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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 3 |
GO:0043226 | organelle | 2 | 3 |
GO:0043227 | membrane-bounded organelle | 3 | 3 |
GO:0043229 | intracellular organelle | 3 | 3 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 3 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
Related structures:
AlphaFold database: A4HP86
Term | Name | Level | Count |
---|---|---|---|
GO:0001510 | RNA methylation | 4 | 8 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 8 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 8 |
GO:0006807 | nitrogen compound metabolic process | 2 | 8 |
GO:0008152 | metabolic process | 1 | 8 |
GO:0009451 | RNA modification | 5 | 8 |
GO:0009987 | cellular process | 1 | 8 |
GO:0016070 | RNA metabolic process | 5 | 8 |
GO:0032259 | methylation | 2 | 8 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 8 |
GO:0043170 | macromolecule metabolic process | 3 | 8 |
GO:0043412 | macromolecule modification | 4 | 8 |
GO:0043414 | macromolecule methylation | 3 | 8 |
GO:0044237 | cellular metabolic process | 2 | 8 |
GO:0044238 | primary metabolic process | 2 | 8 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 8 |
GO:0046483 | heterocycle metabolic process | 3 | 8 |
GO:0071704 | organic substance metabolic process | 2 | 8 |
GO:0090304 | nucleic acid metabolic process | 4 | 8 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 11 |
GO:0003723 | RNA binding | 4 | 11 |
GO:0003824 | catalytic activity | 1 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0008168 | methyltransferase activity | 4 | 11 |
GO:0016740 | transferase activity | 2 | 11 |
GO:0016741 | transferase activity, transferring one-carbon groups | 3 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
GO:0000049 | tRNA binding | 5 | 3 |
GO:0008173 | RNA methyltransferase activity | 4 | 3 |
GO:0008175 | tRNA methyltransferase activity | 5 | 3 |
GO:0008757 | S-adenosylmethionine-dependent methyltransferase activity | 5 | 3 |
GO:0016427 | tRNA (cytosine) methyltransferase activity | 6 | 3 |
GO:0016428 | tRNA (cytosine-5-)-methyltransferase activity | 7 | 3 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 3 |
GO:0140101 | catalytic activity, acting on a tRNA | 4 | 3 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 409 | 413 | PF00656 | 0.506 |
CLV_C14_Caspase3-7 | 441 | 445 | PF00656 | 0.422 |
CLV_C14_Caspase3-7 | 69 | 73 | PF00656 | 0.592 |
CLV_NRD_NRD_1 | 15 | 17 | PF00675 | 0.566 |
CLV_NRD_NRD_1 | 157 | 159 | PF00675 | 0.372 |
CLV_NRD_NRD_1 | 321 | 323 | PF00675 | 0.212 |
CLV_NRD_NRD_1 | 41 | 43 | PF00675 | 0.315 |
CLV_NRD_NRD_1 | 5 | 7 | PF00675 | 0.625 |
CLV_NRD_NRD_1 | 653 | 655 | PF00675 | 0.484 |
CLV_NRD_NRD_1 | 691 | 693 | PF00675 | 0.249 |
CLV_PCSK_KEX2_1 | 15 | 17 | PF00082 | 0.530 |
CLV_PCSK_KEX2_1 | 159 | 161 | PF00082 | 0.385 |
CLV_PCSK_KEX2_1 | 252 | 254 | PF00082 | 0.212 |
CLV_PCSK_KEX2_1 | 262 | 264 | PF00082 | 0.212 |
CLV_PCSK_KEX2_1 | 41 | 43 | PF00082 | 0.315 |
CLV_PCSK_KEX2_1 | 5 | 7 | PF00082 | 0.587 |
CLV_PCSK_KEX2_1 | 513 | 515 | PF00082 | 0.626 |
CLV_PCSK_KEX2_1 | 653 | 655 | PF00082 | 0.482 |
CLV_PCSK_KEX2_1 | 690 | 692 | PF00082 | 0.266 |
CLV_PCSK_PC1ET2_1 | 159 | 161 | PF00082 | 0.403 |
CLV_PCSK_PC1ET2_1 | 252 | 254 | PF00082 | 0.212 |
CLV_PCSK_PC1ET2_1 | 262 | 264 | PF00082 | 0.212 |
CLV_PCSK_PC1ET2_1 | 5 | 7 | PF00082 | 0.468 |
CLV_PCSK_PC1ET2_1 | 513 | 515 | PF00082 | 0.626 |
CLV_PCSK_SKI1_1 | 16 | 20 | PF00082 | 0.556 |
CLV_PCSK_SKI1_1 | 265 | 269 | PF00082 | 0.214 |
CLV_PCSK_SKI1_1 | 384 | 388 | PF00082 | 0.259 |
CLV_PCSK_SKI1_1 | 393 | 397 | PF00082 | 0.221 |
CLV_PCSK_SKI1_1 | 478 | 482 | PF00082 | 0.417 |
CLV_PCSK_SKI1_1 | 488 | 492 | PF00082 | 0.417 |
CLV_PCSK_SKI1_1 | 6 | 10 | PF00082 | 0.522 |
CLV_Separin_Metazoa | 302 | 306 | PF03568 | 0.415 |
DEG_APCC_DBOX_1 | 383 | 391 | PF00400 | 0.459 |
DEG_APCC_DBOX_1 | 392 | 400 | PF00400 | 0.421 |
DEG_APCC_DBOX_1 | 689 | 697 | PF00400 | 0.327 |
DEG_SCF_FBW7_1 | 102 | 109 | PF00400 | 0.388 |
DEG_SCF_FBW7_1 | 541 | 548 | PF00400 | 0.483 |
DEG_SPOP_SBC_1 | 73 | 77 | PF00917 | 0.536 |
DOC_CKS1_1 | 103 | 108 | PF01111 | 0.394 |
DOC_CKS1_1 | 32 | 37 | PF01111 | 0.537 |
DOC_CKS1_1 | 432 | 437 | PF01111 | 0.412 |
DOC_CYCLIN_yCln2_LP_2 | 266 | 272 | PF00134 | 0.430 |
DOC_MAPK_gen_1 | 13 | 21 | PF00069 | 0.478 |
DOC_MAPK_gen_1 | 252 | 258 | PF00069 | 0.423 |
DOC_MAPK_gen_1 | 262 | 268 | PF00069 | 0.455 |
DOC_MAPK_gen_1 | 382 | 389 | PF00069 | 0.425 |
DOC_MAPK_gen_1 | 476 | 485 | PF00069 | 0.366 |
DOC_MAPK_gen_1 | 613 | 622 | PF00069 | 0.500 |
DOC_MAPK_gen_1 | 653 | 663 | PF00069 | 0.331 |
DOC_MAPK_gen_1 | 690 | 698 | PF00069 | 0.402 |
DOC_MAPK_HePTP_8 | 651 | 663 | PF00069 | 0.383 |
DOC_MAPK_HePTP_8 | 718 | 730 | PF00069 | 0.275 |
DOC_MAPK_MEF2A_6 | 211 | 219 | PF00069 | 0.292 |
DOC_MAPK_MEF2A_6 | 279 | 286 | PF00069 | 0.384 |
DOC_MAPK_MEF2A_6 | 341 | 348 | PF00069 | 0.422 |
DOC_MAPK_MEF2A_6 | 654 | 663 | PF00069 | 0.323 |
DOC_MAPK_MEF2A_6 | 721 | 730 | PF00069 | 0.335 |
DOC_MIT_MIM_1 | 686 | 696 | PF04212 | 0.413 |
DOC_PP1_RVXF_1 | 263 | 269 | PF00149 | 0.412 |
DOC_PP1_RVXF_1 | 625 | 632 | PF00149 | 0.425 |
DOC_PP2B_LxvP_1 | 429 | 432 | PF13499 | 0.412 |
DOC_PP4_FxxP_1 | 103 | 106 | PF00568 | 0.317 |
DOC_PP4_FxxP_1 | 418 | 421 | PF00568 | 0.466 |
DOC_PP4_MxPP_1 | 187 | 190 | PF00568 | 0.282 |
DOC_USP7_MATH_1 | 118 | 122 | PF00917 | 0.270 |
DOC_USP7_MATH_1 | 226 | 230 | PF00917 | 0.389 |
DOC_USP7_MATH_1 | 630 | 634 | PF00917 | 0.268 |
DOC_USP7_MATH_1 | 73 | 77 | PF00917 | 0.693 |
DOC_USP7_MATH_1 | 78 | 82 | PF00917 | 0.701 |
DOC_USP7_MATH_1 | 91 | 95 | PF00917 | 0.238 |
DOC_USP7_UBL2_3 | 484 | 488 | PF12436 | 0.554 |
DOC_USP7_UBL2_3 | 5 | 9 | PF12436 | 0.598 |
DOC_USP7_UBL2_3 | 675 | 679 | PF12436 | 0.485 |
DOC_WW_Pin1_4 | 102 | 107 | PF00397 | 0.408 |
DOC_WW_Pin1_4 | 204 | 209 | PF00397 | 0.313 |
DOC_WW_Pin1_4 | 229 | 234 | PF00397 | 0.376 |
DOC_WW_Pin1_4 | 31 | 36 | PF00397 | 0.659 |
DOC_WW_Pin1_4 | 329 | 334 | PF00397 | 0.412 |
DOC_WW_Pin1_4 | 431 | 436 | PF00397 | 0.412 |
DOC_WW_Pin1_4 | 541 | 546 | PF00397 | 0.591 |
DOC_WW_Pin1_4 | 593 | 598 | PF00397 | 0.547 |
DOC_WW_Pin1_4 | 749 | 754 | PF00397 | 0.578 |
LIG_14-3-3_CanoR_1 | 172 | 179 | PF00244 | 0.430 |
LIG_14-3-3_CanoR_1 | 359 | 369 | PF00244 | 0.412 |
LIG_14-3-3_CanoR_1 | 50 | 56 | PF00244 | 0.419 |
LIG_14-3-3_CanoR_1 | 566 | 575 | PF00244 | 0.376 |
LIG_14-3-3_CanoR_1 | 613 | 622 | PF00244 | 0.432 |
LIG_14-3-3_CanoR_1 | 639 | 648 | PF00244 | 0.319 |
LIG_14-3-3_CanoR_1 | 653 | 661 | PF00244 | 0.348 |
LIG_Actin_WH2_2 | 306 | 324 | PF00022 | 0.443 |
LIG_Actin_WH2_2 | 339 | 357 | PF00022 | 0.445 |
LIG_Actin_WH2_2 | 372 | 390 | PF00022 | 0.354 |
LIG_BIR_III_2 | 230 | 234 | PF00653 | 0.458 |
LIG_BIR_III_2 | 391 | 395 | PF00653 | 0.354 |
LIG_BIR_III_4 | 412 | 416 | PF00653 | 0.506 |
LIG_BIR_III_4 | 531 | 535 | PF00653 | 0.481 |
LIG_CaM_IQ_9 | 374 | 390 | PF13499 | 0.354 |
LIG_Clathr_ClatBox_1 | 702 | 706 | PF01394 | 0.288 |
LIG_CSL_BTD_1 | 330 | 333 | PF09270 | 0.412 |
LIG_eIF4E_1 | 238 | 244 | PF01652 | 0.249 |
LIG_FHA_1 | 103 | 109 | PF00498 | 0.334 |
LIG_FHA_1 | 114 | 120 | PF00498 | 0.294 |
LIG_FHA_1 | 362 | 368 | PF00498 | 0.506 |
LIG_FHA_1 | 375 | 381 | PF00498 | 0.506 |
LIG_FHA_1 | 405 | 411 | PF00498 | 0.400 |
LIG_FHA_1 | 614 | 620 | PF00498 | 0.389 |
LIG_FHA_2 | 21 | 27 | PF00498 | 0.557 |
LIG_FHA_2 | 272 | 278 | PF00498 | 0.412 |
LIG_FHA_2 | 407 | 413 | PF00498 | 0.506 |
LIG_FHA_2 | 439 | 445 | PF00498 | 0.428 |
LIG_FHA_2 | 519 | 525 | PF00498 | 0.696 |
LIG_FHA_2 | 67 | 73 | PF00498 | 0.614 |
LIG_LIR_Apic_2 | 569 | 575 | PF02991 | 0.422 |
LIG_LIR_Gen_1 | 49 | 58 | PF02991 | 0.365 |
LIG_LIR_Nem_3 | 139 | 143 | PF02991 | 0.348 |
LIG_LIR_Nem_3 | 46 | 51 | PF02991 | 0.349 |
LIG_LIR_Nem_3 | 569 | 574 | PF02991 | 0.371 |
LIG_PCNA_PIPBox_1 | 163 | 172 | PF02747 | 0.385 |
LIG_PCNA_PIPBox_1 | 565 | 574 | PF02747 | 0.453 |
LIG_PCNA_yPIPBox_3 | 37 | 50 | PF02747 | 0.305 |
LIG_PTB_Apo_2 | 42 | 49 | PF02174 | 0.508 |
LIG_SH2_CRK | 52 | 56 | PF00017 | 0.490 |
LIG_SH2_CRK | 572 | 576 | PF00017 | 0.245 |
LIG_SH2_NCK_1 | 572 | 576 | PF00017 | 0.342 |
LIG_SH2_STAP1 | 438 | 442 | PF00017 | 0.443 |
LIG_SH2_STAP1 | 716 | 720 | PF00017 | 0.283 |
LIG_SH2_STAT5 | 169 | 172 | PF00017 | 0.469 |
LIG_SH2_STAT5 | 280 | 283 | PF00017 | 0.425 |
LIG_SH2_STAT5 | 557 | 560 | PF00017 | 0.287 |
LIG_SH3_1 | 279 | 285 | PF00018 | 0.422 |
LIG_SH3_1 | 572 | 578 | PF00018 | 0.331 |
LIG_SH3_3 | 279 | 285 | PF00018 | 0.376 |
LIG_SH3_3 | 29 | 35 | PF00018 | 0.616 |
LIG_SH3_3 | 391 | 397 | PF00018 | 0.499 |
LIG_SH3_3 | 429 | 435 | PF00018 | 0.435 |
LIG_SH3_3 | 544 | 550 | PF00018 | 0.650 |
LIG_SH3_3 | 555 | 561 | PF00018 | 0.350 |
LIG_SH3_3 | 572 | 578 | PF00018 | 0.331 |
LIG_SH3_3 | 656 | 662 | PF00018 | 0.434 |
LIG_SUMO_SIM_anti_2 | 131 | 136 | PF11976 | 0.237 |
LIG_SUMO_SIM_anti_2 | 616 | 623 | PF11976 | 0.359 |
LIG_SUMO_SIM_par_1 | 17 | 24 | PF11976 | 0.425 |
LIG_SUMO_SIM_par_1 | 616 | 623 | PF11976 | 0.329 |
LIG_SUMO_SIM_par_1 | 701 | 706 | PF11976 | 0.313 |
LIG_TRAF2_1 | 748 | 751 | PF00917 | 0.446 |
LIG_TRAF2_1 | 83 | 86 | PF00917 | 0.469 |
LIG_UBA3_1 | 215 | 223 | PF00899 | 0.316 |
LIG_UBA3_1 | 702 | 709 | PF00899 | 0.448 |
LIG_WRC_WIRS_1 | 108 | 113 | PF05994 | 0.408 |
LIG_WW_1 | 554 | 557 | PF00397 | 0.323 |
MOD_CDK_SPK_2 | 329 | 334 | PF00069 | 0.412 |
MOD_CDK_SPK_2 | 541 | 546 | PF00069 | 0.487 |
MOD_CDK_SPxxK_3 | 204 | 211 | PF00069 | 0.310 |
MOD_CK1_1 | 20 | 26 | PF00069 | 0.563 |
MOD_CK1_1 | 207 | 213 | PF00069 | 0.327 |
MOD_CK1_1 | 229 | 235 | PF00069 | 0.369 |
MOD_CK1_1 | 363 | 369 | PF00069 | 0.412 |
MOD_CK1_1 | 596 | 602 | PF00069 | 0.368 |
MOD_CK1_1 | 749 | 755 | PF00069 | 0.466 |
MOD_CK1_1 | 76 | 82 | PF00069 | 0.754 |
MOD_CK2_1 | 130 | 136 | PF00069 | 0.354 |
MOD_CK2_1 | 21 | 27 | PF00069 | 0.603 |
MOD_CK2_1 | 329 | 335 | PF00069 | 0.430 |
MOD_GlcNHglycan | 315 | 318 | PF01048 | 0.223 |
MOD_GlcNHglycan | 412 | 416 | PF01048 | 0.310 |
MOD_GlcNHglycan | 521 | 524 | PF01048 | 0.591 |
MOD_GlcNHglycan | 622 | 625 | PF01048 | 0.411 |
MOD_GlcNHglycan | 643 | 646 | PF01048 | 0.367 |
MOD_GlcNHglycan | 671 | 674 | PF01048 | 0.432 |
MOD_GlcNHglycan | 76 | 79 | PF01048 | 0.601 |
MOD_GlcNHglycan | 80 | 83 | PF01048 | 0.605 |
MOD_GlcNHglycan | 86 | 90 | PF01048 | 0.499 |
MOD_GSK3_1 | 102 | 109 | PF00069 | 0.430 |
MOD_GSK3_1 | 126 | 133 | PF00069 | 0.356 |
MOD_GSK3_1 | 17 | 24 | PF00069 | 0.649 |
MOD_GSK3_1 | 171 | 178 | PF00069 | 0.334 |
MOD_GSK3_1 | 313 | 320 | PF00069 | 0.424 |
MOD_GSK3_1 | 404 | 411 | PF00069 | 0.493 |
MOD_GSK3_1 | 502 | 509 | PF00069 | 0.629 |
MOD_GSK3_1 | 515 | 522 | PF00069 | 0.758 |
MOD_GSK3_1 | 541 | 548 | PF00069 | 0.530 |
MOD_GSK3_1 | 68 | 75 | PF00069 | 0.637 |
MOD_GSK3_1 | 680 | 687 | PF00069 | 0.453 |
MOD_N-GLC_1 | 113 | 118 | PF02516 | 0.322 |
MOD_N-GLC_1 | 44 | 49 | PF02516 | 0.392 |
MOD_NEK2_1 | 107 | 112 | PF00069 | 0.397 |
MOD_NEK2_1 | 130 | 135 | PF00069 | 0.272 |
MOD_NEK2_1 | 19 | 24 | PF00069 | 0.521 |
MOD_NEK2_1 | 360 | 365 | PF00069 | 0.443 |
MOD_NEK2_1 | 446 | 451 | PF00069 | 0.514 |
MOD_NEK2_1 | 583 | 588 | PF00069 | 0.464 |
MOD_NEK2_1 | 652 | 657 | PF00069 | 0.449 |
MOD_NEK2_1 | 669 | 674 | PF00069 | 0.477 |
MOD_NEK2_2 | 317 | 322 | PF00069 | 0.423 |
MOD_PIKK_1 | 118 | 124 | PF00454 | 0.260 |
MOD_PIKK_1 | 374 | 380 | PF00454 | 0.354 |
MOD_PIKK_1 | 684 | 690 | PF00454 | 0.369 |
MOD_PKA_1 | 653 | 659 | PF00069 | 0.388 |
MOD_PKA_2 | 171 | 177 | PF00069 | 0.462 |
MOD_PKA_2 | 638 | 644 | PF00069 | 0.450 |
MOD_PKA_2 | 652 | 658 | PF00069 | 0.432 |
MOD_Plk_1 | 130 | 136 | PF00069 | 0.266 |
MOD_Plk_1 | 183 | 189 | PF00069 | 0.310 |
MOD_Plk_1 | 44 | 50 | PF00069 | 0.285 |
MOD_Plk_1 | 446 | 452 | PF00069 | 0.466 |
MOD_Plk_1 | 684 | 690 | PF00069 | 0.480 |
MOD_Plk_4 | 107 | 113 | PF00069 | 0.211 |
MOD_Plk_4 | 130 | 136 | PF00069 | 0.344 |
MOD_Plk_4 | 183 | 189 | PF00069 | 0.288 |
MOD_Plk_4 | 599 | 605 | PF00069 | 0.302 |
MOD_Plk_4 | 661 | 667 | PF00069 | 0.354 |
MOD_Plk_4 | 91 | 97 | PF00069 | 0.396 |
MOD_ProDKin_1 | 102 | 108 | PF00069 | 0.504 |
MOD_ProDKin_1 | 204 | 210 | PF00069 | 0.313 |
MOD_ProDKin_1 | 229 | 235 | PF00069 | 0.369 |
MOD_ProDKin_1 | 31 | 37 | PF00069 | 0.654 |
MOD_ProDKin_1 | 329 | 335 | PF00069 | 0.412 |
MOD_ProDKin_1 | 431 | 437 | PF00069 | 0.412 |
MOD_ProDKin_1 | 541 | 547 | PF00069 | 0.589 |
MOD_ProDKin_1 | 593 | 599 | PF00069 | 0.535 |
MOD_ProDKin_1 | 749 | 755 | PF00069 | 0.580 |
MOD_SUMO_for_1 | 483 | 486 | PF00179 | 0.566 |
MOD_SUMO_for_1 | 512 | 515 | PF00179 | 0.710 |
MOD_SUMO_rev_2 | 248 | 254 | PF00179 | 0.412 |
MOD_SUMO_rev_2 | 482 | 490 | PF00179 | 0.606 |
TRG_DiLeu_BaLyEn_6 | 103 | 108 | PF01217 | 0.460 |
TRG_DiLeu_BaLyEn_6 | 262 | 267 | PF01217 | 0.412 |
TRG_DiLeu_BaLyEn_6 | 391 | 396 | PF01217 | 0.354 |
TRG_ENDOCYTIC_2 | 52 | 55 | PF00928 | 0.346 |
TRG_ER_diArg_1 | 157 | 160 | PF00400 | 0.366 |
TRG_ER_diArg_1 | 263 | 266 | PF00400 | 0.439 |
TRG_ER_diArg_1 | 40 | 42 | PF00400 | 0.312 |
TRG_ER_diArg_1 | 652 | 654 | PF00400 | 0.480 |
TRG_ER_diArg_1 | 689 | 692 | PF00400 | 0.379 |
TRG_NLS_Bipartite_1 | 252 | 266 | PF00514 | 0.412 |
TRG_NLS_MonoExtC_3 | 4 | 9 | PF00514 | 0.521 |
TRG_NLS_MonoExtN_4 | 2 | 9 | PF00514 | 0.522 |
TRG_Pf-PMV_PEXEL_1 | 149 | 153 | PF00026 | 0.397 |
TRG_Pf-PMV_PEXEL_1 | 478 | 482 | PF00026 | 0.566 |
TRG_Pf-PMV_PEXEL_1 | 566 | 570 | PF00026 | 0.526 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZE7 | Leptomonas seymouri | 73% | 98% |
A0A1X0P7M3 | Trypanosomatidae | 58% | 100% |
A0A3Q8INR5 | Leishmania donovani | 85% | 99% |
A0A3R7NNX1 | Trypanosoma rangeli | 58% | 100% |
A4IDJ1 | Leishmania infantum | 85% | 99% |
D0A386 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 56% | 100% |
E9ASZ4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |
O13935 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 30% | 100% |
P38205 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 30% | 100% |
Q08J23 | Homo sapiens | 31% | 99% |
Q1HFZ0 | Mus musculus | 31% | 100% |
Q28E61 | Xenopus tropicalis | 31% | 95% |
Q4Q1K4 | Leishmania major | 84% | 100% |
Q4V7N2 | Xenopus laevis | 31% | 100% |
Q5ZLV4 | Gallus gallus | 31% | 96% |
Q9HGQ2 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 33% | 100% |
V5DCJ5 | Trypanosoma cruzi | 63% | 100% |