UniProt ID | MEIS2_HUMAN | |
---|---|---|
UniProt AC | O14770 | |
Protein Name | Homeobox protein Meis2 | |
Gene Name | MEIS2 | |
Organism | Homo sapiens (Human). | |
Sequence Length | 477 | |
Subcellular Localization | Nucleus . Cytoplasm, perinuclear region . | |
Protein Description | Involved in transcriptional regulation. Binds to HOX or PBX proteins to form dimers, or to a DNA-bound dimer of PBX and HOX proteins and thought to have a role in stabilization of the homeoprotein-DNA complex. Isoform 3 is required for the activity of a PDX1:PBX1b:MEIS2b complex in pancreatic acinar cells involved in the transcriptional activation of the ELA1 enhancer; the complex binds to the enhancer B element and cooperates with the transcription factor 1 complex (PTF1) bound to the enhancer A element; MEIS2 is not involved in complex DNA-binding. Probably in complex with PBX1, is involved in transcriptional regulation by KLF4. Isoform 3 and isoform 4 can bind to a EPHA8 promoter sequence containing the DNA motif 5'-CGGTCA-3'; in cooperation with a PBX protein (such as PBX2) is proposed to be involved in the transcriptional activation of EPHA8 in the developing midbrain. May be involved in regulation of myeloid differentiation. Can bind to the DNA sequence 5'-TGACAG-3'in the activator ACT sequence of the D(1A) dopamine receptor (DRD1) promoter and activate DRD1 transcription; isoform 5 cannot activate DRD1 transcription.. | |
Protein Sequence | MAQRYDELPHYGGMDGVGVPASMYGDPHAPRPIPPVHHLNHGPPLHATQHYGAHAPHPNVMPASMGSAVNDALKRDKDAIYGHPLFPLLALVFEKCELATCTPREPGVAGGDVCSSDSFNEDIAVFAKQVRAEKPLFSSNPELDNLMIQAIQVLRFHLLELEKVHELCDNFCHRYISCLKGKMPIDLVIDERDGSSKSDHEELSGSSTNLADHNPSSWRDHDDATSTHSAGTPGPSSGGHASQSGDNSSEQGDGLDNSVASPGTGDDDDPDKDKKRQKKRGIFPKVATNIMRAWLFQHLTHPYPSEEQKKQLAQDTGLTILQVNNWFINARRRIVQPMIDQSNRAGFLLDPSVSQGAAYSPEGQPMGSFVLDGQQHMGIRPAGLQSMPGDYVSQGGPMGMSMAQPSYTPPQMTPHPTQLRHGPPMHSYLPSHPHHPAMMMHGGPPTHPGMTMSAQSPTMLNSVDPNVGGQVMDIHAQ | |
Overview of Protein Modification Sites with Functional and Structural Information | ||
* ASA = Accessible Surface Area
Locations | Modification | Substrate Peptides & Secondary Structure |
ASA (%) | Reference | Orthologous Protein Cluster |
---|---|---|---|---|---|
138 | Phosphorylation | RAEKPLFSSNPELDN HCCCCCCCCCHHHHH | 36.57 | 27732954 | |
139 | Phosphorylation | AEKPLFSSNPELDNL CCCCCCCCCHHHHHH | 49.41 | 27732954 | |
180 | Ubiquitination | HRYISCLKGKMPIDL HHHHHHHCCCCCEEE | 61.89 | - | |
195 | Phosphorylation | VIDERDGSSKSDHEE EEECCCCCCCCCCCH | 38.59 | 27794612 | |
196 | Phosphorylation | IDERDGSSKSDHEEL EECCCCCCCCCCCHH | 41.53 | 27794612 | |
198 | Phosphorylation | ERDGSSKSDHEELSG CCCCCCCCCCCHHCC | 46.26 | 22617229 | |
204 | Phosphorylation | KSDHEELSGSSTNLA CCCCCHHCCCCCCCC | 39.65 | 23663014 | |
206 | Phosphorylation | DHEELSGSSTNLADH CCCHHCCCCCCCCCC | 30.52 | 23663014 | |
207 | Phosphorylation | HEELSGSSTNLADHN CCHHCCCCCCCCCCC | 25.49 | 23663014 | |
208 | Phosphorylation | EELSGSSTNLADHNP CHHCCCCCCCCCCCC | 35.63 | 23663014 | |
216 | Phosphorylation | NLADHNPSSWRDHDD CCCCCCCCCCCCCCC | 48.10 | 24117733 | |
217 | Phosphorylation | LADHNPSSWRDHDDA CCCCCCCCCCCCCCC | 27.64 | 24117733 |
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 MEIS2_HUMAN !! |
Modified Location | Modified Residue | Modification | Function | Reference | ||
---|---|---|---|---|---|---|
Oops, there are no descriptions of PTM sites of MEIS2_HUMAN !! |
* 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 MEIS2_HUMAN !! |
Interacting Protein | Gene Name | Interaction Type | PPI Reference | Domain-Domain Interactions |
---|---|---|---|---|
PBX1_HUMAN | PBX1 | physical | 20211142 | |
TRI25_HUMAN | TRIM25 | physical | 20211142 | |
ZNHI3_HUMAN | ZNHIT3 | physical | 20211142 | |
A4_HUMAN | APP | physical | 21832049 | |
MEIS2_HUMAN | MEIS2 | physical | 25416956 | |
OSGI1_HUMAN | OSGIN1 | physical | 25416956 | |
CA094_HUMAN | C1orf94 | physical | 25416956 | |
MEIS3_HUMAN | MEIS3 | physical | 26186194 | |
MEIS1_HUMAN | MEIS1 | physical | 26186194 | |
PBX1_HUMAN | PBX1 | physical | 26186194 | |
PBX2_HUMAN | PBX2 | physical | 26186194 | |
PBX4_HUMAN | PBX4 | physical | 26186194 | |
PBX3_HUMAN | PBX3 | physical | 26186194 | |
GBB4_HUMAN | GNB4 | physical | 26186194 | |
PIGL_HUMAN | PIGL | physical | 26186194 | |
MEIS3_HUMAN | MEIS3 | physical | 28514442 | |
PBX2_HUMAN | PBX2 | physical | 28514442 | |
PBX4_HUMAN | PBX4 | physical | 28514442 | |
PBX3_HUMAN | PBX3 | physical | 28514442 | |
PBX1_HUMAN | PBX1 | physical | 28514442 | |
MEIS1_HUMAN | MEIS1 | physical | 28514442 | |
PIGL_HUMAN | PIGL | physical | 28514442 | |
ACTB_HUMAN | ACTB | physical | 28514442 |
Kegg Disease | ||||||
---|---|---|---|---|---|---|
There are no disease associations of PTM sites. | ||||||
OMIM Disease | ||||||
There are no disease associations of PTM sites. | ||||||
Kegg Drug | ||||||
There are no disease associations of PTM sites. | ||||||
DrugBank | ||||||
There are no disease associations of PTM sites. |
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