SL9A9_HUMAN - dbPTM
SL9A9_HUMAN - PTM Information in dbPTM
Basic Information of Protein
UniProt ID SL9A9_HUMAN
UniProt AC Q8IVB4
Protein Name Sodium/hydrogen exchanger 9
Gene Name SLC9A9
Organism Homo sapiens (Human).
Sequence Length 645
Subcellular Localization Late endosome membrane
Multi-pass membrane protein .
Protein Description May act in electroneutral exchange of protons for Na(+) across membranes. Involved in the effusion of Golgi luminal H(+) in exchange for cytosolic cations. Involved in organelle ion homeostasis by contributing to the maintenance of the unique acidic pH values of the Golgi and post-Golgi compartments in the cell..
Protein Sequence MERQSRVMSEKDEYQFQHQGAVELLVFNFLLILTILTIWLFKNHRFRFLHETGGAMVYGLIMGLILRYATAPTDIESGTVYDCVKLTFSPSTLLVNITDQVYEYKYKREISQHNINPHQGNAILEKMTFDPEIFFNVLLPPIIFHAGYSLKKRHFFQNLGSILTYAFLGTAISCIVIGLIMYGFVKAMIHAGQLKNGDFHFTDCLFFGSLMSATDPVTVLAIFHELHVDPDLYTLLFGESVLNDAVAIVLTYSISIYSPKENPNAFDAAAFFQSVGNFLGIFAGSFAMGSAYAIITALLTKFTKLCEFPMLETGLFFLLSWSAFLSAEAAGLTGIVAVLFCGVTQAHYTYNNLSSDSKIRTKQLFEFMNFLAENVIFCYMGLALFTFQNHIFNALFILGAFLAIFVARACNIYPLSFLLNLGRKQKIPWNFQHMMMFSGLRGAIAFALAIRNTESQPKQMMFTTTLLLVFFTVWVFGGGTTPMLTWLQIRVGVDLDENLKEDPSSQHQEANNLDKNMTKAESARLFRMWYSFDHKYLKPILTHSGPPLTTTLPEWCGPISRLLTSPQAYGEQLKEDDVECIVNQDELAINYQEQASSPCSPPARLGLDQKASPQTPGKENIYEGDLGLGGYELKLEQTLGQSQLN
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
9PhosphorylationERQSRVMSEKDEYQF
CCCCCCCCCCCCHHH
38.3424719451
96N-linked_GlycosylationSPSTLLVNITDQVYE
CCCEEEEECHHHHHH
31.2617660510
148PhosphorylationPIIFHAGYSLKKRHF
HHHHHCCCCCHHHHH
16.18-
149PhosphorylationIIFHAGYSLKKRHFF
HHHHCCCCCHHHHHH
32.5624719451
355PhosphorylationYTYNNLSSDSKIRTK
HCCCCCCCCCCCCHH
49.41-
463PhosphorylationQPKQMMFTTTLLLVF
CHHHHHHHHHHHHHH
10.8524043423
464PhosphorylationPKQMMFTTTLLLVFF
HHHHHHHHHHHHHHH
12.2724043423
465PhosphorylationKQMMFTTTLLLVFFT
HHHHHHHHHHHHHHH
16.6124043423
472PhosphorylationTLLLVFFTVWVFGGG
HHHHHHHHHHHHCCC
11.2924043423
480PhosphorylationVWVFGGGTTPMLTWL
HHHHCCCCCCCCHHH
30.8824043423
481PhosphorylationWVFGGGTTPMLTWLQ
HHHCCCCCCCCHHHH
15.2424043423
485PhosphorylationGGTTPMLTWLQIRVG
CCCCCCCHHHHEEEC
20.2024043423
500UbiquitinationVDLDENLKEDPSSQH
CCCCCCCCCCCCHHH
72.20-
530PhosphorylationARLFRMWYSFDHKYL
HHHHHHHHHCCCCCH
7.07-
591PhosphorylationQDELAINYQEQASSP
HHHHHCCHHHHCCCC
13.8128270605
596PhosphorylationINYQEQASSPCSPPA
CCHHHHCCCCCCCCH
34.2128270605
597PhosphorylationNYQEQASSPCSPPAR
CHHHHCCCCCCCCHH
32.7028270605
600PhosphorylationEQASSPCSPPARLGL
HHCCCCCCCCHHCCC
36.9828270605
610UbiquitinationARLGLDQKASPQTPG
HHCCCCCCCCCCCCC
50.9632142685
612PhosphorylationLGLDQKASPQTPGKE
CCCCCCCCCCCCCCC
25.2830108239
615PhosphorylationDQKASPQTPGKENIY
CCCCCCCCCCCCCCC
37.0824400094
622PhosphorylationTPGKENIYEGDLGLG
CCCCCCCCCCCCCCC
25.9928796482
631PhosphorylationGDLGLGGYELKLEQT
CCCCCCCEEEEEEEE
19.1128796482

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 SL9A9_HUMAN !!

Functions of PTM Sites
Modified Location Modified Residue Modification Function Reference

Oops, there are no descriptions of PTM sites of SL9A9_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 SL9A9_HUMAN !!

Protein-Protein Interaction
Interacting Protein Gene Name Interaction Type PPI Reference Domain-Domain Interactions

Oops, there are no PPI records of SL9A9_HUMAN !!

Drug and Disease Associations
Kegg Disease
There are no disease associations of PTM sites.
OMIM Disease
q21). The inversion disrupts DOCK3 and SLC9A9.Note=A chromosomal aberration involving SLC9A9 has been found in a family with early-onset behavioral/developmental disorder with features of attention deficit-hyperactivity disorder and intellectual disability. Inversion inv(3)(p14
613410
Kegg Drug
There are no disease associations of PTM sites.
DrugBank
There are no disease associations of PTM sites.
Regulatory Network of SL9A9_HUMAN

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Related Literatures of Post-Translational Modification
N-linked Glycosylation
ReferencePubMed
"Glycoproteomics analysis of human liver tissue by combination ofmultiple enzyme digestion and hydrazide chemistry.";
Chen R., Jiang X., Sun D., Han G., Wang F., Ye M., Wang L., Zou H.;
J. Proteome Res. 8:651-661(2009).
Cited for: GLYCOSYLATION [LARGE SCALE ANALYSIS] AT ASN-96, AND MASS SPECTROMETRY.

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