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: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 3 |
GO:0043226 | organelle | 2 | 3 |
GO:0043227 | membrane-bounded organelle | 3 | 3 |
GO:0043229 | intracellular organelle | 3 | 3 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 3 |
GO:0110165 | cellular anatomical entity | 1 | 3 |
Related structures:
AlphaFold database: Q4Q9M0
Term | Name | Level | Count |
---|---|---|---|
GO:0000394 | RNA splicing, via endonucleolytic cleavage and ligation | 8 | 2 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 11 |
GO:0006378 | mRNA polyadenylation | 7 | 2 |
GO:0006388 | tRNA splicing, via endonucleolytic cleavage and ligation | 9 | 2 |
GO:0006396 | RNA processing | 6 | 11 |
GO:0006397 | mRNA processing | 7 | 2 |
GO:0006399 | tRNA metabolic process | 7 | 2 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 11 |
GO:0006807 | nitrogen compound metabolic process | 2 | 11 |
GO:0008033 | tRNA processing | 8 | 2 |
GO:0008152 | metabolic process | 1 | 11 |
GO:0008380 | RNA splicing | 7 | 2 |
GO:0009987 | cellular process | 1 | 11 |
GO:0016070 | RNA metabolic process | 5 | 11 |
GO:0016071 | mRNA metabolic process | 6 | 2 |
GO:0031123 | RNA 3'-end processing | 7 | 2 |
GO:0031124 | mRNA 3'-end processing | 8 | 2 |
GO:0034470 | ncRNA processing | 7 | 2 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 11 |
GO:0034660 | ncRNA metabolic process | 6 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 11 |
GO:0043631 | RNA polyadenylation | 6 | 2 |
GO:0044237 | cellular metabolic process | 2 | 11 |
GO:0044238 | primary metabolic process | 2 | 11 |
GO:0046483 | heterocycle metabolic process | 3 | 11 |
GO:0071704 | organic substance metabolic process | 2 | 11 |
GO:0090304 | nucleic acid metabolic process | 4 | 11 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 11 |
GO:0006793 | phosphorus metabolic process | 3 | 1 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 1 |
GO:0016310 | phosphorylation | 5 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 11 |
GO:0016301 | kinase activity | 4 | 11 |
GO:0016740 | transferase activity | 2 | 11 |
GO:0016772 | transferase activity, transferring phosphorus-containing groups | 3 | 11 |
GO:0016773 | phosphotransferase activity, alcohol group as acceptor | 4 | 11 |
GO:0019205 | nucleobase-containing compound kinase activity | 5 | 11 |
GO:0051731 | polynucleotide 5'-hydroxyl-kinase activity | 5 | 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_PCSK_SKI1_1 | 103 | 107 | PF00082 | 0.419 |
CLV_PCSK_SKI1_1 | 160 | 164 | PF00082 | 0.425 |
CLV_PCSK_SKI1_1 | 231 | 235 | PF00082 | 0.385 |
CLV_PCSK_SKI1_1 | 440 | 444 | PF00082 | 0.486 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.501 |
DEG_SPOP_SBC_1 | 79 | 83 | PF00917 | 0.452 |
DOC_CYCLIN_RxL_1 | 228 | 235 | PF00134 | 0.412 |
DOC_CYCLIN_yCln2_LP_2 | 185 | 191 | PF00134 | 0.342 |
DOC_MAPK_FxFP_2 | 425 | 428 | PF00069 | 0.572 |
DOC_MAPK_MEF2A_6 | 353 | 362 | PF00069 | 0.397 |
DOC_PP4_FxxP_1 | 4 | 7 | PF00568 | 0.692 |
DOC_PP4_FxxP_1 | 425 | 428 | PF00568 | 0.572 |
DOC_USP7_MATH_1 | 35 | 39 | PF00917 | 0.465 |
DOC_USP7_MATH_1 | 354 | 358 | PF00917 | 0.492 |
DOC_USP7_MATH_1 | 49 | 53 | PF00917 | 0.337 |
DOC_WW_Pin1_4 | 370 | 375 | PF00397 | 0.505 |
DOC_WW_Pin1_4 | 399 | 404 | PF00397 | 0.489 |
DOC_WW_Pin1_4 | 56 | 61 | PF00397 | 0.458 |
LIG_14-3-3_CanoR_1 | 240 | 248 | PF00244 | 0.404 |
LIG_14-3-3_CanoR_1 | 300 | 309 | PF00244 | 0.497 |
LIG_14-3-3_CanoR_1 | 313 | 321 | PF00244 | 0.377 |
LIG_14-3-3_CanoR_1 | 333 | 339 | PF00244 | 0.405 |
LIG_14-3-3_CanoR_1 | 99 | 105 | PF00244 | 0.356 |
LIG_14-3-3_CterR_2 | 440 | 445 | PF00244 | 0.463 |
LIG_Actin_WH2_2 | 80 | 97 | PF00022 | 0.458 |
LIG_BRCT_BRCA1_1 | 314 | 318 | PF00533 | 0.411 |
LIG_BRCT_BRCA1_1 | 334 | 338 | PF00533 | 0.473 |
LIG_BRCT_BRCA1_1 | 351 | 355 | PF00533 | 0.496 |
LIG_BRCT_BRCA1_1 | 421 | 425 | PF00533 | 0.547 |
LIG_Clathr_ClatBox_1 | 163 | 167 | PF01394 | 0.323 |
LIG_FHA_1 | 100 | 106 | PF00498 | 0.469 |
LIG_FHA_1 | 11 | 17 | PF00498 | 0.543 |
LIG_FHA_1 | 116 | 122 | PF00498 | 0.193 |
LIG_FHA_1 | 139 | 145 | PF00498 | 0.416 |
LIG_FHA_1 | 171 | 177 | PF00498 | 0.429 |
LIG_FHA_1 | 201 | 207 | PF00498 | 0.360 |
LIG_FHA_1 | 278 | 284 | PF00498 | 0.392 |
LIG_FHA_1 | 291 | 297 | PF00498 | 0.453 |
LIG_FHA_1 | 431 | 437 | PF00498 | 0.433 |
LIG_FHA_1 | 72 | 78 | PF00498 | 0.372 |
LIG_FHA_1 | 79 | 85 | PF00498 | 0.350 |
LIG_FHA_2 | 207 | 213 | PF00498 | 0.469 |
LIG_GBD_Chelix_1 | 61 | 69 | PF00786 | 0.458 |
LIG_LIR_Apic_2 | 186 | 190 | PF02991 | 0.380 |
LIG_LIR_Apic_2 | 349 | 354 | PF02991 | 0.498 |
LIG_LIR_Apic_2 | 422 | 428 | PF02991 | 0.531 |
LIG_LIR_Apic_2 | 66 | 71 | PF02991 | 0.439 |
LIG_LIR_Gen_1 | 111 | 116 | PF02991 | 0.356 |
LIG_LIR_Gen_1 | 212 | 222 | PF02991 | 0.404 |
LIG_LIR_Gen_1 | 288 | 296 | PF02991 | 0.419 |
LIG_LIR_Gen_1 | 307 | 314 | PF02991 | 0.508 |
LIG_LIR_Gen_1 | 315 | 326 | PF02991 | 0.502 |
LIG_LIR_Gen_1 | 352 | 363 | PF02991 | 0.455 |
LIG_LIR_Nem_3 | 111 | 115 | PF02991 | 0.334 |
LIG_LIR_Nem_3 | 212 | 217 | PF02991 | 0.372 |
LIG_LIR_Nem_3 | 288 | 294 | PF02991 | 0.311 |
LIG_LIR_Nem_3 | 307 | 311 | PF02991 | 0.515 |
LIG_LIR_Nem_3 | 315 | 321 | PF02991 | 0.489 |
LIG_LIR_Nem_3 | 332 | 337 | PF02991 | 0.526 |
LIG_LIR_Nem_3 | 352 | 358 | PF02991 | 0.438 |
LIG_LIR_Nem_3 | 64 | 70 | PF02991 | 0.335 |
LIG_MLH1_MIPbox_1 | 334 | 338 | PF16413 | 0.473 |
LIG_Pex14_1 | 351 | 355 | PF04695 | 0.496 |
LIG_RPA_C_Fungi | 143 | 155 | PF08784 | 0.342 |
LIG_SH2_CRK | 112 | 116 | PF00017 | 0.356 |
LIG_SH2_CRK | 406 | 410 | PF00017 | 0.497 |
LIG_SH2_NCK_1 | 406 | 410 | PF00017 | 0.464 |
LIG_SH2_PTP2 | 308 | 311 | PF00017 | 0.531 |
LIG_SH2_STAP1 | 153 | 157 | PF00017 | 0.386 |
LIG_SH2_STAP1 | 334 | 338 | PF00017 | 0.473 |
LIG_SH2_STAT5 | 204 | 207 | PF00017 | 0.386 |
LIG_SH2_STAT5 | 226 | 229 | PF00017 | 0.336 |
LIG_SH2_STAT5 | 295 | 298 | PF00017 | 0.501 |
LIG_SH2_STAT5 | 308 | 311 | PF00017 | 0.498 |
LIG_SH2_STAT5 | 337 | 340 | PF00017 | 0.382 |
LIG_SH2_STAT5 | 418 | 421 | PF00017 | 0.472 |
LIG_SH2_STAT5 | 68 | 71 | PF00017 | 0.458 |
LIG_SH3_3 | 15 | 21 | PF00018 | 0.558 |
LIG_SH3_3 | 171 | 177 | PF00018 | 0.402 |
LIG_SH3_3 | 368 | 374 | PF00018 | 0.521 |
LIG_SUMO_SIM_anti_2 | 357 | 362 | PF11976 | 0.392 |
LIG_SUMO_SIM_anti_2 | 429 | 436 | PF11976 | 0.415 |
LIG_SUMO_SIM_par_1 | 160 | 165 | PF11976 | 0.327 |
LIG_SUMO_SIM_par_1 | 25 | 32 | PF11976 | 0.427 |
LIG_SUMO_SIM_par_1 | 254 | 260 | PF11976 | 0.356 |
LIG_SUMO_SIM_par_1 | 359 | 366 | PF11976 | 0.387 |
LIG_SUMO_SIM_par_1 | 432 | 438 | PF11976 | 0.351 |
LIG_TRAF2_1 | 376 | 379 | PF00917 | 0.572 |
LIG_TRFH_1 | 67 | 71 | PF08558 | 0.333 |
LIG_TYR_ITIM | 110 | 115 | PF00017 | 0.356 |
LIG_TYR_ITIM | 65 | 70 | PF00017 | 0.386 |
LIG_WRC_WIRS_1 | 211 | 216 | PF05994 | 0.458 |
MOD_CDK_SPxxK_3 | 370 | 377 | PF00069 | 0.547 |
MOD_CK1_1 | 101 | 107 | PF00069 | 0.458 |
MOD_CK1_1 | 12 | 18 | PF00069 | 0.589 |
MOD_CK1_1 | 198 | 204 | PF00069 | 0.369 |
MOD_CK1_1 | 332 | 338 | PF00069 | 0.495 |
MOD_CK1_1 | 349 | 355 | PF00069 | 0.447 |
MOD_CK1_1 | 392 | 398 | PF00069 | 0.552 |
MOD_CK2_1 | 19 | 25 | PF00069 | 0.385 |
MOD_CK2_1 | 206 | 212 | PF00069 | 0.462 |
MOD_GlcNHglycan | 251 | 254 | PF01048 | 0.324 |
MOD_GlcNHglycan | 264 | 267 | PF01048 | 0.314 |
MOD_GlcNHglycan | 334 | 337 | PF01048 | 0.423 |
MOD_GlcNHglycan | 340 | 343 | PF01048 | 0.365 |
MOD_GlcNHglycan | 37 | 40 | PF01048 | 0.386 |
MOD_GlcNHglycan | 394 | 397 | PF01048 | 0.520 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.324 |
MOD_GSK3_1 | 206 | 213 | PF00069 | 0.297 |
MOD_GSK3_1 | 312 | 319 | PF00069 | 0.477 |
MOD_GSK3_1 | 325 | 332 | PF00069 | 0.336 |
MOD_GSK3_1 | 408 | 415 | PF00069 | 0.417 |
MOD_GSK3_1 | 419 | 426 | PF00069 | 0.378 |
MOD_GSK3_1 | 43 | 50 | PF00069 | 0.425 |
MOD_GSK3_1 | 56 | 63 | PF00069 | 0.243 |
MOD_GSK3_1 | 8 | 15 | PF00069 | 0.580 |
MOD_GSK3_1 | 97 | 104 | PF00069 | 0.424 |
MOD_LATS_1 | 298 | 304 | PF00433 | 0.441 |
MOD_N-GLC_1 | 316 | 321 | PF02516 | 0.544 |
MOD_NEK2_1 | 195 | 200 | PF00069 | 0.425 |
MOD_NEK2_1 | 232 | 237 | PF00069 | 0.297 |
MOD_NEK2_1 | 26 | 31 | PF00069 | 0.376 |
MOD_NEK2_1 | 290 | 295 | PF00069 | 0.385 |
MOD_NEK2_1 | 338 | 343 | PF00069 | 0.530 |
MOD_NEK2_1 | 390 | 395 | PF00069 | 0.394 |
MOD_NEK2_1 | 419 | 424 | PF00069 | 0.352 |
MOD_NEK2_1 | 435 | 440 | PF00069 | 0.348 |
MOD_NEK2_1 | 78 | 83 | PF00069 | 0.370 |
MOD_NEK2_2 | 37 | 42 | PF00069 | 0.377 |
MOD_PIKK_1 | 115 | 121 | PF00454 | 0.458 |
MOD_PIKK_1 | 123 | 129 | PF00454 | 0.271 |
MOD_PIKK_1 | 346 | 352 | PF00454 | 0.506 |
MOD_PK_1 | 14 | 20 | PF00069 | 0.559 |
MOD_PKA_2 | 239 | 245 | PF00069 | 0.412 |
MOD_PKA_2 | 312 | 318 | PF00069 | 0.459 |
MOD_PKA_2 | 332 | 338 | PF00069 | 0.407 |
MOD_PKA_2 | 98 | 104 | PF00069 | 0.333 |
MOD_PKB_1 | 238 | 246 | PF00069 | 0.412 |
MOD_Plk_1 | 316 | 322 | PF00069 | 0.552 |
MOD_Plk_1 | 63 | 69 | PF00069 | 0.356 |
MOD_Plk_4 | 130 | 136 | PF00069 | 0.402 |
MOD_Plk_4 | 195 | 201 | PF00069 | 0.425 |
MOD_Plk_4 | 290 | 296 | PF00069 | 0.414 |
MOD_Plk_4 | 325 | 331 | PF00069 | 0.506 |
MOD_Plk_4 | 430 | 436 | PF00069 | 0.438 |
MOD_Plk_4 | 80 | 86 | PF00069 | 0.429 |
MOD_ProDKin_1 | 370 | 376 | PF00069 | 0.506 |
MOD_ProDKin_1 | 399 | 405 | PF00069 | 0.485 |
MOD_ProDKin_1 | 56 | 62 | PF00069 | 0.458 |
MOD_SUMO_for_1 | 363 | 366 | PF00179 | 0.511 |
MOD_SUMO_for_1 | 376 | 379 | PF00179 | 0.539 |
MOD_SUMO_for_1 | 41 | 44 | PF00179 | 0.458 |
MOD_SUMO_rev_2 | 32 | 38 | PF00179 | 0.458 |
TRG_DiLeu_BaEn_1 | 430 | 435 | PF01217 | 0.401 |
TRG_DiLeu_BaEn_3 | 378 | 384 | PF01217 | 0.538 |
TRG_ENDOCYTIC_2 | 112 | 115 | PF00928 | 0.356 |
TRG_ENDOCYTIC_2 | 226 | 229 | PF00928 | 0.343 |
TRG_ENDOCYTIC_2 | 308 | 311 | PF00928 | 0.505 |
TRG_ENDOCYTIC_2 | 406 | 409 | PF00928 | 0.459 |
TRG_ENDOCYTIC_2 | 67 | 70 | PF00928 | 0.356 |
TRG_Pf-PMV_PEXEL_1 | 107 | 111 | PF00026 | 0.386 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I6Q0 | Leptomonas seymouri | 74% | 100% |
A0A0S4J450 | Bodo saltans | 32% | 100% |
A0A1X0NYA9 | Trypanosomatidae | 44% | 100% |
A0A3S5H7F2 | Leishmania donovani | 96% | 100% |
A1DE49 | Neosartorya fischeri (strain ATCC 1020 / DSM 3700 / CBS 544.65 / FGSC A1164 / JCM 1740 / NRRL 181 / WB 181) | 26% | 80% |
A4HEC1 | Leishmania braziliensis | 87% | 100% |
A4I1R6 | Leishmania infantum | 96% | 100% |
A6S936 | Botryotinia fuckeliana (strain B05.10) | 25% | 97% |
A7RG82 | Nematostella vectensis | 25% | 100% |
A8X9U4 | Caenorhabditis briggsae | 22% | 100% |
B0VZR4 | Culex quinquefasciatus | 24% | 100% |
C9ZKC3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
E7F3I6 | Danio rerio | 23% | 100% |
E9AXV1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 96% | 100% |
Q0U2G5 | Phaeosphaeria nodorum (strain SN15 / ATCC MYA-4574 / FGSC 10173) | 22% | 95% |
Q16WA6 | Aedes aegypti | 24% | 100% |
Q2H1L0 | Chaetomium globosum (strain ATCC 6205 / CBS 148.51 / DSM 1962 / NBRC 6347 / NRRL 1970) | 23% | 90% |
Q59ST8 | Candida albicans (strain SC5314 / ATCC MYA-2876) | 25% | 91% |
Q6NS21 | Xenopus laevis | 26% | 100% |
Q7QJW7 | Anopheles gambiae | 24% | 100% |
Q9SR06 | Arabidopsis thaliana | 24% | 100% |
V5BCI8 | Trypanosoma cruzi | 43% | 100% |