P07196

PTMD Annotation Information


※ Protein Information

Tag Content
UniProt Accession NFL_HUMAN; P07196;
Entrez ID 4747
GenBank Protein ID
GenBank Nucleotide ID
Protein Name Neurofilament light polypeptide (NF-L) (68 kDa neurofilament protein) (Neurofilament triplet L protein)
Gene Name NEFL; NF68; NFL
Organism Homo sapiens
NCBI Taxa ID 9606
Functional DescriptionNeurofilaments usually contain three intermediate filament proteins: L, M, and H which are involved in the maintenance of neuronal caliber.
Sequence
(Fasta)
MSSFSYEPYY STSYKRRYVE TPRVHISSVR SGYSTARSAY SSYSAPVSSS LSVRRSYSSS 60
SGSLMPSLEN LDLSQVAAIS NDLKSIRTQE KAQLQDLNDR FASFIERVHE LEQQNKVLEA 120
ELLVLRQKHS EPSRFRALYE QEIRDLRLAA EDATNEKQAL QGEREGLEET LRNLQARYEE 180
EVLSREDAEG RLMEARKGAD EAALARAELE KRIDSLMDEI SFLKKVHEEE IAELQAQIQY 240
AQISVEMDVT KPDLSAALKD IRAQYEKLAA KNMQNAEEWF KSRFTVLTES AAKNTDAVRA 300
AKDEVSESRR LLKAKTLEIE ACRGMNEALE KQLQELEDKQ NADISAMQDT INKLENELRT 360
TKSEMARYLK EYQDLLNVKM ALDIEIAAYR KLLEGEETRL SFTSVGSITS GYSQSSQVFG 420
RSAYGGLQTS SYLMSTRSFP SYYTSHVQEE QIEVEETIEA AKAEEAKDEP PSEGEAEEEE 480
KDKEEAEEEE AAEEEEAAKE ESEEAKEEEE GGEGEEGEET KEAEEEEKKV EGAGEEQAAK 540
KKD 544

※ PTM-Disease Association

NumPTMDiseaseCell TypeTypePTM SitePMID
1Serine PhosphorylationTropical spastic paraparesisUS10319678766
[Reference]: Comparative study of CSF neurofilaments in HTLV-1-associated myelopathy/tropical spastic paraparesis and other neurological disorders.
2Serine PhosphorylationTropical spastic paraparesisUS21519678766
[Reference]: Comparative study of CSF neurofilaments in HTLV-1-associated myelopathy/tropical spastic paraparesis and other neurological disorders.
3Serine PhosphorylationTropical spastic paraparesisUS22119678766
[Reference]: Comparative study of CSF neurofilaments in HTLV-1-associated myelopathy/tropical spastic paraparesis and other neurological disorders.
4Serine PhosphorylationTropical spastic paraparesisUS47219678766
[Reference]: Comparative study of CSF neurofilaments in HTLV-1-associated myelopathy/tropical spastic paraparesis and other neurological disorders.

※ Disease Cross-ref Annotation

DatabaseAnnotation
CTD (Curated)
(count: 2)
MESH:C537987 ; Charcot-Marie-Tooth disease, Type 1F
MESH:C537994 ; Charcot-Marie-Tooth disease, Type 2E

※ PTM Sites

PTM Modification Sites
Phosphorylation
(count: 18)
(view all)
103       DLNDRFASFIERVHE     dbPAF
14        EPYYSTSYKRRYVET     dbPAF
154       RLAAEDATNEKQALQ     dbPAF
21        YKRRYVETPRVHISS     dbPAF
215       ELEKRIDSLMDEISF     dbPAF
221       DSLMDEISFLKKVHE     dbPAF
Ubiquitination
(count: 5)
15        PYYSTSYKRRYVETP     PLMD
157       AEDATNEKQALQGER     PLMD
271       QYEKLAAKNMQNAEE     PLMD
370       SEMARYLKEYQDLLN     PLMD
91        KSIRTQEKAQLQDLN     PLMD
Glycation
(count: 1)
379       YQDLLNVKMALDIEI     PLMD

※ Protein-Protein Interaction

NetworkInteraction
ABSource