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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005730 | nucleolus | 5 | 1 |
GO:0030684 | preribosome | 3 | 1 |
GO:0032040 | small-subunit processome | 4 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
GO:1990904 | ribonucleoprotein complex | 2 | 1 |
Related structures:
AlphaFold database: A4HGB3
Term | Name | Level | Count |
---|---|---|---|
GO:0000462 | maturation of SSU-rRNA from tricistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, LSU-rRNA) | 10 | 1 |
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006364 | rRNA processing | 8 | 1 |
GO:0006396 | RNA processing | 6 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0016072 | rRNA metabolic process | 7 | 1 |
GO:0030490 | maturation of SSU-rRNA | 9 | 1 |
GO:0034470 | ncRNA processing | 7 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0034660 | ncRNA metabolic process | 6 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 116 | 120 | PF00656 | 0.503 |
CLV_C14_Caspase3-7 | 128 | 132 | PF00656 | 0.476 |
CLV_C14_Caspase3-7 | 15 | 19 | PF00656 | 0.687 |
CLV_C14_Caspase3-7 | 27 | 31 | PF00656 | 0.680 |
CLV_C14_Caspase3-7 | 50 | 54 | PF00656 | 0.614 |
CLV_NRD_NRD_1 | 117 | 119 | PF00675 | 0.546 |
CLV_NRD_NRD_1 | 12 | 14 | PF00675 | 0.604 |
CLV_NRD_NRD_1 | 189 | 191 | PF00675 | 0.234 |
CLV_NRD_NRD_1 | 228 | 230 | PF00675 | 0.336 |
CLV_NRD_NRD_1 | 302 | 304 | PF00675 | 0.454 |
CLV_NRD_NRD_1 | 380 | 382 | PF00675 | 0.528 |
CLV_NRD_NRD_1 | 44 | 46 | PF00675 | 0.567 |
CLV_NRD_NRD_1 | 460 | 462 | PF00675 | 0.525 |
CLV_NRD_NRD_1 | 472 | 474 | PF00675 | 0.471 |
CLV_NRD_NRD_1 | 481 | 483 | PF00675 | 0.230 |
CLV_NRD_NRD_1 | 501 | 503 | PF00675 | 0.183 |
CLV_NRD_NRD_1 | 51 | 53 | PF00675 | 0.590 |
CLV_NRD_NRD_1 | 510 | 512 | PF00675 | 0.334 |
CLV_NRD_NRD_1 | 95 | 97 | PF00675 | 0.472 |
CLV_PCSK_FUR_1 | 300 | 304 | PF00082 | 0.601 |
CLV_PCSK_KEX2_1 | 10 | 12 | PF00082 | 0.609 |
CLV_PCSK_KEX2_1 | 117 | 119 | PF00082 | 0.548 |
CLV_PCSK_KEX2_1 | 123 | 125 | PF00082 | 0.612 |
CLV_PCSK_KEX2_1 | 228 | 230 | PF00082 | 0.176 |
CLV_PCSK_KEX2_1 | 302 | 304 | PF00082 | 0.561 |
CLV_PCSK_KEX2_1 | 379 | 381 | PF00082 | 0.509 |
CLV_PCSK_KEX2_1 | 44 | 46 | PF00082 | 0.499 |
CLV_PCSK_KEX2_1 | 472 | 474 | PF00082 | 0.540 |
CLV_PCSK_KEX2_1 | 481 | 483 | PF00082 | 0.235 |
CLV_PCSK_KEX2_1 | 51 | 53 | PF00082 | 0.513 |
CLV_PCSK_KEX2_1 | 510 | 512 | PF00082 | 0.314 |
CLV_PCSK_PC1ET2_1 | 10 | 12 | PF00082 | 0.609 |
CLV_PCSK_PC1ET2_1 | 123 | 125 | PF00082 | 0.606 |
CLV_PCSK_PC7_1 | 47 | 53 | PF00082 | 0.550 |
CLV_PCSK_PC7_1 | 506 | 512 | PF00082 | 0.314 |
CLV_PCSK_PC7_1 | 6 | 12 | PF00082 | 0.493 |
CLV_PCSK_SKI1_1 | 124 | 128 | PF00082 | 0.518 |
CLV_PCSK_SKI1_1 | 292 | 296 | PF00082 | 0.563 |
CLV_PCSK_SKI1_1 | 307 | 311 | PF00082 | 0.558 |
CLV_PCSK_SKI1_1 | 47 | 51 | PF00082 | 0.636 |
CLV_PCSK_SKI1_1 | 492 | 496 | PF00082 | 0.281 |
CLV_Separin_Metazoa | 376 | 380 | PF03568 | 0.623 |
DEG_APCC_DBOX_1 | 123 | 131 | PF00400 | 0.417 |
DEG_APCC_DBOX_1 | 242 | 250 | PF00400 | 0.431 |
DEG_APCC_DBOX_1 | 302 | 310 | PF00400 | 0.469 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 197 | 203 | PF00134 | 0.456 |
DOC_MAPK_gen_1 | 510 | 519 | PF00069 | 0.314 |
DOC_PP4_FxxP_1 | 288 | 291 | PF00568 | 0.449 |
DOC_USP7_MATH_1 | 107 | 111 | PF00917 | 0.537 |
DOC_USP7_MATH_1 | 112 | 116 | PF00917 | 0.414 |
DOC_USP7_MATH_1 | 279 | 283 | PF00917 | 0.651 |
DOC_USP7_MATH_1 | 403 | 407 | PF00917 | 0.784 |
DOC_USP7_UBL2_3 | 10 | 14 | PF12436 | 0.598 |
DOC_USP7_UBL2_3 | 483 | 487 | PF12436 | 0.281 |
DOC_USP7_UBL2_3 | 93 | 97 | PF12436 | 0.538 |
DOC_WW_Pin1_4 | 156 | 161 | PF00397 | 0.401 |
DOC_WW_Pin1_4 | 287 | 292 | PF00397 | 0.449 |
LIG_14-3-3_CanoR_1 | 190 | 199 | PF00244 | 0.373 |
LIG_14-3-3_CanoR_1 | 267 | 274 | PF00244 | 0.675 |
LIG_14-3-3_CanoR_1 | 461 | 467 | PF00244 | 0.425 |
LIG_14-3-3_CanoR_1 | 96 | 104 | PF00244 | 0.510 |
LIG_Actin_WH2_2 | 319 | 337 | PF00022 | 0.389 |
LIG_APCC_ABBA_1 | 242 | 247 | PF00400 | 0.431 |
LIG_BIR_III_2 | 131 | 135 | PF00653 | 0.554 |
LIG_BRCT_BRCA1_1 | 289 | 293 | PF00533 | 0.442 |
LIG_BRCT_BRCA1_1 | 523 | 527 | PF00533 | 0.411 |
LIG_eIF4E_1 | 258 | 264 | PF01652 | 0.392 |
LIG_FHA_1 | 216 | 222 | PF00498 | 0.431 |
LIG_FHA_1 | 383 | 389 | PF00498 | 0.497 |
LIG_FHA_2 | 145 | 151 | PF00498 | 0.469 |
LIG_FHA_2 | 48 | 54 | PF00498 | 0.721 |
LIG_FHA_2 | 97 | 103 | PF00498 | 0.545 |
LIG_LIR_Gen_1 | 140 | 149 | PF02991 | 0.449 |
LIG_LIR_Gen_1 | 218 | 226 | PF02991 | 0.431 |
LIG_LIR_Gen_1 | 354 | 364 | PF02991 | 0.538 |
LIG_LIR_Gen_1 | 412 | 421 | PF02991 | 0.507 |
LIG_LIR_Gen_1 | 441 | 450 | PF02991 | 0.515 |
LIG_LIR_Gen_1 | 57 | 67 | PF02991 | 0.605 |
LIG_LIR_Nem_3 | 140 | 146 | PF02991 | 0.460 |
LIG_LIR_Nem_3 | 218 | 223 | PF02991 | 0.431 |
LIG_LIR_Nem_3 | 354 | 360 | PF02991 | 0.530 |
LIG_LIR_Nem_3 | 441 | 447 | PF02991 | 0.518 |
LIG_LIR_Nem_3 | 532 | 538 | PF02991 | 0.281 |
LIG_LIR_Nem_3 | 57 | 63 | PF02991 | 0.616 |
LIG_NRBOX | 161 | 167 | PF00104 | 0.503 |
LIG_NRBOX | 259 | 265 | PF00104 | 0.300 |
LIG_PCNA_yPIPBox_3 | 255 | 264 | PF02747 | 0.382 |
LIG_PDZ_Class_1 | 546 | 551 | PF00595 | 0.411 |
LIG_REV1ctd_RIR_1 | 354 | 363 | PF16727 | 0.629 |
LIG_SH2_STAP1 | 188 | 192 | PF00017 | 0.550 |
LIG_SH2_STAP1 | 444 | 448 | PF00017 | 0.502 |
LIG_SH2_STAT5 | 213 | 216 | PF00017 | 0.431 |
LIG_SH2_STAT5 | 220 | 223 | PF00017 | 0.431 |
LIG_SH2_STAT5 | 245 | 248 | PF00017 | 0.431 |
LIG_SH2_STAT5 | 34 | 37 | PF00017 | 0.627 |
LIG_SUMO_SIM_anti_2 | 150 | 156 | PF11976 | 0.479 |
LIG_SUMO_SIM_anti_2 | 366 | 376 | PF11976 | 0.636 |
LIG_SUMO_SIM_anti_2 | 83 | 92 | PF11976 | 0.521 |
LIG_TRAF2_1 | 251 | 254 | PF00917 | 0.370 |
LIG_TRAF2_1 | 348 | 351 | PF00917 | 0.691 |
LIG_TRAF2_1 | 474 | 477 | PF00917 | 0.653 |
LIG_TRAF2_1 | 99 | 102 | PF00917 | 0.582 |
LIG_UBA3_1 | 162 | 170 | PF00899 | 0.300 |
LIG_UBA3_1 | 374 | 383 | PF00899 | 0.585 |
LIG_WRC_WIRS_1 | 199 | 204 | PF05994 | 0.535 |
MOD_CDK_SPK_2 | 287 | 292 | PF00069 | 0.449 |
MOD_CK1_1 | 265 | 271 | PF00069 | 0.542 |
MOD_CK1_1 | 358 | 364 | PF00069 | 0.466 |
MOD_CK1_1 | 396 | 402 | PF00069 | 0.511 |
MOD_CK2_1 | 144 | 150 | PF00069 | 0.428 |
MOD_CK2_1 | 198 | 204 | PF00069 | 0.570 |
MOD_CK2_1 | 345 | 351 | PF00069 | 0.698 |
MOD_CK2_1 | 370 | 376 | PF00069 | 0.524 |
MOD_CK2_1 | 96 | 102 | PF00069 | 0.587 |
MOD_Cter_Amidation | 226 | 229 | PF01082 | 0.242 |
MOD_Cter_Amidation | 45 | 48 | PF01082 | 0.495 |
MOD_Cter_Amidation | 484 | 487 | PF01082 | 0.421 |
MOD_Cter_Amidation | 7 | 10 | PF01082 | 0.707 |
MOD_GlcNHglycan | 192 | 195 | PF01048 | 0.287 |
MOD_GlcNHglycan | 264 | 267 | PF01048 | 0.474 |
MOD_GlcNHglycan | 281 | 284 | PF01048 | 0.583 |
MOD_GlcNHglycan | 30 | 34 | PF01048 | 0.536 |
MOD_GlcNHglycan | 331 | 334 | PF01048 | 0.504 |
MOD_GlcNHglycan | 341 | 344 | PF01048 | 0.569 |
MOD_GlcNHglycan | 5 | 9 | PF01048 | 0.490 |
MOD_GSK3_1 | 198 | 205 | PF00069 | 0.558 |
MOD_GSK3_1 | 262 | 269 | PF00069 | 0.488 |
MOD_GSK3_1 | 321 | 328 | PF00069 | 0.536 |
MOD_GSK3_1 | 334 | 341 | PF00069 | 0.489 |
MOD_GSK3_1 | 387 | 394 | PF00069 | 0.695 |
MOD_GSK3_1 | 519 | 526 | PF00069 | 0.411 |
MOD_N-GLC_1 | 334 | 339 | PF02516 | 0.599 |
MOD_NEK2_1 | 202 | 207 | PF00069 | 0.447 |
MOD_NEK2_1 | 209 | 214 | PF00069 | 0.435 |
MOD_NEK2_1 | 215 | 220 | PF00069 | 0.431 |
MOD_NEK2_1 | 256 | 261 | PF00069 | 0.390 |
MOD_NEK2_1 | 334 | 339 | PF00069 | 0.601 |
MOD_PIKK_1 | 519 | 525 | PF00454 | 0.360 |
MOD_PK_1 | 462 | 468 | PF00069 | 0.361 |
MOD_PKA_1 | 190 | 196 | PF00069 | 0.373 |
MOD_PKA_1 | 329 | 335 | PF00069 | 0.619 |
MOD_PKA_1 | 47 | 53 | PF00069 | 0.724 |
MOD_PKA_1 | 96 | 102 | PF00069 | 0.544 |
MOD_PKA_2 | 266 | 272 | PF00069 | 0.688 |
MOD_PKA_2 | 358 | 364 | PF00069 | 0.750 |
MOD_PKA_2 | 392 | 398 | PF00069 | 0.767 |
MOD_PKB_1 | 391 | 399 | PF00069 | 0.593 |
MOD_PKB_1 | 45 | 53 | PF00069 | 0.490 |
MOD_Plk_1 | 29 | 35 | PF00069 | 0.513 |
MOD_Plk_1 | 319 | 325 | PF00069 | 0.382 |
MOD_Plk_2-3 | 345 | 351 | PF00069 | 0.590 |
MOD_Plk_2-3 | 370 | 376 | PF00069 | 0.646 |
MOD_Plk_4 | 168 | 174 | PF00069 | 0.541 |
MOD_Plk_4 | 198 | 204 | PF00069 | 0.506 |
MOD_Plk_4 | 215 | 221 | PF00069 | 0.366 |
MOD_Plk_4 | 370 | 376 | PF00069 | 0.556 |
MOD_Plk_4 | 462 | 468 | PF00069 | 0.626 |
MOD_ProDKin_1 | 156 | 162 | PF00069 | 0.392 |
MOD_ProDKin_1 | 287 | 293 | PF00069 | 0.446 |
MOD_SUMO_for_1 | 155 | 158 | PF00179 | 0.451 |
MOD_SUMO_for_1 | 223 | 226 | PF00179 | 0.431 |
MOD_SUMO_for_1 | 529 | 532 | PF00179 | 0.331 |
MOD_SUMO_rev_2 | 185 | 193 | PF00179 | 0.526 |
MOD_SUMO_rev_2 | 201 | 207 | PF00179 | 0.508 |
MOD_SUMO_rev_2 | 247 | 256 | PF00179 | 0.499 |
TRG_DiLeu_BaEn_1 | 158 | 163 | PF01217 | 0.404 |
TRG_DiLeu_BaEn_1 | 370 | 375 | PF01217 | 0.612 |
TRG_DiLeu_BaLyEn_6 | 259 | 264 | PF01217 | 0.386 |
TRG_ENDOCYTIC_2 | 220 | 223 | PF00928 | 0.431 |
TRG_ENDOCYTIC_2 | 444 | 447 | PF00928 | 0.539 |
TRG_ER_diArg_1 | 228 | 230 | PF00400 | 0.376 |
TRG_ER_diArg_1 | 378 | 381 | PF00400 | 0.546 |
TRG_ER_diArg_1 | 44 | 47 | PF00400 | 0.491 |
TRG_ER_diArg_1 | 472 | 474 | PF00400 | 0.689 |
TRG_ER_diArg_1 | 496 | 499 | PF00400 | 0.347 |
TRG_NLS_MonoExtC_3 | 8 | 13 | PF00514 | 0.607 |
TRG_NLS_MonoExtC_3 | 95 | 101 | PF00514 | 0.593 |
TRG_NLS_MonoExtN_4 | 6 | 13 | PF00514 | 0.598 |
TRG_NLS_MonoExtN_4 | 93 | 100 | PF00514 | 0.585 |
TRG_PTS1 | 548 | 551 | PF00515 | 0.411 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDH2 | Leptomonas seymouri | 71% | 100% |
A0A0S4JBP1 | Bodo saltans | 38% | 100% |
A0A1X0NYI2 | Trypanosomatidae | 49% | 100% |
A0A3S7X1D4 | Leishmania donovani | 85% | 98% |
A0A422P1Q1 | Trypanosoma rangeli | 51% | 100% |
A4I3E7 | Leishmania infantum | 85% | 98% |
D0A800 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 48% | 100% |
E9AZN4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 83% | 98% |
Q4Q8J7 | Leishmania major | 84% | 100% |
V5BG83 | Trypanosoma cruzi | 50% | 100% |