ARMC7_HUMAN - dbPTM
ARMC7_HUMAN - PTM Information in dbPTM
Basic Information of Protein
UniProt ID ARMC7_HUMAN
UniProt AC Q9H6L4
Protein Name Armadillo repeat-containing protein 7
Gene Name ARMC7
Organism Homo sapiens (Human).
Sequence Length 198
Subcellular Localization
Protein Description
Protein Sequence MAQKPKVDPHVGRLGYLQALVTEFQETQSQDAKEQVLANLANFAYDPSNYEYLRQLQVLDLFLDSLSEENETLVEFAIGGLCNLCPDRANKEHILHAGGVPLIINCLSSPNEETVLSAITTLMHLSPPGRSFLPELTATPVVQCMLRFSLSASARLRNLAQIFLEDFCSPRQVAEARSRQAHSALGIPLPRSVAPRQR
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
169PhosphorylationIFLEDFCSPRQVAEA
HHHHHCCCHHHHHHH
24.1024260401
183PhosphorylationARSRQAHSALGIPLP
HHHHHHHHHHCCCCC
28.3624425749
191MethylationALGIPLPRSVAPRQR
HHCCCCCCCCCCCCC
51.99-
192PhosphorylationLGIPLPRSVAPRQR-
HCCCCCCCCCCCCC-
22.2328634298

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 ARMC7_HUMAN !!

Functions of PTM Sites
Modified Location Modified Residue Modification Function Reference

Oops, there are no descriptions of PTM sites of ARMC7_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 ARMC7_HUMAN !!

Protein-Protein Interaction
Interacting Protein Gene Name Interaction Type PPI Reference Domain-Domain Interactions
BACD1_HUMANKCTD13physical
16189514
A4_HUMANAPPphysical
21832049
SMAKA_HUMANC2orf88physical
21988832
CPSF7_HUMANCPSF7physical
25416956
CCD33_HUMANCCDC33physical
25416956
EFHC2_HUMANEFHC2physical
25416956
SPC1L_HUMANSPATC1Lphysical
25416956
LZTS2_HUMANLZTS2physical
25416956
K1C40_HUMANKRT40physical
25416956
SPERT_HUMANSPERTphysical
25416956
TRI42_HUMANTRIM42physical
25416956
INCA1_HUMANINCA1physical
25416956
ARMC7_HUMANARMC7physical
26472760
CKAP4_HUMANCKAP4physical
26472760
RBM48_HUMANRBM48physical
26472760
MPRIP_HUMANMPRIPphysical
26472760
PHB_HUMANPHBphysical
26472760
PHB2_HUMANPHB2physical
26472760
RBM48_HUMANRBM48physical
26627737

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 ARMC7_HUMAN

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Related Literatures of Post-Translational Modification

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