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:0005654 | nucleoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9ARV1
Term | Name | Level | Count |
---|---|---|---|
GO:0006518 | peptide metabolic process | 4 | 12 |
GO:0006575 | cellular modified amino acid metabolic process | 3 | 12 |
GO:0006749 | glutathione metabolic process | 4 | 12 |
GO:0006750 | glutathione biosynthetic process | 5 | 12 |
GO:0006790 | sulfur compound metabolic process | 3 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009058 | biosynthetic process | 2 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0019184 | nonribosomal peptide biosynthetic process | 6 | 12 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0042398 | cellular modified amino acid biosynthetic process | 4 | 12 |
GO:0043043 | peptide biosynthetic process | 5 | 12 |
GO:0043603 | amide metabolic process | 3 | 12 |
GO:0043604 | amide biosynthetic process | 4 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044249 | cellular biosynthetic process | 3 | 12 |
GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 12 |
GO:0044272 | sulfur compound biosynthetic process | 4 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 12 |
GO:1901566 | organonitrogen compound biosynthetic process | 4 | 12 |
GO:1901576 | organic substance biosynthetic process | 3 | 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 12 |
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004357 | glutamate-cysteine ligase activity | 5 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0005524 | ATP binding | 5 | 12 |
GO:0016874 | ligase activity | 2 | 12 |
GO:0016879 | ligase activity, forming carbon-nitrogen bonds | 3 | 12 |
GO:0016881 | acid-amino acid ligase activity | 4 | 12 |
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:1901265 | nucleoside phosphate binding | 3 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 111 | 115 | PF00656 | 0.434 |
CLV_C14_Caspase3-7 | 413 | 417 | PF00656 | 0.372 |
CLV_NRD_NRD_1 | 122 | 124 | PF00675 | 0.300 |
CLV_NRD_NRD_1 | 189 | 191 | PF00675 | 0.294 |
CLV_NRD_NRD_1 | 384 | 386 | PF00675 | 0.252 |
CLV_NRD_NRD_1 | 556 | 558 | PF00675 | 0.256 |
CLV_NRD_NRD_1 | 632 | 634 | PF00675 | 0.325 |
CLV_PCSK_FUR_1 | 187 | 191 | PF00082 | 0.294 |
CLV_PCSK_KEX2_1 | 122 | 124 | PF00082 | 0.301 |
CLV_PCSK_KEX2_1 | 189 | 191 | PF00082 | 0.294 |
CLV_PCSK_KEX2_1 | 384 | 386 | PF00082 | 0.294 |
CLV_PCSK_KEX2_1 | 604 | 606 | PF00082 | 0.293 |
CLV_PCSK_KEX2_1 | 632 | 634 | PF00082 | 0.215 |
CLV_PCSK_PC1ET2_1 | 604 | 606 | PF00082 | 0.456 |
CLV_PCSK_SKI1_1 | 271 | 275 | PF00082 | 0.464 |
CLV_PCSK_SKI1_1 | 364 | 368 | PF00082 | 0.233 |
CLV_PCSK_SKI1_1 | 373 | 377 | PF00082 | 0.233 |
CLV_PCSK_SKI1_1 | 391 | 395 | PF00082 | 0.233 |
CLV_PCSK_SKI1_1 | 558 | 562 | PF00082 | 0.267 |
CLV_PCSK_SKI1_1 | 633 | 637 | PF00082 | 0.327 |
CLV_Separin_Metazoa | 388 | 392 | PF03568 | 0.229 |
DEG_COP1_1 | 162 | 170 | PF00400 | 0.311 |
DOC_CKS1_1 | 273 | 278 | PF01111 | 0.310 |
DOC_CKS1_1 | 503 | 508 | PF01111 | 0.233 |
DOC_CKS1_1 | 624 | 629 | PF01111 | 0.254 |
DOC_CYCLIN_RxL_1 | 268 | 278 | PF00134 | 0.472 |
DOC_CYCLIN_RxL_1 | 361 | 371 | PF00134 | 0.327 |
DOC_CYCLIN_yCln2_LP_2 | 273 | 279 | PF00134 | 0.355 |
DOC_MAPK_DCC_7 | 193 | 202 | PF00069 | 0.347 |
DOC_MAPK_gen_1 | 187 | 196 | PF00069 | 0.289 |
DOC_MAPK_gen_1 | 38 | 48 | PF00069 | 0.463 |
DOC_MAPK_gen_1 | 394 | 402 | PF00069 | 0.267 |
DOC_MAPK_GRA24_9 | 186 | 202 | PF00069 | 0.352 |
DOC_MAPK_HePTP_8 | 186 | 198 | PF00069 | 0.286 |
DOC_MAPK_MEF2A_6 | 189 | 198 | PF00069 | 0.286 |
DOC_MAPK_MEF2A_6 | 396 | 404 | PF00069 | 0.267 |
DOC_MAPK_MEF2A_6 | 430 | 438 | PF00069 | 0.244 |
DOC_PP1_RVXF_1 | 492 | 498 | PF00149 | 0.233 |
DOC_PP2B_LxvP_1 | 165 | 168 | PF13499 | 0.309 |
DOC_PP4_FxxP_1 | 248 | 251 | PF00568 | 0.394 |
DOC_PP4_FxxP_1 | 482 | 485 | PF00568 | 0.327 |
DOC_USP7_MATH_1 | 254 | 258 | PF00917 | 0.524 |
DOC_USP7_MATH_1 | 306 | 310 | PF00917 | 0.294 |
DOC_USP7_MATH_1 | 355 | 359 | PF00917 | 0.233 |
DOC_USP7_MATH_1 | 486 | 490 | PF00917 | 0.297 |
DOC_USP7_MATH_1 | 573 | 577 | PF00917 | 0.254 |
DOC_USP7_MATH_1 | 620 | 624 | PF00917 | 0.134 |
DOC_WW_Pin1_4 | 156 | 161 | PF00397 | 0.355 |
DOC_WW_Pin1_4 | 217 | 222 | PF00397 | 0.422 |
DOC_WW_Pin1_4 | 272 | 277 | PF00397 | 0.301 |
DOC_WW_Pin1_4 | 357 | 362 | PF00397 | 0.233 |
DOC_WW_Pin1_4 | 502 | 507 | PF00397 | 0.233 |
DOC_WW_Pin1_4 | 603 | 608 | PF00397 | 0.379 |
DOC_WW_Pin1_4 | 623 | 628 | PF00397 | 0.254 |
DOC_WW_Pin1_4 | 98 | 103 | PF00397 | 0.428 |
LIG_14-3-3_CanoR_1 | 235 | 242 | PF00244 | 0.571 |
LIG_14-3-3_CanoR_1 | 632 | 641 | PF00244 | 0.331 |
LIG_Actin_WH2_2 | 175 | 191 | PF00022 | 0.313 |
LIG_APCC_ABBA_1 | 198 | 203 | PF00400 | 0.290 |
LIG_deltaCOP1_diTrp_1 | 490 | 497 | PF00928 | 0.293 |
LIG_eIF4E_1 | 589 | 595 | PF01652 | 0.248 |
LIG_FHA_1 | 136 | 142 | PF00498 | 0.292 |
LIG_FHA_1 | 181 | 187 | PF00498 | 0.286 |
LIG_FHA_1 | 236 | 242 | PF00498 | 0.677 |
LIG_FHA_1 | 265 | 271 | PF00498 | 0.422 |
LIG_FHA_1 | 328 | 334 | PF00498 | 0.248 |
LIG_FHA_1 | 406 | 412 | PF00498 | 0.304 |
LIG_FHA_1 | 518 | 524 | PF00498 | 0.267 |
LIG_FHA_1 | 63 | 69 | PF00498 | 0.461 |
LIG_FHA_1 | 646 | 652 | PF00498 | 0.246 |
LIG_FHA_2 | 235 | 241 | PF00498 | 0.505 |
LIG_FHA_2 | 462 | 468 | PF00498 | 0.248 |
LIG_FHA_2 | 503 | 509 | PF00498 | 0.233 |
LIG_FHA_2 | 564 | 570 | PF00498 | 0.293 |
LIG_FHA_2 | 635 | 641 | PF00498 | 0.419 |
LIG_FHA_2 | 68 | 74 | PF00498 | 0.377 |
LIG_GBD_Chelix_1 | 651 | 659 | PF00786 | 0.254 |
LIG_HCF-1_HBM_1 | 103 | 106 | PF13415 | 0.356 |
LIG_Integrin_isoDGR_2 | 233 | 235 | PF01839 | 0.500 |
LIG_LIR_Apic_2 | 245 | 251 | PF02991 | 0.398 |
LIG_LIR_Apic_2 | 479 | 485 | PF02991 | 0.379 |
LIG_LIR_Gen_1 | 138 | 146 | PF02991 | 0.474 |
LIG_LIR_Gen_1 | 371 | 381 | PF02991 | 0.233 |
LIG_LIR_Gen_1 | 395 | 404 | PF02991 | 0.242 |
LIG_LIR_Gen_1 | 424 | 429 | PF02991 | 0.297 |
LIG_LIR_Gen_1 | 474 | 485 | PF02991 | 0.233 |
LIG_LIR_Gen_1 | 611 | 620 | PF02991 | 0.237 |
LIG_LIR_Nem_3 | 138 | 143 | PF02991 | 0.479 |
LIG_LIR_Nem_3 | 371 | 377 | PF02991 | 0.233 |
LIG_LIR_Nem_3 | 395 | 400 | PF02991 | 0.242 |
LIG_LIR_Nem_3 | 424 | 428 | PF02991 | 0.272 |
LIG_LIR_Nem_3 | 466 | 472 | PF02991 | 0.234 |
LIG_LIR_Nem_3 | 585 | 591 | PF02991 | 0.247 |
LIG_LIR_Nem_3 | 611 | 615 | PF02991 | 0.237 |
LIG_LIR_Nem_3 | 92 | 96 | PF02991 | 0.302 |
LIG_Pex14_1 | 493 | 497 | PF04695 | 0.233 |
LIG_Pex14_1 | 89 | 93 | PF04695 | 0.306 |
LIG_Pex14_2 | 33 | 37 | PF04695 | 0.411 |
LIG_PTB_Apo_2 | 506 | 513 | PF02174 | 0.237 |
LIG_PTB_Apo_2 | 87 | 94 | PF02174 | 0.339 |
LIG_PTB_Phospho_1 | 87 | 93 | PF10480 | 0.342 |
LIG_SH2_CRK | 124 | 128 | PF00017 | 0.376 |
LIG_SH2_CRK | 343 | 347 | PF00017 | 0.233 |
LIG_SH2_CRK | 397 | 401 | PF00017 | 0.267 |
LIG_SH2_CRK | 531 | 535 | PF00017 | 0.286 |
LIG_SH2_CRK | 589 | 593 | PF00017 | 0.248 |
LIG_SH2_NCK_1 | 397 | 401 | PF00017 | 0.280 |
LIG_SH2_NCK_1 | 531 | 535 | PF00017 | 0.298 |
LIG_SH2_SRC | 598 | 601 | PF00017 | 0.178 |
LIG_SH2_STAP1 | 161 | 165 | PF00017 | 0.365 |
LIG_SH2_STAP1 | 282 | 286 | PF00017 | 0.338 |
LIG_SH2_STAP1 | 343 | 347 | PF00017 | 0.293 |
LIG_SH2_STAP1 | 454 | 458 | PF00017 | 0.267 |
LIG_SH2_STAT3 | 281 | 284 | PF00017 | 0.310 |
LIG_SH2_STAT5 | 285 | 288 | PF00017 | 0.423 |
LIG_SH2_STAT5 | 425 | 428 | PF00017 | 0.355 |
LIG_SH2_STAT5 | 531 | 534 | PF00017 | 0.233 |
LIG_SH2_STAT5 | 554 | 557 | PF00017 | 0.233 |
LIG_SH2_STAT5 | 598 | 601 | PF00017 | 0.364 |
LIG_SH2_STAT5 | 612 | 615 | PF00017 | 0.123 |
LIG_SH2_STAT5 | 672 | 675 | PF00017 | 0.374 |
LIG_SH3_3 | 138 | 144 | PF00018 | 0.278 |
LIG_SH3_3 | 248 | 254 | PF00018 | 0.463 |
LIG_SH3_3 | 305 | 311 | PF00018 | 0.341 |
LIG_SH3_3 | 511 | 517 | PF00018 | 0.327 |
LIG_SH3_3 | 99 | 105 | PF00018 | 0.264 |
LIG_SH3_5 | 260 | 264 | PF00018 | 0.682 |
LIG_SUMO_SIM_anti_2 | 344 | 350 | PF11976 | 0.327 |
LIG_SUMO_SIM_anti_2 | 532 | 539 | PF11976 | 0.327 |
LIG_SUMO_SIM_par_1 | 455 | 464 | PF11976 | 0.244 |
LIG_SUMO_SIM_par_1 | 63 | 73 | PF11976 | 0.469 |
LIG_TRAF2_1 | 568 | 571 | PF00917 | 0.254 |
LIG_TRFH_1 | 589 | 593 | PF08558 | 0.248 |
LIG_WRC_WIRS_1 | 93 | 98 | PF05994 | 0.295 |
MOD_CDK_SPK_2 | 217 | 222 | PF00069 | 0.229 |
MOD_CDK_SPxxK_3 | 357 | 364 | PF00069 | 0.233 |
MOD_CK1_1 | 109 | 115 | PF00069 | 0.343 |
MOD_CK1_1 | 155 | 161 | PF00069 | 0.372 |
MOD_CK1_1 | 357 | 363 | PF00069 | 0.213 |
MOD_CK1_1 | 405 | 411 | PF00069 | 0.304 |
MOD_CK1_1 | 623 | 629 | PF00069 | 0.307 |
MOD_CK1_1 | 645 | 651 | PF00069 | 0.255 |
MOD_CK1_1 | 661 | 667 | PF00069 | 0.332 |
MOD_CK1_1 | 69 | 75 | PF00069 | 0.467 |
MOD_CK2_1 | 226 | 232 | PF00069 | 0.488 |
MOD_CK2_1 | 234 | 240 | PF00069 | 0.549 |
MOD_CK2_1 | 414 | 420 | PF00069 | 0.276 |
MOD_CK2_1 | 421 | 427 | PF00069 | 0.305 |
MOD_CK2_1 | 461 | 467 | PF00069 | 0.245 |
MOD_CK2_1 | 502 | 508 | PF00069 | 0.233 |
MOD_CK2_1 | 532 | 538 | PF00069 | 0.134 |
MOD_CK2_1 | 565 | 571 | PF00069 | 0.290 |
MOD_CK2_1 | 573 | 579 | PF00069 | 0.206 |
MOD_CK2_1 | 67 | 73 | PF00069 | 0.357 |
MOD_Cter_Amidation | 602 | 605 | PF01082 | 0.254 |
MOD_GlcNHglycan | 324 | 327 | PF01048 | 0.298 |
MOD_GlcNHglycan | 357 | 360 | PF01048 | 0.293 |
MOD_GlcNHglycan | 431 | 434 | PF01048 | 0.270 |
MOD_GlcNHglycan | 620 | 623 | PF01048 | 0.341 |
MOD_GSK3_1 | 12 | 19 | PF00069 | 0.420 |
MOD_GSK3_1 | 135 | 142 | PF00069 | 0.291 |
MOD_GSK3_1 | 152 | 159 | PF00069 | 0.409 |
MOD_GSK3_1 | 203 | 210 | PF00069 | 0.343 |
MOD_GSK3_1 | 392 | 399 | PF00069 | 0.364 |
MOD_GSK3_1 | 472 | 479 | PF00069 | 0.251 |
MOD_GSK3_1 | 565 | 572 | PF00069 | 0.279 |
MOD_GSK3_1 | 614 | 621 | PF00069 | 0.291 |
MOD_GSK3_1 | 62 | 69 | PF00069 | 0.407 |
MOD_GSK3_1 | 679 | 686 | PF00069 | 0.547 |
MOD_N-GLC_1 | 106 | 111 | PF02516 | 0.278 |
MOD_N-GLC_1 | 172 | 177 | PF02516 | 0.326 |
MOD_N-GLC_1 | 180 | 185 | PF02516 | 0.274 |
MOD_N-GLC_1 | 235 | 240 | PF02516 | 0.665 |
MOD_N-GLC_1 | 414 | 419 | PF02516 | 0.276 |
MOD_N-GLC_1 | 421 | 426 | PF02516 | 0.257 |
MOD_N-GLC_1 | 539 | 544 | PF02516 | 0.234 |
MOD_N-GLC_2 | 299 | 301 | PF02516 | 0.425 |
MOD_N-GLC_2 | 563 | 565 | PF02516 | 0.178 |
MOD_NEK2_1 | 322 | 327 | PF00069 | 0.248 |
MOD_NEK2_1 | 354 | 359 | PF00069 | 0.233 |
MOD_NEK2_1 | 414 | 419 | PF00069 | 0.292 |
MOD_NEK2_1 | 429 | 434 | PF00069 | 0.187 |
MOD_NEK2_1 | 608 | 613 | PF00069 | 0.338 |
MOD_NEK2_1 | 618 | 623 | PF00069 | 0.275 |
MOD_NEK2_1 | 634 | 639 | PF00069 | 0.222 |
MOD_NEK2_1 | 647 | 652 | PF00069 | 0.271 |
MOD_NEK2_1 | 97 | 102 | PF00069 | 0.283 |
MOD_NEK2_2 | 161 | 166 | PF00069 | 0.338 |
MOD_NEK2_2 | 266 | 271 | PF00069 | 0.338 |
MOD_PIKK_1 | 159 | 165 | PF00454 | 0.379 |
MOD_PK_1 | 396 | 402 | PF00069 | 0.267 |
MOD_PK_1 | 679 | 685 | PF00069 | 0.347 |
MOD_PKA_2 | 234 | 240 | PF00069 | 0.401 |
MOD_PKA_2 | 254 | 260 | PF00069 | 0.379 |
MOD_PKA_2 | 573 | 579 | PF00069 | 0.329 |
MOD_PKA_2 | 618 | 624 | PF00069 | 0.293 |
MOD_PKA_2 | 645 | 651 | PF00069 | 0.264 |
MOD_PKB_1 | 80 | 88 | PF00069 | 0.220 |
MOD_Plk_1 | 106 | 112 | PF00069 | 0.273 |
MOD_Plk_1 | 207 | 213 | PF00069 | 0.295 |
MOD_Plk_1 | 414 | 420 | PF00069 | 0.281 |
MOD_Plk_1 | 421 | 427 | PF00069 | 0.253 |
MOD_Plk_1 | 62 | 68 | PF00069 | 0.388 |
MOD_Plk_2-3 | 203 | 209 | PF00069 | 0.366 |
MOD_Plk_4 | 136 | 142 | PF00069 | 0.301 |
MOD_Plk_4 | 161 | 167 | PF00069 | 0.335 |
MOD_Plk_4 | 608 | 614 | PF00069 | 0.383 |
MOD_Plk_4 | 673 | 679 | PF00069 | 0.335 |
MOD_Plk_4 | 92 | 98 | PF00069 | 0.300 |
MOD_ProDKin_1 | 156 | 162 | PF00069 | 0.345 |
MOD_ProDKin_1 | 217 | 223 | PF00069 | 0.417 |
MOD_ProDKin_1 | 272 | 278 | PF00069 | 0.300 |
MOD_ProDKin_1 | 357 | 363 | PF00069 | 0.233 |
MOD_ProDKin_1 | 502 | 508 | PF00069 | 0.233 |
MOD_ProDKin_1 | 603 | 609 | PF00069 | 0.379 |
MOD_ProDKin_1 | 623 | 629 | PF00069 | 0.254 |
MOD_ProDKin_1 | 98 | 104 | PF00069 | 0.439 |
MOD_SUMO_rev_2 | 600 | 606 | PF00179 | 0.287 |
TRG_DiLeu_BaEn_2 | 91 | 97 | PF01217 | 0.302 |
TRG_DiLeu_BaEn_3 | 387 | 393 | PF01217 | 0.213 |
TRG_DiLeu_BaLyEn_6 | 514 | 519 | PF01217 | 0.327 |
TRG_DiLeu_BaLyEn_6 | 604 | 609 | PF01217 | 0.134 |
TRG_ENDOCYTIC_2 | 124 | 127 | PF00928 | 0.323 |
TRG_ENDOCYTIC_2 | 343 | 346 | PF00928 | 0.233 |
TRG_ENDOCYTIC_2 | 397 | 400 | PF00928 | 0.241 |
TRG_ENDOCYTIC_2 | 425 | 428 | PF00928 | 0.268 |
TRG_ENDOCYTIC_2 | 454 | 457 | PF00928 | 0.267 |
TRG_ENDOCYTIC_2 | 531 | 534 | PF00928 | 0.283 |
TRG_ENDOCYTIC_2 | 589 | 592 | PF00928 | 0.247 |
TRG_ENDOCYTIC_2 | 612 | 615 | PF00928 | 0.233 |
TRG_ENDOCYTIC_2 | 672 | 675 | PF00928 | 0.504 |
TRG_ENDOCYTIC_2 | 93 | 96 | PF00928 | 0.297 |
TRG_ER_diArg_1 | 122 | 124 | PF00400 | 0.306 |
TRG_ER_diArg_1 | 186 | 189 | PF00400 | 0.280 |
TRG_ER_diArg_1 | 631 | 633 | PF00400 | 0.208 |
TRG_ER_diArg_1 | 79 | 82 | PF00400 | 0.337 |
TRG_Pf-PMV_PEXEL_1 | 597 | 602 | PF00026 | 0.293 |
TRG_Pf-PMV_PEXEL_1 | 653 | 657 | PF00026 | 0.298 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1P9N5 | Leptomonas seymouri | 72% | 100% |
A0A0S4IM75 | Bodo saltans | 53% | 100% |
A0A1X0P757 | Trypanosomatidae | 58% | 100% |
A0A3S5IRL4 | Trypanosoma rangeli | 60% | 100% |
A0A3S7WV51 | Leishmania donovani | 91% | 100% |
A4H9R8 | Leishmania braziliensis | 76% | 100% |
A4HY37 | Leishmania infantum | 91% | 100% |
D0A548 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 57% | 100% |
Q09768 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 34% | 100% |
Q4QDM2 | Leishmania major | 89% | 100% |
Q9HF78 | Candida albicans | 33% | 100% |
V5BDE4 | Trypanosoma cruzi | 59% | 100% |