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: 36 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 26 |
NetGPI | no | yes: 0, no: 26 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 27 |
GO:0110165 | cellular anatomical entity | 1 | 27 |
GO:0005635 | nuclear envelope | 4 | 4 |
GO:0005783 | endoplasmic reticulum | 5 | 4 |
GO:0031967 | organelle envelope | 3 | 4 |
GO:0031975 | envelope | 2 | 4 |
GO:0043226 | organelle | 2 | 4 |
GO:0043227 | membrane-bounded organelle | 3 | 4 |
GO:0043229 | intracellular organelle | 3 | 4 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 4 |
Related structures:
AlphaFold database: A4HMD5
Term | Name | Level | Count |
---|---|---|---|
GO:0006486 | protein glycosylation | 4 | 27 |
GO:0006807 | nitrogen compound metabolic process | 2 | 27 |
GO:0008152 | metabolic process | 1 | 27 |
GO:0019538 | protein metabolic process | 3 | 27 |
GO:0036211 | protein modification process | 4 | 27 |
GO:0043170 | macromolecule metabolic process | 3 | 27 |
GO:0043412 | macromolecule modification | 4 | 27 |
GO:0043413 | macromolecule glycosylation | 3 | 27 |
GO:0044238 | primary metabolic process | 2 | 27 |
GO:0070085 | glycosylation | 2 | 27 |
GO:0071704 | organic substance metabolic process | 2 | 27 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 27 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 27 |
GO:0004576 | oligosaccharyl transferase activity | 5 | 27 |
GO:0004579 | dolichyl-diphosphooligosaccharide-protein glycotransferase activity | 6 | 27 |
GO:0005488 | binding | 1 | 27 |
GO:0016740 | transferase activity | 2 | 27 |
GO:0016757 | glycosyltransferase activity | 3 | 27 |
GO:0016758 | hexosyltransferase activity | 4 | 27 |
GO:0043167 | ion binding | 2 | 27 |
GO:0043169 | cation binding | 3 | 27 |
GO:0046872 | metal ion binding | 4 | 27 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 574 | 578 | PF00656 | 0.297 |
CLV_NRD_NRD_1 | 338 | 340 | PF00675 | 0.375 |
CLV_NRD_NRD_1 | 372 | 374 | PF00675 | 0.283 |
CLV_NRD_NRD_1 | 436 | 438 | PF00675 | 0.450 |
CLV_PCSK_KEX2_1 | 448 | 450 | PF00082 | 0.516 |
CLV_PCSK_PC1ET2_1 | 448 | 450 | PF00082 | 0.509 |
CLV_PCSK_SKI1_1 | 318 | 322 | PF00082 | 0.434 |
CLV_PCSK_SKI1_1 | 521 | 525 | PF00082 | 0.552 |
CLV_PCSK_SKI1_1 | 591 | 595 | PF00082 | 0.496 |
CLV_PCSK_SKI1_1 | 697 | 701 | PF00082 | 0.597 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.230 |
DEG_SPOP_SBC_1 | 61 | 65 | PF00917 | 0.411 |
DOC_AGCK_PIF_1 | 349 | 354 | PF00069 | 0.210 |
DOC_AGCK_PIF_2 | 46 | 51 | PF00069 | 0.280 |
DOC_CKS1_1 | 498 | 503 | PF01111 | 0.210 |
DOC_CYCLIN_RxL_1 | 315 | 325 | PF00134 | 0.242 |
DOC_CYCLIN_yCln2_LP_2 | 400 | 406 | PF00134 | 0.239 |
DOC_MAPK_gen_1 | 166 | 175 | PF00069 | 0.351 |
DOC_MAPK_gen_1 | 270 | 277 | PF00069 | 0.471 |
DOC_MAPK_gen_1 | 373 | 382 | PF00069 | 0.392 |
DOC_MAPK_gen_1 | 464 | 473 | PF00069 | 0.662 |
DOC_MAPK_gen_1 | 9 | 17 | PF00069 | 0.164 |
DOC_MAPK_MEF2A_6 | 486 | 493 | PF00069 | 0.481 |
DOC_MAPK_RevD_3 | 361 | 374 | PF00069 | 0.157 |
DOC_PP1_RVXF_1 | 519 | 525 | PF00149 | 0.372 |
DOC_PP1_RVXF_1 | 553 | 560 | PF00149 | 0.288 |
DOC_PP2B_LxvP_1 | 413 | 416 | PF13499 | 0.180 |
DOC_PP4_FxxP_1 | 517 | 520 | PF00568 | 0.360 |
DOC_USP7_MATH_1 | 244 | 248 | PF00917 | 0.266 |
DOC_USP7_MATH_1 | 369 | 373 | PF00917 | 0.437 |
DOC_USP7_MATH_1 | 430 | 434 | PF00917 | 0.601 |
DOC_USP7_MATH_1 | 672 | 676 | PF00917 | 0.380 |
DOC_WW_Pin1_4 | 240 | 245 | PF00397 | 0.266 |
DOC_WW_Pin1_4 | 302 | 307 | PF00397 | 0.181 |
DOC_WW_Pin1_4 | 426 | 431 | PF00397 | 0.499 |
DOC_WW_Pin1_4 | 497 | 502 | PF00397 | 0.468 |
DOC_WW_Pin1_4 | 547 | 552 | PF00397 | 0.312 |
DOC_WW_Pin1_4 | 592 | 597 | PF00397 | 0.290 |
DOC_WW_Pin1_4 | 621 | 626 | PF00397 | 0.332 |
LIG_14-3-3_CanoR_1 | 11 | 16 | PF00244 | 0.266 |
LIG_14-3-3_CanoR_1 | 166 | 172 | PF00244 | 0.290 |
LIG_14-3-3_CanoR_1 | 212 | 216 | PF00244 | 0.521 |
LIG_14-3-3_CanoR_1 | 288 | 293 | PF00244 | 0.445 |
LIG_14-3-3_CanoR_1 | 452 | 456 | PF00244 | 0.611 |
LIG_14-3-3_CanoR_1 | 464 | 474 | PF00244 | 0.583 |
LIG_14-3-3_CanoR_1 | 509 | 519 | PF00244 | 0.353 |
LIG_14-3-3_CanoR_1 | 555 | 560 | PF00244 | 0.254 |
LIG_14-3-3_CanoR_1 | 572 | 576 | PF00244 | 0.317 |
LIG_14-3-3_CanoR_1 | 629 | 635 | PF00244 | 0.310 |
LIG_14-3-3_CanoR_1 | 662 | 666 | PF00244 | 0.355 |
LIG_14-3-3_CanoR_1 | 765 | 770 | PF00244 | 0.502 |
LIG_Actin_WH2_2 | 516 | 531 | PF00022 | 0.222 |
LIG_AP2alpha_2 | 26 | 28 | PF02296 | 0.266 |
LIG_BRCT_BRCA1_1 | 42 | 46 | PF00533 | 0.336 |
LIG_BRCT_BRCA1_1 | 513 | 517 | PF00533 | 0.270 |
LIG_deltaCOP1_diTrp_1 | 418 | 427 | PF00928 | 0.581 |
LIG_FHA_1 | 119 | 125 | PF00498 | 0.294 |
LIG_FHA_1 | 155 | 161 | PF00498 | 0.259 |
LIG_FHA_1 | 312 | 318 | PF00498 | 0.381 |
LIG_FHA_1 | 466 | 472 | PF00498 | 0.525 |
LIG_FHA_1 | 498 | 504 | PF00498 | 0.489 |
LIG_FHA_1 | 531 | 537 | PF00498 | 0.292 |
LIG_FHA_1 | 592 | 598 | PF00498 | 0.296 |
LIG_FHA_2 | 103 | 109 | PF00498 | 0.271 |
LIG_FHA_2 | 455 | 461 | PF00498 | 0.596 |
LIG_FHA_2 | 474 | 480 | PF00498 | 0.494 |
LIG_FHA_2 | 548 | 554 | PF00498 | 0.296 |
LIG_FHA_2 | 766 | 772 | PF00498 | 0.387 |
LIG_GBD_Chelix_1 | 103 | 111 | PF00786 | 0.240 |
LIG_LIR_Apic_2 | 307 | 312 | PF02991 | 0.293 |
LIG_LIR_Apic_2 | 425 | 430 | PF02991 | 0.545 |
LIG_LIR_Apic_2 | 514 | 520 | PF02991 | 0.364 |
LIG_LIR_Apic_2 | 652 | 657 | PF02991 | 0.360 |
LIG_LIR_Apic_2 | 725 | 729 | PF02991 | 0.426 |
LIG_LIR_Gen_1 | 157 | 165 | PF02991 | 0.313 |
LIG_LIR_Gen_1 | 347 | 356 | PF02991 | 0.218 |
LIG_LIR_Gen_1 | 418 | 428 | PF02991 | 0.533 |
LIG_LIR_Gen_1 | 43 | 52 | PF02991 | 0.323 |
LIG_LIR_Gen_1 | 541 | 551 | PF02991 | 0.289 |
LIG_LIR_Gen_1 | 609 | 615 | PF02991 | 0.338 |
LIG_LIR_Gen_1 | 633 | 643 | PF02991 | 0.388 |
LIG_LIR_Gen_1 | 683 | 693 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 157 | 162 | PF02991 | 0.298 |
LIG_LIR_Nem_3 | 243 | 248 | PF02991 | 0.260 |
LIG_LIR_Nem_3 | 26 | 31 | PF02991 | 0.266 |
LIG_LIR_Nem_3 | 307 | 313 | PF02991 | 0.287 |
LIG_LIR_Nem_3 | 347 | 352 | PF02991 | 0.237 |
LIG_LIR_Nem_3 | 418 | 424 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 43 | 49 | PF02991 | 0.261 |
LIG_LIR_Nem_3 | 53 | 57 | PF02991 | 0.249 |
LIG_LIR_Nem_3 | 541 | 546 | PF02991 | 0.298 |
LIG_LIR_Nem_3 | 558 | 562 | PF02991 | 0.244 |
LIG_LIR_Nem_3 | 609 | 613 | PF02991 | 0.276 |
LIG_LIR_Nem_3 | 63 | 69 | PF02991 | 0.235 |
LIG_LIR_Nem_3 | 633 | 638 | PF02991 | 0.314 |
LIG_LIR_Nem_3 | 683 | 688 | PF02991 | 0.343 |
LIG_LIR_Nem_3 | 690 | 696 | PF02991 | 0.287 |
LIG_LYPXL_yS_3 | 66 | 69 | PF13949 | 0.358 |
LIG_MLH1_MIPbox_1 | 42 | 46 | PF16413 | 0.336 |
LIG_NRBOX | 253 | 259 | PF00104 | 0.365 |
LIG_Pex14_1 | 42 | 46 | PF04695 | 0.266 |
LIG_Pex14_1 | 560 | 564 | PF04695 | 0.278 |
LIG_Pex14_2 | 25 | 29 | PF04695 | 0.245 |
LIG_Pex14_2 | 45 | 49 | PF04695 | 0.202 |
LIG_PTB_Apo_2 | 629 | 636 | PF02174 | 0.305 |
LIG_PTB_Phospho_1 | 629 | 635 | PF10480 | 0.300 |
LIG_SH2_CRK | 100 | 104 | PF00017 | 0.181 |
LIG_SH2_CRK | 18 | 22 | PF00017 | 0.280 |
LIG_SH2_CRK | 654 | 658 | PF00017 | 0.392 |
LIG_SH2_CRK | 693 | 697 | PF00017 | 0.276 |
LIG_SH2_NCK_1 | 383 | 387 | PF00017 | 0.186 |
LIG_SH2_PTP2 | 191 | 194 | PF00017 | 0.333 |
LIG_SH2_PTP2 | 610 | 613 | PF00017 | 0.268 |
LIG_SH2_SRC | 20 | 23 | PF00017 | 0.281 |
LIG_SH2_SRC | 539 | 542 | PF00017 | 0.274 |
LIG_SH2_STAP1 | 223 | 227 | PF00017 | 0.333 |
LIG_SH2_STAP1 | 346 | 350 | PF00017 | 0.234 |
LIG_SH2_STAP1 | 354 | 358 | PF00017 | 0.207 |
LIG_SH2_STAP1 | 417 | 421 | PF00017 | 0.440 |
LIG_SH2_STAP1 | 515 | 519 | PF00017 | 0.234 |
LIG_SH2_STAP1 | 689 | 693 | PF00017 | 0.329 |
LIG_SH2_STAT3 | 502 | 505 | PF00017 | 0.459 |
LIG_SH2_STAT3 | 562 | 565 | PF00017 | 0.270 |
LIG_SH2_STAT5 | 159 | 162 | PF00017 | 0.358 |
LIG_SH2_STAT5 | 191 | 194 | PF00017 | 0.333 |
LIG_SH2_STAT5 | 2 | 5 | PF00017 | 0.307 |
LIG_SH2_STAT5 | 20 | 23 | PF00017 | 0.336 |
LIG_SH2_STAT5 | 227 | 230 | PF00017 | 0.424 |
LIG_SH2_STAT5 | 309 | 312 | PF00017 | 0.253 |
LIG_SH2_STAT5 | 348 | 351 | PF00017 | 0.238 |
LIG_SH2_STAT5 | 389 | 392 | PF00017 | 0.304 |
LIG_SH2_STAT5 | 502 | 505 | PF00017 | 0.326 |
LIG_SH2_STAT5 | 539 | 542 | PF00017 | 0.305 |
LIG_SH2_STAT5 | 610 | 613 | PF00017 | 0.281 |
LIG_SH3_3 | 300 | 306 | PF00018 | 0.306 |
LIG_SH3_3 | 495 | 501 | PF00018 | 0.473 |
LIG_SH3_3 | 637 | 643 | PF00018 | 0.395 |
LIG_SH3_3 | 709 | 715 | PF00018 | 0.346 |
LIG_SH3_3 | 716 | 722 | PF00018 | 0.358 |
LIG_SH3_3 | 91 | 97 | PF00018 | 0.358 |
LIG_SUMO_SIM_anti_2 | 395 | 401 | PF11976 | 0.199 |
LIG_SUMO_SIM_par_1 | 532 | 538 | PF11976 | 0.264 |
LIG_TYR_ITSM | 155 | 162 | PF00017 | 0.298 |
LIG_WRC_WIRS_1 | 155 | 160 | PF05994 | 0.298 |
MOD_CDC14_SPxK_1 | 243 | 246 | PF00782 | 0.336 |
MOD_CDK_SPxK_1 | 240 | 246 | PF00069 | 0.266 |
MOD_CK1_1 | 118 | 124 | PF00069 | 0.366 |
MOD_CK1_1 | 164 | 170 | PF00069 | 0.333 |
MOD_CK1_1 | 384 | 390 | PF00069 | 0.210 |
MOD_CK1_1 | 429 | 435 | PF00069 | 0.606 |
MOD_CK1_1 | 513 | 519 | PF00069 | 0.336 |
MOD_CK1_1 | 705 | 711 | PF00069 | 0.319 |
MOD_CK2_1 | 102 | 108 | PF00069 | 0.157 |
MOD_CK2_1 | 331 | 337 | PF00069 | 0.234 |
MOD_CK2_1 | 369 | 375 | PF00069 | 0.392 |
MOD_CK2_1 | 430 | 436 | PF00069 | 0.572 |
MOD_CK2_1 | 473 | 479 | PF00069 | 0.490 |
MOD_CK2_1 | 765 | 771 | PF00069 | 0.401 |
MOD_Cter_Amidation | 751 | 754 | PF01082 | 0.568 |
MOD_GlcNHglycan | 117 | 120 | PF01048 | 0.318 |
MOD_GlcNHglycan | 37 | 40 | PF01048 | 0.497 |
MOD_GlcNHglycan | 42 | 45 | PF01048 | 0.527 |
MOD_GlcNHglycan | 432 | 435 | PF01048 | 0.377 |
MOD_GlcNHglycan | 674 | 677 | PF01048 | 0.598 |
MOD_GlcNHglycan | 704 | 707 | PF01048 | 0.552 |
MOD_GSK3_1 | 211 | 218 | PF00069 | 0.509 |
MOD_GSK3_1 | 228 | 235 | PF00069 | 0.201 |
MOD_GSK3_1 | 240 | 247 | PF00069 | 0.284 |
MOD_GSK3_1 | 384 | 391 | PF00069 | 0.257 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.341 |
MOD_GSK3_1 | 422 | 429 | PF00069 | 0.624 |
MOD_GSK3_1 | 523 | 530 | PF00069 | 0.348 |
MOD_N-GLC_1 | 115 | 120 | PF02516 | 0.354 |
MOD_N-GLC_1 | 430 | 435 | PF02516 | 0.291 |
MOD_N-GLC_1 | 570 | 575 | PF02516 | 0.492 |
MOD_N-GLC_1 | 702 | 707 | PF02516 | 0.515 |
MOD_N-GLC_2 | 146 | 148 | PF02516 | 0.266 |
MOD_N-GLC_2 | 91 | 93 | PF02516 | 0.424 |
MOD_NEK2_1 | 136 | 141 | PF00069 | 0.337 |
MOD_NEK2_1 | 154 | 159 | PF00069 | 0.203 |
MOD_NEK2_1 | 322 | 327 | PF00069 | 0.277 |
MOD_NEK2_1 | 331 | 336 | PF00069 | 0.239 |
MOD_NEK2_1 | 350 | 355 | PF00069 | 0.333 |
MOD_NEK2_1 | 473 | 478 | PF00069 | 0.667 |
MOD_NEK2_1 | 523 | 528 | PF00069 | 0.322 |
MOD_NEK2_1 | 661 | 666 | PF00069 | 0.303 |
MOD_NEK2_1 | 69 | 74 | PF00069 | 0.313 |
MOD_NEK2_1 | 763 | 768 | PF00069 | 0.394 |
MOD_NEK2_2 | 161 | 166 | PF00069 | 0.298 |
MOD_PIKK_1 | 419 | 425 | PF00454 | 0.415 |
MOD_PIKK_1 | 523 | 529 | PF00454 | 0.285 |
MOD_PK_1 | 11 | 17 | PF00069 | 0.302 |
MOD_PK_1 | 288 | 294 | PF00069 | 0.403 |
MOD_PKA_2 | 167 | 173 | PF00069 | 0.303 |
MOD_PKA_2 | 211 | 217 | PF00069 | 0.521 |
MOD_PKA_2 | 338 | 344 | PF00069 | 0.234 |
MOD_PKA_2 | 392 | 398 | PF00069 | 0.473 |
MOD_PKA_2 | 436 | 442 | PF00069 | 0.601 |
MOD_PKA_2 | 451 | 457 | PF00069 | 0.753 |
MOD_PKA_2 | 465 | 471 | PF00069 | 0.626 |
MOD_PKA_2 | 571 | 577 | PF00069 | 0.296 |
MOD_PKA_2 | 661 | 667 | PF00069 | 0.351 |
MOD_PKB_1 | 286 | 294 | PF00069 | 0.481 |
MOD_PKB_1 | 9 | 17 | PF00069 | 0.154 |
MOD_Plk_1 | 350 | 356 | PF00069 | 0.213 |
MOD_Plk_1 | 570 | 576 | PF00069 | 0.292 |
MOD_Plk_4 | 154 | 160 | PF00069 | 0.298 |
MOD_Plk_4 | 203 | 209 | PF00069 | 0.410 |
MOD_Plk_4 | 215 | 221 | PF00069 | 0.413 |
MOD_Plk_4 | 352 | 358 | PF00069 | 0.301 |
MOD_Plk_4 | 384 | 390 | PF00069 | 0.301 |
MOD_Plk_4 | 50 | 56 | PF00069 | 0.266 |
MOD_Plk_4 | 530 | 536 | PF00069 | 0.351 |
MOD_Plk_4 | 555 | 561 | PF00069 | 0.240 |
MOD_Plk_4 | 599 | 605 | PF00069 | 0.350 |
MOD_Plk_4 | 630 | 636 | PF00069 | 0.290 |
MOD_Plk_4 | 661 | 667 | PF00069 | 0.349 |
MOD_Plk_4 | 680 | 686 | PF00069 | 0.259 |
MOD_Plk_4 | 722 | 728 | PF00069 | 0.365 |
MOD_ProDKin_1 | 240 | 246 | PF00069 | 0.266 |
MOD_ProDKin_1 | 302 | 308 | PF00069 | 0.181 |
MOD_ProDKin_1 | 426 | 432 | PF00069 | 0.501 |
MOD_ProDKin_1 | 497 | 503 | PF00069 | 0.468 |
MOD_ProDKin_1 | 547 | 553 | PF00069 | 0.313 |
MOD_ProDKin_1 | 592 | 598 | PF00069 | 0.296 |
MOD_ProDKin_1 | 621 | 627 | PF00069 | 0.329 |
MOD_SUMO_rev_2 | 433 | 439 | PF00179 | 0.562 |
TRG_DiLeu_BaEn_1 | 599 | 604 | PF01217 | 0.306 |
TRG_DiLeu_BaEn_2 | 374 | 380 | PF01217 | 0.392 |
TRG_ENDOCYTIC_2 | 100 | 103 | PF00928 | 0.181 |
TRG_ENDOCYTIC_2 | 159 | 162 | PF00928 | 0.298 |
TRG_ENDOCYTIC_2 | 18 | 21 | PF00928 | 0.280 |
TRG_ENDOCYTIC_2 | 181 | 184 | PF00928 | 0.298 |
TRG_ENDOCYTIC_2 | 191 | 194 | PF00928 | 0.298 |
TRG_ENDOCYTIC_2 | 223 | 226 | PF00928 | 0.298 |
TRG_ENDOCYTIC_2 | 346 | 349 | PF00928 | 0.248 |
TRG_ENDOCYTIC_2 | 543 | 546 | PF00928 | 0.290 |
TRG_ENDOCYTIC_2 | 610 | 613 | PF00928 | 0.281 |
TRG_ENDOCYTIC_2 | 635 | 638 | PF00928 | 0.325 |
TRG_ENDOCYTIC_2 | 66 | 69 | PF00928 | 0.406 |
TRG_ENDOCYTIC_2 | 693 | 696 | PF00928 | 0.271 |
TRG_ER_diArg_1 | 165 | 168 | PF00400 | 0.332 |
TRG_ER_diArg_1 | 269 | 272 | PF00400 | 0.484 |
TRG_ER_diArg_1 | 277 | 280 | PF00400 | 0.454 |
TRG_ER_diArg_1 | 285 | 288 | PF00400 | 0.401 |
TRG_ER_diArg_1 | 8 | 11 | PF00400 | 0.291 |
TRG_NES_CRM1_1 | 249 | 264 | PF08389 | 0.336 |
TRG_Pf-PMV_PEXEL_1 | 246 | 250 | PF00026 | 0.390 |
TRG_Pf-PMV_PEXEL_1 | 318 | 323 | PF00026 | 0.455 |
TRG_Pf-PMV_PEXEL_1 | 767 | 771 | PF00026 | 0.582 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0S4IZ72 | Bodo saltans | 51% | 94% |
A0A1X0NFU7 | Trypanosomatidae | 57% | 91% |
A0A3Q8IHT0 | Leishmania donovani | 72% | 89% |
A0A3Q8II34 | Leishmania donovani | 54% | 97% |
A0A3Q8ILY7 | Leishmania donovani | 82% | 98% |
A0A3Q8IV37 | Leishmania donovani | 71% | 92% |
A0A422MX14 | Trypanosoma rangeli | 57% | 93% |
A4HFF9 | Leishmania braziliensis | 76% | 100% |
A4HMD6 | Leishmania braziliensis | 59% | 94% |
A4HMD7 | Leishmania braziliensis | 74% | 90% |
A4IB08 | Leishmania infantum | 73% | 89% |
A4IB09 | Leishmania infantum | 83% | 98% |
A4IB10 | Leishmania infantum | 54% | 97% |
C9ZNL1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 54% | 94% |
C9ZQ40 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 51% | 100% |
E2RG47 | Canis lupus familiaris | 31% | 93% |
E9AET6 | Leishmania major | 72% | 100% |
E9AET7 | Leishmania major | 82% | 100% |
E9AET8 | Leishmania major | 54% | 100% |
E9AET9 | Leishmania major | 71% | 100% |
E9AHU4 | Leishmania infantum | 71% | 92% |
E9B5Z2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 71% | 89% |
E9B5Z3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 92% |
E9B5Z4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 54% | 97% |
E9B5Z5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 69% | 91% |
F1PJP5 | Canis lupus familiaris | 29% | 100% |
O94335 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 32% | 100% |
P39007 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 29% | 100% |
P46975 | Caenorhabditis elegans | 31% | 100% |
P46977 | Homo sapiens | 29% | 100% |
P46978 | Mus musculus | 29% | 100% |
Q2KJI2 | Bos taurus | 29% | 100% |
Q3TDQ1 | Mus musculus | 31% | 94% |
Q54NM9 | Dictyostelium discoideum | 30% | 100% |
Q5RCE2 | Pongo abelii | 29% | 100% |
Q6F2Z1 | Oryza sativa subsp. japonica | 29% | 98% |
Q7XQ88 | Oryza sativa subsp. japonica | 32% | 100% |
Q8TCJ2 | Homo sapiens | 31% | 93% |
Q93ZY3 | Arabidopsis thaliana | 31% | 99% |
Q9FX21 | Arabidopsis thaliana | 31% | 100% |
V5BDM6 | Trypanosoma cruzi | 56% | 93% |