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:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4HB07
Term | Name | Level | Count |
---|---|---|---|
GO:0001514 | selenocysteine incorporation | 7 | 1 |
GO:0006414 | translational elongation | 5 | 1 |
GO:0006417 | regulation of translation | 6 | 1 |
GO:0006451 | translational readthrough | 6 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009058 | biosynthetic process | 2 | 1 |
GO:0009059 | macromolecule biosynthetic process | 4 | 1 |
GO:0009889 | regulation of biosynthetic process | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0010468 | regulation of gene expression | 5 | 1 |
GO:0010556 | regulation of macromolecule biosynthetic process | 5 | 1 |
GO:0010608 | post-transcriptional regulation of gene expression | 6 | 1 |
GO:0019222 | regulation of metabolic process | 3 | 1 |
GO:0031323 | regulation of cellular metabolic process | 4 | 1 |
GO:0031326 | regulation of cellular biosynthetic process | 5 | 1 |
GO:0034248 | regulation of amide metabolic process | 5 | 1 |
GO:0034645 | obsolete cellular macromolecule biosynthetic process | 4 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044249 | cellular biosynthetic process | 3 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 1 |
GO:0051246 | regulation of protein metabolic process | 5 | 1 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0080090 | regulation of primary metabolic process | 4 | 1 |
GO:1901576 | organic substance biosynthetic process | 3 | 1 |
GO:2000112 | obsolete regulation of cellular macromolecule biosynthetic process | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 11 |
GO:0003824 | catalytic activity | 1 | 11 |
GO:0003924 | GTPase activity | 7 | 11 |
GO:0005488 | binding | 1 | 11 |
GO:0005525 | GTP binding | 5 | 11 |
GO:0016462 | pyrophosphatase activity | 5 | 11 |
GO:0016787 | hydrolase activity | 2 | 11 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 11 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 11 |
GO:0017076 | purine nucleotide binding | 4 | 11 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 11 |
GO:0019001 | guanyl nucleotide binding | 5 | 11 |
GO:0032553 | ribonucleotide binding | 3 | 11 |
GO:0032555 | purine ribonucleotide binding | 4 | 11 |
GO:0032561 | guanyl ribonucleotide binding | 5 | 11 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 11 |
GO:0036094 | small molecule binding | 2 | 11 |
GO:0043167 | ion binding | 2 | 11 |
GO:0043168 | anion binding | 3 | 11 |
GO:0097159 | organic cyclic compound binding | 2 | 11 |
GO:0097367 | carbohydrate derivative binding | 2 | 11 |
GO:1901265 | nucleoside phosphate binding | 3 | 11 |
GO:1901363 | heterocyclic compound binding | 2 | 11 |
GO:0003676 | nucleic acid binding | 3 | 9 |
GO:0003746 | translation elongation factor activity | 4 | 9 |
GO:0008135 | translation factor activity, RNA binding | 3 | 9 |
GO:0045182 | translation regulator activity | 1 | 9 |
GO:0090079 | translation regulator activity, nucleic acid binding | 2 | 9 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 473 | 477 | PF00656 | 0.596 |
CLV_C14_Caspase3-7 | 574 | 578 | PF00656 | 0.511 |
CLV_NRD_NRD_1 | 157 | 159 | PF00675 | 0.234 |
CLV_NRD_NRD_1 | 164 | 166 | PF00675 | 0.234 |
CLV_NRD_NRD_1 | 263 | 265 | PF00675 | 0.376 |
CLV_NRD_NRD_1 | 490 | 492 | PF00675 | 0.495 |
CLV_NRD_NRD_1 | 629 | 631 | PF00675 | 0.723 |
CLV_PCSK_KEX2_1 | 156 | 158 | PF00082 | 0.219 |
CLV_PCSK_KEX2_1 | 164 | 166 | PF00082 | 0.231 |
CLV_PCSK_KEX2_1 | 490 | 492 | PF00082 | 0.495 |
CLV_PCSK_KEX2_1 | 541 | 543 | PF00082 | 0.728 |
CLV_PCSK_KEX2_1 | 629 | 631 | PF00082 | 0.744 |
CLV_PCSK_PC1ET2_1 | 156 | 158 | PF00082 | 0.219 |
CLV_PCSK_PC1ET2_1 | 541 | 543 | PF00082 | 0.483 |
CLV_PCSK_SKI1_1 | 148 | 152 | PF00082 | 0.213 |
CLV_PCSK_SKI1_1 | 16 | 20 | PF00082 | 0.301 |
CLV_PCSK_SKI1_1 | 210 | 214 | PF00082 | 0.424 |
CLV_PCSK_SKI1_1 | 264 | 268 | PF00082 | 0.330 |
CLV_PCSK_SKI1_1 | 299 | 303 | PF00082 | 0.299 |
CLV_PCSK_SKI1_1 | 41 | 45 | PF00082 | 0.207 |
CLV_PCSK_SKI1_1 | 425 | 429 | PF00082 | 0.388 |
CLV_PCSK_SKI1_1 | 449 | 453 | PF00082 | 0.333 |
CLV_PCSK_SKI1_1 | 606 | 610 | PF00082 | 0.330 |
CLV_PCSK_SKI1_1 | 633 | 637 | PF00082 | 0.578 |
CLV_PCSK_SKI1_1 | 655 | 659 | PF00082 | 0.440 |
CLV_Separin_Metazoa | 65 | 69 | PF03568 | 0.349 |
DEG_COP1_1 | 253 | 260 | PF00400 | 0.454 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.440 |
DEG_SPOP_SBC_1 | 619 | 623 | PF00917 | 0.448 |
DOC_CKS1_1 | 521 | 526 | PF01111 | 0.542 |
DOC_CYCLIN_yCln2_LP_2 | 423 | 429 | PF00134 | 0.307 |
DOC_MAPK_gen_1 | 164 | 174 | PF00069 | 0.457 |
DOC_MAPK_gen_1 | 219 | 227 | PF00069 | 0.246 |
DOC_MAPK_gen_1 | 264 | 271 | PF00069 | 0.326 |
DOC_MAPK_gen_1 | 356 | 366 | PF00069 | 0.467 |
DOC_MAPK_gen_1 | 496 | 504 | PF00069 | 0.349 |
DOC_MAPK_gen_1 | 563 | 571 | PF00069 | 0.414 |
DOC_MAPK_gen_1 | 601 | 609 | PF00069 | 0.340 |
DOC_MAPK_gen_1 | 652 | 660 | PF00069 | 0.368 |
DOC_MAPK_MEF2A_6 | 164 | 173 | PF00069 | 0.408 |
DOC_MAPK_MEF2A_6 | 280 | 289 | PF00069 | 0.215 |
DOC_MAPK_MEF2A_6 | 41 | 49 | PF00069 | 0.410 |
DOC_MAPK_MEF2A_6 | 563 | 571 | PF00069 | 0.334 |
DOC_MAPK_MEF2A_6 | 601 | 609 | PF00069 | 0.340 |
DOC_MAPK_MEF2A_6 | 652 | 660 | PF00069 | 0.456 |
DOC_MAPK_RevD_3 | 649 | 662 | PF00069 | 0.449 |
DOC_PP1_RVXF_1 | 604 | 610 | PF00149 | 0.329 |
DOC_PP2B_LxvP_1 | 409 | 412 | PF13499 | 0.305 |
DOC_PP2B_LxvP_1 | 428 | 431 | PF13499 | 0.337 |
DOC_PP4_FxxP_1 | 272 | 275 | PF00568 | 0.369 |
DOC_PP4_FxxP_1 | 354 | 357 | PF00568 | 0.301 |
DOC_PP4_FxxP_1 | 609 | 612 | PF00568 | 0.360 |
DOC_PP4_FxxP_1 | 614 | 617 | PF00568 | 0.393 |
DOC_PP4_FxxP_1 | 650 | 653 | PF00568 | 0.513 |
DOC_USP7_MATH_1 | 305 | 309 | PF00917 | 0.503 |
DOC_USP7_MATH_1 | 313 | 317 | PF00917 | 0.384 |
DOC_USP7_MATH_1 | 536 | 540 | PF00917 | 0.657 |
DOC_USP7_MATH_1 | 576 | 580 | PF00917 | 0.564 |
DOC_USP7_MATH_1 | 583 | 587 | PF00917 | 0.641 |
DOC_USP7_MATH_1 | 666 | 670 | PF00917 | 0.459 |
DOC_WW_Pin1_4 | 141 | 146 | PF00397 | 0.438 |
DOC_WW_Pin1_4 | 32 | 37 | PF00397 | 0.407 |
DOC_WW_Pin1_4 | 461 | 466 | PF00397 | 0.385 |
DOC_WW_Pin1_4 | 468 | 473 | PF00397 | 0.449 |
DOC_WW_Pin1_4 | 520 | 525 | PF00397 | 0.523 |
DOC_WW_Pin1_4 | 529 | 534 | PF00397 | 0.506 |
LIG_14-3-3_CanoR_1 | 158 | 164 | PF00244 | 0.361 |
LIG_14-3-3_CanoR_1 | 25 | 32 | PF00244 | 0.405 |
LIG_14-3-3_CanoR_1 | 41 | 46 | PF00244 | 0.408 |
LIG_14-3-3_CanoR_1 | 498 | 503 | PF00244 | 0.384 |
LIG_14-3-3_CanoR_1 | 630 | 638 | PF00244 | 0.785 |
LIG_Actin_WH2_2 | 119 | 137 | PF00022 | 0.478 |
LIG_Actin_WH2_2 | 194 | 212 | PF00022 | 0.463 |
LIG_AP2alpha_2 | 374 | 376 | PF02296 | 0.268 |
LIG_APCC_ABBA_1 | 373 | 378 | PF00400 | 0.266 |
LIG_APCC_ABBAyCdc20_2 | 554 | 560 | PF00400 | 0.391 |
LIG_eIF4E_1 | 417 | 423 | PF01652 | 0.281 |
LIG_FHA_1 | 168 | 174 | PF00498 | 0.499 |
LIG_FHA_1 | 191 | 197 | PF00498 | 0.535 |
LIG_FHA_1 | 239 | 245 | PF00498 | 0.297 |
LIG_FHA_1 | 252 | 258 | PF00498 | 0.320 |
LIG_FHA_1 | 261 | 267 | PF00498 | 0.512 |
LIG_FHA_1 | 42 | 48 | PF00498 | 0.407 |
LIG_FHA_1 | 469 | 475 | PF00498 | 0.561 |
LIG_FHA_1 | 499 | 505 | PF00498 | 0.328 |
LIG_FHA_1 | 514 | 520 | PF00498 | 0.351 |
LIG_FHA_1 | 583 | 589 | PF00498 | 0.580 |
LIG_FHA_1 | 600 | 606 | PF00498 | 0.341 |
LIG_FHA_2 | 293 | 299 | PF00498 | 0.501 |
LIG_FHA_2 | 378 | 384 | PF00498 | 0.345 |
LIG_FHA_2 | 471 | 477 | PF00498 | 0.688 |
LIG_FHA_2 | 521 | 527 | PF00498 | 0.447 |
LIG_FHA_2 | 76 | 82 | PF00498 | 0.407 |
LIG_LIR_Apic_2 | 611 | 617 | PF02991 | 0.393 |
LIG_LIR_Gen_1 | 221 | 232 | PF02991 | 0.228 |
LIG_LIR_Gen_1 | 416 | 426 | PF02991 | 0.300 |
LIG_LIR_Gen_1 | 445 | 453 | PF02991 | 0.461 |
LIG_LIR_Gen_1 | 556 | 565 | PF02991 | 0.495 |
LIG_LIR_Nem_3 | 166 | 171 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 221 | 227 | PF02991 | 0.328 |
LIG_LIR_Nem_3 | 371 | 376 | PF02991 | 0.432 |
LIG_LIR_Nem_3 | 414 | 420 | PF02991 | 0.321 |
LIG_LIR_Nem_3 | 445 | 450 | PF02991 | 0.483 |
LIG_LIR_Nem_3 | 556 | 561 | PF02991 | 0.503 |
LIG_SH2_CRK | 327 | 331 | PF00017 | 0.476 |
LIG_SH2_CRK | 418 | 422 | PF00017 | 0.299 |
LIG_SH2_CRK | 499 | 503 | PF00017 | 0.533 |
LIG_SH2_STAP1 | 418 | 422 | PF00017 | 0.299 |
LIG_SH2_STAT5 | 353 | 356 | PF00017 | 0.321 |
LIG_SH3_3 | 252 | 258 | PF00018 | 0.415 |
LIG_SH3_3 | 401 | 407 | PF00018 | 0.463 |
LIG_SH3_3 | 567 | 573 | PF00018 | 0.439 |
LIG_SH3_3 | 577 | 583 | PF00018 | 0.615 |
LIG_SH3_3 | 77 | 83 | PF00018 | 0.407 |
LIG_SUMO_SIM_anti_2 | 170 | 175 | PF11976 | 0.495 |
LIG_SUMO_SIM_par_1 | 100 | 107 | PF11976 | 0.407 |
LIG_SUMO_SIM_par_1 | 169 | 175 | PF11976 | 0.495 |
LIG_SUMO_SIM_par_1 | 253 | 259 | PF11976 | 0.454 |
LIG_SUMO_SIM_par_1 | 419 | 424 | PF11976 | 0.289 |
LIG_SUMO_SIM_par_1 | 516 | 523 | PF11976 | 0.555 |
LIG_SUMO_SIM_par_1 | 566 | 572 | PF11976 | 0.384 |
LIG_TYR_ITIM | 325 | 330 | PF00017 | 0.472 |
LIG_UBA3_1 | 656 | 662 | PF00899 | 0.443 |
LIG_ULM_U2AF65_1 | 164 | 169 | PF00076 | 0.501 |
MOD_CDK_SPxK_1 | 529 | 535 | PF00069 | 0.477 |
MOD_CDK_SPxxK_3 | 141 | 148 | PF00069 | 0.438 |
MOD_CK1_1 | 14 | 20 | PF00069 | 0.407 |
MOD_CK1_1 | 304 | 310 | PF00069 | 0.551 |
MOD_CK1_1 | 35 | 41 | PF00069 | 0.400 |
MOD_CK1_1 | 392 | 398 | PF00069 | 0.618 |
MOD_CK1_1 | 399 | 405 | PF00069 | 0.548 |
MOD_CK1_1 | 461 | 467 | PF00069 | 0.413 |
MOD_CK1_1 | 477 | 483 | PF00069 | 0.638 |
MOD_CK1_1 | 520 | 526 | PF00069 | 0.564 |
MOD_CK2_1 | 292 | 298 | PF00069 | 0.494 |
MOD_CK2_1 | 377 | 383 | PF00069 | 0.320 |
MOD_CK2_1 | 47 | 53 | PF00069 | 0.501 |
MOD_CK2_1 | 666 | 672 | PF00069 | 0.508 |
MOD_GlcNHglycan | 13 | 16 | PF01048 | 0.207 |
MOD_GlcNHglycan | 280 | 283 | PF01048 | 0.397 |
MOD_GlcNHglycan | 303 | 306 | PF01048 | 0.374 |
MOD_GlcNHglycan | 307 | 310 | PF01048 | 0.446 |
MOD_GlcNHglycan | 366 | 369 | PF01048 | 0.553 |
MOD_GlcNHglycan | 401 | 404 | PF01048 | 0.454 |
MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.207 |
MOD_GlcNHglycan | 529 | 532 | PF01048 | 0.625 |
MOD_GlcNHglycan | 538 | 541 | PF01048 | 0.601 |
MOD_GlcNHglycan | 633 | 636 | PF01048 | 0.695 |
MOD_GlcNHglycan | 637 | 641 | PF01048 | 0.653 |
MOD_GlcNHglycan | 645 | 648 | PF01048 | 0.529 |
MOD_GlcNHglycan | 668 | 671 | PF01048 | 0.611 |
MOD_GlcNHglycan | 68 | 71 | PF01048 | 0.207 |
MOD_GSK3_1 | 159 | 166 | PF00069 | 0.403 |
MOD_GSK3_1 | 21 | 28 | PF00069 | 0.438 |
MOD_GSK3_1 | 301 | 308 | PF00069 | 0.468 |
MOD_GSK3_1 | 343 | 350 | PF00069 | 0.357 |
MOD_GSK3_1 | 37 | 44 | PF00069 | 0.407 |
MOD_GSK3_1 | 389 | 396 | PF00069 | 0.429 |
MOD_GSK3_1 | 461 | 468 | PF00069 | 0.439 |
MOD_GSK3_1 | 470 | 477 | PF00069 | 0.585 |
MOD_GSK3_1 | 509 | 516 | PF00069 | 0.242 |
MOD_GSK3_1 | 578 | 585 | PF00069 | 0.606 |
MOD_GSK3_1 | 595 | 602 | PF00069 | 0.492 |
MOD_GSK3_1 | 619 | 626 | PF00069 | 0.574 |
MOD_GSK3_1 | 66 | 73 | PF00069 | 0.470 |
MOD_GSK3_1 | 84 | 91 | PF00069 | 0.386 |
MOD_N-GLC_1 | 313 | 318 | PF02516 | 0.268 |
MOD_N-GLC_1 | 364 | 369 | PF02516 | 0.629 |
MOD_N-GLC_1 | 393 | 398 | PF02516 | 0.365 |
MOD_N-GLC_1 | 481 | 486 | PF02516 | 0.678 |
MOD_N-GLC_1 | 619 | 624 | PF02516 | 0.465 |
MOD_N-GLC_2 | 446 | 448 | PF02516 | 0.368 |
MOD_NEK2_1 | 159 | 164 | PF00069 | 0.408 |
MOD_NEK2_1 | 23 | 28 | PF00069 | 0.420 |
MOD_NEK2_1 | 240 | 245 | PF00069 | 0.300 |
MOD_NEK2_1 | 260 | 265 | PF00069 | 0.214 |
MOD_NEK2_1 | 312 | 317 | PF00069 | 0.396 |
MOD_NEK2_1 | 338 | 343 | PF00069 | 0.340 |
MOD_NEK2_1 | 364 | 369 | PF00069 | 0.426 |
MOD_NEK2_1 | 376 | 381 | PF00069 | 0.261 |
MOD_NEK2_1 | 452 | 457 | PF00069 | 0.387 |
MOD_NEK2_1 | 47 | 52 | PF00069 | 0.407 |
MOD_NEK2_1 | 599 | 604 | PF00069 | 0.376 |
MOD_NEK2_1 | 88 | 93 | PF00069 | 0.424 |
MOD_NEK2_2 | 235 | 240 | PF00069 | 0.307 |
MOD_PIKK_1 | 313 | 319 | PF00454 | 0.453 |
MOD_PIKK_1 | 35 | 41 | PF00454 | 0.420 |
MOD_PIKK_1 | 481 | 487 | PF00454 | 0.403 |
MOD_PKA_1 | 631 | 637 | PF00069 | 0.560 |
MOD_PKA_2 | 163 | 169 | PF00069 | 0.501 |
MOD_PKB_1 | 165 | 173 | PF00069 | 0.420 |
MOD_PKB_1 | 496 | 504 | PF00069 | 0.352 |
MOD_Plk_1 | 313 | 319 | PF00069 | 0.400 |
MOD_Plk_1 | 377 | 383 | PF00069 | 0.376 |
MOD_Plk_1 | 481 | 487 | PF00069 | 0.471 |
MOD_Plk_1 | 52 | 58 | PF00069 | 0.461 |
MOD_Plk_1 | 576 | 582 | PF00069 | 0.503 |
MOD_Plk_1 | 595 | 601 | PF00069 | 0.487 |
MOD_Plk_4 | 167 | 173 | PF00069 | 0.349 |
MOD_Plk_4 | 235 | 241 | PF00069 | 0.304 |
MOD_Plk_4 | 251 | 257 | PF00069 | 0.319 |
MOD_Plk_4 | 343 | 349 | PF00069 | 0.308 |
MOD_Plk_4 | 377 | 383 | PF00069 | 0.309 |
MOD_Plk_4 | 75 | 81 | PF00069 | 0.407 |
MOD_Plk_4 | 84 | 90 | PF00069 | 0.407 |
MOD_ProDKin_1 | 141 | 147 | PF00069 | 0.438 |
MOD_ProDKin_1 | 32 | 38 | PF00069 | 0.407 |
MOD_ProDKin_1 | 461 | 467 | PF00069 | 0.392 |
MOD_ProDKin_1 | 468 | 474 | PF00069 | 0.452 |
MOD_ProDKin_1 | 520 | 526 | PF00069 | 0.530 |
MOD_ProDKin_1 | 529 | 535 | PF00069 | 0.509 |
TRG_DiLeu_BaEn_2 | 559 | 565 | PF01217 | 0.349 |
TRG_DiLeu_BaLyEn_6 | 404 | 409 | PF01217 | 0.297 |
TRG_ENDOCYTIC_2 | 224 | 227 | PF00928 | 0.367 |
TRG_ENDOCYTIC_2 | 327 | 330 | PF00928 | 0.473 |
TRG_ENDOCYTIC_2 | 417 | 420 | PF00928 | 0.281 |
TRG_ENDOCYTIC_2 | 499 | 502 | PF00928 | 0.529 |
TRG_ER_diArg_1 | 157 | 159 | PF00400 | 0.437 |
TRG_ER_diArg_1 | 163 | 165 | PF00400 | 0.441 |
TRG_ER_diArg_1 | 324 | 327 | PF00400 | 0.354 |
TRG_ER_diArg_1 | 489 | 491 | PF00400 | 0.486 |
TRG_NLS_MonoCore_2 | 629 | 634 | PF00514 | 0.760 |
TRG_NLS_MonoExtN_4 | 629 | 635 | PF00514 | 0.632 |
TRG_Pf-PMV_PEXEL_1 | 157 | 161 | PF00026 | 0.301 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZH5 | Leptomonas seymouri | 67% | 95% |
A0A1X0PAN1 | Trypanosomatidae | 50% | 100% |
A0A3Q8IIB7 | Leishmania donovani | 81% | 99% |
A0A3S5IRQ8 | Trypanosoma rangeli | 50% | 100% |
A0A3S7WV40 | Leishmania donovani | 26% | 100% |
A4H9I5 | Leishmania braziliensis | 25% | 100% |
A4IA63 | Leishmania infantum | 81% | 99% |
C9ZM43 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 50% | 100% |
E9AGQ3 | Leishmania infantum | 26% | 100% |
E9ARL1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
E9B575 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 99% |
P57772 | Homo sapiens | 35% | 100% |
Q4Q2R0 | Leishmania major | 79% | 100% |
Q4QDW8 | Leishmania major | 25% | 100% |
Q9JHW4 | Mus musculus | 35% | 100% |
V5BQE1 | Trypanosoma cruzi | 49% | 100% |