PHX2A_HUMAN - dbPTM
PHX2A_HUMAN - PTM Information in dbPTM
Basic Information of Protein
UniProt ID PHX2A_HUMAN
UniProt AC O14813
Protein Name Paired mesoderm homeobox protein 2A
Gene Name PHOX2A
Organism Homo sapiens (Human).
Sequence Length 284
Subcellular Localization Nucleus .
Protein Description May be involved in regulating the specificity of expression of the catecholamine biosynthetic genes. Acts as a transcription activator/factor. Could maintain the noradrenergic phenotype..
Protein Sequence MDYSYLNSYDSCVAAMEASAYGDFGACSQPGGFQYSPLRPAFPAAGPPCPALGSSNCALGALRDHQPAPYSAVPYKFFPEPSGLHEKRKQRRIRTTFTSAQLKELERVFAETHYPDIYTREELALKIDLTEARVQVWFQNRRAKFRKQERAASAKGAAGAAGAKKGEARCSSEDDDSKESTCSPTPDSTASLPPPPAPGLASPRLSPSPLPVALGSGPGPGPGPQPLKGALWAGVAGGGGGGPGAGAAELLKAWQPAESGPGPFSGVLSSFHRKPGPALKTNLF
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
54PhosphorylationPPCPALGSSNCALGA
CCCCCCCCCCCHHHH
21.1627732954
55PhosphorylationPCPALGSSNCALGAL
CCCCCCCCCCHHHHH
33.8427732954
76UbiquitinationPYSAVPYKFFPEPSG
CCCCCCCCCCCCCCC
34.1623503661
87UbiquitinationEPSGLHEKRKQRRIR
CCCCHHHHHHHHHHH
54.9023503661
89UbiquitinationSGLHEKRKQRRIRTT
CCHHHHHHHHHHHHH
60.2623503661
103UbiquitinationTFTSAQLKELERVFA
HHCHHHHHHHHHHHH
48.4423503661
153PhosphorylationRKQERAASAKGAAGA
HHHHHHHHHHHHHHH
29.5422817900
155AcetylationQERAASAKGAAGAAG
HHHHHHHHHHHHHHH
46.7312436251
155UbiquitinationQERAASAKGAAGAAG
HHHHHHHHHHHHHHH
46.7323503661
171PhosphorylationKKGEARCSSEDDDSK
CCCCCCCCCCCCCCC
31.0730177828
172PhosphorylationKGEARCSSEDDDSKE
CCCCCCCCCCCCCCC
48.9830177828
180PhosphorylationEDDDSKESTCSPTPD
CCCCCCCCCCCCCCC
38.1527732954
181PhosphorylationDDDSKESTCSPTPDS
CCCCCCCCCCCCCCC
20.3527732954
183PhosphorylationDSKESTCSPTPDSTA
CCCCCCCCCCCCCCC
31.7127732954
185PhosphorylationKESTCSPTPDSTASL
CCCCCCCCCCCCCCC
24.3527732954
188PhosphorylationTCSPTPDSTASLPPP
CCCCCCCCCCCCCCC
27.3827732954
189PhosphorylationCSPTPDSTASLPPPP
CCCCCCCCCCCCCCC
27.8727732954
191PhosphorylationPTPDSTASLPPPPAP
CCCCCCCCCCCCCCC
41.3127732954
202PhosphorylationPPAPGLASPRLSPSP
CCCCCCCCCCCCCCC
18.6527732954
206PhosphorylationGLASPRLSPSPLPVA
CCCCCCCCCCCCCCC
25.3129900121
208PhosphorylationASPRLSPSPLPVALG
CCCCCCCCCCCCCCC
35.3824117733
216PhosphorylationPLPVALGSGPGPGPG
CCCCCCCCCCCCCCC
42.5427732954
269PhosphorylationGPFSGVLSSFHRKPG
CCCCCHHHHHCCCCC
28.6624117733
270PhosphorylationPFSGVLSSFHRKPGP
CCCCHHHHHCCCCCC
22.4024117733

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
153SPhosphorylationKinasePRKACAP17612
GPS

Functions of PTM Sites
Modified Location Modified Residue Modification Function Reference

Oops, there are no descriptions of PTM sites of PHX2A_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 PHX2A_HUMAN !!

Protein-Protein Interaction
Interacting Protein Gene Name Interaction Type PPI Reference Domain-Domain Interactions
HAND2_HUMANHAND2physical
14506227
JUN_HUMANJUNphysical
14506227
PHX2A_HUMANPHOX2Aphysical
10644760
SP1_HUMANSP1physical
17344216

Drug and Disease Associations
Kegg Disease
There are no disease associations of PTM sites.
OMIM Disease
602078Fibrosis of extraocular muscles, congenital, 2 (CFEOM2)
Kegg Drug
There are no disease associations of PTM sites.
DrugBank
There are no disease associations of PTM sites.
Regulatory Network of PHX2A_HUMAN

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Related Literatures of Post-Translational Modification

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