NDUF5_HUMAN - dbPTM
NDUF5_HUMAN - PTM Information in dbPTM
Basic Information of Protein
UniProt ID NDUF5_HUMAN
UniProt AC Q5TEU4
Protein Name Arginine-hydroxylase NDUFAF5, mitochondrial {ECO:0000305}
Gene Name NDUFAF5 {ECO:0000312|HGNC:HGNC:15899}
Organism Homo sapiens (Human).
Sequence Length 345
Subcellular Localization Mitochondrion inner membrane . Peripherally localized on the matrix face of the mitochondrial inner membrane.
Protein Description Arginine hydroxylase involved in the assembly of mitochondrial NADH:ubiquinone oxidoreductase complex (complex I, MT-ND1) at early stages. [PubMed: 18940309]
Protein Sequence MLRPAGLWRLCRRPWAARVPAENLGRREVTSGVSPRGSTSPRTLNIFDRDLKRKQKNWAARQPEPTKFDYLKEEVGSRIADRVYDIPRNFPLALDLGCGRGYIAQYLNKETIGKFFQADIAENALKNSSETEIPTVSVLADEEFLPFKENTFDLVVSSLSLHWVNDLPRALEQIHYILKPDGVFIGAMFGGDTLYELRCSLQLAETEREGGFSPHISPFTAVNDLGHLLGRAGFNTLTVDTDEIQVNYPGMFELMEDLQGMGESNCAWNRKALLHRDTMLAAAAVYREMYRNEDGSVPATYQIYYMIGWKYHESQARPAERGSATVSFGELGKINNLMPPGKKSQ
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
30PhosphorylationNLGRREVTSGVSPRG
HCCCCCCCCCCCCCC
18.27-
31PhosphorylationLGRREVTSGVSPRGS
CCCCCCCCCCCCCCC
42.2322817900
34PhosphorylationREVTSGVSPRGSTSP
CCCCCCCCCCCCCCC
16.6522817900
67AcetylationARQPEPTKFDYLKEE
HCCCCCCCHHHHHHH
47.137683747
72UbiquitinationPTKFDYLKEEVGSRI
CCCHHHHHHHHHHHH
45.6724816145
77PhosphorylationYLKEEVGSRIADRVY
HHHHHHHHHHHHHHC
26.20-
84PhosphorylationSRIADRVYDIPRNFP
HHHHHHHCCCCCCCC
14.7325839225
109UbiquitinationYIAQYLNKETIGKFF
HHHHHCCHHHHHHHH
54.3522817900
109 (in isoform 1)Ubiquitination-54.3521890473
114UbiquitinationLNKETIGKFFQADIA
CCHHHHHHHHHHHHH
38.8722817900
286PhosphorylationMLAAAAVYREMYRNE
HHHHHHHHHHHHHCC
8.98-
290PhosphorylationAAVYREMYRNEDGSV
HHHHHHHHHCCCCCC
12.92-

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 NDUF5_HUMAN !!

Functions of PTM Sites
Modified Location Modified Residue Modification Function Reference

Oops, there are no descriptions of PTM sites of NDUF5_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 NDUF5_HUMAN !!

Protein-Protein Interaction
Interacting Protein Gene Name Interaction Type PPI Reference Domain-Domain Interactions
PPM1E_HUMANPPM1Ephysical
26186194
XRCC2_HUMANXRCC2physical
26186194
RA51D_HUMANRAD51Dphysical
26186194
HBB_HUMANHBBphysical
26186194
NDUF5_HUMANNDUFAF5physical
27499296
BOLA3_HUMANBOLA3physical
27499296
NDUF8_HUMANC17orf89physical
27499296
STAR7_HUMANSTARD7physical
27499296
ECH1_HUMANECH1physical
27499296
ATP5E_HUMANATP5Ephysical
27499296
ACPM_HUMANNDUFAB1physical
27499296
ATPG_HUMANATP5C1physical
27499296
XRCC2_HUMANXRCC2physical
28514442
HBB_HUMANHBBphysical
28514442
RA51D_HUMANRAD51Dphysical
28514442
PPM1E_HUMANPPM1Ephysical
28514442
FPPS_HUMANFDPSphysical
28514442
CGL_HUMANCTHphysical
28514442

Drug and Disease Associations
Kegg Disease
H00473 Mitochondrial respiratory chain deficiencies (MRCD), including: Mitochondrial complex I deficiency (
OMIM Disease
252010Mitochondrial complex I deficiency (MT-C1D)
256000Leigh syndrome (LS)
Kegg Drug
There are no disease associations of PTM sites.
DrugBank
There are no disease associations of PTM sites.
Regulatory Network of NDUF5_HUMAN

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Related Literatures of Post-Translational Modification

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