PLCB_HUMAN - dbPTM
PLCB_HUMAN - PTM Information in dbPTM
Basic Information of Protein
UniProt ID PLCB_HUMAN
UniProt AC O15120
Protein Name 1-acyl-sn-glycerol-3-phosphate acyltransferase beta
Gene Name AGPAT2
Organism Homo sapiens (Human).
Sequence Length 278
Subcellular Localization Endoplasmic reticulum membrane
Multi-pass membrane protein .
Protein Description Converts lysophosphatidic acid (LPA) into phosphatidic acid by incorporating an acyl moiety at the sn-2 position of the glycerol backbone..
Protein Sequence MELWPCLAAALLLLLLLVQLSRAAEFYAKVALYCALCFTVSAVASLVCLLRHGGRTVENMSIIGWFVRSFKYFYGLRFEVRDPRRLQEARPCVIVSNHQSILDMMGLMEVLPERCVQIAKRELLFLGPVGLIMYLGGVFFINRQRSSTAMTVMADLGERMVRENLKVWIYPEGTRNDNGDLLPFKKGAFYLAVQAQVPIVPVVYSSFSSFYNTKKKFFTSGTVTVQVLEAIPTSGLTAADVPALVDTCHRAMRTTFLHISKTPQENGATAGSGVQPAQ
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
71UbiquitinationGWFVRSFKYFYGLRF
HHHHHHHHHHHCCEE
35.38-
72PhosphorylationWFVRSFKYFYGLRFE
HHHHHHHHHHCCEEE
10.467331443
74PhosphorylationVRSFKYFYGLRFEVR
HHHHHHHHCCEEEEC
16.507331453
146PhosphorylationFFINRQRSSTAMTVM
EEEECCCCCCCHHHC
24.5725954137
147PhosphorylationFINRQRSSTAMTVMA
EEECCCCCCCHHHCH
23.5225954137
148PhosphorylationINRQRSSTAMTVMAD
EECCCCCCCHHHCHH
22.9925954137
151PhosphorylationQRSSTAMTVMADLGE
CCCCCCHHHCHHHHH
12.5025954137
166UbiquitinationRMVRENLKVWIYPEG
HHHHHCCEEEEECCC
47.2921890473
167 (in isoform 1)Ubiquitination-4.1821890473
185UbiquitinationNGDLLPFKKGAFYLA
CCCEECCCCCCEEEE
48.6421890473
186 (in isoform 1)Ubiquitination-56.7121890473
186UbiquitinationGDLLPFKKGAFYLAV
CCEECCCCCCEEEEE
56.71-
220PhosphorylationTKKKFFTSGTVTVQV
CCCCEECCCEEEEEE
27.5846160457
224PhosphorylationFFTSGTVTVQVLEAI
EECCCEEEEEEEEEC
12.6922210691
229 (in isoform 2)Ubiquitination-45.7721906983
233PhosphorylationQVLEAIPTSGLTAAD
EEEEECCCCCCCHHH
29.3446160469
234PhosphorylationVLEAIPTSGLTAADV
EEEECCCCCCCHHHH
26.8422210691
237PhosphorylationAIPTSGLTAADVPAL
ECCCCCCCHHHHHHH
24.2746160475
261UbiquitinationTTFLHISKTPQENGA
HHHEEEECCCCCCCC
64.722190698
262PhosphorylationTFLHISKTPQENGAT
HHEEEECCCCCCCCC
24.3450563993
262 (in isoform 1)Ubiquitination-24.3421890473
272PhosphorylationENGATAGSGVQPAQ-
CCCCCCCCCCCCCC-
33.0750563999

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 PLCB_HUMAN !!

Functions of PTM Sites
Modified Location Modified Residue Modification Function Reference

Oops, there are no descriptions of PTM sites of PLCB_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 PLCB_HUMAN !!

Protein-Protein Interaction
Interacting Protein Gene Name Interaction Type PPI Reference Domain-Domain Interactions
PHF11_HUMANPHF11physical
21988832
S23A2_HUMANSLC23A2physical
21988832
GUAA_HUMANGMPSphysical
21988832
ANR28_HUMANANKRD28physical
21988832
PHRF1_HUMANPHRF1physical
21988832
H13_HUMANHIST1H1Dphysical
26186194
H13_HUMANHIST1H1Dphysical
28514442
INTU_HUMANINTUphysical
27173435

Drug and Disease Associations
Kegg Disease
H00419 Congenital generalized lipodystrophy (CGL)
OMIM Disease
608594Congenital generalized lipodystrophy 1 (CGL1)
Kegg Drug
There are no disease associations of PTM sites.
DrugBank
There are no disease associations of PTM sites.
Regulatory Network of PLCB_HUMAN

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Related Literatures of Post-Translational Modification

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