BDNF_HUMAN - dbPTM
BDNF_HUMAN - PTM Information in dbPTM
Basic Information of Protein
UniProt ID BDNF_HUMAN
UniProt AC P23560
Protein Name Brain-derived neurotrophic factor
Gene Name BDNF
Organism Homo sapiens (Human).
Sequence Length 247
Subcellular Localization Secreted.
Protein Description During development, promotes the survival and differentiation of selected neuronal populations of the peripheral and central nervous systems. Participates in axonal growth, pathfinding and in the modulation of dendritic growth and morphology. Major regulator of synaptic transmission and plasticity at adult synapses in many regions of the CNS. The versatility of BDNF is emphasized by its contribution to a range of adaptive neuronal responses including long-term potentiation (LTP), long-term depression (LTD), certain forms of short-term synaptic plasticity, as well as homeostatic regulation of intrinsic neuronal excitability..
Protein Sequence MTILFLTMVISYFGCMKAAPMKEANIRGQGGLAYPGVRTHGTLESVNGPKAGSRGLTSLADTFEHVIEELLDEDQKVRPNEENNKDADLYTSRVMLSSQVPLEPPLLFLLEEYKNYLDAANMSMRVRRHSDPARRGELSVCDSISEWVTAADKKTAVDMSGGTVTVLEKVPVSKGQLKQYFYETKCNPMGYTKEGCRGIDKRHWNSQCRTTQSYVRALTMDSKKRIGWRFIRIDTSCVCTLTIKRGR
Overview of Protein Modification Sites with Functional and Structural Information
Experimental Post-Translational Modification Sites

* ASA = Accessible Surface Area

Locations Modification Substrate Peptides
&
Secondary Structure
ASA (%) Reference Orthologous
Protein Cluster
2Phosphorylation------MTILFLTMV
------CCHHHHHHH
26.7929759185
7Phosphorylation-MTILFLTMVISYFG
-CCHHHHHHHHHHHC
11.3224043423
10 (in isoform 2)Phosphorylation-1.6029523821
11PhosphorylationLFLTMVISYFGCMKA
HHHHHHHHHHCHHHH
11.7326552605
12PhosphorylationFLTMVISYFGCMKAA
HHHHHHHHHCHHHHC
7.8926552605
15 (in isoform 2)Phosphorylation-1.4929523821
17 (in isoform 3)Phosphorylation-45.5329523821
19 (in isoform 2)Phosphorylation-10.1329523821
20 (in isoform 2)Phosphorylation-38.9629523821
22 (in isoform 3)Phosphorylation-53.2529523821
26 (in isoform 3)Phosphorylation-7.2529523821
27 (in isoform 3)Phosphorylation-31.0529523821
31 (in isoform 5)Phosphorylation-10.1529523821
36 (in isoform 5)Phosphorylation-14.6329523821
40 (in isoform 5)Phosphorylation-19.3729523821
41 (in isoform 5)Phosphorylation-31.2329523821
50UbiquitinationLESVNGPKAGSRGLT
EHHCCCCCCCCCCHH
67.77-
62PhosphorylationGLTSLADTFEHVIEE
CHHHHHHHHHHHHHH
25.89-
84 (in isoform 4)Phosphorylation-47.0329523821
85UbiquitinationRPNEENNKDADLYTS
CCCCCCCCCCCHHHH
66.91-
85AcetylationRPNEENNKDADLYTS
CCCCCCCCCCCHHHH
66.917678523
89 (in isoform 4)Phosphorylation-5.5729523821
93 (in isoform 4)Phosphorylation-15.2929523821
94 (in isoform 4)Phosphorylation-4.5429523821
121N-linked_GlycosylationKNYLDAANMSMRVRR
HHHHHHHHHHHHHHH
25.4519467646
155PhosphorylationVTAADKKTAVDMSGG
CHHCCCCEEEECCCC
37.34-
174UbiquitinationLEKVPVSKGQLKQYF
EEEECCCCHHHHHEE
51.41-
191PhosphorylationTKCNPMGYTKEGCRG
ECCCCCCCCCCCCCC
14.3718083107

Upstream regulatory proteins (kinases for phosphorylation sites, E3 ubiquitin ligases of ubiquitination sites, ...)
Modified Location Modified Residue Modification Type of Upstream Proteins Gene Name of Upstream Proteins UniProt AC of Upstream Proteins Sources
62TPhosphorylationKinaseCHEK2O96017
GPS

Functions of PTM Sites
Modified Location Modified Residue Modification Function Reference

Oops, there are no descriptions of PTM sites of BDNF_HUMAN !!

Disease-associated PTM Sites based on SAP

* Distance = the distance between SAP position and PTM sites.

Modified Location Modification Variant Position
(Distance <= 10)
Residue Change SAP Related Disease Reference

Oops, there are no SNP-PTM records of BDNF_HUMAN !!

Protein-Protein Interaction
Interacting Protein Gene Name Interaction Type PPI Reference Domain-Domain Interactions
NTRK2_HUMANNTRK2physical
9312147
NTRK2_HUMANNTRK2physical
11855816
A4_HUMANAPPphysical
21832049
AGO3_HUMANAGO3physical
21988832
JAM1_HUMANF11Rphysical
21988832
JUNB_HUMANJUNBphysical
21988832
INP5K_HUMANINPP5Kphysical
21988832
NTF4_HUMANNTF4physical
25241761
NTRK2_HUMANNTRK2physical
21651720

Drug and Disease Associations
Kegg Disease
There are no disease associations of PTM sites.
OMIM Disease
209880Congenital central hypoventilation syndrome (CCHS)
Kegg Drug
There are no disease associations of PTM sites.
DrugBank
There are no disease associations of PTM sites.
Regulatory Network of BDNF_HUMAN

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Related Literatures of Post-Translational Modification

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