| 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: 9 |
| NetGPI | no | yes: 0, no: 9 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0005737 | cytoplasm | 2 | 10 |
| GO:0110165 | cellular anatomical entity | 1 | 10 |
Related structures:
AlphaFold database: A4HLD7
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0000166 | nucleotide binding | 3 | 10 |
| GO:0003824 | catalytic activity | 1 | 10 |
| GO:0005488 | binding | 1 | 10 |
| GO:0008670 | 2,4-dienoyl-CoA reductase (NADPH) activity | 5 | 6 |
| GO:0010181 | FMN binding | 4 | 10 |
| GO:0016491 | oxidoreductase activity | 2 | 10 |
| GO:0016627 | oxidoreductase activity, acting on the CH-CH group of donors | 3 | 6 |
| GO:0016628 | oxidoreductase activity, acting on the CH-CH group of donors, NAD or NADP as acceptor | 4 | 6 |
| GO:0032553 | ribonucleotide binding | 3 | 10 |
| GO:0036094 | small molecule binding | 2 | 10 |
| GO:0043167 | ion binding | 2 | 10 |
| GO:0043168 | anion binding | 3 | 10 |
| GO:0097159 | organic cyclic compound binding | 2 | 10 |
| GO:0097367 | carbohydrate derivative binding | 2 | 10 |
| GO:1901265 | nucleoside phosphate binding | 3 | 10 |
| GO:1901363 | heterocyclic compound binding | 2 | 10 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 319 | 323 | PF00656 | 0.485 |
| CLV_C14_Caspase3-7 | 472 | 476 | PF00656 | 0.228 |
| CLV_MEL_PAP_1 | 225 | 231 | PF00089 | 0.256 |
| CLV_NRD_NRD_1 | 294 | 296 | PF00675 | 0.302 |
| CLV_NRD_NRD_1 | 521 | 523 | PF00675 | 0.287 |
| CLV_NRD_NRD_1 | 566 | 568 | PF00675 | 0.333 |
| CLV_PCSK_KEX2_1 | 151 | 153 | PF00082 | 0.163 |
| CLV_PCSK_KEX2_1 | 294 | 296 | PF00082 | 0.284 |
| CLV_PCSK_KEX2_1 | 521 | 523 | PF00082 | 0.287 |
| CLV_PCSK_PC1ET2_1 | 151 | 153 | PF00082 | 0.163 |
| CLV_PCSK_PC7_1 | 290 | 296 | PF00082 | 0.276 |
| CLV_PCSK_SKI1_1 | 216 | 220 | PF00082 | 0.276 |
| CLV_PCSK_SKI1_1 | 330 | 334 | PF00082 | 0.221 |
| CLV_PCSK_SKI1_1 | 384 | 388 | PF00082 | 0.483 |
| CLV_PCSK_SKI1_1 | 458 | 462 | PF00082 | 0.378 |
| CLV_PCSK_SKI1_1 | 614 | 618 | PF00082 | 0.243 |
| CLV_PCSK_SKI1_1 | 694 | 698 | PF00082 | 0.457 |
| CLV_Separin_Metazoa | 210 | 214 | PF03568 | 0.456 |
| DEG_APCC_DBOX_1 | 205 | 213 | PF00400 | 0.421 |
| DEG_APCC_DBOX_1 | 227 | 235 | PF00400 | 0.504 |
| DEG_SPOP_SBC_1 | 542 | 546 | PF00917 | 0.374 |
| DOC_CKS1_1 | 298 | 303 | PF01111 | 0.460 |
| DOC_CYCLIN_yCln2_LP_2 | 31 | 37 | PF00134 | 0.476 |
| DOC_CYCLIN_yCln2_LP_2 | 333 | 339 | PF00134 | 0.464 |
| DOC_CYCLIN_yCln2_LP_2 | 604 | 610 | PF00134 | 0.334 |
| DOC_MAPK_gen_1 | 139 | 147 | PF00069 | 0.363 |
| DOC_MAPK_gen_1 | 204 | 211 | PF00069 | 0.421 |
| DOC_MAPK_gen_1 | 455 | 464 | PF00069 | 0.274 |
| DOC_MAPK_gen_1 | 57 | 66 | PF00069 | 0.438 |
| DOC_MAPK_gen_1 | 669 | 677 | PF00069 | 0.379 |
| DOC_MAPK_gen_1 | 713 | 721 | PF00069 | 0.443 |
| DOC_MAPK_MEF2A_6 | 140 | 149 | PF00069 | 0.453 |
| DOC_MAPK_MEF2A_6 | 455 | 464 | PF00069 | 0.404 |
| DOC_MAPK_MEF2A_6 | 59 | 68 | PF00069 | 0.418 |
| DOC_MAPK_MEF2A_6 | 6 | 15 | PF00069 | 0.282 |
| DOC_PP1_RVXF_1 | 202 | 208 | PF00149 | 0.464 |
| DOC_PP2B_PxIxI_1 | 300 | 306 | PF00149 | 0.504 |
| DOC_PP4_FxxP_1 | 185 | 188 | PF00568 | 0.363 |
| DOC_USP7_MATH_1 | 218 | 222 | PF00917 | 0.504 |
| DOC_USP7_MATH_1 | 236 | 240 | PF00917 | 0.424 |
| DOC_USP7_MATH_1 | 288 | 292 | PF00917 | 0.530 |
| DOC_USP7_MATH_1 | 37 | 41 | PF00917 | 0.512 |
| DOC_USP7_MATH_1 | 403 | 407 | PF00917 | 0.393 |
| DOC_USP7_MATH_1 | 587 | 591 | PF00917 | 0.310 |
| DOC_USP7_UBL2_3 | 2 | 6 | PF12436 | 0.450 |
| DOC_USP7_UBL2_3 | 569 | 573 | PF12436 | 0.367 |
| DOC_USP7_UBL2_3 | 57 | 61 | PF12436 | 0.363 |
| DOC_USP7_UBL2_3 | 690 | 694 | PF12436 | 0.274 |
| DOC_USP7_UBL2_3 | 714 | 718 | PF12436 | 0.450 |
| DOC_WW_Pin1_4 | 126 | 131 | PF00397 | 0.466 |
| DOC_WW_Pin1_4 | 297 | 302 | PF00397 | 0.460 |
| DOC_WW_Pin1_4 | 30 | 35 | PF00397 | 0.504 |
| DOC_WW_Pin1_4 | 538 | 543 | PF00397 | 0.322 |
| DOC_WW_Pin1_4 | 571 | 576 | PF00397 | 0.236 |
| DOC_WW_Pin1_4 | 694 | 699 | PF00397 | 0.526 |
| DOC_WW_Pin1_4 | 70 | 75 | PF00397 | 0.439 |
| LIG_14-3-3_CanoR_1 | 228 | 232 | PF00244 | 0.424 |
| LIG_14-3-3_CanoR_1 | 279 | 285 | PF00244 | 0.449 |
| LIG_14-3-3_CanoR_1 | 330 | 336 | PF00244 | 0.439 |
| LIG_14-3-3_CanoR_1 | 39 | 44 | PF00244 | 0.363 |
| LIG_14-3-3_CanoR_1 | 467 | 471 | PF00244 | 0.467 |
| LIG_14-3-3_CanoR_1 | 596 | 600 | PF00244 | 0.386 |
| LIG_Actin_WH2_2 | 198 | 215 | PF00022 | 0.464 |
| LIG_BIR_III_4 | 217 | 221 | PF00653 | 0.476 |
| LIG_CtBP_PxDLS_1 | 10 | 14 | PF00389 | 0.439 |
| LIG_CtBP_PxDLS_1 | 142 | 146 | PF00389 | 0.504 |
| LIG_eIF4E_1 | 81 | 87 | PF01652 | 0.363 |
| LIG_FHA_1 | 136 | 142 | PF00498 | 0.502 |
| LIG_FHA_1 | 284 | 290 | PF00498 | 0.510 |
| LIG_FHA_1 | 298 | 304 | PF00498 | 0.486 |
| LIG_FHA_1 | 449 | 455 | PF00498 | 0.326 |
| LIG_FHA_1 | 459 | 465 | PF00498 | 0.339 |
| LIG_FHA_1 | 632 | 638 | PF00498 | 0.271 |
| LIG_FHA_1 | 672 | 678 | PF00498 | 0.382 |
| LIG_FHA_1 | 695 | 701 | PF00498 | 0.475 |
| LIG_FHA_1 | 710 | 716 | PF00498 | 0.546 |
| LIG_FHA_2 | 151 | 157 | PF00498 | 0.433 |
| LIG_FHA_2 | 238 | 244 | PF00498 | 0.439 |
| LIG_FHA_2 | 27 | 33 | PF00498 | 0.439 |
| LIG_FHA_2 | 40 | 46 | PF00498 | 0.439 |
| LIG_FHA_2 | 408 | 414 | PF00498 | 0.293 |
| LIG_FHA_2 | 417 | 423 | PF00498 | 0.222 |
| LIG_FHA_2 | 467 | 473 | PF00498 | 0.307 |
| LIG_FHA_2 | 543 | 549 | PF00498 | 0.386 |
| LIG_FHA_2 | 557 | 563 | PF00498 | 0.435 |
| LIG_IBAR_NPY_1 | 47 | 49 | PF08397 | 0.504 |
| LIG_LIR_Gen_1 | 12 | 23 | PF02991 | 0.464 |
| LIG_LIR_Gen_1 | 155 | 164 | PF02991 | 0.504 |
| LIG_LIR_Gen_1 | 221 | 231 | PF02991 | 0.360 |
| LIG_LIR_Gen_1 | 475 | 484 | PF02991 | 0.311 |
| LIG_LIR_LC3C_4 | 672 | 677 | PF02991 | 0.177 |
| LIG_LIR_Nem_3 | 12 | 18 | PF02991 | 0.464 |
| LIG_LIR_Nem_3 | 155 | 160 | PF02991 | 0.467 |
| LIG_LIR_Nem_3 | 221 | 226 | PF02991 | 0.369 |
| LIG_LIR_Nem_3 | 475 | 481 | PF02991 | 0.311 |
| LIG_LIR_Nem_3 | 654 | 658 | PF02991 | 0.282 |
| LIG_LYPXL_yS_3 | 4 | 7 | PF13949 | 0.251 |
| LIG_PCNA_yPIPBox_3 | 358 | 368 | PF02747 | 0.276 |
| LIG_PCNA_yPIPBox_3 | 430 | 440 | PF02747 | 0.292 |
| LIG_PDZ_Class_2 | 726 | 731 | PF00595 | 0.300 |
| LIG_Pex14_2 | 223 | 227 | PF04695 | 0.439 |
| LIG_Pex14_2 | 566 | 570 | PF04695 | 0.258 |
| LIG_SH2_CRK | 49 | 53 | PF00017 | 0.504 |
| LIG_SH2_GRB2like | 119 | 122 | PF00017 | 0.418 |
| LIG_SH2_SRC | 119 | 122 | PF00017 | 0.368 |
| LIG_SH2_SRC | 478 | 481 | PF00017 | 0.318 |
| LIG_SH2_SRC | 509 | 512 | PF00017 | 0.171 |
| LIG_SH2_STAP1 | 421 | 425 | PF00017 | 0.253 |
| LIG_SH2_STAP1 | 478 | 482 | PF00017 | 0.318 |
| LIG_SH2_STAP1 | 49 | 53 | PF00017 | 0.504 |
| LIG_SH2_STAT5 | 180 | 183 | PF00017 | 0.421 |
| LIG_SH2_STAT5 | 282 | 285 | PF00017 | 0.490 |
| LIG_SH2_STAT5 | 337 | 340 | PF00017 | 0.504 |
| LIG_SH2_STAT5 | 509 | 512 | PF00017 | 0.258 |
| LIG_SH2_STAT5 | 555 | 558 | PF00017 | 0.451 |
| LIG_SH2_STAT5 | 665 | 668 | PF00017 | 0.318 |
| LIG_SH3_3 | 604 | 610 | PF00018 | 0.334 |
| LIG_SH3_4 | 2 | 9 | PF00018 | 0.273 |
| LIG_SUMO_SIM_anti_2 | 170 | 178 | PF11976 | 0.421 |
| LIG_SUMO_SIM_anti_2 | 230 | 236 | PF11976 | 0.424 |
| LIG_SUMO_SIM_par_1 | 672 | 678 | PF11976 | 0.334 |
| LIG_TRAF2_1 | 379 | 382 | PF00917 | 0.323 |
| LIG_TRAF2_1 | 559 | 562 | PF00917 | 0.182 |
| LIG_UBA3_1 | 131 | 140 | PF00899 | 0.253 |
| LIG_WRC_WIRS_1 | 655 | 660 | PF05994 | 0.248 |
| MOD_CK1_1 | 133 | 139 | PF00069 | 0.325 |
| MOD_CK1_1 | 26 | 32 | PF00069 | 0.282 |
| MOD_CK1_1 | 541 | 547 | PF00069 | 0.374 |
| MOD_CK1_1 | 595 | 601 | PF00069 | 0.177 |
| MOD_CK2_1 | 237 | 243 | PF00069 | 0.284 |
| MOD_CK2_1 | 26 | 32 | PF00069 | 0.282 |
| MOD_CK2_1 | 39 | 45 | PF00069 | 0.282 |
| MOD_CK2_1 | 416 | 422 | PF00069 | 0.258 |
| MOD_CK2_1 | 505 | 511 | PF00069 | 0.440 |
| MOD_CK2_1 | 542 | 548 | PF00069 | 0.386 |
| MOD_CK2_1 | 556 | 562 | PF00069 | 0.435 |
| MOD_CK2_1 | 685 | 691 | PF00069 | 0.334 |
| MOD_Cter_Amidation | 519 | 522 | PF01082 | 0.299 |
| MOD_GlcNHglycan | 253 | 256 | PF01048 | 0.355 |
| MOD_GlcNHglycan | 260 | 263 | PF01048 | 0.180 |
| MOD_GlcNHglycan | 343 | 346 | PF01048 | 0.378 |
| MOD_GlcNHglycan | 405 | 408 | PF01048 | 0.322 |
| MOD_GlcNHglycan | 422 | 426 | PF01048 | 0.374 |
| MOD_GlcNHglycan | 545 | 548 | PF01048 | 0.400 |
| MOD_GlcNHglycan | 590 | 593 | PF01048 | 0.409 |
| MOD_GlcNHglycan | 74 | 77 | PF01048 | 0.274 |
| MOD_GSK3_1 | 126 | 133 | PF00069 | 0.244 |
| MOD_GSK3_1 | 187 | 194 | PF00069 | 0.380 |
| MOD_GSK3_1 | 26 | 33 | PF00069 | 0.374 |
| MOD_GSK3_1 | 269 | 276 | PF00069 | 0.257 |
| MOD_GSK3_1 | 35 | 42 | PF00069 | 0.374 |
| MOD_GSK3_1 | 403 | 410 | PF00069 | 0.381 |
| MOD_GSK3_1 | 537 | 544 | PF00069 | 0.329 |
| MOD_GSK3_1 | 583 | 590 | PF00069 | 0.426 |
| MOD_GSK3_1 | 66 | 73 | PF00069 | 0.282 |
| MOD_GSK3_1 | 681 | 688 | PF00069 | 0.374 |
| MOD_GSK3_1 | 694 | 701 | PF00069 | 0.485 |
| MOD_LATS_1 | 490 | 496 | PF00433 | 0.177 |
| MOD_N-GLC_1 | 236 | 241 | PF02516 | 0.250 |
| MOD_N-GLC_1 | 458 | 463 | PF02516 | 0.370 |
| MOD_N-GLC_1 | 592 | 597 | PF02516 | 0.177 |
| MOD_N-GLC_1 | 709 | 714 | PF02516 | 0.458 |
| MOD_N-GLC_2 | 351 | 353 | PF02516 | 0.281 |
| MOD_NEK2_1 | 13 | 18 | PF00069 | 0.248 |
| MOD_NEK2_1 | 227 | 232 | PF00069 | 0.282 |
| MOD_NEK2_1 | 619 | 624 | PF00069 | 0.330 |
| MOD_NEK2_1 | 66 | 71 | PF00069 | 0.282 |
| MOD_NEK2_2 | 450 | 455 | PF00069 | 0.380 |
| MOD_PIKK_1 | 133 | 139 | PF00454 | 0.311 |
| MOD_PIKK_1 | 237 | 243 | PF00454 | 0.318 |
| MOD_PK_1 | 492 | 498 | PF00069 | 0.177 |
| MOD_PKA_2 | 227 | 233 | PF00069 | 0.258 |
| MOD_PKA_2 | 38 | 44 | PF00069 | 0.177 |
| MOD_PKA_2 | 466 | 472 | PF00069 | 0.373 |
| MOD_PKA_2 | 595 | 601 | PF00069 | 0.313 |
| MOD_PKA_2 | 642 | 648 | PF00069 | 0.298 |
| MOD_Plk_1 | 143 | 149 | PF00069 | 0.343 |
| MOD_Plk_1 | 339 | 345 | PF00069 | 0.177 |
| MOD_Plk_1 | 421 | 427 | PF00069 | 0.252 |
| MOD_Plk_1 | 458 | 464 | PF00069 | 0.355 |
| MOD_Plk_1 | 592 | 598 | PF00069 | 0.177 |
| MOD_Plk_1 | 614 | 620 | PF00069 | 0.318 |
| MOD_Plk_1 | 671 | 677 | PF00069 | 0.334 |
| MOD_Plk_4 | 219 | 225 | PF00069 | 0.189 |
| MOD_Plk_4 | 227 | 233 | PF00069 | 0.282 |
| MOD_Plk_4 | 416 | 422 | PF00069 | 0.258 |
| MOD_Plk_4 | 492 | 498 | PF00069 | 0.196 |
| MOD_Plk_4 | 614 | 620 | PF00069 | 0.290 |
| MOD_Plk_4 | 671 | 677 | PF00069 | 0.299 |
| MOD_ProDKin_1 | 126 | 132 | PF00069 | 0.321 |
| MOD_ProDKin_1 | 297 | 303 | PF00069 | 0.313 |
| MOD_ProDKin_1 | 30 | 36 | PF00069 | 0.374 |
| MOD_ProDKin_1 | 538 | 544 | PF00069 | 0.322 |
| MOD_ProDKin_1 | 571 | 577 | PF00069 | 0.236 |
| MOD_ProDKin_1 | 694 | 700 | PF00069 | 0.519 |
| MOD_ProDKin_1 | 70 | 76 | PF00069 | 0.282 |
| MOD_SUMO_rev_2 | 580 | 584 | PF00179 | 0.322 |
| TRG_DiLeu_BaEn_4 | 382 | 388 | PF01217 | 0.286 |
| TRG_DiLeu_BaLyEn_6 | 145 | 150 | PF01217 | 0.365 |
| TRG_DiLeu_BaLyEn_6 | 298 | 303 | PF01217 | 0.374 |
| TRG_DiLeu_BaLyEn_6 | 82 | 87 | PF01217 | 0.177 |
| TRG_ENDOCYTIC_2 | 4 | 7 | PF00928 | 0.357 |
| TRG_ENDOCYTIC_2 | 478 | 481 | PF00928 | 0.318 |
| TRG_ENDOCYTIC_2 | 49 | 52 | PF00928 | 0.374 |
| TRG_ENDOCYTIC_2 | 555 | 558 | PF00928 | 0.451 |
| TRG_ENDOCYTIC_2 | 613 | 616 | PF00928 | 0.334 |
| TRG_ENDOCYTIC_2 | 655 | 658 | PF00928 | 0.258 |
| TRG_ER_diArg_1 | 18 | 21 | PF00400 | 0.282 |
| TRG_ER_diArg_1 | 204 | 207 | PF00400 | 0.258 |
| TRG_ER_diArg_1 | 293 | 295 | PF00400 | 0.346 |
| TRG_ER_diArg_1 | 521 | 523 | PF00400 | 0.287 |
| TRG_Pf-PMV_PEXEL_1 | 96 | 100 | PF00026 | 0.177 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N0P302 | Leptomonas seymouri | 74% | 100% |
| A0A0N0P5L6 | Leptomonas seymouri | 31% | 100% |
| A0A0S4JCH5 | Bodo saltans | 33% | 100% |
| A0A0S4JST7 | Bodo saltans | 46% | 100% |
| A0A1X0NKW1 | Trypanosomatidae | 30% | 100% |
| A0A1X0NU55 | Trypanosomatidae | 53% | 100% |
| A0A3S5H5T4 | Leishmania donovani | 31% | 100% |
| A0A3S7X6G9 | Leishmania donovani | 87% | 100% |
| A4H4Q6 | Leishmania braziliensis | 31% | 100% |
| A4HSY5 | Leishmania infantum | 31% | 100% |
| A4I8U6 | Leishmania infantum | 87% | 100% |
| A4J778 | Desulforamulus reducens (strain ATCC BAA-1160 / DSM 100696 / MI-1) | 34% | 100% |
| C9ZTL4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 100% |
| E9AKX1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 30% | 100% |
| E9B3R5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 85% | 100% |
| G9F1Y9 | Clostridium sporogenes (strain ATCC 7955 / DSM 767 / NBRC 16411 / NCIMB 8053 / NCTC 8594 / PA 3679) | 30% | 100% |
| O87278 | Rhizobium meliloti (strain 1021) | 29% | 100% |
| P16099 | Methylophilus methylotrophus | 28% | 100% |
| P19410 | Clostridium scindens (strain JCM 10418 / VPI 12708) | 31% | 100% |
| P32370 | Clostridium scindens (strain JCM 10418 / VPI 12708) | 29% | 100% |
| P32382 | Thermoanaerobacter brockii | 33% | 100% |
| P42593 | Escherichia coli (strain K12) | 43% | 100% |
| Q48303 | Hyphomicrobium sp. (strain x) | 26% | 99% |
| Q4Q4A9 | Leishmania major | 86% | 100% |
| Q4QIY4 | Leishmania major | 31% | 100% |
| V5AR23 | Trypanosoma cruzi | 53% | 100% |
| V5BNI9 | Trypanosoma cruzi | 32% | 100% |