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: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 16 |
NetGPI | no | yes: 0, no: 16 |
Related structures:
AlphaFold database: A4HAT8
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 9 |
GO:0006396 | RNA processing | 6 | 9 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 9 |
GO:0006807 | nitrogen compound metabolic process | 2 | 9 |
GO:0008152 | metabolic process | 1 | 9 |
GO:0008380 | RNA splicing | 7 | 9 |
GO:0009987 | cellular process | 1 | 9 |
GO:0016070 | RNA metabolic process | 5 | 9 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 9 |
GO:0043170 | macromolecule metabolic process | 3 | 9 |
GO:0044237 | cellular metabolic process | 2 | 9 |
GO:0044238 | primary metabolic process | 2 | 9 |
GO:0046483 | heterocycle metabolic process | 3 | 9 |
GO:0071704 | organic substance metabolic process | 2 | 9 |
GO:0090304 | nucleic acid metabolic process | 4 | 9 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 17 |
GO:0003676 | nucleic acid binding | 3 | 14 |
GO:0003824 | catalytic activity | 1 | 17 |
GO:0004386 | helicase activity | 2 | 17 |
GO:0005488 | binding | 1 | 17 |
GO:0005524 | ATP binding | 5 | 17 |
GO:0016787 | hydrolase activity | 2 | 17 |
GO:0017076 | purine nucleotide binding | 4 | 17 |
GO:0030554 | adenyl nucleotide binding | 5 | 17 |
GO:0032553 | ribonucleotide binding | 3 | 17 |
GO:0032555 | purine ribonucleotide binding | 4 | 17 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 17 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 17 |
GO:0036094 | small molecule binding | 2 | 17 |
GO:0043167 | ion binding | 2 | 17 |
GO:0043168 | anion binding | 3 | 17 |
GO:0097159 | organic cyclic compound binding | 2 | 17 |
GO:0097367 | carbohydrate derivative binding | 2 | 17 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 17 |
GO:0140657 | ATP-dependent activity | 1 | 17 |
GO:1901265 | nucleoside phosphate binding | 3 | 17 |
GO:1901363 | heterocyclic compound binding | 2 | 17 |
GO:0003723 | RNA binding | 4 | 1 |
GO:0003724 | RNA helicase activity | 3 | 9 |
GO:0008186 | ATP-dependent activity, acting on RNA | 2 | 9 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 9 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 565 | 569 | PF00656 | 0.477 |
CLV_C14_Caspase3-7 | 675 | 679 | PF00656 | 0.410 |
CLV_C14_Caspase3-7 | 741 | 745 | PF00656 | 0.341 |
CLV_NRD_NRD_1 | 118 | 120 | PF00675 | 0.226 |
CLV_NRD_NRD_1 | 149 | 151 | PF00675 | 0.189 |
CLV_NRD_NRD_1 | 206 | 208 | PF00675 | 0.207 |
CLV_NRD_NRD_1 | 362 | 364 | PF00675 | 0.211 |
CLV_NRD_NRD_1 | 416 | 418 | PF00675 | 0.190 |
CLV_NRD_NRD_1 | 507 | 509 | PF00675 | 0.280 |
CLV_NRD_NRD_1 | 639 | 641 | PF00675 | 0.209 |
CLV_NRD_NRD_1 | 752 | 754 | PF00675 | 0.437 |
CLV_NRD_NRD_1 | 757 | 759 | PF00675 | 0.474 |
CLV_PCSK_KEX2_1 | 118 | 120 | PF00082 | 0.226 |
CLV_PCSK_KEX2_1 | 206 | 208 | PF00082 | 0.223 |
CLV_PCSK_KEX2_1 | 29 | 31 | PF00082 | 0.700 |
CLV_PCSK_KEX2_1 | 4 | 6 | PF00082 | 0.584 |
CLV_PCSK_KEX2_1 | 507 | 509 | PF00082 | 0.280 |
CLV_PCSK_KEX2_1 | 589 | 591 | PF00082 | 0.361 |
CLV_PCSK_KEX2_1 | 69 | 71 | PF00082 | 0.448 |
CLV_PCSK_KEX2_1 | 752 | 754 | PF00082 | 0.423 |
CLV_PCSK_PC1ET2_1 | 29 | 31 | PF00082 | 0.700 |
CLV_PCSK_PC1ET2_1 | 4 | 6 | PF00082 | 0.689 |
CLV_PCSK_PC1ET2_1 | 589 | 591 | PF00082 | 0.361 |
CLV_PCSK_PC1ET2_1 | 69 | 71 | PF00082 | 0.460 |
CLV_PCSK_SKI1_1 | 167 | 171 | PF00082 | 0.220 |
CLV_PCSK_SKI1_1 | 201 | 205 | PF00082 | 0.245 |
CLV_PCSK_SKI1_1 | 431 | 435 | PF00082 | 0.416 |
CLV_PCSK_SKI1_1 | 520 | 524 | PF00082 | 0.257 |
CLV_PCSK_SKI1_1 | 55 | 59 | PF00082 | 0.570 |
CLV_PCSK_SKI1_1 | 641 | 645 | PF00082 | 0.207 |
CLV_PCSK_SKI1_1 | 677 | 681 | PF00082 | 0.243 |
CLV_Separin_Metazoa | 250 | 254 | PF03568 | 0.246 |
CLV_Separin_Metazoa | 448 | 452 | PF03568 | 0.326 |
DEG_APCC_DBOX_1 | 314 | 322 | PF00400 | 0.424 |
DEG_SCF_FBW7_1 | 318 | 323 | PF00400 | 0.414 |
DEG_SCF_FBW7_1 | 654 | 659 | PF00400 | 0.334 |
DOC_CYCLIN_RxL_1 | 198 | 205 | PF00134 | 0.510 |
DOC_CYCLIN_yCln2_LP_2 | 328 | 334 | PF00134 | 0.388 |
DOC_MAPK_gen_1 | 118 | 125 | PF00069 | 0.410 |
DOC_MAPK_gen_1 | 206 | 214 | PF00069 | 0.413 |
DOC_MAPK_gen_1 | 428 | 438 | PF00069 | 0.187 |
DOC_MAPK_gen_1 | 507 | 514 | PF00069 | 0.480 |
DOC_MAPK_gen_1 | 674 | 684 | PF00069 | 0.390 |
DOC_MAPK_HePTP_8 | 125 | 137 | PF00069 | 0.420 |
DOC_MAPK_MEF2A_6 | 128 | 137 | PF00069 | 0.421 |
DOC_MAPK_MEF2A_6 | 333 | 342 | PF00069 | 0.264 |
DOC_MAPK_MEF2A_6 | 677 | 684 | PF00069 | 0.495 |
DOC_MAPK_MEF2A_6 | 78 | 86 | PF00069 | 0.358 |
DOC_MAPK_RevD_3 | 16 | 30 | PF00069 | 0.424 |
DOC_PP2B_LxvP_1 | 328 | 331 | PF13499 | 0.378 |
DOC_PP2B_LxvP_1 | 523 | 526 | PF13499 | 0.505 |
DOC_PP2B_LxvP_1 | 619 | 622 | PF13499 | 0.501 |
DOC_PP4_FxxP_1 | 170 | 173 | PF00568 | 0.431 |
DOC_PP4_FxxP_1 | 246 | 249 | PF00568 | 0.403 |
DOC_PP4_FxxP_1 | 474 | 477 | PF00568 | 0.336 |
DOC_PP4_FxxP_1 | 547 | 550 | PF00568 | 0.435 |
DOC_USP7_MATH_1 | 258 | 262 | PF00917 | 0.316 |
DOC_USP7_MATH_1 | 295 | 299 | PF00917 | 0.518 |
DOC_USP7_MATH_1 | 301 | 305 | PF00917 | 0.614 |
DOC_USP7_MATH_1 | 372 | 376 | PF00917 | 0.413 |
DOC_USP7_MATH_1 | 622 | 626 | PF00917 | 0.449 |
DOC_USP7_MATH_1 | 656 | 660 | PF00917 | 0.503 |
DOC_USP7_MATH_1 | 693 | 697 | PF00917 | 0.466 |
DOC_USP7_UBL2_3 | 349 | 353 | PF12436 | 0.360 |
DOC_WW_Pin1_4 | 316 | 321 | PF00397 | 0.705 |
DOC_WW_Pin1_4 | 40 | 45 | PF00397 | 0.483 |
DOC_WW_Pin1_4 | 652 | 657 | PF00397 | 0.483 |
LIG_14-3-3_CanoR_1 | 431 | 436 | PF00244 | 0.359 |
LIG_14-3-3_CanoR_1 | 598 | 603 | PF00244 | 0.477 |
LIG_14-3-3_CanoR_1 | 613 | 617 | PF00244 | 0.370 |
LIG_14-3-3_CanoR_1 | 624 | 628 | PF00244 | 0.476 |
LIG_14-3-3_CanoR_1 | 671 | 677 | PF00244 | 0.476 |
LIG_14-3-3_CanoR_1 | 686 | 690 | PF00244 | 0.434 |
LIG_14-3-3_CanoR_1 | 719 | 728 | PF00244 | 0.427 |
LIG_Actin_WH2_2 | 153 | 169 | PF00022 | 0.413 |
LIG_Actin_WH2_2 | 599 | 615 | PF00022 | 0.216 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.449 |
LIG_BIR_III_4 | 566 | 570 | PF00653 | 0.380 |
LIG_BRCT_BRCA1_1 | 483 | 487 | PF00533 | 0.430 |
LIG_deltaCOP1_diTrp_1 | 725 | 735 | PF00928 | 0.421 |
LIG_EH1_1 | 79 | 87 | PF00400 | 0.176 |
LIG_FHA_1 | 107 | 113 | PF00498 | 0.432 |
LIG_FHA_1 | 153 | 159 | PF00498 | 0.415 |
LIG_FHA_1 | 191 | 197 | PF00498 | 0.413 |
LIG_FHA_1 | 216 | 222 | PF00498 | 0.514 |
LIG_FHA_1 | 333 | 339 | PF00498 | 0.386 |
LIG_FHA_1 | 360 | 366 | PF00498 | 0.420 |
LIG_FHA_1 | 450 | 456 | PF00498 | 0.329 |
LIG_FHA_1 | 461 | 467 | PF00498 | 0.286 |
LIG_FHA_1 | 532 | 538 | PF00498 | 0.334 |
LIG_FHA_1 | 634 | 640 | PF00498 | 0.327 |
LIG_FHA_1 | 667 | 673 | PF00498 | 0.500 |
LIG_FHA_1 | 77 | 83 | PF00498 | 0.396 |
LIG_FHA_1 | 92 | 98 | PF00498 | 0.395 |
LIG_FHA_2 | 169 | 175 | PF00498 | 0.409 |
LIG_FHA_2 | 321 | 327 | PF00498 | 0.524 |
LIG_FHA_2 | 432 | 438 | PF00498 | 0.330 |
LIG_FHA_2 | 673 | 679 | PF00498 | 0.420 |
LIG_GBD_Chelix_1 | 195 | 203 | PF00786 | 0.310 |
LIG_LIR_Apic_2 | 168 | 173 | PF02991 | 0.431 |
LIG_LIR_Apic_2 | 244 | 249 | PF02991 | 0.401 |
LIG_LIR_Apic_2 | 402 | 406 | PF02991 | 0.421 |
LIG_LIR_Apic_2 | 471 | 477 | PF02991 | 0.384 |
LIG_LIR_Gen_1 | 176 | 186 | PF02991 | 0.477 |
LIG_LIR_Gen_1 | 437 | 445 | PF02991 | 0.299 |
LIG_LIR_Gen_1 | 485 | 496 | PF02991 | 0.319 |
LIG_LIR_Gen_1 | 645 | 656 | PF02991 | 0.410 |
LIG_LIR_Gen_1 | 733 | 743 | PF02991 | 0.418 |
LIG_LIR_LC3C_4 | 209 | 214 | PF02991 | 0.441 |
LIG_LIR_Nem_3 | 176 | 181 | PF02991 | 0.440 |
LIG_LIR_Nem_3 | 209 | 213 | PF02991 | 0.408 |
LIG_LIR_Nem_3 | 437 | 441 | PF02991 | 0.302 |
LIG_LIR_Nem_3 | 471 | 475 | PF02991 | 0.410 |
LIG_LIR_Nem_3 | 484 | 490 | PF02991 | 0.313 |
LIG_LIR_Nem_3 | 51 | 57 | PF02991 | 0.403 |
LIG_LIR_Nem_3 | 645 | 651 | PF02991 | 0.410 |
LIG_LIR_Nem_3 | 670 | 676 | PF02991 | 0.419 |
LIG_LIR_Nem_3 | 733 | 739 | PF02991 | 0.378 |
LIG_NRBOX | 199 | 205 | PF00104 | 0.510 |
LIG_PCNA_TLS_4 | 641 | 648 | PF02747 | 0.435 |
LIG_RPA_C_Fungi | 681 | 693 | PF08784 | 0.361 |
LIG_SH2_CRK | 178 | 182 | PF00017 | 0.337 |
LIG_SH2_CRK | 343 | 347 | PF00017 | 0.254 |
LIG_SH2_CRK | 488 | 492 | PF00017 | 0.341 |
LIG_SH2_CRK | 609 | 613 | PF00017 | 0.372 |
LIG_SH2_CRK | 673 | 677 | PF00017 | 0.390 |
LIG_SH2_SRC | 255 | 258 | PF00017 | 0.337 |
LIG_SH2_STAP1 | 178 | 182 | PF00017 | 0.322 |
LIG_SH2_STAT3 | 389 | 392 | PF00017 | 0.290 |
LIG_SH2_STAT5 | 227 | 230 | PF00017 | 0.330 |
LIG_SH2_STAT5 | 255 | 258 | PF00017 | 0.353 |
LIG_SH2_STAT5 | 383 | 386 | PF00017 | 0.265 |
LIG_SH2_STAT5 | 403 | 406 | PF00017 | 0.111 |
LIG_SH2_STAT5 | 492 | 495 | PF00017 | 0.283 |
LIG_SH2_STAT5 | 581 | 584 | PF00017 | 0.482 |
LIG_SH2_STAT5 | 596 | 599 | PF00017 | 0.347 |
LIG_SH2_STAT5 | 627 | 630 | PF00017 | 0.548 |
LIG_SH2_STAT5 | 633 | 636 | PF00017 | 0.347 |
LIG_SH2_STAT5 | 736 | 739 | PF00017 | 0.387 |
LIG_SH3_3 | 226 | 232 | PF00018 | 0.341 |
LIG_SH3_3 | 328 | 334 | PF00018 | 0.501 |
LIG_SH3_3 | 335 | 341 | PF00018 | 0.304 |
LIG_SH3_3 | 463 | 469 | PF00018 | 0.362 |
LIG_SH3_5 | 251 | 255 | PF00018 | 0.341 |
LIG_SH3_5 | 629 | 633 | PF00018 | 0.262 |
LIG_Sin3_3 | 210 | 217 | PF02671 | 0.343 |
LIG_SUMO_SIM_anti_2 | 179 | 185 | PF11976 | 0.275 |
LIG_SUMO_SIM_anti_2 | 335 | 341 | PF11976 | 0.234 |
LIG_SUMO_SIM_anti_2 | 457 | 463 | PF11976 | 0.299 |
LIG_SUMO_SIM_par_1 | 179 | 185 | PF11976 | 0.254 |
LIG_SUMO_SIM_par_1 | 457 | 463 | PF11976 | 0.282 |
LIG_SUMO_SIM_par_1 | 727 | 733 | PF11976 | 0.265 |
LIG_SUMO_SIM_par_1 | 82 | 89 | PF11976 | 0.273 |
LIG_TYR_ITSM | 174 | 181 | PF00017 | 0.143 |
LIG_UBA3_1 | 521 | 527 | PF00899 | 0.390 |
MOD_CK1_1 | 124 | 130 | PF00069 | 0.343 |
MOD_CK1_1 | 40 | 46 | PF00069 | 0.521 |
MOD_CK1_1 | 410 | 416 | PF00069 | 0.254 |
MOD_CK1_1 | 8 | 14 | PF00069 | 0.433 |
MOD_CK1_1 | 91 | 97 | PF00069 | 0.261 |
MOD_CK2_1 | 320 | 326 | PF00069 | 0.416 |
MOD_CK2_1 | 719 | 725 | PF00069 | 0.298 |
MOD_Cter_Amidation | 505 | 508 | PF01082 | 0.309 |
MOD_Cter_Amidation | 587 | 590 | PF01082 | 0.358 |
MOD_GlcNHglycan | 215 | 218 | PF01048 | 0.254 |
MOD_GlcNHglycan | 236 | 239 | PF01048 | 0.469 |
MOD_GlcNHglycan | 299 | 302 | PF01048 | 0.617 |
MOD_GlcNHglycan | 39 | 42 | PF01048 | 0.579 |
MOD_GlcNHglycan | 412 | 415 | PF01048 | 0.254 |
MOD_GlcNHglycan | 50 | 53 | PF01048 | 0.507 |
MOD_GlcNHglycan | 658 | 661 | PF01048 | 0.224 |
MOD_GlcNHglycan | 721 | 724 | PF01048 | 0.309 |
MOD_GlcNHglycan | 90 | 93 | PF01048 | 0.277 |
MOD_GSK3_1 | 202 | 209 | PF00069 | 0.327 |
MOD_GSK3_1 | 297 | 304 | PF00069 | 0.663 |
MOD_GSK3_1 | 316 | 323 | PF00069 | 0.668 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.592 |
MOD_GSK3_1 | 390 | 397 | PF00069 | 0.277 |
MOD_GSK3_1 | 652 | 659 | PF00069 | 0.342 |
MOD_GSK3_1 | 713 | 720 | PF00069 | 0.326 |
MOD_GSK3_1 | 730 | 737 | PF00069 | 0.374 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.414 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.193 |
MOD_LATS_1 | 144 | 150 | PF00433 | 0.309 |
MOD_N-GLC_1 | 152 | 157 | PF02516 | 0.143 |
MOD_N-GLC_1 | 176 | 181 | PF02516 | 0.200 |
MOD_NEK2_1 | 104 | 109 | PF00069 | 0.236 |
MOD_NEK2_1 | 21 | 26 | PF00069 | 0.669 |
MOD_NEK2_1 | 296 | 301 | PF00069 | 0.465 |
MOD_NEK2_1 | 342 | 347 | PF00069 | 0.287 |
MOD_NEK2_1 | 460 | 465 | PF00069 | 0.372 |
MOD_NEK2_1 | 612 | 617 | PF00069 | 0.342 |
MOD_NEK2_1 | 680 | 685 | PF00069 | 0.341 |
MOD_NEK2_1 | 717 | 722 | PF00069 | 0.390 |
MOD_NEK2_1 | 730 | 735 | PF00069 | 0.244 |
MOD_NEK2_2 | 344 | 349 | PF00069 | 0.279 |
MOD_PIKK_1 | 112 | 118 | PF00454 | 0.254 |
MOD_PIKK_1 | 21 | 27 | PF00454 | 0.521 |
MOD_PIKK_1 | 43 | 49 | PF00454 | 0.327 |
MOD_PIKK_1 | 646 | 652 | PF00454 | 0.250 |
MOD_PIKK_1 | 92 | 98 | PF00454 | 0.217 |
MOD_PKA_1 | 206 | 212 | PF00069 | 0.279 |
MOD_PKA_2 | 206 | 212 | PF00069 | 0.223 |
MOD_PKA_2 | 332 | 338 | PF00069 | 0.467 |
MOD_PKA_2 | 612 | 618 | PF00069 | 0.320 |
MOD_PKA_2 | 623 | 629 | PF00069 | 0.492 |
MOD_PKA_2 | 685 | 691 | PF00069 | 0.313 |
MOD_Plk_1 | 152 | 158 | PF00069 | 0.351 |
MOD_Plk_1 | 176 | 182 | PF00069 | 0.250 |
MOD_Plk_1 | 187 | 193 | PF00069 | 0.318 |
MOD_Plk_1 | 256 | 262 | PF00069 | 0.374 |
MOD_Plk_1 | 372 | 378 | PF00069 | 0.254 |
MOD_Plk_1 | 730 | 736 | PF00069 | 0.399 |
MOD_Plk_2-3 | 168 | 174 | PF00069 | 0.309 |
MOD_Plk_2-3 | 437 | 443 | PF00069 | 0.355 |
MOD_Plk_4 | 176 | 182 | PF00069 | 0.320 |
MOD_Plk_4 | 223 | 229 | PF00069 | 0.412 |
MOD_Plk_4 | 390 | 396 | PF00069 | 0.252 |
MOD_Plk_4 | 454 | 460 | PF00069 | 0.320 |
MOD_Plk_4 | 623 | 629 | PF00069 | 0.519 |
MOD_Plk_4 | 685 | 691 | PF00069 | 0.270 |
MOD_Plk_4 | 713 | 719 | PF00069 | 0.264 |
MOD_Plk_4 | 80 | 86 | PF00069 | 0.300 |
MOD_ProDKin_1 | 316 | 322 | PF00069 | 0.704 |
MOD_ProDKin_1 | 40 | 46 | PF00069 | 0.479 |
MOD_ProDKin_1 | 652 | 658 | PF00069 | 0.353 |
TRG_DiLeu_BaEn_1 | 68 | 73 | PF01217 | 0.446 |
TRG_DiLeu_BaEn_1 | 725 | 730 | PF01217 | 0.309 |
TRG_ENDOCYTIC_2 | 178 | 181 | PF00928 | 0.337 |
TRG_ENDOCYTIC_2 | 343 | 346 | PF00928 | 0.254 |
TRG_ENDOCYTIC_2 | 488 | 491 | PF00928 | 0.270 |
TRG_ENDOCYTIC_2 | 54 | 57 | PF00928 | 0.395 |
TRG_ENDOCYTIC_2 | 609 | 612 | PF00928 | 0.366 |
TRG_ENDOCYTIC_2 | 673 | 676 | PF00928 | 0.265 |
TRG_ENDOCYTIC_2 | 736 | 739 | PF00928 | 0.322 |
TRG_ER_diArg_1 | 117 | 119 | PF00400 | 0.251 |
TRG_ER_diArg_1 | 206 | 208 | PF00400 | 0.267 |
TRG_ER_diArg_1 | 423 | 426 | PF00400 | 0.412 |
TRG_ER_diArg_1 | 507 | 509 | PF00400 | 0.346 |
TRG_ER_diArg_1 | 61 | 64 | PF00400 | 0.456 |
TRG_ER_diArg_1 | 751 | 753 | PF00400 | 0.478 |
TRG_NLS_MonoExtC_3 | 3 | 9 | PF00514 | 0.580 |
TRG_Pf-PMV_PEXEL_1 | 70 | 74 | PF00026 | 0.431 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P5V0 | Leptomonas seymouri | 41% | 100% |
A0A0N0P8Y1 | Leptomonas seymouri | 74% | 98% |
A0A0N0P9D2 | Leptomonas seymouri | 38% | 100% |
A0A0N1I0Z0 | Leptomonas seymouri | 36% | 70% |
A0A0N1IKA7 | Leptomonas seymouri | 34% | 84% |
A0A0N1PEU4 | Leptomonas seymouri | 37% | 80% |
A0A0S4IQ76 | Bodo saltans | 48% | 100% |
A0A0S4IR78 | Bodo saltans | 37% | 86% |
A0A0S4IS51 | Bodo saltans | 37% | 98% |
A0A0S4ITR4 | Bodo saltans | 33% | 71% |
A0A0S4IWU8 | Bodo saltans | 37% | 89% |
A0A0S4J157 | Bodo saltans | 42% | 100% |
A0A0S4JCY8 | Bodo saltans | 36% | 74% |
A0A1X0NJ46 | Trypanosomatidae | 44% | 100% |
A0A1X0NKY7 | Trypanosomatidae | 35% | 71% |
A0A1X0NVG5 | Trypanosomatidae | 35% | 71% |
A0A1X0P0D7 | Trypanosomatidae | 34% | 100% |
A0A1X0P872 | Trypanosomatidae | 38% | 86% |
A0A1X0P9K6 | Trypanosomatidae | 57% | 100% |
A0A3Q8IEC9 | Leishmania donovani | 30% | 70% |
A0A3Q8II71 | Leishmania donovani | 88% | 94% |
A0A3Q8IJ24 | Leishmania donovani | 35% | 80% |
A0A3Q8IWG4 | Leishmania donovani | 36% | 100% |
A0A3R7MA90 | Trypanosoma rangeli | 44% | 100% |
A0A3R7MM88 | Trypanosoma rangeli | 34% | 100% |
A0A3R7NT42 | Trypanosoma rangeli | 59% | 100% |
A0A3S7WYA1 | Leishmania donovani | 36% | 70% |
A0A3S7X8Z5 | Leishmania donovani | 42% | 100% |
A0A3S7XB01 | Leishmania donovani | 34% | 70% |
A0A422MXB1 | Trypanosoma rangeli | 34% | 72% |
A0A422N8L3 | Trypanosoma rangeli | 34% | 75% |
A0A422NK53 | Trypanosoma rangeli | 37% | 100% |
A4HDG6 | Leishmania braziliensis | 34% | 70% |
A4HME2 | Leishmania braziliensis | 42% | 100% |
A4HNU7 | Leishmania braziliensis | 34% | 80% |
A4HPE9 | Leishmania braziliensis | 34% | 70% |
A4HQ83 | Leishmania braziliensis | 32% | 100% |
A4I009 | Leishmania infantum | 29% | 70% |
A4I0U7 | Leishmania infantum | 36% | 70% |
A4IA06 | Leishmania infantum | 88% | 94% |
A4IB14 | Leishmania infantum | 42% | 100% |
A4ICJ0 | Leishmania infantum | 35% | 70% |
A4ICP7 | Leishmania infantum | 35% | 80% |
A4IDY1 | Leishmania infantum | 36% | 100% |
C9ZMN0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 57% | 100% |
C9ZN47 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 70% |
C9ZNP6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 100% |
D0A2R5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 40% | 86% |
D0A3F8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 71% |
D0A429 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 100% |
D0A778 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 73% |
D4A2Z8 | Rattus norvegicus | 29% | 76% |
E9AEU3 | Leishmania major | 42% | 96% |
E9AIQ7 | Leishmania braziliensis | 29% | 70% |
E9ASK7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 89% |
E9AT60 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 70% |
E9AU01 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 37% | 100% |
E9AVY2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 70% |
E9B512 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 94% |
E9B5Z9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 42% | 100% |
F4IE66 | Arabidopsis thaliana | 34% | 100% |
F4IJV4 | Arabidopsis thaliana | 38% | 73% |
F4ILR7 | Arabidopsis thaliana | 36% | 76% |
F4JMJ3 | Arabidopsis thaliana | 38% | 86% |
F4JRJ6 | Arabidopsis thaliana | 37% | 100% |
O22899 | Arabidopsis thaliana | 42% | 100% |
O35286 | Mus musculus | 40% | 95% |
O42945 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 42% | 100% |
O43143 | Homo sapiens | 40% | 95% |
O45244 | Caenorhabditis elegans | 40% | 75% |
O51767 | Borreliella burgdorferi (strain ATCC 35210 / DSM 4680 / CIP 102532 / B31) | 30% | 92% |
O60231 | Homo sapiens | 40% | 73% |
P0C9A2 | African swine fever virus (isolate Tick/South Africa/Pretoriuskop Pr4/1996) | 29% | 79% |
P0C9A3 | African swine fever virus (isolate Warthog/Namibia/Wart80/1980) | 29% | 79% |
P0C9A4 | African swine fever virus (isolate Pig/Kenya/KEN-50/1950) | 29% | 79% |
P15938 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 36% | 71% |
P20095 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 35% | 87% |
P24384 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 36% | 66% |
P34305 | Caenorhabditis elegans | 31% | 66% |
P34498 | Caenorhabditis elegans | 35% | 67% |
P36009 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 35% | 100% |
P53131 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 42% | 99% |
Q03319 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 35% | 100% |
Q05B79 | Bos taurus | 30% | 75% |
Q10752 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 38% | 72% |
Q14147 | Homo sapiens | 36% | 66% |
Q1EHT7 | Oryza sativa subsp. japonica | 29% | 75% |
Q20875 | Caenorhabditis elegans | 41% | 100% |
Q3ZBE0 | Bos taurus | 29% | 100% |
Q4Q0J4 | Leishmania major | 37% | 100% |
Q4Q1D7 | Leishmania major | 35% | 70% |
Q4Q1Y9 | Leishmania major | 36% | 100% |
Q4Q2X4 | Leishmania major | 87% | 100% |
Q4QAM3 | Leishmania major | 36% | 67% |
Q4QBJ7 | Leishmania major | 30% | 100% |
Q54MH3 | Dictyostelium discoideum | 39% | 69% |
Q54NJ4 | Dictyostelium discoideum | 41% | 100% |
Q5R864 | Pongo abelii | 34% | 97% |
Q5RAZ4 | Pongo abelii | 40% | 95% |
Q5RBD4 | Pongo abelii | 37% | 100% |
Q5UQ96 | Acanthamoeba polyphaga mimivirus | 26% | 100% |
Q5XH12 | Xenopus laevis | 27% | 100% |
Q5XI69 | Rattus norvegicus | 34% | 97% |
Q6PE54 | Mus musculus | 34% | 97% |
Q767K6 | Sus scrofa | 40% | 73% |
Q7K3M5 | Drosophila melanogaster | 41% | 100% |
Q7L7V1 | Homo sapiens | 27% | 100% |
Q7YR39 | Pan troglodytes | 40% | 73% |
Q80VY9 | Mus musculus | 35% | 100% |
Q89443 | African swine fever virus (strain Badajoz 1971 Vero-adapted) | 29% | 79% |
Q8BZS9 | Mus musculus | 27% | 100% |
Q8IX18 | Homo sapiens | 34% | 97% |
Q8TE96 | Homo sapiens | 29% | 100% |
Q8V9U2 | African swine fever virus (isolate Tick/Malawi/Lil 20-1/1983) | 29% | 79% |
Q8VHK9 | Mus musculus | 30% | 76% |
Q8VY00 | Arabidopsis thaliana | 39% | 73% |
Q924H9 | Mus musculus | 29% | 100% |
Q93Y16 | Arabidopsis thaliana | 36% | 100% |
Q9BKQ8 | Caenorhabditis elegans | 34% | 100% |
Q9DBV3 | Mus musculus | 35% | 66% |
Q9H2U1 | Homo sapiens | 30% | 75% |
Q9H5Z1 | Homo sapiens | 37% | 100% |
Q9H6R0 | Homo sapiens | 36% | 100% |
Q9HE06 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 34% | 100% |
Q9LZQ9 | Arabidopsis thaliana | 42% | 100% |
V5B3L7 | Trypanosoma cruzi | 33% | 100% |
V5B7H6 | Trypanosoma cruzi | 32% | 70% |
V5BKH2 | Trypanosoma cruzi | 56% | 99% |
V5BPV3 | Trypanosoma cruzi | 36% | 72% |
V5BV22 | Trypanosoma cruzi | 34% | 86% |
V5C0I9 | Trypanosoma cruzi | 34% | 97% |
V5D886 | Trypanosoma cruzi | 42% | 100% |