RM03_HUMAN - dbPTM
RM03_HUMAN - PTM Information in dbPTM
Basic Information of Protein
UniProt ID RM03_HUMAN
UniProt AC P09001
Protein Name 39S ribosomal protein L3, mitochondrial
Gene Name MRPL3
Organism Homo sapiens (Human).
Sequence Length 348
Subcellular Localization Mitochondrion .
Protein Description
Protein Sequence MPGWRLLTQVGAQVLGRLGDGLGAALGPGNRTHIWLFVRGLHGKSGTWWDEHLSEENVPFIKQLVSDEDKAQLASKLCPLKDEPWPIHPWEPGSFRVGLIALKLGMMPLWTKDGQKHVVTLLQVQDCHVLKYTSKENCNGKMATLSVGGKTVSRFRKATSILEFYRELGLPPKQTVKIFNITDNAAIKPGTPLYAAHFRPGQYVDVTAKTIGKGFQGVMKRWGFKGQPATHGQTKTHRRPGAVATGDIGRVWPGTKMPGKMGNIYRTEYGLKVWRINTKHNIIYVNGSVPGHKNCLVKVKDSKLPAYKDLGKNLPFPTYFPDGDEEELPEDLYDENVCQPGAPSITFA
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
44UbiquitinationFVRGLHGKSGTWWDE
EEECCCCCCCCCHHH
34.6623503661
62UbiquitinationEENVPFIKQLVSDED
CCCCCHHHHHCCHHH
37.6522817900
70UbiquitinationQLVSDEDKAQLASKL
HHCCHHHHHHHHHHH
35.6629967540
76UbiquitinationDKAQLASKLCPLKDE
HHHHHHHHHCCCCCC
48.8027667366
81AcetylationASKLCPLKDEPWPIH
HHHHCCCCCCCCCCC
45.2326051181
111PhosphorylationLGMMPLWTKDGQKHV
HCCCEEECCCCCEEE
27.2620068231
112UbiquitinationGMMPLWTKDGQKHVV
CCCEEECCCCCEEEE
48.5629967540
131AcetylationVQDCHVLKYTSKENC
EECCEEEEEECCCCC
45.4526051181
150AcetylationATLSVGGKTVSRFRK
EEEEECCEEHHHHHH
39.5627452117
150UbiquitinationATLSVGGKTVSRFRK
EEEEECCEEHHHHHH
39.5629967540
153PhosphorylationSVGGKTVSRFRKATS
EECCEEHHHHHHHHH
30.82-
157UbiquitinationKTVSRFRKATSILEF
EEHHHHHHHHHHHHH
53.9924816145
159PhosphorylationVSRFRKATSILEFYR
HHHHHHHHHHHHHHH
21.2330108239
160PhosphorylationSRFRKATSILEFYRE
HHHHHHHHHHHHHHH
30.0030108239
188UbiquitinationITDNAAIKPGTPLYA
ECCCCCCCCCCCEEE
32.4429967540
209UbiquitinationQYVDVTAKTIGKGFQ
CEEEEEEEECCCCHH
31.1729967540
213UbiquitinationVTAKTIGKGFQGVMK
EEEEECCCCHHHHHH
53.34-
235UbiquitinationPATHGQTKTHRRPGA
CCCCCCCCCCCCCCC
34.1529967540
260UbiquitinationPGTKMPGKMGNIYRT
CCCCCCCCCCCEEEE
37.45-
265PhosphorylationPGKMGNIYRTEYGLK
CCCCCCEEEECCEEE
18.58-
303UbiquitinationLVKVKDSKLPAYKDL
EEEECCCCCCCHHCC
69.4929967540
308UbiquitinationDSKLPAYKDLGKNLP
CCCCCCHHCCCCCCC
48.8929967540

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 RM03_HUMAN !!

Functions of PTM Sites
Modified Location Modified Residue Modification Function Reference

Oops, there are no descriptions of PTM sites of RM03_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 RM03_HUMAN !!

Protein-Protein Interaction
Interacting Protein Gene Name Interaction Type PPI Reference Domain-Domain Interactions
A4_HUMANAPPphysical
21832049
RM09_HUMANMRPL9physical
22939629
RM04_HUMANMRPL4physical
22939629
RM12_HUMANMRPL12physical
22939629
RT09_HUMANMRPS9physical
22939629
RM39_HUMANMRPL39physical
22939629
RM23_HUMANMRPL23physical
22939629
RM13_HUMANMRPL13physical
22939629
RM17_HUMANMRPL17physical
22939629
RM10_HUMANMRPL10physical
22939629
RM46_HUMANMRPL46physical
22939629
RM42_HUMANMRPL42physical
22939629
RM55_HUMANMRPL55physical
22939629
RM52_HUMANMRPL52physical
22939629
RM19_HUMANMRPL19physical
22939629
RM41_HUMANMRPL41physical
22939629
RS18_HUMANRPS18physical
22939629
RS15_HUMANRPS15physical
22939629
RM15_HUMANMRPL15physical
26344197
RM37_HUMANMRPL37physical
26344197
RM38_HUMANMRPL38physical
26344197
RM09_HUMANMRPL9physical
26344197
RS14_HUMANRPS14physical
26344197
RS5_HUMANRPS5physical
26344197
EFTU_HUMANTUFMphysical
26344197

Drug and Disease Associations
Kegg Disease
There are no disease associations of PTM sites.
OMIM Disease
614582Combined oxidative phosphorylation deficiency 9 (COXPD9)
Kegg Drug
There are no disease associations of PTM sites.
DrugBank
There are no disease associations of PTM sites.
Regulatory Network of RM03_HUMAN

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Related Literatures of Post-Translational Modification

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