CRX_HUMAN - dbPTM
CRX_HUMAN - PTM Information in dbPTM
Basic Information of Protein
UniProt ID CRX_HUMAN
UniProt AC O43186
Protein Name Cone-rod homeobox protein
Gene Name CRX
Organism Homo sapiens (Human).
Sequence Length 299
Subcellular Localization Nucleus .
Protein Description Transcription factor that binds and transactivates the sequence 5'-TAATC[CA]-3' which is found upstream of several photoreceptor-specific genes, including the opsin genes. Acts synergistically with other transcription factors, such as NRL, RORB and RAX, to regulate photoreceptor cell-specific gene transcription. Essential for the maintenance of mammalian photoreceptors..
Protein Sequence MMAYMNPGPHYSVNALALSGPSVDLMHQAVPYPSAPRKQRRERTTFTRSQLEELEALFAKTQYPDVYAREEVALKINLPESRVQVWFKNRRAKCRQQRQQQKQQQQPPGGQAKARPAKRKAGTSPRPSTDVCPDPLGISDSYSPPLPGPSGSPTTAVATVSIWSPASESPLPEAQRAGLVASGPSLTSAPYAMTYAPASAFCSSPSAYGSPSSYFSGLDPYLSPMVPQLGGPALSPLSGPSVGPSLAQSPTSLSGQSYGAYSPVDSLEFKDPTGTWKFTYNPMDPLDYKDQSAWKFQIL
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
4Phosphorylation----MMAYMNPGPHY
----CCCCCCCCCCC
4.5924043423
11PhosphorylationYMNPGPHYSVNALAL
CCCCCCCCCCEEHHH
19.9024043423
12PhosphorylationMNPGPHYSVNALALS
CCCCCCCCCEEHHHC
13.0824043423
19PhosphorylationSVNALALSGPSVDLM
CCEEHHHCCCCCCHH
42.9524043423
22PhosphorylationALALSGPSVDLMHQA
EHHHCCCCCCHHHHC
31.6124043423
32PhosphorylationLMHQAVPYPSAPRKQ
HHHHCCCCCCCCHHH
11.8324043423
34PhosphorylationHQAVPYPSAPRKQRR
HHCCCCCCCCHHHHH
45.0924043423
61PhosphorylationLEALFAKTQYPDVYA
HHHHHHHCCCCCCCC
29.8824043423
63PhosphorylationALFAKTQYPDVYARE
HHHHHCCCCCCCCCC
13.4622817900
67PhosphorylationKTQYPDVYAREEVAL
HCCCCCCCCCCEEEH
13.8122817900

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 CRX_HUMAN !!

Functions of PTM Sites
Modified Location Modified Residue Modification Function Reference

Oops, there are no descriptions of PTM sites of CRX_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 CRX_HUMAN !!

Protein-Protein Interaction
Interacting Protein Gene Name Interaction Type PPI Reference Domain-Domain Interactions
M1AP_HUMANM1APphysical
16189514
MDFI_HUMANMDFIphysical
16189514
IPO13_HUMANIPO13physical
15143176
ATX7_HUMANATXN7physical
11580893
KAT2A_HUMANKAT2Aphysical
15932940
SP4_HUMANSP4physical
15781457
SP1_HUMANSP1physical
15781457
SP3_HUMANSP3physical
15781457
BAF_HUMANBANF1physical
12215455
KPCI_HUMANPRKCIphysical
23718855
IF5A1_HUMANEIF5Aphysical
25416956
AF17_HUMANMLLT6physical
25416956
ROR2_HUMANROR2physical
25416956
AAKB2_HUMANPRKAB2physical
25416956
PSB10_HUMANPSMB10physical
25416956
SOX5_HUMANSOX5physical
25416956
STK16_HUMANSTK16physical
25416956
ATG12_HUMANATG12physical
25416956
GCM2_HUMANGCM2physical
25416956
DELE_HUMANKIAA0141physical
25416956
SFI1_HUMANSFI1physical
25416956
ABI2_HUMANABI2physical
25416956
SZT2_HUMANSZT2physical
25416956
PP16B_HUMANPPP1R16Bphysical
25416956
OSGI1_HUMANOSGIN1physical
25416956
NIP7_HUMANNIP7physical
25416956
QRIC1_HUMANQRICH1physical
25416956
CA109_HUMANC1orf109physical
25416956
PCLI1_HUMANPID1physical
25416956
GUCD1_HUMANGUCD1physical
25416956
LONF1_HUMANLONRF1physical
25416956
LARP4_HUMANLARP4physical
25416956
KLH32_HUMANKLHL32physical
25416956
UBX2B_HUMANUBXN2Bphysical
25416956
CI072_HUMANC9orf72physical
25416956
NRL_HUMANNRLphysical
25703721
NR2E3_HUMANNR2E3physical
25703721

Drug and Disease Associations
Kegg Disease
There are no disease associations of PTM sites.
OMIM Disease
613829Leber congenital amaurosis 7 (LCA7)
120970Cone-rod dystrophy 2 (CORD2)
268000Retinitis pigmentosa (RP)
Kegg Drug
There are no disease associations of PTM sites.
DrugBank
There are no disease associations of PTM sites.
Regulatory Network of CRX_HUMAN

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Related Literatures of Post-Translational Modification

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