CISD2_HUMAN - dbPTM
CISD2_HUMAN - PTM Information in dbPTM
Basic Information of Protein
UniProt ID CISD2_HUMAN
UniProt AC Q8N5K1
Protein Name CDGSH iron-sulfur domain-containing protein 2
Gene Name CISD2
Organism Homo sapiens (Human).
Sequence Length 135
Subcellular Localization Endoplasmic reticulum membrane
Single-pass membrane protein. Mitochondrion outer membrane
Single-pass membrane protein. According to PubMed:20010695, it mainly localizes to the endoplasmic reticulum. However, experiments in mouse showed that it mai
Protein Description Regulator of autophagy that contributes to antagonize BECN1-mediated cellular autophagy at the endoplasmic reticulum. Participates in the interaction of BCL2 with BECN1 and is required for BCL2-mediated depression of endoplasmic reticulum Ca(2+) stores during autophagy. Contributes to BIK-initiated autophagy, while it is not involved in BIK-dependent activation of caspases. Involved in life span control, probably via its function as regulator of autophagy..
Protein Sequence MVLESVARIVKVQLPAYLKRLPVPESITGFARLTVSEWLRLLPFLGVLALLGYLAVRPFLPKKKQQKDSLINLKIQKENPKVVNEINIEDLCLTKAAYCRCWRSKTFPACDGSHNKHNELTGDNVGPLILKKKEV
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
5Phosphorylation---MVLESVARIVKV
---CCHHHHHHHHHC
19.5430001349
192-HydroxyisobutyrylationVQLPAYLKRLPVPES
CHHHHHHHCCCCCCH
38.93-
19UbiquitinationVQLPAYLKRLPVPES
CHHHHHHHCCCCCCH
38.9321890473
34PhosphorylationITGFARLTVSEWLRL
HCCCHHCCHHHHHHH
19.2120068231
36PhosphorylationGFARLTVSEWLRLLP
CCHHCCHHHHHHHHH
20.1620068231
67UbiquitinationLPKKKQQKDSLINLK
CCCCHHCCCCHHCCE
46.9533845483
672-HydroxyisobutyrylationLPKKKQQKDSLINLK
CCCCHHCCCCHHCCE
46.95-
69PhosphorylationKKKQQKDSLINLKIQ
CCHHCCCCHHCCEEC
37.8827499020
74AcetylationKDSLINLKIQKENPK
CCCHHCCEECCCCCC
38.3123236377
74UbiquitinationKDSLINLKIQKENPK
CCCHHCCEECCCCCC
38.3133845483
742-HydroxyisobutyrylationKDSLINLKIQKENPK
CCCHHCCEECCCCCC
38.31-
74MalonylationKDSLINLKIQKENPK
CCCHHCCEECCCCCC
38.3126320211
81AcetylationKIQKENPKVVNEINI
EECCCCCCCCCCCCH
71.0926051181
81UbiquitinationKIQKENPKVVNEINI
EECCCCCCCCCCCCH
71.0933845483
92GlutathionylationEINIEDLCLTKAAYC
CCCHHHHHHHHHHHH
7.5922555962
95AcetylationIEDLCLTKAAYCRCW
HHHHHHHHHHHHHHH
20.3325953088
95UbiquitinationIEDLCLTKAAYCRCW
HHHHHHHHHHHHHHH
20.3321963094
104PhosphorylationAYCRCWRSKTFPACD
HHHHHHHCCCCCCCC
16.1423312004
105UbiquitinationYCRCWRSKTFPACDG
HHHHHHCCCCCCCCC
45.6833845483
106PhosphorylationCRCWRSKTFPACDGS
HHHHHCCCCCCCCCC
35.7826657352
116UbiquitinationACDGSHNKHNELTGD
CCCCCCCCCCCCCCC
42.2433845483
1312-HydroxyisobutyrylationNVGPLILKKKEV---
CCCCEEEEECCC---
55.60-
131UbiquitinationNVGPLILKKKEV---
CCCCEEEEECCC---
55.6033845483
131MethylationNVGPLILKKKEV---
CCCCEEEEECCC---
55.60-
131AcetylationNVGPLILKKKEV---
CCCCEEEEECCC---
55.6023236377
132UbiquitinationVGPLILKKKEV----
CCCEEEEECCC----
51.2024816145
132MethylationVGPLILKKKEV----
CCCEEEEECCC----
51.20-

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 CISD2_HUMAN !!

Functions of PTM Sites
Modified Location Modified Residue Modification Function Reference

Oops, there are no descriptions of PTM sites of CISD2_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 CISD2_HUMAN !!

Protein-Protein Interaction
Interacting Protein Gene Name Interaction Type PPI Reference Domain-Domain Interactions
BCL2_HUMANBCL2physical
20010695
A4_HUMANAPPphysical
21832049

Drug and Disease Associations
Kegg Disease
H00854 Wolfram syndrome (WFS); DIDMOAD syndrome
OMIM Disease
604928Wolfram syndrome 2 (WFS2)
Kegg Drug
There are no disease associations of PTM sites.
DrugBank
There are no disease associations of PTM sites.
Regulatory Network of CISD2_HUMAN

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Related Literatures of Post-Translational Modification

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