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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005730 | nucleolus | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HQ83
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003676 | nucleic acid binding | 3 | 11 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004386 | helicase activity | 2 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0005524 | ATP binding | 5 | 12 |
GO:0016787 | hydrolase activity | 2 | 7 |
GO:0017076 | purine nucleotide binding | 4 | 12 |
GO:0030554 | adenyl nucleotide binding | 5 | 12 |
GO:0032553 | ribonucleotide binding | 3 | 12 |
GO:0032555 | purine ribonucleotide binding | 4 | 12 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 12 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 12 |
GO:0036094 | small molecule binding | 2 | 12 |
GO:0043167 | ion binding | 2 | 12 |
GO:0043168 | anion binding | 3 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:0097367 | carbohydrate derivative binding | 2 | 12 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 12 |
GO:0140657 | ATP-dependent activity | 1 | 12 |
GO:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
GO:0003723 | RNA binding | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 12 | 16 | PF00656 | 0.297 |
CLV_C14_Caspase3-7 | 536 | 540 | PF00656 | 0.441 |
CLV_C14_Caspase3-7 | 572 | 576 | PF00656 | 0.586 |
CLV_C14_Caspase3-7 | 97 | 101 | PF00656 | 0.360 |
CLV_NRD_NRD_1 | 21 | 23 | PF00675 | 0.288 |
CLV_NRD_NRD_1 | 279 | 281 | PF00675 | 0.209 |
CLV_NRD_NRD_1 | 367 | 369 | PF00675 | 0.468 |
CLV_NRD_NRD_1 | 505 | 507 | PF00675 | 0.382 |
CLV_NRD_NRD_1 | 613 | 615 | PF00675 | 0.226 |
CLV_NRD_NRD_1 | 65 | 67 | PF00675 | 0.230 |
CLV_NRD_NRD_1 | 654 | 656 | PF00675 | 0.241 |
CLV_PCSK_KEX2_1 | 237 | 239 | PF00082 | 0.213 |
CLV_PCSK_KEX2_1 | 367 | 369 | PF00082 | 0.468 |
CLV_PCSK_KEX2_1 | 52 | 54 | PF00082 | 0.303 |
CLV_PCSK_KEX2_1 | 568 | 570 | PF00082 | 0.679 |
CLV_PCSK_KEX2_1 | 573 | 575 | PF00082 | 0.587 |
CLV_PCSK_KEX2_1 | 613 | 615 | PF00082 | 0.240 |
CLV_PCSK_KEX2_1 | 65 | 67 | PF00082 | 0.163 |
CLV_PCSK_KEX2_1 | 671 | 673 | PF00082 | 0.236 |
CLV_PCSK_PC1ET2_1 | 237 | 239 | PF00082 | 0.208 |
CLV_PCSK_PC1ET2_1 | 52 | 54 | PF00082 | 0.311 |
CLV_PCSK_PC1ET2_1 | 568 | 570 | PF00082 | 0.619 |
CLV_PCSK_PC1ET2_1 | 573 | 575 | PF00082 | 0.587 |
CLV_PCSK_PC1ET2_1 | 671 | 673 | PF00082 | 0.275 |
CLV_PCSK_PC7_1 | 569 | 575 | PF00082 | 0.483 |
CLV_PCSK_SKI1_1 | 105 | 109 | PF00082 | 0.249 |
CLV_PCSK_SKI1_1 | 237 | 241 | PF00082 | 0.208 |
CLV_PCSK_SKI1_1 | 281 | 285 | PF00082 | 0.232 |
CLV_PCSK_SKI1_1 | 468 | 472 | PF00082 | 0.262 |
CLV_PCSK_SKI1_1 | 478 | 482 | PF00082 | 0.219 |
CLV_PCSK_SKI1_1 | 518 | 522 | PF00082 | 0.372 |
CLV_PCSK_SKI1_1 | 613 | 617 | PF00082 | 0.205 |
CLV_PCSK_SKI1_1 | 657 | 661 | PF00082 | 0.216 |
CLV_PCSK_SKI1_1 | 672 | 676 | PF00082 | 0.186 |
CLV_Separin_Metazoa | 610 | 614 | PF03568 | 0.298 |
DEG_APCC_DBOX_1 | 237 | 245 | PF00400 | 0.457 |
DEG_APCC_DBOX_1 | 367 | 375 | PF00400 | 0.300 |
DOC_CKS1_1 | 692 | 697 | PF01111 | 0.353 |
DOC_CYCLIN_RxL_1 | 235 | 242 | PF00134 | 0.457 |
DOC_MAPK_gen_1 | 152 | 160 | PF00069 | 0.408 |
DOC_MAPK_gen_1 | 19 | 29 | PF00069 | 0.469 |
DOC_MAPK_gen_1 | 367 | 374 | PF00069 | 0.406 |
DOC_MAPK_gen_1 | 65 | 72 | PF00069 | 0.419 |
DOC_MAPK_gen_1 | 655 | 663 | PF00069 | 0.408 |
DOC_MAPK_gen_1 | 671 | 679 | PF00069 | 0.408 |
DOC_MAPK_MEF2A_6 | 154 | 162 | PF00069 | 0.411 |
DOC_MAPK_MEF2A_6 | 367 | 376 | PF00069 | 0.315 |
DOC_MAPK_MEF2A_6 | 655 | 662 | PF00069 | 0.408 |
DOC_PP1_RVXF_1 | 101 | 107 | PF00149 | 0.450 |
DOC_PP1_RVXF_1 | 612 | 619 | PF00149 | 0.511 |
DOC_PP4_FxxP_1 | 692 | 695 | PF00568 | 0.325 |
DOC_USP7_MATH_1 | 13 | 17 | PF00917 | 0.449 |
DOC_USP7_MATH_1 | 289 | 293 | PF00917 | 0.436 |
DOC_USP7_MATH_1 | 456 | 460 | PF00917 | 0.475 |
DOC_USP7_MATH_1 | 559 | 563 | PF00917 | 0.513 |
DOC_USP7_UBL2_3 | 671 | 675 | PF12436 | 0.475 |
DOC_WW_Pin1_4 | 2 | 7 | PF00397 | 0.580 |
DOC_WW_Pin1_4 | 498 | 503 | PF00397 | 0.406 |
DOC_WW_Pin1_4 | 691 | 696 | PF00397 | 0.345 |
LIG_14-3-3_CanoR_1 | 348 | 355 | PF00244 | 0.364 |
LIG_14-3-3_CanoR_1 | 367 | 372 | PF00244 | 0.349 |
LIG_14-3-3_CanoR_1 | 425 | 433 | PF00244 | 0.439 |
LIG_14-3-3_CanoR_1 | 506 | 510 | PF00244 | 0.497 |
LIG_Actin_WH2_2 | 100 | 116 | PF00022 | 0.432 |
LIG_Actin_WH2_2 | 135 | 150 | PF00022 | 0.412 |
LIG_Actin_WH2_2 | 539 | 554 | PF00022 | 0.515 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.659 |
LIG_BIR_III_2 | 687 | 691 | PF00653 | 0.475 |
LIG_BRCT_BRCA1_1 | 466 | 470 | PF00533 | 0.511 |
LIG_BRCT_BRCA1_1 | 648 | 652 | PF00533 | 0.419 |
LIG_Clathr_ClatBox_1 | 269 | 273 | PF01394 | 0.475 |
LIG_eIF4E_1 | 265 | 271 | PF01652 | 0.511 |
LIG_FHA_1 | 106 | 112 | PF00498 | 0.447 |
LIG_FHA_1 | 208 | 214 | PF00498 | 0.408 |
LIG_FHA_1 | 36 | 42 | PF00498 | 0.429 |
LIG_FHA_1 | 404 | 410 | PF00498 | 0.456 |
LIG_FHA_1 | 414 | 420 | PF00498 | 0.461 |
LIG_FHA_2 | 226 | 232 | PF00498 | 0.408 |
LIG_FHA_2 | 320 | 326 | PF00498 | 0.481 |
LIG_FHA_2 | 360 | 366 | PF00498 | 0.338 |
LIG_FHA_2 | 464 | 470 | PF00498 | 0.432 |
LIG_FHA_2 | 506 | 512 | PF00498 | 0.510 |
LIG_FHA_2 | 95 | 101 | PF00498 | 0.429 |
LIG_FXI_DFP_1 | 426 | 430 | PF00024 | 0.219 |
LIG_LIR_Apic_2 | 691 | 695 | PF02991 | 0.341 |
LIG_LIR_Gen_1 | 170 | 180 | PF02991 | 0.318 |
LIG_LIR_Gen_1 | 253 | 262 | PF02991 | 0.412 |
LIG_LIR_Gen_1 | 390 | 399 | PF02991 | 0.330 |
LIG_LIR_Gen_1 | 550 | 560 | PF02991 | 0.437 |
LIG_LIR_Nem_3 | 123 | 128 | PF02991 | 0.438 |
LIG_LIR_Nem_3 | 141 | 147 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 170 | 175 | PF02991 | 0.325 |
LIG_LIR_Nem_3 | 253 | 257 | PF02991 | 0.429 |
LIG_LIR_Nem_3 | 493 | 498 | PF02991 | 0.328 |
LIG_LIR_Nem_3 | 550 | 556 | PF02991 | 0.437 |
LIG_LIR_Nem_3 | 583 | 588 | PF02991 | 0.732 |
LIG_NRBOX | 142 | 148 | PF00104 | 0.408 |
LIG_Pex14_2 | 172 | 176 | PF04695 | 0.287 |
LIG_PTB_Apo_2 | 620 | 627 | PF02174 | 0.450 |
LIG_SH2_CRK | 125 | 129 | PF00017 | 0.408 |
LIG_SH2_CRK | 553 | 557 | PF00017 | 0.386 |
LIG_SH2_CRK | 634 | 638 | PF00017 | 0.419 |
LIG_SH2_GRB2like | 311 | 314 | PF00017 | 0.511 |
LIG_SH2_SRC | 203 | 206 | PF00017 | 0.308 |
LIG_SH2_STAP1 | 265 | 269 | PF00017 | 0.419 |
LIG_SH2_STAP1 | 350 | 354 | PF00017 | 0.310 |
LIG_SH2_STAP1 | 449 | 453 | PF00017 | 0.429 |
LIG_SH2_STAP1 | 90 | 94 | PF00017 | 0.419 |
LIG_SH2_STAT3 | 265 | 268 | PF00017 | 0.408 |
LIG_SH2_STAT5 | 203 | 206 | PF00017 | 0.308 |
LIG_SH2_STAT5 | 300 | 303 | PF00017 | 0.408 |
LIG_SH2_STAT5 | 350 | 353 | PF00017 | 0.353 |
LIG_SH2_STAT5 | 44 | 47 | PF00017 | 0.432 |
LIG_SH2_STAT5 | 498 | 501 | PF00017 | 0.541 |
LIG_SH2_STAT5 | 620 | 623 | PF00017 | 0.457 |
LIG_SH3_3 | 268 | 274 | PF00018 | 0.445 |
LIG_SH3_3 | 3 | 9 | PF00018 | 0.596 |
LIG_SH3_3 | 427 | 433 | PF00018 | 0.409 |
LIG_SH3_5 | 199 | 203 | PF00018 | 0.362 |
LIG_SUMO_SIM_anti_2 | 209 | 215 | PF11976 | 0.311 |
LIG_SUMO_SIM_anti_2 | 369 | 376 | PF11976 | 0.302 |
LIG_SUMO_SIM_anti_2 | 404 | 411 | PF11976 | 0.419 |
LIG_SUMO_SIM_anti_2 | 450 | 456 | PF11976 | 0.511 |
LIG_SUMO_SIM_anti_2 | 676 | 683 | PF11976 | 0.432 |
LIG_SUMO_SIM_par_1 | 26 | 33 | PF11976 | 0.432 |
LIG_TRAF2_1 | 228 | 231 | PF00917 | 0.419 |
LIG_TYR_ITIM | 447 | 452 | PF00017 | 0.352 |
LIG_TYR_ITIM | 551 | 556 | PF00017 | 0.440 |
LIG_UBA3_1 | 143 | 148 | PF00899 | 0.408 |
LIG_UBA3_1 | 240 | 245 | PF00899 | 0.457 |
LIG_UBA3_1 | 407 | 415 | PF00899 | 0.523 |
MOD_CDK_SPK_2 | 498 | 503 | PF00069 | 0.400 |
MOD_CK1_1 | 255 | 261 | PF00069 | 0.530 |
MOD_CK1_1 | 35 | 41 | PF00069 | 0.441 |
MOD_CK1_1 | 359 | 365 | PF00069 | 0.407 |
MOD_CK1_1 | 370 | 376 | PF00069 | 0.247 |
MOD_CK1_1 | 593 | 599 | PF00069 | 0.522 |
MOD_CK2_1 | 1 | 7 | PF00069 | 0.531 |
MOD_CK2_1 | 225 | 231 | PF00069 | 0.408 |
MOD_CK2_1 | 313 | 319 | PF00069 | 0.418 |
MOD_CK2_1 | 359 | 365 | PF00069 | 0.362 |
MOD_CK2_1 | 463 | 469 | PF00069 | 0.432 |
MOD_CK2_1 | 505 | 511 | PF00069 | 0.537 |
MOD_GlcNHglycan | 163 | 166 | PF01048 | 0.208 |
MOD_GlcNHglycan | 303 | 306 | PF01048 | 0.229 |
MOD_GlcNHglycan | 315 | 318 | PF01048 | 0.251 |
MOD_GlcNHglycan | 34 | 37 | PF01048 | 0.244 |
MOD_GlcNHglycan | 458 | 461 | PF01048 | 0.166 |
MOD_GSK3_1 | 189 | 196 | PF00069 | 0.343 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.438 |
MOD_GSK3_1 | 366 | 373 | PF00069 | 0.328 |
MOD_GSK3_1 | 413 | 420 | PF00069 | 0.541 |
MOD_GSK3_1 | 505 | 512 | PF00069 | 0.471 |
MOD_GSK3_1 | 547 | 554 | PF00069 | 0.466 |
MOD_GSK3_1 | 559 | 566 | PF00069 | 0.650 |
MOD_GSK3_1 | 662 | 669 | PF00069 | 0.447 |
MOD_LATS_1 | 567 | 573 | PF00433 | 0.490 |
MOD_N-GLC_1 | 356 | 361 | PF02516 | 0.457 |
MOD_N-GLC_1 | 537 | 542 | PF02516 | 0.355 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.682 |
MOD_NEK2_1 | 163 | 168 | PF00069 | 0.424 |
MOD_NEK2_1 | 413 | 418 | PF00069 | 0.371 |
MOD_NEK2_1 | 463 | 468 | PF00069 | 0.419 |
MOD_NEK2_1 | 481 | 486 | PF00069 | 0.419 |
MOD_NEK2_1 | 551 | 556 | PF00069 | 0.375 |
MOD_NEK2_1 | 633 | 638 | PF00069 | 0.505 |
MOD_NEK2_1 | 94 | 99 | PF00069 | 0.451 |
MOD_PIKK_1 | 329 | 335 | PF00454 | 0.408 |
MOD_PIKK_1 | 36 | 42 | PF00454 | 0.429 |
MOD_PIKK_1 | 525 | 531 | PF00454 | 0.353 |
MOD_PIKK_1 | 59 | 65 | PF00454 | 0.419 |
MOD_PIKK_1 | 593 | 599 | PF00454 | 0.607 |
MOD_PK_1 | 675 | 681 | PF00069 | 0.432 |
MOD_PKA_1 | 367 | 373 | PF00069 | 0.452 |
MOD_PKA_2 | 13 | 19 | PF00069 | 0.368 |
MOD_PKA_2 | 366 | 372 | PF00069 | 0.346 |
MOD_PKA_2 | 424 | 430 | PF00069 | 0.450 |
MOD_PKA_2 | 505 | 511 | PF00069 | 0.506 |
MOD_PKA_2 | 551 | 557 | PF00069 | 0.471 |
MOD_PKA_2 | 667 | 673 | PF00069 | 0.419 |
MOD_PKB_1 | 152 | 160 | PF00069 | 0.432 |
MOD_Plk_1 | 134 | 140 | PF00069 | 0.446 |
MOD_Plk_1 | 154 | 160 | PF00069 | 0.353 |
MOD_Plk_1 | 252 | 258 | PF00069 | 0.511 |
MOD_Plk_1 | 289 | 295 | PF00069 | 0.408 |
MOD_Plk_1 | 359 | 365 | PF00069 | 0.366 |
MOD_Plk_1 | 403 | 409 | PF00069 | 0.440 |
MOD_Plk_1 | 675 | 681 | PF00069 | 0.411 |
MOD_Plk_1 | 99 | 105 | PF00069 | 0.454 |
MOD_Plk_2-3 | 319 | 325 | PF00069 | 0.432 |
MOD_Plk_4 | 13 | 19 | PF00069 | 0.368 |
MOD_Plk_4 | 189 | 195 | PF00069 | 0.371 |
MOD_Plk_4 | 207 | 213 | PF00069 | 0.293 |
MOD_Plk_4 | 255 | 261 | PF00069 | 0.419 |
MOD_Plk_4 | 367 | 373 | PF00069 | 0.345 |
MOD_Plk_4 | 403 | 409 | PF00069 | 0.434 |
MOD_Plk_4 | 487 | 493 | PF00069 | 0.451 |
MOD_Plk_4 | 633 | 639 | PF00069 | 0.419 |
MOD_Plk_4 | 646 | 652 | PF00069 | 0.405 |
MOD_Plk_4 | 662 | 668 | PF00069 | 0.383 |
MOD_Plk_4 | 675 | 681 | PF00069 | 0.417 |
MOD_ProDKin_1 | 2 | 8 | PF00069 | 0.562 |
MOD_ProDKin_1 | 498 | 504 | PF00069 | 0.413 |
MOD_ProDKin_1 | 691 | 697 | PF00069 | 0.361 |
MOD_SUMO_for_1 | 401 | 404 | PF00179 | 0.425 |
MOD_SUMO_for_1 | 521 | 524 | PF00179 | 0.342 |
MOD_SUMO_rev_2 | 231 | 239 | PF00179 | 0.408 |
MOD_SUMO_rev_2 | 467 | 473 | PF00179 | 0.457 |
TRG_DiLeu_BaEn_1 | 242 | 247 | PF01217 | 0.511 |
TRG_DiLeu_BaEn_1 | 266 | 271 | PF01217 | 0.511 |
TRG_DiLeu_BaEn_1 | 405 | 410 | PF01217 | 0.414 |
TRG_DiLeu_BaEn_1 | 577 | 582 | PF01217 | 0.611 |
TRG_ENDOCYTIC_2 | 125 | 128 | PF00928 | 0.410 |
TRG_ENDOCYTIC_2 | 260 | 263 | PF00928 | 0.410 |
TRG_ENDOCYTIC_2 | 449 | 452 | PF00928 | 0.352 |
TRG_ENDOCYTIC_2 | 517 | 520 | PF00928 | 0.358 |
TRG_ENDOCYTIC_2 | 553 | 556 | PF00928 | 0.468 |
TRG_ENDOCYTIC_2 | 585 | 588 | PF00928 | 0.656 |
TRG_ENDOCYTIC_2 | 634 | 637 | PF00928 | 0.419 |
TRG_ER_diArg_1 | 151 | 154 | PF00400 | 0.360 |
TRG_ER_diArg_1 | 366 | 368 | PF00400 | 0.466 |
TRG_ER_diArg_1 | 612 | 614 | PF00400 | 0.440 |
TRG_ER_diArg_1 | 64 | 66 | PF00400 | 0.419 |
TRG_ER_FFAT_1 | 467 | 475 | PF00635 | 0.392 |
TRG_Pf-PMV_PEXEL_1 | 136 | 141 | PF00026 | 0.232 |
TRG_Pf-PMV_PEXEL_1 | 238 | 242 | PF00026 | 0.250 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P437 | Leptomonas seymouri | 28% | 69% |
A0A0N0P5V0 | Leptomonas seymouri | 37% | 99% |
A0A0N0P8Y1 | Leptomonas seymouri | 34% | 90% |
A0A0N0P9D2 | Leptomonas seymouri | 84% | 98% |
A0A0N1IKA7 | Leptomonas seymouri | 38% | 77% |
A0A0N1PEU4 | Leptomonas seymouri | 34% | 73% |
A0A0S4IQ76 | Bodo saltans | 33% | 98% |
A0A0S4IR78 | Bodo saltans | 39% | 79% |
A0A0S4IS51 | Bodo saltans | 61% | 90% |
A0A0S4IWU8 | Bodo saltans | 39% | 82% |
A0A0S4J157 | Bodo saltans | 43% | 100% |
A0A0S4JCY8 | Bodo saltans | 38% | 68% |
A0A1X0NJ46 | Trypanosomatidae | 36% | 98% |
A0A1X0P0D7 | Trypanosomatidae | 71% | 99% |
A0A1X0P872 | Trypanosomatidae | 40% | 79% |
A0A1X0P9K6 | Trypanosomatidae | 38% | 97% |
A0A3Q8II71 | Leishmania donovani | 36% | 87% |
A0A3Q8IJ24 | Leishmania donovani | 36% | 74% |
A0A3Q8IWG4 | Leishmania donovani | 90% | 100% |
A0A3R7MA90 | Trypanosoma rangeli | 36% | 97% |
A0A3R7MM88 | Trypanosoma rangeli | 67% | 100% |
A0A3R7NT42 | Trypanosoma rangeli | 38% | 98% |
A0A3S7X3U3 | Leishmania donovani | 30% | 68% |
A0A3S7X433 | Leishmania donovani | 26% | 76% |
A0A3S7X8Z5 | Leishmania donovani | 37% | 99% |
A0A422N8L3 | Trypanosoma rangeli | 38% | 68% |
A0A422NK53 | Trypanosoma rangeli | 36% | 100% |
A4HAT8 | Leishmania braziliensis | 32% | 100% |
A4HIR4 | Leishmania braziliensis | 29% | 68% |
A4HME2 | Leishmania braziliensis | 37% | 100% |
A4HNU7 | Leishmania braziliensis | 36% | 100% |
A4I609 | Leishmania infantum | 30% | 68% |
A4I6B7 | Leishmania infantum | 26% | 76% |
A4IA06 | Leishmania infantum | 36% | 86% |
A4IB14 | Leishmania infantum | 37% | 99% |
A4ICP7 | Leishmania infantum | 36% | 74% |
A4IDY1 | Leishmania infantum | 90% | 100% |
C9ZMN0 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 94% |
C9ZNP6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 38% | 95% |
D0A2R5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 79% |
D0A429 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 70% | 92% |
D0A778 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 67% |
D4A2Z8 | Rattus norvegicus | 28% | 70% |
E9AEU3 | Leishmania major | 37% | 100% |
E9ASK7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 37% | 81% |
E9AU01 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
E9B1A0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 68% |
E9B1H5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 76% |
E9B512 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 86% |
E9B5Z9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 37% | 99% |
F4IE66 | Arabidopsis thaliana | 38% | 97% |
F4IJV4 | Arabidopsis thaliana | 46% | 67% |
F4JMJ3 | Arabidopsis thaliana | 43% | 79% |
F4JRJ6 | Arabidopsis thaliana | 38% | 100% |
O22243 | Arabidopsis thaliana | 29% | 69% |
O22899 | Arabidopsis thaliana | 45% | 96% |
O35286 | Mus musculus | 44% | 88% |
O42945 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 44% | 95% |
O43143 | Homo sapiens | 44% | 88% |
O45244 | Caenorhabditis elegans | 43% | 69% |
O51767 | Borreliella burgdorferi (strain ATCC 35210 / DSM 4680 / CIP 102532 / B31) | 33% | 85% |
O60231 | Homo sapiens | 39% | 67% |
P0C9A2 | African swine fever virus (isolate Tick/South Africa/Pretoriuskop Pr4/1996) | 26% | 72% |
P0C9A3 | African swine fever virus (isolate Warthog/Namibia/Wart80/1980) | 26% | 72% |
P0C9A4 | African swine fever virus (isolate Pig/Kenya/KEN-50/1950) | 25% | 72% |
P20095 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 43% | 80% |
P36009 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 35% | 95% |
P53131 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 44% | 91% |
Q03319 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 45% | 97% |
Q10752 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 44% | 66% |
Q1EHT7 | Oryza sativa subsp. japonica | 27% | 69% |
Q20875 | Caenorhabditis elegans | 42% | 94% |
Q3ZBE0 | Bos taurus | 27% | 97% |
Q4Q0J4 | Leishmania major | 90% | 100% |
Q4Q1Y9 | Leishmania major | 35% | 100% |
Q4Q2X4 | Leishmania major | 36% | 100% |
Q4Q6N9 | Leishmania major | 26% | 100% |
Q4Q6W4 | Leishmania major | 30% | 68% |
Q54NJ4 | Dictyostelium discoideum | 45% | 96% |
Q5R864 | Pongo abelii | 36% | 89% |
Q5RAZ4 | Pongo abelii | 44% | 88% |
Q5RBD4 | Pongo abelii | 40% | 97% |
Q5UQ96 | Acanthamoeba polyphaga mimivirus | 28% | 100% |
Q5XH12 | Xenopus laevis | 29% | 93% |
Q5XI69 | Rattus norvegicus | 36% | 89% |
Q6PE54 | Mus musculus | 36% | 89% |
Q767K6 | Sus scrofa | 39% | 67% |
Q7K3M5 | Drosophila melanogaster | 40% | 96% |
Q7L7V1 | Homo sapiens | 31% | 94% |
Q7YR39 | Pan troglodytes | 39% | 67% |
Q80VY9 | Mus musculus | 43% | 100% |
Q89443 | African swine fever virus (strain Badajoz 1971 Vero-adapted) | 26% | 72% |
Q8BZS9 | Mus musculus | 27% | 94% |
Q8IX18 | Homo sapiens | 36% | 89% |
Q8TE96 | Homo sapiens | 31% | 97% |
Q8V9U2 | African swine fever virus (isolate Tick/Malawi/Lil 20-1/1983) | 26% | 72% |
Q8VHK9 | Mus musculus | 29% | 70% |
Q8VY00 | Arabidopsis thaliana | 46% | 67% |
Q924H9 | Mus musculus | 29% | 97% |
Q93Y16 | Arabidopsis thaliana | 36% | 100% |
Q9BKQ8 | Caenorhabditis elegans | 41% | 95% |
Q9H2U1 | Homo sapiens | 29% | 69% |
Q9H5Z1 | Homo sapiens | 41% | 99% |
Q9H6R0 | Homo sapiens | 44% | 99% |
Q9HE06 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 36% | 100% |
Q9LZQ9 | Arabidopsis thaliana | 45% | 96% |
V5B3L7 | Trypanosoma cruzi | 69% | 100% |
V5BKH2 | Trypanosoma cruzi | 39% | 91% |
V5BPV3 | Trypanosoma cruzi | 37% | 66% |
V5BV22 | Trypanosoma cruzi | 35% | 79% |
V5C0I9 | Trypanosoma cruzi | 38% | 89% |
V5D886 | Trypanosoma cruzi | 37% | 98% |