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: A0A3Q8ICS9
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_C14_Caspase3-7 | 114 | 118 | PF00656 | 0.754 |
CLV_NRD_NRD_1 | 120 | 122 | PF00675 | 0.696 |
CLV_NRD_NRD_1 | 126 | 128 | PF00675 | 0.662 |
CLV_NRD_NRD_1 | 171 | 173 | PF00675 | 0.603 |
CLV_NRD_NRD_1 | 177 | 179 | PF00675 | 0.571 |
CLV_NRD_NRD_1 | 466 | 468 | PF00675 | 0.435 |
CLV_PCSK_KEX2_1 | 119 | 121 | PF00082 | 0.690 |
CLV_PCSK_KEX2_1 | 126 | 128 | PF00082 | 0.672 |
CLV_PCSK_KEX2_1 | 171 | 173 | PF00082 | 0.600 |
CLV_PCSK_KEX2_1 | 177 | 179 | PF00082 | 0.573 |
CLV_PCSK_KEX2_1 | 465 | 467 | PF00082 | 0.451 |
CLV_PCSK_SKI1_1 | 160 | 164 | PF00082 | 0.537 |
CLV_PCSK_SKI1_1 | 171 | 175 | PF00082 | 0.498 |
CLV_PCSK_SKI1_1 | 246 | 250 | PF00082 | 0.392 |
CLV_PCSK_SKI1_1 | 289 | 293 | PF00082 | 0.489 |
CLV_PCSK_SKI1_1 | 323 | 327 | PF00082 | 0.519 |
CLV_PCSK_SKI1_1 | 6 | 10 | PF00082 | 0.598 |
CLV_Separin_Metazoa | 3 | 7 | PF03568 | 0.578 |
DEG_APCC_DBOX_1 | 126 | 134 | PF00400 | 0.685 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.507 |
DEG_SPOP_SBC_1 | 92 | 96 | PF00917 | 0.669 |
DOC_CKS1_1 | 399 | 404 | PF01111 | 0.519 |
DOC_CYCLIN_RxL_1 | 169 | 179 | PF00134 | 0.579 |
DOC_CYCLIN_RxL_1 | 3 | 12 | PF00134 | 0.530 |
DOC_MAPK_HePTP_8 | 430 | 442 | PF00069 | 0.514 |
DOC_MAPK_MEF2A_6 | 433 | 442 | PF00069 | 0.507 |
DOC_PP1_RVXF_1 | 233 | 239 | PF00149 | 0.451 |
DOC_PP1_RVXF_1 | 321 | 327 | PF00149 | 0.524 |
DOC_PP2B_PxIxI_1 | 435 | 441 | PF00149 | 0.497 |
DOC_PP4_FxxP_1 | 154 | 157 | PF00568 | 0.523 |
DOC_USP7_MATH_1 | 176 | 180 | PF00917 | 0.626 |
DOC_USP7_MATH_1 | 208 | 212 | PF00917 | 0.498 |
DOC_USP7_MATH_1 | 264 | 268 | PF00917 | 0.635 |
DOC_USP7_MATH_1 | 284 | 288 | PF00917 | 0.617 |
DOC_USP7_MATH_1 | 315 | 319 | PF00917 | 0.373 |
DOC_USP7_MATH_1 | 387 | 391 | PF00917 | 0.609 |
DOC_USP7_MATH_1 | 393 | 397 | PF00917 | 0.511 |
DOC_USP7_MATH_1 | 503 | 507 | PF00917 | 0.542 |
DOC_WW_Pin1_4 | 378 | 383 | PF00397 | 0.626 |
DOC_WW_Pin1_4 | 398 | 403 | PF00397 | 0.218 |
LIG_14-3-3_CanoR_1 | 126 | 130 | PF00244 | 0.639 |
LIG_14-3-3_CanoR_1 | 296 | 302 | PF00244 | 0.462 |
LIG_14-3-3_CanoR_1 | 77 | 86 | PF00244 | 0.773 |
LIG_BRCT_BRCA1_1 | 416 | 420 | PF00533 | 0.501 |
LIG_EH_1 | 434 | 438 | PF12763 | 0.452 |
LIG_FHA_1 | 210 | 216 | PF00498 | 0.460 |
LIG_FHA_1 | 320 | 326 | PF00498 | 0.504 |
LIG_FHA_1 | 339 | 345 | PF00498 | 0.333 |
LIG_FHA_1 | 421 | 427 | PF00498 | 0.494 |
LIG_FHA_1 | 472 | 478 | PF00498 | 0.403 |
LIG_FHA_1 | 510 | 516 | PF00498 | 0.539 |
LIG_FHA_2 | 112 | 118 | PF00498 | 0.707 |
LIG_FHA_2 | 364 | 370 | PF00498 | 0.517 |
LIG_FHA_2 | 457 | 463 | PF00498 | 0.479 |
LIG_GBD_Chelix_1 | 442 | 450 | PF00786 | 0.512 |
LIG_LIR_Apic_2 | 153 | 157 | PF02991 | 0.571 |
LIG_LIR_Gen_1 | 195 | 203 | PF02991 | 0.390 |
LIG_LIR_Gen_1 | 37 | 47 | PF02991 | 0.610 |
LIG_LIR_Nem_3 | 106 | 112 | PF02991 | 0.755 |
LIG_LIR_Nem_3 | 195 | 201 | PF02991 | 0.480 |
LIG_LIR_Nem_3 | 35 | 39 | PF02991 | 0.635 |
LIG_LIR_Nem_3 | 448 | 454 | PF02991 | 0.533 |
LIG_LIR_Nem_3 | 59 | 63 | PF02991 | 0.658 |
LIG_LYPXL_S_1 | 46 | 50 | PF13949 | 0.620 |
LIG_LYPXL_yS_3 | 47 | 50 | PF13949 | 0.616 |
LIG_MLH1_MIPbox_1 | 416 | 420 | PF16413 | 0.501 |
LIG_MYND_1 | 138 | 142 | PF01753 | 0.613 |
LIG_NBox_RRM_1 | 163 | 173 | PF00076 | 0.513 |
LIG_SH2_CRK | 39 | 43 | PF00017 | 0.627 |
LIG_SH2_CRK | 451 | 455 | PF00017 | 0.543 |
LIG_SH2_STAT5 | 419 | 422 | PF00017 | 0.444 |
LIG_SH3_3 | 330 | 336 | PF00018 | 0.544 |
LIG_SH3_3 | 339 | 345 | PF00018 | 0.530 |
LIG_SH3_3 | 396 | 402 | PF00018 | 0.491 |
LIG_SUMO_SIM_anti_2 | 372 | 377 | PF11976 | 0.432 |
LIG_SUMO_SIM_par_1 | 340 | 346 | PF11976 | 0.561 |
LIG_TRAF2_1 | 202 | 205 | PF00917 | 0.536 |
LIG_WRC_WIRS_1 | 504 | 509 | PF05994 | 0.554 |
MOD_CK1_1 | 111 | 117 | PF00069 | 0.700 |
MOD_CK1_1 | 266 | 272 | PF00069 | 0.664 |
MOD_CK1_1 | 297 | 303 | PF00069 | 0.547 |
MOD_CK1_1 | 381 | 387 | PF00069 | 0.577 |
MOD_CK1_1 | 444 | 450 | PF00069 | 0.535 |
MOD_CK1_1 | 70 | 76 | PF00069 | 0.729 |
MOD_CK1_1 | 81 | 87 | PF00069 | 0.750 |
MOD_CK2_1 | 363 | 369 | PF00069 | 0.513 |
MOD_CK2_1 | 456 | 462 | PF00069 | 0.478 |
MOD_CMANNOS | 238 | 241 | PF00535 | 0.460 |
MOD_Cter_Amidation | 124 | 127 | PF01082 | 0.628 |
MOD_GlcNHglycan | 135 | 138 | PF01048 | 0.627 |
MOD_GlcNHglycan | 265 | 269 | PF01048 | 0.598 |
MOD_GlcNHglycan | 275 | 278 | PF01048 | 0.525 |
MOD_GlcNHglycan | 285 | 289 | PF01048 | 0.529 |
MOD_GlcNHglycan | 296 | 299 | PF01048 | 0.453 |
MOD_GlcNHglycan | 35 | 39 | PF01048 | 0.584 |
MOD_GlcNHglycan | 383 | 386 | PF01048 | 0.683 |
MOD_GlcNHglycan | 72 | 75 | PF01048 | 0.766 |
MOD_GlcNHglycan | 80 | 83 | PF01048 | 0.779 |
MOD_GSK3_1 | 158 | 165 | PF00069 | 0.554 |
MOD_GSK3_1 | 188 | 195 | PF00069 | 0.521 |
MOD_GSK3_1 | 315 | 322 | PF00069 | 0.520 |
MOD_GSK3_1 | 34 | 41 | PF00069 | 0.606 |
MOD_GSK3_1 | 383 | 390 | PF00069 | 0.560 |
MOD_GSK3_1 | 441 | 448 | PF00069 | 0.537 |
MOD_GSK3_1 | 66 | 73 | PF00069 | 0.662 |
MOD_GSK3_1 | 76 | 83 | PF00069 | 0.723 |
MOD_N-GLC_1 | 66 | 71 | PF02516 | 0.768 |
MOD_NEK2_1 | 133 | 138 | PF00069 | 0.634 |
MOD_NEK2_1 | 263 | 268 | PF00069 | 0.484 |
MOD_NEK2_1 | 299 | 304 | PF00069 | 0.459 |
MOD_NEK2_1 | 363 | 368 | PF00069 | 0.502 |
MOD_NEK2_1 | 420 | 425 | PF00069 | 0.467 |
MOD_NEK2_1 | 445 | 450 | PF00069 | 0.384 |
MOD_NEK2_1 | 461 | 466 | PF00069 | 0.407 |
MOD_NEK2_1 | 93 | 98 | PF00069 | 0.763 |
MOD_NEK2_2 | 158 | 163 | PF00069 | 0.588 |
MOD_PKA_1 | 119 | 125 | PF00069 | 0.717 |
MOD_PKA_2 | 119 | 125 | PF00069 | 0.714 |
MOD_PKA_2 | 176 | 182 | PF00069 | 0.548 |
MOD_PKA_2 | 185 | 191 | PF00069 | 0.400 |
MOD_PKA_2 | 409 | 415 | PF00069 | 0.511 |
MOD_PKA_2 | 76 | 82 | PF00069 | 0.792 |
MOD_Plk_1 | 34 | 40 | PF00069 | 0.613 |
MOD_Plk_4 | 192 | 198 | PF00069 | 0.405 |
MOD_Plk_4 | 234 | 240 | PF00069 | 0.542 |
MOD_Plk_4 | 338 | 344 | PF00069 | 0.535 |
MOD_Plk_4 | 414 | 420 | PF00069 | 0.489 |
MOD_Plk_4 | 441 | 447 | PF00069 | 0.542 |
MOD_Plk_4 | 511 | 517 | PF00069 | 0.419 |
MOD_ProDKin_1 | 378 | 384 | PF00069 | 0.633 |
MOD_ProDKin_1 | 398 | 404 | PF00069 | 0.217 |
TRG_DiLeu_BaEn_1 | 473 | 478 | PF01217 | 0.426 |
TRG_DiLeu_BaLyEn_6 | 169 | 174 | PF01217 | 0.504 |
TRG_DiLeu_BaLyEn_6 | 45 | 50 | PF01217 | 0.550 |
TRG_ENDOCYTIC_2 | 196 | 199 | PF00928 | 0.510 |
TRG_ENDOCYTIC_2 | 39 | 42 | PF00928 | 0.600 |
TRG_ENDOCYTIC_2 | 451 | 454 | PF00928 | 0.542 |
TRG_ENDOCYTIC_2 | 47 | 50 | PF00928 | 0.535 |
TRG_ER_diArg_1 | 119 | 121 | PF00400 | 0.707 |
TRG_ER_diArg_1 | 171 | 173 | PF00400 | 0.603 |
TRG_ER_diArg_1 | 177 | 180 | PF00400 | 0.577 |
TRG_ER_diArg_1 | 293 | 296 | PF00400 | 0.337 |
TRG_ER_diArg_1 | 376 | 379 | PF00400 | 0.528 |
TRG_ER_diArg_1 | 465 | 467 | PF00400 | 0.469 |
TRG_Pf-PMV_PEXEL_1 | 21 | 25 | PF00026 | 0.529 |
TRG_Pf-PMV_PEXEL_1 | 466 | 471 | PF00026 | 0.532 |
TRG_Pf-PMV_PEXEL_1 | 6 | 11 | PF00026 | 0.539 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6I3 | Leptomonas seymouri | 55% | 100% |
A0A0S4JJV4 | Bodo saltans | 26% | 100% |
A0A1X0NPX8 | Trypanosomatidae | 42% | 100% |
A0A3R7KGG9 | Trypanosoma rangeli | 37% | 100% |
A4HHS4 | Leishmania braziliensis | 83% | 100% |
A4HVH0 | Leishmania infantum | 100% | 100% |
D0A6U9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 100% |
E9AP59 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
Q4QGC9 | Leishmania major | 95% | 100% |
V5D9X2 | Trypanosoma cruzi | 37% | 100% |