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: E9B3K7
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 | 0.456 |
CLV_NRD_NRD_1 | 113 | 115 | PF00675 | 0.594 |
CLV_NRD_NRD_1 | 212 | 214 | PF00675 | 0.354 |
CLV_NRD_NRD_1 | 409 | 411 | PF00675 | 0.423 |
CLV_NRD_NRD_1 | 78 | 80 | PF00675 | 0.595 |
CLV_NRD_NRD_1 | 8 | 10 | PF00675 | 0.542 |
CLV_PCSK_KEX2_1 | 10 | 12 | PF00082 | 0.533 |
CLV_PCSK_KEX2_1 | 113 | 115 | PF00082 | 0.594 |
CLV_PCSK_KEX2_1 | 212 | 214 | PF00082 | 0.354 |
CLV_PCSK_KEX2_1 | 409 | 411 | PF00082 | 0.425 |
CLV_PCSK_KEX2_1 | 78 | 80 | PF00082 | 0.511 |
CLV_PCSK_PC1ET2_1 | 10 | 12 | PF00082 | 0.533 |
CLV_PCSK_SKI1_1 | 253 | 257 | PF00082 | 0.550 |
CLV_PCSK_SKI1_1 | 294 | 298 | PF00082 | 0.465 |
CLV_PCSK_SKI1_1 | 438 | 442 | PF00082 | 0.474 |
CLV_Separin_Metazoa | 222 | 226 | PF03568 | 0.467 |
DEG_SCF_FBW7_1 | 295 | 301 | PF00400 | 0.624 |
DOC_CKS1_1 | 295 | 300 | PF01111 | 0.502 |
DOC_CKS1_1 | 503 | 508 | PF01111 | 0.371 |
DOC_CYCLIN_yCln2_LP_2 | 503 | 509 | PF00134 | 0.474 |
DOC_CYCLIN_yCln2_LP_2 | 99 | 105 | PF00134 | 0.509 |
DOC_MAPK_gen_1 | 9 | 18 | PF00069 | 0.563 |
DOC_MAPK_MEF2A_6 | 98 | 105 | PF00069 | 0.492 |
DOC_MAPK_NFAT4_5 | 98 | 106 | PF00069 | 0.533 |
DOC_PP1_RVXF_1 | 130 | 137 | PF00149 | 0.380 |
DOC_PP2B_LxvP_1 | 296 | 299 | PF13499 | 0.617 |
DOC_PP2B_LxvP_1 | 99 | 102 | PF13499 | 0.486 |
DOC_PP4_FxxP_1 | 426 | 429 | PF00568 | 0.387 |
DOC_USP7_MATH_1 | 194 | 198 | PF00917 | 0.565 |
DOC_USP7_MATH_1 | 2 | 6 | PF00917 | 0.653 |
DOC_USP7_MATH_1 | 332 | 336 | PF00917 | 0.547 |
DOC_USP7_MATH_1 | 337 | 341 | PF00917 | 0.466 |
DOC_USP7_MATH_1 | 381 | 385 | PF00917 | 0.455 |
DOC_USP7_MATH_1 | 40 | 44 | PF00917 | 0.470 |
DOC_USP7_MATH_1 | 443 | 447 | PF00917 | 0.417 |
DOC_USP7_MATH_1 | 457 | 461 | PF00917 | 0.245 |
DOC_USP7_MATH_1 | 467 | 471 | PF00917 | 0.439 |
DOC_USP7_UBL2_3 | 253 | 257 | PF12436 | 0.388 |
DOC_WW_Pin1_4 | 134 | 139 | PF00397 | 0.311 |
DOC_WW_Pin1_4 | 246 | 251 | PF00397 | 0.269 |
DOC_WW_Pin1_4 | 294 | 299 | PF00397 | 0.498 |
DOC_WW_Pin1_4 | 417 | 422 | PF00397 | 0.568 |
DOC_WW_Pin1_4 | 483 | 488 | PF00397 | 0.457 |
DOC_WW_Pin1_4 | 502 | 507 | PF00397 | 0.353 |
LIG_14-3-3_CanoR_1 | 108 | 112 | PF00244 | 0.518 |
LIG_14-3-3_CanoR_1 | 121 | 130 | PF00244 | 0.285 |
LIG_14-3-3_CanoR_1 | 410 | 418 | PF00244 | 0.545 |
LIG_14-3-3_CanoR_1 | 438 | 448 | PF00244 | 0.382 |
LIG_14-3-3_CanoR_1 | 92 | 101 | PF00244 | 0.494 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.585 |
LIG_BIR_III_4 | 47 | 51 | PF00653 | 0.419 |
LIG_BRCT_BRCA1_1 | 339 | 343 | PF00533 | 0.467 |
LIG_CSL_BTD_1 | 503 | 506 | PF09270 | 0.352 |
LIG_CSL_BTD_1 | 507 | 510 | PF09270 | 0.432 |
LIG_CtBP_PxDLS_1 | 102 | 106 | PF00389 | 0.618 |
LIG_FHA_1 | 146 | 152 | PF00498 | 0.307 |
LIG_FHA_1 | 216 | 222 | PF00498 | 0.355 |
LIG_FHA_1 | 259 | 265 | PF00498 | 0.400 |
LIG_FHA_1 | 290 | 296 | PF00498 | 0.427 |
LIG_FHA_1 | 356 | 362 | PF00498 | 0.465 |
LIG_FHA_1 | 381 | 387 | PF00498 | 0.476 |
LIG_FHA_1 | 388 | 394 | PF00498 | 0.470 |
LIG_FHA_1 | 400 | 406 | PF00498 | 0.461 |
LIG_FHA_1 | 463 | 469 | PF00498 | 0.473 |
LIG_FHA_1 | 47 | 53 | PF00498 | 0.425 |
LIG_FHA_1 | 85 | 91 | PF00498 | 0.510 |
LIG_FHA_2 | 157 | 163 | PF00498 | 0.344 |
LIG_FHA_2 | 351 | 357 | PF00498 | 0.451 |
LIG_FHA_2 | 428 | 434 | PF00498 | 0.485 |
LIG_FHA_2 | 492 | 498 | PF00498 | 0.434 |
LIG_LIR_Apic_2 | 415 | 421 | PF02991 | 0.514 |
LIG_LIR_Apic_2 | 424 | 429 | PF02991 | 0.392 |
LIG_LIR_Gen_1 | 24 | 33 | PF02991 | 0.480 |
LIG_LIR_Gen_1 | 272 | 279 | PF02991 | 0.425 |
LIG_LIR_Gen_1 | 83 | 94 | PF02991 | 0.536 |
LIG_LIR_Nem_3 | 272 | 278 | PF02991 | 0.331 |
LIG_LIR_Nem_3 | 356 | 362 | PF02991 | 0.464 |
LIG_LIR_Nem_3 | 460 | 464 | PF02991 | 0.374 |
LIG_LIR_Nem_3 | 83 | 89 | PF02991 | 0.488 |
LIG_LIR_Nem_3 | 97 | 103 | PF02991 | 0.472 |
LIG_SH2_CRK | 100 | 104 | PF00017 | 0.548 |
LIG_SH2_CRK | 362 | 366 | PF00017 | 0.364 |
LIG_SH2_NCK_1 | 247 | 251 | PF00017 | 0.280 |
LIG_SH2_PTP2 | 275 | 278 | PF00017 | 0.378 |
LIG_SH2_STAT5 | 142 | 145 | PF00017 | 0.409 |
LIG_SH2_STAT5 | 243 | 246 | PF00017 | 0.324 |
LIG_SH2_STAT5 | 275 | 278 | PF00017 | 0.328 |
LIG_SH2_STAT5 | 461 | 464 | PF00017 | 0.378 |
LIG_SH3_1 | 225 | 231 | PF00018 | 0.451 |
LIG_SH3_3 | 225 | 231 | PF00018 | 0.373 |
LIG_SH3_3 | 292 | 298 | PF00018 | 0.553 |
LIG_SUMO_SIM_anti_2 | 220 | 225 | PF11976 | 0.466 |
LIG_SUMO_SIM_par_1 | 101 | 107 | PF11976 | 0.616 |
LIG_SUMO_SIM_par_1 | 452 | 460 | PF11976 | 0.375 |
LIG_TRAF2_1 | 80 | 83 | PF00917 | 0.628 |
LIG_Vh1_VBS_1 | 38 | 56 | PF01044 | 0.539 |
LIG_WRC_WIRS_1 | 423 | 428 | PF05994 | 0.382 |
MOD_CDK_SPxxK_3 | 246 | 253 | PF00069 | 0.271 |
MOD_CK1_1 | 104 | 110 | PF00069 | 0.574 |
MOD_CK1_1 | 156 | 162 | PF00069 | 0.330 |
MOD_CK1_1 | 249 | 255 | PF00069 | 0.289 |
MOD_CK1_1 | 315 | 321 | PF00069 | 0.705 |
MOD_CK1_1 | 339 | 345 | PF00069 | 0.290 |
MOD_CK1_1 | 470 | 476 | PF00069 | 0.391 |
MOD_CK2_1 | 422 | 428 | PF00069 | 0.385 |
MOD_CK2_1 | 439 | 445 | PF00069 | 0.430 |
MOD_CK2_1 | 69 | 75 | PF00069 | 0.611 |
MOD_Cter_Amidation | 111 | 114 | PF01082 | 0.602 |
MOD_GlcNHglycan | 123 | 126 | PF01048 | 0.449 |
MOD_GlcNHglycan | 161 | 166 | PF01048 | 0.492 |
MOD_GlcNHglycan | 196 | 199 | PF01048 | 0.562 |
MOD_GlcNHglycan | 234 | 237 | PF01048 | 0.438 |
MOD_GlcNHglycan | 271 | 274 | PF01048 | 0.396 |
MOD_GlcNHglycan | 316 | 320 | PF01048 | 0.647 |
MOD_GlcNHglycan | 334 | 337 | PF01048 | 0.445 |
MOD_GlcNHglycan | 365 | 368 | PF01048 | 0.481 |
MOD_GlcNHglycan | 377 | 380 | PF01048 | 0.295 |
MOD_GlcNHglycan | 42 | 45 | PF01048 | 0.449 |
MOD_GlcNHglycan | 441 | 444 | PF01048 | 0.465 |
MOD_GlcNHglycan | 94 | 97 | PF01048 | 0.508 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.448 |
MOD_GSK3_1 | 265 | 272 | PF00069 | 0.456 |
MOD_GSK3_1 | 294 | 301 | PF00069 | 0.521 |
MOD_GSK3_1 | 302 | 309 | PF00069 | 0.563 |
MOD_GSK3_1 | 317 | 324 | PF00069 | 0.670 |
MOD_GSK3_1 | 332 | 339 | PF00069 | 0.430 |
MOD_GSK3_1 | 346 | 353 | PF00069 | 0.367 |
MOD_GSK3_1 | 381 | 388 | PF00069 | 0.472 |
MOD_GSK3_1 | 417 | 424 | PF00069 | 0.522 |
MOD_GSK3_1 | 439 | 446 | PF00069 | 0.353 |
MOD_GSK3_1 | 467 | 474 | PF00069 | 0.383 |
MOD_N-GLC_1 | 443 | 448 | PF02516 | 0.368 |
MOD_NEK2_1 | 103 | 108 | PF00069 | 0.371 |
MOD_NEK2_1 | 123 | 128 | PF00069 | 0.462 |
MOD_NEK2_1 | 232 | 237 | PF00069 | 0.321 |
MOD_NEK2_1 | 350 | 355 | PF00069 | 0.353 |
MOD_NEK2_1 | 399 | 404 | PF00069 | 0.469 |
MOD_NEK2_1 | 411 | 416 | PF00069 | 0.597 |
MOD_NEK2_1 | 84 | 89 | PF00069 | 0.514 |
MOD_NEK2_1 | 94 | 99 | PF00069 | 0.424 |
MOD_PIKK_1 | 2 | 8 | PF00454 | 0.680 |
MOD_PIKK_1 | 215 | 221 | PF00454 | 0.375 |
MOD_PIKK_1 | 471 | 477 | PF00454 | 0.431 |
MOD_PIKK_1 | 84 | 90 | PF00454 | 0.595 |
MOD_PKA_2 | 107 | 113 | PF00069 | 0.519 |
MOD_PKA_2 | 325 | 331 | PF00069 | 0.616 |
MOD_PKB_1 | 119 | 127 | PF00069 | 0.354 |
MOD_Plk_1 | 132 | 138 | PF00069 | 0.414 |
MOD_Plk_1 | 161 | 167 | PF00069 | 0.506 |
MOD_Plk_1 | 265 | 271 | PF00069 | 0.385 |
MOD_Plk_1 | 421 | 427 | PF00069 | 0.420 |
MOD_Plk_1 | 443 | 449 | PF00069 | 0.362 |
MOD_Plk_1 | 451 | 457 | PF00069 | 0.381 |
MOD_Plk_1 | 468 | 474 | PF00069 | 0.452 |
MOD_Plk_1 | 496 | 502 | PF00069 | 0.390 |
MOD_Plk_2-3 | 422 | 428 | PF00069 | 0.400 |
MOD_Plk_4 | 355 | 361 | PF00069 | 0.321 |
MOD_Plk_4 | 381 | 387 | PF00069 | 0.533 |
MOD_Plk_4 | 451 | 457 | PF00069 | 0.343 |
MOD_Plk_4 | 474 | 480 | PF00069 | 0.446 |
MOD_ProDKin_1 | 134 | 140 | PF00069 | 0.312 |
MOD_ProDKin_1 | 246 | 252 | PF00069 | 0.269 |
MOD_ProDKin_1 | 294 | 300 | PF00069 | 0.508 |
MOD_ProDKin_1 | 417 | 423 | PF00069 | 0.561 |
MOD_ProDKin_1 | 483 | 489 | PF00069 | 0.465 |
MOD_ProDKin_1 | 502 | 508 | PF00069 | 0.364 |
MOD_SUMO_rev_2 | 249 | 255 | PF00179 | 0.373 |
TRG_DiLeu_BaLyEn_6 | 283 | 288 | PF01217 | 0.351 |
TRG_ENDOCYTIC_2 | 100 | 103 | PF00928 | 0.496 |
TRG_ENDOCYTIC_2 | 26 | 29 | PF00928 | 0.386 |
TRG_ENDOCYTIC_2 | 275 | 278 | PF00928 | 0.407 |
TRG_ENDOCYTIC_2 | 362 | 365 | PF00928 | 0.395 |
TRG_ER_diArg_1 | 116 | 119 | PF00400 | 0.397 |
TRG_ER_diArg_1 | 211 | 213 | PF00400 | 0.374 |
TRG_ER_diArg_1 | 408 | 410 | PF00400 | 0.416 |
TRG_ER_diArg_1 | 500 | 503 | PF00400 | 0.327 |
TRG_ER_diArg_1 | 9 | 12 | PF00400 | 0.555 |
TRG_NES_CRM1_1 | 19 | 32 | PF08389 | 0.465 |
TRG_NES_CRM1_1 | 61 | 77 | PF08389 | 0.482 |
TRG_NLS_MonoCore_2 | 9 | 14 | PF00514 | 0.564 |
TRG_NLS_MonoExtC_3 | 8 | 13 | PF00514 | 0.551 |
TRG_NLS_MonoExtN_4 | 7 | 14 | PF00514 | 0.539 |
TRG_Pf-PMV_PEXEL_1 | 23 | 27 | PF00026 | 0.408 |
TRG_Pf-PMV_PEXEL_1 | 31 | 36 | PF00026 | 0.415 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IHC2 | Leptomonas seymouri | 81% | 94% |
A0A0S4IHN1 | Bodo saltans | 39% | 92% |
A0A0S4JL38 | Bodo saltans | 23% | 95% |
A0A1X0P742 | Trypanosomatidae | 54% | 100% |
A0A3Q8ITT7 | Leishmania donovani | 97% | 100% |
A0A422NAT5 | Trypanosoma rangeli | 53% | 97% |
A4HL64 | Leishmania braziliensis | 94% | 100% |
A4I8P5 | Leishmania infantum | 98% | 100% |
D0A0R2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 53% | 99% |
Q4Q4J2 | Leishmania major | 97% | 100% |
Q8L4J2 | Arabidopsis thaliana | 24% | 100% |
V5BJ28 | Trypanosoma cruzi | 52% | 94% |