1C07_HUMAN - dbPTM
1C07_HUMAN - PTM Information in dbPTM
Basic Information of Protein
UniProt ID 1C07_HUMAN
UniProt AC P10321
Protein Name HLA class I histocompatibility antigen, Cw-7 alpha chain
Gene Name HLA-C
Organism Homo sapiens (Human).
Sequence Length 366
Subcellular Localization Membrane
Single-pass type I membrane protein.
Protein Description Involved in the presentation of foreign antigens to the immune system..
Protein Sequence MRVMAPRALLLLLSGGLALTETWACSHSMRYFDTAVSRPGRGEPRFISVGYVDDTQFVRFDSDAASPRGEPRAPWVEQEGPEYWDRETQKYKRQAQADRVSLRNLRGYYNQSEDGSHTLQRMSGCDLGPDGRLLRGYDQSAYDGKDYIALNEDLRSWTAADTAAQITQRKLEAARAAEQLRAYLEGTCVEWLRRYLENGKETLQRAEPPKTHVTHHPLSDHEATLRCWALGFYPAEITLTWQRDGEDQTQDTELVETRPAGDGTFQKWAAVVVPSGQEQRYTCHMQHEGLQEPLTLSWEPSSQPTIPIMGIVAGLAVLVVLAVLGAVVTAMMCRRKSSGGKGGSCSQAACSNSAQGSDESLITCKA
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
188GlutathionylationRAYLEGTCVEWLRRY
HHHHHCHHHHHHHHH
3.7222555962

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 1C07_HUMAN !!

Functions of PTM Sites
Modified Location Modified Residue Modification Function Reference

Oops, there are no descriptions of PTM sites of 1C07_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 1C07_HUMAN !!

Protein-Protein Interaction
Interacting Protein Gene Name Interaction Type PPI Reference Domain-Domain Interactions
1C07_HUMANHLA-Cphysical
12794140
CD8A_HUMANCD8Aphysical
10809759
KI2L1_HUMANKIR2DL1physical
11163076
KI2L1_HUMANKIR2DL1physical
9768753
KI2L3_HUMANKIR2DL3physical
9768753
KI2S2_HUMANKIR2DL3physical
9768753
GRP78_HUMANHSPA5physical
7957306
YBOX1_HUMANYBX1physical
21988832
TANK_HUMANTANKphysical
21988832
TMG4_HUMANPRRG4physical
21988832
F213A_HUMANFAM213Aphysical
26186194
AT1A3_HUMANATP1A3physical
26186194
HLAF_HUMANHLA-Fphysical
26186194
1A02_HUMANHLA-Aphysical
26186194
1A03_HUMANHLA-Aphysical
26186194
1A01_HUMANHLA-Aphysical
26186194
1A26_HUMANHLA-Aphysical
26186194
HLAG_HUMANHLA-Gphysical
26186194
HLAE_HUMANHLA-Ephysical
26186194
SCAP_HUMANSCAPphysical
26186194
E2AK3_HUMANEIF2AK3physical
26186194
ARV1_HUMANARV1physical
26186194
NSDHL_HUMANNSDHLphysical
26186194
CNNM1_HUMANCNNM1physical
26186194
SCRB1_HUMANSCARB1physical
26186194
DJC16_HUMANDNAJC16physical
26186194
PMGT1_HUMANPOMGNT1physical
26186194
HMR1_HUMANMR1physical
26186194
UFSP2_HUMANUFSP2physical
26186194
NETO2_HUMANNETO2physical
26186194
NEK4_HUMANNEK4physical
26186194
TECT2_HUMANTCTN2physical
26186194
TIP_HUMANITFG1physical
26186194
ITA6_HUMANITGA6physical
26186194
TM223_HUMANTMEM223physical
26186194
FAM3C_HUMANFAM3Cphysical
26186194
MD2L2_HUMANMAD2L2physical
26186194
DNJC1_HUMANDNAJC1physical
26186194
TM206_HUMANTMEM206physical
26186194
B2MG_HUMANB2Mphysical
26186194
CISD2_HUMANCISD2physical
26186194
MTR1L_HUMANGPR50physical
26186194
LRFN3_HUMANLRFN3physical
26186194
1A02_HUMANHLA-Aphysical
28514442
1A03_HUMANHLA-Aphysical
28514442
1A01_HUMANHLA-Aphysical
28514442
1A26_HUMANHLA-Aphysical
28514442
HLAE_HUMANHLA-Ephysical
28514442
CNNM1_HUMANCNNM1physical
28514442
HLAF_HUMANHLA-Fphysical
28514442
UFSP2_HUMANUFSP2physical
28514442
MTR1L_HUMANGPR50physical
28514442
MD2L2_HUMANMAD2L2physical
28514442
ITA6_HUMANITGA6physical
28514442
B2MG_HUMANB2Mphysical
28514442
CISD2_HUMANCISD2physical
28514442
FAM3C_HUMANFAM3Cphysical
28514442
SCRB1_HUMANSCARB1physical
28514442
F213A_HUMANFAM213Aphysical
28514442
NEK4_HUMANNEK4physical
28514442
NETO2_HUMANNETO2physical
28514442
NGBR_HUMANNUS1physical
28514442
TECT2_HUMANTCTN2physical
28514442

Drug and Disease Associations
Kegg Disease
OMIM Disease
There are no disease associations of PTM sites.
Kegg Drug
DrugBank
There are no disease associations of PTM sites.
Regulatory Network of 1C07_HUMAN

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Related Literatures of Post-Translational Modification

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