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: 22 |
NetGPI | no | yes: 0, no: 22 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 3 |
GO:0005737 | cytoplasm | 2 | 3 |
GO:0005819 | spindle | 5 | 2 |
GO:0032991 | protein-containing complex | 1 | 3 |
GO:0033588 | elongator holoenzyme complex | 3 | 3 |
GO:0043226 | organelle | 2 | 3 |
GO:0043227 | membrane-bounded organelle | 3 | 3 |
GO:0043228 | non-membrane-bounded organelle | 3 | 3 |
GO:0043229 | intracellular organelle | 3 | 3 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 3 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 3 |
GO:0110165 | cellular anatomical entity | 1 | 4 |
GO:0140535 | intracellular protein-containing complex | 2 | 3 |
GO:1902494 | catalytic complex | 2 | 3 |
GO:0016020 | membrane | 2 | 1 |
GO:0005635 | nuclear envelope | 4 | 1 |
GO:0005730 | nucleolus | 5 | 1 |
GO:0031967 | organelle envelope | 3 | 1 |
GO:0031975 | envelope | 2 | 1 |
Related structures:
AlphaFold database: Q4QB17
Term | Name | Level | Count |
---|---|---|---|
GO:0002097 | tRNA wobble base modification | 7 | 3 |
GO:0002098 | tRNA wobble uridine modification | 8 | 3 |
GO:0002926 | tRNA wobble base 5-methoxycarbonylmethyl-2-thiouridinylation | 9 | 3 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 3 |
GO:0006396 | RNA processing | 6 | 3 |
GO:0006399 | tRNA metabolic process | 7 | 3 |
GO:0006400 | tRNA modification | 6 | 3 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 3 |
GO:0006807 | nitrogen compound metabolic process | 2 | 3 |
GO:0008033 | tRNA processing | 8 | 3 |
GO:0008152 | metabolic process | 1 | 3 |
GO:0009451 | RNA modification | 5 | 3 |
GO:0009987 | cellular process | 1 | 3 |
GO:0016070 | RNA metabolic process | 5 | 3 |
GO:0034470 | ncRNA processing | 7 | 3 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 3 |
GO:0034660 | ncRNA metabolic process | 6 | 3 |
GO:0043170 | macromolecule metabolic process | 3 | 3 |
GO:0043412 | macromolecule modification | 4 | 3 |
GO:0044237 | cellular metabolic process | 2 | 3 |
GO:0044238 | primary metabolic process | 2 | 3 |
GO:0046483 | heterocycle metabolic process | 3 | 3 |
GO:0071704 | organic substance metabolic process | 2 | 3 |
GO:0090304 | nucleic acid metabolic process | 4 | 3 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 3 |
GO:0006259 | DNA metabolic process | 4 | 1 |
GO:0006473 | protein acetylation | 6 | 1 |
GO:0006475 | internal protein amino acid acetylation | 7 | 1 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0016570 | histone modification | 5 | 1 |
GO:0016573 | histone acetylation | 6 | 1 |
GO:0018193 | peptidyl-amino acid modification | 5 | 1 |
GO:0018205 | peptidyl-lysine modification | 6 | 1 |
GO:0018393 | internal peptidyl-lysine acetylation | 8 | 1 |
GO:0018394 | peptidyl-lysine acetylation | 7 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0036211 | protein modification process | 4 | 1 |
GO:0043007 | maintenance of rDNA | 6 | 1 |
GO:0043543 | protein acylation | 5 | 1 |
GO:0043570 | maintenance of DNA repeat elements | 5 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0051276 | chromosome organization | 5 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000049 | tRNA binding | 5 | 23 |
GO:0003676 | nucleic acid binding | 3 | 23 |
GO:0003723 | RNA binding | 4 | 23 |
GO:0003824 | catalytic activity | 1 | 23 |
GO:0005488 | binding | 1 | 23 |
GO:0016407 | acetyltransferase activity | 5 | 23 |
GO:0016740 | transferase activity | 2 | 23 |
GO:0016746 | acyltransferase activity | 3 | 23 |
GO:0016747 | acyltransferase activity, transferring groups other than amino-acyl groups | 4 | 23 |
GO:0043167 | ion binding | 2 | 23 |
GO:0043169 | cation binding | 3 | 23 |
GO:0046872 | metal ion binding | 4 | 23 |
GO:0051536 | iron-sulfur cluster binding | 3 | 23 |
GO:0051539 | 4 iron, 4 sulfur cluster binding | 4 | 23 |
GO:0051540 | metal cluster binding | 2 | 23 |
GO:0097159 | organic cyclic compound binding | 2 | 23 |
GO:0106261 | tRNA uridine(34) acetyltransferase activity | 6 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 23 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 11 | 13 | PF00675 | 0.499 |
CLV_NRD_NRD_1 | 120 | 122 | PF00675 | 0.432 |
CLV_NRD_NRD_1 | 161 | 163 | PF00675 | 0.430 |
CLV_NRD_NRD_1 | 190 | 192 | PF00675 | 0.429 |
CLV_NRD_NRD_1 | 344 | 346 | PF00675 | 0.240 |
CLV_NRD_NRD_1 | 644 | 646 | PF00675 | 0.279 |
CLV_PCSK_KEX2_1 | 120 | 122 | PF00082 | 0.429 |
CLV_PCSK_KEX2_1 | 13 | 15 | PF00082 | 0.683 |
CLV_PCSK_KEX2_1 | 344 | 346 | PF00082 | 0.233 |
CLV_PCSK_KEX2_1 | 496 | 498 | PF00082 | 0.228 |
CLV_PCSK_KEX2_1 | 644 | 646 | PF00082 | 0.287 |
CLV_PCSK_PC1ET2_1 | 13 | 15 | PF00082 | 0.683 |
CLV_PCSK_PC1ET2_1 | 496 | 498 | PF00082 | 0.293 |
CLV_PCSK_SKI1_1 | 121 | 125 | PF00082 | 0.417 |
CLV_PCSK_SKI1_1 | 625 | 629 | PF00082 | 0.398 |
CLV_PCSK_SKI1_1 | 694 | 698 | PF00082 | 0.617 |
DEG_APCC_DBOX_1 | 475 | 483 | PF00400 | 0.428 |
DEG_APCC_DBOX_1 | 496 | 504 | PF00400 | 0.428 |
DOC_CYCLIN_yCln2_LP_2 | 27 | 33 | PF00134 | 0.449 |
DOC_MAPK_gen_1 | 191 | 202 | PF00069 | 0.403 |
DOC_MAPK_gen_1 | 341 | 351 | PF00069 | 0.481 |
DOC_MAPK_gen_1 | 628 | 637 | PF00069 | 0.405 |
DOC_MAPK_HePTP_8 | 189 | 205 | PF00069 | 0.386 |
DOC_PIKK_1 | 98 | 106 | PF02985 | 0.462 |
DOC_PP2B_LxvP_1 | 25 | 28 | PF13499 | 0.496 |
DOC_PP4_FxxP_1 | 206 | 209 | PF00568 | 0.305 |
DOC_PP4_FxxP_1 | 21 | 24 | PF00568 | 0.474 |
DOC_PP4_FxxP_1 | 212 | 215 | PF00568 | 0.359 |
DOC_USP7_MATH_1 | 136 | 140 | PF00917 | 0.515 |
DOC_USP7_MATH_1 | 161 | 165 | PF00917 | 0.407 |
DOC_USP7_MATH_1 | 308 | 312 | PF00917 | 0.442 |
DOC_USP7_MATH_1 | 401 | 405 | PF00917 | 0.441 |
DOC_USP7_MATH_1 | 685 | 689 | PF00917 | 0.621 |
DOC_WW_Pin1_4 | 20 | 25 | PF00397 | 0.533 |
LIG_14-3-3_CanoR_1 | 162 | 170 | PF00244 | 0.430 |
LIG_14-3-3_CanoR_1 | 307 | 313 | PF00244 | 0.453 |
LIG_14-3-3_CanoR_1 | 344 | 350 | PF00244 | 0.453 |
LIG_14-3-3_CanoR_1 | 541 | 549 | PF00244 | 0.263 |
LIG_AP2alpha_1 | 536 | 540 | PF02296 | 0.290 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.774 |
LIG_EH1_1 | 460 | 468 | PF00400 | 0.493 |
LIG_eIF4E_1 | 461 | 467 | PF01652 | 0.461 |
LIG_EVH1_1 | 25 | 29 | PF00568 | 0.495 |
LIG_FHA_1 | 431 | 437 | PF00498 | 0.428 |
LIG_FHA_1 | 486 | 492 | PF00498 | 0.439 |
LIG_FHA_1 | 608 | 614 | PF00498 | 0.344 |
LIG_FHA_1 | 655 | 661 | PF00498 | 0.335 |
LIG_FHA_2 | 297 | 303 | PF00498 | 0.433 |
LIG_FHA_2 | 315 | 321 | PF00498 | 0.423 |
LIG_FHA_2 | 331 | 337 | PF00498 | 0.432 |
LIG_FHA_2 | 604 | 610 | PF00498 | 0.313 |
LIG_LIR_Apic_2 | 18 | 24 | PF02991 | 0.473 |
LIG_LIR_Apic_2 | 204 | 209 | PF02991 | 0.283 |
LIG_LIR_Apic_2 | 211 | 215 | PF02991 | 0.378 |
LIG_LIR_Apic_2 | 93 | 97 | PF02991 | 0.484 |
LIG_LIR_Gen_1 | 111 | 119 | PF02991 | 0.537 |
LIG_LIR_Gen_1 | 410 | 418 | PF02991 | 0.310 |
LIG_LIR_Gen_1 | 435 | 446 | PF02991 | 0.428 |
LIG_LIR_Gen_1 | 546 | 556 | PF02991 | 0.295 |
LIG_LIR_Gen_1 | 629 | 639 | PF02991 | 0.311 |
LIG_LIR_Gen_1 | 684 | 693 | PF02991 | 0.454 |
LIG_LIR_Gen_1 | 86 | 94 | PF02991 | 0.494 |
LIG_LIR_LC3C_4 | 198 | 203 | PF02991 | 0.384 |
LIG_LIR_Nem_3 | 111 | 116 | PF02991 | 0.470 |
LIG_LIR_Nem_3 | 167 | 173 | PF02991 | 0.392 |
LIG_LIR_Nem_3 | 277 | 281 | PF02991 | 0.430 |
LIG_LIR_Nem_3 | 410 | 415 | PF02991 | 0.316 |
LIG_LIR_Nem_3 | 426 | 431 | PF02991 | 0.441 |
LIG_LIR_Nem_3 | 435 | 441 | PF02991 | 0.428 |
LIG_LIR_Nem_3 | 546 | 552 | PF02991 | 0.279 |
LIG_LIR_Nem_3 | 558 | 564 | PF02991 | 0.261 |
LIG_LIR_Nem_3 | 594 | 598 | PF02991 | 0.329 |
LIG_LIR_Nem_3 | 684 | 689 | PF02991 | 0.639 |
LIG_LIR_Nem_3 | 695 | 699 | PF02991 | 0.650 |
LIG_LIR_Nem_3 | 86 | 90 | PF02991 | 0.479 |
LIG_PCNA_yPIPBox_3 | 175 | 189 | PF02747 | 0.431 |
LIG_Pex14_2 | 242 | 246 | PF04695 | 0.522 |
LIG_Pex14_2 | 412 | 416 | PF04695 | 0.335 |
LIG_Pex14_2 | 536 | 540 | PF04695 | 0.274 |
LIG_PTB_Apo_2 | 455 | 462 | PF02174 | 0.545 |
LIG_PTB_Phospho_1 | 455 | 461 | PF10480 | 0.545 |
LIG_SH2_CRK | 170 | 174 | PF00017 | 0.388 |
LIG_SH2_CRK | 595 | 599 | PF00017 | 0.290 |
LIG_SH2_CRK | 647 | 651 | PF00017 | 0.299 |
LIG_SH2_NCK_1 | 253 | 257 | PF00017 | 0.439 |
LIG_SH2_NCK_1 | 301 | 305 | PF00017 | 0.441 |
LIG_SH2_NCK_1 | 94 | 98 | PF00017 | 0.440 |
LIG_SH2_STAP1 | 285 | 289 | PF00017 | 0.453 |
LIG_SH2_STAP1 | 686 | 690 | PF00017 | 0.457 |
LIG_SH2_STAT5 | 220 | 223 | PF00017 | 0.428 |
LIG_SH2_STAT5 | 231 | 234 | PF00017 | 0.428 |
LIG_SH2_STAT5 | 337 | 340 | PF00017 | 0.439 |
LIG_SH2_STAT5 | 468 | 471 | PF00017 | 0.432 |
LIG_SH2_STAT5 | 490 | 493 | PF00017 | 0.432 |
LIG_SH2_STAT5 | 549 | 552 | PF00017 | 0.268 |
LIG_SH3_2 | 305 | 310 | PF14604 | 0.493 |
LIG_SH3_3 | 219 | 225 | PF00018 | 0.428 |
LIG_SH3_3 | 23 | 29 | PF00018 | 0.515 |
LIG_SH3_3 | 30 | 36 | PF00018 | 0.491 |
LIG_SH3_3 | 302 | 308 | PF00018 | 0.452 |
LIG_SH3_3 | 395 | 401 | PF00018 | 0.428 |
LIG_SUMO_SIM_anti_2 | 198 | 204 | PF11976 | 0.355 |
LIG_SUMO_SIM_anti_2 | 267 | 273 | PF11976 | 0.428 |
LIG_SUMO_SIM_par_1 | 198 | 204 | PF11976 | 0.355 |
LIG_SUMO_SIM_par_1 | 597 | 602 | PF11976 | 0.274 |
LIG_TRAF2_1 | 573 | 576 | PF00917 | 0.361 |
LIG_WRC_WIRS_1 | 686 | 691 | PF05994 | 0.597 |
LIG_WRC_WIRS_1 | 693 | 698 | PF05994 | 0.549 |
LIG_WRPW_2 | 450 | 453 | PF00400 | 0.274 |
MOD_CK1_1 | 127 | 133 | PF00069 | 0.483 |
MOD_CK1_1 | 164 | 170 | PF00069 | 0.406 |
MOD_CK1_1 | 543 | 549 | PF00069 | 0.297 |
MOD_CK1_1 | 64 | 70 | PF00069 | 0.719 |
MOD_CK1_1 | 668 | 674 | PF00069 | 0.549 |
MOD_CK1_1 | 684 | 690 | PF00069 | 0.345 |
MOD_CK1_1 | 86 | 92 | PF00069 | 0.493 |
MOD_CK2_1 | 136 | 142 | PF00069 | 0.564 |
MOD_CK2_1 | 254 | 260 | PF00069 | 0.307 |
MOD_CK2_1 | 308 | 314 | PF00069 | 0.263 |
MOD_CK2_1 | 336 | 342 | PF00069 | 0.327 |
MOD_CK2_1 | 400 | 406 | PF00069 | 0.304 |
MOD_CK2_1 | 570 | 576 | PF00069 | 0.335 |
MOD_CK2_1 | 603 | 609 | PF00069 | 0.298 |
MOD_CK2_1 | 69 | 75 | PF00069 | 0.543 |
MOD_GlcNHglycan | 139 | 142 | PF01048 | 0.556 |
MOD_GlcNHglycan | 197 | 200 | PF01048 | 0.396 |
MOD_GlcNHglycan | 256 | 259 | PF01048 | 0.290 |
MOD_GlcNHglycan | 302 | 305 | PF01048 | 0.316 |
MOD_GlcNHglycan | 338 | 341 | PF01048 | 0.267 |
MOD_GlcNHglycan | 416 | 419 | PF01048 | 0.508 |
MOD_GlcNHglycan | 44 | 47 | PF01048 | 0.543 |
MOD_GlcNHglycan | 55 | 58 | PF01048 | 0.749 |
MOD_GlcNHglycan | 667 | 670 | PF01048 | 0.541 |
MOD_GlcNHglycan | 682 | 686 | PF01048 | 0.496 |
MOD_GlcNHglycan | 71 | 74 | PF01048 | 0.455 |
MOD_GSK3_1 | 157 | 164 | PF00069 | 0.452 |
MOD_GSK3_1 | 296 | 303 | PF00069 | 0.279 |
MOD_GSK3_1 | 345 | 352 | PF00069 | 0.301 |
MOD_GSK3_1 | 432 | 439 | PF00069 | 0.279 |
MOD_GSK3_1 | 530 | 537 | PF00069 | 0.227 |
MOD_GSK3_1 | 570 | 577 | PF00069 | 0.368 |
MOD_GSK3_1 | 599 | 606 | PF00069 | 0.275 |
MOD_GSK3_1 | 61 | 68 | PF00069 | 0.653 |
MOD_GSK3_1 | 681 | 688 | PF00069 | 0.544 |
MOD_N-GLC_1 | 419 | 424 | PF02516 | 0.436 |
MOD_NEK2_1 | 124 | 129 | PF00069 | 0.430 |
MOD_NEK2_1 | 157 | 162 | PF00069 | 0.502 |
MOD_NEK2_1 | 201 | 206 | PF00069 | 0.325 |
MOD_NEK2_1 | 274 | 279 | PF00069 | 0.279 |
MOD_NEK2_1 | 290 | 295 | PF00069 | 0.292 |
MOD_NEK2_1 | 349 | 354 | PF00069 | 0.282 |
MOD_NEK2_1 | 411 | 416 | PF00069 | 0.463 |
MOD_NEK2_1 | 53 | 58 | PF00069 | 0.724 |
MOD_NEK2_1 | 654 | 659 | PF00069 | 0.348 |
MOD_NEK2_1 | 689 | 694 | PF00069 | 0.585 |
MOD_NEK2_1 | 69 | 74 | PF00069 | 0.474 |
MOD_NEK2_2 | 276 | 281 | PF00069 | 0.274 |
MOD_PIKK_1 | 247 | 253 | PF00454 | 0.290 |
MOD_PIKK_1 | 555 | 561 | PF00454 | 0.406 |
MOD_PIKK_1 | 599 | 605 | PF00454 | 0.390 |
MOD_PIKK_1 | 607 | 613 | PF00454 | 0.239 |
MOD_PIKK_1 | 614 | 620 | PF00454 | 0.193 |
MOD_PK_1 | 61 | 67 | PF00069 | 0.549 |
MOD_PKA_2 | 161 | 167 | PF00069 | 0.431 |
MOD_PKA_2 | 254 | 260 | PF00069 | 0.290 |
MOD_PKA_2 | 540 | 546 | PF00069 | 0.271 |
MOD_PKA_2 | 607 | 613 | PF00069 | 0.451 |
MOD_Plk_1 | 314 | 320 | PF00069 | 0.277 |
MOD_Plk_1 | 419 | 425 | PF00069 | 0.432 |
MOD_Plk_1 | 555 | 561 | PF00069 | 0.338 |
MOD_Plk_1 | 61 | 67 | PF00069 | 0.479 |
MOD_Plk_1 | 654 | 660 | PF00069 | 0.356 |
MOD_Plk_1 | 681 | 687 | PF00069 | 0.646 |
MOD_Plk_2-3 | 314 | 320 | PF00069 | 0.309 |
MOD_Plk_4 | 201 | 207 | PF00069 | 0.344 |
MOD_Plk_4 | 290 | 296 | PF00069 | 0.265 |
MOD_Plk_4 | 375 | 381 | PF00069 | 0.344 |
MOD_Plk_4 | 411 | 417 | PF00069 | 0.448 |
MOD_Plk_4 | 486 | 492 | PF00069 | 0.274 |
MOD_Plk_4 | 654 | 660 | PF00069 | 0.341 |
MOD_Plk_4 | 685 | 691 | PF00069 | 0.574 |
MOD_Plk_4 | 692 | 698 | PF00069 | 0.540 |
MOD_Plk_4 | 86 | 92 | PF00069 | 0.523 |
MOD_ProDKin_1 | 20 | 26 | PF00069 | 0.531 |
MOD_SUMO_rev_2 | 93 | 103 | PF00179 | 0.499 |
TRG_DiLeu_BaEn_4 | 575 | 581 | PF01217 | 0.262 |
TRG_DiLeu_BaLyEn_6 | 30 | 35 | PF01217 | 0.518 |
TRG_DiLeu_BaLyEn_6 | 381 | 386 | PF01217 | 0.261 |
TRG_ENDOCYTIC_2 | 170 | 173 | PF00928 | 0.376 |
TRG_ENDOCYTIC_2 | 453 | 456 | PF00928 | 0.377 |
TRG_ENDOCYTIC_2 | 549 | 552 | PF00928 | 0.253 |
TRG_ENDOCYTIC_2 | 561 | 564 | PF00928 | 0.241 |
TRG_ENDOCYTIC_2 | 595 | 598 | PF00928 | 0.274 |
TRG_ENDOCYTIC_2 | 632 | 635 | PF00928 | 0.315 |
TRG_ENDOCYTIC_2 | 647 | 650 | PF00928 | 0.228 |
TRG_ENDOCYTIC_2 | 686 | 689 | PF00928 | 0.638 |
TRG_ER_diArg_1 | 12 | 15 | PF00400 | 0.689 |
TRG_ER_diArg_1 | 323 | 326 | PF00400 | 0.274 |
TRG_ER_diArg_1 | 343 | 345 | PF00400 | 0.290 |
TRG_ER_diArg_1 | 475 | 478 | PF00400 | 0.239 |
TRG_ER_diArg_1 | 508 | 511 | PF00400 | 0.428 |
TRG_ER_diArg_1 | 564 | 567 | PF00400 | 0.274 |
TRG_ER_diArg_1 | 643 | 645 | PF00400 | 0.259 |
TRG_ER_FFAT_2 | 332 | 342 | PF00635 | 0.262 |
TRG_NES_CRM1_1 | 342 | 355 | PF08389 | 0.299 |
TRG_NLS_MonoExtC_3 | 11 | 16 | PF00514 | 0.516 |
TRG_NLS_MonoExtC_3 | 190 | 195 | PF00514 | 0.430 |
TRG_NLS_MonoExtN_4 | 12 | 17 | PF00514 | 0.510 |
TRG_NLS_MonoExtN_4 | 191 | 196 | PF00514 | 0.431 |
TRG_Pf-PMV_PEXEL_1 | 171 | 176 | PF00026 | 0.399 |
TRG_Pf-PMV_PEXEL_1 | 310 | 314 | PF00026 | 0.365 |
TRG_Pf-PMV_PEXEL_1 | 481 | 485 | PF00026 | 0.299 |
TRG_Pf-PMV_PEXEL_1 | 661 | 665 | PF00026 | 0.468 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P567 | Leptomonas seymouri | 87% | 100% |
A0A0N1PFU7 | Leptomonas seymouri | 45% | 94% |
A0A0S4IQT9 | Bodo saltans | 69% | 100% |
A0A0S4KPU1 | Bodo saltans | 45% | 100% |
A0A1X0NG94 | Trypanosomatidae | 41% | 96% |
A0A1X0NX69 | Trypanosomatidae | 75% | 100% |
A0A3Q8ICG0 | Leishmania donovani | 46% | 93% |
A0A3R7KUY9 | Trypanosoma rangeli | 74% | 100% |
A0A3S7WXV4 | Leishmania donovani | 96% | 99% |
A0A422NDG5 | Trypanosoma rangeli | 41% | 94% |
A4H8F0 | Leishmania braziliensis | 44% | 93% |
A4HD08 | Leishmania braziliensis | 94% | 100% |
A4HWS3 | Leishmania infantum | 46% | 93% |
A4I0J4 | Leishmania infantum | 96% | 99% |
C9ZVC1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 76% | 100% |
C9ZW50 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
D5VRB9 | Methanocaldococcus infernus (strain DSM 11812 / JCM 15783 / ME) | 36% | 100% |
E9AQI1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 46% | 92% |
E9AWF5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
O14023 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 34% | 100% |
Q02908 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 34% | 100% |
Q1ZXC6 | Dictyostelium discoideum | 34% | 100% |
Q23651 | Caenorhabditis elegans | 34% | 100% |
Q2KJ61 | Bos taurus | 34% | 100% |
Q4QEZ6 | Leishmania major | 45% | 92% |
Q58536 | Methanocaldococcus jannaschii (strain ATCC 43067 / DSM 2661 / JAL-1 / JCM 10045 / NBRC 100440) | 36% | 100% |
Q5HZM6 | Xenopus laevis | 33% | 100% |
Q5RIC0 | Danio rerio | 33% | 100% |
Q5ZHS1 | Gallus gallus | 33% | 100% |
Q60LW7 | Caenorhabditis briggsae | 34% | 100% |
Q6NVL5 | Xenopus tropicalis | 32% | 100% |
Q7X7L3 | Oryza sativa subsp. japonica | 35% | 100% |
Q93ZR1 | Arabidopsis thaliana | 34% | 100% |
Q9CZX0 | Mus musculus | 32% | 100% |
Q9H9T3 | Homo sapiens | 32% | 100% |
Q9VQZ6 | Drosophila melanogaster | 33% | 100% |
V5B5L2 | Trypanosoma cruzi | 42% | 100% |
V5BNQ5 | Trypanosoma cruzi | 76% | 100% |