Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 4 |
Forrest at al. (procyclic) | no | yes: 4 |
Silverman et al. | no | yes: 0 |
Pissara et al. | yes | yes: 15 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | yes | yes: 5 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 10 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 2 |
GO:0005852 | eukaryotic translation initiation factor 3 complex | 2 | 12 |
GO:0016020 | membrane | 2 | 3 |
GO:0016282 | eukaryotic 43S preinitiation complex | 4 | 6 |
GO:0032991 | protein-containing complex | 1 | 12 |
GO:0033290 | eukaryotic 48S preinitiation complex | 4 | 6 |
GO:0070993 | translation preinitiation complex | 3 | 6 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
GO:1990904 | ribonucleoprotein complex | 2 | 6 |
Related structures:
AlphaFold database: Q4Q253
Term | Name | Level | Count |
---|---|---|---|
GO:0001732 | formation of cytoplasmic translation initiation complex | 7 | 6 |
GO:0006413 | translational initiation | 3 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009987 | cellular process | 1 | 6 |
GO:0016043 | cellular component organization | 3 | 6 |
GO:0022607 | cellular component assembly | 4 | 6 |
GO:0022618 | ribonucleoprotein complex assembly | 6 | 6 |
GO:0043933 | protein-containing complex organization | 4 | 6 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0065003 | protein-containing complex assembly | 5 | 6 |
GO:0071826 | ribonucleoprotein complex subunit organization | 5 | 6 |
GO:0071840 | cellular component organization or biogenesis | 2 | 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003676 | nucleic acid binding | 3 | 12 |
GO:0003743 | translation initiation factor activity | 4 | 12 |
GO:0005488 | binding | 1 | 12 |
GO:0008135 | translation factor activity, RNA binding | 3 | 12 |
GO:0045182 | translation regulator activity | 1 | 12 |
GO:0090079 | translation regulator activity, nucleic acid binding | 2 | 12 |
GO:0097159 | organic cyclic compound binding | 2 | 12 |
GO:1901363 | heterocyclic compound binding | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 116 | 120 | PF00656 | 0.613 |
CLV_C14_Caspase3-7 | 251 | 255 | PF00656 | 0.625 |
CLV_C14_Caspase3-7 | 391 | 395 | PF00656 | 0.617 |
CLV_MEL_PAP_1 | 318 | 324 | PF00089 | 0.425 |
CLV_NRD_NRD_1 | 117 | 119 | PF00675 | 0.614 |
CLV_NRD_NRD_1 | 351 | 353 | PF00675 | 0.353 |
CLV_NRD_NRD_1 | 361 | 363 | PF00675 | 0.407 |
CLV_NRD_NRD_1 | 395 | 397 | PF00675 | 0.332 |
CLV_NRD_NRD_1 | 452 | 454 | PF00675 | 0.336 |
CLV_NRD_NRD_1 | 561 | 563 | PF00675 | 0.582 |
CLV_NRD_NRD_1 | 576 | 578 | PF00675 | 0.599 |
CLV_NRD_NRD_1 | 585 | 587 | PF00675 | 0.644 |
CLV_PCSK_KEX2_1 | 117 | 119 | PF00082 | 0.614 |
CLV_PCSK_KEX2_1 | 351 | 353 | PF00082 | 0.353 |
CLV_PCSK_KEX2_1 | 361 | 363 | PF00082 | 0.407 |
CLV_PCSK_KEX2_1 | 452 | 454 | PF00082 | 0.345 |
CLV_PCSK_KEX2_1 | 561 | 563 | PF00082 | 0.600 |
CLV_PCSK_KEX2_1 | 576 | 578 | PF00082 | 0.589 |
CLV_PCSK_KEX2_1 | 584 | 586 | PF00082 | 0.657 |
CLV_PCSK_PC1ET2_1 | 561 | 563 | PF00082 | 0.677 |
CLV_PCSK_PC1ET2_1 | 576 | 578 | PF00082 | 0.709 |
CLV_PCSK_PC1ET2_1 | 584 | 586 | PF00082 | 0.820 |
CLV_PCSK_PC7_1 | 113 | 119 | PF00082 | 0.589 |
CLV_PCSK_PC7_1 | 581 | 587 | PF00082 | 0.781 |
CLV_PCSK_SKI1_1 | 177 | 181 | PF00082 | 0.418 |
CLV_PCSK_SKI1_1 | 316 | 320 | PF00082 | 0.332 |
CLV_PCSK_SKI1_1 | 352 | 356 | PF00082 | 0.425 |
CLV_PCSK_SKI1_1 | 417 | 421 | PF00082 | 0.369 |
CLV_PCSK_SKI1_1 | 426 | 430 | PF00082 | 0.315 |
CLV_PCSK_SKI1_1 | 81 | 85 | PF00082 | 0.471 |
CLV_PCSK_SKI1_1 | 89 | 93 | PF00082 | 0.431 |
DEG_APCC_DBOX_1 | 315 | 323 | PF00400 | 0.545 |
DEG_SPOP_SBC_1 | 515 | 519 | PF00917 | 0.625 |
DOC_CKS1_1 | 30 | 35 | PF01111 | 0.579 |
DOC_CYCLIN_RxL_1 | 174 | 182 | PF00134 | 0.432 |
DOC_CYCLIN_yClb3_PxF_3 | 29 | 35 | PF00134 | 0.449 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 384 | 393 | PF00134 | 0.625 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 475 | 482 | PF00134 | 0.625 |
DOC_CYCLIN_yCln2_LP_2 | 14 | 17 | PF00134 | 0.463 |
DOC_MAPK_gen_1 | 289 | 296 | PF00069 | 0.600 |
DOC_MAPK_gen_1 | 351 | 358 | PF00069 | 0.582 |
DOC_MAPK_MEF2A_6 | 147 | 154 | PF00069 | 0.481 |
DOC_MAPK_MEF2A_6 | 289 | 296 | PF00069 | 0.597 |
DOC_MAPK_MEF2A_6 | 351 | 358 | PF00069 | 0.625 |
DOC_PP2B_LxvP_1 | 14 | 17 | PF13499 | 0.463 |
DOC_PP2B_LxvP_1 | 428 | 431 | PF13499 | 0.532 |
DOC_USP7_MATH_1 | 243 | 247 | PF00917 | 0.619 |
DOC_USP7_MATH_1 | 603 | 607 | PF00917 | 0.632 |
DOC_USP7_MATH_1 | 62 | 66 | PF00917 | 0.449 |
DOC_USP7_MATH_1 | 622 | 626 | PF00917 | 0.673 |
DOC_USP7_UBL2_3 | 545 | 549 | PF12436 | 0.666 |
DOC_WW_Pin1_4 | 29 | 34 | PF00397 | 0.577 |
DOC_WW_Pin1_4 | 320 | 325 | PF00397 | 0.614 |
DOC_WW_Pin1_4 | 421 | 426 | PF00397 | 0.521 |
DOC_WW_Pin1_4 | 433 | 438 | PF00397 | 0.521 |
DOC_WW_Pin1_4 | 70 | 75 | PF00397 | 0.510 |
LIG_14-3-3_CanoR_1 | 351 | 357 | PF00244 | 0.545 |
LIG_14-3-3_CanoR_1 | 69 | 74 | PF00244 | 0.508 |
LIG_14-3-3_CanoR_1 | 77 | 83 | PF00244 | 0.467 |
LIG_Actin_WH2_2 | 535 | 550 | PF00022 | 0.757 |
LIG_AP2alpha_1 | 416 | 420 | PF02296 | 0.576 |
LIG_BIR_III_4 | 190 | 194 | PF00653 | 0.555 |
LIG_BRCT_BRCA1_1 | 157 | 161 | PF00533 | 0.514 |
LIG_BRCT_BRCA1_1 | 171 | 175 | PF00533 | 0.480 |
LIG_BRCT_BRCA1_1 | 346 | 350 | PF00533 | 0.532 |
LIG_BRCT_BRCA1_1 | 423 | 427 | PF00533 | 0.521 |
LIG_BRCT_BRCA1_1 | 518 | 522 | PF00533 | 0.588 |
LIG_BRCT_BRCA1_1 | 535 | 539 | PF00533 | 0.608 |
LIG_BRCT_BRCA1_1 | 624 | 628 | PF00533 | 0.770 |
LIG_BRCT_BRCA1_2 | 171 | 177 | PF00533 | 0.521 |
LIG_Clathr_ClatBox_1 | 482 | 486 | PF01394 | 0.607 |
LIG_FHA_1 | 234 | 240 | PF00498 | 0.571 |
LIG_FHA_1 | 275 | 281 | PF00498 | 0.597 |
LIG_FHA_1 | 353 | 359 | PF00498 | 0.607 |
LIG_FHA_1 | 388 | 394 | PF00498 | 0.625 |
LIG_FHA_1 | 506 | 512 | PF00498 | 0.599 |
LIG_FHA_1 | 622 | 628 | PF00498 | 0.823 |
LIG_FHA_2 | 195 | 201 | PF00498 | 0.607 |
LIG_FHA_2 | 302 | 308 | PF00498 | 0.632 |
LIG_FHA_2 | 408 | 414 | PF00498 | 0.582 |
LIG_FHA_2 | 479 | 485 | PF00498 | 0.542 |
LIG_FHA_2 | 551 | 557 | PF00498 | 0.632 |
LIG_FHA_2 | 90 | 96 | PF00498 | 0.602 |
LIG_Integrin_isoDGR_2 | 359 | 361 | PF01839 | 0.407 |
LIG_LIR_Apic_2 | 207 | 211 | PF02991 | 0.607 |
LIG_LIR_Apic_2 | 237 | 243 | PF02991 | 0.588 |
LIG_LIR_Gen_1 | 103 | 111 | PF02991 | 0.454 |
LIG_LIR_Gen_1 | 128 | 139 | PF02991 | 0.562 |
LIG_LIR_Gen_1 | 168 | 179 | PF02991 | 0.420 |
LIG_LIR_Gen_1 | 197 | 205 | PF02991 | 0.555 |
LIG_LIR_Gen_1 | 217 | 226 | PF02991 | 0.523 |
LIG_LIR_Gen_1 | 227 | 235 | PF02991 | 0.585 |
LIG_LIR_Gen_1 | 281 | 292 | PF02991 | 0.638 |
LIG_LIR_Gen_1 | 298 | 308 | PF02991 | 0.452 |
LIG_LIR_Gen_1 | 336 | 343 | PF02991 | 0.532 |
LIG_LIR_Gen_1 | 370 | 381 | PF02991 | 0.532 |
LIG_LIR_Gen_1 | 424 | 432 | PF02991 | 0.521 |
LIG_LIR_Gen_1 | 519 | 526 | PF02991 | 0.607 |
LIG_LIR_Gen_1 | 84 | 94 | PF02991 | 0.741 |
LIG_LIR_Nem_3 | 103 | 108 | PF02991 | 0.458 |
LIG_LIR_Nem_3 | 128 | 134 | PF02991 | 0.463 |
LIG_LIR_Nem_3 | 148 | 152 | PF02991 | 0.532 |
LIG_LIR_Nem_3 | 168 | 174 | PF02991 | 0.214 |
LIG_LIR_Nem_3 | 192 | 198 | PF02991 | 0.393 |
LIG_LIR_Nem_3 | 217 | 222 | PF02991 | 0.523 |
LIG_LIR_Nem_3 | 227 | 233 | PF02991 | 0.585 |
LIG_LIR_Nem_3 | 27 | 31 | PF02991 | 0.455 |
LIG_LIR_Nem_3 | 281 | 287 | PF02991 | 0.605 |
LIG_LIR_Nem_3 | 298 | 303 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 32 | 38 | PF02991 | 0.428 |
LIG_LIR_Nem_3 | 328 | 333 | PF02991 | 0.540 |
LIG_LIR_Nem_3 | 336 | 340 | PF02991 | 0.498 |
LIG_LIR_Nem_3 | 370 | 376 | PF02991 | 0.521 |
LIG_LIR_Nem_3 | 413 | 419 | PF02991 | 0.524 |
LIG_LIR_Nem_3 | 424 | 430 | PF02991 | 0.519 |
LIG_LIR_Nem_3 | 486 | 492 | PF02991 | 0.567 |
LIG_LIR_Nem_3 | 519 | 525 | PF02991 | 0.600 |
LIG_LIR_Nem_3 | 536 | 542 | PF02991 | 0.459 |
LIG_MYND_1 | 12 | 16 | PF01753 | 0.474 |
LIG_NRBOX | 291 | 297 | PF00104 | 0.582 |
LIG_NRBOX | 478 | 484 | PF00104 | 0.607 |
LIG_PCNA_yPIPBox_3 | 255 | 263 | PF02747 | 0.625 |
LIG_PCNA_yPIPBox_3 | 289 | 300 | PF02747 | 0.557 |
LIG_PCNA_yPIPBox_3 | 75 | 87 | PF02747 | 0.478 |
LIG_Pex14_2 | 416 | 420 | PF04695 | 0.529 |
LIG_REV1ctd_RIR_1 | 105 | 113 | PF16727 | 0.478 |
LIG_SH2_CRK | 171 | 175 | PF00017 | 0.395 |
LIG_SH2_CRK | 230 | 234 | PF00017 | 0.607 |
LIG_SH2_CRK | 284 | 288 | PF00017 | 0.636 |
LIG_SH2_CRK | 300 | 304 | PF00017 | 0.489 |
LIG_SH2_CRK | 373 | 377 | PF00017 | 0.582 |
LIG_SH2_CRK | 489 | 493 | PF00017 | 0.624 |
LIG_SH2_GRB2like | 471 | 474 | PF00017 | 0.607 |
LIG_SH2_NCK_1 | 208 | 212 | PF00017 | 0.607 |
LIG_SH2_NCK_1 | 284 | 288 | PF00017 | 0.607 |
LIG_SH2_SRC | 284 | 287 | PF00017 | 0.625 |
LIG_SH2_SRC | 392 | 395 | PF00017 | 0.625 |
LIG_SH2_SRC | 4 | 7 | PF00017 | 0.467 |
LIG_SH2_STAP1 | 127 | 131 | PF00017 | 0.465 |
LIG_SH2_STAP1 | 171 | 175 | PF00017 | 0.515 |
LIG_SH2_STAP1 | 198 | 202 | PF00017 | 0.607 |
LIG_SH2_STAT3 | 127 | 130 | PF00017 | 0.492 |
LIG_SH2_STAT5 | 31 | 34 | PF00017 | 0.544 |
LIG_SH2_STAT5 | 337 | 340 | PF00017 | 0.529 |
LIG_SH2_STAT5 | 375 | 378 | PF00017 | 0.607 |
LIG_SH2_STAT5 | 392 | 395 | PF00017 | 0.607 |
LIG_SH2_STAT5 | 467 | 470 | PF00017 | 0.545 |
LIG_SH3_3 | 183 | 189 | PF00018 | 0.631 |
LIG_SH3_3 | 259 | 265 | PF00018 | 0.581 |
LIG_SH3_3 | 27 | 33 | PF00018 | 0.452 |
LIG_SUMO_SIM_anti_2 | 528 | 536 | PF11976 | 0.563 |
LIG_SUMO_SIM_par_1 | 46 | 53 | PF11976 | 0.541 |
LIG_SUMO_SIM_par_1 | 480 | 487 | PF11976 | 0.534 |
LIG_TYR_ITIM | 169 | 174 | PF00017 | 0.478 |
LIG_TYR_ITIM | 228 | 233 | PF00017 | 0.607 |
LIG_UBA3_1 | 201 | 206 | PF00899 | 0.625 |
LIG_UBA3_1 | 258 | 263 | PF00899 | 0.607 |
LIG_UBA3_1 | 461 | 469 | PF00899 | 0.607 |
LIG_UBA3_1 | 492 | 496 | PF00899 | 0.545 |
LIG_UBA3_1 | 546 | 551 | PF00899 | 0.677 |
LIG_WRC_WIRS_1 | 170 | 175 | PF05994 | 0.410 |
MOD_CDC14_SPxK_1 | 436 | 439 | PF00782 | 0.600 |
MOD_CDK_SPK_2 | 421 | 426 | PF00069 | 0.521 |
MOD_CDK_SPK_2 | 70 | 75 | PF00069 | 0.510 |
MOD_CDK_SPxK_1 | 433 | 439 | PF00069 | 0.600 |
MOD_CDK_SPxxK_3 | 70 | 77 | PF00069 | 0.508 |
MOD_CK1_1 | 301 | 307 | PF00069 | 0.590 |
MOD_CK1_1 | 407 | 413 | PF00069 | 0.599 |
MOD_CK1_1 | 433 | 439 | PF00069 | 0.588 |
MOD_CK1_1 | 63 | 69 | PF00069 | 0.466 |
MOD_CK1_1 | 73 | 79 | PF00069 | 0.487 |
MOD_CK2_1 | 194 | 200 | PF00069 | 0.589 |
MOD_CK2_1 | 301 | 307 | PF00069 | 0.607 |
MOD_CK2_1 | 407 | 413 | PF00069 | 0.555 |
MOD_CK2_1 | 478 | 484 | PF00069 | 0.542 |
MOD_CK2_1 | 515 | 521 | PF00069 | 0.632 |
MOD_CMANNOS | 213 | 216 | PF00535 | 0.332 |
MOD_Cter_Amidation | 359 | 362 | PF01082 | 0.407 |
MOD_GlcNHglycan | 280 | 283 | PF01048 | 0.380 |
MOD_GlcNHglycan | 300 | 303 | PF01048 | 0.342 |
MOD_GlcNHglycan | 601 | 604 | PF01048 | 0.800 |
MOD_GSK3_1 | 274 | 281 | PF00069 | 0.599 |
MOD_GSK3_1 | 388 | 395 | PF00069 | 0.612 |
MOD_GSK3_1 | 426 | 433 | PF00069 | 0.604 |
MOD_GSK3_1 | 599 | 606 | PF00069 | 0.626 |
MOD_GSK3_1 | 65 | 72 | PF00069 | 0.567 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.567 |
MOD_N-GLC_1 | 182 | 187 | PF02516 | 0.624 |
MOD_N-GLC_1 | 387 | 392 | PF02516 | 0.332 |
MOD_N-GLC_1 | 564 | 569 | PF02516 | 0.665 |
MOD_N-GLC_1 | 603 | 608 | PF02516 | 0.811 |
MOD_NEK2_1 | 126 | 131 | PF00069 | 0.565 |
MOD_NEK2_1 | 169 | 174 | PF00069 | 0.513 |
MOD_NEK2_1 | 478 | 483 | PF00069 | 0.512 |
MOD_NEK2_1 | 564 | 569 | PF00069 | 0.665 |
MOD_NEK2_2 | 325 | 330 | PF00069 | 0.582 |
MOD_PIKK_1 | 126 | 132 | PF00454 | 0.502 |
MOD_PIKK_1 | 550 | 556 | PF00454 | 0.603 |
MOD_PIKK_1 | 76 | 82 | PF00454 | 0.628 |
MOD_PKA_1 | 361 | 367 | PF00069 | 0.532 |
MOD_PKA_2 | 361 | 367 | PF00069 | 0.562 |
MOD_PKA_2 | 404 | 410 | PF00069 | 0.582 |
MOD_PKA_2 | 604 | 610 | PF00069 | 0.687 |
MOD_PKA_2 | 76 | 82 | PF00069 | 0.481 |
MOD_Plk_1 | 182 | 188 | PF00069 | 0.600 |
MOD_Plk_1 | 243 | 249 | PF00069 | 0.571 |
MOD_Plk_1 | 253 | 259 | PF00069 | 0.582 |
MOD_Plk_1 | 387 | 393 | PF00069 | 0.545 |
MOD_Plk_1 | 63 | 69 | PF00069 | 0.466 |
MOD_Plk_4 | 169 | 175 | PF00069 | 0.410 |
MOD_Plk_4 | 224 | 230 | PF00069 | 0.521 |
MOD_Plk_4 | 325 | 331 | PF00069 | 0.528 |
MOD_Plk_4 | 388 | 394 | PF00069 | 0.548 |
MOD_Plk_4 | 478 | 484 | PF00069 | 0.521 |
MOD_ProDKin_1 | 29 | 35 | PF00069 | 0.578 |
MOD_ProDKin_1 | 320 | 326 | PF00069 | 0.614 |
MOD_ProDKin_1 | 421 | 427 | PF00069 | 0.521 |
MOD_ProDKin_1 | 433 | 439 | PF00069 | 0.521 |
MOD_ProDKin_1 | 70 | 76 | PF00069 | 0.508 |
TRG_DiLeu_BaEn_1 | 244 | 249 | PF01217 | 0.562 |
TRG_DiLeu_BaLyEn_6 | 254 | 259 | PF01217 | 0.581 |
TRG_DiLeu_LyEn_5 | 244 | 249 | PF01217 | 0.607 |
TRG_ENDOCYTIC_2 | 105 | 108 | PF00928 | 0.473 |
TRG_ENDOCYTIC_2 | 171 | 174 | PF00928 | 0.393 |
TRG_ENDOCYTIC_2 | 176 | 179 | PF00928 | 0.408 |
TRG_ENDOCYTIC_2 | 198 | 201 | PF00928 | 0.607 |
TRG_ENDOCYTIC_2 | 230 | 233 | PF00928 | 0.586 |
TRG_ENDOCYTIC_2 | 284 | 287 | PF00928 | 0.636 |
TRG_ENDOCYTIC_2 | 300 | 303 | PF00928 | 0.489 |
TRG_ENDOCYTIC_2 | 337 | 340 | PF00928 | 0.534 |
TRG_ENDOCYTIC_2 | 373 | 376 | PF00928 | 0.545 |
TRG_ENDOCYTIC_2 | 467 | 470 | PF00928 | 0.545 |
TRG_ENDOCYTIC_2 | 489 | 492 | PF00928 | 0.604 |
TRG_ER_diArg_1 | 350 | 352 | PF00400 | 0.553 |
TRG_ER_diArg_1 | 361 | 363 | PF00400 | 0.568 |
TRG_ER_diArg_1 | 451 | 453 | PF00400 | 0.545 |
TRG_ER_diArg_1 | 497 | 500 | PF00400 | 0.563 |
TRG_ER_diArg_1 | 585 | 587 | PF00400 | 0.756 |
TRG_NES_CRM1_1 | 217 | 231 | PF08389 | 0.532 |
TRG_NES_CRM1_1 | 460 | 472 | PF08389 | 0.548 |
TRG_NLS_MonoExtN_4 | 581 | 588 | PF00514 | 0.784 |
TRG_Pf-PMV_PEXEL_1 | 247 | 251 | PF00026 | 0.407 |
TRG_Pf-PMV_PEXEL_1 | 500 | 505 | PF00026 | 0.332 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDA7 | Leptomonas seymouri | 79% | 100% |
A0A0S4KNQ8 | Bodo saltans | 34% | 100% |
A0A1X0P8D7 | Trypanosomatidae | 53% | 100% |
A0A3Q8IIN0 | Leishmania donovani | 98% | 100% |
A0A3R7KQY4 | Trypanosoma rangeli | 53% | 100% |
A4HNN3 | Leishmania braziliensis | 96% | 100% |
A4ICW2 | Leishmania infantum | 98% | 100% |
A5A6M4 | Pan troglodytes | 25% | 100% |
A7SDW5 | Nematostella vectensis | 24% | 100% |
A8PHP4 | Brugia malayi | 22% | 100% |
A8X419 | Caenorhabditis briggsae | 23% | 100% |
A9VCY6 | Monosiga brevicollis | 25% | 100% |
B0WR18 | Culex quinquefasciatus | 22% | 100% |
B3M7W0 | Drosophila ananassae | 24% | 100% |
B3NH71 | Drosophila erecta | 24% | 100% |
B4GR63 | Drosophila persimilis | 25% | 100% |
B4HFJ3 | Drosophila sechellia | 24% | 100% |
B4IWN1 | Drosophila grimshawi | 23% | 100% |
B4KZ45 | Drosophila mojavensis | 24% | 100% |
B4LEJ0 | Drosophila virilis | 24% | 100% |
B4MX71 | Drosophila willistoni | 23% | 100% |
B4PG99 | Drosophila yakuba | 24% | 100% |
B4QR64 | Drosophila simulans | 24% | 100% |
D0A2I7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 50% | 100% |
E9ASE2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 97% | 100% |
P0CN56 | Cryptococcus neoformans var. neoformans serotype D (strain JEC21 / ATCC MYA-565) | 23% | 100% |
P0CN57 | Cryptococcus neoformans var. neoformans serotype D (strain B-3501A) | 23% | 100% |
Q16FL6 | Aedes aegypti | 22% | 100% |
Q2M0S3 | Drosophila pseudoobscura pseudoobscura | 25% | 100% |
Q3ZCK1 | Bos taurus | 25% | 100% |
Q4PF85 | Ustilago maydis (strain 521 / FGSC 9021) | 22% | 95% |
Q5F428 | Gallus gallus | 25% | 100% |
Q6CAE9 | Yarrowia lipolytica (strain CLIB 122 / E 150) | 24% | 100% |
Q6P878 | Xenopus tropicalis | 25% | 100% |
Q7Q5Y8 | Anopheles gambiae | 24% | 100% |
Q7T2A5 | Danio rerio | 25% | 100% |
Q8AVJ0 | Xenopus laevis | 24% | 100% |
Q8QZY1 | Mus musculus | 25% | 100% |
Q95QW0 | Caenorhabditis elegans | 24% | 100% |
Q9VTU4 | Drosophila melanogaster | 24% | 100% |
Q9Y262 | Homo sapiens | 25% | 100% |
V5BV76 | Trypanosoma cruzi | 52% | 100% |