blastp_kegg |
lcl|pper:PRUPE_ppa004543mg
|
1 |
506 |
+ |
506 |
Gaps:5 |
99.80 |
504 |
71.77 |
0.0 |
hypothetical protein
|
blastp_kegg |
lcl|pxb:103957734
|
1 |
506 |
+ |
506 |
Gaps:5 |
99.80 |
504 |
70.97 |
0.0 |
diphthamide biosynthesis protein 2-like
|
blastp_kegg |
lcl|pxb:103957701
|
1 |
506 |
+ |
506 |
Gaps:5 |
99.80 |
504 |
70.97 |
0.0 |
diphthamide biosynthesis protein 2
|
blastp_kegg |
lcl|pmum:103323579
|
1 |
506 |
+ |
506 |
Gaps:5 |
99.80 |
504 |
71.37 |
0.0 |
diphthamide biosynthesis protein 2
|
blastp_kegg |
lcl|vvi:100262956
|
1 |
504 |
+ |
504 |
Gaps:8 |
99.60 |
506 |
73.41 |
0.0 |
diphthamide biosynthesis protein 2-like
|
blastp_kegg |
lcl|mdm:103427470
|
1 |
506 |
+ |
506 |
Gaps:5 |
99.80 |
504 |
70.58 |
0.0 |
diphthamide biosynthesis protein 2-like
|
blastp_kegg |
lcl|cam:101501182
|
1 |
504 |
+ |
504 |
Gaps:3 |
100.00 |
501 |
70.26 |
0.0 |
diphthamide biosynthesis protein 2-like
|
blastp_kegg |
lcl|rcu:RCOM_0547500
|
1 |
504 |
+ |
504 |
Gaps:9 |
100.00 |
499 |
70.94 |
0.0 |
diphteria toxin resistance protein 2 dph2 putative
|
blastp_kegg |
lcl|tcc:TCM_012451
|
1 |
505 |
+ |
505 |
Gaps:20 |
58.70 |
833 |
73.42 |
0.0 |
Diphthamide synthesis DPH2 family protein
|
blastp_kegg |
lcl|pvu:PHAVU_005G177500g
|
1 |
504 |
+ |
504 |
Gaps:12 |
99.80 |
501 |
70.00 |
0.0 |
hypothetical protein
|
blastp_pdb |
3lzd_B
|
2 |
160 |
+ |
159 |
Gaps:13 |
44.44 |
378 |
23.81 |
9e-06 |
mol:protein length:378 Dph2
|
blastp_pdb |
3lzd_A
|
2 |
160 |
+ |
159 |
Gaps:13 |
44.44 |
378 |
23.81 |
9e-06 |
mol:protein length:378 Dph2
|
blastp_pdb |
3lzc_B
|
2 |
160 |
+ |
159 |
Gaps:13 |
44.44 |
378 |
23.81 |
9e-06 |
mol:protein length:378 Dph2
|
blastp_pdb |
3lzc_A
|
2 |
160 |
+ |
159 |
Gaps:13 |
44.44 |
378 |
23.81 |
9e-06 |
mol:protein length:378 Dph2
|
blastp_uniprot_sprot |
sp|A4QN59|DPH2_DANRE
|
2 |
500 |
+ |
499 |
Gaps:63 |
92.37 |
498 |
37.17 |
1e-85 |
Diphthamide biosynthesis protein 2 OS Danio rerio GN dph2 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|A7SKJ3|DPH2_NEMVE
|
7 |
500 |
+ |
494 |
Gaps:50 |
91.53 |
531 |
35.60 |
8e-85 |
Diphthamide biosynthesis protein 2 OS Nematostella vectensis GN dph2 PE 3 SV 1
|
blastp_uniprot_sprot |
sp|Q5ZKI2|DPH2_CHICK
|
2 |
504 |
+ |
503 |
Gaps:55 |
94.34 |
477 |
36.67 |
1e-76 |
Diphthamide biosynthesis protein 2 OS Gallus gallus GN DPH2 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q10206|DPH2_SCHPO
|
2 |
505 |
+ |
504 |
Gaps:71 |
92.45 |
503 |
33.12 |
2e-75 |
Diphthamide biosynthesis protein 2 OS Schizosaccharomyces pombe (strain 972 / ATCC 24843) GN dph2 PE 3 SV 1
|
blastp_uniprot_sprot |
sp|Q6DE00|DPH2_XENLA
|
2 |
500 |
+ |
499 |
Gaps:77 |
92.89 |
478 |
36.04 |
1e-71 |
Diphthamide biosynthesis protein 2 OS Xenopus laevis GN dph2 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|P0CN20|DPH2_CRYNJ
|
1 |
501 |
+ |
501 |
Gaps:60 |
92.62 |
515 |
30.40 |
2e-59 |
Diphthamide biosynthesis protein 2 OS Cryptococcus neoformans var. neoformans serotype D (strain JEC21 / ATCC MYA-565) GN DPH2 PE 3 SV 1
|
blastp_uniprot_sprot |
sp|P0CN21|DPH2_CRYNB
|
1 |
501 |
+ |
501 |
Gaps:60 |
92.62 |
515 |
30.40 |
2e-59 |
Diphthamide biosynthesis protein 2 OS Cryptococcus neoformans var. neoformans serotype D (strain B-3501A) GN DPH2 PE 3 SV 1
|
blastp_uniprot_sprot |
sp|Q568Y2|DPH2_RAT
|
2 |
502 |
+ |
501 |
Gaps:74 |
94.27 |
489 |
33.19 |
6e-51 |
Diphthamide biosynthesis protein 2 OS Rattus norvegicus GN Dph2 PE 2 SV 1
|
blastp_uniprot_sprot |
sp|Q5B2Q1|DPH2_EMENI
|
2 |
398 |
+ |
397 |
Gaps:75 |
66.32 |
582 |
32.64 |
2e-49 |
Diphthamide biosynthesis protein 2 OS Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) GN dph2 PE 3 SV 1
|
blastp_uniprot_sprot |
sp|Q002B5|DPH2_CRIGR
|
2 |
502 |
+ |
501 |
Gaps:72 |
94.27 |
489 |
31.67 |
3e-49 |
Diphthamide biosynthesis protein 2 OS Cricetulus griseus GN DPH2 PE 2 SV 1
|
rpsblast_cdd |
gnl|CDD|188040
|
6 |
376 |
+ |
371 |
Gaps:55 |
99.69 |
319 |
37.11 |
2e-91 |
TIGR00322 diphth2_R diphthamide biosynthesis enzyme Dph1/Dph2 domain. Archaea and Eukaryotes but not Eubacteria share the property of having a covalently modified residue 2'-[3-carboxamido-3-(trimethylammonio)propyl]histidine as a part of a cytosolic protein. The modified His termed diphthamide is part of translation elongation factor EF-2 and is the site for ADP-ribosylation by diphtheria toxin. This model includes both Dph1 and Dph2 from Saccharomyces cerevisiae although only Dph2 is found in the Archaea (see TIGR03682). Dph2 has been shown to act analogously to the radical SAM (rSAM) family (pfam04055) with 4Fe-4S-assisted cleavage of S-adenosylmethionine to create a free radical but a different organic radical than in rSAM.
|
rpsblast_cdd |
gnl|CDD|161796
|
2 |
497 |
+ |
496 |
Gaps:60 |
93.15 |
496 |
31.82 |
3e-69 |
TIGR00272 DPH2 diphthamide biosynthesis protein 2. This protein has been shown in Saccharomyces cerevisiae to be one of several required for the modification of a particular histidine residue of translation elongation factor 2 to diphthamide. This modified site can then become the target for ADP-ribosylation by diphtheria toxin.
|
rpsblast_cdd |
gnl|CDD|190143
|
28 |
390 |
+ |
363 |
Gaps:66 |
99.67 |
300 |
30.77 |
2e-54 |
pfam01866 Diphthamide_syn Putative diphthamide synthesis protein. Human DPH1 is a candidate tumour suppressor gene. DPH2 from yeast which confers resistance to diphtheria toxin has been found to be involved in diphthamide synthesis. Diphtheria toxin inhibits eukaryotic protein synthesis by ADP-ribosylating diphthamide a posttranslationally modified histidine residue present in EF2. The exact function of the members of this family is unknown.
|
rpsblast_cdd |
gnl|CDD|31922
|
6 |
390 |
+ |
385 |
Gaps:63 |
93.95 |
347 |
26.38 |
8e-48 |
COG1736 DPH2 Diphthamide synthase subunit DPH2 [Translation ribosomal structure and biogenesis].
|
rpsblast_cdd |
gnl|CDD|188369
|
23 |
389 |
+ |
367 |
Gaps:28 |
74.35 |
308 |
27.51 |
2e-11 |
TIGR03682 arCOG04112 diphthamide biosynthesis enzyme Dph2. Members of this family are the archaeal protein Dph2 members of the universal archaeal protein family designated arCOG04112. The chemical function of this protein is analogous to the radical SAM family (pfam04055) although the sequence is not homologous. The chemistry involves [4Fe-4S]-aided formation of a 3-amino-3-carboxypropyl radical rather than the canonical 5'-deoxyadenosyl radical of the radical SAM family.
|
rpsblast_kog |
gnl|CDD|37859
|
6 |
500 |
+ |
495 |
Gaps:80 |
92.49 |
453 |
38.90 |
1e-101 |
KOG2648 KOG2648 KOG2648 Diphthamide biosynthesis protein [Translation ribosomal structure and biogenesis].
|