HCN1_HUMAN - dbPTM
HCN1_HUMAN - PTM Information in dbPTM
Basic Information of Protein
UniProt ID HCN1_HUMAN
UniProt AC O60741
Protein Name Potassium/sodium hyperpolarization-activated cyclic nucleotide-gated channel 1
Gene Name HCN1
Organism Homo sapiens (Human).
Sequence Length 890
Subcellular Localization Cell membrane
Multi-pass membrane protein .
Protein Description Hyperpolarization-activated ion channel exhibiting weak selectivity for potassium over sodium ions. [PubMed: 28086084 Contributes to the native pacemaker currents in heart (If) and in neurons (Ih May mediate responses to sour stimuli.]
Protein Sequence MEGGGKPNSSSNSRDDGNSVFPAKASATGAGPAAAEKRLGTPPGGGGAGAKEHGNSVCFKVDGGGGGGGGGGGGEEPAGGFEDAEGPRRQYGFMQRQFTSMLQPGVNKFSLRMFGSQKAVEKEQERVKTAGFWIIHPYSDFRFYWDLIMLIMMVGNLVIIPVGITFFTEQTTTPWIIFNVASDTVFLLDLIMNFRTGTVNEDSSEIILDPKVIKMNYLKSWFVVDFISSIPVDYIFLIVEKGMDSEVYKTARALRIVRFTKILSLLRLLRLSRLIRYIHQWEEIFHMTYDLASAVVRIFNLIGMMLLLCHWDGCLQFLVPLLQDFPPDCWVSLNEMVNDSWGKQYSYALFKAMSHMLCIGYGAQAPVSMSDLWITMLSMIVGATCYAMFVGHATALIQSLDSSRRQYQEKYKQVEQYMSFHKLPADMRQKIHDYYEHRYQGKIFDEENILNELNDPLREEIVNFNCRKLVATMPLFANADPNFVTAMLSKLRFEVFQPGDYIIREGAVGKKMYFIQHGVAGVITKSSKEMKLTDGSYFGEICLLTKGRRTASVRADTYCRLYSLSVDNFNEVLEEYPMMRRAFETVAIDRLDRIGKKNSILLQKFQKDLNTGVFNNQENEILKQIVKHDREMVQAIAPINYPQMTTLNSTSSTTTPTSRMRTQSPPVYTATSLSHSNLHSPSPSTQTPQPSAILSPCSYTTAVCSPPVQSPLAARTFHYASPTASQLSLMQQQPQQQVQQSQPPQTQPQQPSPQPQTPGSSTPKNEVHKSTQALHNTNLTREVRPLSASQPSLPHEVSTLISRPHPTVGESLASIPQPVTAVPGTGLQAGGRSTVPQRVTLFRQMSSGAIPPNRGVPPAPPPPAAALPRESSSVLNTDPDAEKPRFASNL
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
26PhosphorylationSVFPAKASATGAGPA
CCCCCCCCCCCCCHH
26.1720068231
28PhosphorylationFPAKASATGAGPAAA
CCCCCCCCCCCHHHH
25.6820068231
41PhosphorylationAAEKRLGTPPGGGGA
HHHHHHCCCCCCCCC
30.7920068231
91PhosphorylationAEGPRRQYGFMQRQF
CCCHHHHHHHHHHHH
15.5429978859
99PhosphorylationGFMQRQFTSMLQPGV
HHHHHHHHHHHCCCC
12.6130576142
100PhosphorylationFMQRQFTSMLQPGVN
HHHHHHHHHHCCCCC
20.8429978859
110PhosphorylationQPGVNKFSLRMFGSQ
CCCCCHHHHHHHCCH
19.3725394399
116PhosphorylationFSLRMFGSQKAVEKE
HHHHHHCCHHHHHHH
19.7630576142
217PhosphorylationPKVIKMNYLKSWFVV
HHHEEHHHCCHHHHH
16.41-
338N-linked_GlycosylationVSLNEMVNDSWGKQY
EEHHHHHCCCCHHHH
35.97UniProtKB CARBOHYD
407PhosphorylationLDSSRRQYQEKYKQV
HHHHHHHHHHHHHHH
19.48-
411PhosphorylationRRQYQEKYKQVEQYM
HHHHHHHHHHHHHHH
13.1017977941
417PhosphorylationKYKQVEQYMSFHKLP
HHHHHHHHHHHCCCC
4.92-
513PhosphorylationGAVGKKMYFIQHGVA
CCCCCEEEEEECCCE
13.3522496350
623UbiquitinationNQENEILKQIVKHDR
CHHHHHHHHHHHCCH
43.57-
645O-linked_GlycosylationPINYPQMTTLNSTSS
CCCCCCCEECCCCCC
23.9228657654
700O-linked_GlycosylationILSPCSYTTAVCSPP
EECCCCCEEECCCCC
7.6228657654
807O-linked_GlycosylationLISRPHPTVGESLAS
HHCCCCCCCCHHHHC
37.8028657654
846PhosphorylationVTLFRQMSSGAIPPN
HHHHHHHCCCCCCCC
19.79-
847PhosphorylationTLFRQMSSGAIPPNR
HHHHHHCCCCCCCCC
27.23-

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 HCN1_HUMAN !!

Functions of PTM Sites
Modified Location Modified Residue Modification Function Reference

Oops, there are no descriptions of PTM sites of HCN1_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 HCN1_HUMAN !!

Protein-Protein Interaction
Interacting Protein Gene Name Interaction Type PPI Reference Domain-Domain Interactions
HCN2_HUMANHCN2physical
12928435
HCN3_HUMANHCN3physical
12928435
HCN4_HUMANHCN4physical
12928435
HCN1_HUMANHCN1physical
12034718
HCN2_HUMANHCN2physical
12034718
NED4L_HUMANNEDD4Lphysical
24451387

Drug and Disease Associations
Kegg Disease
There are no disease associations of PTM sites.
OMIM Disease
615871Epileptic encephalopathy, early infantile, 24 (EIEE24)
Kegg Drug
There are no disease associations of PTM sites.
DrugBank
There are no disease associations of PTM sites.
Regulatory Network of HCN1_HUMAN

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Related Literatures of Post-Translational Modification

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