TRM7_HUMAN - dbPTM
TRM7_HUMAN - PTM Information in dbPTM
Basic Information of Protein
UniProt ID TRM7_HUMAN
UniProt AC Q9UET6
Protein Name Putative tRNA (cytidine(32)/guanosine(34)-2'-O)-methyltransferase {ECO:0000255|HAMAP-Rule:MF_03162}
Gene Name FTSJ1 {ECO:0000255|HAMAP-Rule:MF_03162}
Organism Homo sapiens (Human).
Sequence Length 329
Subcellular Localization Cytoplasm .
Protein Description Methylates the 2'-O-ribose of nucleotides at positions 32 and 34 of the tRNA anticodon loop of substrate tRNAs..
Protein Sequence MGRTSKDKRDVYYRLAKENGWRARSAFKLLQLDKEFQLFQGVTRAVDLCAAPGSWSQVLSQKIGGQGSGHVVAVDLQAMAPLPGVVQIQGDITQLSTAKEIIQHFKGCPADLVVCDGAPDVTGLHDVDEYMQAQLLLAALNIATHVLKPGGCFVAKIFRGRDVTLLYSQLQVFFSSVLCAKPRSSRNSSIEAFAVCQGYDPPEGFIPDLSKPLLDHSYDPDFNQLDGPTRIIVPFVTCGDLSSYDSDRSYPLDLEGGSEYKYTPPTQPPISPPYQEACTLKRKGQLAKEIRPQDCPISRVDTFPQPLAAPQCHTLLAPEMEDNEMSCSP
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
12PhosphorylationSKDKRDVYYRLAKEN
CCCHHHHHHHHHHHH
-
28UbiquitinationWRARSAFKLLQLDKE
CCHHHHHHHHHHCHH
-
34UbiquitinationFKLLQLDKEFQLFQG
HHHHHHCHHHHHHHC
21890473
43PhosphorylationFQLFQGVTRAVDLCA
HHHHHCCHHHHHHHC
27251275
164PhosphorylationIFRGRDVTLLYSQLQ
ECCCCCCEEEHHHHH
22115753
167PhosphorylationGRDVTLLYSQLQVFF
CCCCEEEHHHHHHHH
22115753
168PhosphorylationRDVTLLYSQLQVFFS
CCCEEEHHHHHHHHH
22115753
175PhosphorylationSQLQVFFSSVLCAKP
HHHHHHHHHHHCCCC
22115753
176PhosphorylationQLQVFFSSVLCAKPR
HHHHHHHHHHCCCCC
22115753
210PhosphorylationEGFIPDLSKPLLDHS
CCCCCCCCCCCCCCC
24719451
217 (in isoform 2)Phosphorylation-25159151
217PhosphorylationSKPLLDHSYDPDFNQ
CCCCCCCCCCCCHHH
25159151
258PhosphorylationPLDLEGGSEYKYTPP
CCCCCCCCCCCCCCC
29978859
260PhosphorylationDLEGGSEYKYTPPTQ
CCCCCCCCCCCCCCC
18669648
261SumoylationLEGGSEYKYTPPTQP
CCCCCCCCCCCCCCC
-
261UbiquitinationLEGGSEYKYTPPTQP
CCCCCCCCCCCCCCC
-
262PhosphorylationEGGSEYKYTPPTQPP
CCCCCCCCCCCCCCC
25159151
263PhosphorylationGGSEYKYTPPTQPPI
CCCCCCCCCCCCCCC
28796482
266PhosphorylationEYKYTPPTQPPISPP
CCCCCCCCCCCCCCC
28796482
271PhosphorylationPPTQPPISPPYQEAC
CCCCCCCCCCHHHHH
25159151
274PhosphorylationQPPISPPYQEACTLK
CCCCCCCHHHHHCHH
21712546
279PhosphorylationPPYQEACTLKRKGQL
CCHHHHHCHHHCCCH
25159151
281MethylationYQEACTLKRKGQLAK
HHHHHCHHHCCCHHH
-
288UbiquitinationKRKGQLAKEIRPQDC
HHCCCHHHHCCCCCC
-
298PhosphorylationRPQDCPISRVDTFPQ
CCCCCCCCCCCCCCC
26074081
302PhosphorylationCPISRVDTFPQPLAA
CCCCCCCCCCCCCCC
20068231
314PhosphorylationLAAPQCHTLLAPEME
CCCCCCCCEECCCCC
20068231
326PhosphorylationEMEDNEMSCSP----
CCCCCCCCCCC----
25159151
328PhosphorylationEDNEMSCSP------
CCCCCCCCC------
25159151

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 TRM7_HUMAN !!

Functions of PTM Sites
Modified Location Modified Residue Modification Function Reference

Oops, there are no descriptions of PTM sites of TRM7_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 TRM7_HUMAN !!

Protein-Protein Interaction
Interacting Protein Gene Name Interaction Type PPI Reference Domain-Domain Interactions
A4_HUMANAPPphysical
21832049
WDR6_HUMANWDR6physical
26344197
DYSF_HUMANDYSFphysical
26496610
CDC37_HUMANCDC37physical
26496610
WDR6_HUMANWDR6physical
26496610
IBTK_HUMANIBTKphysical
26496610
SIR6_HUMANSIRT6physical
26496610
GNL3L_HUMANGNL3Lphysical
26496610
MRM1_HUMANMRM1physical
26496610
ZFP91_HUMANZFP91physical
26496610
AROS_HUMANRPS19BP1physical
26496610

Drug and Disease Associations
Kegg Disease
There are no disease associations of PTM sites.
OMIM Disease
309549Mental retardation, X-linked 44 (MRX44)
Kegg Drug
There are no disease associations of PTM sites.
DrugBank
There are no disease associations of PTM sites.
Regulatory Network of TRM7_HUMAN

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Related Literatures of Post-Translational Modification

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