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:0005634 | nucleus | 5 | 12 |
GO:0043226 | organelle | 2 | 12 |
GO:0043227 | membrane-bounded organelle | 3 | 12 |
GO:0043229 | intracellular organelle | 3 | 12 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
Related structures:
AlphaFold database: A4HIZ6
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006396 | RNA processing | 6 | 12 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 12 |
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0016070 | RNA metabolic process | 5 | 12 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0044237 | cellular metabolic process | 2 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0046483 | heterocycle metabolic process | 3 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:0090304 | nucleic acid metabolic process | 4 | 12 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 12 |
GO:0000394 | RNA splicing, via endonucleolytic cleavage and ligation | 8 | 1 |
GO:0006378 | mRNA polyadenylation | 7 | 1 |
GO:0006388 | tRNA splicing, via endonucleolytic cleavage and ligation | 9 | 1 |
GO:0006397 | mRNA processing | 7 | 1 |
GO:0006399 | tRNA metabolic process | 7 | 1 |
GO:0008033 | tRNA processing | 8 | 1 |
GO:0008380 | RNA splicing | 7 | 1 |
GO:0016071 | mRNA metabolic process | 6 | 1 |
GO:0031123 | RNA 3'-end processing | 7 | 1 |
GO:0031124 | mRNA 3'-end processing | 8 | 1 |
GO:0034470 | ncRNA processing | 7 | 1 |
GO:0034660 | ncRNA metabolic process | 6 | 1 |
GO:0043631 | RNA polyadenylation | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 12 |
GO:0016301 | kinase activity | 4 | 12 |
GO:0016740 | transferase activity | 2 | 12 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 12 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 12 |
GO:0019205 | nucleobase-containing compound kinase activity | 5 | 12 |
GO:0051731 | polynucleotide 5'-hydroxyl-kinase activity | 5 | 12 |
GO:0000166 | nucleotide binding | 3 | 2 |
GO:0005488 | binding | 1 | 2 |
GO:0005524 | ATP binding | 5 | 2 |
GO:0017076 | purine nucleotide binding | 4 | 2 |
GO:0030554 | adenyl nucleotide binding | 5 | 2 |
GO:0032553 | ribonucleotide binding | 3 | 2 |
GO:0032555 | purine ribonucleotide binding | 4 | 2 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 2 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 2 |
GO:0036094 | small molecule binding | 2 | 2 |
GO:0043167 | ion binding | 2 | 2 |
GO:0043168 | anion binding | 3 | 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 |
GO:0046404 | polydeoxyribonucleotide 5'-hydroxyl-kinase activity | 7 | 1 |
GO:0051733 | polydeoxyribonucleotide kinase activity | 6 | 1 |
GO:0051734 | polynucleotide kinase activity | 6 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 32 | 34 | PF00675 | 0.452 |
CLV_PCSK_KEX2_1 | 371 | 373 | PF00082 | 0.313 |
CLV_PCSK_PC1ET2_1 | 371 | 373 | PF00082 | 0.404 |
CLV_PCSK_SKI1_1 | 101 | 105 | PF00082 | 0.413 |
CLV_PCSK_SKI1_1 | 126 | 130 | PF00082 | 0.403 |
CLV_PCSK_SKI1_1 | 17 | 21 | PF00082 | 0.431 |
CLV_PCSK_SKI1_1 | 352 | 356 | PF00082 | 0.504 |
CLV_PCSK_SKI1_1 | 400 | 404 | PF00082 | 0.436 |
DOC_CKS1_1 | 163 | 168 | PF01111 | 0.487 |
DOC_CKS1_1 | 380 | 385 | PF01111 | 0.534 |
DOC_CYCLIN_yCln2_LP_2 | 163 | 169 | PF00134 | 0.487 |
DOC_MAPK_FxFP_2 | 168 | 171 | PF00069 | 0.340 |
DOC_MAPK_gen_1 | 230 | 238 | PF00069 | 0.340 |
DOC_MAPK_gen_1 | 475 | 485 | PF00069 | 0.400 |
DOC_MAPK_MEF2A_6 | 120 | 129 | PF00069 | 0.526 |
DOC_PP1_RVXF_1 | 124 | 130 | PF00149 | 0.427 |
DOC_PP2B_LxvP_1 | 80 | 83 | PF13499 | 0.439 |
DOC_PP4_FxxP_1 | 168 | 171 | PF00568 | 0.340 |
DOC_PP4_FxxP_1 | 380 | 383 | PF00568 | 0.532 |
DOC_USP7_MATH_1 | 257 | 261 | PF00917 | 0.662 |
DOC_USP7_MATH_1 | 264 | 268 | PF00917 | 0.709 |
DOC_USP7_MATH_1 | 270 | 274 | PF00917 | 0.707 |
DOC_USP7_MATH_1 | 432 | 436 | PF00917 | 0.453 |
DOC_USP7_MATH_1 | 64 | 68 | PF00917 | 0.383 |
DOC_WW_Pin1_4 | 162 | 167 | PF00397 | 0.487 |
DOC_WW_Pin1_4 | 189 | 194 | PF00397 | 0.452 |
DOC_WW_Pin1_4 | 266 | 271 | PF00397 | 0.687 |
DOC_WW_Pin1_4 | 379 | 384 | PF00397 | 0.527 |
DOC_WW_Pin1_4 | 489 | 494 | PF00397 | 0.503 |
LIG_14-3-3_CanoR_1 | 17 | 23 | PF00244 | 0.384 |
LIG_14-3-3_CanoR_1 | 336 | 340 | PF00244 | 0.483 |
LIG_14-3-3_CanoR_1 | 400 | 405 | PF00244 | 0.492 |
LIG_14-3-3_CanoR_1 | 495 | 499 | PF00244 | 0.439 |
LIG_14-3-3_CanoR_1 | 89 | 99 | PF00244 | 0.435 |
LIG_APCC_ABBA_1 | 10 | 15 | PF00400 | 0.277 |
LIG_BRCT_BRCA1_1 | 466 | 470 | PF00533 | 0.336 |
LIG_Clathr_ClatBox_1 | 353 | 357 | PF01394 | 0.286 |
LIG_Clathr_ClatBox_1 | 391 | 395 | PF01394 | 0.473 |
LIG_EH1_1 | 211 | 219 | PF00400 | 0.452 |
LIG_FHA_1 | 190 | 196 | PF00498 | 0.427 |
LIG_FHA_1 | 280 | 286 | PF00498 | 0.529 |
LIG_FHA_1 | 356 | 362 | PF00498 | 0.493 |
LIG_FHA_1 | 382 | 388 | PF00498 | 0.453 |
LIG_FHA_1 | 495 | 501 | PF00498 | 0.454 |
LIG_FHA_1 | 50 | 56 | PF00498 | 0.355 |
LIG_FHA_1 | 75 | 81 | PF00498 | 0.405 |
LIG_FHA_2 | 285 | 291 | PF00498 | 0.430 |
LIG_FHA_2 | 43 | 49 | PF00498 | 0.401 |
LIG_FHA_2 | 436 | 442 | PF00498 | 0.516 |
LIG_FHA_2 | 451 | 457 | PF00498 | 0.338 |
LIG_FHA_2 | 514 | 520 | PF00498 | 0.280 |
LIG_LIR_Apic_2 | 165 | 171 | PF02991 | 0.487 |
LIG_LIR_Apic_2 | 334 | 340 | PF02991 | 0.564 |
LIG_LIR_Gen_1 | 435 | 444 | PF02991 | 0.532 |
LIG_LIR_Gen_1 | 467 | 477 | PF02991 | 0.306 |
LIG_LIR_Nem_3 | 239 | 243 | PF02991 | 0.369 |
LIG_LIR_Nem_3 | 435 | 439 | PF02991 | 0.522 |
LIG_LIR_Nem_3 | 467 | 473 | PF02991 | 0.320 |
LIG_NRBOX | 510 | 516 | PF00104 | 0.484 |
LIG_Pex14_1 | 144 | 148 | PF04695 | 0.452 |
LIG_Pex14_1 | 375 | 379 | PF04695 | 0.387 |
LIG_SH2_CRK | 154 | 158 | PF00017 | 0.340 |
LIG_SH2_PTP2 | 196 | 199 | PF00017 | 0.224 |
LIG_SH2_STAP1 | 91 | 95 | PF00017 | 0.487 |
LIG_SH2_STAT5 | 141 | 144 | PF00017 | 0.332 |
LIG_SH2_STAT5 | 196 | 199 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 378 | 381 | PF00017 | 0.399 |
LIG_SH2_STAT5 | 8 | 11 | PF00017 | 0.437 |
LIG_SH3_2 | 383 | 388 | PF14604 | 0.559 |
LIG_SH3_3 | 201 | 207 | PF00018 | 0.478 |
LIG_SH3_3 | 239 | 245 | PF00018 | 0.494 |
LIG_SH3_3 | 380 | 386 | PF00018 | 0.460 |
LIG_SH3_3 | 53 | 59 | PF00018 | 0.355 |
LIG_SH3_3 | 6 | 12 | PF00018 | 0.509 |
LIG_SH3_3 | 78 | 84 | PF00018 | 0.371 |
LIG_SUMO_SIM_anti_2 | 494 | 501 | PF11976 | 0.427 |
LIG_SUMO_SIM_anti_2 | 77 | 82 | PF11976 | 0.452 |
LIG_SUMO_SIM_par_1 | 155 | 160 | PF11976 | 0.340 |
LIG_SUMO_SIM_par_1 | 390 | 395 | PF11976 | 0.477 |
LIG_SUMO_SIM_par_1 | 446 | 453 | PF11976 | 0.422 |
LIG_SUMO_SIM_par_1 | 496 | 501 | PF11976 | 0.525 |
LIG_TRAF2_1 | 516 | 519 | PF00917 | 0.413 |
LIG_TRFH_1 | 8 | 12 | PF08558 | 0.407 |
LIG_TYR_ITIM | 152 | 157 | PF00017 | 0.340 |
LIG_ULM_U2AF65_1 | 371 | 376 | PF00076 | 0.275 |
MOD_CDC14_SPxK_1 | 385 | 388 | PF00782 | 0.556 |
MOD_CDK_SPxK_1 | 382 | 388 | PF00069 | 0.551 |
MOD_CDK_SPxK_1 | 489 | 495 | PF00069 | 0.504 |
MOD_CK1_1 | 21 | 27 | PF00069 | 0.452 |
MOD_CK1_1 | 277 | 283 | PF00069 | 0.639 |
MOD_CK1_1 | 28 | 34 | PF00069 | 0.452 |
MOD_CK1_1 | 42 | 48 | PF00069 | 0.253 |
MOD_CK1_1 | 435 | 441 | PF00069 | 0.498 |
MOD_CK1_1 | 452 | 458 | PF00069 | 0.290 |
MOD_CK1_1 | 69 | 75 | PF00069 | 0.435 |
MOD_CK2_1 | 105 | 111 | PF00069 | 0.327 |
MOD_CK2_1 | 42 | 48 | PF00069 | 0.414 |
MOD_CK2_1 | 450 | 456 | PF00069 | 0.404 |
MOD_CK2_1 | 468 | 474 | PF00069 | 0.537 |
MOD_CK2_1 | 513 | 519 | PF00069 | 0.399 |
MOD_CMANNOS | 307 | 310 | PF00535 | 0.496 |
MOD_GlcNHglycan | 266 | 269 | PF01048 | 0.733 |
MOD_GlcNHglycan | 272 | 275 | PF01048 | 0.772 |
MOD_GlcNHglycan | 500 | 503 | PF01048 | 0.579 |
MOD_GSK3_1 | 17 | 24 | PF00069 | 0.441 |
MOD_GSK3_1 | 258 | 265 | PF00069 | 0.650 |
MOD_GSK3_1 | 266 | 273 | PF00069 | 0.731 |
MOD_GSK3_1 | 284 | 291 | PF00069 | 0.546 |
MOD_GSK3_1 | 361 | 368 | PF00069 | 0.519 |
MOD_GSK3_1 | 390 | 397 | PF00069 | 0.434 |
MOD_GSK3_1 | 464 | 471 | PF00069 | 0.473 |
MOD_GSK3_1 | 494 | 501 | PF00069 | 0.445 |
MOD_GSK3_1 | 66 | 73 | PF00069 | 0.402 |
MOD_GSK3_1 | 91 | 98 | PF00069 | 0.389 |
MOD_N-GLC_1 | 189 | 194 | PF02516 | 0.452 |
MOD_NEK2_1 | 22 | 27 | PF00069 | 0.359 |
MOD_NEK2_1 | 288 | 293 | PF00069 | 0.434 |
MOD_NEK2_1 | 355 | 360 | PF00069 | 0.522 |
MOD_NEK2_1 | 361 | 366 | PF00069 | 0.586 |
MOD_NEK2_1 | 394 | 399 | PF00069 | 0.485 |
MOD_NEK2_1 | 468 | 473 | PF00069 | 0.508 |
MOD_NEK2_1 | 487 | 492 | PF00069 | 0.398 |
MOD_NEK2_1 | 498 | 503 | PF00069 | 0.375 |
MOD_NEK2_1 | 71 | 76 | PF00069 | 0.370 |
MOD_NEK2_1 | 95 | 100 | PF00069 | 0.437 |
MOD_PIKK_1 | 22 | 28 | PF00454 | 0.452 |
MOD_PIKK_1 | 277 | 283 | PF00454 | 0.538 |
MOD_PIKK_1 | 394 | 400 | PF00454 | 0.524 |
MOD_PK_1 | 66 | 72 | PF00069 | 0.452 |
MOD_PKA_2 | 335 | 341 | PF00069 | 0.494 |
MOD_PKA_2 | 494 | 500 | PF00069 | 0.446 |
MOD_Plk_1 | 322 | 328 | PF00069 | 0.401 |
MOD_Plk_1 | 394 | 400 | PF00069 | 0.432 |
MOD_Plk_1 | 473 | 479 | PF00069 | 0.439 |
MOD_Plk_4 | 137 | 143 | PF00069 | 0.338 |
MOD_Plk_4 | 284 | 290 | PF00069 | 0.464 |
MOD_Plk_4 | 303 | 309 | PF00069 | 0.317 |
MOD_Plk_4 | 365 | 371 | PF00069 | 0.316 |
MOD_Plk_4 | 387 | 393 | PF00069 | 0.442 |
MOD_Plk_4 | 411 | 417 | PF00069 | 0.603 |
MOD_Plk_4 | 432 | 438 | PF00069 | 0.398 |
MOD_Plk_4 | 478 | 484 | PF00069 | 0.510 |
MOD_Plk_4 | 494 | 500 | PF00069 | 0.422 |
MOD_Plk_4 | 66 | 72 | PF00069 | 0.379 |
MOD_Plk_4 | 74 | 80 | PF00069 | 0.308 |
MOD_Plk_4 | 95 | 101 | PF00069 | 0.416 |
MOD_ProDKin_1 | 162 | 168 | PF00069 | 0.487 |
MOD_ProDKin_1 | 189 | 195 | PF00069 | 0.452 |
MOD_ProDKin_1 | 266 | 272 | PF00069 | 0.691 |
MOD_ProDKin_1 | 379 | 385 | PF00069 | 0.527 |
MOD_ProDKin_1 | 489 | 495 | PF00069 | 0.504 |
MOD_SUMO_rev_2 | 517 | 522 | PF00179 | 0.326 |
TRG_DiLeu_BaEn_1 | 494 | 499 | PF01217 | 0.552 |
TRG_DiLeu_BaEn_4 | 186 | 192 | PF01217 | 0.452 |
TRG_DiLeu_BaLyEn_6 | 153 | 158 | PF01217 | 0.340 |
TRG_ENDOCYTIC_2 | 154 | 157 | PF00928 | 0.352 |
TRG_ENDOCYTIC_2 | 196 | 199 | PF00928 | 0.487 |
TRG_ENDOCYTIC_2 | 240 | 243 | PF00928 | 0.252 |
TRG_ER_diArg_1 | 112 | 115 | PF00400 | 0.415 |
TRG_ER_diArg_1 | 230 | 233 | PF00400 | 0.324 |
TRG_ER_diArg_1 | 372 | 375 | PF00400 | 0.431 |
TRG_Pf-PMV_PEXEL_1 | 101 | 105 | PF00026 | 0.383 |
TRG_Pf-PMV_PEXEL_1 | 475 | 479 | PF00026 | 0.495 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IA46 | Leptomonas seymouri | 76% | 100% |
A0A1X0NKV9 | Trypanosomatidae | 47% | 100% |
A0A3S7X444 | Leishmania donovani | 91% | 100% |
A0A422MZS5 | Trypanosoma rangeli | 47% | 100% |
A4I6B3 | Leishmania infantum | 91% | 100% |
C9ZN71 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 100% |
E9B1G9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
E9B1H1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
Q4Q6P3 | Leishmania major | 90% | 100% |
V5BBI5 | Trypanosoma cruzi | 47% | 100% |