| 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:0005654 | nucleoplasm | 2 | 2 |
| GO:0005829 | cytosol | 2 | 2 |
| GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: Q4QD65
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0000166 | nucleotide binding | 3 | 2 |
| GO:0003824 | catalytic activity | 1 | 10 |
| GO:0004497 | monooxygenase activity | 3 | 5 |
| GO:0004517 | nitric-oxide synthase activity | 5 | 5 |
| GO:0005488 | binding | 1 | 2 |
| GO:0010181 | FMN binding | 4 | 2 |
| GO:0016491 | oxidoreductase activity | 2 | 10 |
| GO:0016705 | oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen | 3 | 5 |
| GO:0016709 | oxidoreductase activity, acting on paired donors, with incorporation or reduction of molecular oxygen, NAD(P)H as one donor, and incorporation of one atom of oxygen | 4 | 5 |
| GO:0032553 | ribonucleotide binding | 3 | 2 |
| GO:0036094 | small molecule binding | 2 | 2 |
| GO:0043167 | ion binding | 2 | 2 |
| GO:0043168 | anion binding | 3 | 2 |
| GO:0050660 | flavin adenine dinucleotide binding | 4 | 2 |
| GO:0097159 | organic cyclic compound binding | 2 | 2 |
| GO:0097367 | carbohydrate derivative binding | 2 | 2 |
| GO:1901265 | nucleoside phosphate binding | 3 | 2 |
| GO:1901363 | heterocyclic compound binding | 2 | 2 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_NRD_NRD_1 | 2 | 4 | PF00675 | 0.586 |
| CLV_NRD_NRD_1 | 298 | 300 | PF00675 | 0.550 |
| CLV_NRD_NRD_1 | 325 | 327 | PF00675 | 0.609 |
| CLV_NRD_NRD_1 | 447 | 449 | PF00675 | 0.361 |
| CLV_PCSK_KEX2_1 | 2 | 4 | PF00082 | 0.531 |
| CLV_PCSK_KEX2_1 | 298 | 300 | PF00082 | 0.593 |
| CLV_PCSK_KEX2_1 | 325 | 327 | PF00082 | 0.609 |
| CLV_PCSK_KEX2_1 | 447 | 449 | PF00082 | 0.363 |
| CLV_PCSK_SKI1_1 | 125 | 129 | PF00082 | 0.659 |
| CLV_PCSK_SKI1_1 | 185 | 189 | PF00082 | 0.583 |
| CLV_PCSK_SKI1_1 | 375 | 379 | PF00082 | 0.707 |
| CLV_PCSK_SKI1_1 | 479 | 483 | PF00082 | 0.308 |
| CLV_PCSK_SKI1_1 | 505 | 509 | PF00082 | 0.294 |
| CLV_PCSK_SKI1_1 | 88 | 92 | PF00082 | 0.647 |
| CLV_Separin_Metazoa | 476 | 480 | PF03568 | 0.424 |
| DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.346 |
| DEG_ODPH_VHL_1 | 434 | 446 | PF01847 | 0.444 |
| DEG_SPOP_SBC_1 | 226 | 230 | PF00917 | 0.590 |
| DOC_CYCLIN_RxL_1 | 151 | 159 | PF00134 | 0.414 |
| DOC_CYCLIN_yCln2_LP_2 | 183 | 189 | PF00134 | 0.376 |
| DOC_CYCLIN_yCln2_LP_2 | 412 | 418 | PF00134 | 0.455 |
| DOC_CYCLIN_yCln2_LP_2 | 421 | 427 | PF00134 | 0.310 |
| DOC_MAPK_RevD_3 | 283 | 299 | PF00069 | 0.356 |
| DOC_MAPK_RevD_3 | 310 | 326 | PF00069 | 0.282 |
| DOC_PP1_RVXF_1 | 569 | 575 | PF00149 | 0.599 |
| DOC_PP2B_PxIxI_1 | 110 | 116 | PF00149 | 0.426 |
| DOC_USP7_MATH_1 | 245 | 249 | PF00917 | 0.428 |
| DOC_USP7_MATH_1 | 324 | 328 | PF00917 | 0.421 |
| DOC_USP7_MATH_1 | 373 | 377 | PF00917 | 0.431 |
| DOC_USP7_MATH_1 | 452 | 456 | PF00917 | 0.541 |
| DOC_USP7_MATH_1 | 536 | 540 | PF00917 | 0.518 |
| DOC_WW_Pin1_4 | 104 | 109 | PF00397 | 0.436 |
| DOC_WW_Pin1_4 | 166 | 171 | PF00397 | 0.361 |
| DOC_WW_Pin1_4 | 229 | 234 | PF00397 | 0.550 |
| DOC_WW_Pin1_4 | 261 | 266 | PF00397 | 0.440 |
| DOC_WW_Pin1_4 | 310 | 315 | PF00397 | 0.445 |
| DOC_WW_Pin1_4 | 331 | 336 | PF00397 | 0.360 |
| DOC_WW_Pin1_4 | 420 | 425 | PF00397 | 0.460 |
| DOC_WW_Pin1_4 | 73 | 78 | PF00397 | 0.477 |
| LIG_14-3-3_CanoR_1 | 216 | 223 | PF00244 | 0.396 |
| LIG_14-3-3_CanoR_1 | 298 | 303 | PF00244 | 0.351 |
| LIG_14-3-3_CanoR_1 | 325 | 331 | PF00244 | 0.455 |
| LIG_14-3-3_CanoR_1 | 447 | 457 | PF00244 | 0.545 |
| LIG_Actin_WH2_2 | 434 | 449 | PF00022 | 0.485 |
| LIG_Actin_WH2_2 | 470 | 485 | PF00022 | 0.424 |
| LIG_APCC_ABBA_1 | 215 | 220 | PF00400 | 0.447 |
| LIG_BRCT_BRCA1_1 | 422 | 426 | PF00533 | 0.361 |
| LIG_BRCT_BRCA1_1 | 454 | 458 | PF00533 | 0.583 |
| LIG_Clathr_ClatBox_1 | 563 | 567 | PF01394 | 0.645 |
| LIG_CSL_BTD_1 | 179 | 182 | PF09270 | 0.357 |
| LIG_deltaCOP1_diTrp_1 | 575 | 583 | PF00928 | 0.596 |
| LIG_eIF4E_1 | 390 | 396 | PF01652 | 0.339 |
| LIG_FHA_1 | 16 | 22 | PF00498 | 0.361 |
| LIG_FHA_1 | 307 | 313 | PF00498 | 0.431 |
| LIG_FHA_1 | 482 | 488 | PF00498 | 0.575 |
| LIG_FHA_1 | 506 | 512 | PF00498 | 0.505 |
| LIG_FHA_1 | 517 | 523 | PF00498 | 0.591 |
| LIG_FHA_1 | 577 | 583 | PF00498 | 0.638 |
| LIG_FHA_2 | 466 | 472 | PF00498 | 0.556 |
| LIG_LIR_Gen_1 | 194 | 204 | PF02991 | 0.367 |
| LIG_LIR_Gen_1 | 209 | 218 | PF02991 | 0.372 |
| LIG_LIR_Gen_1 | 23 | 32 | PF02991 | 0.331 |
| LIG_LIR_Gen_1 | 276 | 285 | PF02991 | 0.372 |
| LIG_LIR_Gen_1 | 392 | 401 | PF02991 | 0.438 |
| LIG_LIR_Gen_1 | 471 | 482 | PF02991 | 0.424 |
| LIG_LIR_Nem_3 | 194 | 199 | PF02991 | 0.342 |
| LIG_LIR_Nem_3 | 209 | 214 | PF02991 | 0.314 |
| LIG_LIR_Nem_3 | 23 | 29 | PF02991 | 0.331 |
| LIG_LIR_Nem_3 | 276 | 281 | PF02991 | 0.367 |
| LIG_LIR_Nem_3 | 392 | 396 | PF02991 | 0.429 |
| LIG_LIR_Nem_3 | 471 | 477 | PF02991 | 0.565 |
| LIG_LYPXL_yS_3 | 268 | 271 | PF13949 | 0.361 |
| LIG_NRBOX | 188 | 194 | PF00104 | 0.416 |
| LIG_NRBOX | 254 | 260 | PF00104 | 0.332 |
| LIG_Pex14_1 | 22 | 26 | PF04695 | 0.308 |
| LIG_Pex14_2 | 211 | 215 | PF04695 | 0.370 |
| LIG_PTB_Apo_2 | 395 | 402 | PF02174 | 0.437 |
| LIG_SH2_NCK_1 | 300 | 304 | PF00017 | 0.425 |
| LIG_SH2_PTP2 | 196 | 199 | PF00017 | 0.351 |
| LIG_SH2_PTP2 | 65 | 68 | PF00017 | 0.446 |
| LIG_SH2_SRC | 196 | 199 | PF00017 | 0.351 |
| LIG_SH2_SRC | 474 | 477 | PF00017 | 0.583 |
| LIG_SH2_SRC | 490 | 493 | PF00017 | 0.551 |
| LIG_SH2_SRC | 65 | 68 | PF00017 | 0.416 |
| LIG_SH2_STAP1 | 26 | 30 | PF00017 | 0.348 |
| LIG_SH2_STAP1 | 474 | 478 | PF00017 | 0.577 |
| LIG_SH2_STAP1 | 490 | 494 | PF00017 | 0.415 |
| LIG_SH2_STAT5 | 196 | 199 | PF00017 | 0.304 |
| LIG_SH2_STAT5 | 204 | 207 | PF00017 | 0.310 |
| LIG_SH2_STAT5 | 390 | 393 | PF00017 | 0.350 |
| LIG_SH2_STAT5 | 506 | 509 | PF00017 | 0.531 |
| LIG_SH2_STAT5 | 65 | 68 | PF00017 | 0.403 |
| LIG_SH3_3 | 1 | 7 | PF00018 | 0.311 |
| LIG_SH3_3 | 105 | 111 | PF00018 | 0.456 |
| LIG_SH3_3 | 167 | 173 | PF00018 | 0.357 |
| LIG_SH3_3 | 176 | 182 | PF00018 | 0.328 |
| LIG_SH3_3 | 278 | 284 | PF00018 | 0.375 |
| LIG_SH3_3 | 288 | 294 | PF00018 | 0.293 |
| LIG_SH3_3 | 308 | 314 | PF00018 | 0.309 |
| LIG_SH3_3 | 527 | 533 | PF00018 | 0.561 |
| LIG_SH3_3 | 66 | 72 | PF00018 | 0.443 |
| LIG_SUMO_SIM_anti_2 | 131 | 138 | PF11976 | 0.439 |
| LIG_SUMO_SIM_anti_2 | 270 | 276 | PF11976 | 0.414 |
| LIG_SUMO_SIM_par_1 | 270 | 276 | PF11976 | 0.414 |
| LIG_SUMO_SIM_par_1 | 286 | 292 | PF11976 | 0.202 |
| LIG_SUMO_SIM_par_1 | 562 | 568 | PF11976 | 0.593 |
| LIG_TRAF2_1 | 48 | 51 | PF00917 | 0.595 |
| LIG_TRAF2_1 | 495 | 498 | PF00917 | 0.461 |
| LIG_TRAF2_1 | 557 | 560 | PF00917 | 0.638 |
| LIG_TYR_ITIM | 24 | 29 | PF00017 | 0.336 |
| LIG_TYR_ITIM | 266 | 271 | PF00017 | 0.393 |
| LIG_TYR_ITIM | 472 | 477 | PF00017 | 0.424 |
| LIG_UBA3_1 | 214 | 222 | PF00899 | 0.412 |
| LIG_UBA3_1 | 255 | 261 | PF00899 | 0.474 |
| LIG_WRC_WIRS_1 | 277 | 282 | PF05994 | 0.388 |
| LIG_WRC_WIRS_1 | 390 | 395 | PF05994 | 0.410 |
| MOD_CK1_1 | 100 | 106 | PF00069 | 0.450 |
| MOD_CK1_1 | 140 | 146 | PF00069 | 0.516 |
| MOD_CK1_1 | 15 | 21 | PF00069 | 0.339 |
| MOD_CK1_1 | 200 | 206 | PF00069 | 0.375 |
| MOD_CK1_1 | 221 | 227 | PF00069 | 0.505 |
| MOD_CK1_1 | 228 | 234 | PF00069 | 0.493 |
| MOD_CK1_1 | 248 | 254 | PF00069 | 0.236 |
| MOD_CK1_1 | 260 | 266 | PF00069 | 0.445 |
| MOD_CK1_1 | 420 | 426 | PF00069 | 0.418 |
| MOD_CK2_1 | 206 | 212 | PF00069 | 0.394 |
| MOD_CK2_1 | 45 | 51 | PF00069 | 0.593 |
| MOD_CK2_1 | 465 | 471 | PF00069 | 0.527 |
| MOD_CK2_1 | 492 | 498 | PF00069 | 0.462 |
| MOD_CK2_1 | 554 | 560 | PF00069 | 0.583 |
| MOD_CK2_1 | 73 | 79 | PF00069 | 0.480 |
| MOD_GlcNHglycan | 120 | 123 | PF01048 | 0.691 |
| MOD_GlcNHglycan | 14 | 17 | PF01048 | 0.508 |
| MOD_GlcNHglycan | 193 | 196 | PF01048 | 0.596 |
| MOD_GlcNHglycan | 224 | 227 | PF01048 | 0.774 |
| MOD_GlcNHglycan | 290 | 294 | PF01048 | 0.577 |
| MOD_GlcNHglycan | 326 | 329 | PF01048 | 0.615 |
| MOD_GlcNHglycan | 379 | 382 | PF01048 | 0.699 |
| MOD_GlcNHglycan | 454 | 457 | PF01048 | 0.391 |
| MOD_GSK3_1 | 206 | 213 | PF00069 | 0.382 |
| MOD_GSK3_1 | 218 | 225 | PF00069 | 0.380 |
| MOD_GSK3_1 | 227 | 234 | PF00069 | 0.475 |
| MOD_GSK3_1 | 257 | 264 | PF00069 | 0.467 |
| MOD_GSK3_1 | 294 | 301 | PF00069 | 0.393 |
| MOD_GSK3_1 | 306 | 313 | PF00069 | 0.402 |
| MOD_GSK3_1 | 373 | 380 | PF00069 | 0.404 |
| MOD_GSK3_1 | 448 | 455 | PF00069 | 0.565 |
| MOD_GSK3_1 | 97 | 104 | PF00069 | 0.368 |
| MOD_NEK2_1 | 118 | 123 | PF00069 | 0.441 |
| MOD_NEK2_1 | 206 | 211 | PF00069 | 0.355 |
| MOD_NEK2_1 | 259 | 264 | PF00069 | 0.460 |
| MOD_NEK2_1 | 289 | 294 | PF00069 | 0.353 |
| MOD_NEK2_1 | 363 | 368 | PF00069 | 0.390 |
| MOD_NEK2_1 | 377 | 382 | PF00069 | 0.466 |
| MOD_NEK2_1 | 389 | 394 | PF00069 | 0.290 |
| MOD_NEK2_1 | 396 | 401 | PF00069 | 0.271 |
| MOD_NEK2_2 | 101 | 106 | PF00069 | 0.405 |
| MOD_NEK2_2 | 536 | 541 | PF00069 | 0.596 |
| MOD_PIKK_1 | 140 | 146 | PF00454 | 0.524 |
| MOD_PIKK_1 | 43 | 49 | PF00454 | 0.574 |
| MOD_PIKK_1 | 439 | 445 | PF00454 | 0.395 |
| MOD_PKA_1 | 298 | 304 | PF00069 | 0.334 |
| MOD_PKA_2 | 298 | 304 | PF00069 | 0.379 |
| MOD_PKA_2 | 324 | 330 | PF00069 | 0.441 |
| MOD_Plk_1 | 554 | 560 | PF00069 | 0.568 |
| MOD_Plk_2-3 | 554 | 560 | PF00069 | 0.568 |
| MOD_Plk_4 | 101 | 107 | PF00069 | 0.404 |
| MOD_Plk_4 | 200 | 206 | PF00069 | 0.346 |
| MOD_Plk_4 | 210 | 216 | PF00069 | 0.317 |
| MOD_Plk_4 | 267 | 273 | PF00069 | 0.374 |
| MOD_Plk_4 | 396 | 402 | PF00069 | 0.421 |
| MOD_Plk_4 | 57 | 63 | PF00069 | 0.384 |
| MOD_ProDKin_1 | 104 | 110 | PF00069 | 0.435 |
| MOD_ProDKin_1 | 166 | 172 | PF00069 | 0.359 |
| MOD_ProDKin_1 | 229 | 235 | PF00069 | 0.538 |
| MOD_ProDKin_1 | 261 | 267 | PF00069 | 0.430 |
| MOD_ProDKin_1 | 310 | 316 | PF00069 | 0.438 |
| MOD_ProDKin_1 | 331 | 337 | PF00069 | 0.356 |
| MOD_ProDKin_1 | 420 | 426 | PF00069 | 0.449 |
| MOD_ProDKin_1 | 73 | 79 | PF00069 | 0.473 |
| MOD_SUMO_for_1 | 488 | 491 | PF00179 | 0.591 |
| MOD_SUMO_rev_2 | 219 | 224 | PF00179 | 0.444 |
| MOD_SUMO_rev_2 | 79 | 87 | PF00179 | 0.451 |
| TRG_DiLeu_BaEn_1 | 238 | 243 | PF01217 | 0.432 |
| TRG_DiLeu_BaEn_1 | 560 | 565 | PF01217 | 0.603 |
| TRG_DiLeu_BaEn_2 | 275 | 281 | PF01217 | 0.393 |
| TRG_DiLeu_BaEn_2 | 524 | 530 | PF01217 | 0.536 |
| TRG_DiLeu_BaLyEn_6 | 254 | 259 | PF01217 | 0.444 |
| TRG_DiLeu_BaLyEn_6 | 284 | 289 | PF01217 | 0.331 |
| TRG_DiLeu_BaLyEn_6 | 433 | 438 | PF01217 | 0.427 |
| TRG_DiLeu_BaLyEn_6 | 559 | 564 | PF01217 | 0.662 |
| TRG_DiLeu_LyEn_5 | 238 | 243 | PF01217 | 0.418 |
| TRG_ENDOCYTIC_2 | 196 | 199 | PF00928 | 0.342 |
| TRG_ENDOCYTIC_2 | 26 | 29 | PF00928 | 0.391 |
| TRG_ENDOCYTIC_2 | 268 | 271 | PF00928 | 0.378 |
| TRG_ENDOCYTIC_2 | 390 | 393 | PF00928 | 0.413 |
| TRG_ENDOCYTIC_2 | 474 | 477 | PF00928 | 0.424 |
| TRG_ER_diArg_1 | 1 | 3 | PF00400 | 0.336 |
| TRG_ER_diArg_1 | 298 | 300 | PF00400 | 0.359 |
| TRG_ER_diArg_1 | 446 | 448 | PF00400 | 0.563 |
| TRG_ER_diArg_1 | 569 | 572 | PF00400 | 0.606 |
| TRG_NES_CRM1_1 | 273 | 286 | PF08389 | 0.394 |
| TRG_Pf-PMV_PEXEL_1 | 562 | 567 | PF00026 | 0.388 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1IB19 | Leptomonas seymouri | 60% | 100% |
| A0A0S4INF0 | Bodo saltans | 26% | 100% |
| A0A1X0P608 | Trypanosomatidae | 38% | 94% |
| A0A3Q8IK79 | Leishmania donovani | 95% | 100% |
| A4HA95 | Leishmania braziliensis | 84% | 100% |
| A4HYH5 | Leishmania infantum | 95% | 100% |
| D0A0U9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 93% |
| E9AS99 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |