| Source | Evidence on protein | Close homologs |
|---|---|---|
| Cuervo et al. | no | yes: 0 |
| Hassani et al. | no | yes: 0 |
| Forrest at al. (metacyclic) | no | yes: 6 |
| Forrest at al. (procyclic) | no | yes: 6 |
| Silverman et al. | no | yes: 0 |
| Pissara et al. | yes | yes: 18 |
| Source | Evidence on protein | Close homologs |
|---|---|---|
| Pires et al. | no | yes: 0 |
| Source | Evidence on protein | Close homologs |
|---|---|---|
| Silverman et al. | no | yes: 15 |
| Source | Evidence on protein | Close homologs |
|---|---|---|
| Jamdhade et al. | no | yes: 15 |
| Source | Evidence on protein | Close homologs |
|---|---|---|
| DeepLoc | ||
| SignalP6 | no | yes: 1, no: 11 |
| NetGPI | no | yes: 0, no: 12 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0032991 | protein-containing complex | 1 | 13 |
| GO:0033178 | proton-transporting two-sector ATPase complex, catalytic domain | 3 | 13 |
| GO:0045261 | proton-transporting ATP synthase complex, catalytic core F(1) | 4 | 13 |
| GO:0098796 | membrane protein complex | 2 | 13 |
| GO:0000275 | mitochondrial proton-transporting ATP synthase complex, catalytic sector F(1) | 4 | 1 |
| GO:0098798 | mitochondrial protein-containing complex | 2 | 1 |
| GO:0098800 | inner mitochondrial membrane protein complex | 3 | 1 |
Related structures:
AlphaFold database: E9AKF7
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
| GO:0006163 | purine nucleotide metabolic process | 5 | 1 |
| GO:0006164 | purine nucleotide biosynthetic process | 6 | 1 |
| GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
| GO:0006753 | nucleoside phosphate metabolic process | 4 | 1 |
| GO:0006754 | ATP biosynthetic process | 8 | 1 |
| GO:0006793 | phosphorus metabolic process | 3 | 1 |
| GO:0006796 | phosphate-containing compound metabolic process | 4 | 1 |
| GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
| GO:0008152 | metabolic process | 1 | 1 |
| GO:0009058 | biosynthetic process | 2 | 1 |
| GO:0009117 | nucleotide metabolic process | 5 | 1 |
| GO:0009141 | nucleoside triphosphate metabolic process | 5 | 1 |
| GO:0009142 | nucleoside triphosphate biosynthetic process | 6 | 1 |
| GO:0009144 | purine nucleoside triphosphate metabolic process | 6 | 1 |
| GO:0009145 | purine nucleoside triphosphate biosynthetic process | 7 | 1 |
| GO:0009150 | purine ribonucleotide metabolic process | 6 | 1 |
| GO:0009152 | purine ribonucleotide biosynthetic process | 7 | 1 |
| GO:0009165 | nucleotide biosynthetic process | 6 | 1 |
| GO:0009199 | ribonucleoside triphosphate metabolic process | 6 | 1 |
| GO:0009201 | ribonucleoside triphosphate biosynthetic process | 7 | 1 |
| GO:0009205 | purine ribonucleoside triphosphate metabolic process | 7 | 1 |
| GO:0009206 | purine ribonucleoside triphosphate biosynthetic process | 8 | 1 |
| GO:0009259 | ribonucleotide metabolic process | 5 | 1 |
| GO:0009260 | ribonucleotide biosynthetic process | 6 | 1 |
| GO:0009987 | cellular process | 1 | 1 |
| GO:0015986 | proton motive force-driven ATP synthesis | 9 | 1 |
| GO:0018130 | heterocycle biosynthetic process | 4 | 1 |
| GO:0019438 | aromatic compound biosynthetic process | 4 | 1 |
| GO:0019637 | organophosphate metabolic process | 3 | 1 |
| GO:0019693 | ribose phosphate metabolic process | 4 | 1 |
| GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
| GO:0034654 | nucleobase-containing compound biosynthetic process | 4 | 1 |
| GO:0044237 | cellular metabolic process | 2 | 1 |
| GO:0044238 | primary metabolic process | 2 | 1 |
| GO:0044249 | cellular biosynthetic process | 3 | 1 |
| GO:0044271 | cellular nitrogen compound biosynthetic process | 4 | 1 |
| GO:0044281 | small molecule metabolic process | 2 | 1 |
| GO:0046034 | ATP metabolic process | 7 | 1 |
| GO:0046390 | ribose phosphate biosynthetic process | 5 | 1 |
| GO:0046483 | heterocycle metabolic process | 3 | 1 |
| GO:0055086 | nucleobase-containing small molecule metabolic process | 3 | 1 |
| GO:0071704 | organic substance metabolic process | 2 | 1 |
| GO:0072521 | purine-containing compound metabolic process | 4 | 1 |
| GO:0072522 | purine-containing compound biosynthetic process | 5 | 1 |
| GO:0090407 | organophosphate biosynthetic process | 4 | 1 |
| GO:1901135 | carbohydrate derivative metabolic process | 3 | 1 |
| GO:1901137 | carbohydrate derivative biosynthetic process | 4 | 1 |
| GO:1901293 | nucleoside phosphate biosynthetic process | 5 | 1 |
| GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
| GO:1901362 | organic cyclic compound biosynthetic process | 4 | 1 |
| GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
| GO:1901566 | organonitrogen compound biosynthetic process | 4 | 1 |
| GO:1901576 | organic substance biosynthetic process | 3 | 1 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0000166 | nucleotide binding | 3 | 13 |
| GO:0003824 | catalytic activity | 1 | 13 |
| GO:0005215 | transporter activity | 1 | 13 |
| GO:0005216 | monoatomic ion channel activity | 4 | 13 |
| GO:0005261 | monoatomic cation channel activity | 5 | 13 |
| GO:0005488 | binding | 1 | 13 |
| GO:0005524 | ATP binding | 5 | 13 |
| GO:0008324 | monoatomic cation transmembrane transporter activity | 4 | 13 |
| GO:0015075 | monoatomic ion transmembrane transporter activity | 3 | 13 |
| GO:0015078 | proton transmembrane transporter activity | 5 | 13 |
| GO:0015252 | proton channel activity | 6 | 13 |
| GO:0015267 | channel activity | 4 | 13 |
| GO:0015318 | inorganic molecular entity transmembrane transporter activity | 3 | 13 |
| GO:0016874 | ligase activity | 2 | 13 |
| GO:0017076 | purine nucleotide binding | 4 | 13 |
| GO:0022803 | passive transmembrane transporter activity | 3 | 13 |
| GO:0022857 | transmembrane transporter activity | 2 | 13 |
| GO:0022890 | inorganic cation transmembrane transporter activity | 4 | 13 |
| GO:0030554 | adenyl nucleotide binding | 5 | 13 |
| GO:0032553 | ribonucleotide binding | 3 | 13 |
| GO:0032555 | purine ribonucleotide binding | 4 | 13 |
| GO:0032559 | adenyl ribonucleotide binding | 5 | 13 |
| GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 13 |
| GO:0036094 | small molecule binding | 2 | 13 |
| GO:0043167 | ion binding | 2 | 13 |
| GO:0043168 | anion binding | 3 | 13 |
| GO:0046933 | proton-transporting ATP synthase activity, rotational mechanism | 3 | 13 |
| GO:0097159 | organic cyclic compound binding | 2 | 13 |
| GO:0097367 | carbohydrate derivative binding | 2 | 13 |
| GO:1901265 | nucleoside phosphate binding | 3 | 13 |
| GO:1901363 | heterocyclic compound binding | 2 | 13 |
| GO:0016787 | hydrolase activity | 2 | 3 |
| GO:0043531 | ADP binding | 4 | 1 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 466 | 470 | PF00656 | 0.292 |
| CLV_NRD_NRD_1 | 13 | 15 | PF00675 | 0.460 |
| CLV_NRD_NRD_1 | 28 | 30 | PF00675 | 0.476 |
| CLV_NRD_NRD_1 | 408 | 410 | PF00675 | 0.317 |
| CLV_NRD_NRD_1 | 519 | 521 | PF00675 | 0.292 |
| CLV_NRD_NRD_1 | 97 | 99 | PF00675 | 0.618 |
| CLV_PCSK_KEX2_1 | 13 | 15 | PF00082 | 0.460 |
| CLV_PCSK_KEX2_1 | 28 | 30 | PF00082 | 0.476 |
| CLV_PCSK_KEX2_1 | 408 | 410 | PF00082 | 0.317 |
| CLV_PCSK_KEX2_1 | 666 | 668 | PF00082 | 0.382 |
| CLV_PCSK_KEX2_1 | 97 | 99 | PF00082 | 0.618 |
| CLV_PCSK_PC1ET2_1 | 666 | 668 | PF00082 | 0.382 |
| CLV_PCSK_SKI1_1 | 126 | 130 | PF00082 | 0.490 |
| CLV_PCSK_SKI1_1 | 239 | 243 | PF00082 | 0.465 |
| CLV_PCSK_SKI1_1 | 477 | 481 | PF00082 | 0.292 |
| CLV_PCSK_SKI1_1 | 49 | 53 | PF00082 | 0.498 |
| CLV_PCSK_SKI1_1 | 513 | 517 | PF00082 | 0.292 |
| CLV_PCSK_SKI1_1 | 614 | 618 | PF00082 | 0.342 |
| CLV_PCSK_SKI1_1 | 653 | 657 | PF00082 | 0.384 |
| CLV_PCSK_SKI1_1 | 659 | 663 | PF00082 | 0.359 |
| DOC_CYCLIN_RxL_1 | 236 | 245 | PF00134 | 0.480 |
| DOC_CYCLIN_RxL_1 | 653 | 664 | PF00134 | 0.367 |
| DOC_CYCLIN_yCln2_LP_2 | 210 | 216 | PF00134 | 0.378 |
| DOC_MAPK_gen_1 | 182 | 190 | PF00069 | 0.353 |
| DOC_MAPK_gen_1 | 382 | 389 | PF00069 | 0.292 |
| DOC_MAPK_MEF2A_6 | 182 | 190 | PF00069 | 0.353 |
| DOC_MAPK_MEF2A_6 | 318 | 326 | PF00069 | 0.292 |
| DOC_MAPK_MEF2A_6 | 484 | 493 | PF00069 | 0.292 |
| DOC_PP2B_LxvP_1 | 210 | 213 | PF13499 | 0.331 |
| DOC_PP4_FxxP_1 | 27 | 30 | PF00568 | 0.488 |
| DOC_USP7_MATH_1 | 117 | 121 | PF00917 | 0.694 |
| DOC_USP7_MATH_1 | 523 | 527 | PF00917 | 0.292 |
| DOC_USP7_MATH_1 | 558 | 562 | PF00917 | 0.292 |
| DOC_USP7_UBL2_3 | 126 | 130 | PF12436 | 0.482 |
| DOC_WW_Pin1_4 | 165 | 170 | PF00397 | 0.402 |
| DOC_WW_Pin1_4 | 259 | 264 | PF00397 | 0.366 |
| DOC_WW_Pin1_4 | 40 | 45 | PF00397 | 0.485 |
| DOC_WW_Pin1_4 | 432 | 437 | PF00397 | 0.300 |
| DOC_WW_Pin1_4 | 56 | 61 | PF00397 | 0.452 |
| LIG_14-3-3_CanoR_1 | 340 | 346 | PF00244 | 0.311 |
| LIG_14-3-3_CanoR_1 | 349 | 354 | PF00244 | 0.311 |
| LIG_14-3-3_CanoR_1 | 401 | 406 | PF00244 | 0.310 |
| LIG_14-3-3_CanoR_1 | 495 | 505 | PF00244 | 0.356 |
| LIG_14-3-3_CanoR_1 | 614 | 619 | PF00244 | 0.347 |
| LIG_Actin_WH2_2 | 334 | 351 | PF00022 | 0.292 |
| LIG_APCC_ABBA_1 | 387 | 392 | PF00400 | 0.292 |
| LIG_CaM_IQ_9 | 194 | 210 | PF13499 | 0.383 |
| LIG_EH1_1 | 553 | 561 | PF00400 | 0.292 |
| LIG_eIF4E_1 | 400 | 406 | PF01652 | 0.292 |
| LIG_eIF4E_1 | 422 | 428 | PF01652 | 0.292 |
| LIG_eIF4E_1 | 473 | 479 | PF01652 | 0.292 |
| LIG_EVH1_1 | 57 | 61 | PF00568 | 0.464 |
| LIG_FHA_1 | 130 | 136 | PF00498 | 0.405 |
| LIG_FHA_1 | 204 | 210 | PF00498 | 0.359 |
| LIG_FHA_1 | 455 | 461 | PF00498 | 0.292 |
| LIG_FHA_2 | 355 | 361 | PF00498 | 0.292 |
| LIG_FHA_2 | 372 | 378 | PF00498 | 0.292 |
| LIG_FHA_2 | 649 | 655 | PF00498 | 0.474 |
| LIG_GBD_Chelix_1 | 508 | 516 | PF00786 | 0.292 |
| LIG_LIR_Apic_2 | 24 | 30 | PF02991 | 0.485 |
| LIG_LIR_Gen_1 | 561 | 570 | PF02991 | 0.292 |
| LIG_LIR_Gen_1 | 576 | 585 | PF02991 | 0.292 |
| LIG_LIR_Nem_3 | 270 | 275 | PF02991 | 0.292 |
| LIG_LIR_Nem_3 | 323 | 328 | PF02991 | 0.292 |
| LIG_LIR_Nem_3 | 344 | 348 | PF02991 | 0.338 |
| LIG_LIR_Nem_3 | 518 | 522 | PF02991 | 0.292 |
| LIG_LIR_Nem_3 | 561 | 566 | PF02991 | 0.292 |
| LIG_LIR_Nem_3 | 576 | 580 | PF02991 | 0.292 |
| LIG_LIR_Nem_3 | 582 | 586 | PF02991 | 0.288 |
| LIG_MYND_1 | 85 | 89 | PF01753 | 0.501 |
| LIG_NRBOX | 657 | 663 | PF00104 | 0.360 |
| LIG_PCNA_PIPBox_1 | 556 | 565 | PF02747 | 0.292 |
| LIG_PCNA_yPIPBox_3 | 624 | 632 | PF02747 | 0.436 |
| LIG_Pex14_2 | 543 | 547 | PF04695 | 0.292 |
| LIG_PTB_Apo_2 | 548 | 555 | PF02174 | 0.433 |
| LIG_PTB_Apo_2 | 657 | 664 | PF02174 | 0.359 |
| LIG_PTB_Phospho_1 | 657 | 663 | PF10480 | 0.360 |
| LIG_REV1ctd_RIR_1 | 126 | 134 | PF16727 | 0.470 |
| LIG_SH2_CRK | 159 | 163 | PF00017 | 0.354 |
| LIG_SH2_CRK | 266 | 270 | PF00017 | 0.331 |
| LIG_SH2_CRK | 345 | 349 | PF00017 | 0.323 |
| LIG_SH2_CRK | 350 | 354 | PF00017 | 0.323 |
| LIG_SH2_CRK | 370 | 374 | PF00017 | 0.155 |
| LIG_SH2_CRK | 400 | 404 | PF00017 | 0.292 |
| LIG_SH2_CRK | 519 | 523 | PF00017 | 0.292 |
| LIG_SH2_CRK | 563 | 567 | PF00017 | 0.308 |
| LIG_SH2_CRK | 603 | 607 | PF00017 | 0.351 |
| LIG_SH2_PTP2 | 103 | 106 | PF00017 | 0.619 |
| LIG_SH2_PTP2 | 211 | 214 | PF00017 | 0.423 |
| LIG_SH2_PTP2 | 325 | 328 | PF00017 | 0.292 |
| LIG_SH2_SRC | 137 | 140 | PF00017 | 0.359 |
| LIG_SH2_SRC | 211 | 214 | PF00017 | 0.423 |
| LIG_SH2_SRC | 422 | 425 | PF00017 | 0.292 |
| LIG_SH2_STAP1 | 350 | 354 | PF00017 | 0.292 |
| LIG_SH2_STAP1 | 577 | 581 | PF00017 | 0.308 |
| LIG_SH2_STAT3 | 605 | 608 | PF00017 | 0.500 |
| LIG_SH2_STAT5 | 103 | 106 | PF00017 | 0.619 |
| LIG_SH2_STAT5 | 137 | 140 | PF00017 | 0.366 |
| LIG_SH2_STAT5 | 211 | 214 | PF00017 | 0.423 |
| LIG_SH2_STAT5 | 325 | 328 | PF00017 | 0.292 |
| LIG_SH2_STAT5 | 350 | 353 | PF00017 | 0.292 |
| LIG_SH2_STAT5 | 366 | 369 | PF00017 | 0.370 |
| LIG_SH2_STAT5 | 378 | 381 | PF00017 | 0.320 |
| LIG_SH2_STAT5 | 422 | 425 | PF00017 | 0.292 |
| LIG_SH2_STAT5 | 459 | 462 | PF00017 | 0.292 |
| LIG_SH2_STAT5 | 473 | 476 | PF00017 | 0.292 |
| LIG_SH2_STAT5 | 569 | 572 | PF00017 | 0.376 |
| LIG_SH2_STAT5 | 583 | 586 | PF00017 | 0.292 |
| LIG_SH2_STAT5 | 605 | 608 | PF00017 | 0.363 |
| LIG_SH2_STAT5 | 611 | 614 | PF00017 | 0.330 |
| LIG_SH3_3 | 149 | 155 | PF00018 | 0.406 |
| LIG_SH3_3 | 219 | 225 | PF00018 | 0.334 |
| LIG_SH3_3 | 55 | 61 | PF00018 | 0.469 |
| LIG_SH3_3 | 78 | 84 | PF00018 | 0.473 |
| LIG_SUMO_SIM_anti_2 | 589 | 594 | PF11976 | 0.364 |
| LIG_SUMO_SIM_par_1 | 462 | 469 | PF11976 | 0.292 |
| LIG_TYR_ITIM | 157 | 162 | PF00017 | 0.365 |
| LIG_TYR_ITIM | 209 | 214 | PF00017 | 0.427 |
| LIG_TYR_ITIM | 264 | 269 | PF00017 | 0.346 |
| LIG_TYR_ITIM | 348 | 353 | PF00017 | 0.292 |
| LIG_TYR_ITIM | 398 | 403 | PF00017 | 0.292 |
| MOD_CDC14_SPxK_1 | 435 | 438 | PF00782 | 0.292 |
| MOD_CDK_SPxK_1 | 432 | 438 | PF00069 | 0.292 |
| MOD_CK1_1 | 168 | 174 | PF00069 | 0.429 |
| MOD_CK1_1 | 19 | 25 | PF00069 | 0.469 |
| MOD_CK1_1 | 371 | 377 | PF00069 | 0.386 |
| MOD_CK1_1 | 43 | 49 | PF00069 | 0.491 |
| MOD_CK2_1 | 354 | 360 | PF00069 | 0.292 |
| MOD_CK2_1 | 371 | 377 | PF00069 | 0.292 |
| MOD_CK2_1 | 648 | 654 | PF00069 | 0.450 |
| MOD_GlcNHglycan | 119 | 122 | PF01048 | 0.617 |
| MOD_GlcNHglycan | 198 | 201 | PF01048 | 0.382 |
| MOD_GlcNHglycan | 370 | 373 | PF01048 | 0.408 |
| MOD_GlcNHglycan | 498 | 501 | PF01048 | 0.361 |
| MOD_GlcNHglycan | 72 | 75 | PF01048 | 0.455 |
| MOD_GSK3_1 | 137 | 144 | PF00069 | 0.378 |
| MOD_GSK3_1 | 15 | 22 | PF00069 | 0.456 |
| MOD_GSK3_1 | 192 | 199 | PF00069 | 0.376 |
| MOD_GSK3_1 | 292 | 299 | PF00069 | 0.302 |
| MOD_GSK3_1 | 320 | 327 | PF00069 | 0.292 |
| MOD_GSK3_1 | 450 | 457 | PF00069 | 0.292 |
| MOD_GSK3_1 | 459 | 466 | PF00069 | 0.292 |
| MOD_GSK3_1 | 473 | 480 | PF00069 | 0.292 |
| MOD_GSK3_1 | 491 | 498 | PF00069 | 0.370 |
| MOD_GSK3_1 | 523 | 530 | PF00069 | 0.381 |
| MOD_GSK3_1 | 56 | 63 | PF00069 | 0.460 |
| MOD_LATS_1 | 88 | 94 | PF00433 | 0.498 |
| MOD_N-GLC_1 | 16 | 21 | PF02516 | 0.458 |
| MOD_N-GLC_1 | 192 | 197 | PF02516 | 0.369 |
| MOD_NEK2_1 | 111 | 116 | PF00069 | 0.757 |
| MOD_NEK2_1 | 16 | 21 | PF00069 | 0.458 |
| MOD_NEK2_1 | 235 | 240 | PF00069 | 0.526 |
| MOD_NEK2_1 | 341 | 346 | PF00069 | 0.297 |
| MOD_NEK2_1 | 348 | 353 | PF00069 | 0.285 |
| MOD_NEK2_1 | 354 | 359 | PF00069 | 0.280 |
| MOD_NEK2_1 | 491 | 496 | PF00069 | 0.292 |
| MOD_NEK2_1 | 593 | 598 | PF00069 | 0.408 |
| MOD_NEK2_1 | 661 | 666 | PF00069 | 0.350 |
| MOD_NEK2_2 | 124 | 129 | PF00069 | 0.515 |
| MOD_NEK2_2 | 320 | 325 | PF00069 | 0.292 |
| MOD_NEK2_2 | 558 | 563 | PF00069 | 0.292 |
| MOD_OFUCOSY | 64 | 71 | PF10250 | 0.457 |
| MOD_PIKK_1 | 527 | 533 | PF00454 | 0.381 |
| MOD_PK_1 | 588 | 594 | PF00069 | 0.380 |
| MOD_PKA_1 | 28 | 34 | PF00069 | 0.484 |
| MOD_PKA_2 | 28 | 34 | PF00069 | 0.484 |
| MOD_PKA_2 | 292 | 298 | PF00069 | 0.292 |
| MOD_PKA_2 | 330 | 336 | PF00069 | 0.292 |
| MOD_PKA_2 | 348 | 354 | PF00069 | 0.292 |
| MOD_Plk_1 | 16 | 22 | PF00069 | 0.458 |
| MOD_Plk_1 | 454 | 460 | PF00069 | 0.292 |
| MOD_Plk_1 | 588 | 594 | PF00069 | 0.380 |
| MOD_Plk_4 | 124 | 130 | PF00069 | 0.493 |
| MOD_Plk_4 | 144 | 150 | PF00069 | 0.221 |
| MOD_Plk_4 | 158 | 164 | PF00069 | 0.356 |
| MOD_Plk_4 | 22 | 28 | PF00069 | 0.482 |
| MOD_Plk_4 | 274 | 280 | PF00069 | 0.292 |
| MOD_Plk_4 | 301 | 307 | PF00069 | 0.292 |
| MOD_Plk_4 | 349 | 355 | PF00069 | 0.292 |
| MOD_Plk_4 | 550 | 556 | PF00069 | 0.292 |
| MOD_Plk_4 | 558 | 564 | PF00069 | 0.292 |
| MOD_Plk_4 | 588 | 594 | PF00069 | 0.380 |
| MOD_ProDKin_1 | 165 | 171 | PF00069 | 0.403 |
| MOD_ProDKin_1 | 259 | 265 | PF00069 | 0.369 |
| MOD_ProDKin_1 | 40 | 46 | PF00069 | 0.487 |
| MOD_ProDKin_1 | 432 | 438 | PF00069 | 0.300 |
| MOD_ProDKin_1 | 56 | 62 | PF00069 | 0.449 |
| MOD_SUMO_for_1 | 649 | 652 | PF00179 | 0.389 |
| MOD_SUMO_rev_2 | 469 | 479 | PF00179 | 0.292 |
| MOD_SUMO_rev_2 | 571 | 576 | PF00179 | 0.292 |
| MOD_SUMO_rev_2 | 652 | 658 | PF00179 | 0.394 |
| TRG_DiLeu_BaLyEn_6 | 337 | 342 | PF01217 | 0.292 |
| TRG_DiLeu_BaLyEn_6 | 423 | 428 | PF01217 | 0.292 |
| TRG_ENDOCYTIC_2 | 159 | 162 | PF00928 | 0.360 |
| TRG_ENDOCYTIC_2 | 211 | 214 | PF00928 | 0.423 |
| TRG_ENDOCYTIC_2 | 266 | 269 | PF00928 | 0.337 |
| TRG_ENDOCYTIC_2 | 325 | 328 | PF00928 | 0.292 |
| TRG_ENDOCYTIC_2 | 345 | 348 | PF00928 | 0.250 |
| TRG_ENDOCYTIC_2 | 350 | 353 | PF00928 | 0.323 |
| TRG_ENDOCYTIC_2 | 370 | 373 | PF00928 | 0.155 |
| TRG_ENDOCYTIC_2 | 390 | 393 | PF00928 | 0.155 |
| TRG_ENDOCYTIC_2 | 400 | 403 | PF00928 | 0.305 |
| TRG_ENDOCYTIC_2 | 519 | 522 | PF00928 | 0.292 |
| TRG_ENDOCYTIC_2 | 563 | 566 | PF00928 | 0.303 |
| TRG_ENDOCYTIC_2 | 577 | 580 | PF00928 | 0.266 |
| TRG_ENDOCYTIC_2 | 581 | 584 | PF00928 | 0.235 |
| TRG_ENDOCYTIC_2 | 603 | 606 | PF00928 | 0.335 |
| TRG_ER_diArg_1 | 12 | 14 | PF00400 | 0.470 |
| TRG_ER_diArg_1 | 27 | 29 | PF00400 | 0.481 |
| TRG_ER_diArg_1 | 407 | 409 | PF00400 | 0.292 |
| TRG_ER_diArg_1 | 96 | 98 | PF00400 | 0.618 |
| TRG_Pf-PMV_PEXEL_1 | 239 | 243 | PF00026 | 0.480 |
| TRG_Pf-PMV_PEXEL_1 | 520 | 525 | PF00026 | 0.292 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1PBM9 | Leptomonas seymouri | 97% | 100% |
| A0A0S4JQS7 | Bodo saltans | 89% | 100% |
| A0A1X0NJW9 | Trypanosomatidae | 93% | 100% |
| A0A381MM20 | Leishmania infantum | 25% | 100% |
| A0A3Q8IE37 | Leishmania donovani | 27% | 100% |
| A0A3Q8IFA8 | Leishmania donovani | 25% | 100% |
| A0A3S5H5I2 | Leishmania donovani | 99% | 100% |
| A0A422N2S4 | Trypanosoma rangeli | 89% | 100% |
| A0LSL4 | Acidothermus cellulolyticus (strain ATCC 43068 / DSM 8971 / 11B) | 47% | 100% |
| A0RR28 | Campylobacter fetus subsp. fetus (strain 82-40) | 46% | 100% |
| A1A3C7 | Bifidobacterium adolescentis (strain ATCC 15703 / DSM 20083 / NCTC 11814 / E194a) | 48% | 100% |
| A1B8N8 | Paracoccus denitrificans (strain Pd 1222) | 47% | 100% |
| A1UR47 | Bartonella bacilliformis (strain ATCC 35685 / NCTC 12138 / KC583) | 48% | 100% |
| A3DIM7 | Acetivibrio thermocellus (strain ATCC 27405 / DSM 1237 / JCM 9322 / NBRC 103400 / NCIMB 10682 / NRRL B-4536 / VPI 7372) | 47% | 100% |
| A4GYP3 | Populus trichocarpa | 48% | 100% |
| A4H497 | Leishmania braziliensis | 97% | 100% |
| A4HE61 | Leishmania braziliensis | 25% | 100% |
| A4HGU6 | Leishmania braziliensis | 25% | 100% |
| A4HSH2 | Leishmania infantum | 99% | 100% |
| A4I3X4 | Leishmania infantum | 27% | 100% |
| A5CQ58 | Clavibacter michiganensis subsp. michiganensis (strain NCPPB 382) | 47% | 100% |
| A5ILX0 | Thermotoga petrophila (strain ATCC BAA-488 / DSM 13995 / JCM 10881 / RKU-1) | 48% | 100% |
| A6H5F1 | Cycas taitungensis | 47% | 100% |
| A6LQH4 | Clostridium beijerinckii (strain ATCC 51743 / NCIMB 8052) | 48% | 100% |
| A6MMA7 | Chloranthus spicatus | 47% | 100% |
| A6Q4C2 | Nitratiruptor sp. (strain SB155-2) | 45% | 100% |
| A6W7G7 | Kineococcus radiotolerans (strain ATCC BAA-149 / DSM 14245 / SRS30216) | 47% | 100% |
| A7H019 | Campylobacter curvus (strain 525.92) | 46% | 100% |
| A7NIR1 | Roseiflexus castenholzii (strain DSM 13941 / HLO8) | 47% | 100% |
| A7ZC35 | Campylobacter concisus (strain 13826) | 46% | 100% |
| A8F3K0 | Pseudothermotoga lettingae (strain ATCC BAA-301 / DSM 14385 / NBRC 107922 / TMO) | 48% | 100% |
| A8M2J5 | Salinispora arenicola (strain CNS-205) | 46% | 100% |
| A9BCD9 | Prochlorococcus marinus (strain MIT 9211) | 46% | 100% |
| A9BFX5 | Petrotoga mobilis (strain DSM 10674 / SJ95) | 49% | 100% |
| A9L981 | Lemna minor | 48% | 100% |
| A9WNC6 | Renibacterium salmoninarum (strain ATCC 33209 / DSM 20767 / JCM 11484 / NBRC 15589 / NCIMB 2235) | 48% | 100% |
| B0RED6 | Clavibacter michiganensis subsp. sepedonicus (strain ATCC 33113 / DSM 20744 / JCM 9667 / LMG 2889 / C-1) | 47% | 100% |
| B1LBC1 | Thermotoga sp. (strain RQ2) | 48% | 100% |
| B3CSS9 | Orientia tsutsugamushi (strain Ikeda) | 47% | 100% |
| B3DTV2 | Bifidobacterium longum (strain DJO10A) | 49% | 100% |
| B3EHU6 | Chlorobium limicola (strain DSM 245 / NBRC 103803 / 6330) | 44% | 100% |
| B4U989 | Hydrogenobaculum sp. (strain Y04AAS1) | 50% | 100% |
| B5ER44 | Acidithiobacillus ferrooxidans (strain ATCC 53993 / BNL-5-31) | 47% | 100% |
| B7GTZ1 | Bifidobacterium longum subsp. infantis (strain ATCC 15697 / DSM 20088 / JCM 1222 / NCTC 11817 / S12) | 49% | 100% |
| B7IG42 | Thermosipho africanus (strain TCF52B) | 49% | 100% |
| B7JB86 | Acidithiobacillus ferrooxidans (strain ATCC 23270 / DSM 14882 / CIP 104768 / NCIMB 8455) | 47% | 100% |
| B8DRD0 | Desulfovibrio vulgaris (strain DSM 19637 / Miyazaki F) | 46% | 100% |
| B8DWS4 | Bifidobacterium animalis subsp. lactis (strain AD011) | 44% | 100% |
| B8FZ36 | Desulfitobacterium hafniense (strain DSM 10664 / DCB-2) | 48% | 100% |
| B9L1H1 | Thermomicrobium roseum (strain ATCC 27502 / DSM 5159 / P-2) | 48% | 100% |
| C0QW65 | Brachyspira hyodysenteriae (strain ATCC 49526 / WA1) | 49% | 100% |
| C1F3N8 | Acidobacterium capsulatum (strain ATCC 51196 / DSM 11244 / BCRC 80197 / JCM 7670 / NBRC 15755 / NCIMB 13165 / 161) | 47% | 100% |
| C5C1U6 | Beutenbergia cavernae (strain ATCC BAA-8 / DSM 12333 / NBRC 16432) | 48% | 100% |
| C9ZUD8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 93% | 100% |
| E8NHQ7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 100% | 100% |
| E9AXJ6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
| E9AXJ7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 25% | 100% |
| E9B064 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
| O50288 | Rickettsia prowazekii (strain Madrid E) | 47% | 100% |
| O66907 | Aquifex aeolicus (strain VF5) | 47% | 100% |
| P26526 | Chlamydomonas reinhardtii | 48% | 100% |
| P26679 | Enterococcus hirae (strain ATCC 9790 / DSM 20160 / JCM 8729 / LMG 6399 / NBRC 3181 / NCIMB 6459 / NCDO 1258 / NCTC 12367 / WDCM 00089 / R) | 45% | 100% |
| P27179 | Synechocystis sp. (strain PCC 6803 / Kazusa) | 47% | 100% |
| P35009 | Galdieria sulphuraria | 47% | 100% |
| P41167 | Acidithiobacillus ferridurans | 47% | 100% |
| P72245 | Rhodobacter capsulatus | 47% | 100% |
| Q06FX6 | Pelargonium hortorum | 47% | 100% |
| Q0RDB2 | Frankia alni (strain ACN14a) | 49% | 100% |
| Q14FH2 | Populus alba | 48% | 100% |
| Q17Y80 | Helicobacter acinonychis (strain Sheeba) | 46% | 100% |
| Q1AVH7 | Rubrobacter xylanophilus (strain DSM 9941 / NBRC 16129 / PRD-1) | 49% | 100% |
| Q1IIG6 | Koribacter versatilis (strain Ellin345) | 46% | 100% |
| Q1MRB9 | Lawsonia intracellularis (strain PHE/MN1-00) | 48% | 100% |
| Q24MN9 | Desulfitobacterium hafniense (strain Y51) | 48% | 100% |
| Q2J6N1 | Frankia casuarinae (strain DSM 45818 / CECT 9043 / CcI3) | 47% | 100% |
| Q2JIG0 | Synechococcus sp. (strain JA-2-3B'a(2-13)) | 49% | 100% |
| Q2JSW1 | Synechococcus sp. (strain JA-3-3Ab) | 49% | 100% |
| Q2PMS8 | Glycine max | 47% | 100% |
| Q32RS8 | Staurastrum punctulatum | 48% | 100% |
| Q37380 | Acanthamoeba castellanii | 47% | 100% |
| Q3B1F4 | Chlorobium luteolum (strain DSM 273 / BCRC 81028 / 2530) | 45% | 100% |
| Q3BAQ7 | Phalaenopsis aphrodite subsp. formosana | 47% | 100% |
| Q4Q821 | Leishmania major | 27% | 100% |
| Q4Q9X5 | Leishmania major | 24% | 100% |
| Q4Q9X6 | Leishmania major | 25% | 100% |
| Q4QJF1 | Leishmania major | 99% | 100% |
| Q5FF66 | Ehrlichia ruminantium (strain Gardel) | 50% | 100% |
| Q5HC95 | Ehrlichia ruminantium (strain Welgevonden) | 50% | 100% |
| Q5SCX6 | Huperzia lucidula | 47% | 100% |
| Q6AG60 | Leifsonia xyli subsp. xyli (strain CTCB07) | 47% | 100% |
| Q6B8Q8 | Gracilaria tenuistipitata var. liui | 48% | 100% |
| Q6C326 | Yarrowia lipolytica (strain CLIB 122 / E 150) | 49% | 100% |
| Q6EW63 | Nymphaea alba | 48% | 100% |
| Q6G1W7 | Bartonella henselae (strain ATCC 49882 / DSM 28221 / Houston 1) | 47% | 100% |
| Q6YXK3 | Physcomitrium patens | 48% | 100% |
| Q7V5S7 | Prochlorococcus marinus (strain MIT 9313) | 46% | 100% |
| Q85AU2 | Anthoceros angustus | 48% | 100% |
| Q85FN4 | Adiantum capillus-veneris | 48% | 100% |
| Q8G7B1 | Bifidobacterium longum (strain NCC 2705) | 49% | 100% |
| Q8MA05 | Chaetosphaeridium globosum | 47% | 100% |
| Q8RC17 | Caldanaerobacter subterraneus subsp. tengcongensis (strain DSM 15242 / JCM 11007 / NBRC 100824 / MB4) | 46% | 100% |
| Q9BBS3 | Lotus japonicus | 47% | 100% |
| Q9GS23 | Trypanosoma brucei brucei | 93% | 100% |
| Q9X1U7 | Thermotoga maritima (strain ATCC 43589 / DSM 3109 / JCM 10099 / NBRC 100826 / MSB8) | 48% | 100% |
| V5AVB0 | Trypanosoma cruzi | 89% | 100% |