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:0005739 | mitochondrion | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A0A3S7WX31
Term | Name | Level | Count |
---|---|---|---|
GO:0006082 | organic acid metabolic process | 3 | 7 |
GO:0006629 | lipid metabolic process | 3 | 7 |
GO:0006631 | fatty acid metabolic process | 4 | 7 |
GO:0008152 | metabolic process | 1 | 7 |
GO:0009987 | cellular process | 1 | 7 |
GO:0019752 | carboxylic acid metabolic process | 5 | 7 |
GO:0032787 | monocarboxylic acid metabolic process | 6 | 7 |
GO:0043436 | oxoacid metabolic process | 4 | 7 |
GO:0044237 | cellular metabolic process | 2 | 7 |
GO:0044238 | primary metabolic process | 2 | 7 |
GO:0044255 | cellular lipid metabolic process | 3 | 7 |
GO:0044281 | small molecule metabolic process | 2 | 7 |
GO:0071704 | organic substance metabolic process | 2 | 7 |
GO:0006635 | fatty acid beta-oxidation | 6 | 1 |
GO:0009056 | catabolic process | 2 | 1 |
GO:0009062 | fatty acid catabolic process | 5 | 1 |
GO:0016042 | lipid catabolic process | 4 | 1 |
GO:0016054 | organic acid catabolic process | 4 | 1 |
GO:0019395 | fatty acid oxidation | 5 | 1 |
GO:0030258 | lipid modification | 4 | 1 |
GO:0034440 | lipid oxidation | 5 | 1 |
GO:0044242 | cellular lipid catabolic process | 4 | 1 |
GO:0044248 | cellular catabolic process | 3 | 1 |
GO:0044282 | small molecule catabolic process | 3 | 1 |
GO:0046395 | carboxylic acid catabolic process | 5 | 1 |
GO:0072329 | monocarboxylic acid catabolic process | 6 | 1 |
GO:1901575 | organic substance catabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 12 |
GO:0004095 | carnitine O-palmitoyltransferase activity | 7 | 8 |
GO:0008374 | O-acyltransferase activity | 5 | 8 |
GO:0016406 | carnitine O-acyltransferase activity | 6 | 8 |
GO:0016409 | palmitoyltransferase activity | 5 | 8 |
GO:0016416 | O-palmitoyltransferase activity | 6 | 8 |
GO:0016740 | transferase activity | 2 | 12 |
GO:0016746 | acyltransferase activity | 3 | 12 |
GO:0016747 | acyltransferase activity, transferring groups other than amino-acyl groups | 4 | 8 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 275 | 279 | PF00656 | 0.364 |
CLV_C14_Caspase3-7 | 352 | 356 | PF00656 | 0.392 |
CLV_C14_Caspase3-7 | 401 | 405 | PF00656 | 0.342 |
CLV_NRD_NRD_1 | 112 | 114 | PF00675 | 0.428 |
CLV_NRD_NRD_1 | 409 | 411 | PF00675 | 0.396 |
CLV_NRD_NRD_1 | 427 | 429 | PF00675 | 0.189 |
CLV_NRD_NRD_1 | 457 | 459 | PF00675 | 0.343 |
CLV_NRD_NRD_1 | 516 | 518 | PF00675 | 0.428 |
CLV_PCSK_KEX2_1 | 112 | 114 | PF00082 | 0.428 |
CLV_PCSK_KEX2_1 | 195 | 197 | PF00082 | 0.438 |
CLV_PCSK_KEX2_1 | 409 | 411 | PF00082 | 0.371 |
CLV_PCSK_KEX2_1 | 457 | 459 | PF00082 | 0.363 |
CLV_PCSK_KEX2_1 | 516 | 518 | PF00082 | 0.428 |
CLV_PCSK_PC1ET2_1 | 195 | 197 | PF00082 | 0.438 |
CLV_PCSK_SKI1_1 | 136 | 140 | PF00082 | 0.438 |
CLV_PCSK_SKI1_1 | 19 | 23 | PF00082 | 0.600 |
CLV_PCSK_SKI1_1 | 323 | 327 | PF00082 | 0.422 |
CLV_PCSK_SKI1_1 | 457 | 461 | PF00082 | 0.450 |
DEG_APCC_DBOX_1 | 1 | 9 | PF00400 | 0.530 |
DEG_SCF_FBW7_2 | 479 | 484 | PF00400 | 0.449 |
DEG_SPOP_SBC_1 | 651 | 655 | PF00917 | 0.557 |
DOC_ANK_TNKS_1 | 185 | 192 | PF00023 | 0.453 |
DOC_CDC14_PxL_1 | 584 | 592 | PF14671 | 0.411 |
DOC_CKS1_1 | 216 | 221 | PF01111 | 0.428 |
DOC_CKS1_1 | 46 | 51 | PF01111 | 0.530 |
DOC_CYCLIN_yCln2_LP_2 | 64 | 70 | PF00134 | 0.467 |
DOC_MAPK_gen_1 | 134 | 141 | PF00069 | 0.434 |
DOC_MAPK_gen_1 | 457 | 468 | PF00069 | 0.405 |
DOC_MAPK_gen_1 | 516 | 525 | PF00069 | 0.415 |
DOC_MAPK_MEF2A_6 | 59 | 66 | PF00069 | 0.522 |
DOC_PP1_RVXF_1 | 253 | 260 | PF00149 | 0.428 |
DOC_PP1_RVXF_1 | 436 | 443 | PF00149 | 0.323 |
DOC_PP2B_LxvP_1 | 64 | 67 | PF13499 | 0.311 |
DOC_PP2B_LxvP_1 | 672 | 675 | PF13499 | 0.469 |
DOC_PP2B_LxvP_1 | 83 | 86 | PF13499 | 0.307 |
DOC_USP7_MATH_1 | 119 | 123 | PF00917 | 0.453 |
DOC_USP7_MATH_1 | 140 | 144 | PF00917 | 0.428 |
DOC_USP7_MATH_1 | 398 | 402 | PF00917 | 0.428 |
DOC_USP7_MATH_1 | 421 | 425 | PF00917 | 0.428 |
DOC_USP7_MATH_1 | 652 | 656 | PF00917 | 0.460 |
DOC_USP7_MATH_1 | 90 | 94 | PF00917 | 0.453 |
DOC_USP7_UBL2_3 | 557 | 561 | PF12436 | 0.328 |
DOC_WW_Pin1_4 | 215 | 220 | PF00397 | 0.346 |
DOC_WW_Pin1_4 | 35 | 40 | PF00397 | 0.598 |
DOC_WW_Pin1_4 | 359 | 364 | PF00397 | 0.445 |
DOC_WW_Pin1_4 | 367 | 372 | PF00397 | 0.403 |
DOC_WW_Pin1_4 | 45 | 50 | PF00397 | 0.521 |
DOC_WW_Pin1_4 | 475 | 480 | PF00397 | 0.445 |
DOC_WW_Pin1_4 | 640 | 645 | PF00397 | 0.512 |
DOC_WW_Pin1_4 | 78 | 83 | PF00397 | 0.350 |
LIG_14-3-3_CanoR_1 | 112 | 119 | PF00244 | 0.404 |
LIG_14-3-3_CanoR_1 | 142 | 148 | PF00244 | 0.459 |
LIG_14-3-3_CanoR_1 | 40 | 44 | PF00244 | 0.523 |
LIG_14-3-3_CanoR_1 | 516 | 525 | PF00244 | 0.447 |
LIG_14-3-3_CanoR_1 | 565 | 571 | PF00244 | 0.447 |
LIG_14-3-3_CanoR_1 | 577 | 584 | PF00244 | 0.334 |
LIG_14-3-3_CanoR_1 | 632 | 638 | PF00244 | 0.529 |
LIG_Actin_WH2_2 | 279 | 296 | PF00022 | 0.428 |
LIG_BRCT_BRCA1_1 | 125 | 129 | PF00533 | 0.428 |
LIG_BRCT_BRCA1_1 | 168 | 172 | PF00533 | 0.307 |
LIG_BRCT_BRCA1_1 | 216 | 220 | PF00533 | 0.404 |
LIG_BRCT_BRCA1_1 | 529 | 533 | PF00533 | 0.295 |
LIG_BRCT_BRCA1_1 | 654 | 658 | PF00533 | 0.498 |
LIG_BRCT_BRCA1_2 | 168 | 174 | PF00533 | 0.392 |
LIG_CtBP_PxDLS_1 | 231 | 235 | PF00389 | 0.307 |
LIG_eIF4E_1 | 123 | 129 | PF01652 | 0.428 |
LIG_FHA_1 | 119 | 125 | PF00498 | 0.307 |
LIG_FHA_1 | 144 | 150 | PF00498 | 0.389 |
LIG_FHA_1 | 206 | 212 | PF00498 | 0.295 |
LIG_FHA_1 | 216 | 222 | PF00498 | 0.326 |
LIG_FHA_1 | 322 | 328 | PF00498 | 0.342 |
LIG_FHA_1 | 359 | 365 | PF00498 | 0.251 |
LIG_FHA_1 | 432 | 438 | PF00498 | 0.304 |
LIG_FHA_1 | 454 | 460 | PF00498 | 0.386 |
LIG_FHA_1 | 46 | 52 | PF00498 | 0.449 |
LIG_FHA_1 | 478 | 484 | PF00498 | 0.399 |
LIG_FHA_1 | 529 | 535 | PF00498 | 0.372 |
LIG_FHA_1 | 95 | 101 | PF00498 | 0.234 |
LIG_FHA_2 | 273 | 279 | PF00498 | 0.317 |
LIG_FHA_2 | 40 | 46 | PF00498 | 0.582 |
LIG_FHA_2 | 524 | 530 | PF00498 | 0.417 |
LIG_Integrin_RGD_1 | 391 | 393 | PF01839 | 0.453 |
LIG_LIR_Apic_2 | 589 | 594 | PF02991 | 0.392 |
LIG_LIR_Gen_1 | 235 | 241 | PF02991 | 0.353 |
LIG_LIR_Gen_1 | 25 | 36 | PF02991 | 0.490 |
LIG_LIR_Gen_1 | 287 | 297 | PF02991 | 0.307 |
LIG_LIR_Gen_1 | 309 | 315 | PF02991 | 0.361 |
LIG_LIR_Gen_1 | 567 | 578 | PF02991 | 0.268 |
LIG_LIR_Gen_1 | 593 | 604 | PF02991 | 0.312 |
LIG_LIR_Nem_3 | 169 | 175 | PF02991 | 0.396 |
LIG_LIR_Nem_3 | 235 | 240 | PF02991 | 0.333 |
LIG_LIR_Nem_3 | 25 | 31 | PF02991 | 0.450 |
LIG_LIR_Nem_3 | 287 | 293 | PF02991 | 0.307 |
LIG_LIR_Nem_3 | 309 | 314 | PF02991 | 0.343 |
LIG_LIR_Nem_3 | 567 | 573 | PF02991 | 0.268 |
LIG_LIR_Nem_3 | 593 | 599 | PF02991 | 0.276 |
LIG_MYND_1 | 49 | 53 | PF01753 | 0.558 |
LIG_Pex14_2 | 237 | 241 | PF04695 | 0.416 |
LIG_Pex14_2 | 658 | 662 | PF04695 | 0.463 |
LIG_PTB_Apo_2 | 410 | 417 | PF02174 | 0.453 |
LIG_PTB_Phospho_1 | 410 | 416 | PF10480 | 0.453 |
LIG_SH2_CRK | 290 | 294 | PF00017 | 0.299 |
LIG_SH2_GRB2like | 411 | 414 | PF00017 | 0.453 |
LIG_SH2_STAP1 | 222 | 226 | PF00017 | 0.417 |
LIG_SH2_STAP1 | 570 | 574 | PF00017 | 0.268 |
LIG_SH2_STAT5 | 123 | 126 | PF00017 | 0.323 |
LIG_SH2_STAT5 | 176 | 179 | PF00017 | 0.307 |
LIG_SH2_STAT5 | 215 | 218 | PF00017 | 0.369 |
LIG_SH2_STAT5 | 23 | 26 | PF00017 | 0.567 |
LIG_SH2_STAT5 | 411 | 414 | PF00017 | 0.293 |
LIG_SH2_STAT5 | 76 | 79 | PF00017 | 0.307 |
LIG_SH3_1 | 59 | 65 | PF00018 | 0.523 |
LIG_SH3_3 | 213 | 219 | PF00018 | 0.440 |
LIG_SH3_3 | 225 | 231 | PF00018 | 0.420 |
LIG_SH3_3 | 357 | 363 | PF00018 | 0.453 |
LIG_SH3_3 | 59 | 65 | PF00018 | 0.523 |
LIG_SH3_3 | 596 | 602 | PF00018 | 0.453 |
LIG_SH3_3 | 638 | 644 | PF00018 | 0.521 |
LIG_SUMO_SIM_par_1 | 282 | 288 | PF11976 | 0.392 |
LIG_SUMO_SIM_par_1 | 471 | 478 | PF11976 | 0.412 |
LIG_TRAF2_1 | 338 | 341 | PF00917 | 0.415 |
LIG_TRAF2_1 | 42 | 45 | PF00917 | 0.592 |
LIG_TRAF2_1 | 665 | 668 | PF00917 | 0.473 |
LIG_TRFH_1 | 619 | 623 | PF08558 | 0.453 |
MOD_CDK_SPK_2 | 35 | 40 | PF00069 | 0.539 |
MOD_CDK_SPxxK_3 | 367 | 374 | PF00069 | 0.428 |
MOD_CK1_1 | 122 | 128 | PF00069 | 0.307 |
MOD_CK1_1 | 143 | 149 | PF00069 | 0.397 |
MOD_CK1_1 | 194 | 200 | PF00069 | 0.394 |
MOD_CK1_1 | 309 | 315 | PF00069 | 0.428 |
MOD_CK1_1 | 387 | 393 | PF00069 | 0.443 |
MOD_CK1_1 | 397 | 403 | PF00069 | 0.330 |
MOD_CK1_1 | 536 | 542 | PF00069 | 0.463 |
MOD_CK1_1 | 564 | 570 | PF00069 | 0.371 |
MOD_CK1_1 | 654 | 660 | PF00069 | 0.514 |
MOD_CK2_1 | 282 | 288 | PF00069 | 0.453 |
MOD_CK2_1 | 39 | 45 | PF00069 | 0.597 |
MOD_CK2_1 | 523 | 529 | PF00069 | 0.393 |
MOD_CK2_1 | 537 | 543 | PF00069 | 0.230 |
MOD_GlcNHglycan | 136 | 139 | PF01048 | 0.391 |
MOD_GlcNHglycan | 15 | 18 | PF01048 | 0.649 |
MOD_GlcNHglycan | 161 | 164 | PF01048 | 0.453 |
MOD_GlcNHglycan | 196 | 199 | PF01048 | 0.420 |
MOD_GlcNHglycan | 222 | 225 | PF01048 | 0.264 |
MOD_GlcNHglycan | 24 | 27 | PF01048 | 0.593 |
MOD_GlcNHglycan | 396 | 399 | PF01048 | 0.422 |
MOD_GlcNHglycan | 654 | 657 | PF01048 | 0.417 |
MOD_GlcNHglycan | 668 | 672 | PF01048 | 0.412 |
MOD_GlcNHglycan | 90 | 93 | PF01048 | 0.418 |
MOD_GSK3_1 | 118 | 125 | PF00069 | 0.315 |
MOD_GSK3_1 | 194 | 201 | PF00069 | 0.407 |
MOD_GSK3_1 | 35 | 42 | PF00069 | 0.541 |
MOD_GSK3_1 | 380 | 387 | PF00069 | 0.344 |
MOD_GSK3_1 | 394 | 401 | PF00069 | 0.286 |
MOD_GSK3_1 | 453 | 460 | PF00069 | 0.392 |
MOD_GSK3_1 | 47 | 54 | PF00069 | 0.314 |
MOD_GSK3_1 | 523 | 530 | PF00069 | 0.305 |
MOD_GSK3_1 | 533 | 540 | PF00069 | 0.270 |
MOD_GSK3_1 | 561 | 568 | PF00069 | 0.453 |
MOD_GSK3_1 | 622 | 629 | PF00069 | 0.481 |
MOD_GSK3_1 | 640 | 647 | PF00069 | 0.375 |
MOD_GSK3_1 | 650 | 657 | PF00069 | 0.533 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.418 |
MOD_N-GLC_1 | 241 | 246 | PF02516 | 0.342 |
MOD_NEK2_1 | 129 | 134 | PF00069 | 0.405 |
MOD_NEK2_1 | 159 | 164 | PF00069 | 0.342 |
MOD_NEK2_1 | 166 | 171 | PF00069 | 0.299 |
MOD_NEK2_1 | 205 | 210 | PF00069 | 0.307 |
MOD_NEK2_1 | 22 | 27 | PF00069 | 0.623 |
MOD_NEK2_1 | 220 | 225 | PF00069 | 0.307 |
MOD_NEK2_1 | 232 | 237 | PF00069 | 0.284 |
MOD_NEK2_1 | 240 | 245 | PF00069 | 0.307 |
MOD_NEK2_1 | 272 | 277 | PF00069 | 0.424 |
MOD_NEK2_1 | 384 | 389 | PF00069 | 0.388 |
MOD_NEK2_1 | 528 | 533 | PF00069 | 0.430 |
MOD_NEK2_1 | 537 | 542 | PF00069 | 0.444 |
MOD_NEK2_1 | 628 | 633 | PF00069 | 0.392 |
MOD_NEK2_1 | 69 | 74 | PF00069 | 0.380 |
MOD_PIKK_1 | 232 | 238 | PF00454 | 0.335 |
MOD_PIKK_1 | 541 | 547 | PF00454 | 0.404 |
MOD_PK_1 | 369 | 375 | PF00069 | 0.389 |
MOD_PK_1 | 382 | 388 | PF00069 | 0.221 |
MOD_PKA_1 | 457 | 463 | PF00069 | 0.371 |
MOD_PKA_2 | 111 | 117 | PF00069 | 0.404 |
MOD_PKA_2 | 39 | 45 | PF00069 | 0.580 |
MOD_PKA_2 | 453 | 459 | PF00069 | 0.369 |
MOD_PKA_2 | 462 | 468 | PF00069 | 0.358 |
MOD_PKA_2 | 541 | 547 | PF00069 | 0.423 |
MOD_PKA_2 | 564 | 570 | PF00069 | 0.445 |
MOD_PKA_2 | 576 | 582 | PF00069 | 0.362 |
MOD_Plk_1 | 129 | 135 | PF00069 | 0.433 |
MOD_Plk_1 | 232 | 238 | PF00069 | 0.290 |
MOD_Plk_1 | 241 | 247 | PF00069 | 0.293 |
MOD_Plk_1 | 306 | 312 | PF00069 | 0.380 |
MOD_Plk_1 | 339 | 345 | PF00069 | 0.411 |
MOD_Plk_1 | 380 | 386 | PF00069 | 0.332 |
MOD_Plk_1 | 398 | 404 | PF00069 | 0.307 |
MOD_Plk_1 | 483 | 489 | PF00069 | 0.418 |
MOD_Plk_1 | 528 | 534 | PF00069 | 0.453 |
MOD_Plk_1 | 667 | 673 | PF00069 | 0.509 |
MOD_Plk_2-3 | 462 | 468 | PF00069 | 0.350 |
MOD_Plk_4 | 119 | 125 | PF00069 | 0.316 |
MOD_Plk_4 | 306 | 312 | PF00069 | 0.463 |
MOD_Plk_4 | 339 | 345 | PF00069 | 0.417 |
MOD_Plk_4 | 47 | 53 | PF00069 | 0.440 |
MOD_Plk_4 | 633 | 639 | PF00069 | 0.494 |
MOD_ProDKin_1 | 215 | 221 | PF00069 | 0.346 |
MOD_ProDKin_1 | 35 | 41 | PF00069 | 0.593 |
MOD_ProDKin_1 | 359 | 365 | PF00069 | 0.445 |
MOD_ProDKin_1 | 367 | 373 | PF00069 | 0.403 |
MOD_ProDKin_1 | 45 | 51 | PF00069 | 0.522 |
MOD_ProDKin_1 | 475 | 481 | PF00069 | 0.445 |
MOD_ProDKin_1 | 640 | 646 | PF00069 | 0.530 |
MOD_ProDKin_1 | 78 | 84 | PF00069 | 0.350 |
MOD_SUMO_for_1 | 100 | 103 | PF00179 | 0.268 |
MOD_SUMO_rev_2 | 252 | 257 | PF00179 | 0.397 |
TRG_DiLeu_BaEn_1 | 340 | 345 | PF01217 | 0.440 |
TRG_DiLeu_BaEn_1 | 668 | 673 | PF01217 | 0.511 |
TRG_DiLeu_BaEn_2 | 528 | 534 | PF01217 | 0.453 |
TRG_ENDOCYTIC_2 | 290 | 293 | PF00928 | 0.307 |
TRG_ENDOCYTIC_2 | 570 | 573 | PF00928 | 0.268 |
TRG_ER_diArg_1 | 111 | 113 | PF00400 | 0.428 |
TRG_ER_diArg_1 | 408 | 410 | PF00400 | 0.412 |
TRG_ER_diArg_1 | 457 | 459 | PF00400 | 0.332 |
TRG_ER_diArg_1 | 515 | 517 | PF00400 | 0.345 |
TRG_Pf-PMV_PEXEL_1 | 410 | 414 | PF00026 | 0.397 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IK11 | Leptomonas seymouri | 60% | 100% |
A0A0S4JAG1 | Bodo saltans | 23% | 93% |
A0A0S4JRH6 | Bodo saltans | 37% | 99% |
A0A0S4JRL8 | Bodo saltans | 23% | 84% |
A0A0S4KE24 | Bodo saltans | 21% | 82% |
A0A1X0NT49 | Trypanosomatidae | 22% | 91% |
A0A1X0NT60 | Trypanosomatidae | 40% | 99% |
A0A1X0P523 | Trypanosomatidae | 22% | 89% |
A0A1X0P5Y2 | Trypanosomatidae | 27% | 85% |
A0A3S5IQT1 | Trypanosoma rangeli | 24% | 90% |
A0A422NSK2 | Trypanosoma rangeli | 36% | 100% |
A4HC81 | Leishmania braziliensis | 84% | 100% |
A4HHE2 | Leishmania braziliensis | 23% | 100% |
A4HZQ9 | Leishmania infantum | 99% | 100% |
B2ZGJ1 | Danio rerio | 23% | 100% |
C9ZRI9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 100% |
D0A627 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 22% | 88% |
E9AVL5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
O19094 | Bos taurus | 25% | 100% |
P07668 | Drosophila melanogaster | 24% | 94% |
P11466 | Rattus norvegicus | 25% | 100% |
P13222 | Sus scrofa | 24% | 100% |
P18886 | Rattus norvegicus | 30% | 100% |
P23786 | Homo sapiens | 29% | 100% |
P28329 | Homo sapiens | 24% | 90% |
P32198 | Rattus norvegicus | 24% | 87% |
P32738 | Rattus norvegicus | 24% | 100% |
P43155 | Homo sapiens | 22% | 100% |
P47934 | Mus musculus | 22% | 100% |
P52825 | Mus musculus | 29% | 100% |
P52826 | Columba livia | 25% | 100% |
P80235 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 22% | 98% |
Q00614 | Candida tropicalis | 21% | 100% |
Q03059 | Mus musculus | 25% | 100% |
Q2KJB7 | Bos taurus | 29% | 100% |
Q4QBW4 | Leishmania major | 92% | 100% |
Q58DK1 | Bos taurus | 22% | 88% |
Q5U3U3 | Danio rerio | 29% | 100% |
Q60HG9 | Macaca fascicularis | 29% | 100% |
Q63704 | Rattus norvegicus | 23% | 88% |
Q68Y62 | Equus caballus | 23% | 87% |
Q6P4X5 | Xenopus tropicalis | 27% | 100% |
Q704S8 | Rattus norvegicus | 23% | 100% |
Q7ZXE1 | Xenopus laevis | 27% | 100% |
Q8HY46 | Sus scrofa | 23% | 88% |
Q90YJ9 | Gallus gallus | 25% | 100% |
Q924X2 | Mus musculus | 22% | 88% |
Q92523 | Homo sapiens | 23% | 88% |
Q9DC50 | Mus musculus | 25% | 100% |
Q9UKG9 | Homo sapiens | 24% | 100% |
V5BH74 | Trypanosoma cruzi | 25% | 100% |
V5BQH8 | Trypanosoma cruzi | 22% | 85% |
V5D4R1 | Trypanosoma cruzi | 25% | 85% |
V5DBT5 | Trypanosoma cruzi | 39% | 100% |