| 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: 8 |
| NetGPI | no | yes: 0, no: 8 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0005634 | nucleus | 5 | 1 |
| GO:0005737 | cytoplasm | 2 | 1 |
| GO:0043226 | organelle | 2 | 1 |
| GO:0043227 | membrane-bounded organelle | 3 | 1 |
| GO:0043229 | intracellular organelle | 3 | 1 |
| GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
| GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9AUJ4
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0008152 | metabolic process | 1 | 4 |
| GO:0009058 | biosynthetic process | 2 | 4 |
| GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
| GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
| GO:0006753 | nucleoside phosphate metabolic process | 4 | 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:0009117 | nucleotide metabolic process | 5 | 1 |
| GO:0009165 | nucleotide biosynthetic process | 6 | 1 |
| GO:0009435 | NAD biosynthetic process | 8 | 1 |
| GO:0009987 | cellular process | 1 | 1 |
| GO:0018130 | heterocycle biosynthetic process | 4 | 1 |
| GO:0019359 | nicotinamide nucleotide biosynthetic process | 7 | 1 |
| GO:0019362 | pyridine nucleotide metabolic process | 5 | 1 |
| GO:0019363 | pyridine nucleotide biosynthetic process | 6 | 1 |
| GO:0019438 | aromatic compound biosynthetic process | 4 | 1 |
| GO:0019637 | organophosphate metabolic process | 3 | 1 |
| GO:0034356 | NAD biosynthesis via nicotinamide riboside salvage pathway | 9 | 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:0046483 | heterocycle metabolic process | 3 | 1 |
| GO:0046496 | nicotinamide nucleotide metabolic process | 6 | 1 |
| GO:0055086 | nucleobase-containing small molecule metabolic process | 3 | 1 |
| GO:0071704 | organic substance metabolic process | 2 | 1 |
| GO:0072524 | pyridine-containing compound metabolic process | 4 | 1 |
| GO:0072525 | pyridine-containing compound biosynthetic process | 5 | 1 |
| GO:0090407 | organophosphate 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:0003824 | catalytic activity | 1 | 4 |
| GO:0000309 | nicotinamide-nucleotide adenylyltransferase activity | 6 | 1 |
| GO:0016462 | pyrophosphatase activity | 5 | 1 |
| GO:0016740 | transferase activity | 2 | 1 |
| GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 1 |
| GO:0016779 | nucleotidyltransferase activity | 4 | 1 |
| GO:0016787 | hydrolase activity | 2 | 1 |
| GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 1 |
| GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 1 |
| GO:0016887 | ATP hydrolysis activity | 7 | 1 |
| GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 1 |
| GO:0070566 | adenylyltransferase activity | 5 | 1 |
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 148 | 152 | PF00656 | 0.513 |
| CLV_NRD_NRD_1 | 130 | 132 | PF00675 | 0.525 |
| CLV_NRD_NRD_1 | 30 | 32 | PF00675 | 0.512 |
| CLV_NRD_NRD_1 | 423 | 425 | PF00675 | 0.314 |
| CLV_NRD_NRD_1 | 430 | 432 | PF00675 | 0.287 |
| CLV_NRD_NRD_1 | 503 | 505 | PF00675 | 0.296 |
| CLV_PCSK_FUR_1 | 128 | 132 | PF00082 | 0.593 |
| CLV_PCSK_KEX2_1 | 130 | 132 | PF00082 | 0.525 |
| CLV_PCSK_KEX2_1 | 30 | 32 | PF00082 | 0.512 |
| CLV_PCSK_KEX2_1 | 423 | 425 | PF00082 | 0.282 |
| CLV_PCSK_KEX2_1 | 430 | 432 | PF00082 | 0.265 |
| CLV_PCSK_SKI1_1 | 223 | 227 | PF00082 | 0.568 |
| CLV_PCSK_SKI1_1 | 283 | 287 | PF00082 | 0.493 |
| CLV_PCSK_SKI1_1 | 30 | 34 | PF00082 | 0.518 |
| CLV_PCSK_SKI1_1 | 40 | 44 | PF00082 | 0.366 |
| CLV_PCSK_SKI1_1 | 525 | 529 | PF00082 | 0.274 |
| DEG_APCC_DBOX_1 | 282 | 290 | PF00400 | 0.534 |
| DOC_CKS1_1 | 396 | 401 | PF01111 | 0.453 |
| DOC_CYCLIN_RxL_1 | 34 | 44 | PF00134 | 0.431 |
| DOC_CYCLIN_yCln2_LP_2 | 396 | 402 | PF00134 | 0.453 |
| DOC_MAPK_gen_1 | 128 | 138 | PF00069 | 0.502 |
| DOC_MAPK_gen_1 | 430 | 439 | PF00069 | 0.510 |
| DOC_MAPK_MEF2A_6 | 131 | 140 | PF00069 | 0.505 |
| DOC_MAPK_MEF2A_6 | 430 | 439 | PF00069 | 0.385 |
| DOC_PP1_RVXF_1 | 81 | 88 | PF00149 | 0.569 |
| DOC_PP2B_LxvP_1 | 518 | 521 | PF13499 | 0.496 |
| DOC_USP7_MATH_1 | 197 | 201 | PF00917 | 0.276 |
| DOC_USP7_MATH_1 | 237 | 241 | PF00917 | 0.618 |
| DOC_USP7_MATH_1 | 266 | 270 | PF00917 | 0.710 |
| DOC_USP7_MATH_1 | 296 | 300 | PF00917 | 0.603 |
| DOC_USP7_MATH_1 | 350 | 354 | PF00917 | 0.656 |
| DOC_USP7_MATH_1 | 36 | 40 | PF00917 | 0.477 |
| DOC_USP7_UBL2_3 | 409 | 413 | PF12436 | 0.536 |
| DOC_WW_Pin1_4 | 10 | 15 | PF00397 | 0.363 |
| DOC_WW_Pin1_4 | 156 | 161 | PF00397 | 0.735 |
| DOC_WW_Pin1_4 | 395 | 400 | PF00397 | 0.528 |
| LIG_14-3-3_CanoR_1 | 16 | 20 | PF00244 | 0.429 |
| LIG_14-3-3_CanoR_1 | 261 | 266 | PF00244 | 0.598 |
| LIG_14-3-3_CanoR_1 | 434 | 440 | PF00244 | 0.508 |
| LIG_14-3-3_CanoR_1 | 504 | 509 | PF00244 | 0.555 |
| LIG_14-3-3_CanoR_1 | 51 | 58 | PF00244 | 0.570 |
| LIG_Actin_WH2_2 | 302 | 319 | PF00022 | 0.518 |
| LIG_Actin_WH2_2 | 414 | 432 | PF00022 | 0.510 |
| LIG_APCC_ABBA_1 | 321 | 326 | PF00400 | 0.428 |
| LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.439 |
| LIG_CaM_IQ_9 | 373 | 389 | PF13499 | 0.510 |
| LIG_Clathr_ClatBox_1 | 456 | 460 | PF01394 | 0.536 |
| LIG_deltaCOP1_diTrp_1 | 305 | 310 | PF00928 | 0.288 |
| LIG_eIF4E_1 | 370 | 376 | PF01652 | 0.555 |
| LIG_FHA_1 | 109 | 115 | PF00498 | 0.507 |
| LIG_FHA_1 | 119 | 125 | PF00498 | 0.334 |
| LIG_FHA_1 | 371 | 377 | PF00498 | 0.562 |
| LIG_FHA_1 | 378 | 384 | PF00498 | 0.510 |
| LIG_FHA_1 | 401 | 407 | PF00498 | 0.465 |
| LIG_FHA_1 | 439 | 445 | PF00498 | 0.526 |
| LIG_FHA_1 | 487 | 493 | PF00498 | 0.555 |
| LIG_FHA_2 | 39 | 45 | PF00498 | 0.419 |
| LIG_FHA_2 | 396 | 402 | PF00498 | 0.442 |
| LIG_FHA_2 | 471 | 477 | PF00498 | 0.533 |
| LIG_LIR_Gen_1 | 224 | 234 | PF02991 | 0.559 |
| LIG_LIR_LC3C_4 | 187 | 190 | PF02991 | 0.448 |
| LIG_LIR_Nem_3 | 224 | 229 | PF02991 | 0.517 |
| LIG_LIR_Nem_3 | 364 | 368 | PF02991 | 0.484 |
| LIG_SH2_SRC | 404 | 407 | PF00017 | 0.471 |
| LIG_SH2_STAP1 | 344 | 348 | PF00017 | 0.639 |
| LIG_SH2_STAP1 | 404 | 408 | PF00017 | 0.471 |
| LIG_SH2_STAT5 | 498 | 501 | PF00017 | 0.471 |
| LIG_SH3_3 | 462 | 468 | PF00018 | 0.536 |
| LIG_SH3_3 | 526 | 532 | PF00018 | 0.487 |
| LIG_SH3_3 | 97 | 103 | PF00018 | 0.615 |
| LIG_SUMO_SIM_anti_2 | 183 | 190 | PF11976 | 0.462 |
| LIG_SUMO_SIM_anti_2 | 2 | 8 | PF11976 | 0.522 |
| LIG_SUMO_SIM_par_1 | 398 | 403 | PF11976 | 0.498 |
| MOD_CDC14_SPxK_1 | 13 | 16 | PF00782 | 0.369 |
| MOD_CDK_SPxK_1 | 10 | 16 | PF00069 | 0.362 |
| MOD_CK1_1 | 129 | 135 | PF00069 | 0.604 |
| MOD_CK1_1 | 238 | 244 | PF00069 | 0.728 |
| MOD_CK1_1 | 254 | 260 | PF00069 | 0.659 |
| MOD_CK1_1 | 264 | 270 | PF00069 | 0.639 |
| MOD_CK1_1 | 299 | 305 | PF00069 | 0.525 |
| MOD_CK1_1 | 325 | 331 | PF00069 | 0.487 |
| MOD_CK2_1 | 129 | 135 | PF00069 | 0.604 |
| MOD_CK2_1 | 229 | 235 | PF00069 | 0.664 |
| MOD_CK2_1 | 299 | 305 | PF00069 | 0.499 |
| MOD_CK2_1 | 38 | 44 | PF00069 | 0.487 |
| MOD_CK2_1 | 395 | 401 | PF00069 | 0.273 |
| MOD_CK2_1 | 469 | 475 | PF00069 | 0.432 |
| MOD_CK2_1 | 538 | 544 | PF00069 | 0.350 |
| MOD_CMANNOS | 307 | 310 | PF00535 | 0.268 |
| MOD_Cter_Amidation | 502 | 505 | PF01082 | 0.350 |
| MOD_GlcNHglycan | 121 | 124 | PF01048 | 0.421 |
| MOD_GlcNHglycan | 147 | 150 | PF01048 | 0.525 |
| MOD_GlcNHglycan | 215 | 218 | PF01048 | 0.710 |
| MOD_GlcNHglycan | 231 | 234 | PF01048 | 0.658 |
| MOD_GlcNHglycan | 237 | 240 | PF01048 | 0.755 |
| MOD_GlcNHglycan | 258 | 261 | PF01048 | 0.690 |
| MOD_GlcNHglycan | 268 | 271 | PF01048 | 0.723 |
| MOD_GlcNHglycan | 277 | 281 | PF01048 | 0.552 |
| MOD_GlcNHglycan | 345 | 349 | PF01048 | 0.688 |
| MOD_GlcNHglycan | 66 | 69 | PF01048 | 0.476 |
| MOD_GSK3_1 | 119 | 126 | PF00069 | 0.433 |
| MOD_GSK3_1 | 141 | 148 | PF00069 | 0.440 |
| MOD_GSK3_1 | 213 | 220 | PF00069 | 0.617 |
| MOD_GSK3_1 | 221 | 228 | PF00069 | 0.499 |
| MOD_GSK3_1 | 238 | 245 | PF00069 | 0.770 |
| MOD_GSK3_1 | 391 | 398 | PF00069 | 0.382 |
| MOD_N-GLC_1 | 235 | 240 | PF02516 | 0.565 |
| MOD_N-GLC_2 | 550 | 552 | PF02516 | 0.542 |
| MOD_NEK2_1 | 484 | 489 | PF00069 | 0.193 |
| MOD_NEK2_1 | 79 | 84 | PF00069 | 0.508 |
| MOD_PIKK_1 | 51 | 57 | PF00454 | 0.545 |
| MOD_PK_1 | 261 | 267 | PF00069 | 0.636 |
| MOD_PKA_1 | 30 | 36 | PF00069 | 0.530 |
| MOD_PKA_1 | 504 | 510 | PF00069 | 0.432 |
| MOD_PKA_2 | 129 | 135 | PF00069 | 0.578 |
| MOD_PKA_2 | 15 | 21 | PF00069 | 0.429 |
| MOD_PKA_2 | 210 | 216 | PF00069 | 0.618 |
| MOD_PKA_2 | 30 | 36 | PF00069 | 0.504 |
| MOD_PKA_2 | 50 | 56 | PF00069 | 0.303 |
| MOD_Plk_1 | 391 | 397 | PF00069 | 0.372 |
| MOD_Plk_1 | 400 | 406 | PF00069 | 0.236 |
| MOD_Plk_1 | 513 | 519 | PF00069 | 0.319 |
| MOD_Plk_4 | 225 | 231 | PF00069 | 0.407 |
| MOD_Plk_4 | 251 | 257 | PF00069 | 0.702 |
| MOD_Plk_4 | 438 | 444 | PF00069 | 0.353 |
| MOD_ProDKin_1 | 10 | 16 | PF00069 | 0.362 |
| MOD_ProDKin_1 | 156 | 162 | PF00069 | 0.728 |
| MOD_ProDKin_1 | 395 | 401 | PF00069 | 0.394 |
| TRG_DiLeu_BaEn_1 | 184 | 189 | PF01217 | 0.498 |
| TRG_DiLeu_BaEn_1 | 417 | 422 | PF01217 | 0.353 |
| TRG_DiLeu_BaLyEn_6 | 355 | 360 | PF01217 | 0.478 |
| TRG_ENDOCYTIC_2 | 168 | 171 | PF00928 | 0.560 |
| TRG_ENDOCYTIC_2 | 498 | 501 | PF00928 | 0.316 |
| TRG_ER_diArg_1 | 128 | 131 | PF00400 | 0.542 |
| TRG_ER_diArg_1 | 29 | 31 | PF00400 | 0.516 |
| TRG_ER_diArg_1 | 383 | 386 | PF00400 | 0.369 |
| TRG_ER_diArg_1 | 422 | 424 | PF00400 | 0.370 |
| TRG_ER_diArg_1 | 429 | 431 | PF00400 | 0.314 |
| TRG_Pf-PMV_PEXEL_1 | 381 | 385 | PF00026 | 0.372 |
| TRG_Pf-PMV_PEXEL_1 | 40 | 44 | PF00026 | 0.426 |
| TRG_Pf-PMV_PEXEL_1 | 72 | 76 | PF00026 | 0.451 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N0P7H4 | Leptomonas seymouri | 54% | 100% |
| A0A0S4ILY4 | Bodo saltans | 34% | 100% |
| A0A3S7WVU1 | Leishmania donovani | 89% | 100% |
| A4HYR1 | Leishmania infantum | 90% | 100% |
| E9AIA7 | Leishmania braziliensis | 77% | 100% |
| Q4QCZ0 | Leishmania major | 87% | 100% |
| V5C0A1 | Trypanosoma cruzi | 34% | 100% |