UniProt ID | TEX11_HUMAN | |
---|---|---|
UniProt AC | Q8IYF3 | |
Protein Name | Testis-expressed protein 11 | |
Gene Name | TEX11 | |
Organism | Homo sapiens (Human). | |
Sequence Length | 940 | |
Subcellular Localization | Chromosome. Forms arrays of discrete foci along synaptonemal complexes in spermatocytes and fetal oocytes.. | |
Protein Description | Regulator of crossing-over during meiosis. Involved in initiation and/or maintenance of chromosome synapsis and formation of crossovers (By similarity).. | |
Protein Sequence | MISAHCNLRLLCSSDSSASASQVAGTTEVVENLVTNDNSPNIPEAIDRLFSDIANINRESMAEITDIQIEEMAVNLWNWALTIGGGWLVNEEQKIRLHYVACKLLSMCEASFASEQSIQRLIMMNMRIGKEWLDAGNFLIADECFQAAVASLEQLYVKLIQRSSPEADLTMEKITVESDHFRVLSYQAESAVAQGDFQRASMCVLQCKDMLMRLPQMTSSLHHLCYNFGVETQKNNKYEESSFWLSQSYDIGKMDKKSTGPEMLAKVLRLLATNYLDWDDTKYYDKALNAVNLANKEHLSSPGLFLKMKILLKGETSNEELLEAVMEILHLDMPLDFCLNIAKLLMDHERESVGFHFLTIIHERFKSSENIGKVLILHTDMLLQRKEELLAKEKIEEIFLAHQTGRQLTAESMNWLHNILWRQAASSFEVQNYTDALQWYYYSLRFYSTDEMDLDFTKLQRNMACCYLNLQQLDKAKEAVAEAERHDPRNVFTQFYIFKIAVIEGNSERALQAIITLENILTDEESEDNDLVAERGSPTMLLSLAAQFALENGQQIVAEKALEYLAQHSEDQEQVLTAVKCLLRFLLPKIAEMPESEDKKKEMDRLLTCLNRAFVKLSQPFGEEALSLESRANEAQWFRKTAWNLAVQCDKDPVMMREFFILSYKMSQFCPSDQVILIARKTCLLMAVAVDLEQGRKASTAFEQTMFLSRALEEIQTCNDIHNFLKQTGTFSNDSCEKLLLLYEFEVRAKLNDPLLESFLESVWELPHLETKTFETIAIIAMEKPAHYPLIALKALKKALLLYKKEEPIDISQYSKCMHNLVNLSVPDGASNVELCPLEEVWGYFEDALSHISRTKDYPEMEILWLMVKSWNTGVLMFSRSKYASAEKWCGLALRFLNHLTSFKESYETQMNMLYSQLVEALSNNKGPVFHEHGYWSKSD | |
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 |
---|---|---|---|---|---|
175 | Phosphorylation | DLTMEKITVESDHFR CCEEEEEEEECCCEE | 29.32 | - | |
284 | Phosphorylation | DWDDTKYYDKALNAV CCCCCHHHHHHHHHH | 16.72 | 22817900 | |
368 | Phosphorylation | IHERFKSSENIGKVL HHHHHHCCCCHHHHE | 34.94 | 23532336 | |
443 | Phosphorylation | ALQWYYYSLRFYSTD HHHHHHHHCCCCCCC | 9.28 | 24719451 | |
507 | Phosphorylation | IAVIEGNSERALQAI EEEECCCHHHHHHHH | 39.04 | 21659604 | |
682 | Phosphorylation | VILIARKTCLLMAVA HHEEEHHHHHHHHHH | 11.66 | - | |
743 | Phosphorylation | CEKLLLLYEFEVRAK HHHHHHHHEEHHHHH | 20.67 | - |
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 TEX11_HUMAN !! |
Modified Location | Modified Residue | Modification | Function | Reference | ||
---|---|---|---|---|---|---|
Oops, there are no descriptions of PTM sites of TEX11_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 TEX11_HUMAN !! |
Interacting Protein | Gene Name | Interaction Type | PPI Reference | Domain-Domain Interactions |
---|---|---|---|---|
EFHC1_HUMAN | EFHC1 | physical | 16189514 | |
CJ082_HUMAN | C10orf82 | physical | 16189514 | |
ZN414_HUMAN | ZNF414 | physical | 16189514 | |
T22D4_HUMAN | TSC22D4 | physical | 16189514 | |
COKA1_HUMAN | COL20A1 | physical | 16189514 | |
CFA53_HUMAN | CFAP53 | physical | 16189514 | |
HYI_HUMAN | HYI | physical | 16189514 | |
SKT_HUMAN | KIAA1217 | physical | 16189514 | |
TCHP_HUMAN | TCHP | physical | 16189514 | |
C2CD6_HUMAN | ALS2CR11 | physical | 16189514 | |
P66B_HUMAN | GATAD2B | physical | 25416956 | |
COKA1_HUMAN | COL20A1 | physical | 25416956 | |
DUS21_HUMAN | DUSP21 | physical | 25416956 | |
T22D4_HUMAN | TSC22D4 | physical | 25416956 | |
HYI_HUMAN | HYI | physical | 25416956 | |
FBF1_HUMAN | FBF1 | physical | 25416956 | |
RIBC1_HUMAN | RIBC1 | physical | 25416956 | |
PPR18_HUMAN | PPP1R18 | physical | 25416956 | |
SPERT_HUMAN | SPERT | physical | 25416956 | |
CENPP_HUMAN | CENPP | physical | 25416956 | |
CF226_HUMAN | C6orf226 | physical | 25416956 | |
BORC8_HUMAN | MEF2BNB | physical | 25416956 |
Kegg Disease | ||||||
---|---|---|---|---|---|---|
There are no disease associations of PTM sites. | ||||||
OMIM Disease | ||||||
309120 | Spermatogenic failure, X-linked, 2 (SPGFX2) | |||||
Kegg Drug | ||||||
There are no disease associations of PTM sites. | ||||||
DrugBank | ||||||
There are no disease associations of PTM sites. |
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