PMID-sentid Pub_year Sent_text comp_official_name comp_offsetprotein_name organism prot_offset 6461667-1 1982 H (beta 1H) controls the C3b amplification loop by its ability to displace Bb from the alternative pathway convertase, C3b,Bb, and acts as a cofactor with I (C3b inactivator) to produce inactive C3b. boeravinone B 75-77 complement factor H Homo sapiens 3-10 11694537-9 2002 Mutations at the C3b.Bb interface interfere with the normal dissociation of C3b from Bb, whether it is spontaneous or promoted by DAF, CR1, or factor H. boeravinone B 21-23 complement factor H Homo sapiens 143-151 11694537-9 2002 Mutations at the C3b.Bb interface interfere with the normal dissociation of C3b from Bb, whether it is spontaneous or promoted by DAF, CR1, or factor H. boeravinone B 85-87 complement factor H Homo sapiens 143-151 2964038-3 1988 However, the activity of the serum control protein of the alternative complement pathway, factor H, in controlling streptococcus-bound C3b and C3b,Bb was 6-8 times stronger on M+ organisms than on M- organisms. boeravinone B 147-149 complement factor H Homo sapiens 90-98 390986-6 1979 Sialic acid residues on C3b-bearing particles augment binding of beta 1H to favor competition with B, inactivation of C3b and decay-dissociation of C3b, Bb. boeravinone B 153-155 complement factor H Homo sapiens 65-72 6459381-4 1982 C3b bound to cells that had been treated with virus, and P-stabilized amplification convertase sites P,C3b,Bb formed on these cells, exhibited increased resistance to the action of the regulatory proteins beta-1H and C3b Ina compared with C3b and P,C3b,Bb on untreated, nonactivating cells. boeravinone B 107-109 complement factor H Homo sapiens 205-212 77846-5 1978 Cell-bound beta1H was also dissociated by the action of B (or Bb). boeravinone B 62-64 complement factor H Homo sapiens 11-17 77846-7 1978 The C3b site-bearing cell could bind beta1H on the C3c region of C3b molecules facilitating the C3bINA action on C3b, and beta1H shared the same binding site with B (or Bb) inhibiting the generation of the alternative pathway convertases competitively. boeravinone B 169-171 complement factor H Homo sapiens 122-128 30248148-5 2018 RESULTS: In adjusted analyses, HF1, HF2 and CKD273 (p <= 0.024) were higher in BB users than non-users with a similar trend for ACSP75 (p = 0.06). boeravinone B 82-84 complement factor H Homo sapiens 31-34 30248148-5 2018 RESULTS: In adjusted analyses, HF1, HF2 and CKD273 (p <= 0.024) were higher in BB users than non-users with a similar trend for ACSP75 (p = 0.06). boeravinone B 82-84 complement factor H Homo sapiens 36-39 30248148-6 2018 Patients started on BB within 1 year after HTx and non-users had similar HF1 and HF2 levels (p >= 0.098), whereas starting BB later was associated with higher HF1 and HF2 compared with non-users (p <= 0.014). boeravinone B 20-22 complement factor H Homo sapiens 73-76 30248148-6 2018 Patients started on BB within 1 year after HTx and non-users had similar HF1 and HF2 levels (p >= 0.098), whereas starting BB later was associated with higher HF1 and HF2 compared with non-users (p <= 0.014). boeravinone B 20-22 complement factor H Homo sapiens 81-84 30248148-6 2018 Patients started on BB within 1 year after HTx and non-users had similar HF1 and HF2 levels (p >= 0.098), whereas starting BB later was associated with higher HF1 and HF2 compared with non-users (p <= 0.014). boeravinone B 126-128 complement factor H Homo sapiens 162-165 30248148-6 2018 Patients started on BB within 1 year after HTx and non-users had similar HF1 and HF2 levels (p >= 0.098), whereas starting BB later was associated with higher HF1 and HF2 compared with non-users (p <= 0.014). boeravinone B 126-128 complement factor H Homo sapiens 170-173 29174517-7 2018 Positive associations were also observed for C3a (beta=0.64 [0.31; 0.97]), FD (beta=1.00 [0.59; 1.42]), FH (beta=1.17 [0.82; 1.53]), and properdin (beta=0.60 [0.28; 0.92]), but not for Bb, C5a or sC5b-9. boeravinone B 185-187 complement factor H Homo sapiens 104-106