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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005643 | nuclear pore | 3 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:0140513 | nuclear protein-containing complex | 2 | 1 |
Related structures:
AlphaFold database: A4HHS4
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 1 |
GO:0006913 | nucleocytoplasmic transport | 5 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0046907 | intracellular transport | 3 | 1 |
GO:0051169 | nuclear transport | 4 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0051641 | cellular localization | 2 | 1 |
GO:0051649 | establishment of localization in cell | 3 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 120 | 122 | PF00675 | 0.652 |
CLV_NRD_NRD_1 | 177 | 179 | PF00675 | 0.642 |
CLV_NRD_NRD_1 | 466 | 468 | PF00675 | 0.356 |
CLV_PCSK_FUR_1 | 175 | 179 | PF00082 | 0.405 |
CLV_PCSK_KEX2_1 | 120 | 122 | PF00082 | 0.608 |
CLV_PCSK_KEX2_1 | 177 | 179 | PF00082 | 0.644 |
CLV_PCSK_KEX2_1 | 465 | 467 | PF00082 | 0.372 |
CLV_PCSK_SKI1_1 | 160 | 164 | PF00082 | 0.573 |
CLV_PCSK_SKI1_1 | 246 | 250 | PF00082 | 0.337 |
CLV_PCSK_SKI1_1 | 289 | 293 | PF00082 | 0.450 |
CLV_PCSK_SKI1_1 | 323 | 327 | PF00082 | 0.507 |
DEG_APCC_DBOX_1 | 126 | 134 | PF00400 | 0.676 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.546 |
DEG_SPOP_SBC_1 | 92 | 96 | PF00917 | 0.578 |
DOC_CKS1_1 | 399 | 404 | PF01111 | 0.497 |
DOC_CYCLIN_RxL_1 | 286 | 296 | PF00134 | 0.279 |
DOC_MAPK_HePTP_8 | 430 | 442 | PF00069 | 0.489 |
DOC_MAPK_MEF2A_6 | 433 | 442 | PF00069 | 0.474 |
DOC_PP1_RVXF_1 | 148 | 155 | PF00149 | 0.435 |
DOC_PP1_RVXF_1 | 232 | 239 | PF00149 | 0.405 |
DOC_PP1_RVXF_1 | 287 | 293 | PF00149 | 0.275 |
DOC_PP1_RVXF_1 | 321 | 327 | PF00149 | 0.400 |
DOC_PP2B_PxIxI_1 | 435 | 441 | PF00149 | 0.461 |
DOC_PP4_FxxP_1 | 154 | 157 | PF00568 | 0.498 |
DOC_USP7_MATH_1 | 166 | 170 | PF00917 | 0.436 |
DOC_USP7_MATH_1 | 176 | 180 | PF00917 | 0.630 |
DOC_USP7_MATH_1 | 208 | 212 | PF00917 | 0.468 |
DOC_USP7_MATH_1 | 264 | 268 | PF00917 | 0.608 |
DOC_USP7_MATH_1 | 271 | 275 | PF00917 | 0.633 |
DOC_USP7_MATH_1 | 294 | 298 | PF00917 | 0.514 |
DOC_USP7_MATH_1 | 315 | 319 | PF00917 | 0.322 |
DOC_USP7_MATH_1 | 393 | 397 | PF00917 | 0.550 |
DOC_USP7_MATH_1 | 78 | 82 | PF00917 | 0.695 |
DOC_WW_Pin1_4 | 378 | 383 | PF00397 | 0.607 |
DOC_WW_Pin1_4 | 398 | 403 | PF00397 | 0.501 |
LIG_14-3-3_CanoR_1 | 107 | 113 | PF00244 | 0.666 |
LIG_14-3-3_CanoR_1 | 75 | 85 | PF00244 | 0.728 |
LIG_Actin_WH2_2 | 145 | 162 | PF00022 | 0.337 |
LIG_BRCT_BRCA1_1 | 380 | 384 | PF00533 | 0.398 |
LIG_BRCT_BRCA1_1 | 416 | 420 | PF00533 | 0.466 |
LIG_deltaCOP1_diTrp_1 | 235 | 241 | PF00928 | 0.357 |
LIG_EH_1 | 434 | 438 | PF12763 | 0.408 |
LIG_eIF4E_1 | 143 | 149 | PF01652 | 0.495 |
LIG_FHA_1 | 143 | 149 | PF00498 | 0.533 |
LIG_FHA_1 | 210 | 216 | PF00498 | 0.431 |
LIG_FHA_1 | 339 | 345 | PF00498 | 0.518 |
LIG_FHA_1 | 421 | 427 | PF00498 | 0.438 |
LIG_FHA_1 | 472 | 478 | PF00498 | 0.371 |
LIG_FHA_1 | 510 | 516 | PF00498 | 0.489 |
LIG_FHA_2 | 112 | 118 | PF00498 | 0.568 |
LIG_FHA_2 | 364 | 370 | PF00498 | 0.397 |
LIG_FHA_2 | 457 | 463 | PF00498 | 0.371 |
LIG_FHA_2 | 495 | 501 | PF00498 | 0.259 |
LIG_GBD_Chelix_1 | 442 | 450 | PF00786 | 0.504 |
LIG_Integrin_isoDGR_2 | 73 | 75 | PF01839 | 0.515 |
LIG_LIR_Apic_2 | 151 | 157 | PF02991 | 0.564 |
LIG_LIR_Gen_1 | 106 | 116 | PF02991 | 0.528 |
LIG_LIR_Gen_1 | 194 | 203 | PF02991 | 0.314 |
LIG_LIR_Gen_1 | 37 | 47 | PF02991 | 0.518 |
LIG_LIR_Nem_3 | 106 | 112 | PF02991 | 0.605 |
LIG_LIR_Nem_3 | 194 | 199 | PF02991 | 0.441 |
LIG_LIR_Nem_3 | 35 | 39 | PF02991 | 0.623 |
LIG_LIR_Nem_3 | 448 | 454 | PF02991 | 0.538 |
LIG_LYPXL_S_1 | 46 | 50 | PF13949 | 0.578 |
LIG_LYPXL_yS_3 | 47 | 50 | PF13949 | 0.586 |
LIG_MLH1_MIPbox_1 | 416 | 420 | PF16413 | 0.466 |
LIG_MYND_1 | 138 | 142 | PF01753 | 0.512 |
LIG_NRBOX | 258 | 264 | PF00104 | 0.255 |
LIG_SH2_CRK | 39 | 43 | PF00017 | 0.603 |
LIG_SH2_CRK | 451 | 455 | PF00017 | 0.526 |
LIG_SH2_STAT5 | 143 | 146 | PF00017 | 0.329 |
LIG_SH2_STAT5 | 419 | 422 | PF00017 | 0.441 |
LIG_SH3_3 | 330 | 336 | PF00018 | 0.570 |
LIG_SH3_3 | 339 | 345 | PF00018 | 0.559 |
LIG_SH3_3 | 396 | 402 | PF00018 | 0.455 |
LIG_SH3_3 | 43 | 49 | PF00018 | 0.473 |
LIG_SH3_3 | 7 | 13 | PF00018 | 0.456 |
LIG_SUMO_SIM_anti_2 | 372 | 377 | PF11976 | 0.384 |
LIG_SUMO_SIM_par_1 | 340 | 346 | PF11976 | 0.523 |
LIG_TRAF2_1 | 202 | 205 | PF00917 | 0.410 |
LIG_WRC_WIRS_1 | 504 | 509 | PF05994 | 0.405 |
MOD_CK1_1 | 111 | 117 | PF00069 | 0.631 |
MOD_CK1_1 | 191 | 197 | PF00069 | 0.255 |
MOD_CK1_1 | 267 | 273 | PF00069 | 0.632 |
MOD_CK1_1 | 297 | 303 | PF00069 | 0.544 |
MOD_CK1_1 | 444 | 450 | PF00069 | 0.576 |
MOD_CK1_1 | 81 | 87 | PF00069 | 0.737 |
MOD_CK2_1 | 111 | 117 | PF00069 | 0.436 |
MOD_CK2_1 | 363 | 369 | PF00069 | 0.388 |
MOD_CK2_1 | 456 | 462 | PF00069 | 0.372 |
MOD_CK2_1 | 494 | 500 | PF00069 | 0.264 |
MOD_CMANNOS | 238 | 241 | PF00535 | 0.459 |
MOD_GlcNHglycan | 135 | 138 | PF01048 | 0.620 |
MOD_GlcNHglycan | 168 | 171 | PF01048 | 0.396 |
MOD_GlcNHglycan | 282 | 285 | PF01048 | 0.538 |
MOD_GlcNHglycan | 296 | 299 | PF01048 | 0.466 |
MOD_GlcNHglycan | 35 | 39 | PF01048 | 0.580 |
MOD_GlcNHglycan | 385 | 388 | PF01048 | 0.532 |
MOD_GlcNHglycan | 389 | 392 | PF01048 | 0.472 |
MOD_GlcNHglycan | 80 | 83 | PF01048 | 0.742 |
MOD_GlcNHglycan | 85 | 88 | PF01048 | 0.748 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.671 |
MOD_GSK3_1 | 158 | 165 | PF00069 | 0.558 |
MOD_GSK3_1 | 188 | 195 | PF00069 | 0.490 |
MOD_GSK3_1 | 263 | 270 | PF00069 | 0.410 |
MOD_GSK3_1 | 273 | 280 | PF00069 | 0.432 |
MOD_GSK3_1 | 293 | 300 | PF00069 | 0.322 |
MOD_GSK3_1 | 315 | 322 | PF00069 | 0.526 |
MOD_GSK3_1 | 383 | 390 | PF00069 | 0.524 |
MOD_GSK3_1 | 441 | 448 | PF00069 | 0.430 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.692 |
MOD_N-GLC_1 | 66 | 71 | PF02516 | 0.645 |
MOD_NEK2_1 | 133 | 138 | PF00069 | 0.622 |
MOD_NEK2_1 | 148 | 153 | PF00069 | 0.379 |
MOD_NEK2_1 | 192 | 197 | PF00069 | 0.260 |
MOD_NEK2_1 | 363 | 368 | PF00069 | 0.395 |
MOD_NEK2_1 | 420 | 425 | PF00069 | 0.488 |
MOD_NEK2_1 | 445 | 450 | PF00069 | 0.381 |
MOD_NEK2_1 | 461 | 466 | PF00069 | 0.429 |
MOD_NEK2_1 | 66 | 71 | PF00069 | 0.684 |
MOD_NEK2_1 | 93 | 98 | PF00069 | 0.649 |
MOD_NEK2_2 | 158 | 163 | PF00069 | 0.606 |
MOD_PKA_2 | 176 | 182 | PF00069 | 0.552 |
MOD_PKA_2 | 185 | 191 | PF00069 | 0.341 |
MOD_PKA_2 | 409 | 415 | PF00069 | 0.495 |
MOD_PKA_2 | 76 | 82 | PF00069 | 0.768 |
MOD_Plk_1 | 234 | 240 | PF00069 | 0.255 |
MOD_Plk_1 | 271 | 277 | PF00069 | 0.417 |
MOD_Plk_1 | 34 | 40 | PF00069 | 0.610 |
MOD_Plk_4 | 150 | 156 | PF00069 | 0.344 |
MOD_Plk_4 | 192 | 198 | PF00069 | 0.382 |
MOD_Plk_4 | 234 | 240 | PF00069 | 0.412 |
MOD_Plk_4 | 338 | 344 | PF00069 | 0.482 |
MOD_Plk_4 | 414 | 420 | PF00069 | 0.469 |
MOD_Plk_4 | 441 | 447 | PF00069 | 0.520 |
MOD_Plk_4 | 511 | 517 | PF00069 | 0.348 |
MOD_ProDKin_1 | 378 | 384 | PF00069 | 0.615 |
MOD_ProDKin_1 | 398 | 404 | PF00069 | 0.498 |
TRG_DiLeu_BaEn_1 | 473 | 478 | PF01217 | 0.373 |
TRG_DiLeu_BaLyEn_6 | 258 | 263 | PF01217 | 0.243 |
TRG_ENDOCYTIC_2 | 196 | 199 | PF00928 | 0.468 |
TRG_ENDOCYTIC_2 | 39 | 42 | PF00928 | 0.571 |
TRG_ENDOCYTIC_2 | 451 | 454 | PF00928 | 0.542 |
TRG_ENDOCYTIC_2 | 47 | 50 | PF00928 | 0.579 |
TRG_ER_diArg_1 | 120 | 123 | PF00400 | 0.672 |
TRG_ER_diArg_1 | 174 | 177 | PF00400 | 0.564 |
TRG_ER_diArg_1 | 376 | 379 | PF00400 | 0.419 |
TRG_ER_diArg_1 | 465 | 467 | PF00400 | 0.391 |
TRG_Pf-PMV_PEXEL_1 | 21 | 25 | PF00026 | 0.526 |
TRG_Pf-PMV_PEXEL_1 | 466 | 471 | PF00026 | 0.388 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6I3 | Leptomonas seymouri | 55% | 100% |
A0A0S4JJV4 | Bodo saltans | 26% | 100% |
A0A1X0NPX8 | Trypanosomatidae | 41% | 100% |
A0A3Q8ICS9 | Leishmania donovani | 83% | 100% |
A0A3R7KGG9 | Trypanosoma rangeli | 37% | 100% |
A4HVH0 | Leishmania infantum | 84% | 100% |
D0A6U9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 100% |
E9AP59 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 100% |
Q4QGC9 | Leishmania major | 84% | 100% |
V5D9X2 | Trypanosoma cruzi | 36% | 100% |