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. | yes | 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: A0A3Q8II34
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 | 572 | 576 | PF00656 | 0.246 |
CLV_C14_Caspase3-7 | 777 | 781 | PF00656 | 0.315 |
CLV_NRD_NRD_1 | 289 | 291 | PF00675 | 0.202 |
CLV_NRD_NRD_1 | 470 | 472 | PF00675 | 0.354 |
CLV_PCSK_KEX2_1 | 288 | 290 | PF00082 | 0.219 |
CLV_PCSK_KEX2_1 | 470 | 472 | PF00082 | 0.283 |
CLV_PCSK_KEX2_1 | 652 | 654 | PF00082 | 0.534 |
CLV_PCSK_KEX2_1 | 660 | 662 | PF00082 | 0.576 |
CLV_PCSK_PC1ET2_1 | 470 | 472 | PF00082 | 0.276 |
CLV_PCSK_PC1ET2_1 | 652 | 654 | PF00082 | 0.534 |
CLV_PCSK_PC1ET2_1 | 660 | 662 | PF00082 | 0.576 |
CLV_PCSK_SKI1_1 | 430 | 434 | PF00082 | 0.357 |
CLV_PCSK_SKI1_1 | 482 | 486 | PF00082 | 0.302 |
CLV_PCSK_SKI1_1 | 589 | 593 | PF00082 | 0.478 |
CLV_PCSK_SKI1_1 | 647 | 651 | PF00082 | 0.456 |
CLV_PCSK_SKI1_1 | 723 | 727 | PF00082 | 0.603 |
CLV_PCSK_SKI1_1 | 776 | 780 | PF00082 | 0.535 |
CLV_Separin_Metazoa | 384 | 388 | PF03568 | 0.372 |
DEG_APCC_DBOX_1 | 429 | 437 | PF00400 | 0.202 |
DEG_ODPH_VHL_1 | 321 | 332 | PF01847 | 0.301 |
DEG_SPOP_SBC_1 | 79 | 83 | PF00917 | 0.375 |
DOC_AGCK_PIF_2 | 64 | 69 | PF00069 | 0.272 |
DOC_CYCLIN_RxL_1 | 325 | 335 | PF00134 | 0.243 |
DOC_MAPK_FxFP_2 | 367 | 370 | PF00069 | 0.247 |
DOC_MAPK_gen_1 | 184 | 193 | PF00069 | 0.347 |
DOC_MAPK_gen_1 | 295 | 305 | PF00069 | 0.476 |
DOC_MAPK_gen_1 | 660 | 667 | PF00069 | 0.385 |
DOC_MAPK_MEF2A_6 | 298 | 307 | PF00069 | 0.461 |
DOC_MAPK_MEF2A_6 | 487 | 496 | PF00069 | 0.307 |
DOC_MAPK_MEF2A_6 | 512 | 521 | PF00069 | 0.205 |
DOC_MAPK_RevD_3 | 517 | 533 | PF00069 | 0.181 |
DOC_PP1_RVXF_1 | 551 | 558 | PF00149 | 0.258 |
DOC_PP4_FxxP_1 | 326 | 329 | PF00568 | 0.281 |
DOC_PP4_FxxP_1 | 367 | 370 | PF00568 | 0.434 |
DOC_USP7_MATH_1 | 138 | 142 | PF00917 | 0.315 |
DOC_USP7_MATH_1 | 262 | 266 | PF00917 | 0.258 |
DOC_USP7_MATH_1 | 376 | 380 | PF00917 | 0.392 |
DOC_USP7_MATH_1 | 407 | 411 | PF00917 | 0.407 |
DOC_USP7_MATH_1 | 643 | 647 | PF00917 | 0.286 |
DOC_USP7_MATH_1 | 659 | 663 | PF00917 | 0.400 |
DOC_USP7_MATH_1 | 78 | 82 | PF00917 | 0.334 |
DOC_WW_Pin1_4 | 258 | 263 | PF00397 | 0.258 |
DOC_WW_Pin1_4 | 545 | 550 | PF00397 | 0.247 |
DOC_WW_Pin1_4 | 590 | 595 | PF00397 | 0.285 |
DOC_WW_Pin1_4 | 621 | 626 | PF00397 | 0.317 |
LIG_14-3-3_CanoR_1 | 184 | 190 | PF00244 | 0.282 |
LIG_14-3-3_CanoR_1 | 230 | 234 | PF00244 | 0.514 |
LIG_14-3-3_CanoR_1 | 239 | 244 | PF00244 | 0.380 |
LIG_14-3-3_CanoR_1 | 343 | 349 | PF00244 | 0.295 |
LIG_14-3-3_CanoR_1 | 387 | 392 | PF00244 | 0.414 |
LIG_14-3-3_CanoR_1 | 570 | 574 | PF00244 | 0.273 |
LIG_14-3-3_CanoR_1 | 629 | 635 | PF00244 | 0.301 |
LIG_14-3-3_CanoR_1 | 663 | 668 | PF00244 | 0.387 |
LIG_AP2alpha_2 | 44 | 46 | PF02296 | 0.258 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.491 |
LIG_BRCT_BRCA1_1 | 10 | 14 | PF00533 | 0.261 |
LIG_BRCT_BRCA1_1 | 143 | 147 | PF00533 | 0.391 |
LIG_BRCT_BRCA1_1 | 60 | 64 | PF00533 | 0.311 |
LIG_eIF4E_1 | 435 | 441 | PF01652 | 0.390 |
LIG_eIF4E_1 | 681 | 687 | PF01652 | 0.266 |
LIG_FAT_LD_1 | 433 | 441 | PF03623 | 0.381 |
LIG_FHA_1 | 3 | 9 | PF00498 | 0.572 |
LIG_FHA_1 | 381 | 387 | PF00498 | 0.366 |
LIG_FHA_1 | 423 | 429 | PF00498 | 0.277 |
LIG_FHA_1 | 476 | 482 | PF00498 | 0.399 |
LIG_FHA_1 | 484 | 490 | PF00498 | 0.329 |
LIG_FHA_1 | 590 | 596 | PF00498 | 0.291 |
LIG_FHA_2 | 345 | 351 | PF00498 | 0.269 |
LIG_FHA_2 | 459 | 465 | PF00498 | 0.387 |
LIG_FHA_2 | 546 | 552 | PF00498 | 0.237 |
LIG_FHA_2 | 703 | 709 | PF00498 | 0.314 |
LIG_GBD_Chelix_1 | 129 | 137 | PF00786 | 0.453 |
LIG_LIR_Apic_2 | 751 | 755 | PF02991 | 0.393 |
LIG_LIR_Gen_1 | 144 | 155 | PF02991 | 0.411 |
LIG_LIR_Gen_1 | 175 | 183 | PF02991 | 0.302 |
LIG_LIR_Gen_1 | 392 | 402 | PF02991 | 0.400 |
LIG_LIR_Gen_1 | 439 | 449 | PF02991 | 0.440 |
LIG_LIR_Gen_1 | 473 | 484 | PF02991 | 0.395 |
LIG_LIR_Gen_1 | 57 | 67 | PF02991 | 0.342 |
LIG_LIR_Gen_1 | 607 | 613 | PF02991 | 0.334 |
LIG_LIR_Gen_1 | 615 | 625 | PF02991 | 0.396 |
LIG_LIR_Gen_1 | 708 | 718 | PF02991 | 0.405 |
LIG_LIR_Nem_3 | 144 | 150 | PF02991 | 0.326 |
LIG_LIR_Nem_3 | 175 | 180 | PF02991 | 0.287 |
LIG_LIR_Nem_3 | 242 | 247 | PF02991 | 0.271 |
LIG_LIR_Nem_3 | 261 | 266 | PF02991 | 0.252 |
LIG_LIR_Nem_3 | 43 | 49 | PF02991 | 0.268 |
LIG_LIR_Nem_3 | 535 | 541 | PF02991 | 0.235 |
LIG_LIR_Nem_3 | 57 | 63 | PF02991 | 0.307 |
LIG_LIR_Nem_3 | 607 | 611 | PF02991 | 0.261 |
LIG_LIR_Nem_3 | 615 | 621 | PF02991 | 0.341 |
LIG_LIR_Nem_3 | 633 | 638 | PF02991 | 0.301 |
LIG_LIR_Nem_3 | 65 | 69 | PF02991 | 0.281 |
LIG_LIR_Nem_3 | 708 | 714 | PF02991 | 0.343 |
LIG_LIR_Nem_3 | 71 | 75 | PF02991 | 0.262 |
LIG_LIR_Nem_3 | 773 | 778 | PF02991 | 0.340 |
LIG_LIR_Nem_3 | 81 | 87 | PF02991 | 0.229 |
LIG_LYPXL_yS_3 | 84 | 87 | PF13949 | 0.346 |
LIG_MLH1_MIPbox_1 | 60 | 64 | PF16413 | 0.311 |
LIG_NRBOX | 268 | 274 | PF00104 | 0.348 |
LIG_NRBOX | 432 | 438 | PF00104 | 0.202 |
LIG_PCNA_PIPBox_1 | 398 | 407 | PF02747 | 0.173 |
LIG_PCNA_yPIPBox_3 | 343 | 353 | PF02747 | 0.166 |
LIG_Pex14_1 | 431 | 435 | PF04695 | 0.202 |
LIG_Pex14_1 | 558 | 562 | PF04695 | 0.247 |
LIG_Pex14_1 | 60 | 64 | PF04695 | 0.258 |
LIG_Pex14_2 | 63 | 67 | PF04695 | 0.196 |
LIG_Pex14_2 | 711 | 715 | PF04695 | 0.235 |
LIG_PTB_Apo_2 | 385 | 392 | PF02174 | 0.387 |
LIG_PTB_Apo_2 | 629 | 636 | PF02174 | 0.304 |
LIG_PTB_Phospho_1 | 385 | 391 | PF10480 | 0.387 |
LIG_PTB_Phospho_1 | 629 | 635 | PF10480 | 0.301 |
LIG_REV1ctd_RIR_1 | 324 | 328 | PF16727 | 0.196 |
LIG_SH2_CRK | 36 | 40 | PF00017 | 0.294 |
LIG_SH2_CRK | 399 | 403 | PF00017 | 0.274 |
LIG_SH2_PTP2 | 209 | 212 | PF00017 | 0.321 |
LIG_SH2_PTP2 | 608 | 611 | PF00017 | 0.260 |
LIG_SH2_SRC | 681 | 684 | PF00017 | 0.277 |
LIG_SH2_STAP1 | 10 | 14 | PF00017 | 0.223 |
LIG_SH2_STAP1 | 241 | 245 | PF00017 | 0.321 |
LIG_SH2_STAP1 | 26 | 30 | PF00017 | 0.255 |
LIG_SH2_STAP1 | 308 | 312 | PF00017 | 0.194 |
LIG_SH2_STAP1 | 391 | 395 | PF00017 | 0.482 |
LIG_SH2_STAT3 | 560 | 563 | PF00017 | 0.247 |
LIG_SH2_STAT5 | 177 | 180 | PF00017 | 0.346 |
LIG_SH2_STAT5 | 209 | 212 | PF00017 | 0.321 |
LIG_SH2_STAT5 | 241 | 244 | PF00017 | 0.437 |
LIG_SH2_STAT5 | 245 | 248 | PF00017 | 0.416 |
LIG_SH2_STAT5 | 38 | 41 | PF00017 | 0.348 |
LIG_SH2_STAT5 | 389 | 392 | PF00017 | 0.444 |
LIG_SH2_STAT5 | 405 | 408 | PF00017 | 0.293 |
LIG_SH2_STAT5 | 435 | 438 | PF00017 | 0.457 |
LIG_SH2_STAT5 | 541 | 544 | PF00017 | 0.256 |
LIG_SH2_STAT5 | 608 | 611 | PF00017 | 0.260 |
LIG_SH2_STAT5 | 617 | 620 | PF00017 | 0.335 |
LIG_SH3_3 | 109 | 115 | PF00018 | 0.346 |
LIG_SH3_3 | 250 | 256 | PF00018 | 0.334 |
LIG_SH3_3 | 637 | 643 | PF00018 | 0.385 |
LIG_SH3_3 | 677 | 683 | PF00018 | 0.315 |
LIG_SH3_3 | 735 | 741 | PF00018 | 0.342 |
LIG_SH3_3 | 742 | 748 | PF00018 | 0.347 |
LIG_SUMO_SIM_anti_2 | 299 | 305 | PF11976 | 0.464 |
LIG_SUMO_SIM_anti_2 | 358 | 364 | PF11976 | 0.176 |
LIG_SUMO_SIM_par_1 | 314 | 320 | PF11976 | 0.194 |
LIG_TRAF2_1 | 461 | 464 | PF00917 | 0.559 |
LIG_TYR_ITIM | 397 | 402 | PF00017 | 0.226 |
LIG_TYR_ITSM | 173 | 180 | PF00017 | 0.286 |
LIG_UBA3_1 | 721 | 726 | PF00899 | 0.290 |
LIG_WRC_WIRS_1 | 173 | 178 | PF05994 | 0.286 |
MOD_CDC14_SPxK_1 | 261 | 264 | PF00782 | 0.311 |
MOD_CDK_SPxK_1 | 258 | 264 | PF00069 | 0.258 |
MOD_CK1_1 | 119 | 125 | PF00069 | 0.229 |
MOD_CK1_1 | 141 | 147 | PF00069 | 0.328 |
MOD_CK1_1 | 182 | 188 | PF00069 | 0.321 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.563 |
MOD_CK1_1 | 731 | 737 | PF00069 | 0.314 |
MOD_CK2_1 | 279 | 285 | PF00069 | 0.459 |
MOD_CK2_1 | 458 | 464 | PF00069 | 0.498 |
MOD_CK2_1 | 663 | 669 | PF00069 | 0.372 |
MOD_CK2_1 | 702 | 708 | PF00069 | 0.270 |
MOD_GlcNHglycan | 122 | 125 | PF01048 | 0.402 |
MOD_GlcNHglycan | 132 | 136 | PF01048 | 0.476 |
MOD_GlcNHglycan | 334 | 337 | PF01048 | 0.506 |
MOD_GlcNHglycan | 378 | 381 | PF01048 | 0.198 |
MOD_GlcNHglycan | 500 | 503 | PF01048 | 0.304 |
MOD_GlcNHglycan | 522 | 525 | PF01048 | 0.449 |
MOD_GlcNHglycan | 60 | 63 | PF01048 | 0.551 |
MOD_GlcNHglycan | 696 | 699 | PF01048 | 0.536 |
MOD_GlcNHglycan | 716 | 719 | PF01048 | 0.613 |
MOD_GSK3_1 | 116 | 123 | PF00069 | 0.343 |
MOD_GSK3_1 | 141 | 148 | PF00069 | 0.342 |
MOD_GSK3_1 | 229 | 236 | PF00069 | 0.502 |
MOD_GSK3_1 | 258 | 265 | PF00069 | 0.276 |
MOD_GSK3_1 | 328 | 335 | PF00069 | 0.172 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.199 |
MOD_GSK3_1 | 376 | 383 | PF00069 | 0.258 |
MOD_GSK3_1 | 387 | 394 | PF00069 | 0.397 |
MOD_GSK3_1 | 4 | 11 | PF00069 | 0.553 |
MOD_GSK3_1 | 54 | 61 | PF00069 | 0.327 |
MOD_GSK3_1 | 659 | 666 | PF00069 | 0.466 |
MOD_GSK3_1 | 702 | 709 | PF00069 | 0.325 |
MOD_N-GLC_1 | 387 | 392 | PF02516 | 0.193 |
MOD_N-GLC_1 | 568 | 573 | PF02516 | 0.446 |
MOD_N-GLC_1 | 621 | 626 | PF02516 | 0.446 |
MOD_N-GLC_1 | 706 | 711 | PF02516 | 0.444 |
MOD_N-GLC_1 | 728 | 733 | PF02516 | 0.511 |
MOD_N-GLC_2 | 109 | 111 | PF02516 | 0.416 |
MOD_N-GLC_2 | 164 | 166 | PF02516 | 0.258 |
MOD_NEK2_1 | 120 | 125 | PF00069 | 0.362 |
MOD_NEK2_1 | 154 | 159 | PF00069 | 0.365 |
MOD_NEK2_1 | 172 | 177 | PF00069 | 0.223 |
MOD_NEK2_1 | 279 | 284 | PF00069 | 0.194 |
MOD_NEK2_1 | 332 | 337 | PF00069 | 0.245 |
MOD_NEK2_1 | 348 | 353 | PF00069 | 0.229 |
MOD_NEK2_1 | 436 | 441 | PF00069 | 0.447 |
MOD_NEK2_1 | 498 | 503 | PF00069 | 0.277 |
MOD_NEK2_1 | 687 | 692 | PF00069 | 0.282 |
MOD_NEK2_1 | 706 | 711 | PF00069 | 0.217 |
MOD_NEK2_1 | 87 | 92 | PF00069 | 0.302 |
MOD_NEK2_2 | 179 | 184 | PF00069 | 0.286 |
MOD_NEK2_2 | 407 | 412 | PF00069 | 0.264 |
MOD_PIKK_1 | 405 | 411 | PF00454 | 0.215 |
MOD_PK_1 | 29 | 35 | PF00069 | 0.342 |
MOD_PK_1 | 663 | 669 | PF00069 | 0.381 |
MOD_PKA_1 | 482 | 488 | PF00069 | 0.393 |
MOD_PKA_2 | 185 | 191 | PF00069 | 0.295 |
MOD_PKA_2 | 229 | 235 | PF00069 | 0.514 |
MOD_PKA_2 | 294 | 300 | PF00069 | 0.485 |
MOD_PKA_2 | 498 | 504 | PF00069 | 0.317 |
MOD_PKA_2 | 569 | 575 | PF00069 | 0.247 |
MOD_PKB_1 | 661 | 669 | PF00069 | 0.387 |
MOD_Plk_1 | 387 | 393 | PF00069 | 0.387 |
MOD_Plk_1 | 568 | 574 | PF00069 | 0.256 |
MOD_Plk_1 | 706 | 712 | PF00069 | 0.250 |
MOD_Plk_4 | 141 | 147 | PF00069 | 0.292 |
MOD_Plk_4 | 172 | 178 | PF00069 | 0.286 |
MOD_Plk_4 | 221 | 227 | PF00069 | 0.401 |
MOD_Plk_4 | 233 | 239 | PF00069 | 0.407 |
MOD_Plk_4 | 344 | 350 | PF00069 | 0.353 |
MOD_Plk_4 | 391 | 397 | PF00069 | 0.417 |
MOD_Plk_4 | 436 | 442 | PF00069 | 0.478 |
MOD_Plk_4 | 597 | 603 | PF00069 | 0.347 |
MOD_Plk_4 | 613 | 619 | PF00069 | 0.355 |
MOD_Plk_4 | 630 | 636 | PF00069 | 0.290 |
MOD_Plk_4 | 68 | 74 | PF00069 | 0.258 |
MOD_Plk_4 | 682 | 688 | PF00069 | 0.355 |
MOD_Plk_4 | 706 | 712 | PF00069 | 0.250 |
MOD_Plk_4 | 748 | 754 | PF00069 | 0.350 |
MOD_ProDKin_1 | 258 | 264 | PF00069 | 0.258 |
MOD_ProDKin_1 | 545 | 551 | PF00069 | 0.247 |
MOD_ProDKin_1 | 590 | 596 | PF00069 | 0.291 |
MOD_ProDKin_1 | 621 | 627 | PF00069 | 0.314 |
MOD_SUMO_rev_2 | 530 | 534 | PF00179 | 0.181 |
TRG_DiLeu_BaEn_1 | 299 | 304 | PF01217 | 0.396 |
TRG_DiLeu_BaEn_1 | 597 | 602 | PF01217 | 0.302 |
TRG_DiLeu_BaEn_1 | 682 | 687 | PF01217 | 0.250 |
TRG_ENDOCYTIC_2 | 177 | 180 | PF00928 | 0.286 |
TRG_ENDOCYTIC_2 | 199 | 202 | PF00928 | 0.286 |
TRG_ENDOCYTIC_2 | 209 | 212 | PF00928 | 0.286 |
TRG_ENDOCYTIC_2 | 241 | 244 | PF00928 | 0.286 |
TRG_ENDOCYTIC_2 | 308 | 311 | PF00928 | 0.306 |
TRG_ENDOCYTIC_2 | 36 | 39 | PF00928 | 0.281 |
TRG_ENDOCYTIC_2 | 399 | 402 | PF00928 | 0.237 |
TRG_ENDOCYTIC_2 | 476 | 479 | PF00928 | 0.396 |
TRG_ENDOCYTIC_2 | 541 | 544 | PF00928 | 0.247 |
TRG_ENDOCYTIC_2 | 608 | 611 | PF00928 | 0.260 |
TRG_ENDOCYTIC_2 | 635 | 638 | PF00928 | 0.309 |
TRG_ENDOCYTIC_2 | 84 | 87 | PF00928 | 0.399 |
TRG_ER_diArg_1 | 183 | 186 | PF00400 | 0.308 |
TRG_ER_diArg_1 | 28 | 31 | PF00400 | 0.330 |
TRG_ER_diArg_1 | 288 | 290 | PF00400 | 0.475 |
TRG_NES_CRM1_1 | 267 | 281 | PF08389 | 0.311 |
TRG_NES_CRM1_1 | 719 | 733 | PF08389 | 0.231 |
TRG_NLS_MonoCore_2 | 651 | 656 | PF00514 | 0.328 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0S4IZ72 | Bodo saltans | 43% | 96% |
A0A1X0NFU7 | Trypanosomatidae | 47% | 94% |
A0A3Q8IHT0 | Leishmania donovani | 56% | 100% |
A0A3Q8ILY7 | Leishmania donovani | 57% | 100% |
A0A3Q8IV37 | Leishmania donovani | 57% | 95% |
A0A422MX14 | Trypanosoma rangeli | 49% | 96% |
A4HFF9 | Leishmania braziliensis | 54% | 100% |
A4HMD5 | Leishmania braziliensis | 54% | 97% |
A4HMD6 | Leishmania braziliensis | 80% | 100% |
A4HMD7 | Leishmania braziliensis | 55% | 100% |
A4IB08 | Leishmania infantum | 56% | 100% |
A4IB09 | Leishmania infantum | 57% | 100% |
A4IB10 | Leishmania infantum | 100% | 100% |
C9ZNL1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 47% | 97% |
C9ZQ40 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 100% |
E2RG47 | Canis lupus familiaris | 32% | 96% |
E9AET6 | Leishmania major | 56% | 100% |
E9AET7 | Leishmania major | 58% | 100% |
E9AET8 | Leishmania major | 94% | 100% |
E9AET9 | Leishmania major | 55% | 100% |
E9AHU4 | Leishmania infantum | 56% | 100% |
E9B5Z2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 55% | 100% |
E9B5Z3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 57% | 100% |
E9B5Z4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
E9B5Z5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 55% | 100% |
F1PJP5 | Canis lupus familiaris | 29% | 100% |
O94335 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 31% | 100% |
P39007 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 28% | 100% |
P46975 | Caenorhabditis elegans | 30% | 100% |
P46977 | Homo sapiens | 29% | 100% |
P46978 | Mus musculus | 29% | 100% |
Q2KJI2 | Bos taurus | 29% | 100% |
Q3TDQ1 | Mus musculus | 32% | 96% |
Q54NM9 | Dictyostelium discoideum | 28% | 100% |
Q5RCE2 | Pongo abelii | 29% | 100% |
Q6F2Z1 | Oryza sativa subsp. japonica | 28% | 100% |
Q7XQ88 | Oryza sativa subsp. japonica | 30% | 100% |
Q8TCJ2 | Homo sapiens | 32% | 96% |
Q93ZY3 | Arabidopsis thaliana | 32% | 100% |
Q9FX21 | Arabidopsis thaliana | 30% | 100% |
V5BDM6 | Trypanosoma cruzi | 48% | 96% |