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: 5 |
NetGPI | no | yes: 0, no: 5 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005643 | nuclear pore | 3 | 6 |
GO:0032991 | protein-containing complex | 1 | 6 |
GO:0140513 | nuclear protein-containing complex | 2 | 6 |
GO:0044613 | nuclear pore central transport channel | 3 | 1 |
Related structures:
AlphaFold database: A0A3S7X5T9
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 6 |
GO:0008104 | protein localization | 4 | 6 |
GO:0009987 | cellular process | 1 | 6 |
GO:0015031 | protein transport | 4 | 6 |
GO:0033036 | macromolecule localization | 2 | 6 |
GO:0045184 | establishment of protein localization | 3 | 6 |
GO:0051179 | localization | 1 | 6 |
GO:0051234 | establishment of localization | 2 | 6 |
GO:0051641 | cellular localization | 2 | 6 |
GO:0070727 | cellular macromolecule localization | 3 | 6 |
GO:0071702 | organic substance transport | 4 | 6 |
GO:0071705 | nitrogen compound transport | 4 | 6 |
GO:0006405 | RNA export from nucleus | 5 | 1 |
GO:0006606 | protein import into nucleus | 5 | 1 |
GO:0006886 | intracellular protein transport | 4 | 1 |
GO:0006913 | nucleocytoplasmic transport | 5 | 1 |
GO:0015931 | nucleobase-containing compound transport | 5 | 1 |
GO:0033365 | protein localization to organelle | 5 | 1 |
GO:0034504 | protein localization to nucleus | 6 | 1 |
GO:0046907 | intracellular transport | 3 | 1 |
GO:0050657 | nucleic acid transport | 6 | 1 |
GO:0050658 | RNA transport | 4 | 1 |
GO:0051168 | nuclear export | 6 | 1 |
GO:0051169 | nuclear transport | 4 | 1 |
GO:0051170 | import into nucleus | 6 | 1 |
GO:0051236 | establishment of RNA localization | 3 | 1 |
GO:0051649 | establishment of localization in cell | 3 | 1 |
GO:0072594 | establishment of protein localization to organelle | 4 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005198 | structural molecule activity | 1 | 6 |
GO:0017056 | structural constituent of nuclear pore | 2 | 6 |
GO:0005488 | binding | 1 | 1 |
GO:0005543 | phospholipid binding | 3 | 1 |
GO:0008289 | lipid binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 470 | 472 | PF00675 | 0.405 |
CLV_PCSK_KEX2_1 | 439 | 441 | PF00082 | 0.673 |
CLV_PCSK_PC1ET2_1 | 439 | 441 | PF00082 | 0.673 |
CLV_PCSK_SKI1_1 | 513 | 517 | PF00082 | 0.441 |
CLV_PCSK_SKI1_1 | 573 | 577 | PF00082 | 0.544 |
DEG_APCC_DBOX_1 | 604 | 612 | PF00400 | 0.578 |
DEG_SCF_FBW7_1 | 69 | 74 | PF00400 | 0.554 |
DEG_SPOP_SBC_1 | 381 | 385 | PF00917 | 0.586 |
DEG_SPOP_SBC_1 | 86 | 90 | PF00917 | 0.611 |
DOC_CYCLIN_yCln2_LP_2 | 177 | 183 | PF00134 | 0.668 |
DOC_MAPK_gen_1 | 471 | 479 | PF00069 | 0.405 |
DOC_MAPK_MEF2A_6 | 471 | 479 | PF00069 | 0.405 |
DOC_PP2B_LxvP_1 | 177 | 180 | PF13499 | 0.662 |
DOC_PP2B_LxvP_1 | 323 | 326 | PF13499 | 0.619 |
DOC_USP7_MATH_1 | 124 | 128 | PF00917 | 0.784 |
DOC_USP7_MATH_1 | 132 | 136 | PF00917 | 0.590 |
DOC_USP7_MATH_1 | 202 | 206 | PF00917 | 0.652 |
DOC_USP7_MATH_1 | 207 | 211 | PF00917 | 0.623 |
DOC_USP7_MATH_1 | 274 | 278 | PF00917 | 0.611 |
DOC_USP7_MATH_1 | 337 | 341 | PF00917 | 0.575 |
DOC_USP7_MATH_1 | 357 | 361 | PF00917 | 0.633 |
DOC_USP7_MATH_1 | 380 | 384 | PF00917 | 0.741 |
DOC_USP7_MATH_1 | 396 | 400 | PF00917 | 0.578 |
DOC_USP7_MATH_1 | 434 | 438 | PF00917 | 0.700 |
DOC_USP7_MATH_1 | 455 | 459 | PF00917 | 0.441 |
DOC_USP7_MATH_1 | 5 | 9 | PF00917 | 0.712 |
DOC_USP7_MATH_1 | 518 | 522 | PF00917 | 0.405 |
DOC_USP7_MATH_1 | 633 | 637 | PF00917 | 0.485 |
DOC_USP7_MATH_1 | 71 | 75 | PF00917 | 0.680 |
DOC_USP7_MATH_1 | 87 | 91 | PF00917 | 0.637 |
DOC_WW_Pin1_4 | 104 | 109 | PF00397 | 0.671 |
DOC_WW_Pin1_4 | 133 | 138 | PF00397 | 0.682 |
DOC_WW_Pin1_4 | 16 | 21 | PF00397 | 0.678 |
DOC_WW_Pin1_4 | 161 | 166 | PF00397 | 0.742 |
DOC_WW_Pin1_4 | 190 | 195 | PF00397 | 0.646 |
DOC_WW_Pin1_4 | 226 | 231 | PF00397 | 0.618 |
DOC_WW_Pin1_4 | 328 | 333 | PF00397 | 0.617 |
DOC_WW_Pin1_4 | 346 | 351 | PF00397 | 0.640 |
DOC_WW_Pin1_4 | 368 | 373 | PF00397 | 0.631 |
DOC_WW_Pin1_4 | 414 | 419 | PF00397 | 0.716 |
DOC_WW_Pin1_4 | 425 | 430 | PF00397 | 0.594 |
DOC_WW_Pin1_4 | 453 | 458 | PF00397 | 0.405 |
DOC_WW_Pin1_4 | 65 | 70 | PF00397 | 0.657 |
LIG_14-3-3_CanoR_1 | 532 | 540 | PF00244 | 0.356 |
LIG_14-3-3_CanoR_1 | 573 | 578 | PF00244 | 0.543 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.657 |
LIG_BRCT_BRCA1_1 | 134 | 138 | PF00533 | 0.682 |
LIG_BRCT_BRCA1_1 | 195 | 199 | PF00533 | 0.601 |
LIG_BRCT_BRCA1_1 | 276 | 280 | PF00533 | 0.672 |
LIG_BRCT_BRCA1_1 | 339 | 343 | PF00533 | 0.561 |
LIG_BRCT_BRCA1_1 | 384 | 388 | PF00533 | 0.647 |
LIG_BRCT_BRCA1_1 | 457 | 461 | PF00533 | 0.405 |
LIG_FHA_1 | 201 | 207 | PF00498 | 0.601 |
LIG_FHA_1 | 268 | 274 | PF00498 | 0.761 |
LIG_FHA_1 | 425 | 431 | PF00498 | 0.633 |
LIG_FHA_2 | 523 | 529 | PF00498 | 0.405 |
LIG_GBD_Chelix_1 | 634 | 642 | PF00786 | 0.495 |
LIG_LIR_Gen_1 | 576 | 584 | PF02991 | 0.453 |
LIG_LIR_Nem_3 | 164 | 169 | PF02991 | 0.644 |
LIG_LIR_Nem_3 | 216 | 221 | PF02991 | 0.544 |
LIG_LIR_Nem_3 | 576 | 580 | PF02991 | 0.454 |
LIG_LIR_Nem_3 | 75 | 81 | PF02991 | 0.645 |
LIG_NRBOX | 641 | 647 | PF00104 | 0.517 |
LIG_PCNA_PIPBox_1 | 533 | 542 | PF02747 | 0.405 |
LIG_PCNA_yPIPBox_3 | 530 | 540 | PF02747 | 0.405 |
LIG_SH2_CRK | 577 | 581 | PF00017 | 0.454 |
LIG_SH2_GRB2like | 577 | 580 | PF00017 | 0.515 |
LIG_SH2_SRC | 577 | 580 | PF00017 | 0.515 |
LIG_SH2_STAP1 | 577 | 581 | PF00017 | 0.514 |
LIG_SH2_STAT3 | 550 | 553 | PF00017 | 0.405 |
LIG_SH2_STAT5 | 539 | 542 | PF00017 | 0.405 |
LIG_SH3_3 | 141 | 147 | PF00018 | 0.642 |
LIG_SH3_3 | 31 | 37 | PF00018 | 0.615 |
LIG_SH3_3 | 442 | 448 | PF00018 | 0.572 |
LIG_SH3_3 | 98 | 104 | PF00018 | 0.654 |
LIG_SUMO_SIM_par_1 | 231 | 236 | PF11976 | 0.635 |
LIG_TRAF2_1 | 457 | 460 | PF00917 | 0.417 |
LIG_TRAF2_2 | 457 | 462 | PF00917 | 0.356 |
LIG_TYR_ITIM | 575 | 580 | PF00017 | 0.431 |
LIG_WW_2 | 445 | 448 | PF00397 | 0.572 |
MOD_CK1_1 | 106 | 112 | PF00069 | 0.594 |
MOD_CK1_1 | 193 | 199 | PF00069 | 0.612 |
MOD_CK1_1 | 205 | 211 | PF00069 | 0.615 |
MOD_CK1_1 | 254 | 260 | PF00069 | 0.644 |
MOD_CK1_1 | 284 | 290 | PF00069 | 0.550 |
MOD_CK1_1 | 318 | 324 | PF00069 | 0.641 |
MOD_CK1_1 | 400 | 406 | PF00069 | 0.614 |
MOD_CK1_1 | 412 | 418 | PF00069 | 0.657 |
MOD_CK1_1 | 53 | 59 | PF00069 | 0.724 |
MOD_CK1_1 | 95 | 101 | PF00069 | 0.707 |
MOD_CK2_1 | 522 | 528 | PF00069 | 0.405 |
MOD_CK2_1 | 601 | 607 | PF00069 | 0.582 |
MOD_CK2_1 | 609 | 615 | PF00069 | 0.491 |
MOD_CK2_1 | 633 | 639 | PF00069 | 0.489 |
MOD_GlcNHglycan | 111 | 114 | PF01048 | 0.553 |
MOD_GlcNHglycan | 126 | 129 | PF01048 | 0.622 |
MOD_GlcNHglycan | 148 | 151 | PF01048 | 0.699 |
MOD_GlcNHglycan | 159 | 162 | PF01048 | 0.581 |
MOD_GlcNHglycan | 166 | 169 | PF01048 | 0.516 |
MOD_GlcNHglycan | 190 | 193 | PF01048 | 0.641 |
MOD_GlcNHglycan | 195 | 198 | PF01048 | 0.611 |
MOD_GlcNHglycan | 207 | 210 | PF01048 | 0.556 |
MOD_GlcNHglycan | 237 | 240 | PF01048 | 0.640 |
MOD_GlcNHglycan | 253 | 256 | PF01048 | 0.647 |
MOD_GlcNHglycan | 259 | 262 | PF01048 | 0.652 |
MOD_GlcNHglycan | 270 | 273 | PF01048 | 0.608 |
MOD_GlcNHglycan | 276 | 279 | PF01048 | 0.538 |
MOD_GlcNHglycan | 282 | 286 | PF01048 | 0.559 |
MOD_GlcNHglycan | 290 | 293 | PF01048 | 0.476 |
MOD_GlcNHglycan | 317 | 320 | PF01048 | 0.744 |
MOD_GlcNHglycan | 339 | 342 | PF01048 | 0.571 |
MOD_GlcNHglycan | 359 | 362 | PF01048 | 0.582 |
MOD_GlcNHglycan | 368 | 371 | PF01048 | 0.627 |
MOD_GlcNHglycan | 384 | 387 | PF01048 | 0.636 |
MOD_GlcNHglycan | 411 | 414 | PF01048 | 0.752 |
MOD_GlcNHglycan | 436 | 439 | PF01048 | 0.657 |
MOD_GlcNHglycan | 48 | 51 | PF01048 | 0.746 |
MOD_GlcNHglycan | 52 | 55 | PF01048 | 0.701 |
MOD_GlcNHglycan | 520 | 523 | PF01048 | 0.405 |
MOD_GlcNHglycan | 562 | 565 | PF01048 | 0.512 |
MOD_GlcNHglycan | 58 | 61 | PF01048 | 0.627 |
MOD_GlcNHglycan | 631 | 634 | PF01048 | 0.490 |
MOD_GlcNHglycan | 635 | 638 | PF01048 | 0.442 |
MOD_GlcNHglycan | 94 | 97 | PF01048 | 0.724 |
MOD_GSK3_1 | 132 | 139 | PF00069 | 0.613 |
MOD_GSK3_1 | 157 | 164 | PF00069 | 0.679 |
MOD_GSK3_1 | 184 | 191 | PF00069 | 0.726 |
MOD_GSK3_1 | 284 | 291 | PF00069 | 0.563 |
MOD_GSK3_1 | 303 | 310 | PF00069 | 0.631 |
MOD_GSK3_1 | 324 | 331 | PF00069 | 0.557 |
MOD_GSK3_1 | 337 | 344 | PF00069 | 0.560 |
MOD_GSK3_1 | 382 | 389 | PF00069 | 0.718 |
MOD_GSK3_1 | 396 | 403 | PF00069 | 0.677 |
MOD_GSK3_1 | 420 | 427 | PF00069 | 0.639 |
MOD_GSK3_1 | 428 | 435 | PF00069 | 0.670 |
MOD_GSK3_1 | 446 | 453 | PF00069 | 0.548 |
MOD_GSK3_1 | 46 | 53 | PF00069 | 0.764 |
MOD_GSK3_1 | 514 | 521 | PF00069 | 0.365 |
MOD_GSK3_1 | 629 | 636 | PF00069 | 0.498 |
MOD_GSK3_1 | 65 | 72 | PF00069 | 0.552 |
MOD_GSK3_1 | 85 | 92 | PF00069 | 0.538 |
MOD_N-GLC_1 | 328 | 333 | PF02516 | 0.617 |
MOD_N-GLC_1 | 601 | 606 | PF02516 | 0.549 |
MOD_NEK2_1 | 111 | 116 | PF00069 | 0.758 |
MOD_NEK2_1 | 154 | 159 | PF00069 | 0.721 |
MOD_NEK2_1 | 365 | 370 | PF00069 | 0.676 |
MOD_NEK2_1 | 390 | 395 | PF00069 | 0.694 |
MOD_NEK2_1 | 6 | 11 | PF00069 | 0.666 |
MOD_PIKK_1 | 455 | 461 | PF00454 | 0.429 |
MOD_PKA_2 | 531 | 537 | PF00069 | 0.359 |
MOD_Plk_1 | 475 | 481 | PF00069 | 0.356 |
MOD_Plk_1 | 522 | 528 | PF00069 | 0.405 |
MOD_Plk_2-3 | 565 | 571 | PF00069 | 0.450 |
MOD_Plk_4 | 507 | 513 | PF00069 | 0.441 |
MOD_ProDKin_1 | 104 | 110 | PF00069 | 0.666 |
MOD_ProDKin_1 | 133 | 139 | PF00069 | 0.683 |
MOD_ProDKin_1 | 16 | 22 | PF00069 | 0.677 |
MOD_ProDKin_1 | 161 | 167 | PF00069 | 0.743 |
MOD_ProDKin_1 | 190 | 196 | PF00069 | 0.646 |
MOD_ProDKin_1 | 226 | 232 | PF00069 | 0.615 |
MOD_ProDKin_1 | 328 | 334 | PF00069 | 0.613 |
MOD_ProDKin_1 | 346 | 352 | PF00069 | 0.637 |
MOD_ProDKin_1 | 368 | 374 | PF00069 | 0.630 |
MOD_ProDKin_1 | 414 | 420 | PF00069 | 0.719 |
MOD_ProDKin_1 | 425 | 431 | PF00069 | 0.594 |
MOD_ProDKin_1 | 453 | 459 | PF00069 | 0.405 |
MOD_ProDKin_1 | 65 | 71 | PF00069 | 0.653 |
MOD_SUMO_rev_2 | 456 | 466 | PF00179 | 0.356 |
MOD_SUMO_rev_2 | 538 | 547 | PF00179 | 0.405 |
MOD_SUMO_rev_2 | 585 | 594 | PF00179 | 0.516 |
TRG_DiLeu_BaEn_1 | 641 | 646 | PF01217 | 0.514 |
TRG_DiLeu_BaLyEn_6 | 616 | 621 | PF01217 | 0.514 |
TRG_DiLeu_LyEn_5 | 641 | 646 | PF01217 | 0.514 |
TRG_ENDOCYTIC_2 | 577 | 580 | PF00928 | 0.455 |
TRG_Pf-PMV_PEXEL_1 | 471 | 476 | PF00026 | 0.405 |
TRG_Pf-PMV_PEXEL_1 | 503 | 507 | PF00026 | 0.405 |