PHEX_HUMAN - dbPTM
PHEX_HUMAN - PTM Information in dbPTM
Basic Information of Protein
UniProt ID PHEX_HUMAN
UniProt AC P78562
Protein Name Phosphate-regulating neutral endopeptidase
Gene Name PHEX
Organism Homo sapiens (Human).
Sequence Length 749
Subcellular Localization Membrane
Single-pass type II membrane protein .
Protein Description Probably involved in bone and dentin mineralization and renal phosphate reabsorption..
Protein Sequence MEAETGSSVETGKKANRGTRIALVVFVGGTLVLGTILFLVSQGLLSLQAKQEYCLKPECIEAAAAILSKVNLSVDPCDNFFRFACDGWISNNPIPEDMPSYGVYPWLRHNVDLKLKELLEKSISRRRDTEAIQKAKILYSSCMNEKAIEKADAKPLLHILRHSPFRWPVLESNIGPEGVWSERKFSLLQTLATFRGQYSNSVFIRLYVSPDDKASNEHILKLDQATLSLAVREDYLDNSTEAKSYRDALYKFMVDTAVLLGANSSRAEHDMKSVLRLEIKIAEIMIPHENRTSEAMYNKMNISELSAMIPQFDWLGYIKKVIDTRLYPHLKDISPSENVVVRVPQYFKDLFRILGSERKKTIANYLVWRMVYSRIPNLSRRFQYRWLEFSRVIQGTTTLLPQWDKCVNFIESALPYVVGKMFVDVYFQEDKKEMMEELVEGVRWAFIDMLEKENEWMDAGTKRKAKEKARAVLAKVGYPEFIMNDTHVNEDLKAIKFSEADYFGNVLQTRKYLAQSDFFWLRKAVPKTEWFTNPTTVNAFYSASTNQIRFPAGELQKPFFWGTEYPRSLSYGAIGVIVGHEFTHGFDNNGRKYDKNGNLDPWWSTESEEKFKEKTKCMINQYSNYYWKKAGLNVKGKRTLGENIADNGGLREAFRAYRKWINDRRQGLEEPLLPGITFTNNQLFFLSYAHVRCNSYRPEAAREQVQIGAHSPPQFRVNGAISNFEEFQKAFNCPPNSTMNRGMDSCRLW
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---MEAETGSSVETG
---CCCCCCCCHHHC
49.78-
7Phosphorylation-MEAETGSSVETGKK
-CCCCCCCCHHHCCC
38.33-
8PhosphorylationMEAETGSSVETGKKA
CCCCCCCCHHHCCCC
25.89-
11PhosphorylationETGSSVETGKKANRG
CCCCCHHHCCCCCCC
52.74-
71N-linked_GlycosylationAAILSKVNLSVDPCD
HHHHHHCCCCCCCCC
30.27UniProtKB CARBOHYD
129PhosphorylationSISRRRDTEAIQKAK
HHHCCCCHHHHHHHH
26.04-
140PhosphorylationQKAKILYSSCMNEKA
HHHHHHHHHHCCHHH
17.39-
141PhosphorylationKAKILYSSCMNEKAI
HHHHHHHHHCCHHHH
12.11-
186PhosphorylationVWSERKFSLLQTLAT
CCCHHHHHHHHHHHH
31.07-
190PhosphorylationRKFSLLQTLATFRGQ
HHHHHHHHHHHHCCC
20.5218491316
193PhosphorylationSLLQTLATFRGQYSN
HHHHHHHHHCCCCCC
19.5818491316
238N-linked_GlycosylationVREDYLDNSTEAKSY
HCHHHCCCCCCHHHH
48.51UniProtKB CARBOHYD
263N-linked_GlycosylationTAVLLGANSSRAEHD
HHHHHCCCCCCCCCC
38.43UniProtKB CARBOHYD
290N-linked_GlycosylationEIMIPHENRTSEAMY
EEECCCCCCCCHHHH
49.88UniProtKB CARBOHYD
293PhosphorylationIPHENRTSEAMYNKM
CCCCCCCCHHHHHCC
21.8124275569
297PhosphorylationNRTSEAMYNKMNISE
CCCCHHHHHCCCHHH
20.7624275569
301N-linked_GlycosylationEAMYNKMNISELSAM
HHHHHCCCHHHHHHH
35.92UniProtKB CARBOHYD
346PhosphorylationVVVRVPQYFKDLFRI
EEEECCHHHHHHHHH
13.41-
356PhosphorylationDLFRILGSERKKTIA
HHHHHHCCCHHHHHH
30.6824043423
377N-linked_GlycosylationMVYSRIPNLSRRFQY
HHHHCCCCHHHHHHH
48.56UniProtKB CARBOHYD
484N-linked_GlycosylationGYPEFIMNDTHVNED
CCCHHHCCCCCCCCC
46.33UniProtKB CARBOHYD
623PhosphorylationKCMINQYSNYYWKKA
HHHHHHCCCCCHHHC
14.4827251275
639PhosphorylationLNVKGKRTLGENIAD
CCCCCCEECCCCCCC
42.47-
736N-linked_GlycosylationKAFNCPPNSTMNRGM
HHHCCCCCCCCCCCC
34.94UniProtKB CARBOHYD

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 PHEX_HUMAN !!

Functions of PTM Sites
Modified Location Modified Residue Modification Function Reference

Oops, there are no descriptions of PTM sites of PHEX_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 PHEX_HUMAN !!

Protein-Protein Interaction
Interacting Protein Gene Name Interaction Type PPI Reference Domain-Domain Interactions
NNRD_HUMANCARKDphysical
28514442

Drug and Disease Associations
Kegg Disease
H00214 Hypophosphatemic rickets, including: X-Linked dominant hypophosphatemia (XLH); X-Linked recessive hy
OMIM Disease
307800Hypophosphatemic rickets, X-linked dominant (XLHR)
Kegg Drug
There are no disease associations of PTM sites.
DrugBank
There are no disease associations of PTM sites.
Regulatory Network of PHEX_HUMAN

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Related Literatures of Post-Translational Modification

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