Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 1 |
Forrest at al. (metacyclic) | no | yes: 2 |
Forrest at al. (procyclic) | no | yes: 3 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 34 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 16 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 16 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 1, no: 78 |
NetGPI | no | yes: 0, no: 79 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 5 |
GO:0005737 | cytoplasm | 2 | 3 |
GO:0005930 | axoneme | 2 | 1 |
GO:0005815 | microtubule organizing center | 2 | 1 |
GO:0005856 | cytoskeleton | 5 | 1 |
GO:0020016 | ciliary pocket | 2 | 1 |
GO:0020038 | subpellicular network | 2 | 1 |
GO:0030863 | cortical cytoskeleton | 6 | 1 |
GO:0036064 | ciliary basal body | 3 | 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 |
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 80 |
GO:0006807 | nitrogen compound metabolic process | 2 | 80 |
GO:0008152 | metabolic process | 1 | 80 |
GO:0019538 | protein metabolic process | 3 | 80 |
GO:0043170 | macromolecule metabolic process | 3 | 80 |
GO:0044238 | primary metabolic process | 2 | 80 |
GO:0071704 | organic substance metabolic process | 2 | 80 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 80 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 80 |
GO:0004175 | endopeptidase activity | 4 | 80 |
GO:0004197 | cysteine-type endopeptidase activity | 5 | 80 |
GO:0004198 | calcium-dependent cysteine-type endopeptidase activity | 6 | 80 |
GO:0008233 | peptidase activity | 3 | 80 |
GO:0008234 | cysteine-type peptidase activity | 4 | 80 |
GO:0016787 | hydrolase activity | 2 | 80 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 80 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 361 | 365 | PF00656 | 0.521 |
CLV_NRD_NRD_1 | 142 | 144 | PF00675 | 0.234 |
CLV_NRD_NRD_1 | 253 | 255 | PF00675 | 0.375 |
CLV_NRD_NRD_1 | 345 | 347 | PF00675 | 0.274 |
CLV_NRD_NRD_1 | 403 | 405 | PF00675 | 0.397 |
CLV_NRD_NRD_1 | 418 | 420 | PF00675 | 0.466 |
CLV_NRD_NRD_1 | 43 | 45 | PF00675 | 0.401 |
CLV_NRD_NRD_1 | 80 | 82 | PF00675 | 0.268 |
CLV_PCSK_KEX2_1 | 142 | 144 | PF00082 | 0.235 |
CLV_PCSK_KEX2_1 | 345 | 347 | PF00082 | 0.273 |
CLV_PCSK_KEX2_1 | 418 | 420 | PF00082 | 0.475 |
CLV_PCSK_KEX2_1 | 554 | 556 | PF00082 | 0.532 |
CLV_PCSK_KEX2_1 | 63 | 65 | PF00082 | 0.325 |
CLV_PCSK_KEX2_1 | 80 | 82 | PF00082 | 0.260 |
CLV_PCSK_PC1ET2_1 | 554 | 556 | PF00082 | 0.562 |
CLV_PCSK_PC1ET2_1 | 63 | 65 | PF00082 | 0.331 |
CLV_PCSK_SKI1_1 | 13 | 17 | PF00082 | 0.547 |
CLV_PCSK_SKI1_1 | 131 | 135 | PF00082 | 0.250 |
CLV_PCSK_SKI1_1 | 248 | 252 | PF00082 | 0.232 |
CLV_PCSK_SKI1_1 | 313 | 317 | PF00082 | 0.273 |
CLV_PCSK_SKI1_1 | 408 | 412 | PF00082 | 0.456 |
CLV_PCSK_SKI1_1 | 431 | 435 | PF00082 | 0.526 |
CLV_PCSK_SKI1_1 | 491 | 495 | PF00082 | 0.555 |
CLV_PCSK_SKI1_1 | 501 | 505 | PF00082 | 0.543 |
DEG_APCC_DBOX_1 | 310 | 318 | PF00400 | 0.518 |
DEG_MDM2_SWIB_1 | 358 | 366 | PF02201 | 0.449 |
DEG_Nend_UBRbox_1 | 1 | 3 | PF02207 | 0.261 |
DEG_ODPH_VHL_1 | 508 | 520 | PF01847 | 0.304 |
DEG_SPOP_SBC_1 | 124 | 128 | PF00917 | 0.500 |
DOC_AGCK_PIF_1 | 224 | 229 | PF00069 | 0.507 |
DOC_CKS1_1 | 262 | 267 | PF01111 | 0.462 |
DOC_CYCLIN_RxL_1 | 404 | 414 | PF00134 | 0.504 |
DOC_CYCLIN_RxL_1 | 428 | 438 | PF00134 | 0.522 |
DOC_MAPK_DCC_7 | 305 | 314 | PF00069 | 0.571 |
DOC_MAPK_gen_1 | 252 | 262 | PF00069 | 0.437 |
DOC_MAPK_gen_1 | 404 | 411 | PF00069 | 0.370 |
DOC_MAPK_gen_1 | 42 | 51 | PF00069 | 0.337 |
DOC_MAPK_gen_1 | 516 | 525 | PF00069 | 0.547 |
DOC_MAPK_gen_1 | 560 | 567 | PF00069 | 0.323 |
DOC_MAPK_HePTP_8 | 302 | 314 | PF00069 | 0.480 |
DOC_MAPK_MEF2A_6 | 305 | 314 | PF00069 | 0.480 |
DOC_MAPK_MEF2A_6 | 44 | 53 | PF00069 | 0.303 |
DOC_MAPK_MEF2A_6 | 471 | 479 | PF00069 | 0.474 |
DOC_MAPK_RevD_3 | 391 | 405 | PF00069 | 0.454 |
DOC_PP1_RVXF_1 | 406 | 412 | PF00149 | 0.435 |
DOC_PP1_RVXF_1 | 517 | 523 | PF00149 | 0.455 |
DOC_PP4_FxxP_1 | 134 | 137 | PF00568 | 0.448 |
DOC_PP4_FxxP_1 | 307 | 310 | PF00568 | 0.497 |
DOC_USP7_MATH_1 | 241 | 245 | PF00917 | 0.461 |
DOC_USP7_MATH_1 | 30 | 34 | PF00917 | 0.496 |
DOC_USP7_MATH_1 | 320 | 324 | PF00917 | 0.499 |
DOC_USP7_MATH_1 | 510 | 514 | PF00917 | 0.517 |
DOC_USP7_UBL2_3 | 197 | 201 | PF12436 | 0.448 |
DOC_WW_Pin1_4 | 261 | 266 | PF00397 | 0.469 |
LIG_14-3-3_CanoR_1 | 345 | 353 | PF00244 | 0.563 |
LIG_14-3-3_CanoR_1 | 491 | 500 | PF00244 | 0.494 |
LIG_14-3-3_CanoR_1 | 519 | 523 | PF00244 | 0.472 |
LIG_14-3-3_CanoR_1 | 533 | 539 | PF00244 | 0.424 |
LIG_14-3-3_CanoR_1 | 98 | 106 | PF00244 | 0.506 |
LIG_Actin_WH2_2 | 518 | 535 | PF00022 | 0.285 |
LIG_BRCT_BRCA1_1 | 243 | 247 | PF00533 | 0.502 |
LIG_deltaCOP1_diTrp_1 | 325 | 331 | PF00928 | 0.442 |
LIG_deltaCOP1_diTrp_1 | 361 | 369 | PF00928 | 0.454 |
LIG_FHA_1 | 125 | 131 | PF00498 | 0.436 |
LIG_FHA_1 | 21 | 27 | PF00498 | 0.484 |
LIG_FHA_1 | 288 | 294 | PF00498 | 0.464 |
LIG_FHA_1 | 444 | 450 | PF00498 | 0.519 |
LIG_FHA_2 | 564 | 570 | PF00498 | 0.505 |
LIG_IRF3_LxIS_1 | 429 | 436 | PF10401 | 0.498 |
LIG_LIR_Apic_2 | 132 | 137 | PF02991 | 0.462 |
LIG_LIR_Apic_2 | 574 | 580 | PF02991 | 0.547 |
LIG_LIR_Apic_2 | 78 | 82 | PF02991 | 0.427 |
LIG_LIR_Gen_1 | 189 | 199 | PF02991 | 0.432 |
LIG_LIR_Gen_1 | 205 | 214 | PF02991 | 0.457 |
LIG_LIR_Gen_1 | 298 | 307 | PF02991 | 0.485 |
LIG_LIR_Gen_1 | 463 | 473 | PF02991 | 0.440 |
LIG_LIR_Gen_1 | 521 | 530 | PF02991 | 0.403 |
LIG_LIR_Nem_3 | 173 | 177 | PF02991 | 0.478 |
LIG_LIR_Nem_3 | 189 | 194 | PF02991 | 0.440 |
LIG_LIR_Nem_3 | 196 | 202 | PF02991 | 0.448 |
LIG_LIR_Nem_3 | 205 | 209 | PF02991 | 0.448 |
LIG_LIR_Nem_3 | 222 | 227 | PF02991 | 0.455 |
LIG_LIR_Nem_3 | 244 | 250 | PF02991 | 0.430 |
LIG_LIR_Nem_3 | 298 | 302 | PF02991 | 0.481 |
LIG_LIR_Nem_3 | 427 | 433 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 463 | 468 | PF02991 | 0.470 |
LIG_LIR_Nem_3 | 521 | 525 | PF02991 | 0.433 |
LIG_MLH1_MIPbox_1 | 243 | 247 | PF16413 | 0.516 |
LIG_Pex14_2 | 229 | 233 | PF04695 | 0.441 |
LIG_Pex14_2 | 358 | 362 | PF04695 | 0.453 |
LIG_Pex14_2 | 386 | 390 | PF04695 | 0.400 |
LIG_REV1ctd_RIR_1 | 244 | 252 | PF16727 | 0.467 |
LIG_SH2_CRK | 174 | 178 | PF00017 | 0.569 |
LIG_SH2_CRK | 199 | 203 | PF00017 | 0.447 |
LIG_SH2_CRK | 206 | 210 | PF00017 | 0.451 |
LIG_SH2_CRK | 299 | 303 | PF00017 | 0.461 |
LIG_SH2_CRK | 384 | 388 | PF00017 | 0.342 |
LIG_SH2_CRK | 430 | 434 | PF00017 | 0.479 |
LIG_SH2_SRC | 258 | 261 | PF00017 | 0.448 |
LIG_SH2_SRC | 465 | 468 | PF00017 | 0.524 |
LIG_SH2_SRC | 577 | 580 | PF00017 | 0.318 |
LIG_SH2_SRC | 85 | 88 | PF00017 | 0.462 |
LIG_SH2_STAP1 | 188 | 192 | PF00017 | 0.488 |
LIG_SH2_STAP1 | 206 | 210 | PF00017 | 0.441 |
LIG_SH2_STAP1 | 299 | 303 | PF00017 | 0.471 |
LIG_SH2_STAP1 | 465 | 469 | PF00017 | 0.516 |
LIG_SH2_STAT5 | 170 | 173 | PF00017 | 0.459 |
LIG_SH2_STAT5 | 179 | 182 | PF00017 | 0.460 |
LIG_SH2_STAT5 | 258 | 261 | PF00017 | 0.459 |
LIG_SH2_STAT5 | 467 | 470 | PF00017 | 0.422 |
LIG_SH2_STAT5 | 50 | 53 | PF00017 | 0.476 |
LIG_SH2_STAT5 | 577 | 580 | PF00017 | 0.501 |
LIG_SH2_STAT5 | 85 | 88 | PF00017 | 0.432 |
LIG_SH3_3 | 420 | 426 | PF00018 | 0.530 |
LIG_SH3_3 | 456 | 462 | PF00018 | 0.524 |
LIG_SH3_3 | 520 | 526 | PF00018 | 0.480 |
LIG_SH3_3 | 533 | 539 | PF00018 | 0.487 |
LIG_SUMO_SIM_anti_2 | 119 | 128 | PF11976 | 0.486 |
LIG_SUMO_SIM_par_1 | 258 | 264 | PF11976 | 0.421 |
LIG_SUMO_SIM_par_1 | 433 | 438 | PF11976 | 0.434 |
LIG_TRAF2_1 | 237 | 240 | PF00917 | 0.492 |
LIG_TRAF2_1 | 90 | 93 | PF00917 | 0.351 |
LIG_UBA3_1 | 409 | 416 | PF00899 | 0.475 |
LIG_WRC_WIRS_1 | 226 | 231 | PF05994 | 0.485 |
MOD_CK1_1 | 205 | 211 | PF00069 | 0.429 |
MOD_CK1_1 | 261 | 267 | PF00069 | 0.427 |
MOD_CK1_1 | 351 | 357 | PF00069 | 0.488 |
MOD_CK1_1 | 70 | 76 | PF00069 | 0.477 |
MOD_CK2_1 | 138 | 144 | PF00069 | 0.434 |
MOD_CK2_1 | 190 | 196 | PF00069 | 0.445 |
MOD_CK2_1 | 30 | 36 | PF00069 | 0.440 |
MOD_CK2_1 | 320 | 326 | PF00069 | 0.458 |
MOD_CMANNOS | 359 | 362 | PF00535 | 0.244 |
MOD_GlcNHglycan | 101 | 104 | PF01048 | 0.308 |
MOD_GlcNHglycan | 268 | 272 | PF01048 | 0.252 |
MOD_GlcNHglycan | 275 | 278 | PF01048 | 0.262 |
MOD_GlcNHglycan | 322 | 325 | PF01048 | 0.304 |
MOD_GSK3_1 | 166 | 173 | PF00069 | 0.481 |
MOD_GSK3_1 | 225 | 232 | PF00069 | 0.456 |
MOD_GSK3_1 | 260 | 267 | PF00069 | 0.463 |
MOD_GSK3_1 | 287 | 294 | PF00069 | 0.515 |
MOD_GSK3_1 | 344 | 351 | PF00069 | 0.478 |
MOD_N-GLC_1 | 333 | 338 | PF02516 | 0.292 |
MOD_N-GLC_1 | 510 | 515 | PF02516 | 0.566 |
MOD_NEK2_1 | 116 | 121 | PF00069 | 0.461 |
MOD_NEK2_1 | 180 | 185 | PF00069 | 0.458 |
MOD_NEK2_1 | 190 | 195 | PF00069 | 0.453 |
MOD_NEK2_1 | 20 | 25 | PF00069 | 0.504 |
MOD_NEK2_1 | 202 | 207 | PF00069 | 0.463 |
MOD_NEK2_1 | 229 | 234 | PF00069 | 0.507 |
MOD_NEK2_1 | 409 | 414 | PF00069 | 0.396 |
MOD_NEK2_1 | 433 | 438 | PF00069 | 0.381 |
MOD_NEK2_1 | 518 | 523 | PF00069 | 0.432 |
MOD_NEK2_1 | 568 | 573 | PF00069 | 0.436 |
MOD_NEK2_2 | 563 | 568 | PF00069 | 0.318 |
MOD_PIKK_1 | 136 | 142 | PF00454 | 0.579 |
MOD_PIKK_1 | 20 | 26 | PF00454 | 0.517 |
MOD_PIKK_1 | 241 | 247 | PF00454 | 0.520 |
MOD_PIKK_1 | 411 | 417 | PF00454 | 0.440 |
MOD_PIKK_1 | 443 | 449 | PF00454 | 0.611 |
MOD_PKA_2 | 181 | 187 | PF00069 | 0.475 |
MOD_PKA_2 | 344 | 350 | PF00069 | 0.499 |
MOD_PKA_2 | 43 | 49 | PF00069 | 0.470 |
MOD_PKA_2 | 518 | 524 | PF00069 | 0.457 |
MOD_Plk_1 | 124 | 130 | PF00069 | 0.471 |
MOD_Plk_1 | 267 | 273 | PF00069 | 0.464 |
MOD_Plk_1 | 280 | 286 | PF00069 | 0.508 |
MOD_Plk_1 | 501 | 507 | PF00069 | 0.580 |
MOD_Plk_1 | 568 | 574 | PF00069 | 0.464 |
MOD_Plk_4 | 125 | 131 | PF00069 | 0.485 |
MOD_Plk_4 | 166 | 172 | PF00069 | 0.483 |
MOD_Plk_4 | 190 | 196 | PF00069 | 0.430 |
MOD_Plk_4 | 205 | 211 | PF00069 | 0.448 |
MOD_Plk_4 | 297 | 303 | PF00069 | 0.472 |
MOD_Plk_4 | 339 | 345 | PF00069 | 0.482 |
MOD_Plk_4 | 354 | 360 | PF00069 | 0.444 |
MOD_Plk_4 | 393 | 399 | PF00069 | 0.337 |
MOD_Plk_4 | 518 | 524 | PF00069 | 0.531 |
MOD_Plk_4 | 573 | 579 | PF00069 | 0.473 |
MOD_ProDKin_1 | 261 | 267 | PF00069 | 0.469 |
MOD_SUMO_for_1 | 399 | 402 | PF00179 | 0.384 |
MOD_SUMO_rev_2 | 92 | 97 | PF00179 | 0.351 |
TRG_ENDOCYTIC_2 | 174 | 177 | PF00928 | 0.497 |
TRG_ENDOCYTIC_2 | 199 | 202 | PF00928 | 0.450 |
TRG_ENDOCYTIC_2 | 206 | 209 | PF00928 | 0.451 |
TRG_ENDOCYTIC_2 | 299 | 302 | PF00928 | 0.470 |
TRG_ENDOCYTIC_2 | 430 | 433 | PF00928 | 0.439 |
TRG_ENDOCYTIC_2 | 465 | 468 | PF00928 | 0.483 |
TRG_ENDOCYTIC_2 | 50 | 53 | PF00928 | 0.462 |
TRG_ER_diArg_1 | 344 | 346 | PF00400 | 0.486 |
TRG_ER_diArg_1 | 418 | 420 | PF00400 | 0.541 |
TRG_ER_diArg_1 | 79 | 81 | PF00400 | 0.470 |
TRG_NLS_MonoExtC_3 | 403 | 408 | PF00514 | 0.390 |
TRG_NLS_MonoExtN_4 | 404 | 409 | PF00514 | 0.398 |
TRG_NLS_MonoExtN_4 | 42 | 48 | PF00514 | 0.469 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8T6 | Leptomonas seymouri | 67% | 83% |
A0A0N1IGQ2 | Leptomonas seymouri | 36% | 82% |
A0A0N1ILF1 | Leptomonas seymouri | 35% | 84% |
A0A0N1IMH1 | Leptomonas seymouri | 35% | 74% |
A0A0N1P9P1 | Leptomonas seymouri | 34% | 68% |
A0A0N1PCA9 | Leptomonas seymouri | 30% | 79% |
A0A0N1PFI4 | Leptomonas seymouri | 33% | 75% |
A0A0S4JLK6 | Bodo saltans | 32% | 72% |
A0A0S4JS70 | Bodo saltans | 26% | 76% |
A0A0S4KGT2 | Bodo saltans | 40% | 77% |
A0A0S4KKP7 | Bodo saltans | 22% | 78% |
A0A1X0NJ61 | Trypanosomatidae | 42% | 100% |
A0A1X0NJK2 | Trypanosomatidae | 45% | 77% |
A0A1X0NJX8 | Trypanosomatidae | 36% | 75% |
A0A1X0NKT7 | Trypanosomatidae | 29% | 73% |
A0A1X0NKX8 | Trypanosomatidae | 33% | 71% |
A0A1X0NMT3 | Trypanosomatidae | 35% | 68% |
A0A1X0NW84 | Trypanosomatidae | 34% | 84% |
A0A1X0NW85 | Trypanosomatidae | 32% | 86% |
A0A1X0NW89 | Trypanosomatidae | 34% | 67% |
A0A1X0NWA6 | Trypanosomatidae | 26% | 67% |
A0A1X0NWW1 | Trypanosomatidae | 33% | 80% |
A0A3Q8IDD4 | Leishmania donovani | 36% | 82% |
A0A3Q8IJT4 | Leishmania donovani | 25% | 77% |
A0A3S5H5A5 | Leishmania donovani | 32% | 68% |
A0A3S5ISG2 | Trypanosoma rangeli | 35% | 75% |
A0A3S7WW18 | Leishmania donovani | 34% | 71% |
A0A3S7WW41 | Leishmania donovani | 30% | 78% |
A0A3S7WW71 | Leishmania donovani | 34% | 85% |
A0A3S7X430 | Leishmania donovani | 35% | 74% |
A0A3S7X460 | Leishmania donovani | 88% | 75% |
A0A3S7X470 | Leishmania donovani | 33% | 80% |
A0A422MYX0 | Trypanosoma rangeli | 33% | 80% |
A4H3W4 | Leishmania braziliensis | 31% | 68% |
A4HE81 | Leishmania braziliensis | 39% | 100% |
A4HJ14 | Leishmania braziliensis | 34% | 100% |
A4HJ23 | Leishmania braziliensis | 34% | 100% |
A4HJ24 | Leishmania braziliensis | 81% | 100% |
A4HS39 | Leishmania infantum | 32% | 68% |
A4HYN0 | Leishmania infantum | 35% | 71% |
A4HYW2 | Leishmania infantum | 34% | 85% |
A4HYW3 | Leishmania infantum | 29% | 78% |
A4I1J4 | Leishmania infantum | 36% | 82% |
A4I6E4 | Leishmania infantum | 33% | 80% |
A4I6E6 | Leishmania infantum | 88% | 75% |
A4I6K4 | Leishmania infantum | 34% | 74% |
A4I6K6 | Leishmania infantum | 26% | 77% |
C9ZIE8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 85% |
C9ZIE9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 79% |
C9ZN52 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 73% |
C9ZN53 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 68% |
C9ZWY4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 72% |
C9ZY36 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 68% |
E8NHF1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 98% | 100% |
E8NHG6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 100% |
E8NHG8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 99% | 100% |
E8NHM2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 99% | 100% |
E8NHM4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 99% | 100% |
E8NHQ2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 100% |
E9AIH1 | Leishmania braziliensis | 35% | 100% |
E9AIH3 | Leishmania braziliensis | 35% | 100% |
E9AIH4 | Leishmania braziliensis | 29% | 100% |
E9AIH6 | Leishmania braziliensis | 29% | 100% |
E9AK26 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 31% | 73% |
E9AUQ8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 89% |
E9AUQ9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 85% |
E9AUR0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 78% |
E9AUR1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 100% |
E9AXM9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 37% | 82% |
E9B1J0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 34% | 74% |
E9B1J2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 77% |
E9B1J6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 99% | 82% |
O08688 | Mus musculus | 27% | 91% |
O15484 | Homo sapiens | 26% | 91% |
Q4Q6L7 | Leishmania major | 88% | 100% |
Q4Q6L9 | Leishmania major | 33% | 100% |
Q4Q6M2 | Leishmania major | 25% | 100% |
Q4Q6M4 | Leishmania major | 35% | 68% |
Q4Q9U3 | Leishmania major | 38% | 100% |
Q4QCS5 | Leishmania major | 28% | 97% |
Q4QCS6 | Leishmania major | 30% | 100% |
Q4QCS7 | Leishmania major | 35% | 100% |
Q4QCS8 | Leishmania major | 35% | 100% |
Q5BK10 | Rattus norvegicus | 25% | 87% |
Q8R4C0 | Rattus norvegicus | 27% | 91% |
Q9TTH8 | Ovis aries | 29% | 71% |
Q9U0T9 | Leishmania major | 31% | 68% |
V5AYJ1 | Trypanosoma cruzi | 40% | 81% |
V5B5I4 | Trypanosoma cruzi | 34% | 69% |
V5BA05 | Trypanosoma cruzi | 35% | 87% |
V5BEL3 | Trypanosoma cruzi | 35% | 84% |
V5BN20 | Trypanosoma cruzi | 36% | 75% |
V5D5V8 | Trypanosoma cruzi | 30% | 78% |
V5D9Y2 | Trypanosoma cruzi | 31% | 68% |
V5DES7 | Trypanosoma cruzi | 36% | 73% |