| 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 |
Related structures:
AlphaFold database: E9AZ31
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0006508 | proteolysis | 4 | 11 |
| GO:0006511 | ubiquitin-dependent protein catabolic process | 7 | 11 |
| GO:0006807 | nitrogen compound metabolic process | 2 | 11 |
| GO:0008152 | metabolic process | 1 | 11 |
| GO:0009056 | catabolic process | 2 | 11 |
| GO:0009057 | macromolecule catabolic process | 4 | 11 |
| GO:0009987 | cellular process | 1 | 11 |
| GO:0016579 | protein deubiquitination | 6 | 11 |
| GO:0019538 | protein metabolic process | 3 | 11 |
| GO:0019941 | modification-dependent protein catabolic process | 6 | 11 |
| GO:0036211 | protein modification process | 4 | 11 |
| GO:0043170 | macromolecule metabolic process | 3 | 11 |
| GO:0043412 | macromolecule modification | 4 | 11 |
| GO:0043632 | modification-dependent macromolecule catabolic process | 5 | 11 |
| GO:0044237 | cellular metabolic process | 2 | 11 |
| GO:0044238 | primary metabolic process | 2 | 11 |
| GO:0044248 | cellular catabolic process | 3 | 11 |
| GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 11 |
| GO:0044265 | obsolete cellular macromolecule catabolic process | 4 | 11 |
| GO:0051603 | proteolysis involved in protein catabolic process | 5 | 11 |
| GO:0070646 | protein modification by small protein removal | 5 | 11 |
| GO:0070647 | protein modification by small protein conjugation or removal | 5 | 11 |
| GO:0071704 | organic substance metabolic process | 2 | 11 |
| GO:1901564 | organonitrogen compound metabolic process | 3 | 11 |
| GO:1901575 | organic substance catabolic process | 3 | 11 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0003824 | catalytic activity | 1 | 11 |
| GO:0004843 | cysteine-type deubiquitinase activity | 5 | 11 |
| GO:0008233 | peptidase activity | 3 | 11 |
| GO:0008234 | cysteine-type peptidase activity | 4 | 11 |
| GO:0016787 | hydrolase activity | 2 | 11 |
| GO:0019783 | ubiquitin-like protein peptidase activity | 4 | 11 |
| GO:0101005 | deubiquitinase activity | 5 | 11 |
| GO:0140096 | catalytic activity, acting on a protein | 2 | 11 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 132 | 136 | PF00656 | 0.721 |
| CLV_C14_Caspase3-7 | 333 | 337 | PF00656 | 0.326 |
| CLV_C14_Caspase3-7 | 445 | 449 | PF00656 | 0.265 |
| CLV_C14_Caspase3-7 | 561 | 565 | PF00656 | 0.341 |
| CLV_NRD_NRD_1 | 116 | 118 | PF00675 | 0.543 |
| CLV_NRD_NRD_1 | 122 | 124 | PF00675 | 0.551 |
| CLV_NRD_NRD_1 | 246 | 248 | PF00675 | 0.320 |
| CLV_NRD_NRD_1 | 377 | 379 | PF00675 | 0.330 |
| CLV_NRD_NRD_1 | 464 | 466 | PF00675 | 0.330 |
| CLV_PCSK_KEX2_1 | 116 | 118 | PF00082 | 0.543 |
| CLV_PCSK_KEX2_1 | 121 | 123 | PF00082 | 0.544 |
| CLV_PCSK_KEX2_1 | 245 | 247 | PF00082 | 0.357 |
| CLV_PCSK_KEX2_1 | 377 | 379 | PF00082 | 0.388 |
| CLV_PCSK_KEX2_1 | 482 | 484 | PF00082 | 0.256 |
| CLV_PCSK_KEX2_1 | 51 | 53 | PF00082 | 0.443 |
| CLV_PCSK_KEX2_1 | 85 | 87 | PF00082 | 0.424 |
| CLV_PCSK_PC1ET2_1 | 482 | 484 | PF00082 | 0.256 |
| CLV_PCSK_PC1ET2_1 | 51 | 53 | PF00082 | 0.443 |
| CLV_PCSK_PC1ET2_1 | 85 | 87 | PF00082 | 0.424 |
| CLV_PCSK_PC7_1 | 117 | 123 | PF00082 | 0.598 |
| CLV_PCSK_SKI1_1 | 180 | 184 | PF00082 | 0.743 |
| CLV_PCSK_SKI1_1 | 218 | 222 | PF00082 | 0.509 |
| CLV_PCSK_SKI1_1 | 319 | 323 | PF00082 | 0.330 |
| CLV_PCSK_SKI1_1 | 342 | 346 | PF00082 | 0.327 |
| CLV_PCSK_SKI1_1 | 359 | 363 | PF00082 | 0.393 |
| CLV_PCSK_SKI1_1 | 466 | 470 | PF00082 | 0.256 |
| CLV_PCSK_SKI1_1 | 63 | 67 | PF00082 | 0.499 |
| CLV_PCSK_SKI1_1 | 85 | 89 | PF00082 | 0.465 |
| DEG_APCC_DBOX_1 | 341 | 349 | PF00400 | 0.299 |
| DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.509 |
| DEG_SPOP_SBC_1 | 426 | 430 | PF00917 | 0.263 |
| DOC_CYCLIN_RxL_1 | 461 | 472 | PF00134 | 0.258 |
| DOC_CYCLIN_RxL_1 | 60 | 71 | PF00134 | 0.459 |
| DOC_CYCLIN_yClb5_NLxxxL_5 | 562 | 571 | PF00134 | 0.330 |
| DOC_MAPK_gen_1 | 245 | 252 | PF00069 | 0.292 |
| DOC_MAPK_gen_1 | 518 | 526 | PF00069 | 0.388 |
| DOC_MAPK_gen_1 | 97 | 105 | PF00069 | 0.557 |
| DOC_MAPK_MEF2A_6 | 413 | 421 | PF00069 | 0.274 |
| DOC_PIKK_1 | 160 | 167 | PF02985 | 0.479 |
| DOC_PP1_RVXF_1 | 168 | 174 | PF00149 | 0.456 |
| DOC_PP1_RVXF_1 | 357 | 363 | PF00149 | 0.388 |
| DOC_PP1_RVXF_1 | 464 | 471 | PF00149 | 0.310 |
| DOC_PP1_RVXF_1 | 61 | 68 | PF00149 | 0.433 |
| DOC_USP7_MATH_1 | 223 | 227 | PF00917 | 0.593 |
| DOC_USP7_MATH_1 | 278 | 282 | PF00917 | 0.218 |
| DOC_USP7_MATH_1 | 317 | 321 | PF00917 | 0.386 |
| DOC_USP7_MATH_1 | 426 | 430 | PF00917 | 0.291 |
| DOC_USP7_UBL2_3 | 140 | 144 | PF12436 | 0.430 |
| DOC_USP7_UBL2_3 | 3 | 7 | PF12436 | 0.458 |
| DOC_USP7_UBL2_3 | 97 | 101 | PF12436 | 0.527 |
| DOC_WW_Pin1_4 | 180 | 185 | PF00397 | 0.655 |
| DOC_WW_Pin1_4 | 204 | 209 | PF00397 | 0.784 |
| DOC_WW_Pin1_4 | 265 | 270 | PF00397 | 0.253 |
| DOC_WW_Pin1_4 | 313 | 318 | PF00397 | 0.288 |
| LIG_14-3-3_CanoR_1 | 228 | 237 | PF00244 | 0.550 |
| LIG_14-3-3_CanoR_1 | 292 | 298 | PF00244 | 0.259 |
| LIG_14-3-3_CanoR_1 | 427 | 434 | PF00244 | 0.411 |
| LIG_APCC_ABBAyCdc20_2 | 63 | 69 | PF00400 | 0.442 |
| LIG_BIR_III_4 | 541 | 545 | PF00653 | 0.388 |
| LIG_BRCT_BRCA1_1 | 295 | 299 | PF00533 | 0.335 |
| LIG_BRCT_BRCA1_1 | 411 | 415 | PF00533 | 0.256 |
| LIG_BRCT_BRCA1_1 | 497 | 501 | PF00533 | 0.391 |
| LIG_BRCT_BRCA1_2 | 498 | 504 | PF00533 | 0.370 |
| LIG_Clathr_ClatBox_1 | 65 | 69 | PF01394 | 0.446 |
| LIG_deltaCOP1_diTrp_1 | 546 | 552 | PF00928 | 0.299 |
| LIG_eIF4E_1 | 60 | 66 | PF01652 | 0.430 |
| LIG_EVH1_2 | 474 | 478 | PF00568 | 0.388 |
| LIG_FAT_LD_1 | 164 | 172 | PF03623 | 0.558 |
| LIG_FHA_1 | 177 | 183 | PF00498 | 0.674 |
| LIG_FHA_1 | 229 | 235 | PF00498 | 0.568 |
| LIG_FHA_1 | 289 | 295 | PF00498 | 0.321 |
| LIG_FHA_1 | 503 | 509 | PF00498 | 0.435 |
| LIG_FHA_1 | 82 | 88 | PF00498 | 0.525 |
| LIG_FHA_2 | 369 | 375 | PF00498 | 0.308 |
| LIG_FHA_2 | 556 | 562 | PF00498 | 0.388 |
| LIG_FHA_2 | 76 | 82 | PF00498 | 0.581 |
| LIG_LIR_Apic_2 | 450 | 456 | PF02991 | 0.256 |
| LIG_LIR_Gen_1 | 197 | 206 | PF02991 | 0.614 |
| LIG_LIR_Gen_1 | 296 | 304 | PF02991 | 0.273 |
| LIG_LIR_Gen_1 | 339 | 348 | PF02991 | 0.322 |
| LIG_LIR_Gen_1 | 393 | 402 | PF02991 | 0.330 |
| LIG_LIR_Gen_1 | 519 | 527 | PF02991 | 0.287 |
| LIG_LIR_Gen_1 | 546 | 557 | PF02991 | 0.335 |
| LIG_LIR_Gen_1 | 9 | 18 | PF02991 | 0.393 |
| LIG_LIR_Nem_3 | 197 | 201 | PF02991 | 0.622 |
| LIG_LIR_Nem_3 | 296 | 300 | PF02991 | 0.271 |
| LIG_LIR_Nem_3 | 324 | 329 | PF02991 | 0.265 |
| LIG_LIR_Nem_3 | 339 | 343 | PF02991 | 0.213 |
| LIG_LIR_Nem_3 | 393 | 397 | PF02991 | 0.426 |
| LIG_LIR_Nem_3 | 435 | 441 | PF02991 | 0.388 |
| LIG_LIR_Nem_3 | 519 | 524 | PF02991 | 0.265 |
| LIG_LIR_Nem_3 | 546 | 552 | PF02991 | 0.272 |
| LIG_LIR_Nem_3 | 9 | 13 | PF02991 | 0.354 |
| LIG_LYPXL_SIV_4 | 57 | 65 | PF13949 | 0.427 |
| LIG_MLH1_MIPbox_1 | 498 | 502 | PF16413 | 0.285 |
| LIG_PCNA_yPIPBox_3 | 161 | 170 | PF02747 | 0.467 |
| LIG_Pex14_1 | 380 | 384 | PF04695 | 0.388 |
| LIG_PTB_Apo_2 | 251 | 258 | PF02174 | 0.256 |
| LIG_PTB_Apo_2 | 53 | 60 | PF02174 | 0.445 |
| LIG_PTB_Phospho_1 | 251 | 257 | PF10480 | 0.256 |
| LIG_PTB_Phospho_1 | 53 | 59 | PF10480 | 0.444 |
| LIG_REV1ctd_RIR_1 | 499 | 508 | PF16727 | 0.388 |
| LIG_REV1ctd_RIR_1 | 65 | 73 | PF16727 | 0.491 |
| LIG_SH2_CRK | 198 | 202 | PF00017 | 0.628 |
| LIG_SH2_CRK | 453 | 457 | PF00017 | 0.256 |
| LIG_SH2_CRK | 471 | 475 | PF00017 | 0.256 |
| LIG_SH2_CRK | 521 | 525 | PF00017 | 0.256 |
| LIG_SH2_GRB2like | 257 | 260 | PF00017 | 0.256 |
| LIG_SH2_GRB2like | 54 | 57 | PF00017 | 0.444 |
| LIG_SH2_GRB2like | 60 | 63 | PF00017 | 0.433 |
| LIG_SH2_NCK_1 | 198 | 202 | PF00017 | 0.628 |
| LIG_SH2_NCK_1 | 471 | 475 | PF00017 | 0.363 |
| LIG_SH2_NCK_1 | 54 | 58 | PF00017 | 0.385 |
| LIG_SH2_SRC | 54 | 57 | PF00017 | 0.444 |
| LIG_SH2_STAP1 | 10 | 14 | PF00017 | 0.412 |
| LIG_SH2_STAP1 | 230 | 234 | PF00017 | 0.507 |
| LIG_SH2_STAP1 | 24 | 28 | PF00017 | 0.494 |
| LIG_SH2_STAP1 | 538 | 542 | PF00017 | 0.335 |
| LIG_SH2_STAP1 | 54 | 58 | PF00017 | 0.339 |
| LIG_SH2_STAT3 | 379 | 382 | PF00017 | 0.284 |
| LIG_SH2_STAT5 | 230 | 233 | PF00017 | 0.411 |
| LIG_SH2_STAT5 | 273 | 276 | PF00017 | 0.388 |
| LIG_SH2_STAT5 | 279 | 282 | PF00017 | 0.256 |
| LIG_SH2_STAT5 | 394 | 397 | PF00017 | 0.395 |
| LIG_SH2_STAT5 | 441 | 444 | PF00017 | 0.256 |
| LIG_SH2_STAT5 | 538 | 541 | PF00017 | 0.291 |
| LIG_SH2_STAT5 | 569 | 572 | PF00017 | 0.256 |
| LIG_SH2_STAT5 | 60 | 63 | PF00017 | 0.320 |
| LIG_SH3_3 | 185 | 191 | PF00018 | 0.733 |
| LIG_SH3_3 | 198 | 204 | PF00018 | 0.672 |
| LIG_SH3_3 | 207 | 213 | PF00018 | 0.650 |
| LIG_SH3_3 | 25 | 31 | PF00018 | 0.549 |
| LIG_TRAF2_1 | 396 | 399 | PF00917 | 0.274 |
| LIG_TYR_ITSM | 517 | 524 | PF00017 | 0.274 |
| LIG_UBA3_1 | 1 | 7 | PF00899 | 0.325 |
| LIG_UBA3_1 | 477 | 482 | PF00899 | 0.265 |
| LIG_WRC_WIRS_1 | 294 | 299 | PF05994 | 0.301 |
| LIG_WW_1 | 195 | 198 | PF00397 | 0.544 |
| MOD_CAAXbox | 572 | 575 | PF01239 | 0.419 |
| MOD_CDC14_SPxK_1 | 316 | 319 | PF00782 | 0.335 |
| MOD_CDK_SPxK_1 | 313 | 319 | PF00069 | 0.335 |
| MOD_CK1_1 | 159 | 165 | PF00069 | 0.664 |
| MOD_CK1_1 | 226 | 232 | PF00069 | 0.530 |
| MOD_CK1_1 | 238 | 244 | PF00069 | 0.421 |
| MOD_CK1_1 | 430 | 436 | PF00069 | 0.388 |
| MOD_CK1_1 | 514 | 520 | PF00069 | 0.378 |
| MOD_CK2_1 | 160 | 166 | PF00069 | 0.640 |
| MOD_CK2_1 | 199 | 205 | PF00069 | 0.751 |
| MOD_CK2_1 | 368 | 374 | PF00069 | 0.289 |
| MOD_CK2_1 | 6 | 12 | PF00069 | 0.435 |
| MOD_GlcNHglycan | 132 | 135 | PF01048 | 0.508 |
| MOD_GlcNHglycan | 223 | 226 | PF01048 | 0.653 |
| MOD_GlcNHglycan | 313 | 316 | PF01048 | 0.472 |
| MOD_GlcNHglycan | 319 | 322 | PF01048 | 0.433 |
| MOD_GlcNHglycan | 399 | 403 | PF01048 | 0.330 |
| MOD_GlcNHglycan | 471 | 474 | PF01048 | 0.370 |
| MOD_GlcNHglycan | 513 | 516 | PF01048 | 0.441 |
| MOD_GSK3_1 | 155 | 162 | PF00069 | 0.583 |
| MOD_GSK3_1 | 172 | 179 | PF00069 | 0.656 |
| MOD_GSK3_1 | 309 | 316 | PF00069 | 0.342 |
| MOD_GSK3_1 | 411 | 418 | PF00069 | 0.290 |
| MOD_GSK3_1 | 426 | 433 | PF00069 | 0.237 |
| MOD_GSK3_1 | 491 | 498 | PF00069 | 0.455 |
| MOD_GSK3_1 | 507 | 514 | PF00069 | 0.199 |
| MOD_N-GLC_1 | 160 | 165 | PF02516 | 0.655 |
| MOD_N-GLC_1 | 238 | 243 | PF02516 | 0.505 |
| MOD_N-GLC_1 | 265 | 270 | PF02516 | 0.388 |
| MOD_N-GLC_1 | 304 | 309 | PF02516 | 0.319 |
| MOD_N-GLC_1 | 330 | 335 | PF02516 | 0.388 |
| MOD_N-GLC_1 | 354 | 359 | PF02516 | 0.327 |
| MOD_N-GLC_1 | 386 | 391 | PF02516 | 0.272 |
| MOD_N-GLC_1 | 415 | 420 | PF02516 | 0.330 |
| MOD_N-GLC_1 | 448 | 453 | PF02516 | 0.395 |
| MOD_N-GLC_1 | 496 | 501 | PF02516 | 0.388 |
| MOD_N-GLC_2 | 254 | 256 | PF02516 | 0.256 |
| MOD_N-GLC_2 | 62 | 64 | PF02516 | 0.430 |
| MOD_NEK2_1 | 13 | 18 | PF00069 | 0.411 |
| MOD_NEK2_1 | 148 | 153 | PF00069 | 0.682 |
| MOD_NEK2_1 | 252 | 257 | PF00069 | 0.273 |
| MOD_NEK2_1 | 264 | 269 | PF00069 | 0.256 |
| MOD_NEK2_1 | 283 | 288 | PF00069 | 0.265 |
| MOD_NEK2_1 | 293 | 298 | PF00069 | 0.230 |
| MOD_NEK2_1 | 311 | 316 | PF00069 | 0.401 |
| MOD_NEK2_1 | 329 | 334 | PF00069 | 0.302 |
| MOD_NEK2_1 | 415 | 420 | PF00069 | 0.388 |
| MOD_NEK2_1 | 447 | 452 | PF00069 | 0.285 |
| MOD_NEK2_1 | 469 | 474 | PF00069 | 0.256 |
| MOD_NEK2_1 | 477 | 482 | PF00069 | 0.256 |
| MOD_NEK2_1 | 502 | 507 | PF00069 | 0.312 |
| MOD_NEK2_1 | 516 | 521 | PF00069 | 0.292 |
| MOD_NEK2_2 | 240 | 245 | PF00069 | 0.428 |
| MOD_PIKK_1 | 330 | 336 | PF00454 | 0.299 |
| MOD_PIKK_1 | 75 | 81 | PF00454 | 0.548 |
| MOD_PK_1 | 386 | 392 | PF00069 | 0.335 |
| MOD_PKA_2 | 426 | 432 | PF00069 | 0.316 |
| MOD_Plk_1 | 159 | 165 | PF00069 | 0.574 |
| MOD_Plk_1 | 238 | 244 | PF00069 | 0.490 |
| MOD_Plk_1 | 386 | 392 | PF00069 | 0.297 |
| MOD_Plk_1 | 398 | 404 | PF00069 | 0.297 |
| MOD_Plk_1 | 415 | 421 | PF00069 | 0.246 |
| MOD_Plk_1 | 447 | 453 | PF00069 | 0.380 |
| MOD_Plk_1 | 496 | 502 | PF00069 | 0.388 |
| MOD_Plk_2-3 | 160 | 166 | PF00069 | 0.591 |
| MOD_Plk_4 | 257 | 263 | PF00069 | 0.335 |
| MOD_Plk_4 | 386 | 392 | PF00069 | 0.256 |
| MOD_Plk_4 | 448 | 454 | PF00069 | 0.274 |
| MOD_Plk_4 | 496 | 502 | PF00069 | 0.395 |
| MOD_Plk_4 | 507 | 513 | PF00069 | 0.231 |
| MOD_ProDKin_1 | 180 | 186 | PF00069 | 0.658 |
| MOD_ProDKin_1 | 204 | 210 | PF00069 | 0.785 |
| MOD_ProDKin_1 | 265 | 271 | PF00069 | 0.253 |
| MOD_ProDKin_1 | 313 | 319 | PF00069 | 0.288 |
| MOD_SUMO_for_1 | 45 | 48 | PF00179 | 0.474 |
| MOD_SUMO_rev_2 | 102 | 110 | PF00179 | 0.355 |
| MOD_SUMO_rev_2 | 303 | 312 | PF00179 | 0.285 |
| MOD_SUMO_rev_2 | 90 | 98 | PF00179 | 0.401 |
| TRG_DiLeu_BaLyEn_6 | 289 | 294 | PF01217 | 0.388 |
| TRG_ENDOCYTIC_2 | 10 | 13 | PF00928 | 0.361 |
| TRG_ENDOCYTIC_2 | 107 | 110 | PF00928 | 0.446 |
| TRG_ENDOCYTIC_2 | 198 | 201 | PF00928 | 0.629 |
| TRG_ENDOCYTIC_2 | 326 | 329 | PF00928 | 0.299 |
| TRG_ENDOCYTIC_2 | 394 | 397 | PF00928 | 0.330 |
| TRG_ENDOCYTIC_2 | 487 | 490 | PF00928 | 0.299 |
| TRG_ENDOCYTIC_2 | 521 | 524 | PF00928 | 0.256 |
| TRG_ENDOCYTIC_2 | 58 | 61 | PF00928 | 0.431 |
| TRG_ER_diArg_1 | 121 | 123 | PF00400 | 0.541 |
| TRG_ER_diArg_1 | 244 | 247 | PF00400 | 0.393 |
| TRG_ER_diArg_1 | 377 | 379 | PF00400 | 0.285 |
| TRG_NLS_Bipartite_1 | 465 | 486 | PF00514 | 0.388 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1I1S4 | Leptomonas seymouri | 66% | 97% |
| A0A0S4IVV7 | Bodo saltans | 29% | 98% |
| A0A1X0NIL8 | Trypanosomatidae | 25% | 75% |
| A0A1X0P5M1 | Trypanosomatidae | 42% | 100% |
| A0A3Q8IGB5 | Leishmania donovani | 96% | 100% |
| A0A422NFS3 | Trypanosoma rangeli | 44% | 100% |
| A4HFQ3 | Leishmania braziliensis | 83% | 100% |
| A4I2S8 | Leishmania infantum | 96% | 100% |
| B2GUX4 | Rattus norvegicus | 29% | 100% |
| D0A5Z2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 39% | 100% |
| E9ADA6 | Leishmania major | 95% | 100% |
| O94269 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 24% | 100% |
| P36026 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 24% | 80% |
| Q2KJ72 | Bos taurus | 29% | 100% |
| Q2NL57 | Xenopus laevis | 22% | 73% |
| Q5U349 | Rattus norvegicus | 30% | 93% |
| Q7ZXR7 | Xenopus laevis | 22% | 71% |
| Q91W36 | Mus musculus | 27% | 100% |
| Q9HFS7 | Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) | 28% | 72% |
| Q9UK80 | Homo sapiens | 29% | 100% |
| Q9Y6I4 | Homo sapiens | 27% | 100% |
| V5BQL0 | Trypanosoma cruzi | 44% | 100% |