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: 1, no: 10 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005840 | ribosome | 5 | 11 |
GO:0005848 | mRNA cleavage stimulating factor complex | 4 | 12 |
GO:0005849 | mRNA cleavage factor complex | 3 | 12 |
GO:0032991 | protein-containing complex | 1 | 12 |
GO:0043226 | organelle | 2 | 11 |
GO:0043228 | non-membrane-bounded organelle | 3 | 11 |
GO:0043229 | intracellular organelle | 3 | 11 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
GO:0140513 | nuclear protein-containing complex | 2 | 12 |
GO:1990904 | ribonucleoprotein complex | 2 | 11 |
Related structures:
AlphaFold database: A4HL64
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 12 |
GO:0006396 | RNA processing | 6 | 12 |
GO:0006397 | mRNA processing | 7 | 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:0016071 | mRNA metabolic process | 6 | 12 |
GO:0031123 | RNA 3'-end processing | 7 | 12 |
GO:0031124 | mRNA 3'-end processing | 8 | 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 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 353 | 357 | PF00656 | 0.538 |
CLV_NRD_NRD_1 | 113 | 115 | PF00675 | 0.650 |
CLV_NRD_NRD_1 | 212 | 214 | PF00675 | 0.416 |
CLV_NRD_NRD_1 | 409 | 411 | PF00675 | 0.453 |
CLV_NRD_NRD_1 | 78 | 80 | PF00675 | 0.671 |
CLV_NRD_NRD_1 | 8 | 10 | PF00675 | 0.607 |
CLV_PCSK_KEX2_1 | 10 | 12 | PF00082 | 0.600 |
CLV_PCSK_KEX2_1 | 113 | 115 | PF00082 | 0.650 |
CLV_PCSK_KEX2_1 | 212 | 214 | PF00082 | 0.416 |
CLV_PCSK_KEX2_1 | 409 | 411 | PF00082 | 0.453 |
CLV_PCSK_KEX2_1 | 78 | 80 | PF00082 | 0.696 |
CLV_PCSK_PC1ET2_1 | 10 | 12 | PF00082 | 0.600 |
CLV_PCSK_SKI1_1 | 253 | 257 | PF00082 | 0.555 |
CLV_PCSK_SKI1_1 | 294 | 298 | PF00082 | 0.514 |
CLV_PCSK_SKI1_1 | 438 | 442 | PF00082 | 0.478 |
CLV_Separin_Metazoa | 222 | 226 | PF03568 | 0.495 |
DEG_SCF_FBW7_1 | 295 | 301 | PF00400 | 0.640 |
DEG_SPOP_SBC_1 | 467 | 471 | PF00917 | 0.309 |
DOC_CKS1_1 | 295 | 300 | PF01111 | 0.541 |
DOC_CKS1_1 | 503 | 508 | PF01111 | 0.451 |
DOC_CYCLIN_yCln2_LP_2 | 99 | 105 | PF00134 | 0.576 |
DOC_MAPK_gen_1 | 9 | 18 | PF00069 | 0.632 |
DOC_MAPK_MEF2A_6 | 98 | 105 | PF00069 | 0.559 |
DOC_MAPK_NFAT4_5 | 98 | 106 | PF00069 | 0.601 |
DOC_PP1_RVXF_1 | 130 | 137 | PF00149 | 0.438 |
DOC_PP2B_LxvP_1 | 296 | 299 | PF13499 | 0.634 |
DOC_PP2B_LxvP_1 | 99 | 102 | PF13499 | 0.554 |
DOC_PP4_FxxP_1 | 426 | 429 | PF00568 | 0.458 |
DOC_USP7_MATH_1 | 194 | 198 | PF00917 | 0.705 |
DOC_USP7_MATH_1 | 315 | 319 | PF00917 | 0.748 |
DOC_USP7_MATH_1 | 321 | 325 | PF00917 | 0.650 |
DOC_USP7_MATH_1 | 332 | 336 | PF00917 | 0.404 |
DOC_USP7_MATH_1 | 337 | 341 | PF00917 | 0.466 |
DOC_USP7_MATH_1 | 381 | 385 | PF00917 | 0.466 |
DOC_USP7_MATH_1 | 40 | 44 | PF00917 | 0.507 |
DOC_USP7_MATH_1 | 443 | 447 | PF00917 | 0.476 |
DOC_USP7_MATH_1 | 457 | 461 | PF00917 | 0.300 |
DOC_WW_Pin1_4 | 134 | 139 | PF00397 | 0.383 |
DOC_WW_Pin1_4 | 294 | 299 | PF00397 | 0.522 |
DOC_WW_Pin1_4 | 341 | 346 | PF00397 | 0.473 |
DOC_WW_Pin1_4 | 417 | 422 | PF00397 | 0.610 |
DOC_WW_Pin1_4 | 483 | 488 | PF00397 | 0.506 |
DOC_WW_Pin1_4 | 502 | 507 | PF00397 | 0.430 |
LIG_14-3-3_CanoR_1 | 108 | 112 | PF00244 | 0.612 |
LIG_14-3-3_CanoR_1 | 121 | 130 | PF00244 | 0.349 |
LIG_14-3-3_CanoR_1 | 410 | 418 | PF00244 | 0.606 |
LIG_14-3-3_CanoR_1 | 438 | 448 | PF00244 | 0.441 |
LIG_14-3-3_CanoR_1 | 92 | 101 | PF00244 | 0.576 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.691 |
LIG_BIR_III_4 | 47 | 51 | PF00653 | 0.486 |
LIG_BRCT_BRCA1_1 | 339 | 343 | PF00533 | 0.538 |
LIG_CSL_BTD_1 | 503 | 506 | PF09270 | 0.431 |
LIG_CSL_BTD_1 | 507 | 510 | PF09270 | 0.516 |
LIG_CtBP_PxDLS_1 | 102 | 106 | PF00389 | 0.661 |
LIG_FHA_1 | 146 | 152 | PF00498 | 0.377 |
LIG_FHA_1 | 216 | 222 | PF00498 | 0.405 |
LIG_FHA_1 | 227 | 233 | PF00498 | 0.389 |
LIG_FHA_1 | 259 | 265 | PF00498 | 0.448 |
LIG_FHA_1 | 290 | 296 | PF00498 | 0.477 |
LIG_FHA_1 | 356 | 362 | PF00498 | 0.528 |
LIG_FHA_1 | 381 | 387 | PF00498 | 0.491 |
LIG_FHA_1 | 388 | 394 | PF00498 | 0.466 |
LIG_FHA_1 | 400 | 406 | PF00498 | 0.367 |
LIG_FHA_1 | 463 | 469 | PF00498 | 0.523 |
LIG_FHA_1 | 47 | 53 | PF00498 | 0.488 |
LIG_FHA_1 | 85 | 91 | PF00498 | 0.607 |
LIG_FHA_2 | 157 | 163 | PF00498 | 0.410 |
LIG_FHA_2 | 351 | 357 | PF00498 | 0.538 |
LIG_FHA_2 | 428 | 434 | PF00498 | 0.606 |
LIG_FHA_2 | 492 | 498 | PF00498 | 0.478 |
LIG_LIR_Apic_2 | 415 | 421 | PF02991 | 0.664 |
LIG_LIR_Apic_2 | 424 | 429 | PF02991 | 0.461 |
LIG_LIR_Gen_1 | 24 | 33 | PF02991 | 0.540 |
LIG_LIR_Gen_1 | 272 | 280 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 24 | 29 | PF02991 | 0.578 |
LIG_LIR_Nem_3 | 272 | 278 | PF02991 | 0.382 |
LIG_LIR_Nem_3 | 356 | 362 | PF02991 | 0.527 |
LIG_LIR_Nem_3 | 460 | 464 | PF02991 | 0.430 |
LIG_LIR_Nem_3 | 97 | 103 | PF02991 | 0.539 |
LIG_PTB_Apo_2 | 243 | 250 | PF02174 | 0.505 |
LIG_PTB_Phospho_1 | 243 | 249 | PF10480 | 0.489 |
LIG_SH2_CRK | 100 | 104 | PF00017 | 0.608 |
LIG_SH2_CRK | 26 | 30 | PF00017 | 0.489 |
LIG_SH2_CRK | 362 | 366 | PF00017 | 0.536 |
LIG_SH2_CRK | 464 | 468 | PF00017 | 0.439 |
LIG_SH2_PTP2 | 275 | 278 | PF00017 | 0.513 |
LIG_SH2_SRC | 247 | 250 | PF00017 | 0.527 |
LIG_SH2_STAT5 | 142 | 145 | PF00017 | 0.456 |
LIG_SH2_STAT5 | 243 | 246 | PF00017 | 0.377 |
LIG_SH2_STAT5 | 275 | 278 | PF00017 | 0.382 |
LIG_SH2_STAT5 | 461 | 464 | PF00017 | 0.444 |
LIG_SH3_1 | 225 | 231 | PF00018 | 0.494 |
LIG_SH3_3 | 225 | 231 | PF00018 | 0.425 |
LIG_SH3_3 | 292 | 298 | PF00018 | 0.559 |
LIG_SUMO_SIM_anti_2 | 220 | 225 | PF11976 | 0.494 |
LIG_SUMO_SIM_par_1 | 101 | 107 | PF11976 | 0.661 |
LIG_SUMO_SIM_par_1 | 229 | 235 | PF11976 | 0.401 |
LIG_SUMO_SIM_par_1 | 452 | 460 | PF11976 | 0.520 |
LIG_TRAF2_1 | 80 | 83 | PF00917 | 0.648 |
LIG_Vh1_VBS_1 | 38 | 56 | PF01044 | 0.582 |
LIG_WRC_WIRS_1 | 423 | 428 | PF05994 | 0.452 |
MOD_CDK_SPxxK_3 | 341 | 348 | PF00069 | 0.473 |
MOD_CK1_1 | 104 | 110 | PF00069 | 0.623 |
MOD_CK1_1 | 156 | 162 | PF00069 | 0.385 |
MOD_CK1_1 | 470 | 476 | PF00069 | 0.431 |
MOD_CK2_1 | 422 | 428 | PF00069 | 0.452 |
MOD_CK2_1 | 439 | 445 | PF00069 | 0.315 |
MOD_CK2_1 | 69 | 75 | PF00069 | 0.675 |
MOD_Cter_Amidation | 111 | 114 | PF01082 | 0.662 |
MOD_GlcNHglycan | 123 | 126 | PF01048 | 0.486 |
MOD_GlcNHglycan | 161 | 166 | PF01048 | 0.535 |
MOD_GlcNHglycan | 196 | 199 | PF01048 | 0.613 |
MOD_GlcNHglycan | 234 | 237 | PF01048 | 0.474 |
MOD_GlcNHglycan | 271 | 274 | PF01048 | 0.445 |
MOD_GlcNHglycan | 316 | 320 | PF01048 | 0.699 |
MOD_GlcNHglycan | 334 | 337 | PF01048 | 0.121 |
MOD_GlcNHglycan | 365 | 368 | PF01048 | 0.529 |
MOD_GlcNHglycan | 377 | 380 | PF01048 | 0.297 |
MOD_GlcNHglycan | 42 | 45 | PF01048 | 0.494 |
MOD_GlcNHglycan | 441 | 444 | PF01048 | 0.511 |
MOD_GlcNHglycan | 94 | 97 | PF01048 | 0.578 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.513 |
MOD_GSK3_1 | 141 | 148 | PF00069 | 0.267 |
MOD_GSK3_1 | 265 | 272 | PF00069 | 0.491 |
MOD_GSK3_1 | 294 | 301 | PF00069 | 0.563 |
MOD_GSK3_1 | 302 | 309 | PF00069 | 0.604 |
MOD_GSK3_1 | 315 | 322 | PF00069 | 0.628 |
MOD_GSK3_1 | 332 | 339 | PF00069 | 0.310 |
MOD_GSK3_1 | 346 | 353 | PF00069 | 0.423 |
MOD_GSK3_1 | 381 | 388 | PF00069 | 0.470 |
MOD_GSK3_1 | 417 | 424 | PF00069 | 0.569 |
MOD_GSK3_1 | 439 | 446 | PF00069 | 0.424 |
MOD_GSK3_1 | 462 | 469 | PF00069 | 0.462 |
MOD_GSK3_1 | 470 | 477 | PF00069 | 0.465 |
MOD_N-GLC_1 | 443 | 448 | PF02516 | 0.421 |
MOD_NEK2_1 | 103 | 108 | PF00069 | 0.399 |
MOD_NEK2_1 | 123 | 128 | PF00069 | 0.503 |
MOD_NEK2_1 | 350 | 355 | PF00069 | 0.456 |
MOD_NEK2_1 | 399 | 404 | PF00069 | 0.500 |
MOD_NEK2_1 | 411 | 416 | PF00069 | 0.614 |
MOD_NEK2_1 | 84 | 89 | PF00069 | 0.608 |
MOD_NEK2_1 | 94 | 99 | PF00069 | 0.490 |
MOD_PIKK_1 | 215 | 221 | PF00454 | 0.433 |
MOD_PIKK_1 | 471 | 477 | PF00454 | 0.573 |
MOD_PIKK_1 | 84 | 90 | PF00454 | 0.670 |
MOD_PKA_2 | 107 | 113 | PF00069 | 0.607 |
MOD_PKA_2 | 325 | 331 | PF00069 | 0.632 |
MOD_PKB_1 | 119 | 127 | PF00069 | 0.421 |
MOD_Plk_1 | 132 | 138 | PF00069 | 0.465 |
MOD_Plk_1 | 161 | 167 | PF00069 | 0.541 |
MOD_Plk_1 | 265 | 271 | PF00069 | 0.523 |
MOD_Plk_1 | 421 | 427 | PF00069 | 0.570 |
MOD_Plk_1 | 443 | 449 | PF00069 | 0.404 |
MOD_Plk_1 | 451 | 457 | PF00069 | 0.375 |
MOD_Plk_1 | 496 | 502 | PF00069 | 0.435 |
MOD_Plk_2-3 | 422 | 428 | PF00069 | 0.469 |
MOD_Plk_4 | 355 | 361 | PF00069 | 0.450 |
MOD_Plk_4 | 381 | 387 | PF00069 | 0.562 |
MOD_Plk_4 | 451 | 457 | PF00069 | 0.406 |
MOD_Plk_4 | 474 | 480 | PF00069 | 0.503 |
MOD_ProDKin_1 | 134 | 140 | PF00069 | 0.385 |
MOD_ProDKin_1 | 294 | 300 | PF00069 | 0.529 |
MOD_ProDKin_1 | 341 | 347 | PF00069 | 0.473 |
MOD_ProDKin_1 | 417 | 423 | PF00069 | 0.605 |
MOD_ProDKin_1 | 483 | 489 | PF00069 | 0.514 |
MOD_ProDKin_1 | 502 | 508 | PF00069 | 0.443 |
TRG_DiLeu_BaLyEn_6 | 283 | 288 | PF01217 | 0.409 |
TRG_ENDOCYTIC_2 | 100 | 103 | PF00928 | 0.565 |
TRG_ENDOCYTIC_2 | 26 | 29 | PF00928 | 0.455 |
TRG_ENDOCYTIC_2 | 275 | 278 | PF00928 | 0.451 |
TRG_ENDOCYTIC_2 | 362 | 365 | PF00928 | 0.533 |
TRG_ENDOCYTIC_2 | 464 | 467 | PF00928 | 0.444 |
TRG_ER_diArg_1 | 116 | 119 | PF00400 | 0.471 |
TRG_ER_diArg_1 | 211 | 213 | PF00400 | 0.435 |
TRG_ER_diArg_1 | 408 | 410 | PF00400 | 0.440 |
TRG_ER_diArg_1 | 500 | 503 | PF00400 | 0.384 |
TRG_ER_diArg_1 | 9 | 12 | PF00400 | 0.621 |
TRG_NES_CRM1_1 | 19 | 32 | PF08389 | 0.615 |
TRG_NES_CRM1_1 | 61 | 77 | PF08389 | 0.573 |
TRG_NLS_MonoCore_2 | 9 | 14 | PF00514 | 0.632 |
TRG_NLS_MonoExtC_3 | 8 | 13 | PF00514 | 0.618 |
TRG_NLS_MonoExtN_4 | 7 | 14 | PF00514 | 0.606 |
TRG_Pf-PMV_PEXEL_1 | 23 | 27 | PF00026 | 0.477 |
TRG_Pf-PMV_PEXEL_1 | 31 | 36 | PF00026 | 0.483 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IHC2 | Leptomonas seymouri | 80% | 94% |
A0A0S4IHN1 | Bodo saltans | 39% | 92% |
A0A0S4JL38 | Bodo saltans | 24% | 95% |
A0A1X0P742 | Trypanosomatidae | 52% | 100% |
A0A3Q8ITT7 | Leishmania donovani | 94% | 100% |
A0A422NAT5 | Trypanosoma rangeli | 52% | 97% |
A4I8P5 | Leishmania infantum | 94% | 100% |
D0A0R2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 53% | 99% |
E9B3K7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
Q4Q4J2 | Leishmania major | 94% | 100% |
Q8L4J2 | Arabidopsis thaliana | 24% | 100% |
V5BJ28 | Trypanosoma cruzi | 51% | 94% |