F162A_HUMAN - dbPTM
F162A_HUMAN - PTM Information in dbPTM
Basic Information of Protein
UniProt ID F162A_HUMAN
UniProt AC Q96A26
Protein Name Protein FAM162A
Gene Name FAM162A
Organism Homo sapiens (Human).
Sequence Length 154
Subcellular Localization Membrane
Single-pass membrane protein . Mitochondrion .
Protein Description Proposed to be involved in regulation of apoptosis; the exact mechanism may differ between cell types/tissues. May be involved in hypoxia-induced cell death of transformed cells implicating cytochrome C release and caspase activation (such as CASP9) and inducing mitochondrial permeability transition. May be involved in hypoxia-induced cell death of neuronal cells probably by promoting release of AIFM1 from mitochondria to cytoplasm and its translocation to the nucleus; however, the involvement of caspases has been reported conflictingly..
Protein Sequence MGSLSGLRLAAGSCFRLCERDVSSSLRLTRSSDLKRINGFCTKPQESPGAPSRTYNRVPLHKPTDWQKKILIWSGRFKKEDEIPETVSLEMLDAAKNKMRVKISYLMIALTVVGCIFMVIEGKKAAQRHETLTSLNLEKKARLKEEAAMKAKTE
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
3Phosphorylation-----MGSLSGLRLA
-----CCCCHHHHHH
20.3324043423
5Phosphorylation---MGSLSGLRLAAG
---CCCCHHHHHHHC
37.1624719451
13PhosphorylationGLRLAAGSCFRLCER
HHHHHHCHHHHHHHC
12.8324719451
47PhosphorylationFCTKPQESPGAPSRT
CCCCCCCCCCCCCCC
24.3225849741
62AcetylationYNRVPLHKPTDWQKK
CCCCCCCCCCCHHHH
58.2425953088
62MalonylationYNRVPLHKPTDWQKK
CCCCCCCCCCCHHHH
58.2426320211
62UbiquitinationYNRVPLHKPTDWQKK
CCCCCCCCCCCHHHH
58.24-
64PhosphorylationRVPLHKPTDWQKKIL
CCCCCCCCCHHHHEE
55.4624719451
682-HydroxyisobutyrylationHKPTDWQKKILIWSG
CCCCCHHHHEEEEEC
37.21-
692-HydroxyisobutyrylationKPTDWQKKILIWSGR
CCCCHHHHEEEEECC
27.87-
74PhosphorylationQKKILIWSGRFKKED
HHHEEEEECCCCCCC
17.07-
79UbiquitinationIWSGRFKKEDEIPET
EEECCCCCCCCCCCC
68.6221906983
91SulfoxidationPETVSLEMLDAAKNK
CCCEEHHHHHHHCHH
5.0728465586
962-HydroxyisobutyrylationLEMLDAAKNKMRVKI
HHHHHHHCHHHHHHH
59.84-
96UbiquitinationLEMLDAAKNKMRVKI
HHHHHHHCHHHHHHH
59.8421906983
98UbiquitinationMLDAAKNKMRVKISY
HHHHHCHHHHHHHHH
27.63983
131PhosphorylationKAAQRHETLTSLNLE
HHHHHHHHHHHCCHH
29.2528122231
133PhosphorylationAQRHETLTSLNLEKK
HHHHHHHHHCCHHHH
38.2928122231
134PhosphorylationQRHETLTSLNLEKKA
HHHHHHHHCCHHHHH
20.5524719451
1392-HydroxyisobutyrylationLTSLNLEKKARLKEE
HHHCCHHHHHHHHHH
55.70-
139UbiquitinationLTSLNLEKKARLKEE
HHHCCHHHHHHHHHH
55.7021906983
139MalonylationLTSLNLEKKARLKEE
HHHCCHHHHHHHHHH
55.7032601280
140UbiquitinationTSLNLEKKARLKEEA
HHCCHHHHHHHHHHH
29.39-

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 F162A_HUMAN !!

Functions of PTM Sites
Modified Location Modified Residue Modification Function Reference

Oops, there are no descriptions of PTM sites of F162A_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 F162A_HUMAN !!

Protein-Protein Interaction
Interacting Protein Gene Name Interaction Type PPI Reference Domain-Domain Interactions
SRRT_HUMANSRRTphysical
22939629
TXTP_HUMANSLC25A1physical
22939629
CAVN1_HUMANPTRFphysical
22939629
VDAC2_HUMANVDAC2physical
22939629
RM22_HUMANMRPL22physical
22939629
RMD3_HUMANRMDN3physical
22939629
TM9S4_HUMANTM9SF4physical
22939629
SSRG_HUMANSSR3physical
22939629
HACL1_HUMANHACL1physical
22939629
IWS1_HUMANIWS1physical
22939629
HS90A_HUMANHSP90AA1physical
16698020

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 F162A_HUMAN

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Related Literatures of Post-Translational Modification

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