KEGG   Homo sapiens (human): 5216
Entry
5216              CDS       T01001                                 
Symbol
PFN1, ALS18
Name
(RefSeq) profilin 1
  KO
K05759  profilin
Organism
hsa  Homo sapiens (human)
Pathway
hsa04015  Rap1 signaling pathway
hsa04810  Regulation of actin cytoskeleton
hsa05014  Amyotrophic lateral sclerosis
hsa05131  Shigellosis
hsa05132  Salmonella infection
Network
nt06464  Amyotrophic lateral sclerosis
nt06541  Cytoskeleton in neurons
  Element
N01161  Actin polymerization
N01162  Mutation-caused aberrant PFN1 to actin polymerization
Disease
H00058  Amyotrophic lateral sclerosis (ALS)
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09130 Environmental Information Processing
  09132 Signal transduction
   04015 Rap1 signaling pathway
    5216 (PFN1)
 09140 Cellular Processes
  09142 Cell motility
   04810 Regulation of actin cytoskeleton
    5216 (PFN1)
 09160 Human Diseases
  09171 Infectious disease: bacterial
   05132 Salmonella infection
    5216 (PFN1)
   05131 Shigellosis
    5216 (PFN1)
  09164 Neurodegenerative disease
   05014 Amyotrophic lateral sclerosis
    5216 (PFN1)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   04131 Membrane trafficking [BR:hsa04131]
    5216 (PFN1)
  09183 Protein families: signaling and cellular processes
   04812 Cytoskeleton proteins [BR:hsa04812]
    5216 (PFN1)
   04147 Exosome [BR:hsa04147]
    5216 (PFN1)
Membrane trafficking [BR:hsa04131]
 Others
  Actin-binding proteins
   Others
    5216 (PFN1)
Cytoskeleton proteins [BR:hsa04812]
 Eukaryotic cytoskeleton proteins
  Actin filaments / Microfilaments
   Actin-binding proteins
    Profilin
     5216 (PFN1)
Exosome [BR:hsa04147]
 Exosomal proteins
  Proteins found in most exosomes
   5216 (PFN1)
SSDB
Motif
Pfam: Profilin
Other DBs
NCBI-GeneID: 5216
NCBI-ProteinID: NP_005013
OMIM: 176610
HGNC: 8881
Ensembl: ENSG00000108518
UniProt: P07737
Structure
Position
17:complement(4945652..4948530)
AA seq 140 aa
MAGWNAYIDNLMADGTCQDAAIVGYKDSPSVWAAVPGKTFVNITPAEVGVLVGKDRSSFY
VNGLTLGGQKCSVIRDSLLQDGEFSMDLRTKSTGGAPTFNVTVTKTDKTLVLLMGKEGVH
GGLINKKCYEMASHLRRSQY
NT seq 423 nt   +upstreamnt  +downstreamnt
atggccgggtggaacgcctacatcgacaacctcatggcggacgggacctgtcaggacgcg
gccatcgtgggctacaaggactcgccctccgtctgggccgccgtccccgggaaaacgttc
gtcaacatcacgccagctgaggtgggtgtcctggttggcaaagaccggtcaagtttttac
gtgaatgggctgacacttgggggccagaaatgttcggtgatccgggactcactgctgcag
gatggggaatttagcatggatcttcgtaccaagagcaccggtggggcccccaccttcaat
gtcactgtcaccaagactgacaagacgctagtcctgctgatgggcaaagaaggtgtccac
ggtggtttgatcaacaagaaatgttatgaaatggcctcccaccttcggcgttcccagtac
tga

  All links  
Disease (2)   
   OMIM (2)   
Gene (73)   
   RefGene (3)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (65)   
   OC (1)   
Protein sequence (4)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (2)   
DNA sequence (30)   
   RefSeq(nuc) (2)   
   GenBank (14)   
   EMBL (14)   
3D Structure (22)   
   PDB (22)   
Protein domain (1)   
   Pfam (1)   
All databases (132)   

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