Publication for CRP and CFHR5
| Species | Symbol | Function* | Entrez Gene ID* | Other ID | Gene coexpression |
CoexViewer |
|---|---|---|---|---|---|---|
| hsa | CRP | C-reactive protein | 1401 | [link] | ||
| hsa | CFHR5 | complement factor H related 5 | 81494 |
| Pubmed ID | Priority | Text |
|---|---|---|
| 25855355 | 0.98 | CFHR5 was also shown to bind to C-reactive protein (CRP), an acute phase protein belonging to the family of pentraxins. |
| 0.97 | CRP and incubated with 50 mug/ml FH with or without 20 mug/ml CFHR5, as indicated below the blot, and then C3b and FI were added to each well. | |
| 0.97 | CFHR5 and CRP can further fine-tune these interactions, but this needs to be characterized in more detail. | |
| 0.96 | CRP for the cleavage of C3b in the presence and absence of CFHR5 was measured by Western blot. | |
| 0.93 | CFHR5 when added to heat-inactivated serum significantly reduced the amount of bound FH on PTX3, CRP, and MaxGel (Fig. 8A). | |
| 0.93 | CFHR5 may promote complement activation and complement-mediated damage/inflammation through three mechanisms: 1) by preventing the binding of the complement inhibitor FH to PTX3, CRP, and ECM; 2) by allowing increased binding of the complement activation initiator molecule C1q; and 3) by supporting the assembly of the alternative pathway C3 convertase C3bBb. | |
| 0.92 | CRP can interact with several members of the FH protein family, namely FH, FHL-1, CFHR4, and CFHR5, but the interaction of FH with the denatured monomeric CRP versus native pentameric CRP is still a controversial issue. | |
| 0.92 | CRP (lanes 4-6) were incubated with 50% normal human serum (NHS) (lanes 2 and 5) and a patient serum containing both wild-type CFHR5 and the mutCFHR5 (lanes 3 and 6). | |
| 0.91 | CFHR5 and FH occurs also in serum, wells were coated with PTX3, CRP, and MaxGel and incubated with heat-inactivated serum, which was used to exclude FH binding through deposited C3 fragments. | |
| 0.90 | CFHR5 dose-dependently inhibited FH binding to PTX3 and also to the monomeric, denatured form of the short pentraxin C-reactive protein. | |
| 0.90 | CFHR5 was shown to interact with CRP, but the CRP form that binds to CFHR5 and the functional consequence of this interaction were not investigated. | |
| 0.90 | CRP was localized to CCPs 3-7 of CFHR5. | |
| 0.90 | CFHR5 with CRP was first described by McRae et al. but the type of CRP that binds CFHR5 was not studied. | |
| 0.89 | CRP) and 25% normal human serum (for ECM) were added for 30 min at 37 C, with or without 20 mug/ml CFHR5 or CFHR4A. | |
| 0.78 | CRP, and MaxGel was measured in complement active normal serum when CFHR5 was added to increase its concentration. | |
| 0.68 | CFHR5 binds to denatured, monomeric CRP and inhibits FH binding and cofactor activity | |
| 0.54 | CFHR5 competes with FH in serum for binding to PTX3, CRP, and MaxGel and causes enhanced C3 fragment deposition. | |
| 0.53 | CFHR5 and the mutCFHR5 were incubated in wells coated with PTX3 and the related short pentraxin CRP. | |
| 19365580 | 0.97 | CFHR5, which shows the highest similarity to CFH, has nine SCRs, with the first two being similar to SCRs 6 and 7 of CFH and therefore having CRP and heparin binding properties. |
| 0.95 | CFHR5 has been proposed to rely upon its recruitment to sites of tissue damage by CRP. | |
| 24970127 | 0.97 | CFHR5 were shown to bind to C3b, CFHR1, CFHR3 and CFHR5 to heparin, and CFHR4 and CFHR5 to CRP. |
| 31428091 | 0.96 | FHR-5-CRP interaction, and thereby influence complement activation and control in C3GN. |
| 0.94 | FHR-5 domains 3-7 preferentially interact with the monomeric (mCRP), while FHR-4 domain 1 mainly binds the pentameric form of CRP (pCRP). | |
| 0.92 | FHR-5 domain 1 that is homologous to the short consensus repeat 6 of FH, which interacts with CRP. | |
| 28572805 | 0.95 | FHR-5 can also compete with FH for binding to CRP, PTX3, and extracellular matrix, resulting in enhancement of complement activation. |
| 22622361 | 0.94 | CFHR5 protein fragment containing SCR1-4, however, did not show CRP and heparin binding, while a SCR3-7 fragment did show binding capacity. |
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