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 | 5 |
GO:0043226 | organelle | 2 | 5 |
GO:0043227 | membrane-bounded organelle | 3 | 5 |
GO:0043229 | intracellular organelle | 3 | 5 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 5 |
GO:0110165 | cellular anatomical entity | 1 | 5 |
Related structures:
AlphaFold database: Q4QBU6
Term | Name | Level | Count |
---|---|---|---|
GO:0006405 | RNA export from nucleus | 5 | 2 |
GO:0006406 | mRNA export from nucleus | 6 | 2 |
GO:0006810 | transport | 3 | 2 |
GO:0006913 | nucleocytoplasmic transport | 5 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0015931 | nucleobase-containing compound transport | 5 | 2 |
GO:0016973 | poly(A)+ mRNA export from nucleus | 7 | 2 |
GO:0046907 | intracellular transport | 3 | 2 |
GO:0050657 | nucleic acid transport | 6 | 2 |
GO:0050658 | RNA transport | 4 | 2 |
GO:0051028 | mRNA transport | 5 | 2 |
GO:0051168 | nuclear export | 6 | 2 |
GO:0051169 | nuclear transport | 4 | 2 |
GO:0051179 | localization | 1 | 2 |
GO:0051234 | establishment of localization | 2 | 2 |
GO:0051236 | establishment of RNA localization | 3 | 2 |
GO:0051641 | cellular localization | 2 | 2 |
GO:0051649 | establishment of localization in cell | 3 | 2 |
GO:0071702 | organic substance transport | 4 | 2 |
GO:0071705 | nitrogen compound transport | 4 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 101 | 105 | PF00656 | 0.612 |
CLV_C14_Caspase3-7 | 230 | 234 | PF00656 | 0.545 |
CLV_C14_Caspase3-7 | 405 | 409 | PF00656 | 0.521 |
CLV_C14_Caspase3-7 | 84 | 88 | PF00656 | 0.700 |
CLV_NRD_NRD_1 | 192 | 194 | PF00675 | 0.678 |
CLV_NRD_NRD_1 | 201 | 203 | PF00675 | 0.552 |
CLV_NRD_NRD_1 | 263 | 265 | PF00675 | 0.667 |
CLV_NRD_NRD_1 | 400 | 402 | PF00675 | 0.552 |
CLV_PCSK_KEX2_1 | 146 | 148 | PF00082 | 0.502 |
CLV_PCSK_KEX2_1 | 150 | 152 | PF00082 | 0.417 |
CLV_PCSK_KEX2_1 | 167 | 169 | PF00082 | 0.664 |
CLV_PCSK_KEX2_1 | 201 | 203 | PF00082 | 0.767 |
CLV_PCSK_KEX2_1 | 400 | 402 | PF00082 | 0.590 |
CLV_PCSK_PC1ET2_1 | 146 | 148 | PF00082 | 0.482 |
CLV_PCSK_PC1ET2_1 | 150 | 152 | PF00082 | 0.417 |
CLV_PCSK_PC1ET2_1 | 167 | 169 | PF00082 | 0.664 |
CLV_PCSK_SKI1_1 | 139 | 143 | PF00082 | 0.541 |
CLV_PCSK_SKI1_1 | 244 | 248 | PF00082 | 0.571 |
CLV_PCSK_SKI1_1 | 256 | 260 | PF00082 | 0.617 |
CLV_PCSK_SKI1_1 | 307 | 311 | PF00082 | 0.488 |
DEG_APCC_DBOX_1 | 306 | 314 | PF00400 | 0.440 |
DEG_Kelch_Keap1_1 | 206 | 211 | PF01344 | 0.540 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.722 |
DOC_CYCLIN_yCln2_LP_2 | 225 | 231 | PF00134 | 0.639 |
DOC_MAPK_MEF2A_6 | 354 | 362 | PF00069 | 0.370 |
DOC_PP4_FxxP_1 | 468 | 471 | PF00568 | 0.640 |
DOC_USP7_MATH_1 | 189 | 193 | PF00917 | 0.736 |
DOC_USP7_MATH_1 | 309 | 313 | PF00917 | 0.447 |
DOC_USP7_UBL2_3 | 138 | 142 | PF12436 | 0.467 |
DOC_USP7_UBL2_3 | 146 | 150 | PF12436 | 0.459 |
DOC_USP7_UBL2_3 | 153 | 157 | PF12436 | 0.427 |
DOC_USP7_UBL2_3 | 163 | 167 | PF12436 | 0.539 |
DOC_USP7_UBL2_3 | 171 | 175 | PF12436 | 0.528 |
DOC_USP7_UBL2_3 | 176 | 180 | PF12436 | 0.602 |
DOC_USP7_UBL2_3 | 195 | 199 | PF12436 | 0.726 |
DOC_USP7_UBL2_3 | 439 | 443 | PF12436 | 0.671 |
DOC_WW_Pin1_4 | 34 | 39 | PF00397 | 0.627 |
DOC_WW_Pin1_4 | 449 | 454 | PF00397 | 0.647 |
LIG_14-3-3_CanoR_1 | 264 | 274 | PF00244 | 0.597 |
LIG_14-3-3_CanoR_1 | 294 | 300 | PF00244 | 0.565 |
LIG_14-3-3_CanoR_1 | 354 | 362 | PF00244 | 0.449 |
LIG_Actin_WH2_2 | 235 | 250 | PF00022 | 0.588 |
LIG_APCC_ABBA_1 | 15 | 20 | PF00400 | 0.670 |
LIG_BRCT_BRCA1_1 | 460 | 464 | PF00533 | 0.648 |
LIG_BRCT_BRCA1_2 | 460 | 466 | PF00533 | 0.573 |
LIG_eIF4E_1 | 322 | 328 | PF01652 | 0.508 |
LIG_FHA_1 | 125 | 131 | PF00498 | 0.481 |
LIG_FHA_1 | 353 | 359 | PF00498 | 0.427 |
LIG_FHA_1 | 371 | 377 | PF00498 | 0.618 |
LIG_FHA_2 | 354 | 360 | PF00498 | 0.511 |
LIG_FHA_2 | 457 | 463 | PF00498 | 0.519 |
LIG_GBD_Chelix_1 | 274 | 282 | PF00786 | 0.497 |
LIG_LIR_Apic_2 | 467 | 471 | PF02991 | 0.623 |
LIG_LIR_Gen_1 | 213 | 223 | PF02991 | 0.638 |
LIG_LIR_Gen_1 | 418 | 427 | PF02991 | 0.553 |
LIG_LIR_Gen_1 | 452 | 458 | PF02991 | 0.656 |
LIG_LIR_Gen_1 | 52 | 61 | PF02991 | 0.532 |
LIG_LIR_Nem_3 | 335 | 341 | PF02991 | 0.429 |
LIG_LIR_Nem_3 | 377 | 382 | PF02991 | 0.524 |
LIG_LIR_Nem_3 | 418 | 423 | PF02991 | 0.524 |
LIG_LIR_Nem_3 | 452 | 457 | PF02991 | 0.659 |
LIG_LIR_Nem_3 | 477 | 482 | PF02991 | 0.564 |
LIG_LIR_Nem_3 | 52 | 56 | PF02991 | 0.527 |
LIG_NRP_CendR_1 | 511 | 512 | PF00754 | 0.720 |
LIG_Pex14_2 | 464 | 468 | PF04695 | 0.658 |
LIG_SH2_CRK | 479 | 483 | PF00017 | 0.662 |
LIG_SH2_STAT5 | 502 | 505 | PF00017 | 0.615 |
LIG_SH3_1 | 470 | 476 | PF00018 | 0.557 |
LIG_SH3_3 | 359 | 365 | PF00018 | 0.526 |
LIG_SH3_3 | 447 | 453 | PF00018 | 0.527 |
LIG_SH3_3 | 470 | 476 | PF00018 | 0.532 |
LIG_SH3_3 | 481 | 487 | PF00018 | 0.554 |
LIG_SUMO_SIM_anti_2 | 127 | 134 | PF11976 | 0.506 |
LIG_SUMO_SIM_anti_2 | 355 | 363 | PF11976 | 0.415 |
LIG_SUMO_SIM_par_1 | 131 | 137 | PF11976 | 0.594 |
LIG_TYR_ITSM | 475 | 482 | PF00017 | 0.668 |
LIG_UBA3_1 | 131 | 139 | PF00899 | 0.539 |
LIG_WRC_WIRS_1 | 417 | 422 | PF05994 | 0.520 |
MOD_CK1_1 | 174 | 180 | PF00069 | 0.702 |
MOD_CK1_1 | 21 | 27 | PF00069 | 0.668 |
MOD_CK1_1 | 425 | 431 | PF00069 | 0.700 |
MOD_CK1_1 | 446 | 452 | PF00069 | 0.593 |
MOD_CK1_1 | 49 | 55 | PF00069 | 0.720 |
MOD_CK2_1 | 106 | 112 | PF00069 | 0.776 |
MOD_CK2_1 | 264 | 270 | PF00069 | 0.596 |
MOD_CK2_1 | 449 | 455 | PF00069 | 0.560 |
MOD_CK2_1 | 456 | 462 | PF00069 | 0.499 |
MOD_Cter_Amidation | 144 | 147 | PF01082 | 0.585 |
MOD_GlcNHglycan | 108 | 111 | PF01048 | 0.718 |
MOD_GlcNHglycan | 189 | 192 | PF01048 | 0.738 |
MOD_GlcNHglycan | 267 | 270 | PF01048 | 0.571 |
MOD_GlcNHglycan | 27 | 30 | PF01048 | 0.733 |
MOD_GlcNHglycan | 279 | 282 | PF01048 | 0.481 |
MOD_GlcNHglycan | 34 | 37 | PF01048 | 0.623 |
MOD_GlcNHglycan | 424 | 427 | PF01048 | 0.527 |
MOD_GlcNHglycan | 46 | 51 | PF01048 | 0.748 |
MOD_GlcNHglycan | 495 | 498 | PF01048 | 0.664 |
MOD_GSK3_1 | 158 | 165 | PF00069 | 0.584 |
MOD_GSK3_1 | 21 | 28 | PF00069 | 0.670 |
MOD_GSK3_1 | 366 | 373 | PF00069 | 0.606 |
MOD_GSK3_1 | 418 | 425 | PF00069 | 0.528 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.781 |
MOD_N-GLC_1 | 493 | 498 | PF02516 | 0.667 |
MOD_NEK2_1 | 131 | 136 | PF00069 | 0.570 |
MOD_NEK2_1 | 155 | 160 | PF00069 | 0.457 |
MOD_NEK2_1 | 353 | 358 | PF00069 | 0.496 |
MOD_NEK2_1 | 366 | 371 | PF00069 | 0.495 |
MOD_NEK2_1 | 416 | 421 | PF00069 | 0.485 |
MOD_NEK2_1 | 464 | 469 | PF00069 | 0.634 |
MOD_NEK2_2 | 210 | 215 | PF00069 | 0.656 |
MOD_PKA_1 | 162 | 168 | PF00069 | 0.592 |
MOD_PKA_1 | 195 | 201 | PF00069 | 0.750 |
MOD_PKA_1 | 264 | 270 | PF00069 | 0.533 |
MOD_PKA_2 | 263 | 269 | PF00069 | 0.634 |
MOD_PKA_2 | 295 | 301 | PF00069 | 0.572 |
MOD_PKA_2 | 353 | 359 | PF00069 | 0.447 |
MOD_Plk_1 | 3 | 9 | PF00069 | 0.738 |
MOD_Plk_1 | 334 | 340 | PF00069 | 0.346 |
MOD_Plk_1 | 374 | 380 | PF00069 | 0.635 |
MOD_Plk_1 | 403 | 409 | PF00069 | 0.539 |
MOD_Plk_4 | 21 | 27 | PF00069 | 0.476 |
MOD_Plk_4 | 210 | 216 | PF00069 | 0.654 |
MOD_Plk_4 | 3 | 9 | PF00069 | 0.738 |
MOD_Plk_4 | 309 | 315 | PF00069 | 0.472 |
MOD_Plk_4 | 334 | 340 | PF00069 | 0.358 |
MOD_Plk_4 | 464 | 470 | PF00069 | 0.549 |
MOD_ProDKin_1 | 34 | 40 | PF00069 | 0.631 |
MOD_ProDKin_1 | 449 | 455 | PF00069 | 0.649 |
MOD_SUMO_rev_2 | 134 | 141 | PF00179 | 0.543 |
MOD_SUMO_rev_2 | 429 | 438 | PF00179 | 0.678 |
TRG_DiLeu_BaEn_2 | 210 | 216 | PF01217 | 0.654 |
TRG_DiLeu_BaEn_3 | 2 | 8 | PF01217 | 0.711 |
TRG_DiLeu_BaEn_4 | 3 | 9 | PF01217 | 0.713 |
TRG_ENDOCYTIC_2 | 479 | 482 | PF00928 | 0.574 |
TRG_ER_diArg_1 | 293 | 296 | PF00400 | 0.480 |
TRG_ER_diArg_1 | 399 | 401 | PF00400 | 0.573 |
TRG_ER_diArg_1 | 510 | 512 | PF00400 | 0.723 |
TRG_NLS_Bipartite_1 | 138 | 154 | PF00514 | 0.506 |
TRG_NLS_Bipartite_1 | 162 | 179 | PF00514 | 0.607 |
TRG_NLS_MonoCore_2 | 192 | 197 | PF00514 | 0.631 |
TRG_NLS_MonoExtC_3 | 149 | 154 | PF00514 | 0.427 |
TRG_NLS_MonoExtC_3 | 166 | 171 | PF00514 | 0.595 |
TRG_NLS_MonoExtN_4 | 147 | 154 | PF00514 | 0.497 |
TRG_NLS_MonoExtN_4 | 193 | 198 | PF00514 | 0.654 |
TRG_Pf-PMV_PEXEL_1 | 286 | 290 | PF00026 | 0.519 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PAB7 | Leptomonas seymouri | 58% | 100% |
A0A3Q8IAL9 | Leishmania donovani | 90% | 99% |
A0A422N2J9 | Trypanosoma rangeli | 35% | 100% |
A4HC96 | Leishmania braziliensis | 75% | 100% |
A4HZS8 | Leishmania infantum | 90% | 99% |
C9ZRL3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
E9AVN3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 99% |
V5BLH2 | Trypanosoma cruzi | 34% | 100% |