAT_EZ IBB ARM_ARMC5 HEAT HEAT_2 TMCO6 Adaptin_N ARMC6 HEAT_MROH2B_C TOR1L1_N V-ATPase_H_C Cnd1 TPR_TRIP12_N HEAT_GCN1 ARM_PUB ZER1-like_2nd Arm_2 ScaA_C TPR_DNAAF5 PIK3R4-like_middle CTNNBL Mo25 TPR_LAA1_C
Other DBs
NCBI-GeneID: 3840
NCBI-ProteinID: NP_002259
OMIM: 602970
HGNC: 6397
Ensembl: ENSP00000334373.4
UniProt: O00629
Structure
LinkDB
Position
3:complement(160495007..160565571)
AA seq 521 aa
MADNEKLDNQRLKNFKNKGRDLETMRRQRNEVVVELRKNKRDEHLLKRRNVPHEDICEDS
DIDGDYRVQNTSLEAIVQNASSDNQGIQLSAVQAARKLLSSDRNPPIDDLIKSGILPILV
HCLERDDNPSLQFEAAWALTNIASGTSEQTQAVVQSNAVPLFLRLLHSPHQNVCEQAVWA
LGNIIGDGPQCRDYVISLGVVKPLLSFISPSIPITFLRNVTWVMVNLCRHKDPPPPMETI
QEILPALCVLIHHTDVNILVDTVWALSYLTDAGNEQIQMVIDSGIVPHLVPLLSHQEVKV
QTAALRAVGNIVTGTDEQTQVVLNCDALSHFPALLTHPKEKINKEAVWFLSNITAGNQQQ
VQAVIDANLVPMIIHLLDKGDFGTQKEAAWAISNLTISGRKDQVAYLIQQNVIPPFCNLL
TVKDAQVVQVVLDGLSNILKMAEDEAETIGNLIEECGGLEKIEQLQNHENEDIYKLAYEI
IDQFFSSDDIDEDPSLVPEAIQGGTFGFNSSANVPTEGFQF
NT seq 1566 nt   +upstreamnt  +downstreamnt
atggcggacaacgagaaactggacaaccaacggctcaagaatttcaagaacaaaggccgc
gacttggagactatgagaagacaacgaaatgaagttgtagttgaattaaggaagaataaa
agagatgaacatctcttaaagagaaggaatgtaccacatgaagatatctgtgaagactct
gatatagatggtgattatagagtgcaaaatacctctctagaagctattgttcaaaatgct
tcaagtgataaccaaggaattcaattaagtgcagttcaagctgctaggaagcttttgtcc
agtgatcgaaatccaccaattgatgacttaataaaatctggaatattgcccattttagtc
cattgtcttgaaagagatgacaatccttctttacagtttgaagctgcatgggctttgaca
aacattgcatctggaacttctgaacaaactcaagcagtagttcagtccaatgctgtgcca
cttttcctgaggcttctccattcaccccatcagaatgtctgtgagcaagcagtgtgggca
ttgggaaatatcataggtgatgggccccagtgtagagattatgtcataagtcttggagtt
gtgaaacctttactttccttcataagtccatctattcctataacattcttaagaaatgtt
acttgggttatggtcaacttatgtcgccacaaagacccaccaccaccaatggaaaccatt
caggagattcttccagccctttgtgttttaattcatcacacagatgtaaatatactggta
gacacagtctgggccctctcttaccttactgatgctggcaatgaacaaatacagatggta
atagactctggaatagttcctcatttggttcctctgctcagccaccaggaagttaaagtt
cagactgctgcacttagagctgtgggcaacattgttactggaactgatgagcaaacacaa
gtagttttgaactgtgatgctctttcacacttcccagcactcctgacacatcccaaagag
aaaattaataaagaagcagtgtggttcctctccaacatcactgcaggaaatcagcagcag
gtacaggcagtaattgatgccaatcttgtaccaatgataatacaccttttggataagggg
gattttggcactcaaaaagaagctgcttgggccataagtaacttaacaattagtggaagg
aaagatcaagtggcttaccttatccaacaaaatgttatcccacctttttgcaacttgctg
actgtaaaagatgcacaagttgtgcaagtagtactcgatggactaagtaatatattaaaa
atggctgaagatgaggcagaaaccataggcaatcttatagaagaatgtggagggctggag
aaaattgaacaacttcaaaatcatgaaaatgaagacatctacaaattggcctatgagatc
attgatcagttcttctcttcagatgatattgatgaagaccctagccttgttccagaggca
attcaaggcggaacatttggtttcaattcatctgccaatgtaccaacagaagggttccag
ttttag

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