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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 4 |
GO:0043226 | organelle | 2 | 4 |
GO:0043227 | membrane-bounded organelle | 3 | 4 |
GO:0043229 | intracellular organelle | 3 | 4 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 4 |
GO:0110165 | cellular anatomical entity | 1 | 4 |
Related structures:
AlphaFold database: A0A3Q8IAL9
Term | Name | Level | Count |
---|---|---|---|
GO:0006405 | RNA export from nucleus | 5 | 1 |
GO:0006406 | mRNA export from nucleus | 6 | 1 |
GO:0006810 | transport | 3 | 1 |
GO:0006913 | nucleocytoplasmic transport | 5 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0015931 | nucleobase-containing compound transport | 5 | 1 |
GO:0016973 | poly(A)+ mRNA export from nucleus | 7 | 1 |
GO:0046907 | intracellular transport | 3 | 1 |
GO:0050657 | nucleic acid transport | 6 | 1 |
GO:0050658 | RNA transport | 4 | 1 |
GO:0051028 | mRNA transport | 5 | 1 |
GO:0051168 | nuclear export | 6 | 1 |
GO:0051169 | nuclear transport | 4 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0051236 | establishment of RNA localization | 3 | 1 |
GO:0051641 | cellular localization | 2 | 1 |
GO:0051649 | establishment of localization in cell | 3 | 1 |
GO:0071702 | organic substance transport | 4 | 1 |
GO:0071705 | nitrogen compound transport | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 101 | 105 | PF00656 | 0.645 |
CLV_C14_Caspase3-7 | 217 | 221 | PF00656 | 0.669 |
CLV_C14_Caspase3-7 | 223 | 227 | PF00656 | 0.709 |
CLV_C14_Caspase3-7 | 236 | 240 | PF00656 | 0.576 |
CLV_C14_Caspase3-7 | 411 | 415 | PF00656 | 0.519 |
CLV_C14_Caspase3-7 | 60 | 64 | PF00656 | 0.573 |
CLV_C14_Caspase3-7 | 65 | 69 | PF00656 | 0.623 |
CLV_C14_Caspase3-7 | 87 | 91 | PF00656 | 0.719 |
CLV_NRD_NRD_1 | 192 | 194 | PF00675 | 0.694 |
CLV_NRD_NRD_1 | 201 | 203 | PF00675 | 0.578 |
CLV_NRD_NRD_1 | 269 | 271 | PF00675 | 0.680 |
CLV_NRD_NRD_1 | 406 | 408 | PF00675 | 0.569 |
CLV_PCSK_KEX2_1 | 142 | 144 | PF00082 | 0.537 |
CLV_PCSK_KEX2_1 | 146 | 148 | PF00082 | 0.503 |
CLV_PCSK_KEX2_1 | 150 | 152 | PF00082 | 0.439 |
CLV_PCSK_KEX2_1 | 201 | 203 | PF00082 | 0.786 |
CLV_PCSK_KEX2_1 | 406 | 408 | PF00082 | 0.607 |
CLV_PCSK_PC1ET2_1 | 142 | 144 | PF00082 | 0.517 |
CLV_PCSK_PC1ET2_1 | 146 | 148 | PF00082 | 0.503 |
CLV_PCSK_PC1ET2_1 | 150 | 152 | PF00082 | 0.439 |
CLV_PCSK_SKI1_1 | 139 | 143 | PF00082 | 0.571 |
CLV_PCSK_SKI1_1 | 250 | 254 | PF00082 | 0.603 |
CLV_PCSK_SKI1_1 | 262 | 266 | PF00082 | 0.649 |
CLV_PCSK_SKI1_1 | 313 | 317 | PF00082 | 0.492 |
DEG_APCC_DBOX_1 | 312 | 320 | PF00400 | 0.517 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.750 |
DOC_CYCLIN_yCln2_LP_2 | 231 | 237 | PF00134 | 0.662 |
DOC_MAPK_MEF2A_6 | 360 | 368 | PF00069 | 0.395 |
DOC_PP4_FxxP_1 | 474 | 477 | PF00568 | 0.656 |
DOC_USP7_MATH_1 | 115 | 119 | PF00917 | 0.620 |
DOC_USP7_MATH_1 | 158 | 162 | PF00917 | 0.471 |
DOC_USP7_MATH_1 | 189 | 193 | PF00917 | 0.760 |
DOC_USP7_MATH_1 | 315 | 319 | PF00917 | 0.545 |
DOC_USP7_MATH_1 | 74 | 78 | PF00917 | 0.845 |
DOC_USP7_UBL2_3 | 138 | 142 | PF12436 | 0.501 |
DOC_USP7_UBL2_3 | 146 | 150 | PF12436 | 0.368 |
DOC_USP7_UBL2_3 | 153 | 157 | PF12436 | 0.477 |
DOC_USP7_UBL2_3 | 163 | 167 | PF12436 | 0.559 |
DOC_USP7_UBL2_3 | 176 | 180 | PF12436 | 0.627 |
DOC_USP7_UBL2_3 | 195 | 199 | PF12436 | 0.739 |
DOC_USP7_UBL2_3 | 262 | 266 | PF12436 | 0.626 |
DOC_USP7_UBL2_3 | 445 | 449 | PF12436 | 0.684 |
DOC_USP7_UBL2_3 | 472 | 476 | PF12436 | 0.510 |
DOC_WW_Pin1_4 | 34 | 39 | PF00397 | 0.686 |
DOC_WW_Pin1_4 | 455 | 460 | PF00397 | 0.632 |
LIG_14-3-3_CanoR_1 | 270 | 280 | PF00244 | 0.633 |
LIG_14-3-3_CanoR_1 | 302 | 306 | PF00244 | 0.583 |
LIG_Actin_WH2_2 | 241 | 256 | PF00022 | 0.617 |
LIG_APCC_ABBA_1 | 15 | 20 | PF00400 | 0.702 |
LIG_BRCT_BRCA1_1 | 466 | 470 | PF00533 | 0.681 |
LIG_BRCT_BRCA1_1 | 49 | 53 | PF00533 | 0.515 |
LIG_BRCT_BRCA1_2 | 466 | 472 | PF00533 | 0.599 |
LIG_eIF4E_1 | 328 | 334 | PF01652 | 0.539 |
LIG_FHA_1 | 359 | 365 | PF00498 | 0.448 |
LIG_FHA_1 | 377 | 383 | PF00498 | 0.634 |
LIG_FHA_2 | 17 | 23 | PF00498 | 0.779 |
LIG_FHA_2 | 463 | 469 | PF00498 | 0.545 |
LIG_FHA_2 | 58 | 64 | PF00498 | 0.673 |
LIG_GBD_Chelix_1 | 280 | 288 | PF00786 | 0.518 |
LIG_LIR_Apic_2 | 473 | 477 | PF02991 | 0.654 |
LIG_LIR_Gen_1 | 213 | 222 | PF02991 | 0.676 |
LIG_LIR_Gen_1 | 424 | 433 | PF02991 | 0.576 |
LIG_LIR_Gen_1 | 458 | 464 | PF02991 | 0.676 |
LIG_LIR_Gen_1 | 50 | 61 | PF02991 | 0.590 |
LIG_LIR_Nem_3 | 341 | 347 | PF02991 | 0.454 |
LIG_LIR_Nem_3 | 383 | 388 | PF02991 | 0.551 |
LIG_LIR_Nem_3 | 424 | 429 | PF02991 | 0.548 |
LIG_LIR_Nem_3 | 458 | 463 | PF02991 | 0.680 |
LIG_LIR_Nem_3 | 483 | 488 | PF02991 | 0.568 |
LIG_LIR_Nem_3 | 50 | 56 | PF02991 | 0.599 |
LIG_NRP_CendR_1 | 517 | 518 | PF00754 | 0.774 |
LIG_Pex14_2 | 305 | 309 | PF04695 | 0.511 |
LIG_Pex14_2 | 470 | 474 | PF04695 | 0.692 |
LIG_SH2_CRK | 485 | 489 | PF00017 | 0.681 |
LIG_SH2_STAT5 | 30 | 33 | PF00017 | 0.694 |
LIG_SH2_STAT5 | 328 | 331 | PF00017 | 0.410 |
LIG_SH2_STAT5 | 508 | 511 | PF00017 | 0.610 |
LIG_SH3_1 | 476 | 482 | PF00018 | 0.585 |
LIG_SH3_3 | 32 | 38 | PF00018 | 0.583 |
LIG_SH3_3 | 365 | 371 | PF00018 | 0.559 |
LIG_SH3_3 | 453 | 459 | PF00018 | 0.559 |
LIG_SH3_3 | 476 | 482 | PF00018 | 0.560 |
LIG_SH3_3 | 487 | 493 | PF00018 | 0.585 |
LIG_SUMO_SIM_anti_2 | 128 | 134 | PF11976 | 0.530 |
LIG_SUMO_SIM_par_1 | 131 | 137 | PF11976 | 0.613 |
LIG_TYR_ITSM | 481 | 488 | PF00017 | 0.704 |
LIG_UBA3_1 | 131 | 139 | PF00899 | 0.548 |
LIG_WRC_WIRS_1 | 423 | 428 | PF05994 | 0.544 |
MOD_CK1_1 | 174 | 180 | PF00069 | 0.726 |
MOD_CK1_1 | 21 | 27 | PF00069 | 0.716 |
MOD_CK1_1 | 431 | 437 | PF00069 | 0.673 |
MOD_CK1_1 | 49 | 55 | PF00069 | 0.748 |
MOD_CK2_1 | 106 | 112 | PF00069 | 0.800 |
MOD_CK2_1 | 16 | 22 | PF00069 | 0.685 |
MOD_CK2_1 | 270 | 276 | PF00069 | 0.618 |
MOD_CK2_1 | 455 | 461 | PF00069 | 0.590 |
MOD_CK2_1 | 462 | 468 | PF00069 | 0.526 |
MOD_Cter_Amidation | 144 | 147 | PF01082 | 0.597 |
MOD_GlcNHglycan | 108 | 111 | PF01048 | 0.741 |
MOD_GlcNHglycan | 117 | 120 | PF01048 | 0.630 |
MOD_GlcNHglycan | 189 | 192 | PF01048 | 0.739 |
MOD_GlcNHglycan | 27 | 30 | PF01048 | 0.807 |
MOD_GlcNHglycan | 273 | 276 | PF01048 | 0.576 |
MOD_GlcNHglycan | 299 | 302 | PF01048 | 0.614 |
MOD_GlcNHglycan | 430 | 433 | PF01048 | 0.531 |
MOD_GlcNHglycan | 501 | 504 | PF01048 | 0.681 |
MOD_GlcNHglycan | 76 | 79 | PF01048 | 0.839 |
MOD_GSK3_1 | 189 | 196 | PF00069 | 0.682 |
MOD_GSK3_1 | 21 | 28 | PF00069 | 0.778 |
MOD_GSK3_1 | 210 | 217 | PF00069 | 0.546 |
MOD_GSK3_1 | 253 | 260 | PF00069 | 0.576 |
MOD_GSK3_1 | 297 | 304 | PF00069 | 0.509 |
MOD_GSK3_1 | 372 | 379 | PF00069 | 0.582 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.791 |
MOD_GSK3_1 | 424 | 431 | PF00069 | 0.552 |
MOD_N-GLC_1 | 499 | 504 | PF02516 | 0.683 |
MOD_NEK2_1 | 131 | 136 | PF00069 | 0.561 |
MOD_NEK2_1 | 214 | 219 | PF00069 | 0.537 |
MOD_NEK2_1 | 253 | 258 | PF00069 | 0.654 |
MOD_NEK2_1 | 372 | 377 | PF00069 | 0.487 |
MOD_NEK2_1 | 422 | 427 | PF00069 | 0.512 |
MOD_NEK2_1 | 470 | 475 | PF00069 | 0.609 |
MOD_NEK2_1 | 57 | 62 | PF00069 | 0.623 |
MOD_NEK2_2 | 210 | 215 | PF00069 | 0.693 |
MOD_PIKK_1 | 156 | 162 | PF00454 | 0.455 |
MOD_PIKK_1 | 171 | 177 | PF00454 | 0.492 |
MOD_PKA_1 | 187 | 193 | PF00069 | 0.725 |
MOD_PKA_1 | 270 | 276 | PF00069 | 0.568 |
MOD_PKA_2 | 253 | 259 | PF00069 | 0.566 |
MOD_PKA_2 | 269 | 275 | PF00069 | 0.671 |
MOD_PKA_2 | 301 | 307 | PF00069 | 0.599 |
MOD_PKA_2 | 57 | 63 | PF00069 | 0.630 |
MOD_Plk_1 | 21 | 27 | PF00069 | 0.502 |
MOD_Plk_1 | 3 | 9 | PF00069 | 0.782 |
MOD_Plk_1 | 340 | 346 | PF00069 | 0.377 |
MOD_Plk_1 | 380 | 386 | PF00069 | 0.654 |
MOD_Plk_1 | 409 | 415 | PF00069 | 0.558 |
MOD_Plk_4 | 21 | 27 | PF00069 | 0.757 |
MOD_Plk_4 | 210 | 216 | PF00069 | 0.692 |
MOD_Plk_4 | 3 | 9 | PF00069 | 0.741 |
MOD_Plk_4 | 315 | 321 | PF00069 | 0.492 |
MOD_Plk_4 | 340 | 346 | PF00069 | 0.369 |
MOD_Plk_4 | 470 | 476 | PF00069 | 0.576 |
MOD_ProDKin_1 | 34 | 40 | PF00069 | 0.688 |
MOD_ProDKin_1 | 455 | 461 | PF00069 | 0.633 |
MOD_SUMO_rev_2 | 134 | 141 | PF00179 | 0.553 |
MOD_SUMO_rev_2 | 435 | 444 | PF00179 | 0.697 |
TRG_DiLeu_BaEn_2 | 210 | 216 | PF01217 | 0.692 |
TRG_DiLeu_BaEn_3 | 2 | 8 | PF01217 | 0.741 |
TRG_DiLeu_BaEn_4 | 3 | 9 | PF01217 | 0.741 |
TRG_ENDOCYTIC_2 | 485 | 488 | PF00928 | 0.579 |
TRG_ER_diArg_1 | 405 | 407 | PF00400 | 0.592 |
TRG_ER_diArg_1 | 516 | 518 | PF00400 | 0.758 |
TRG_NLS_Bipartite_1 | 138 | 154 | PF00514 | 0.526 |
TRG_NLS_MonoExtC_3 | 149 | 154 | PF00514 | 0.450 |
TRG_NLS_MonoExtN_4 | 147 | 154 | PF00514 | 0.519 |
TRG_Pf-PMV_PEXEL_1 | 292 | 296 | PF00026 | 0.537 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PAB7 | Leptomonas seymouri | 60% | 100% |
A0A422N2J9 | Trypanosoma rangeli | 35% | 100% |
A4HC96 | Leishmania braziliensis | 76% | 97% |
A4HZS8 | Leishmania infantum | 99% | 100% |
C9ZRL3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
E9AVN3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
Q4QBU6 | Leishmania major | 90% | 99% |
V5BLH2 | Trypanosoma cruzi | 34% | 100% |