P35439

PTMD Annotation Information


※ Protein Information

Tag Content
UniProt Accession NMDZ1_RAT; P35439;
Entrez ID 24408
GenBank Protein ID NM_001270602.1; NM_001270603.1; NM_001270605.1; NM_001270608.1; NM_001270610.1; NM_001287423.1; NM_017010.2;
GenBank Nucleotide ID NP_001257531.1; NP_001257532.1; NP_001257534.1; NP_001257537.1; NP_001257539.1; NP_001274352.1; NP_058706.1;
Protein Name Glutamate receptor ionotropic, NMDA 1 (GluN1) (Glutamate [NMDA] receptor subunit zeta-1) (N-methyl-D-aspartate receptor subunit NR1) (NMD-R1)
Gene Name Grin1; Nmdar1
Organism Rattus norvegicus
NCBI Taxa ID 10116
Functional DescriptionComponent of NMDA receptor complexes that function as heterotetrameric, ligand-gated ion channels with high calcium permeability and voltage-dependent sensitivity to magnesium. Channel activation requires binding of the neurotransmitter glutamate to the epsilon subunit, glycine binding to the zeta subunit, plus membrane depolarization to eliminate channel inhibition by Mg(2+) (PubMed:1350383, PubMed:1834949, PubMed:1388270, PubMed:8428958, PubMed:18177891, PubMed:28384476, PubMed:15996549, PubMed:24876489, PubMed:27135925, PubMed:27618671, PubMed:28468946). Sensitivity to glutamate and channel kinetics depend on the subunit composition (PubMed:28384476).
Sequence
(Fasta)
MSTMHLLTFA LLFSCSFARA ACDPKIVNIG AVLSTRKHEQ MFREAVNQAN KRHGSWKIQL 60
NATSVTHKPN AIQMALSVCE DLISSQVYAI LVSHPPTPND HFTPTPVSYT AGFYRIPVLG 120
LTTRMSIYSD KSIHLSFLRT VPPYSHQSSV WFEMMRVYNW NHIILLVSDD HEGRAAQKRL 180
ETLLEERESK AEKVLQFDPG TKNVTALLME ARELEARVII LSASEDDAAT VYRAAAMLNM 240
TGSGYVWLVG EREISGNALR YAPDGIIGLQ LINGKNESAH ISDAVGVVAQ AVHELLEKEN 300
ITDPPRGCVG NTNIWKTGPL FKRVLMSSKY ADGVTGRVEF NEDGDRKFAN YSIMNLQNRK 360
LVQVGIYNGT HVIPNDRKII WPGGETEKPR GYQMSTRLKI VTIHQEPFVY VKPTMSDGTC 420
KEEFTVNGDP VKKVICTGPN DTSPGSPRHT VPQCCYGFCI DLLIKLARTM NFTYEVHLVA 480
DGKFGTQERV NNSNKKEWNG MMGELLSGQA DMIVAPLTIN NERAQYIEFS KPFKYQGLTI 540
LVKKEIPRST LDSFMQPFQS TLWLLVGLSV HVVAVMLYLL DRFSPFGRFK VNSEEEEEDA 600
LTLSSAMWFS WGVLLNSGIG EGAPRSFSAR ILGMVWAGFA MIIVASYTAN LAAFLVLDRP 660
EERITGINDP RLRNPSDKFI YATVKQSSVD IYFRRQVELS TMYRHMEKHN YESAAEAIQA 720
VRDNKLHAFI WDSAVLEFEA SQKCDLVTTG ELFFRSGFGI GMRKDSPWKQ NVSLSILKSH 780
ENGFMEDLDK TWVRYQECDS RSNAPATLTF ENMAGVFMLV AGGIVAGIFL IFIEIAYKRH 840
KDARRKQMQL AFAAVNVWRK NLQDRKSGRA EPDPKKKATF RAITSTLASS FKRRRSSKDT 900
STGGGRGALQ NQKDTVLPRR AIEREEGQLQ LCSRHRES 939

※ PTM-Disease Association

NumPTMDiseaseCell TypeTypePTM SitePMID
1Serine PhosphorylationParkinson's diseaseDS89019283475
[Reference]: We found a significant reduction in the abundance of both phosphorylated NR1 on serine residues 890 and 896 (pNR1S890 and pNR1S896) and NR1 in the cell plasma membrane of lesioned striatum.
2Serine PhosphorylationParkinson's diseaseDS89619283475
[Reference]: We found a significant reduction in the abundance of both phosphorylated NR1 on serine residues 890 and 896 (pNR1S890 and pNR1S896) and NR1 in the cell plasma membrane of lesioned striatum.
3Serine PhosphorylationParkinson's diseaseDS89719283475
[Reference]: pNR1S897 is dependent on the number of levodopa injections and is paralleled by a sensitization of the rotational response.?

※ Disease Cross-ref Annotation

DatabaseAnnotation
CTD (Curated)
(count: 7)
(view all)
MESH:D019970 ; Cocaine-Related Disorders
MESH:D004195 ; Disease Models, Animal
MESH:D006930 ; Hyperalgesia
OMIM:614254 ; MENTAL RETARDATION, AUTOSOMAL DOMINANT 8
MESH:D010146 ; Pain
MESH:D011618 ; Psychotic Disorders

※ PTM Sites

PTM Modification Sites
Phosphorylation
(count: 7)
(view all)
330       RVLMSSKYADGVTGR     dbPAF
879       PDPKKKATFRAITST     dbPAF
889       AITSTLASSFKRRRS     dbPAF
890       ITSTLASSFKRRRSS     dbPAF
896       SSFKRRRSSKDTSTG     dbPAF
897       SFKRRRSSKDTSTGG     dbPAF
Ubiquitination
(count: 1)
913       RGALQNQKDTVLPRR     PLMD