Homo sapiens (human): 6613
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Entry
6613 CDS
T01001
Symbol
SUMO2, HSMT3, SMT3B, SMT3H2, SUMO3, Smt3A
Name
(RefSeq) small ubiquitin like modifier 2
KO
K12160
small ubiquitin-related modifier
Organism
hsa
Homo sapiens (human)
Pathway
hsa03013
Nucleocytoplasmic transport
hsa05418
Fluid shear stress and atherosclerosis
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09120 Genetic Information Processing
09122 Translation
03013 Nucleocytoplasmic transport
6613 (SUMO2)
09160 Human Diseases
09166 Cardiovascular disease
05418 Fluid shear stress and atherosclerosis
6613 (SUMO2)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
04121 Ubiquitin system [BR:
hsa04121
]
6613 (SUMO2)
03029 Mitochondrial biogenesis [BR:
hsa03029
]
6613 (SUMO2)
09183 Protein families: signaling and cellular processes
04812 Cytoskeleton proteins [BR:
hsa04812
]
6613 (SUMO2)
Ubiquitin system [BR:
hsa04121
]
Ubiquitins and ubiquitin-like proteins
Ubiquitin-like proteins (UBLs)
6613 (SUMO2)
Mitochondrial biogenesis [BR:
hsa03029
]
Mitochondrial quality control factors
Mitochondrial dynamics
Fission and Fusion factors
6613 (SUMO2)
Cytoskeleton proteins [BR:
hsa04812
]
Eukaryotic cytoskeleton proteins
Septins
Septin associated proteins
6613 (SUMO2)
BRITE hierarchy
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
Rad60-SLD
ubiquitin
Motif
Other DBs
NCBI-GeneID:
6613
NCBI-ProteinID:
NP_008868
OMIM:
603042
HGNC:
11125
Ensembl:
ENSG00000188612
UniProt:
P61956
Structure
PDB
PDBj
LinkDB
All DBs
Position
17:complement(75165586..75182959)
Genome browser
AA seq
95 aa
AA seq
DB search
MADEKPKEGVKTENNDHINLKVAGQDGSVVQFKIKRHTPLSKLMKAYCERQGLSMRQIRF
RFDGQPINETDTPAQLEMEDEDTIDVFQQQTGGVY
NT seq
288 nt
NT seq
+upstream
nt +downstream
nt
atggccgacgaaaagcccaaggaaggagtcaagactgagaacaacgatcatattaatttg
aaggtggcggggcaggatggttctgtggtgcagtttaagattaagaggcatacaccactt
agtaaactaatgaaagcctattgtgaacgacagggattgtcaatgaggcagatcagattc
cgatttgacgggcaaccaatcaatgaaacagacacacctgcacagttggaaatggaggat
gaagatacaattgatgtgttccaacagcagacgggaggtgtctactga
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integrated database retrieval system