CXCR2_HUMAN - dbPTM
CXCR2_HUMAN - PTM Information in dbPTM
Basic Information of Protein
UniProt ID CXCR2_HUMAN
UniProt AC P25025
Protein Name C-X-C chemokine receptor type 2
Gene Name CXCR2
Organism Homo sapiens (Human).
Sequence Length 360
Subcellular Localization Cell membrane
Multi-pass membrane protein.
Protein Description Receptor for interleukin-8 which is a powerful neutrophil chemotactic factor. Binding of IL-8 to the receptor causes activation of neutrophils. This response is mediated via a G-protein that activates a phosphatidylinositol-calcium second messenger system. Binds to IL-8 with high affinity. Also binds with high affinity to CXCL3, GRO/MGSA and NAP-2..
Protein Sequence MEDFNMESDSFEDFWKGEDLSNYSYSSTLPPFLLDAAPCEPESLEINKYFVVIIYALVFLLSLLGNSLVMLVILYSRVGRSVTDVYLLNLALADLLFALTLPIWAASKVNGWIFGTFLCKVVSLLKEVNFYSGILLLACISVDRYLAIVHATRTLTQKRYLVKFICLSIWGLSLLLALPVLLFRRTVYSSNVSPACYEDMGNNTANWRMLLRILPQSFGFIVPLLIMLFCYGFTLRTLFKAHMGQKHRAMRVIFAVVLIFLLCWLPYNLVLLADTLMRTQVIQETCERRNHIDRALDATEILGILHSCLNPLIYAFIGQKFRHGLLKILAIHGLISKDSLPKDSRPSFVGSSSGHTSTTL
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
22N-linked_GlycosylationWKGEDLSNYSYSSTL
HCCCCCCCCCCCCCC
36.75UniProtKB CARBOHYD
76PhosphorylationVMLVILYSRVGRSVT
HHHHHHHHCCCCCHH
19.6224719451
123PhosphorylationTFLCKVVSLLKEVNF
HHHHHHHHHHHHCCC
30.8524719451
131PhosphorylationLLKEVNFYSGILLLA
HHHHCCCCCHHHHHH
10.7722210691
145PhosphorylationACISVDRYLAIVHAT
HHHCHHHHHHHHHHH
8.9522210691
154PhosphorylationAIVHATRTLTQKRYL
HHHHHHCCCCCHHHH
29.7829449344
156PhosphorylationVHATRTLTQKRYLVK
HHHHCCCCCHHHHHH
31.2822210691
160PhosphorylationRTLTQKRYLVKFICL
CCCCCHHHHHHHHHH
23.9229449344
234PhosphorylationMLFCYGFTLRTLFKA
HHHHHHHHHHHHHHH
15.8024719451
336PhosphorylationLAIHGLISKDSLPKD
HHHCCCCCCCCCCCC
35.1424719451
339PhosphorylationHGLISKDSLPKDSRP
CCCCCCCCCCCCCCC
50.7528450419
344PhosphorylationKDSLPKDSRPSFVGS
CCCCCCCCCCCCCCC
52.8223312004
347PhosphorylationLPKDSRPSFVGSSSG
CCCCCCCCCCCCCCC
31.3022817900
351PhosphorylationSRPSFVGSSSGHTST
CCCCCCCCCCCCCCC
18.9422817900
352PhosphorylationRPSFVGSSSGHTSTT
CCCCCCCCCCCCCCC
34.1222817900
353PhosphorylationPSFVGSSSGHTSTTL
CCCCCCCCCCCCCCC
35.9722817900
358PhosphorylationSSSGHTSTTL-----
CCCCCCCCCC-----
33.0223312004
359PhosphorylationSSGHTSTTL------
CCCCCCCCC------
30.1823312004

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 CXCR2_HUMAN !!

Functions of PTM Sites
Modified Location Modified Residue Modification Function Reference

Oops, there are no descriptions of PTM sites of CXCR2_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 CXCR2_HUMAN !!

Protein-Protein Interaction
Interacting Protein Gene Name Interaction Type PPI Reference Domain-Domain Interactions
RFIP2_HUMANRAB11FIP2physical
15004234
MYO5B_HUMANMYO5Bphysical
15004234
CXCR2_HUMANCXCR2physical
12888558
TF3A_HUMANGTF3Aphysical
11170396
ARRB1_HUMANARRB1physical
11170396
IL8_HUMANCXCL8physical
9464567
RGS12_RATRgs12physical
9651375
F10A1_HUMANST13physical
11751889

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
D08984 Reparixin (USAN/INN)
D10075 Navarixin (USAN); Navarixin hydrate
D10332 Elubrixin (USAN)
D10387 Danirixin (USAN/INN)
D10420 Elubrixin tosylate (USAN)
DrugBank
There are no disease associations of PTM sites.
Regulatory Network of CXCR2_HUMAN

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Related Literatures of Post-Translational Modification

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