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 | 2 |
GO:0032991 | protein-containing complex | 1 | 2 |
GO:0140513 | nuclear protein-containing complex | 2 | 2 |
Related structures:
AlphaFold database: Q4QGC9
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 2 |
GO:0006913 | nucleocytoplasmic transport | 5 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0046907 | intracellular transport | 3 | 2 |
GO:0051169 | nuclear transport | 4 | 2 |
GO:0051179 | localization | 1 | 2 |
GO:0051234 | establishment of localization | 2 | 2 |
GO:0051641 | cellular localization | 2 | 2 |
GO:0051649 | establishment of localization in cell | 3 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 114 | 118 | PF00656 | 0.749 |
CLV_C14_Caspase3-7 | 269 | 273 | PF00656 | 0.513 |
CLV_NRD_NRD_1 | 120 | 122 | PF00675 | 0.687 |
CLV_NRD_NRD_1 | 126 | 128 | PF00675 | 0.668 |
CLV_NRD_NRD_1 | 171 | 173 | PF00675 | 0.599 |
CLV_NRD_NRD_1 | 177 | 179 | PF00675 | 0.559 |
CLV_NRD_NRD_1 | 466 | 468 | PF00675 | 0.404 |
CLV_PCSK_KEX2_1 | 119 | 121 | PF00082 | 0.682 |
CLV_PCSK_KEX2_1 | 126 | 128 | PF00082 | 0.678 |
CLV_PCSK_KEX2_1 | 171 | 173 | PF00082 | 0.596 |
CLV_PCSK_KEX2_1 | 177 | 179 | PF00082 | 0.562 |
CLV_PCSK_KEX2_1 | 465 | 467 | PF00082 | 0.412 |
CLV_PCSK_SKI1_1 | 160 | 164 | PF00082 | 0.564 |
CLV_PCSK_SKI1_1 | 171 | 175 | PF00082 | 0.493 |
CLV_PCSK_SKI1_1 | 246 | 250 | PF00082 | 0.390 |
CLV_PCSK_SKI1_1 | 289 | 293 | PF00082 | 0.472 |
CLV_PCSK_SKI1_1 | 323 | 327 | PF00082 | 0.507 |
CLV_PCSK_SKI1_1 | 6 | 10 | PF00082 | 0.508 |
CLV_Separin_Metazoa | 3 | 7 | PF03568 | 0.518 |
DEG_APCC_DBOX_1 | 126 | 134 | PF00400 | 0.673 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.456 |
DEG_SPOP_SBC_1 | 208 | 212 | PF00917 | 0.348 |
DOC_CKS1_1 | 399 | 404 | PF01111 | 0.518 |
DOC_CYCLIN_RxL_1 | 169 | 179 | PF00134 | 0.574 |
DOC_CYCLIN_RxL_1 | 3 | 12 | PF00134 | 0.456 |
DOC_MAPK_HePTP_8 | 430 | 442 | PF00069 | 0.514 |
DOC_MAPK_MEF2A_6 | 433 | 442 | PF00069 | 0.508 |
DOC_PP1_RVXF_1 | 233 | 239 | PF00149 | 0.443 |
DOC_PP1_RVXF_1 | 321 | 327 | PF00149 | 0.527 |
DOC_PP2B_PxIxI_1 | 435 | 441 | PF00149 | 0.497 |
DOC_PP4_FxxP_1 | 154 | 157 | PF00568 | 0.538 |
DOC_USP7_MATH_1 | 176 | 180 | PF00917 | 0.614 |
DOC_USP7_MATH_1 | 208 | 212 | PF00917 | 0.496 |
DOC_USP7_MATH_1 | 264 | 268 | PF00917 | 0.643 |
DOC_USP7_MATH_1 | 284 | 288 | PF00917 | 0.659 |
DOC_USP7_MATH_1 | 294 | 298 | PF00917 | 0.545 |
DOC_USP7_MATH_1 | 315 | 319 | PF00917 | 0.375 |
DOC_USP7_MATH_1 | 387 | 391 | PF00917 | 0.621 |
DOC_USP7_MATH_1 | 393 | 397 | PF00917 | 0.549 |
DOC_USP7_MATH_1 | 503 | 507 | PF00917 | 0.482 |
DOC_USP7_MATH_1 | 78 | 82 | PF00917 | 0.722 |
DOC_WW_Pin1_4 | 378 | 383 | PF00397 | 0.637 |
DOC_WW_Pin1_4 | 398 | 403 | PF00397 | 0.216 |
LIG_14-3-3_CanoR_1 | 107 | 113 | PF00244 | 0.710 |
LIG_14-3-3_CanoR_1 | 126 | 130 | PF00244 | 0.644 |
LIG_14-3-3_CanoR_1 | 296 | 302 | PF00244 | 0.460 |
LIG_14-3-3_CanoR_1 | 77 | 85 | PF00244 | 0.766 |
LIG_BRCT_BRCA1_1 | 416 | 420 | PF00533 | 0.497 |
LIG_deltaCOP1_diTrp_1 | 272 | 281 | PF00928 | 0.508 |
LIG_EH_1 | 434 | 438 | PF12763 | 0.454 |
LIG_FHA_1 | 210 | 216 | PF00498 | 0.458 |
LIG_FHA_1 | 320 | 326 | PF00498 | 0.507 |
LIG_FHA_1 | 339 | 345 | PF00498 | 0.405 |
LIG_FHA_1 | 421 | 427 | PF00498 | 0.473 |
LIG_FHA_1 | 472 | 478 | PF00498 | 0.380 |
LIG_FHA_1 | 510 | 516 | PF00498 | 0.511 |
LIG_FHA_2 | 112 | 118 | PF00498 | 0.700 |
LIG_FHA_2 | 364 | 370 | PF00498 | 0.517 |
LIG_FHA_2 | 457 | 463 | PF00498 | 0.470 |
LIG_GBD_Chelix_1 | 442 | 450 | PF00786 | 0.505 |
LIG_LIR_Apic_2 | 151 | 157 | PF02991 | 0.574 |
LIG_LIR_Gen_1 | 106 | 115 | PF02991 | 0.629 |
LIG_LIR_Gen_1 | 37 | 47 | PF02991 | 0.518 |
LIG_LIR_Nem_3 | 106 | 112 | PF02991 | 0.748 |
LIG_LIR_Nem_3 | 191 | 195 | PF02991 | 0.456 |
LIG_LIR_Nem_3 | 37 | 42 | PF02991 | 0.546 |
LIG_LIR_Nem_3 | 448 | 454 | PF02991 | 0.515 |
LIG_LIR_Nem_3 | 514 | 519 | PF02991 | 0.408 |
LIG_LYPXL_S_1 | 46 | 50 | PF13949 | 0.568 |
LIG_LYPXL_yS_3 | 47 | 50 | PF13949 | 0.567 |
LIG_MLH1_MIPbox_1 | 416 | 420 | PF16413 | 0.497 |
LIG_MYND_1 | 138 | 142 | PF01753 | 0.621 |
LIG_NBox_RRM_1 | 163 | 173 | PF00076 | 0.527 |
LIG_SH2_CRK | 39 | 43 | PF00017 | 0.525 |
LIG_SH2_CRK | 451 | 455 | PF00017 | 0.520 |
LIG_SH2_STAT5 | 419 | 422 | PF00017 | 0.469 |
LIG_SH3_3 | 330 | 336 | PF00018 | 0.569 |
LIG_SH3_3 | 339 | 345 | PF00018 | 0.578 |
LIG_SH3_3 | 396 | 402 | PF00018 | 0.488 |
LIG_SUMO_SIM_anti_2 | 371 | 377 | PF11976 | 0.436 |
LIG_SUMO_SIM_par_1 | 340 | 346 | PF11976 | 0.599 |
LIG_TRAF2_1 | 202 | 205 | PF00917 | 0.527 |
LIG_WRC_WIRS_1 | 504 | 509 | PF05994 | 0.522 |
MOD_CK1_1 | 111 | 117 | PF00069 | 0.693 |
MOD_CK1_1 | 297 | 303 | PF00069 | 0.533 |
MOD_CK1_1 | 381 | 387 | PF00069 | 0.597 |
MOD_CK1_1 | 444 | 450 | PF00069 | 0.526 |
MOD_CK1_1 | 70 | 76 | PF00069 | 0.718 |
MOD_CK1_1 | 81 | 87 | PF00069 | 0.745 |
MOD_CK2_1 | 363 | 369 | PF00069 | 0.499 |
MOD_CK2_1 | 456 | 462 | PF00069 | 0.470 |
MOD_CMANNOS | 238 | 241 | PF00535 | 0.486 |
MOD_Cter_Amidation | 124 | 127 | PF01082 | 0.630 |
MOD_GlcNHglycan | 135 | 138 | PF01048 | 0.628 |
MOD_GlcNHglycan | 265 | 269 | PF01048 | 0.607 |
MOD_GlcNHglycan | 285 | 289 | PF01048 | 0.546 |
MOD_GlcNHglycan | 296 | 299 | PF01048 | 0.449 |
MOD_GlcNHglycan | 35 | 39 | PF01048 | 0.494 |
MOD_GlcNHglycan | 383 | 386 | PF01048 | 0.693 |
MOD_GlcNHglycan | 389 | 392 | PF01048 | 0.671 |
MOD_GlcNHglycan | 72 | 75 | PF01048 | 0.758 |
MOD_GlcNHglycan | 80 | 83 | PF01048 | 0.767 |
MOD_GlcNHglycan | 85 | 88 | PF01048 | 0.753 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.710 |
MOD_GSK3_1 | 158 | 165 | PF00069 | 0.570 |
MOD_GSK3_1 | 315 | 322 | PF00069 | 0.527 |
MOD_GSK3_1 | 34 | 41 | PF00069 | 0.515 |
MOD_GSK3_1 | 383 | 390 | PF00069 | 0.584 |
MOD_GSK3_1 | 441 | 448 | PF00069 | 0.542 |
MOD_GSK3_1 | 66 | 73 | PF00069 | 0.653 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.708 |
MOD_N-GLC_1 | 66 | 71 | PF02516 | 0.759 |
MOD_NEK2_1 | 133 | 138 | PF00069 | 0.636 |
MOD_NEK2_1 | 148 | 153 | PF00069 | 0.416 |
MOD_NEK2_1 | 234 | 239 | PF00069 | 0.335 |
MOD_NEK2_1 | 263 | 268 | PF00069 | 0.487 |
MOD_NEK2_1 | 299 | 304 | PF00069 | 0.461 |
MOD_NEK2_1 | 363 | 368 | PF00069 | 0.494 |
MOD_NEK2_1 | 420 | 425 | PF00069 | 0.506 |
MOD_NEK2_1 | 445 | 450 | PF00069 | 0.375 |
MOD_NEK2_1 | 461 | 466 | PF00069 | 0.385 |
MOD_NEK2_1 | 93 | 98 | PF00069 | 0.767 |
MOD_NEK2_2 | 158 | 163 | PF00069 | 0.605 |
MOD_PKA_1 | 119 | 125 | PF00069 | 0.713 |
MOD_PKA_2 | 119 | 125 | PF00069 | 0.711 |
MOD_PKA_2 | 176 | 182 | PF00069 | 0.540 |
MOD_PKA_2 | 185 | 191 | PF00069 | 0.386 |
MOD_PKA_2 | 409 | 415 | PF00069 | 0.510 |
MOD_PKA_2 | 76 | 82 | PF00069 | 0.777 |
MOD_Plk_1 | 34 | 40 | PF00069 | 0.522 |
MOD_Plk_1 | 368 | 374 | PF00069 | 0.370 |
MOD_Plk_4 | 234 | 240 | PF00069 | 0.530 |
MOD_Plk_4 | 338 | 344 | PF00069 | 0.529 |
MOD_Plk_4 | 414 | 420 | PF00069 | 0.500 |
MOD_Plk_4 | 441 | 447 | PF00069 | 0.537 |
MOD_Plk_4 | 511 | 517 | PF00069 | 0.379 |
MOD_ProDKin_1 | 378 | 384 | PF00069 | 0.645 |
MOD_ProDKin_1 | 398 | 404 | PF00069 | 0.214 |
TRG_DiLeu_BaEn_1 | 473 | 478 | PF01217 | 0.401 |
TRG_DiLeu_BaLyEn_6 | 169 | 174 | PF01217 | 0.523 |
TRG_DiLeu_BaLyEn_6 | 45 | 50 | PF01217 | 0.488 |
TRG_ENDOCYTIC_2 | 196 | 199 | PF00928 | 0.496 |
TRG_ENDOCYTIC_2 | 39 | 42 | PF00928 | 0.504 |
TRG_ENDOCYTIC_2 | 451 | 454 | PF00928 | 0.518 |
TRG_ENDOCYTIC_2 | 47 | 50 | PF00928 | 0.486 |
TRG_ER_diArg_1 | 119 | 121 | PF00400 | 0.699 |
TRG_ER_diArg_1 | 171 | 173 | PF00400 | 0.598 |
TRG_ER_diArg_1 | 177 | 180 | PF00400 | 0.566 |
TRG_ER_diArg_1 | 376 | 379 | PF00400 | 0.534 |
TRG_ER_diArg_1 | 465 | 467 | PF00400 | 0.436 |
TRG_Pf-PMV_PEXEL_1 | 21 | 25 | PF00026 | 0.410 |
TRG_Pf-PMV_PEXEL_1 | 466 | 471 | PF00026 | 0.508 |
TRG_Pf-PMV_PEXEL_1 | 6 | 11 | PF00026 | 0.467 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6I3 | Leptomonas seymouri | 56% | 100% |
A0A0S4JJV4 | Bodo saltans | 26% | 100% |
A0A1X0NPX8 | Trypanosomatidae | 41% | 100% |
A0A3Q8ICS9 | Leishmania donovani | 95% | 100% |
A0A3R7KGG9 | Trypanosoma rangeli | 36% | 100% |
A4HHS4 | Leishmania braziliensis | 84% | 100% |
A4HVH0 | Leishmania infantum | 95% | 100% |
D0A6U9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 100% |
E9AP59 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
V5D9X2 | Trypanosoma cruzi | 36% | 100% |