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: 18 |
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:0005730 | nucleolus | 5 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0043226 | organelle | 2 | 4 |
GO:0043227 | membrane-bounded organelle | 3 | 3 |
GO:0043228 | non-membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 4 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 3 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 4 |
GO:1990904 | ribonucleoprotein complex | 2 | 2 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005739 | mitochondrion | 5 | 1 |
GO:0031974 | membrane-enclosed lumen | 2 | 1 |
GO:0031981 | nuclear lumen | 5 | 1 |
GO:0043233 | organelle lumen | 3 | 1 |
GO:0070013 | intracellular organelle lumen | 4 | 1 |
Related structures:
AlphaFold database: A4H5Z5
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 5 |
GO:0006364 | rRNA processing | 8 | 4 |
GO:0006396 | RNA processing | 6 | 4 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 5 |
GO:0006807 | nitrogen compound metabolic process | 2 | 5 |
GO:0008152 | metabolic process | 1 | 5 |
GO:0009987 | cellular process | 1 | 5 |
GO:0016070 | RNA metabolic process | 5 | 5 |
GO:0016072 | rRNA metabolic process | 7 | 4 |
GO:0030490 | maturation of SSU-rRNA | 9 | 4 |
GO:0034470 | ncRNA processing | 7 | 4 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 5 |
GO:0034660 | ncRNA metabolic process | 6 | 4 |
GO:0043170 | macromolecule metabolic process | 3 | 5 |
GO:0044237 | cellular metabolic process | 2 | 5 |
GO:0044238 | primary metabolic process | 2 | 5 |
GO:0046483 | heterocycle metabolic process | 3 | 5 |
GO:0071704 | organic substance metabolic process | 2 | 5 |
GO:0090304 | nucleic acid metabolic process | 4 | 5 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 5 |
GO:0009451 | RNA modification | 5 | 1 |
GO:0016071 | mRNA metabolic process | 6 | 1 |
GO:0016556 | mRNA modification | 6 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 23 |
GO:0003676 | nucleic acid binding | 3 | 23 |
GO:0003824 | catalytic activity | 1 | 23 |
GO:0004386 | helicase activity | 2 | 23 |
GO:0005488 | binding | 1 | 23 |
GO:0005524 | ATP binding | 5 | 23 |
GO:0017076 | purine nucleotide binding | 4 | 23 |
GO:0030554 | adenyl nucleotide binding | 5 | 23 |
GO:0032553 | ribonucleotide binding | 3 | 23 |
GO:0032555 | purine ribonucleotide binding | 4 | 23 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 23 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 23 |
GO:0036094 | small molecule binding | 2 | 23 |
GO:0043167 | ion binding | 2 | 23 |
GO:0043168 | anion binding | 3 | 23 |
GO:0097159 | organic cyclic compound binding | 2 | 23 |
GO:0097367 | carbohydrate derivative binding | 2 | 23 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 23 |
GO:0140657 | ATP-dependent activity | 1 | 23 |
GO:1901265 | nucleoside phosphate binding | 3 | 23 |
GO:1901363 | heterocyclic compound binding | 2 | 23 |
GO:0003724 | RNA helicase activity | 3 | 7 |
GO:0008186 | ATP-dependent activity, acting on RNA | 2 | 7 |
GO:0016787 | hydrolase activity | 2 | 16 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 7 |
GO:0003723 | RNA binding | 4 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 113 | 117 | PF00656 | 0.556 |
CLV_NRD_NRD_1 | 139 | 141 | PF00675 | 0.622 |
CLV_NRD_NRD_1 | 387 | 389 | PF00675 | 0.305 |
CLV_NRD_NRD_1 | 474 | 476 | PF00675 | 0.457 |
CLV_NRD_NRD_1 | 566 | 568 | PF00675 | 0.272 |
CLV_NRD_NRD_1 | 693 | 695 | PF00675 | 0.682 |
CLV_NRD_NRD_1 | 698 | 700 | PF00675 | 0.636 |
CLV_PCSK_FUR_1 | 696 | 700 | PF00082 | 0.614 |
CLV_PCSK_KEX2_1 | 139 | 141 | PF00082 | 0.622 |
CLV_PCSK_KEX2_1 | 525 | 527 | PF00082 | 0.224 |
CLV_PCSK_KEX2_1 | 568 | 570 | PF00082 | 0.225 |
CLV_PCSK_KEX2_1 | 693 | 695 | PF00082 | 0.704 |
CLV_PCSK_KEX2_1 | 698 | 700 | PF00082 | 0.662 |
CLV_PCSK_PC1ET2_1 | 525 | 527 | PF00082 | 0.224 |
CLV_PCSK_PC1ET2_1 | 568 | 570 | PF00082 | 0.245 |
CLV_PCSK_PC7_1 | 694 | 700 | PF00082 | 0.605 |
CLV_PCSK_SKI1_1 | 187 | 191 | PF00082 | 0.522 |
CLV_PCSK_SKI1_1 | 319 | 323 | PF00082 | 0.277 |
CLV_PCSK_SKI1_1 | 448 | 452 | PF00082 | 0.358 |
CLV_PCSK_SKI1_1 | 498 | 502 | PF00082 | 0.602 |
DEG_APCC_DBOX_1 | 497 | 505 | PF00400 | 0.339 |
DEG_SCF_FBW7_1 | 284 | 291 | PF00400 | 0.378 |
DEG_SPOP_SBC_1 | 324 | 328 | PF00917 | 0.418 |
DOC_ANK_TNKS_1 | 138 | 145 | PF00023 | 0.534 |
DOC_CKS1_1 | 396 | 401 | PF01111 | 0.485 |
DOC_CKS1_1 | 676 | 681 | PF01111 | 0.561 |
DOC_MAPK_DCC_7 | 159 | 169 | PF00069 | 0.465 |
DOC_MAPK_gen_1 | 388 | 396 | PF00069 | 0.437 |
DOC_MAPK_gen_1 | 525 | 531 | PF00069 | 0.467 |
DOC_PP2B_LxvP_1 | 466 | 469 | PF13499 | 0.291 |
DOC_PP2B_LxvP_1 | 550 | 553 | PF13499 | 0.424 |
DOC_PP4_FxxP_1 | 263 | 266 | PF00568 | 0.475 |
DOC_PP4_FxxP_1 | 633 | 636 | PF00568 | 0.328 |
DOC_USP7_MATH_1 | 288 | 292 | PF00917 | 0.468 |
DOC_USP7_MATH_1 | 298 | 302 | PF00917 | 0.485 |
DOC_USP7_MATH_1 | 323 | 327 | PF00917 | 0.461 |
DOC_USP7_MATH_1 | 373 | 377 | PF00917 | 0.481 |
DOC_USP7_MATH_1 | 503 | 507 | PF00917 | 0.406 |
DOC_USP7_MATH_1 | 672 | 676 | PF00917 | 0.602 |
DOC_USP7_MATH_1 | 90 | 94 | PF00917 | 0.567 |
DOC_WW_Pin1_4 | 15 | 20 | PF00397 | 0.485 |
DOC_WW_Pin1_4 | 177 | 182 | PF00397 | 0.649 |
DOC_WW_Pin1_4 | 232 | 237 | PF00397 | 0.536 |
DOC_WW_Pin1_4 | 284 | 289 | PF00397 | 0.424 |
DOC_WW_Pin1_4 | 395 | 400 | PF00397 | 0.485 |
DOC_WW_Pin1_4 | 430 | 435 | PF00397 | 0.436 |
DOC_WW_Pin1_4 | 476 | 481 | PF00397 | 0.442 |
DOC_WW_Pin1_4 | 675 | 680 | PF00397 | 0.635 |
DOC_WW_Pin1_4 | 715 | 720 | PF00397 | 0.660 |
LIG_14-3-3_CanoR_1 | 347 | 351 | PF00244 | 0.486 |
LIG_14-3-3_CanoR_1 | 404 | 413 | PF00244 | 0.471 |
LIG_14-3-3_CanoR_1 | 510 | 518 | PF00244 | 0.373 |
LIG_14-3-3_CanoR_1 | 53 | 63 | PF00244 | 0.478 |
LIG_14-3-3_CanoR_1 | 626 | 636 | PF00244 | 0.427 |
LIG_14-3-3_CanoR_1 | 650 | 656 | PF00244 | 0.412 |
LIG_Actin_WH2_2 | 336 | 354 | PF00022 | 0.406 |
LIG_APCC_ABBA_1 | 37 | 42 | PF00400 | 0.563 |
LIG_BRCT_BRCA1_1 | 629 | 633 | PF00533 | 0.327 |
LIG_Clathr_ClatBox_1 | 427 | 431 | PF01394 | 0.408 |
LIG_eIF4E_1 | 63 | 69 | PF01652 | 0.608 |
LIG_EVH1_2 | 165 | 169 | PF00568 | 0.489 |
LIG_FHA_1 | 401 | 407 | PF00498 | 0.442 |
LIG_FHA_1 | 480 | 486 | PF00498 | 0.581 |
LIG_FHA_1 | 541 | 547 | PF00498 | 0.448 |
LIG_FHA_1 | 630 | 636 | PF00498 | 0.294 |
LIG_FHA_1 | 643 | 649 | PF00498 | 0.391 |
LIG_FHA_1 | 676 | 682 | PF00498 | 0.567 |
LIG_FHA_1 | 690 | 696 | PF00498 | 0.608 |
LIG_FHA_1 | 83 | 89 | PF00498 | 0.575 |
LIG_FHA_2 | 16 | 22 | PF00498 | 0.483 |
LIG_FHA_2 | 43 | 49 | PF00498 | 0.490 |
LIG_FHA_2 | 486 | 492 | PF00498 | 0.464 |
LIG_FHA_2 | 536 | 542 | PF00498 | 0.509 |
LIG_KLC1_Yacidic_2 | 592 | 597 | PF13176 | 0.378 |
LIG_LIR_Apic_2 | 24 | 29 | PF02991 | 0.607 |
LIG_LIR_Apic_2 | 260 | 266 | PF02991 | 0.380 |
LIG_LIR_Apic_2 | 294 | 300 | PF02991 | 0.490 |
LIG_LIR_Apic_2 | 630 | 636 | PF02991 | 0.322 |
LIG_LIR_Apic_2 | 673 | 679 | PF02991 | 0.569 |
LIG_LIR_Gen_1 | 379 | 386 | PF02991 | 0.378 |
LIG_LIR_Nem_3 | 21 | 26 | PF02991 | 0.675 |
LIG_LIR_Nem_3 | 34 | 40 | PF02991 | 0.609 |
LIG_LIR_Nem_3 | 379 | 384 | PF02991 | 0.378 |
LIG_LIR_Nem_3 | 571 | 576 | PF02991 | 0.378 |
LIG_PCNA_yPIPBox_3 | 650 | 664 | PF02747 | 0.363 |
LIG_Rb_LxCxE_1 | 460 | 479 | PF01857 | 0.323 |
LIG_Rb_pABgroove_1 | 512 | 520 | PF01858 | 0.347 |
LIG_SH2_CRK | 26 | 30 | PF00017 | 0.459 |
LIG_SH2_CRK | 297 | 301 | PF00017 | 0.479 |
LIG_SH2_CRK | 357 | 361 | PF00017 | 0.486 |
LIG_SH2_CRK | 371 | 375 | PF00017 | 0.486 |
LIG_SH2_CRK | 477 | 481 | PF00017 | 0.352 |
LIG_SH2_CRK | 605 | 609 | PF00017 | 0.461 |
LIG_SH2_NCK_1 | 297 | 301 | PF00017 | 0.410 |
LIG_SH2_NCK_1 | 381 | 385 | PF00017 | 0.378 |
LIG_SH2_NCK_1 | 605 | 609 | PF00017 | 0.445 |
LIG_SH2_SRC | 26 | 29 | PF00017 | 0.505 |
LIG_SH2_SRC | 63 | 66 | PF00017 | 0.480 |
LIG_SH2_STAP1 | 23 | 27 | PF00017 | 0.466 |
LIG_SH2_STAP1 | 357 | 361 | PF00017 | 0.385 |
LIG_SH2_STAP1 | 381 | 385 | PF00017 | 0.378 |
LIG_SH2_STAT3 | 215 | 218 | PF00017 | 0.431 |
LIG_SH2_STAT5 | 442 | 445 | PF00017 | 0.294 |
LIG_SH2_STAT5 | 532 | 535 | PF00017 | 0.457 |
LIG_SH2_STAT5 | 595 | 598 | PF00017 | 0.560 |
LIG_SH2_STAT5 | 614 | 617 | PF00017 | 0.510 |
LIG_SH3_2 | 163 | 168 | PF14604 | 0.472 |
LIG_SH3_3 | 146 | 152 | PF00018 | 0.597 |
LIG_SH3_3 | 160 | 166 | PF00018 | 0.693 |
LIG_SH3_3 | 269 | 275 | PF00018 | 0.436 |
LIG_SH3_3 | 332 | 338 | PF00018 | 0.477 |
LIG_SH3_3 | 393 | 399 | PF00018 | 0.511 |
LIG_SH3_3 | 426 | 432 | PF00018 | 0.378 |
LIG_SUMO_SIM_anti_2 | 245 | 251 | PF11976 | 0.291 |
LIG_SUMO_SIM_anti_2 | 301 | 306 | PF11976 | 0.410 |
LIG_SUMO_SIM_par_1 | 28 | 34 | PF11976 | 0.510 |
LIG_SUMO_SIM_par_1 | 417 | 422 | PF11976 | 0.532 |
LIG_SUMO_SIM_par_1 | 426 | 431 | PF11976 | 0.568 |
LIG_SUMO_SIM_par_1 | 482 | 488 | PF11976 | 0.400 |
LIG_TRAF2_1 | 488 | 491 | PF00917 | 0.469 |
LIG_TRAF2_1 | 538 | 541 | PF00917 | 0.424 |
LIG_UBA3_1 | 305 | 309 | PF00899 | 0.424 |
MOD_CDK_SPxK_1 | 232 | 238 | PF00069 | 0.452 |
MOD_CDK_SPxxK_3 | 177 | 184 | PF00069 | 0.498 |
MOD_CDK_SPxxK_3 | 430 | 437 | PF00069 | 0.483 |
MOD_CDK_SPxxK_3 | 675 | 682 | PF00069 | 0.564 |
MOD_CK1_1 | 261 | 267 | PF00069 | 0.454 |
MOD_CK1_1 | 291 | 297 | PF00069 | 0.503 |
MOD_CK1_1 | 326 | 332 | PF00069 | 0.432 |
MOD_CK1_1 | 479 | 485 | PF00069 | 0.393 |
MOD_CK1_1 | 551 | 557 | PF00069 | 0.486 |
MOD_CK1_1 | 675 | 681 | PF00069 | 0.595 |
MOD_CK1_1 | 689 | 695 | PF00069 | 0.573 |
MOD_CK1_1 | 93 | 99 | PF00069 | 0.573 |
MOD_CK2_1 | 373 | 379 | PF00069 | 0.416 |
MOD_CK2_1 | 42 | 48 | PF00069 | 0.469 |
MOD_CK2_1 | 485 | 491 | PF00069 | 0.483 |
MOD_CK2_1 | 535 | 541 | PF00069 | 0.437 |
MOD_Cter_Amidation | 696 | 699 | PF01082 | 0.649 |
MOD_GlcNHglycan | 260 | 263 | PF01048 | 0.405 |
MOD_GlcNHglycan | 289 | 293 | PF01048 | 0.293 |
MOD_GlcNHglycan | 550 | 553 | PF01048 | 0.286 |
MOD_GlcNHglycan | 56 | 59 | PF01048 | 0.554 |
MOD_GlcNHglycan | 561 | 564 | PF01048 | 0.286 |
MOD_GlcNHglycan | 623 | 626 | PF01048 | 0.239 |
MOD_GlcNHglycan | 712 | 715 | PF01048 | 0.654 |
MOD_GlcNHglycan | 92 | 95 | PF01048 | 0.813 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.646 |
MOD_GSK3_1 | 264 | 271 | PF00069 | 0.345 |
MOD_GSK3_1 | 284 | 291 | PF00069 | 0.444 |
MOD_GSK3_1 | 323 | 330 | PF00069 | 0.414 |
MOD_GSK3_1 | 346 | 353 | PF00069 | 0.476 |
MOD_GSK3_1 | 400 | 407 | PF00069 | 0.389 |
MOD_GSK3_1 | 481 | 488 | PF00069 | 0.474 |
MOD_GSK3_1 | 548 | 555 | PF00069 | 0.459 |
MOD_GSK3_1 | 706 | 713 | PF00069 | 0.529 |
MOD_GSK3_1 | 93 | 100 | PF00069 | 0.561 |
MOD_N-GLC_1 | 197 | 202 | PF02516 | 0.681 |
MOD_N-GLC_1 | 656 | 661 | PF02516 | 0.312 |
MOD_NEK2_1 | 135 | 140 | PF00069 | 0.652 |
MOD_NEK2_1 | 217 | 222 | PF00069 | 0.589 |
MOD_NEK2_1 | 258 | 263 | PF00069 | 0.400 |
MOD_NEK2_1 | 268 | 273 | PF00069 | 0.220 |
MOD_NEK2_1 | 343 | 348 | PF00069 | 0.515 |
MOD_NEK2_1 | 356 | 361 | PF00069 | 0.490 |
MOD_NEK2_1 | 481 | 486 | PF00069 | 0.498 |
MOD_NEK2_1 | 546 | 551 | PF00069 | 0.497 |
MOD_NEK2_1 | 656 | 661 | PF00069 | 0.395 |
MOD_NEK2_2 | 33 | 38 | PF00069 | 0.454 |
MOD_NEK2_2 | 56 | 61 | PF00069 | 0.449 |
MOD_PKA_2 | 264 | 270 | PF00069 | 0.440 |
MOD_PKA_2 | 346 | 352 | PF00069 | 0.486 |
MOD_PKA_2 | 509 | 515 | PF00069 | 0.284 |
MOD_PKA_2 | 535 | 541 | PF00069 | 0.499 |
MOD_PKA_2 | 649 | 655 | PF00069 | 0.370 |
MOD_PKB_1 | 702 | 710 | PF00069 | 0.453 |
MOD_Plk_1 | 197 | 203 | PF00069 | 0.530 |
MOD_Plk_1 | 33 | 39 | PF00069 | 0.526 |
MOD_Plk_1 | 41 | 47 | PF00069 | 0.482 |
MOD_Plk_1 | 656 | 662 | PF00069 | 0.560 |
MOD_Plk_1 | 672 | 678 | PF00069 | 0.592 |
MOD_Plk_2-3 | 42 | 48 | PF00069 | 0.469 |
MOD_Plk_4 | 264 | 270 | PF00069 | 0.353 |
MOD_Plk_4 | 346 | 352 | PF00069 | 0.498 |
MOD_Plk_4 | 469 | 475 | PF00069 | 0.464 |
MOD_Plk_4 | 481 | 487 | PF00069 | 0.380 |
MOD_Plk_4 | 552 | 558 | PF00069 | 0.497 |
MOD_Plk_4 | 629 | 635 | PF00069 | 0.355 |
MOD_Plk_4 | 93 | 99 | PF00069 | 0.578 |
MOD_ProDKin_1 | 15 | 21 | PF00069 | 0.484 |
MOD_ProDKin_1 | 177 | 183 | PF00069 | 0.651 |
MOD_ProDKin_1 | 232 | 238 | PF00069 | 0.541 |
MOD_ProDKin_1 | 284 | 290 | PF00069 | 0.424 |
MOD_ProDKin_1 | 395 | 401 | PF00069 | 0.485 |
MOD_ProDKin_1 | 430 | 436 | PF00069 | 0.436 |
MOD_ProDKin_1 | 476 | 482 | PF00069 | 0.440 |
MOD_ProDKin_1 | 675 | 681 | PF00069 | 0.637 |
MOD_ProDKin_1 | 715 | 721 | PF00069 | 0.666 |
TRG_DiLeu_BaEn_1 | 363 | 368 | PF01217 | 0.451 |
TRG_ENDOCYTIC_2 | 357 | 360 | PF00928 | 0.486 |
TRG_ENDOCYTIC_2 | 371 | 374 | PF00928 | 0.486 |
TRG_ENDOCYTIC_2 | 381 | 384 | PF00928 | 0.394 |
TRG_ER_diArg_1 | 139 | 141 | PF00400 | 0.489 |
TRG_ER_diArg_1 | 566 | 569 | PF00400 | 0.425 |
TRG_ER_diArg_1 | 693 | 696 | PF00400 | 0.655 |
TRG_ER_diArg_1 | 701 | 704 | PF00400 | 0.659 |
TRG_NES_CRM1_1 | 606 | 616 | PF08389 | 0.442 |
TRG_Pf-PMV_PEXEL_1 | 244 | 248 | PF00026 | 0.527 |
TRG_Pf-PMV_PEXEL_1 | 699 | 703 | PF00026 | 0.576 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I5R1 | Leptomonas seymouri | 56% | 91% |
A0A0S4J5D6 | Bodo saltans | 23% | 100% |
A0A1X0NRS9 | Trypanosomatidae | 32% | 93% |
A0A3Q8ID91 | Leishmania donovani | 27% | 100% |
A0A3Q8IQY6 | Leishmania donovani | 25% | 100% |
A0A3S5H5X3 | Leishmania donovani | 22% | 100% |
A0A3S7WR01 | Leishmania donovani | 69% | 92% |
A0A3S7X579 | Leishmania donovani | 25% | 100% |
A0A3S7XAT8 | Leishmania donovani | 23% | 100% |
A1CHL3 | Aspergillus clavatus (strain ATCC 1007 / CBS 513.65 / DSM 816 / NCTC 3887 / NRRL 1 / QM 1276 / 107) | 24% | 90% |
A3GG51 | Scheffersomyces stipitis (strain ATCC 58785 / CBS 6054 / NBRC 10063 / NRRL Y-11545) | 23% | 86% |
A4H4Y0 | Leishmania braziliensis | 23% | 100% |
A4HGR1 | Leishmania braziliensis | 26% | 100% |
A4HK20 | Leishmania braziliensis | 23% | 100% |
A4HK38 | Leishmania braziliensis | 25% | 100% |
A4HP49 | Leishmania braziliensis | 22% | 100% |
A4HP82 | Leishmania braziliensis | 25% | 100% |
A4HT33 | Leishmania infantum | 22% | 100% |
A4HUC1 | Leishmania infantum | 69% | 92% |
A4HZF8 | Leishmania infantum | 20% | 100% |
A4I3T6 | Leishmania infantum | 27% | 100% |
A4I7M5 | Leishmania infantum | 25% | 100% |
A4IDF6 | Leishmania infantum | 23% | 100% |
A4IDI7 | Leishmania infantum | 25% | 100% |
A5DF03 | Meyerozyma guilliermondii (strain ATCC 6260 / CBS 566 / DSM 6381 / JCM 1539 / NBRC 10279 / NRRL Y-324) | 22% | 100% |
E9AN20 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 68% | 98% |
E9ASV7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 23% | 100% |
E9ASZ0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
E9B028 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 100% |
E9B2I0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 24% | 100% |
Q4Q1K8 | Leishmania major | 24% | 100% |
Q4Q1N9 | Leishmania major | 22% | 100% |
Q4Q5M6 | Leishmania major | 25% | 100% |
Q4Q858 | Leishmania major | 27% | 100% |
Q4QHK6 | Leishmania major | 69% | 100% |
Q4QIQ9 | Leishmania major | 23% | 100% |
Q4QJI9 | Leishmania major | 22% | 100% |
Q5N7W4 | Oryza sativa subsp. japonica | 23% | 100% |
Q6CDS6 | Yarrowia lipolytica (strain CLIB 122 / E 150) | 22% | 100% |
Q92841 | Homo sapiens | 24% | 99% |
Q9LYJ9 | Arabidopsis thaliana | 23% | 100% |
V5BII0 | Trypanosoma cruzi | 35% | 100% |
V5D8J9 | Trypanosoma cruzi | 22% | 100% |