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:0005942 | phosphatidylinositol 3-kinase complex | 3 | 12 |
GO:0032991 | protein-containing complex | 1 | 12 |
GO:0035032 | phosphatidylinositol 3-kinase complex, class III | 4 | 12 |
GO:0061695 | transferase complex, transferring phosphorus-containing groups | 4 | 12 |
GO:0070772 | PAS complex | 5 | 12 |
GO:0098796 | membrane protein complex | 2 | 12 |
GO:1902494 | catalytic complex | 2 | 12 |
GO:1990234 | transferase complex | 3 | 12 |
GO:0005737 | cytoplasm | 2 | 1 |
GO:0010008 | endosome membrane | 5 | 1 |
GO:0012506 | vesicle membrane | 4 | 1 |
GO:0016020 | membrane | 2 | 1 |
GO:0030659 | cytoplasmic vesicle membrane | 5 | 1 |
GO:0031090 | organelle membrane | 3 | 1 |
GO:0098588 | bounding membrane of organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4H7W5
Term | Name | Level | Count |
---|---|---|---|
GO:0006629 | lipid metabolic process | 3 | 12 |
GO:0006644 | phospholipid metabolic process | 4 | 12 |
GO:0006650 | glycerophospholipid metabolic process | 5 | 12 |
GO:0006661 | phosphatidylinositol biosynthetic process | 6 | 12 |
GO:0006793 | phosphorus metabolic process | 3 | 12 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0008610 | lipid biosynthetic process | 4 | 12 |
GO:0008654 | phospholipid biosynthetic process | 5 | 12 |
GO:0009058 | biosynthetic process | 2 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0019637 | organophosphate metabolic process | 3 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0044249 | cellular biosynthetic process | 3 | 12 |
GO:0044255 | cellular lipid metabolic process | 3 | 12 |
GO:0045017 | glycerolipid biosynthetic process | 4 | 12 |
GO:0046474 | glycerophospholipid biosynthetic process | 5 | 12 |
GO:0046486 | glycerolipid metabolic process | 4 | 12 |
GO:0046488 | phosphatidylinositol metabolic process | 6 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:0090407 | organophosphate biosynthetic process | 4 | 12 |
GO:1901576 | organic substance biosynthetic process | 3 | 12 |
GO:0009893 | positive regulation of metabolic process | 4 | 1 |
GO:0010562 | positive regulation of phosphorus metabolic process | 6 | 1 |
GO:0019220 | regulation of phosphate metabolic process | 6 | 1 |
GO:0019222 | regulation of metabolic process | 3 | 1 |
GO:0031323 | regulation of cellular metabolic process | 4 | 1 |
GO:0031325 | positive regulation of cellular metabolic process | 5 | 1 |
GO:0033674 | positive regulation of kinase activity | 6 | 1 |
GO:0042325 | regulation of phosphorylation | 7 | 1 |
GO:0042327 | positive regulation of phosphorylation | 8 | 1 |
GO:0043085 | positive regulation of catalytic activity | 4 | 1 |
GO:0043549 | regulation of kinase activity | 5 | 1 |
GO:0044093 | positive regulation of molecular function | 3 | 1 |
GO:0045937 | positive regulation of phosphate metabolic process | 7 | 1 |
GO:0048518 | positive regulation of biological process | 3 | 1 |
GO:0048522 | positive regulation of cellular process | 4 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050790 | regulation of catalytic activity | 3 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0051174 | regulation of phosphorus metabolic process | 5 | 1 |
GO:0051338 | regulation of transferase activity | 4 | 1 |
GO:0051347 | positive regulation of transferase activity | 5 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0065009 | regulation of molecular function | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 104 | 108 | PF00656 | 0.346 |
CLV_C14_Caspase3-7 | 370 | 374 | PF00656 | 0.386 |
CLV_NRD_NRD_1 | 11 | 13 | PF00675 | 0.524 |
CLV_NRD_NRD_1 | 460 | 462 | PF00675 | 0.431 |
CLV_NRD_NRD_1 | 467 | 469 | PF00675 | 0.389 |
CLV_NRD_NRD_1 | 527 | 529 | PF00675 | 0.418 |
CLV_NRD_NRD_1 | 567 | 569 | PF00675 | 0.351 |
CLV_NRD_NRD_1 | 637 | 639 | PF00675 | 0.297 |
CLV_NRD_NRD_1 | 70 | 72 | PF00675 | 0.289 |
CLV_PCSK_FUR_1 | 150 | 154 | PF00082 | 0.413 |
CLV_PCSK_KEX2_1 | 152 | 154 | PF00082 | 0.341 |
CLV_PCSK_KEX2_1 | 460 | 462 | PF00082 | 0.431 |
CLV_PCSK_KEX2_1 | 467 | 469 | PF00082 | 0.389 |
CLV_PCSK_KEX2_1 | 527 | 529 | PF00082 | 0.428 |
CLV_PCSK_KEX2_1 | 567 | 569 | PF00082 | 0.353 |
CLV_PCSK_KEX2_1 | 637 | 639 | PF00082 | 0.297 |
CLV_PCSK_KEX2_1 | 70 | 72 | PF00082 | 0.289 |
CLV_PCSK_PC1ET2_1 | 152 | 154 | PF00082 | 0.341 |
CLV_PCSK_PC7_1 | 523 | 529 | PF00082 | 0.418 |
CLV_PCSK_SKI1_1 | 12 | 16 | PF00082 | 0.461 |
CLV_PCSK_SKI1_1 | 152 | 156 | PF00082 | 0.320 |
CLV_PCSK_SKI1_1 | 217 | 221 | PF00082 | 0.470 |
CLV_PCSK_SKI1_1 | 236 | 240 | PF00082 | 0.358 |
CLV_PCSK_SKI1_1 | 366 | 370 | PF00082 | 0.462 |
CLV_PCSK_SKI1_1 | 504 | 508 | PF00082 | 0.326 |
CLV_PCSK_SKI1_1 | 523 | 527 | PF00082 | 0.149 |
CLV_PCSK_SKI1_1 | 528 | 532 | PF00082 | 0.331 |
CLV_Separin_Metazoa | 122 | 126 | PF03568 | 0.413 |
DEG_APCC_DBOX_1 | 365 | 373 | PF00400 | 0.450 |
DEG_APCC_DBOX_1 | 70 | 78 | PF00400 | 0.317 |
DEG_MDM2_SWIB_1 | 294 | 302 | PF02201 | 0.438 |
DEG_SPOP_SBC_1 | 395 | 399 | PF00917 | 0.268 |
DOC_CYCLIN_RxL_1 | 233 | 243 | PF00134 | 0.366 |
DOC_MAPK_gen_1 | 637 | 644 | PF00069 | 0.413 |
DOC_MAPK_gen_1 | 70 | 77 | PF00069 | 0.341 |
DOC_MAPK_MEF2A_6 | 482 | 489 | PF00069 | 0.418 |
DOC_MAPK_MEF2A_6 | 500 | 509 | PF00069 | 0.341 |
DOC_MAPK_MEF2A_6 | 637 | 646 | PF00069 | 0.503 |
DOC_MAPK_RevD_3 | 554 | 568 | PF00069 | 0.331 |
DOC_PP2B_LxvP_1 | 220 | 223 | PF13499 | 0.393 |
DOC_PP2B_LxvP_1 | 623 | 626 | PF13499 | 0.297 |
DOC_USP7_MATH_1 | 181 | 185 | PF00917 | 0.340 |
DOC_USP7_MATH_1 | 196 | 200 | PF00917 | 0.528 |
DOC_USP7_MATH_1 | 206 | 210 | PF00917 | 0.417 |
DOC_USP7_MATH_1 | 241 | 245 | PF00917 | 0.506 |
DOC_USP7_MATH_1 | 29 | 33 | PF00917 | 0.483 |
DOC_USP7_MATH_1 | 396 | 400 | PF00917 | 0.511 |
DOC_USP7_MATH_1 | 417 | 421 | PF00917 | 0.245 |
DOC_USP7_MATH_1 | 88 | 92 | PF00917 | 0.448 |
DOC_WW_Pin1_4 | 626 | 631 | PF00397 | 0.307 |
LIG_14-3-3_CanoR_1 | 135 | 143 | PF00244 | 0.403 |
LIG_14-3-3_CanoR_1 | 424 | 432 | PF00244 | 0.291 |
LIG_14-3-3_CanoR_1 | 467 | 473 | PF00244 | 0.467 |
LIG_14-3-3_CanoR_1 | 491 | 499 | PF00244 | 0.418 |
LIG_14-3-3_CanoR_1 | 602 | 606 | PF00244 | 0.341 |
LIG_14-3-3_CanoR_1 | 607 | 612 | PF00244 | 0.341 |
LIG_14-3-3_CanoR_1 | 63 | 69 | PF00244 | 0.439 |
LIG_Actin_WH2_2 | 201 | 219 | PF00022 | 0.479 |
LIG_Actin_WH2_2 | 353 | 368 | PF00022 | 0.424 |
LIG_Actin_WH2_2 | 409 | 426 | PF00022 | 0.234 |
LIG_Actin_WH2_2 | 47 | 65 | PF00022 | 0.450 |
LIG_Actin_WH2_2 | 486 | 502 | PF00022 | 0.413 |
LIG_Actin_WH2_2 | 586 | 604 | PF00022 | 0.413 |
LIG_AP2alpha_1 | 136 | 140 | PF02296 | 0.413 |
LIG_APCC_ABBA_1 | 35 | 40 | PF00400 | 0.420 |
LIG_BIR_III_2 | 107 | 111 | PF00653 | 0.413 |
LIG_BRCT_BRCA1_1 | 594 | 598 | PF00533 | 0.341 |
LIG_Clathr_ClatBox_1 | 645 | 649 | PF01394 | 0.474 |
LIG_deltaCOP1_diTrp_1 | 130 | 136 | PF00928 | 0.331 |
LIG_eIF4E_1 | 548 | 554 | PF01652 | 0.413 |
LIG_eIF4E_1 | 619 | 625 | PF01652 | 0.418 |
LIG_eIF4E_1 | 69 | 75 | PF01652 | 0.413 |
LIG_FHA_1 | 32 | 38 | PF00498 | 0.455 |
LIG_FHA_1 | 407 | 413 | PF00498 | 0.374 |
LIG_FHA_1 | 564 | 570 | PF00498 | 0.418 |
LIG_FHA_1 | 615 | 621 | PF00498 | 0.413 |
LIG_FHA_1 | 63 | 69 | PF00498 | 0.441 |
LIG_FHA_1 | 641 | 647 | PF00498 | 0.509 |
LIG_FHA_2 | 162 | 168 | PF00498 | 0.321 |
LIG_FHA_2 | 321 | 327 | PF00498 | 0.384 |
LIG_FHA_2 | 42 | 48 | PF00498 | 0.429 |
LIG_FHA_2 | 513 | 519 | PF00498 | 0.297 |
LIG_GBD_Chelix_1 | 505 | 513 | PF00786 | 0.418 |
LIG_GBD_Chelix_1 | 614 | 622 | PF00786 | 0.413 |
LIG_LIR_Gen_1 | 118 | 129 | PF02991 | 0.418 |
LIG_LIR_Gen_1 | 137 | 147 | PF02991 | 0.312 |
LIG_LIR_Gen_1 | 247 | 255 | PF02991 | 0.478 |
LIG_LIR_Gen_1 | 386 | 395 | PF02991 | 0.330 |
LIG_LIR_Gen_1 | 537 | 543 | PF02991 | 0.466 |
LIG_LIR_Gen_1 | 582 | 590 | PF02991 | 0.377 |
LIG_LIR_Gen_1 | 595 | 606 | PF02991 | 0.247 |
LIG_LIR_Gen_1 | 617 | 626 | PF02991 | 0.418 |
LIG_LIR_Gen_1 | 629 | 639 | PF02991 | 0.341 |
LIG_LIR_LC3C_4 | 197 | 202 | PF02991 | 0.620 |
LIG_LIR_Nem_3 | 118 | 124 | PF02991 | 0.413 |
LIG_LIR_Nem_3 | 137 | 143 | PF02991 | 0.303 |
LIG_LIR_Nem_3 | 247 | 253 | PF02991 | 0.476 |
LIG_LIR_Nem_3 | 386 | 390 | PF02991 | 0.326 |
LIG_LIR_Nem_3 | 515 | 519 | PF02991 | 0.323 |
LIG_LIR_Nem_3 | 537 | 542 | PF02991 | 0.345 |
LIG_LIR_Nem_3 | 582 | 586 | PF02991 | 0.365 |
LIG_LIR_Nem_3 | 595 | 601 | PF02991 | 0.226 |
LIG_LIR_Nem_3 | 617 | 622 | PF02991 | 0.418 |
LIG_LIR_Nem_3 | 629 | 635 | PF02991 | 0.304 |
LIG_LIR_Nem_3 | 667 | 672 | PF02991 | 0.428 |
LIG_NRBOX | 234 | 240 | PF00104 | 0.374 |
LIG_NRBOX | 384 | 390 | PF00104 | 0.442 |
LIG_NRBOX | 445 | 451 | PF00104 | 0.471 |
LIG_NRBOX | 617 | 623 | PF00104 | 0.413 |
LIG_NRBOX | 93 | 99 | PF00104 | 0.418 |
LIG_PCNA_yPIPBox_3 | 443 | 454 | PF02747 | 0.265 |
LIG_Pex14_1 | 132 | 136 | PF04695 | 0.358 |
LIG_Pex14_2 | 136 | 140 | PF04695 | 0.279 |
LIG_Pex14_2 | 294 | 298 | PF04695 | 0.435 |
LIG_SH2_CRK | 548 | 552 | PF00017 | 0.302 |
LIG_SH2_CRK | 632 | 636 | PF00017 | 0.326 |
LIG_SH2_NCK_1 | 548 | 552 | PF00017 | 0.297 |
LIG_SH2_PTP2 | 583 | 586 | PF00017 | 0.406 |
LIG_SH2_PTP2 | 619 | 622 | PF00017 | 0.418 |
LIG_SH2_STAP1 | 682 | 686 | PF00017 | 0.551 |
LIG_SH2_STAT5 | 583 | 586 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 619 | 622 | PF00017 | 0.418 |
LIG_SH2_STAT5 | 672 | 675 | PF00017 | 0.518 |
LIG_SH3_3 | 82 | 88 | PF00018 | 0.417 |
LIG_SUMO_SIM_anti_2 | 274 | 282 | PF11976 | 0.329 |
LIG_SUMO_SIM_anti_2 | 367 | 374 | PF11976 | 0.438 |
LIG_SUMO_SIM_anti_2 | 386 | 392 | PF11976 | 0.335 |
LIG_SUMO_SIM_anti_2 | 408 | 415 | PF11976 | 0.226 |
LIG_SUMO_SIM_anti_2 | 47 | 53 | PF11976 | 0.517 |
LIG_SUMO_SIM_par_1 | 367 | 374 | PF11976 | 0.438 |
LIG_SUMO_SIM_par_1 | 408 | 415 | PF11976 | 0.265 |
LIG_SUMO_SIM_par_1 | 47 | 53 | PF11976 | 0.484 |
LIG_SUMO_SIM_par_1 | 505 | 511 | PF11976 | 0.198 |
LIG_TRAF2_1 | 341 | 344 | PF00917 | 0.476 |
LIG_TRAF2_1 | 376 | 379 | PF00917 | 0.492 |
LIG_TRAF2_1 | 674 | 677 | PF00917 | 0.529 |
LIG_WRC_WIRS_1 | 182 | 187 | PF05994 | 0.339 |
MOD_CK1_1 | 192 | 198 | PF00069 | 0.430 |
MOD_CK1_1 | 230 | 236 | PF00069 | 0.373 |
MOD_CK1_1 | 244 | 250 | PF00069 | 0.350 |
MOD_CK1_1 | 265 | 271 | PF00069 | 0.513 |
MOD_CK1_1 | 288 | 294 | PF00069 | 0.399 |
MOD_CK1_1 | 31 | 37 | PF00069 | 0.485 |
MOD_CK1_1 | 494 | 500 | PF00069 | 0.406 |
MOD_CK1_1 | 508 | 514 | PF00069 | 0.320 |
MOD_CK1_1 | 579 | 585 | PF00069 | 0.317 |
MOD_CK1_1 | 596 | 602 | PF00069 | 0.317 |
MOD_CK2_1 | 161 | 167 | PF00069 | 0.341 |
MOD_CK2_1 | 320 | 326 | PF00069 | 0.381 |
MOD_CK2_1 | 364 | 370 | PF00069 | 0.401 |
MOD_CK2_1 | 394 | 400 | PF00069 | 0.435 |
MOD_CK2_1 | 41 | 47 | PF00069 | 0.402 |
MOD_CK2_1 | 471 | 477 | PF00069 | 0.428 |
MOD_CK2_1 | 512 | 518 | PF00069 | 0.297 |
MOD_GlcNHglycan | 171 | 174 | PF01048 | 0.490 |
MOD_GlcNHglycan | 194 | 197 | PF01048 | 0.582 |
MOD_GlcNHglycan | 264 | 267 | PF01048 | 0.534 |
MOD_GlcNHglycan | 287 | 290 | PF01048 | 0.502 |
MOD_GlcNHglycan | 356 | 359 | PF01048 | 0.501 |
MOD_GlcNHglycan | 373 | 376 | PF01048 | 0.379 |
MOD_GlcNHglycan | 539 | 542 | PF01048 | 0.316 |
MOD_GSK3_1 | 134 | 141 | PF00069 | 0.399 |
MOD_GSK3_1 | 161 | 168 | PF00069 | 0.368 |
MOD_GSK3_1 | 192 | 199 | PF00069 | 0.548 |
MOD_GSK3_1 | 258 | 265 | PF00069 | 0.468 |
MOD_GSK3_1 | 284 | 291 | PF00069 | 0.415 |
MOD_GSK3_1 | 508 | 515 | PF00069 | 0.188 |
MOD_GSK3_1 | 528 | 535 | PF00069 | 0.156 |
MOD_GSK3_1 | 592 | 599 | PF00069 | 0.413 |
MOD_GSK3_1 | 650 | 657 | PF00069 | 0.470 |
MOD_N-GLC_1 | 244 | 249 | PF02516 | 0.508 |
MOD_N-GLC_2 | 271 | 273 | PF02516 | 0.234 |
MOD_NEK2_1 | 165 | 170 | PF00069 | 0.454 |
MOD_NEK2_1 | 227 | 232 | PF00069 | 0.447 |
MOD_NEK2_1 | 279 | 284 | PF00069 | 0.277 |
MOD_NEK2_1 | 320 | 325 | PF00069 | 0.430 |
MOD_NEK2_1 | 364 | 369 | PF00069 | 0.450 |
MOD_NEK2_1 | 371 | 376 | PF00069 | 0.498 |
MOD_NEK2_1 | 512 | 517 | PF00069 | 0.310 |
MOD_NEK2_1 | 530 | 535 | PF00069 | 0.297 |
MOD_NEK2_1 | 563 | 568 | PF00069 | 0.418 |
MOD_NEK2_1 | 593 | 598 | PF00069 | 0.440 |
MOD_NEK2_1 | 601 | 606 | PF00069 | 0.266 |
MOD_NEK2_1 | 614 | 619 | PF00069 | 0.201 |
MOD_NEK2_1 | 62 | 67 | PF00069 | 0.392 |
MOD_NEK2_1 | 8 | 13 | PF00069 | 0.472 |
MOD_PIKK_1 | 206 | 212 | PF00454 | 0.460 |
MOD_PIKK_1 | 258 | 264 | PF00454 | 0.499 |
MOD_PKA_2 | 134 | 140 | PF00069 | 0.413 |
MOD_PKA_2 | 423 | 429 | PF00069 | 0.289 |
MOD_PKA_2 | 481 | 487 | PF00069 | 0.191 |
MOD_PKA_2 | 601 | 607 | PF00069 | 0.341 |
MOD_PKA_2 | 62 | 68 | PF00069 | 0.392 |
MOD_Plk_1 | 377 | 383 | PF00069 | 0.343 |
MOD_Plk_1 | 576 | 582 | PF00069 | 0.413 |
MOD_Plk_1 | 593 | 599 | PF00069 | 0.413 |
MOD_Plk_2-3 | 53 | 59 | PF00069 | 0.256 |
MOD_Plk_4 | 181 | 187 | PF00069 | 0.356 |
MOD_Plk_4 | 230 | 236 | PF00069 | 0.374 |
MOD_Plk_4 | 377 | 383 | PF00069 | 0.495 |
MOD_Plk_4 | 481 | 487 | PF00069 | 0.347 |
MOD_Plk_4 | 508 | 514 | PF00069 | 0.188 |
MOD_Plk_4 | 579 | 585 | PF00069 | 0.320 |
MOD_Plk_4 | 601 | 607 | PF00069 | 0.324 |
MOD_Plk_4 | 614 | 620 | PF00069 | 0.268 |
MOD_Plk_4 | 640 | 646 | PF00069 | 0.481 |
MOD_ProDKin_1 | 626 | 632 | PF00069 | 0.307 |
TRG_DiLeu_BaEn_1 | 440 | 445 | PF01217 | 0.429 |
TRG_DiLeu_BaEn_4 | 47 | 53 | PF01217 | 0.388 |
TRG_DiLeu_BaLyEn_6 | 445 | 450 | PF01217 | 0.462 |
TRG_DiLeu_BaLyEn_6 | 520 | 525 | PF01217 | 0.191 |
TRG_ENDOCYTIC_2 | 121 | 124 | PF00928 | 0.387 |
TRG_ENDOCYTIC_2 | 38 | 41 | PF00928 | 0.475 |
TRG_ENDOCYTIC_2 | 548 | 551 | PF00928 | 0.306 |
TRG_ENDOCYTIC_2 | 583 | 586 | PF00928 | 0.387 |
TRG_ENDOCYTIC_2 | 619 | 622 | PF00928 | 0.418 |
TRG_ENDOCYTIC_2 | 632 | 635 | PF00928 | 0.304 |
TRG_ER_diArg_1 | 290 | 293 | PF00400 | 0.458 |
TRG_ER_diArg_1 | 459 | 461 | PF00400 | 0.431 |
TRG_ER_diArg_1 | 466 | 468 | PF00400 | 0.389 |
TRG_ER_diArg_1 | 472 | 475 | PF00400 | 0.372 |
TRG_ER_diArg_1 | 526 | 528 | PF00400 | 0.418 |
TRG_ER_diArg_1 | 567 | 569 | PF00400 | 0.331 |
TRG_ER_diArg_1 | 637 | 639 | PF00400 | 0.301 |
TRG_ER_diArg_1 | 69 | 71 | PF00400 | 0.300 |
TRG_NES_CRM1_1 | 297 | 310 | PF08389 | 0.476 |
TRG_NES_CRM1_1 | 498 | 510 | PF08389 | 0.421 |
TRG_Pf-PMV_PEXEL_1 | 13 | 17 | PF00026 | 0.473 |
TRG_Pf-PMV_PEXEL_1 | 198 | 203 | PF00026 | 0.356 |
TRG_Pf-PMV_PEXEL_1 | 491 | 495 | PF00026 | 0.226 |
TRG_Pf-PMV_PEXEL_1 | 567 | 571 | PF00026 | 0.418 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PC70 | Leptomonas seymouri | 61% | 99% |
A0A0S4IRF4 | Bodo saltans | 28% | 100% |
A0A1X0NNZ5 | Trypanosomatidae | 28% | 99% |
A0A3Q8IA32 | Leishmania donovani | 84% | 100% |
A0A422N3V6 | Trypanosoma rangeli | 31% | 99% |
A4HW92 | Leishmania infantum | 84% | 100% |
C9ZSR9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 99% |
E9APZ3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |
P87145 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 25% | 85% |
Q4QFI8 | Leishmania major | 84% | 100% |
Q66L58 | Danio rerio | 24% | 89% |
Q9ZU97 | Arabidopsis thaliana | 27% | 92% |
V5AVZ7 | Trypanosoma cruzi | 29% | 99% |