Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0032991 | protein-containing complex | 1 | 11 |
GO:1990904 | ribonucleoprotein complex | 2 | 11 |
GO:0005654 | nucleoplasm | 2 | 1 |
GO:0005681 | spliceosomal complex | 3 | 1 |
GO:0005684 | U2-type spliceosomal complex | 4 | 1 |
GO:0030532 | small nuclear ribonucleoprotein complex | 3 | 1 |
GO:0046540 | U4/U6 x U5 tri-snRNP complex | 6 | 1 |
GO:0071007 | U2-type catalytic step 2 spliceosome | 4 | 1 |
GO:0071013 | catalytic step 2 spliceosome | 3 | 1 |
GO:0097525 | spliceosomal snRNP complex | 4 | 1 |
GO:0097526 | spliceosomal tri-snRNP complex | 5 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
GO:0120114 | Sm-like protein family complex | 2 | 1 |
GO:0140513 | nuclear protein-containing complex | 2 | 1 |
GO:1902494 | catalytic complex | 2 | 1 |
Related structures:
AlphaFold database: E9B301
Term | Name | Level | Count |
---|---|---|---|
GO:0000375 | RNA splicing, via transesterification reactions | 8 | 1 |
GO:0000377 | RNA splicing, via transesterification reactions with bulged adenosine as nucleophile | 9 | 1 |
GO:0000398 | mRNA splicing, via spliceosome | 8 | 1 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006396 | RNA processing | 6 | 1 |
GO:0006397 | mRNA processing | 7 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0008380 | RNA splicing | 7 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0016071 | mRNA metabolic process | 6 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0003924 | GTPase activity | 7 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0005525 | GTP binding | 5 | 12 |
GO:0016462 | pyrophosphatase activity | 5 | 12 |
GO:0016787 | hydrolase activity | 2 | 12 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 12 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 12 |
GO:0017076 | purine nucleotide binding | 4 | 12 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 12 |
GO:0019001 | guanyl nucleotide binding | 5 | 12 |
GO:0032553 | ribonucleotide binding | 3 | 12 |
GO:0032555 | purine ribonucleotide binding | 4 | 12 |
GO:0032561 | guanyl ribonucleotide binding | 5 | 12 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 12 |
GO:0036094 | small molecule binding | 2 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043168 | anion binding | 3 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0097367 | carbohydrate derivative binding | 2 | 12 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003723 | RNA binding | 4 | 1 |
GO:0017069 | snRNA binding | 5 | 1 |
GO:0030623 | U5 snRNA binding | 6 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 15 | 19 | PF00656 | 0.654 |
CLV_C14_Caspase3-7 | 438 | 442 | PF00656 | 0.362 |
CLV_C14_Caspase3-7 | 56 | 60 | PF00656 | 0.677 |
CLV_C14_Caspase3-7 | 663 | 667 | PF00656 | 0.447 |
CLV_C14_Caspase3-7 | 727 | 731 | PF00656 | 0.502 |
CLV_C14_Caspase3-7 | 792 | 796 | PF00656 | 0.431 |
CLV_C14_Caspase3-7 | 867 | 871 | PF00656 | 0.536 |
CLV_NRD_NRD_1 | 1004 | 1006 | PF00675 | 0.395 |
CLV_NRD_NRD_1 | 133 | 135 | PF00675 | 0.685 |
CLV_NRD_NRD_1 | 20 | 22 | PF00675 | 0.713 |
CLV_NRD_NRD_1 | 293 | 295 | PF00675 | 0.231 |
CLV_NRD_NRD_1 | 778 | 780 | PF00675 | 0.570 |
CLV_NRD_NRD_1 | 786 | 788 | PF00675 | 0.257 |
CLV_NRD_NRD_1 | 918 | 920 | PF00675 | 0.231 |
CLV_NRD_NRD_1 | 97 | 99 | PF00675 | 0.621 |
CLV_PCSK_KEX2_1 | 132 | 134 | PF00082 | 0.688 |
CLV_PCSK_KEX2_1 | 185 | 187 | PF00082 | 0.327 |
CLV_PCSK_KEX2_1 | 20 | 22 | PF00082 | 0.713 |
CLV_PCSK_KEX2_1 | 786 | 788 | PF00082 | 0.289 |
CLV_PCSK_KEX2_1 | 918 | 920 | PF00082 | 0.231 |
CLV_PCSK_KEX2_1 | 97 | 99 | PF00082 | 0.643 |
CLV_PCSK_PC1ET2_1 | 185 | 187 | PF00082 | 0.327 |
CLV_PCSK_PC7_1 | 181 | 187 | PF00082 | 0.269 |
CLV_PCSK_SKI1_1 | 192 | 196 | PF00082 | 0.327 |
CLV_PCSK_SKI1_1 | 215 | 219 | PF00082 | 0.327 |
CLV_PCSK_SKI1_1 | 371 | 375 | PF00082 | 0.453 |
CLV_PCSK_SKI1_1 | 754 | 758 | PF00082 | 0.454 |
CLV_PCSK_SKI1_1 | 858 | 862 | PF00082 | 0.242 |
CLV_PCSK_SKI1_1 | 878 | 882 | PF00082 | 0.374 |
CLV_PCSK_SKI1_1 | 953 | 957 | PF00082 | 0.274 |
CLV_Separin_Metazoa | 850 | 854 | PF03568 | 0.482 |
DEG_APCC_DBOX_1 | 417 | 425 | PF00400 | 0.528 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.634 |
DEG_SPOP_SBC_1 | 523 | 527 | PF00917 | 0.440 |
DOC_CKS1_1 | 220 | 225 | PF01111 | 0.456 |
DOC_CYCLIN_yClb1_LxF_4 | 742 | 748 | PF00134 | 0.236 |
DOC_CYCLIN_yCln2_LP_2 | 892 | 898 | PF00134 | 0.439 |
DOC_MAPK_gen_1 | 277 | 287 | PF00069 | 0.423 |
DOC_MAPK_gen_1 | 294 | 300 | PF00069 | 0.442 |
DOC_MAPK_gen_1 | 370 | 379 | PF00069 | 0.543 |
DOC_MAPK_gen_1 | 380 | 388 | PF00069 | 0.367 |
DOC_MAPK_MEF2A_6 | 170 | 178 | PF00069 | 0.474 |
DOC_MAPK_MEF2A_6 | 277 | 285 | PF00069 | 0.444 |
DOC_MAPK_MEF2A_6 | 673 | 680 | PF00069 | 0.527 |
DOC_MAPK_MEF2A_6 | 706 | 715 | PF00069 | 0.620 |
DOC_PP1_RVXF_1 | 373 | 380 | PF00149 | 0.419 |
DOC_PP1_RVXF_1 | 544 | 551 | PF00149 | 0.528 |
DOC_PP1_RVXF_1 | 638 | 645 | PF00149 | 0.508 |
DOC_PP1_RVXF_1 | 856 | 862 | PF00149 | 0.442 |
DOC_PP1_RVXF_1 | 96 | 103 | PF00149 | 0.650 |
DOC_PP2B_LxvP_1 | 447 | 450 | PF13499 | 0.476 |
DOC_PP2B_LxvP_1 | 902 | 905 | PF13499 | 0.458 |
DOC_PP2B_PxIxI_1 | 809 | 815 | PF00149 | 0.496 |
DOC_PP4_FxxP_1 | 644 | 647 | PF00568 | 0.515 |
DOC_USP7_MATH_1 | 140 | 144 | PF00917 | 0.549 |
DOC_USP7_MATH_1 | 248 | 252 | PF00917 | 0.438 |
DOC_USP7_MATH_1 | 349 | 353 | PF00917 | 0.385 |
DOC_USP7_MATH_1 | 451 | 455 | PF00917 | 0.501 |
DOC_USP7_MATH_1 | 465 | 469 | PF00917 | 0.370 |
DOC_USP7_MATH_1 | 496 | 500 | PF00917 | 0.516 |
DOC_USP7_MATH_1 | 532 | 536 | PF00917 | 0.642 |
DOC_USP7_MATH_1 | 54 | 58 | PF00917 | 0.563 |
DOC_USP7_MATH_1 | 595 | 599 | PF00917 | 0.495 |
DOC_USP7_MATH_1 | 833 | 837 | PF00917 | 0.483 |
DOC_USP7_MATH_1 | 942 | 946 | PF00917 | 0.442 |
DOC_USP7_UBL2_3 | 370 | 374 | PF12436 | 0.525 |
DOC_WW_Pin1_4 | 219 | 224 | PF00397 | 0.436 |
DOC_WW_Pin1_4 | 317 | 322 | PF00397 | 0.443 |
DOC_WW_Pin1_4 | 407 | 412 | PF00397 | 0.523 |
DOC_WW_Pin1_4 | 416 | 421 | PF00397 | 0.515 |
DOC_WW_Pin1_4 | 619 | 624 | PF00397 | 0.387 |
DOC_WW_Pin1_4 | 672 | 677 | PF00397 | 0.431 |
LIG_14-3-3_CanoR_1 | 215 | 220 | PF00244 | 0.527 |
LIG_14-3-3_CanoR_1 | 418 | 428 | PF00244 | 0.461 |
LIG_14-3-3_CanoR_1 | 515 | 523 | PF00244 | 0.538 |
LIG_14-3-3_CanoR_1 | 582 | 590 | PF00244 | 0.478 |
LIG_14-3-3_CanoR_1 | 741 | 746 | PF00244 | 0.535 |
LIG_14-3-3_CanoR_1 | 754 | 762 | PF00244 | 0.369 |
LIG_14-3-3_CanoR_1 | 779 | 785 | PF00244 | 0.349 |
LIG_14-3-3_CanoR_1 | 832 | 842 | PF00244 | 0.506 |
LIG_14-3-3_CanoR_1 | 882 | 886 | PF00244 | 0.349 |
LIG_14-3-3_CanoR_1 | 953 | 962 | PF00244 | 0.431 |
LIG_Actin_WH2_2 | 811 | 829 | PF00022 | 0.527 |
LIG_AP2alpha_2 | 975 | 977 | PF02296 | 0.442 |
LIG_APCC_ABBA_1 | 678 | 683 | PF00400 | 0.527 |
LIG_BIR_III_2 | 556 | 560 | PF00653 | 0.405 |
LIG_BIR_III_4 | 49 | 53 | PF00653 | 0.666 |
LIG_BIR_III_4 | 730 | 734 | PF00653 | 0.541 |
LIG_BRCT_BRCA1_1 | 640 | 644 | PF00533 | 0.502 |
LIG_BRCT_BRCA1_1 | 717 | 721 | PF00533 | 0.375 |
LIG_BRCT_BRCA1_1 | 743 | 747 | PF00533 | 0.478 |
LIG_Clathr_ClatBox_1 | 243 | 247 | PF01394 | 0.456 |
LIG_Clathr_ClatBox_1 | 547 | 551 | PF01394 | 0.392 |
LIG_eIF4E_1 | 762 | 768 | PF01652 | 0.448 |
LIG_EVH1_1 | 447 | 451 | PF00568 | 0.404 |
LIG_FHA_1 | 169 | 175 | PF00498 | 0.431 |
LIG_FHA_1 | 518 | 524 | PF00498 | 0.472 |
LIG_FHA_1 | 755 | 761 | PF00498 | 0.390 |
LIG_FHA_1 | 77 | 83 | PF00498 | 0.662 |
LIG_FHA_1 | 929 | 935 | PF00498 | 0.442 |
LIG_FHA_2 | 150 | 156 | PF00498 | 0.453 |
LIG_FHA_2 | 216 | 222 | PF00498 | 0.496 |
LIG_FHA_2 | 274 | 280 | PF00498 | 0.440 |
LIG_FHA_2 | 310 | 316 | PF00498 | 0.557 |
LIG_FHA_2 | 570 | 576 | PF00498 | 0.489 |
LIG_FHA_2 | 721 | 727 | PF00498 | 0.364 |
LIG_FHA_2 | 815 | 821 | PF00498 | 0.442 |
LIG_GBD_Chelix_1 | 358 | 366 | PF00786 | 0.214 |
LIG_LIR_Apic_2 | 630 | 636 | PF02991 | 0.498 |
LIG_LIR_Apic_2 | 641 | 647 | PF02991 | 0.268 |
LIG_LIR_Gen_1 | 143 | 154 | PF02991 | 0.461 |
LIG_LIR_Gen_1 | 312 | 321 | PF02991 | 0.515 |
LIG_LIR_Gen_1 | 325 | 335 | PF02991 | 0.389 |
LIG_LIR_Gen_1 | 384 | 393 | PF02991 | 0.364 |
LIG_LIR_Gen_1 | 718 | 728 | PF02991 | 0.347 |
LIG_LIR_Gen_1 | 761 | 768 | PF02991 | 0.470 |
LIG_LIR_Gen_1 | 788 | 799 | PF02991 | 0.527 |
LIG_LIR_Nem_3 | 143 | 149 | PF02991 | 0.483 |
LIG_LIR_Nem_3 | 2 | 8 | PF02991 | 0.676 |
LIG_LIR_Nem_3 | 27 | 32 | PF02991 | 0.555 |
LIG_LIR_Nem_3 | 291 | 296 | PF02991 | 0.431 |
LIG_LIR_Nem_3 | 312 | 317 | PF02991 | 0.515 |
LIG_LIR_Nem_3 | 325 | 331 | PF02991 | 0.389 |
LIG_LIR_Nem_3 | 372 | 376 | PF02991 | 0.468 |
LIG_LIR_Nem_3 | 384 | 388 | PF02991 | 0.321 |
LIG_LIR_Nem_3 | 391 | 397 | PF02991 | 0.299 |
LIG_LIR_Nem_3 | 558 | 563 | PF02991 | 0.395 |
LIG_LIR_Nem_3 | 574 | 580 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 691 | 696 | PF02991 | 0.442 |
LIG_LIR_Nem_3 | 718 | 724 | PF02991 | 0.360 |
LIG_LIR_Nem_3 | 761 | 765 | PF02991 | 0.443 |
LIG_LIR_Nem_3 | 788 | 794 | PF02991 | 0.527 |
LIG_LYPXL_yS_3 | 350 | 353 | PF13949 | 0.410 |
LIG_MAD2 | 375 | 383 | PF02301 | 0.406 |
LIG_NRBOX | 172 | 178 | PF00104 | 0.458 |
LIG_NRBOX | 667 | 673 | PF00104 | 0.496 |
LIG_PDZ_Class_1 | 1011 | 1016 | PF00595 | 0.595 |
LIG_SH2_CRK | 293 | 297 | PF00017 | 0.431 |
LIG_SH2_CRK | 394 | 398 | PF00017 | 0.341 |
LIG_SH2_NCK_1 | 346 | 350 | PF00017 | 0.476 |
LIG_SH2_SRC | 146 | 149 | PF00017 | 0.550 |
LIG_SH2_STAP1 | 314 | 318 | PF00017 | 0.515 |
LIG_SH2_STAP1 | 346 | 350 | PF00017 | 0.371 |
LIG_SH2_STAP1 | 561 | 565 | PF00017 | 0.363 |
LIG_SH2_STAT5 | 146 | 149 | PF00017 | 0.550 |
LIG_SH2_STAT5 | 430 | 433 | PF00017 | 0.490 |
LIG_SH2_STAT5 | 569 | 572 | PF00017 | 0.437 |
LIG_SH2_STAT5 | 688 | 691 | PF00017 | 0.527 |
LIG_SH3_2 | 448 | 453 | PF14604 | 0.413 |
LIG_SH3_2 | 985 | 990 | PF14604 | 0.436 |
LIG_SH3_3 | 206 | 212 | PF00018 | 0.470 |
LIG_SH3_3 | 220 | 226 | PF00018 | 0.414 |
LIG_SH3_3 | 386 | 392 | PF00018 | 0.357 |
LIG_SH3_3 | 414 | 420 | PF00018 | 0.444 |
LIG_SH3_3 | 445 | 451 | PF00018 | 0.485 |
LIG_SH3_3 | 618 | 624 | PF00018 | 0.557 |
LIG_SH3_3 | 652 | 658 | PF00018 | 0.545 |
LIG_SH3_3 | 708 | 714 | PF00018 | 0.504 |
LIG_SH3_3 | 970 | 976 | PF00018 | 0.431 |
LIG_SH3_3 | 982 | 988 | PF00018 | 0.426 |
LIG_Sin3_3 | 936 | 943 | PF02671 | 0.515 |
LIG_SUMO_SIM_anti_2 | 145 | 152 | PF11976 | 0.318 |
LIG_SUMO_SIM_anti_2 | 171 | 178 | PF11976 | 0.474 |
LIG_SUMO_SIM_anti_2 | 600 | 606 | PF11976 | 0.381 |
LIG_SUMO_SIM_anti_2 | 67 | 74 | PF11976 | 0.579 |
LIG_SUMO_SIM_par_1 | 270 | 276 | PF11976 | 0.443 |
LIG_SUMO_SIM_par_1 | 491 | 499 | PF11976 | 0.514 |
LIG_TRAF2_1 | 31 | 34 | PF00917 | 0.759 |
LIG_TRAF2_1 | 423 | 426 | PF00917 | 0.460 |
LIG_TRAF2_1 | 817 | 820 | PF00917 | 0.360 |
LIG_TRFH_1 | 388 | 392 | PF08558 | 0.368 |
LIG_TYR_ITIM | 760 | 765 | PF00017 | 0.432 |
LIG_UBA3_1 | 281 | 286 | PF00899 | 0.462 |
LIG_WRC_WIRS_1 | 339 | 344 | PF05994 | 0.410 |
LIG_WRC_WIRS_1 | 721 | 726 | PF05994 | 0.310 |
LIG_WRC_WIRS_1 | 943 | 948 | PF05994 | 0.431 |
MOD_CDC14_SPxK_1 | 320 | 323 | PF00782 | 0.527 |
MOD_CDK_SPxK_1 | 317 | 323 | PF00069 | 0.527 |
MOD_CK1_1 | 253 | 259 | PF00069 | 0.494 |
MOD_CK1_1 | 309 | 315 | PF00069 | 0.474 |
MOD_CK1_1 | 338 | 344 | PF00069 | 0.393 |
MOD_CK1_1 | 35 | 41 | PF00069 | 0.665 |
MOD_CK1_1 | 419 | 425 | PF00069 | 0.529 |
MOD_CK1_1 | 526 | 532 | PF00069 | 0.581 |
MOD_CK1_1 | 57 | 63 | PF00069 | 0.653 |
MOD_CK1_1 | 64 | 70 | PF00069 | 0.597 |
MOD_CK2_1 | 169 | 175 | PF00069 | 0.515 |
MOD_CK2_1 | 28 | 34 | PF00069 | 0.720 |
MOD_CK2_1 | 55 | 61 | PF00069 | 0.719 |
MOD_CK2_1 | 619 | 625 | PF00069 | 0.489 |
MOD_CK2_1 | 720 | 726 | PF00069 | 0.338 |
MOD_CK2_1 | 814 | 820 | PF00069 | 0.442 |
MOD_Cter_Amidation | 18 | 21 | PF01082 | 0.582 |
MOD_Cter_Amidation | 95 | 98 | PF01082 | 0.682 |
MOD_GlcNHglycan | 12 | 15 | PF01048 | 0.698 |
MOD_GlcNHglycan | 139 | 143 | PF01048 | 0.652 |
MOD_GlcNHglycan | 233 | 236 | PF01048 | 0.314 |
MOD_GlcNHglycan | 421 | 424 | PF01048 | 0.435 |
MOD_GlcNHglycan | 463 | 466 | PF01048 | 0.542 |
MOD_GlcNHglycan | 597 | 600 | PF01048 | 0.535 |
MOD_GlcNHglycan | 690 | 693 | PF01048 | 0.296 |
MOD_GlcNHglycan | 748 | 751 | PF01048 | 0.471 |
MOD_GlcNHglycan | 835 | 838 | PF01048 | 0.245 |
MOD_GSK3_1 | 117 | 124 | PF00069 | 0.753 |
MOD_GSK3_1 | 138 | 145 | PF00069 | 0.578 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.437 |
MOD_GSK3_1 | 211 | 218 | PF00069 | 0.474 |
MOD_GSK3_1 | 24 | 31 | PF00069 | 0.728 |
MOD_GSK3_1 | 306 | 313 | PF00069 | 0.461 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.683 |
MOD_GSK3_1 | 322 | 329 | PF00069 | 0.456 |
MOD_GSK3_1 | 451 | 458 | PF00069 | 0.426 |
MOD_GSK3_1 | 461 | 468 | PF00069 | 0.476 |
MOD_GSK3_1 | 522 | 529 | PF00069 | 0.630 |
MOD_GSK3_1 | 55 | 62 | PF00069 | 0.605 |
MOD_GSK3_1 | 581 | 588 | PF00069 | 0.424 |
MOD_GSK3_1 | 682 | 689 | PF00069 | 0.431 |
MOD_GSK3_1 | 720 | 727 | PF00069 | 0.338 |
MOD_GSK3_1 | 737 | 744 | PF00069 | 0.416 |
MOD_GSK3_1 | 833 | 840 | PF00069 | 0.440 |
MOD_GSK3_1 | 872 | 879 | PF00069 | 0.397 |
MOD_N-GLC_1 | 523 | 528 | PF02516 | 0.666 |
MOD_N-GLC_1 | 741 | 746 | PF02516 | 0.515 |
MOD_N-GLC_1 | 9 | 14 | PF02516 | 0.669 |
MOD_NEK2_1 | 273 | 278 | PF00069 | 0.438 |
MOD_NEK2_1 | 671 | 676 | PF00069 | 0.434 |
MOD_NEK2_1 | 724 | 729 | PF00069 | 0.356 |
MOD_NEK2_1 | 735 | 740 | PF00069 | 0.427 |
MOD_NEK2_1 | 838 | 843 | PF00069 | 0.527 |
MOD_NEK2_1 | 881 | 886 | PF00069 | 0.457 |
MOD_NEK2_2 | 327 | 332 | PF00069 | 0.401 |
MOD_NEK2_2 | 585 | 590 | PF00069 | 0.489 |
MOD_PIKK_1 | 121 | 127 | PF00454 | 0.626 |
MOD_PIKK_1 | 140 | 146 | PF00454 | 0.626 |
MOD_PIKK_1 | 451 | 457 | PF00454 | 0.392 |
MOD_PIKK_1 | 715 | 721 | PF00454 | 0.399 |
MOD_PIKK_1 | 754 | 760 | PF00454 | 0.476 |
MOD_PIKK_1 | 76 | 82 | PF00454 | 0.713 |
MOD_PIKK_1 | 947 | 953 | PF00454 | 0.431 |
MOD_PK_1 | 660 | 666 | PF00069 | 0.515 |
MOD_PKA_2 | 10 | 16 | PF00069 | 0.663 |
MOD_PKA_2 | 322 | 328 | PF00069 | 0.527 |
MOD_PKA_2 | 35 | 41 | PF00069 | 0.737 |
MOD_PKA_2 | 381 | 387 | PF00069 | 0.437 |
MOD_PKA_2 | 514 | 520 | PF00069 | 0.469 |
MOD_PKA_2 | 581 | 587 | PF00069 | 0.483 |
MOD_PKA_2 | 838 | 844 | PF00069 | 0.515 |
MOD_PKA_2 | 881 | 887 | PF00069 | 0.364 |
MOD_Plk_1 | 179 | 185 | PF00069 | 0.565 |
MOD_Plk_1 | 192 | 198 | PF00069 | 0.442 |
MOD_Plk_1 | 686 | 692 | PF00069 | 0.431 |
MOD_Plk_1 | 741 | 747 | PF00069 | 0.564 |
MOD_Plk_1 | 814 | 820 | PF00069 | 0.438 |
MOD_Plk_2-3 | 28 | 34 | PF00069 | 0.638 |
MOD_Plk_2-3 | 552 | 558 | PF00069 | 0.440 |
MOD_Plk_4 | 142 | 148 | PF00069 | 0.381 |
MOD_Plk_4 | 169 | 175 | PF00069 | 0.431 |
MOD_Plk_4 | 381 | 387 | PF00069 | 0.331 |
MOD_Plk_4 | 442 | 448 | PF00069 | 0.437 |
MOD_Plk_4 | 465 | 471 | PF00069 | 0.305 |
MOD_Plk_4 | 585 | 591 | PF00069 | 0.490 |
MOD_Plk_4 | 881 | 887 | PF00069 | 0.410 |
MOD_Plk_4 | 929 | 935 | PF00069 | 0.502 |
MOD_ProDKin_1 | 219 | 225 | PF00069 | 0.436 |
MOD_ProDKin_1 | 317 | 323 | PF00069 | 0.443 |
MOD_ProDKin_1 | 407 | 413 | PF00069 | 0.515 |
MOD_ProDKin_1 | 416 | 422 | PF00069 | 0.505 |
MOD_ProDKin_1 | 619 | 625 | PF00069 | 0.394 |
MOD_ProDKin_1 | 672 | 678 | PF00069 | 0.431 |
MOD_SUMO_rev_2 | 279 | 288 | PF00179 | 0.442 |
MOD_SUMO_rev_2 | 369 | 376 | PF00179 | 0.502 |
MOD_SUMO_rev_2 | 499 | 509 | PF00179 | 0.533 |
TRG_DiLeu_BaEn_1 | 105 | 110 | PF01217 | 0.687 |
TRG_DiLeu_BaLyEn_6 | 255 | 260 | PF01217 | 0.456 |
TRG_DiLeu_BaLyEn_6 | 543 | 548 | PF01217 | 0.564 |
TRG_DiLeu_BaLyEn_6 | 644 | 649 | PF01217 | 0.509 |
TRG_ENDOCYTIC_2 | 146 | 149 | PF00928 | 0.550 |
TRG_ENDOCYTIC_2 | 293 | 296 | PF00928 | 0.431 |
TRG_ENDOCYTIC_2 | 314 | 317 | PF00928 | 0.515 |
TRG_ENDOCYTIC_2 | 350 | 353 | PF00928 | 0.407 |
TRG_ENDOCYTIC_2 | 394 | 397 | PF00928 | 0.344 |
TRG_ENDOCYTIC_2 | 560 | 563 | PF00928 | 0.417 |
TRG_ENDOCYTIC_2 | 762 | 765 | PF00928 | 0.448 |
TRG_ER_diArg_1 | 132 | 134 | PF00400 | 0.459 |
TRG_ER_diArg_1 | 379 | 382 | PF00400 | 0.467 |
TRG_ER_diArg_1 | 544 | 547 | PF00400 | 0.543 |
TRG_ER_diArg_1 | 785 | 787 | PF00400 | 0.488 |
TRG_ER_diArg_1 | 889 | 892 | PF00400 | 0.464 |
TRG_ER_diArg_1 | 934 | 937 | PF00400 | 0.485 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IJN8 | Leptomonas seymouri | 75% | 100% |
A0A0N1PBS6 | Leptomonas seymouri | 27% | 100% |
A0A0S4JM05 | Bodo saltans | 27% | 100% |
A0A0S4JNU7 | Bodo saltans | 40% | 100% |
A0A1X0NU75 | Trypanosomatidae | 50% | 100% |
A0A1X0P8P3 | Trypanosomatidae | 26% | 100% |
A0A3Q8IFJ7 | Leishmania donovani | 95% | 100% |
A0A3Q8IIX7 | Leishmania donovani | 27% | 100% |
A0A3R7NHC0 | Trypanosoma rangeli | 26% | 100% |
A0A422N8J1 | Trypanosoma rangeli | 48% | 100% |
A4FUD3 | Bos taurus | 29% | 100% |
A4HKL0 | Leishmania braziliensis | 85% | 100% |
A4HNM7 | Leishmania braziliensis | 26% | 100% |
A4I843 | Leishmania infantum | 95% | 100% |
A4ICW8 | Leishmania infantum | 27% | 100% |
A5DI11 | Meyerozyma guilliermondii (strain ATCC 6260 / CBS 566 / DSM 6381 / JCM 1539 / NBRC 10279 / NRRL Y-324) | 25% | 100% |
C4YJQ8 | Candida albicans (strain WO-1) | 25% | 100% |
D0A2I0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
D0AAB0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 49% | 100% |
E9ASD6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
O08810 | Mus musculus | 29% | 100% |
O14460 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 25% | 100% |
O23755 | Beta vulgaris | 25% | 100% |
O74945 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 24% | 100% |
O94316 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 30% | 100% |
P15112 | Dictyostelium discoideum | 26% | 100% |
P32324 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 26% | 100% |
Q06193 | Entamoeba histolytica | 26% | 100% |
Q15029 | Homo sapiens | 29% | 100% |
Q17152 | Blastocystis hominis | 26% | 100% |
Q23716 | Cryptosporidium parvum | 27% | 100% |
Q4Q259 | Leishmania major | 27% | 100% |
Q4Q555 | Leishmania major | 95% | 100% |
Q5A0M4 | Candida albicans (strain SC5314 / ATCC MYA-2876) | 25% | 100% |
Q5F3X4 | Gallus gallus | 30% | 100% |
Q5R6E0 | Pongo abelii | 29% | 100% |
Q6BJ25 | Debaryomyces hansenii (strain ATCC 36239 / CBS 767 / BCRC 21394 / JCM 1990 / NBRC 0083 / IGC 2968) | 25% | 100% |
Q6CPQ9 | Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) | 25% | 100% |
Q6FYA7 | Candida glabrata (strain ATCC 2001 / CBS 138 / JCM 3761 / NBRC 0622 / NRRL Y-65) | 26% | 100% |
Q74M52 | Nanoarchaeum equitans (strain Kin4-M) | 23% | 100% |
Q754C8 | Ashbya gossypii (strain ATCC 10895 / CBS 109.51 / FGSC 9923 / NRRL Y-1056) | 26% | 100% |
Q874B9 | Komagataella pastoris | 26% | 100% |
Q875S0 | Lachancea kluyveri (strain ATCC 58438 / CBS 3082 / BCRC 21498 / NBRC 1685 / JCM 7257 / NCYC 543 / NRRL Y-12651) | 26% | 100% |
Q875Z2 | Naumovozyma castellii (strain ATCC 76901 / BCRC 22586 / CBS 4309 / NBRC 1992 / NRRL Y-12630) | 26% | 100% |
Q96X45 | Neurospora crassa (strain ATCC 24698 / 74-OR23-1A / CBS 708.71 / DSM 1257 / FGSC 987) | 26% | 100% |
V5AW74 | Trypanosoma cruzi | 49% | 100% |
V5DRS6 | Trypanosoma cruzi | 26% | 100% |