MEOX1_HUMAN - dbPTM
MEOX1_HUMAN - PTM Information in dbPTM
Basic Information of Protein
UniProt ID MEOX1_HUMAN
UniProt AC P50221
Protein Name Homeobox protein MOX-1
Gene Name MEOX1
Organism Homo sapiens (Human).
Sequence Length 254
Subcellular Localization Nucleus . Cytoplasm . Localizes predominantly in the nucleus.
Protein Description Mesodermal transcription factor that plays a key role in somitogenesis and is specifically required for sclerotome development. Required for maintenance of the sclerotome polarity and formation of the cranio-cervical joints. [PubMed: 23290072]
Protein Sequence MDPAASSCMRSLQPPAPVWGCLRNPHSEGNGASGLPHYPPTPFSFHQKPDFLATATAAYPDFSASCLAATPHSLPQEEHIFTEQHPAFPQSPNWHFPVSDARRRPNSGPAGGSKEMGTSSLGLVDTTGGPGDDYGVLGSTANETEKKSSRRRKESSDNQENRGKPEGSSKARKERTAFTKEQLRELEAEFAHHNYLTRLRRYEIAVNLDLSERQVKVWFQNRRMKWKRVKGGQPISPNGQDPEDGDSTASPSSE
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
6Phosphorylation--MDPAASSCMRSLQ
--CCHHHHHHHHHCC
26.6122210691
29PhosphorylationLRNPHSEGNGASGLP
CCCCCCCCCCCCCCC
40.6724719451
33PhosphorylationHSEGNGASGLPHYPP
CCCCCCCCCCCCCCC
42.1124719451
107PhosphorylationDARRRPNSGPAGGSK
HHCCCCCCCCCCCCC
49.1627461979
121PhosphorylationKEMGTSSLGLVDTTG
CCCCCCCCCEECCCC
6.5224719451
134PhosphorylationTGGPGDDYGVLGSTA
CCCCCCCCCCCCCCC
17.5527642862
137PhosphorylationPGDDYGVLGSTANET
CCCCCCCCCCCCCHH
3.7824719451
144PhosphorylationLGSTANETEKKSSRR
CCCCCCHHHHHHHHH
53.5724719451
148PhosphorylationANETEKKSSRRRKES
CCHHHHHHHHHHHHC
39.9024719451
155 (in isoform 2)Phosphorylation-46.1327174698
156 (in isoform 2)Phosphorylation-41.4927174698
159 (in isoform 2)Phosphorylation-55.0927174698
236PhosphorylationVKGGQPISPNGQDPE
ECCCCCCCCCCCCCC
20.9922210691
247PhosphorylationQDPEDGDSTASPSSE
CCCCCCCCCCCCCCC
31.2522210691
248PhosphorylationDPEDGDSTASPSSE-
CCCCCCCCCCCCCC-
35.5722210691
252PhosphorylationGDSTASPSSE-----
CCCCCCCCCC-----
44.6027251275
253PhosphorylationDSTASPSSE------
CCCCCCCCC------
51.1927251275

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

Oops, there are no upstream regulatory protein records of MEOX1_HUMAN !!

Functions of PTM Sites
Modified Location Modified Residue Modification Function Reference

Oops, there are no descriptions of PTM sites of MEOX1_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 MEOX1_HUMAN !!

Protein-Protein Interaction
Interacting Protein Gene Name Interaction Type PPI Reference Domain-Domain Interactions
PAX1_HUMANPAX1physical
11423130
PAX3_HUMANPAX3physical
11423130
A4_HUMANAPPphysical
21832049
TRI18_HUMANMID1physical
25416956
MK09_HUMANMAPK9physical
25416956
RANB3_HUMANRANBP3physical
25416956
CIAO1_HUMANCIAO1physical
25416956
MO4L1_HUMANMORF4L1physical
25416956
DP13A_HUMANAPPL1physical
25416956
SYT17_HUMANSYT17physical
25416956
QRIC1_HUMANQRICH1physical
25416956
UB2R2_HUMANUBE2R2physical
25416956
NAGK_HUMANNAGKphysical
25416956
CIB3_HUMANCIB3physical
25416956
UBX2B_HUMANUBXN2Bphysical
25416956
C19L2_HUMANCWF19L2physical
25416956
TEANC_HUMANTCEANCphysical
25416956
TXLNA_HUMANTXLNAphysical
25416956
NEIL2_HUMANNEIL2physical
25416956
NIF3L_HUMANNIF3L1physical
26186194
MEOX2_HUMANMEOX2physical
26186194
CHM1A_HUMANCHMP1Aphysical
26186194
PRPK_HUMANTP53RKphysical
26186194
MEOX2_HUMANMEOX2physical
28514442
CHM1A_HUMANCHMP1Aphysical
28514442
NIF3L_HUMANNIF3L1physical
28514442

Drug and Disease Associations
Kegg Drug
DrugBank
There are no disease associations of PTM sites.
Regulatory Network of MEOX1_HUMAN

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Related Literatures of Post-Translational Modification

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