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: E9AVL5
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 | 277 | 281 | PF00656 | 0.364 |
CLV_C14_Caspase3-7 | 403 | 407 | PF00656 | 0.341 |
CLV_MEL_PAP_1 | 457 | 463 | PF00089 | 0.267 |
CLV_NRD_NRD_1 | 114 | 116 | PF00675 | 0.427 |
CLV_NRD_NRD_1 | 411 | 413 | PF00675 | 0.395 |
CLV_NRD_NRD_1 | 429 | 431 | PF00675 | 0.188 |
CLV_NRD_NRD_1 | 459 | 461 | PF00675 | 0.337 |
CLV_NRD_NRD_1 | 518 | 520 | PF00675 | 0.427 |
CLV_PCSK_KEX2_1 | 114 | 116 | PF00082 | 0.427 |
CLV_PCSK_KEX2_1 | 157 | 159 | PF00082 | 0.242 |
CLV_PCSK_KEX2_1 | 197 | 199 | PF00082 | 0.438 |
CLV_PCSK_KEX2_1 | 411 | 413 | PF00082 | 0.370 |
CLV_PCSK_KEX2_1 | 459 | 461 | PF00082 | 0.364 |
CLV_PCSK_KEX2_1 | 518 | 520 | PF00082 | 0.427 |
CLV_PCSK_PC1ET2_1 | 157 | 159 | PF00082 | 0.307 |
CLV_PCSK_PC1ET2_1 | 197 | 199 | PF00082 | 0.438 |
CLV_PCSK_SKI1_1 | 138 | 142 | PF00082 | 0.438 |
CLV_PCSK_SKI1_1 | 158 | 162 | PF00082 | 0.124 |
CLV_PCSK_SKI1_1 | 77 | 81 | PF00082 | 0.291 |
DEG_APCC_DBOX_1 | 1 | 9 | PF00400 | 0.555 |
DEG_SCF_FBW7_1 | 527 | 533 | PF00400 | 0.243 |
DEG_SCF_FBW7_2 | 481 | 486 | PF00400 | 0.451 |
DEG_SPOP_SBC_1 | 653 | 657 | PF00917 | 0.556 |
DOC_ANK_TNKS_1 | 187 | 194 | PF00023 | 0.453 |
DOC_CDC14_PxL_1 | 586 | 594 | PF14671 | 0.410 |
DOC_CKS1_1 | 218 | 223 | PF01111 | 0.427 |
DOC_CKS1_1 | 527 | 532 | PF01111 | 0.247 |
DOC_CKS1_1 | 85 | 90 | PF01111 | 0.366 |
DOC_CYCLIN_yCln2_LP_2 | 66 | 72 | PF00134 | 0.467 |
DOC_MAPK_DCC_7 | 257 | 267 | PF00069 | 0.281 |
DOC_MAPK_gen_1 | 136 | 143 | PF00069 | 0.433 |
DOC_MAPK_gen_1 | 459 | 470 | PF00069 | 0.404 |
DOC_MAPK_gen_1 | 518 | 527 | PF00069 | 0.414 |
DOC_MAPK_MEF2A_6 | 61 | 68 | PF00069 | 0.523 |
DOC_PP1_RVXF_1 | 255 | 262 | PF00149 | 0.395 |
DOC_PP1_RVXF_1 | 438 | 445 | PF00149 | 0.322 |
DOC_PP2B_LxvP_1 | 48 | 51 | PF13499 | 0.414 |
DOC_PP2B_LxvP_1 | 66 | 69 | PF13499 | 0.311 |
DOC_PP2B_LxvP_1 | 674 | 677 | PF13499 | 0.473 |
DOC_USP7_MATH_1 | 121 | 125 | PF00917 | 0.453 |
DOC_USP7_MATH_1 | 142 | 146 | PF00917 | 0.392 |
DOC_USP7_MATH_1 | 400 | 404 | PF00917 | 0.427 |
DOC_USP7_MATH_1 | 423 | 427 | PF00917 | 0.427 |
DOC_USP7_MATH_1 | 653 | 657 | PF00917 | 0.459 |
DOC_USP7_MATH_1 | 92 | 96 | PF00917 | 0.427 |
DOC_USP7_UBL2_3 | 559 | 563 | PF12436 | 0.328 |
DOC_WW_Pin1_4 | 217 | 222 | PF00397 | 0.346 |
DOC_WW_Pin1_4 | 361 | 366 | PF00397 | 0.444 |
DOC_WW_Pin1_4 | 369 | 374 | PF00397 | 0.403 |
DOC_WW_Pin1_4 | 37 | 42 | PF00397 | 0.644 |
DOC_WW_Pin1_4 | 477 | 482 | PF00397 | 0.446 |
DOC_WW_Pin1_4 | 526 | 531 | PF00397 | 0.388 |
DOC_WW_Pin1_4 | 80 | 85 | PF00397 | 0.350 |
LIG_14-3-3_CanoR_1 | 114 | 121 | PF00244 | 0.403 |
LIG_14-3-3_CanoR_1 | 144 | 150 | PF00244 | 0.458 |
LIG_14-3-3_CanoR_1 | 325 | 329 | PF00244 | 0.189 |
LIG_14-3-3_CanoR_1 | 42 | 46 | PF00244 | 0.516 |
LIG_14-3-3_CanoR_1 | 518 | 527 | PF00244 | 0.409 |
LIG_14-3-3_CanoR_1 | 540 | 544 | PF00244 | 0.364 |
LIG_14-3-3_CanoR_1 | 567 | 573 | PF00244 | 0.446 |
LIG_14-3-3_CanoR_1 | 579 | 586 | PF00244 | 0.334 |
LIG_14-3-3_CanoR_1 | 634 | 640 | PF00244 | 0.544 |
LIG_14-3-3_CanoR_1 | 77 | 85 | PF00244 | 0.247 |
LIG_Actin_WH2_2 | 281 | 298 | PF00022 | 0.427 |
LIG_BRCT_BRCA1_1 | 127 | 131 | PF00533 | 0.427 |
LIG_BRCT_BRCA1_1 | 170 | 174 | PF00533 | 0.307 |
LIG_BRCT_BRCA1_1 | 218 | 222 | PF00533 | 0.404 |
LIG_BRCT_BRCA1_1 | 531 | 535 | PF00533 | 0.295 |
LIG_BRCT_BRCA1_1 | 656 | 660 | PF00533 | 0.505 |
LIG_BRCT_BRCA1_2 | 170 | 176 | PF00533 | 0.392 |
LIG_CtBP_PxDLS_1 | 233 | 237 | PF00389 | 0.307 |
LIG_eIF4E_1 | 125 | 131 | PF01652 | 0.427 |
LIG_FHA_1 | 121 | 127 | PF00498 | 0.296 |
LIG_FHA_1 | 146 | 152 | PF00498 | 0.389 |
LIG_FHA_1 | 208 | 214 | PF00498 | 0.295 |
LIG_FHA_1 | 218 | 224 | PF00498 | 0.326 |
LIG_FHA_1 | 299 | 305 | PF00498 | 0.165 |
LIG_FHA_1 | 324 | 330 | PF00498 | 0.341 |
LIG_FHA_1 | 434 | 440 | PF00498 | 0.301 |
LIG_FHA_1 | 456 | 462 | PF00498 | 0.376 |
LIG_FHA_1 | 480 | 486 | PF00498 | 0.384 |
LIG_FHA_1 | 531 | 537 | PF00498 | 0.372 |
LIG_FHA_2 | 275 | 281 | PF00498 | 0.317 |
LIG_FHA_2 | 42 | 48 | PF00498 | 0.577 |
LIG_FHA_2 | 526 | 532 | PF00498 | 0.391 |
LIG_Integrin_RGD_1 | 393 | 395 | PF01839 | 0.453 |
LIG_LIR_Apic_2 | 591 | 596 | PF02991 | 0.392 |
LIG_LIR_Gen_1 | 237 | 243 | PF02991 | 0.352 |
LIG_LIR_Gen_1 | 27 | 38 | PF02991 | 0.556 |
LIG_LIR_Gen_1 | 289 | 299 | PF02991 | 0.299 |
LIG_LIR_Gen_1 | 311 | 317 | PF02991 | 0.380 |
LIG_LIR_Gen_1 | 569 | 580 | PF02991 | 0.267 |
LIG_LIR_Gen_1 | 595 | 606 | PF02991 | 0.312 |
LIG_LIR_Nem_3 | 171 | 177 | PF02991 | 0.377 |
LIG_LIR_Nem_3 | 237 | 242 | PF02991 | 0.352 |
LIG_LIR_Nem_3 | 27 | 33 | PF02991 | 0.504 |
LIG_LIR_Nem_3 | 289 | 295 | PF02991 | 0.299 |
LIG_LIR_Nem_3 | 311 | 316 | PF02991 | 0.359 |
LIG_LIR_Nem_3 | 569 | 575 | PF02991 | 0.267 |
LIG_LIR_Nem_3 | 595 | 601 | PF02991 | 0.276 |
LIG_MYND_1 | 51 | 55 | PF01753 | 0.557 |
LIG_PCNA_yPIPBox_3 | 588 | 601 | PF02747 | 0.329 |
LIG_Pex14_2 | 239 | 243 | PF04695 | 0.405 |
LIG_Pex14_2 | 660 | 664 | PF04695 | 0.473 |
LIG_PTB_Apo_2 | 412 | 419 | PF02174 | 0.453 |
LIG_PTB_Phospho_1 | 412 | 418 | PF10480 | 0.453 |
LIG_SH2_CRK | 292 | 296 | PF00017 | 0.307 |
LIG_SH2_GRB2like | 413 | 416 | PF00017 | 0.453 |
LIG_SH2_STAP1 | 572 | 576 | PF00017 | 0.267 |
LIG_SH2_STAT5 | 125 | 128 | PF00017 | 0.322 |
LIG_SH2_STAT5 | 178 | 181 | PF00017 | 0.301 |
LIG_SH2_STAT5 | 217 | 220 | PF00017 | 0.402 |
LIG_SH2_STAT5 | 25 | 28 | PF00017 | 0.640 |
LIG_SH2_STAT5 | 413 | 416 | PF00017 | 0.307 |
LIG_SH2_STAT5 | 621 | 624 | PF00017 | 0.350 |
LIG_SH2_STAT5 | 78 | 81 | PF00017 | 0.307 |
LIG_SH3_1 | 61 | 67 | PF00018 | 0.525 |
LIG_SH3_3 | 215 | 221 | PF00018 | 0.453 |
LIG_SH3_3 | 227 | 233 | PF00018 | 0.255 |
LIG_SH3_3 | 300 | 306 | PF00018 | 0.199 |
LIG_SH3_3 | 359 | 365 | PF00018 | 0.456 |
LIG_SH3_3 | 598 | 604 | PF00018 | 0.453 |
LIG_SH3_3 | 61 | 67 | PF00018 | 0.525 |
LIG_SH3_3 | 640 | 646 | PF00018 | 0.512 |
LIG_SUMO_SIM_anti_2 | 395 | 403 | PF11976 | 0.227 |
LIG_SUMO_SIM_par_1 | 284 | 290 | PF11976 | 0.409 |
LIG_TRAF2_1 | 340 | 343 | PF00917 | 0.414 |
LIG_TRAF2_1 | 44 | 47 | PF00917 | 0.594 |
LIG_TRAF2_1 | 667 | 670 | PF00917 | 0.420 |
LIG_TRFH_1 | 621 | 625 | PF08558 | 0.453 |
MOD_CDK_SPK_2 | 37 | 42 | PF00069 | 0.586 |
MOD_CDK_SPxxK_3 | 369 | 376 | PF00069 | 0.427 |
MOD_CK1_1 | 124 | 130 | PF00069 | 0.302 |
MOD_CK1_1 | 145 | 151 | PF00069 | 0.377 |
MOD_CK1_1 | 196 | 202 | PF00069 | 0.377 |
MOD_CK1_1 | 311 | 317 | PF00069 | 0.398 |
MOD_CK1_1 | 389 | 395 | PF00069 | 0.448 |
MOD_CK1_1 | 526 | 532 | PF00069 | 0.374 |
MOD_CK1_1 | 538 | 544 | PF00069 | 0.428 |
MOD_CK1_1 | 566 | 572 | PF00069 | 0.370 |
MOD_CK1_1 | 599 | 605 | PF00069 | 0.308 |
MOD_CK2_1 | 284 | 290 | PF00069 | 0.453 |
MOD_CK2_1 | 41 | 47 | PF00069 | 0.594 |
MOD_CK2_1 | 525 | 531 | PF00069 | 0.438 |
MOD_CK2_1 | 539 | 545 | PF00069 | 0.236 |
MOD_GlcNHglycan | 138 | 141 | PF01048 | 0.391 |
MOD_GlcNHglycan | 15 | 18 | PF01048 | 0.690 |
MOD_GlcNHglycan | 163 | 166 | PF01048 | 0.466 |
MOD_GlcNHglycan | 198 | 201 | PF01048 | 0.395 |
MOD_GlcNHglycan | 26 | 29 | PF01048 | 0.660 |
MOD_GlcNHglycan | 656 | 659 | PF01048 | 0.419 |
MOD_GlcNHglycan | 670 | 674 | PF01048 | 0.452 |
MOD_GlcNHglycan | 94 | 97 | PF01048 | 0.368 |
MOD_GSK3_1 | 120 | 127 | PF00069 | 0.307 |
MOD_GSK3_1 | 192 | 199 | PF00069 | 0.428 |
MOD_GSK3_1 | 37 | 44 | PF00069 | 0.575 |
MOD_GSK3_1 | 382 | 389 | PF00069 | 0.346 |
MOD_GSK3_1 | 455 | 462 | PF00069 | 0.403 |
MOD_GSK3_1 | 49 | 56 | PF00069 | 0.312 |
MOD_GSK3_1 | 519 | 526 | PF00069 | 0.440 |
MOD_GSK3_1 | 535 | 542 | PF00069 | 0.274 |
MOD_GSK3_1 | 563 | 570 | PF00069 | 0.453 |
MOD_GSK3_1 | 624 | 631 | PF00069 | 0.493 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.383 |
MOD_GSK3_1 | 90 | 97 | PF00069 | 0.384 |
MOD_N-GLC_1 | 243 | 248 | PF02516 | 0.318 |
MOD_NEK2_1 | 131 | 136 | PF00069 | 0.405 |
MOD_NEK2_1 | 161 | 166 | PF00069 | 0.341 |
MOD_NEK2_1 | 168 | 173 | PF00069 | 0.299 |
MOD_NEK2_1 | 207 | 212 | PF00069 | 0.307 |
MOD_NEK2_1 | 234 | 239 | PF00069 | 0.288 |
MOD_NEK2_1 | 242 | 247 | PF00069 | 0.274 |
MOD_NEK2_1 | 274 | 279 | PF00069 | 0.423 |
MOD_NEK2_1 | 386 | 391 | PF00069 | 0.390 |
MOD_NEK2_1 | 399 | 404 | PF00069 | 0.291 |
MOD_NEK2_1 | 535 | 540 | PF00069 | 0.439 |
MOD_NEK2_1 | 630 | 635 | PF00069 | 0.403 |
MOD_NEK2_1 | 71 | 76 | PF00069 | 0.380 |
MOD_NEK2_1 | 91 | 96 | PF00069 | 0.124 |
MOD_NEK2_2 | 619 | 624 | PF00069 | 0.267 |
MOD_PIKK_1 | 234 | 240 | PF00454 | 0.332 |
MOD_PIKK_1 | 543 | 549 | PF00454 | 0.453 |
MOD_PK_1 | 371 | 377 | PF00069 | 0.398 |
MOD_PK_1 | 384 | 390 | PF00069 | 0.210 |
MOD_PKA_1 | 459 | 465 | PF00069 | 0.370 |
MOD_PKA_2 | 113 | 119 | PF00069 | 0.403 |
MOD_PKA_2 | 324 | 330 | PF00069 | 0.189 |
MOD_PKA_2 | 41 | 47 | PF00069 | 0.577 |
MOD_PKA_2 | 455 | 461 | PF00069 | 0.379 |
MOD_PKA_2 | 464 | 470 | PF00069 | 0.341 |
MOD_PKA_2 | 539 | 545 | PF00069 | 0.422 |
MOD_PKA_2 | 566 | 572 | PF00069 | 0.445 |
MOD_PKA_2 | 578 | 584 | PF00069 | 0.362 |
MOD_Plk_1 | 131 | 137 | PF00069 | 0.432 |
MOD_Plk_1 | 234 | 240 | PF00069 | 0.302 |
MOD_Plk_1 | 243 | 249 | PF00069 | 0.273 |
MOD_Plk_1 | 308 | 314 | PF00069 | 0.380 |
MOD_Plk_1 | 341 | 347 | PF00069 | 0.410 |
MOD_Plk_1 | 382 | 388 | PF00069 | 0.333 |
MOD_Plk_1 | 400 | 406 | PF00069 | 0.307 |
MOD_Plk_1 | 485 | 491 | PF00069 | 0.392 |
MOD_Plk_1 | 530 | 536 | PF00069 | 0.453 |
MOD_Plk_1 | 613 | 619 | PF00069 | 0.466 |
MOD_Plk_1 | 669 | 675 | PF00069 | 0.512 |
MOD_Plk_2-3 | 464 | 470 | PF00069 | 0.350 |
MOD_Plk_4 | 121 | 127 | PF00069 | 0.316 |
MOD_Plk_4 | 308 | 314 | PF00069 | 0.463 |
MOD_Plk_4 | 324 | 330 | PF00069 | 0.310 |
MOD_Plk_4 | 341 | 347 | PF00069 | 0.416 |
MOD_Plk_4 | 49 | 55 | PF00069 | 0.438 |
MOD_Plk_4 | 635 | 641 | PF00069 | 0.513 |
MOD_ProDKin_1 | 217 | 223 | PF00069 | 0.346 |
MOD_ProDKin_1 | 361 | 367 | PF00069 | 0.444 |
MOD_ProDKin_1 | 369 | 375 | PF00069 | 0.403 |
MOD_ProDKin_1 | 37 | 43 | PF00069 | 0.633 |
MOD_ProDKin_1 | 477 | 483 | PF00069 | 0.446 |
MOD_ProDKin_1 | 526 | 532 | PF00069 | 0.388 |
MOD_ProDKin_1 | 80 | 86 | PF00069 | 0.350 |
MOD_SUMO_for_1 | 102 | 105 | PF00179 | 0.267 |
MOD_SUMO_rev_2 | 254 | 259 | PF00179 | 0.397 |
TRG_DiLeu_BaEn_1 | 342 | 347 | PF01217 | 0.440 |
TRG_DiLeu_BaEn_1 | 670 | 675 | PF01217 | 0.516 |
TRG_DiLeu_BaEn_2 | 530 | 536 | PF01217 | 0.453 |
TRG_ENDOCYTIC_2 | 292 | 295 | PF00928 | 0.307 |
TRG_ENDOCYTIC_2 | 572 | 575 | PF00928 | 0.267 |
TRG_ER_diArg_1 | 113 | 115 | PF00400 | 0.427 |
TRG_ER_diArg_1 | 410 | 412 | PF00400 | 0.412 |
TRG_ER_diArg_1 | 459 | 461 | PF00400 | 0.339 |
TRG_ER_diArg_1 | 517 | 519 | PF00400 | 0.344 |
TRG_ER_diArg_1 | 6 | 9 | PF00400 | 0.619 |
TRG_Pf-PMV_PEXEL_1 | 107 | 111 | PF00026 | 0.281 |
TRG_Pf-PMV_PEXEL_1 | 412 | 416 | PF00026 | 0.427 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IK11 | Leptomonas seymouri | 61% | 100% |
A0A0S4JAG1 | Bodo saltans | 23% | 93% |
A0A0S4JRH6 | Bodo saltans | 38% | 99% |
A0A0S4JRL8 | Bodo saltans | 24% | 84% |
A0A0S4KE24 | Bodo saltans | 21% | 82% |
A0A1X0NT49 | Trypanosomatidae | 22% | 91% |
A0A1X0NT60 | Trypanosomatidae | 38% | 100% |
A0A1X0NZS6 | Trypanosomatidae | 23% | 100% |
A0A1X0P523 | Trypanosomatidae | 22% | 89% |
A0A1X0P5Y2 | Trypanosomatidae | 25% | 86% |
A0A3S5IQT1 | Trypanosoma rangeli | 23% | 91% |
A0A3S7WX31 | Leishmania donovani | 92% | 100% |
A0A422NSK2 | Trypanosoma rangeli | 36% | 100% |
A4HC81 | Leishmania braziliensis | 83% | 100% |
A4HHE2 | Leishmania braziliensis | 24% | 100% |
A4HZQ9 | Leishmania infantum | 92% | 100% |
B2ZGJ1 | Danio rerio | 23% | 100% |
C9ZL75 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 25% | 100% |
C9ZRI9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 100% |
D0A627 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 23% | 88% |
F1LN46 | Rattus norvegicus | 23% | 85% |
O19094 | Bos taurus | 25% | 100% |
P07668 | Drosophila melanogaster | 25% | 94% |
P11466 | Rattus norvegicus | 26% | 100% |
P13222 | Sus scrofa | 25% | 100% |
P18886 | Rattus norvegicus | 30% | 100% |
P23786 | Homo sapiens | 30% | 100% |
P28329 | Homo sapiens | 26% | 91% |
P32198 | Rattus norvegicus | 24% | 88% |
P32738 | Rattus norvegicus | 25% | 100% |
P32756 | Caenorhabditis elegans | 23% | 100% |
P32796 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 22% | 100% |
P43155 | Homo sapiens | 23% | 100% |
P47934 | Mus musculus | 22% | 100% |
P52825 | Mus musculus | 30% | 100% |
P52826 | Columba livia | 25% | 100% |
P80235 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 23% | 99% |
P97742 | Mus musculus | 25% | 88% |
Q00614 | Candida tropicalis | 21% | 100% |
Q03059 | Mus musculus | 26% | 100% |
Q2KJB7 | Bos taurus | 30% | 100% |
Q4QBW4 | Leishmania major | 90% | 100% |
Q58DK1 | Bos taurus | 22% | 88% |
Q5U3U3 | Danio rerio | 30% | 100% |
Q60HG9 | Macaca fascicularis | 30% | 100% |
Q63704 | Rattus norvegicus | 22% | 88% |
Q68Y62 | Equus caballus | 24% | 87% |
Q6P4X5 | Xenopus tropicalis | 27% | 100% |
Q704S8 | Rattus norvegicus | 23% | 100% |
Q7ZXE1 | Xenopus laevis | 28% | 100% |
Q8BGD5 | Mus musculus | 23% | 85% |
Q8HY46 | Sus scrofa | 23% | 88% |
Q8TCG5 | Homo sapiens | 25% | 84% |
Q90YJ9 | Gallus gallus | 25% | 100% |
Q924X2 | Mus musculus | 22% | 88% |
Q92523 | Homo sapiens | 23% | 88% |
Q9DC50 | Mus musculus | 26% | 100% |
Q9UKG9 | Homo sapiens | 25% | 100% |
V5BH74 | Trypanosoma cruzi | 25% | 100% |
V5BQH8 | Trypanosoma cruzi | 22% | 85% |
V5DBT5 | Trypanosoma cruzi | 39% | 100% |