SYRM_HUMAN - dbPTM
SYRM_HUMAN - PTM Information in dbPTM
Basic Information of Protein
UniProt ID SYRM_HUMAN
UniProt AC Q5T160
Protein Name Probable arginine--tRNA ligase, mitochondrial
Gene Name RARS2
Organism Homo sapiens (Human).
Sequence Length 578
Subcellular Localization Mitochondrion matrix.
Protein Description
Protein Sequence MACGFRRAIACQLSRVLNLPPENLITSISAVPISQKEEVADFQLSVDSLLEKDNDHSRPDIQVQAKRLAEKLRCDTVVSEISTGQRTVNFKINRELLTKTVLQQVIEDGSKYGLKSELFSGLPQKKIVVEFSSPNVAKKFHVGHLRSTIIGNFIANLKEALGHQVIRINYLGDWGMQFGLLGTGFQLFGYEEKLQSNPLQHLFEVYVQVNKEAADDKSVAKAAQEFFQRLELGDVQALSLWQKFRDLSIEEYIRVYKRLGVYFDEYSGESFYREKSQEVLKLLESKGLLLKTIKGTAVVDLSGNGDPSSICTVMRSDGTSLYATRDLAAAIDRMDKYNFDTMIYVTDKGQKKHFQQVFQMLKIMGYDWAERCQHVPFGVVQGMKTRRGDVTFLEDVLNEIQLRMLQNMASIKTTKELKNPQETAERVGLAALIIQDFKGLLLSDYKFSWDRVFQSRGDTGVFLQYTHARLHSLEETFGCGYLNDFNTACLQEPQSVSILQHLLRFDEVLYKSSQDFQPRHIVSYLLTLSHLAAVAHKTLQIKDSPPEVAGARLHLFKAVRSVLANGMKLLGITPVCRM
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
45PhosphorylationEVADFQLSVDSLLEK
HHHCEECCHHHHHHH
17.0729083192
48PhosphorylationDFQLSVDSLLEKDND
CEECCHHHHHHHCCC
32.4724719451
57O-linked_GlycosylationLEKDNDHSRPDIQVQ
HHHCCCCCCCCHHHH
48.6630379171
66UbiquitinationPDIQVQAKRLAEKLR
CCHHHHHHHHHHHHC
30.74-
99UbiquitinationINRELLTKTVLQQVI
ECHHHHHHHHHHHHH
36.28-
112PhosphorylationVIEDGSKYGLKSELF
HHHCCHHCCCCHHHC
29.4128842319
115UbiquitinationDGSKYGLKSELFSGL
CCHHCCCCHHHCCCC
37.2121890473
116PhosphorylationGSKYGLKSELFSGLP
CHHCCCCHHHCCCCC
44.5728842319
125AcetylationLFSGLPQKKIVVEFS
HCCCCCCCEEEEEEC
42.3925953088
1252-HydroxyisobutyrylationLFSGLPQKKIVVEFS
HCCCCCCCEEEEEEC
42.39-
138AcetylationFSSPNVAKKFHVGHL
ECCCCHHHHCCCHHH
52.2525953088
138SuccinylationFSSPNVAKKFHVGHL
ECCCCHHHHCCCHHH
52.2523954790
138MalonylationFSSPNVAKKFHVGHL
ECCCCHHHHCCCHHH
52.2526320211
139AcetylationSSPNVAKKFHVGHLR
CCCCHHHHCCCHHHH
30.8525953088
221MalonylationADDKSVAKAAQEFFQ
CCCHHHHHHHHHHHH
41.9426320211
285PhosphorylationEVLKLLESKGLLLKT
HHHHHHHHCCCEEEE
31.8029396449
312PhosphorylationGDPSSICTVMRSDGT
CCHHHCEEEECCCCC
18.7022210691
346PhosphorylationFDTMIYVTDKGQKKH
CCEEEEECCCCCHHH
18.28-
352MalonylationVTDKGQKKHFQQVFQ
ECCCCCHHHHHHHHH
41.5926320211
362AcetylationQQVFQMLKIMGYDWA
HHHHHHHHHHCCCHH
25.8812655243
410PhosphorylationRMLQNMASIKTTKEL
HHHHHHHCCCCHHHH
17.5330631047
446UbiquitinationGLLLSDYKFSWDRVF
CHHHCCCCCCHHHHH
37.6021890473
511MalonylationRFDEVLYKSSQDFQP
HHHHHHHHCCCCCCH
39.2026320211
542MalonylationAHKTLQIKDSPPEVA
HHHHCCCCCCCHHHC
38.9126320211
557AcetylationGARLHLFKAVRSVLA
HHHHHHHHHHHHHHH
52.9425953088
568AcetylationSVLANGMKLLGITPV
HHHHHCHHHCCCCCC
41.79-
573PhosphorylationGMKLLGITPVCRM--
CHHHCCCCCCCCC--
14.10-

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 SYRM_HUMAN !!

Functions of PTM Sites
Modified Location Modified Residue Modification Function Reference

Oops, there are no descriptions of PTM sites of SYRM_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 SYRM_HUMAN !!

Protein-Protein Interaction
Interacting Protein Gene Name Interaction Type PPI Reference Domain-Domain Interactions
CPSM_HUMANCPS1physical
26186194
AT12A_HUMANATP12Aphysical
26186194
RRF2M_HUMANGFM2physical
26186194
PREP_HUMANPITRM1physical
26186194
GLSK_HUMANGLSphysical
26186194
PDPR_HUMANPDPRphysical
26186194
PCCA_HUMANPCCAphysical
26186194
PPCEL_HUMANPREPLphysical
26186194
PXDC2_HUMANPLXDC2physical
26186194
MCCA_HUMANMCCC1physical
26186194
CLN3_HUMANCLN3physical
26186194
ARL8A_HUMANARL8Aphysical
26186194
SYAM_HUMANAARS2physical
26186194
NSDHL_HUMANNSDHLphysical
26186194
RRF2M_HUMANGFM2physical
28514442
AT12A_HUMANATP12Aphysical
28514442
PREP_HUMANPITRM1physical
28514442
PDPR_HUMANPDPRphysical
28514442
CPSM_HUMANCPS1physical
28514442
ARL8A_HUMANARL8Aphysical
28514442
PCCA_HUMANPCCAphysical
28514442

Drug and Disease Associations
Kegg Disease
There are no disease associations of PTM sites.
OMIM Disease
611523Pontocerebellar hypoplasia 6 (PCH6)
Kegg Drug
There are no disease associations of PTM sites.
DrugBank
There are no disease associations of PTM sites.
Regulatory Network of SYRM_HUMAN

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Related Literatures of Post-Translational Modification

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