TMPS3_HUMAN - dbPTM
TMPS3_HUMAN - PTM Information in dbPTM
Basic Information of Protein
UniProt ID TMPS3_HUMAN
UniProt AC P57727
Protein Name Transmembrane protease serine 3
Gene Name TMPRSS3
Organism Homo sapiens (Human).
Sequence Length 454
Subcellular Localization Endoplasmic reticulum membrane
Single-pass type II membrane protein .
Protein Description Probable serine protease that plays a role in hearing. Acts as a permissive factor for cochlear hair cell survival and activation at the onset of hearing and is required for saccular hair cell survival (By similarity). Activates ENaC (in vitro)..
Protein Sequence MGENDPPAVEAPFSFRSLFGLDDLKISPVAPDADAVAAQILSLLPLKFFPIIVIGIIALILALAIGLGIHFDCSGKYRCRSSFKCIELIARCDGVSDCKDGEDEYRCVRVGGQNAVLQVFTAASWKTMCSDDWKGHYANVACAQLGFPSYVSSDNLRVSSLEGQFREEFVSIDHLLPDDKVTALHHSVYVREGCASGHVVTLQCTACGHRRGYSSRIVGGNMSLLSQWPWQASLQFQGYHLCGGSVITPLWIITAAHCVYDLYLPKSWTIQVGLVSLLDNPAPSHLVEKIVYHSKYKPKRLGNDIALMKLAGPLTFNEMIQPVCLPNSEENFPDGKVCWTSGWGATEDGAGDASPVLNHAAVPLISNKICNHRDVYGGIISPSMLCAGYLTGGVDSCQGDSGGPLVCQERRLWKLVGATSFGIGCAEVNKPGVYTRVTSFLDWIHEQMERDLKT
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
14PhosphorylationPAVEAPFSFRSLFGL
CCCCCCCCHHHHHCC
20.7724719451
99UbiquitinationCDGVSDCKDGEDEYR
CCCCCCCCCCCCCEE
73.9921963094
99 (in isoform 1)Ubiquitination-73.9921906983
99 (in isoform 3)Ubiquitination-73.9921906983
99 (in isoform 4)Ubiquitination-73.9921906983
124PhosphorylationLQVFTAASWKTMCSD
EEEEEHHHHHCCCCC
27.0024719451
168UbiquitinationLEGQFREEFVSIDHL
CCCCCHHHEECHHHC
47.2829967540
183 (in isoform 5)Ubiquitination-14.1121906983
187PhosphorylationKVTALHHSVYVREGC
CCEEEEEEEEEECCC
12.3729083192
189PhosphorylationTALHHSVYVREGCAS
EEEEEEEEEECCCCC
9.2329083192
221N-linked_GlycosylationSSRIVGGNMSLLSQW
CCCEECCCCHHHHCC
15.79UniProtKB CARBOHYD
295UbiquitinationEKIVYHSKYKPKRLG
HHHHHCCCCCCHHCC
43.9429967540

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 TMPS3_HUMAN !!

Functions of PTM Sites
Modified Location Modified Residue Modification Function Reference

Oops, there are no descriptions of PTM sites of TMPS3_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 TMPS3_HUMAN !!

Protein-Protein Interaction
Interacting Protein Gene Name Interaction Type PPI Reference Domain-Domain Interactions
RXRA_HUMANRXRAphysical
16169070
EF1A1_HUMANEEF1A1physical
16169070
CISD2_HUMANCISD2physical
28514442
DCAKD_HUMANDCAKDphysical
28514442
DJC18_HUMANDNAJC18physical
28514442
EPHB4_HUMANEPHB4physical
28514442
E2AK3_HUMANEIF2AK3physical
28514442
VRK2_HUMANVRK2physical
28514442
UPK3L_HUMANUPK3BLphysical
28514442
RETST_HUMANRETSATphysical
28514442
PDZD8_HUMANPDZD8physical
28514442
LRIG3_HUMANLRIG3physical
28514442
ALG9_HUMANALG9physical
28514442
K319L_HUMANKIAA0319Lphysical
28514442
LRFN3_HUMANLRFN3physical
28514442
PTN1_HUMANPTPN1physical
28514442
LRP10_HUMANLRP10physical
28514442
TOR3A_HUMANTOR3Aphysical
28514442
TM39A_HUMANTMEM39Aphysical
28514442
PDE3B_HUMANPDE3Bphysical
28514442
NETO2_HUMANNETO2physical
28514442
DHRS7_HUMANDHRS7physical
28514442
CGRF1_HUMANCGRRF1physical
28514442
TYW1_HUMANTYW1physical
28514442
CXA1_HUMANGJA1physical
28514442
S27A3_HUMANSLC27A3physical
28514442
CALX_HUMANCANXphysical
28514442
1A02_HUMANHLA-Aphysical
28514442
1A03_HUMANHLA-Aphysical
28514442
1A01_HUMANHLA-Aphysical
28514442
1A26_HUMANHLA-Aphysical
28514442
PLXB2_HUMANPLXNB2physical
28514442

Drug and Disease Associations
Kegg Disease
H00605 Deafness, autosomal recessive
OMIM Disease
601072Deafness, autosomal recessive, 8 (DFNB8)
Kegg Drug
There are no disease associations of PTM sites.
DrugBank
There are no disease associations of PTM sites.
Regulatory Network of TMPS3_HUMAN

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Related Literatures of Post-Translational Modification

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