KELL_HUMAN - dbPTM
KELL_HUMAN - PTM Information in dbPTM
Basic Information of Protein
UniProt ID KELL_HUMAN
UniProt AC P23276
Protein Name Kell blood group glycoprotein
Gene Name KEL
Organism Homo sapiens (Human).
Sequence Length 732
Subcellular Localization Cell membrane
Single-pass type II membrane protein. Spans the erythrocyte membrane, and is attached to the underlying cytoskeleton.
Protein Description Zinc endopeptidase with endothelin-3-converting enzyme activity. Cleaves EDN1, EDN2 and EDN3, with a marked preference for EDN3..
Protein Sequence MEGGDQSEEEPRERSQAGGMGTLWSQESTPEERLPVEGSRPWAVARRVLTAILILGLLLCFSVLLFYNFQNCGPRPCETSVCLDLRDHYLASGNTSVAPCTDFFSFACGRAKETNNSFQELATKNKNRLRRILEVQNSWHPGSGEEKAFQFYNSCMDTLAIEAAGTGPLRQVIEELGGWRISGKWTSLNFNRTLRLLMSQYGHFPFFRAYLGPHPASPHTPVIQIDQPEFDVPLKQDQEQKIYAQIFREYLTYLNQLGTLLGGDPSKVQEHSSLSISITSRLFQFLRPLEQRRAQGKLFQMVTIDQLKEMAPAIDWLSCLQATFTPMSLSPSQSLVVHDVEYLKNMSQLVEEMLLKQRDFLQSHMILGLVVTLSPALDSQFQEARRKLSQKLRELTEQPPMPARPRWMKCVEETGTFFEPTLAALFVREAFGPSTRSAAMKLFTAIRDALITRLRNLPWMNEETQNMAQDKVAQLQVEMGASEWALKPELARQEYNDIQLGSSFLQSVLSCVRSLRARIVQSFLQPHPQHRWKVSPWDVNAYYSVSDHVVVFPAGLLQPPFFHPGYPRAVNFGAAGSIMAHELLHIFYQLLLPGGCLACDNHALQEAHLCLKRHYAAFPLPSRTSFNDSLTFLENAADVGGLAIALQAYSKRLLRHHGETVLPSLDLSPQQIFFRSYAQVMCRKPSPQDSHDTHSPPHLRVHGPLSSTPAFARYFRCARGALLNPSSRCQLW
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
7Phosphorylation-MEGGDQSEEEPRER
-CCCCCCCCCCHHHH
52.288669078
15PhosphorylationEEEPRERSQAGGMGT
CCCHHHHHHCCCCCC
21.4523025827
94N-linked_GlycosylationDHYLASGNTSVAPCT
HHHHCCCCCCCCCCC
27.04UniProtKB CARBOHYD
115N-linked_GlycosylationCGRAKETNNSFQELA
CCCCHHHCCHHHHHH
43.15UniProtKB CARBOHYD
186PhosphorylationWRISGKWTSLNFNRT
CEEECCEECCCHHHH
27.1629083192
187PhosphorylationRISGKWTSLNFNRTL
EEECCEECCCHHHHH
21.8729083192
191N-linked_GlycosylationKWTSLNFNRTLRLLM
CEECCCHHHHHHHHH
34.6511336649
201PhosphorylationLRLLMSQYGHFPFFR
HHHHHHHHCCCHHHH
12.78-
272PhosphorylationPSKVQEHSSLSISIT
HHHHCCCCCCHHHHH
32.02-
303PhosphorylationGKLFQMVTIDQLKEM
CCEEEEEEHHHHHHH
17.3126074081
345N-linked_GlycosylationHDVEYLKNMSQLVEE
CCHHHHHCHHHHHHH
32.51UniProtKB CARBOHYD
444PhosphorylationSAAMKLFTAIRDALI
HHHHHHHHHHHHHHH
31.4521712546
452PhosphorylationAIRDALITRLRNLPW
HHHHHHHHHHHCCCC
25.2221712546
502PhosphorylationYNDIQLGSSFLQSVL
CCCHHHHHHHHHHHH
26.8922210691
627N-linked_GlycosylationLPSRTSFNDSLTFLE
CCCCCCCCCCCHHHH
37.42UniProtKB CARBOHYD
706PhosphorylationLRVHGPLSSTPAFAR
EEECCCCCCCHHHHH
34.9929449344
707PhosphorylationRVHGPLSSTPAFARY
EECCCCCCCHHHHHH
46.2029449344
708PhosphorylationVHGPLSSTPAFARYF
ECCCCCCCHHHHHHH
18.4329449344
714PhosphorylationSTPAFARYFRCARGA
CCHHHHHHHHHHHCC
7.6129449344

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 KELL_HUMAN !!

Functions of PTM Sites
Modified Location Modified Residue Modification Function Reference

Oops, there are no descriptions of PTM sites of KELL_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
272Phosphorylation281 (9)RWrs8176059
  • Immature fraction of reticulocytes
  • High light scatter reticulocyte count
  • High light scatter reticulocyte percentage of red cells
27863252

Protein-Protein Interaction
Interacting Protein Gene Name Interaction Type PPI Reference Domain-Domain Interactions
TBA1A_HUMANTUBA1Aphysical
21900206

Drug and Disease Associations
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.
Regulatory Network of KELL_HUMAN

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Related Literatures of Post-Translational Modification

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