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:0044613 | nuclear pore central transport channel | 3 | 2 |
GO:0140513 | nuclear protein-containing complex | 2 | 6 |
Related structures:
AlphaFold database: Q4Q540
Term | Name | Level | Count |
---|---|---|---|
GO:0006405 | RNA export from nucleus | 5 | 2 |
GO:0006606 | protein import into nucleus | 5 | 2 |
GO:0006810 | transport | 3 | 6 |
GO:0006886 | intracellular protein transport | 4 | 2 |
GO:0006913 | nucleocytoplasmic transport | 5 | 2 |
GO:0008104 | protein localization | 4 | 6 |
GO:0009987 | cellular process | 1 | 6 |
GO:0015031 | protein transport | 4 | 6 |
GO:0015931 | nucleobase-containing compound transport | 5 | 2 |
GO:0033036 | macromolecule localization | 2 | 6 |
GO:0033365 | protein localization to organelle | 5 | 2 |
GO:0034504 | protein localization to nucleus | 6 | 2 |
GO:0045184 | establishment of protein localization | 3 | 6 |
GO:0046907 | intracellular transport | 3 | 2 |
GO:0050657 | nucleic acid transport | 6 | 2 |
GO:0050658 | RNA transport | 4 | 2 |
GO:0051168 | nuclear export | 6 | 2 |
GO:0051169 | nuclear transport | 4 | 2 |
GO:0051170 | import into nucleus | 6 | 2 |
GO:0051179 | localization | 1 | 6 |
GO:0051234 | establishment of localization | 2 | 6 |
GO:0051236 | establishment of RNA localization | 3 | 2 |
GO:0051641 | cellular localization | 2 | 6 |
GO:0051649 | establishment of localization in cell | 3 | 2 |
GO:0070727 | cellular macromolecule localization | 3 | 6 |
GO:0071702 | organic substance transport | 4 | 6 |
GO:0071705 | nitrogen compound transport | 4 | 6 |
GO:0072594 | establishment of protein localization to organelle | 4 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005198 | structural molecule activity | 1 | 6 |
GO:0005488 | binding | 1 | 2 |
GO:0005543 | phospholipid binding | 3 | 2 |
GO:0008289 | lipid binding | 2 | 2 |
GO:0017056 | structural constituent of nuclear pore | 2 | 6 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 459 | 461 | PF00675 | 0.530 |
CLV_PCSK_KEX2_1 | 428 | 430 | PF00082 | 0.651 |
CLV_PCSK_PC1ET2_1 | 428 | 430 | PF00082 | 0.651 |
CLV_PCSK_SKI1_1 | 502 | 506 | PF00082 | 0.471 |
CLV_PCSK_SKI1_1 | 567 | 571 | PF00082 | 0.494 |
DEG_APCC_DBOX_1 | 598 | 606 | PF00400 | 0.702 |
DEG_SPOP_SBC_1 | 84 | 88 | PF00917 | 0.720 |
DOC_CYCLIN_yCln2_LP_2 | 171 | 177 | PF00134 | 0.766 |
DOC_MAPK_gen_1 | 460 | 468 | PF00069 | 0.530 |
DOC_MAPK_MEF2A_6 | 460 | 468 | PF00069 | 0.530 |
DOC_PP2B_LxvP_1 | 171 | 174 | PF13499 | 0.760 |
DOC_PP2B_LxvP_1 | 313 | 316 | PF13499 | 0.687 |
DOC_USP7_MATH_1 | 118 | 122 | PF00917 | 0.757 |
DOC_USP7_MATH_1 | 126 | 130 | PF00917 | 0.626 |
DOC_USP7_MATH_1 | 133 | 137 | PF00917 | 0.527 |
DOC_USP7_MATH_1 | 196 | 200 | PF00917 | 0.753 |
DOC_USP7_MATH_1 | 201 | 205 | PF00917 | 0.700 |
DOC_USP7_MATH_1 | 262 | 266 | PF00917 | 0.688 |
DOC_USP7_MATH_1 | 346 | 350 | PF00917 | 0.569 |
DOC_USP7_MATH_1 | 369 | 373 | PF00917 | 0.625 |
DOC_USP7_MATH_1 | 385 | 389 | PF00917 | 0.643 |
DOC_USP7_MATH_1 | 444 | 448 | PF00917 | 0.530 |
DOC_USP7_MATH_1 | 5 | 9 | PF00917 | 0.787 |
DOC_USP7_MATH_1 | 507 | 511 | PF00917 | 0.530 |
DOC_USP7_MATH_1 | 627 | 631 | PF00917 | 0.607 |
DOC_USP7_MATH_1 | 69 | 73 | PF00917 | 0.764 |
DOC_USP7_MATH_1 | 85 | 89 | PF00917 | 0.600 |
DOC_USP7_MATH_1 | 90 | 94 | PF00917 | 0.734 |
DOC_WW_Pin1_4 | 102 | 107 | PF00397 | 0.750 |
DOC_WW_Pin1_4 | 127 | 132 | PF00397 | 0.795 |
DOC_WW_Pin1_4 | 155 | 160 | PF00397 | 0.695 |
DOC_WW_Pin1_4 | 16 | 21 | PF00397 | 0.802 |
DOC_WW_Pin1_4 | 184 | 189 | PF00397 | 0.719 |
DOC_WW_Pin1_4 | 318 | 323 | PF00397 | 0.689 |
DOC_WW_Pin1_4 | 337 | 342 | PF00397 | 0.471 |
DOC_WW_Pin1_4 | 357 | 362 | PF00397 | 0.635 |
DOC_WW_Pin1_4 | 403 | 408 | PF00397 | 0.669 |
DOC_WW_Pin1_4 | 442 | 447 | PF00397 | 0.530 |
DOC_WW_Pin1_4 | 65 | 70 | PF00397 | 0.739 |
LIG_14-3-3_CanoR_1 | 521 | 529 | PF00244 | 0.452 |
LIG_14-3-3_CanoR_1 | 567 | 572 | PF00244 | 0.507 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.785 |
LIG_BRCT_BRCA1_1 | 128 | 132 | PF00533 | 0.793 |
LIG_BRCT_BRCA1_1 | 373 | 377 | PF00533 | 0.723 |
LIG_BRCT_BRCA1_1 | 446 | 450 | PF00533 | 0.530 |
LIG_FHA_1 | 195 | 201 | PF00498 | 0.671 |
LIG_FHA_1 | 262 | 268 | PF00498 | 0.762 |
LIG_FHA_1 | 294 | 300 | PF00498 | 0.559 |
LIG_FHA_1 | 418 | 424 | PF00498 | 0.668 |
LIG_FHA_1 | 609 | 615 | PF00498 | 0.516 |
LIG_FHA_2 | 512 | 518 | PF00498 | 0.488 |
LIG_GBD_Chelix_1 | 628 | 636 | PF00786 | 0.621 |
LIG_LIR_Nem_3 | 158 | 163 | PF02991 | 0.731 |
LIG_LIR_Nem_3 | 73 | 79 | PF02991 | 0.732 |
LIG_NRBOX | 635 | 641 | PF00104 | 0.644 |
LIG_PCNA_PIPBox_1 | 522 | 531 | PF02747 | 0.530 |
LIG_PCNA_yPIPBox_3 | 519 | 529 | PF02747 | 0.476 |
LIG_PTAP_UEV_1 | 33 | 38 | PF05743 | 0.550 |
LIG_SH2_GRB2like | 571 | 574 | PF00017 | 0.649 |
LIG_SH2_SRC | 571 | 574 | PF00017 | 0.649 |
LIG_SH2_STAP1 | 571 | 575 | PF00017 | 0.649 |
LIG_SH2_STAT3 | 539 | 542 | PF00017 | 0.530 |
LIG_SH2_STAT5 | 528 | 531 | PF00017 | 0.369 |
LIG_SH3_3 | 135 | 141 | PF00018 | 0.718 |
LIG_SH3_3 | 31 | 37 | PF00018 | 0.687 |
LIG_SH3_3 | 96 | 102 | PF00018 | 0.731 |
LIG_SUMO_SIM_par_1 | 225 | 230 | PF11976 | 0.712 |
LIG_TRAF2_1 | 446 | 449 | PF00917 | 0.530 |
LIG_TRAF2_2 | 446 | 451 | PF00917 | 0.452 |
MOD_CK1_1 | 104 | 110 | PF00069 | 0.628 |
MOD_CK1_1 | 199 | 205 | PF00069 | 0.688 |
MOD_CK1_1 | 248 | 254 | PF00069 | 0.736 |
MOD_CK1_1 | 308 | 314 | PF00069 | 0.724 |
MOD_CK1_1 | 401 | 407 | PF00069 | 0.713 |
MOD_CK1_1 | 415 | 421 | PF00069 | 0.586 |
MOD_CK1_1 | 49 | 55 | PF00069 | 0.698 |
MOD_CK1_1 | 59 | 65 | PF00069 | 0.706 |
MOD_CK1_1 | 93 | 99 | PF00069 | 0.815 |
MOD_CK2_1 | 511 | 517 | PF00069 | 0.530 |
MOD_CK2_1 | 595 | 601 | PF00069 | 0.559 |
MOD_CK2_1 | 603 | 609 | PF00069 | 0.624 |
MOD_CK2_1 | 627 | 633 | PF00069 | 0.497 |
MOD_GlcNHglycan | 111 | 114 | PF01048 | 0.522 |
MOD_GlcNHglycan | 120 | 123 | PF01048 | 0.650 |
MOD_GlcNHglycan | 142 | 145 | PF01048 | 0.814 |
MOD_GlcNHglycan | 153 | 156 | PF01048 | 0.638 |
MOD_GlcNHglycan | 201 | 204 | PF01048 | 0.596 |
MOD_GlcNHglycan | 231 | 234 | PF01048 | 0.734 |
MOD_GlcNHglycan | 247 | 250 | PF01048 | 0.616 |
MOD_GlcNHglycan | 253 | 256 | PF01048 | 0.686 |
MOD_GlcNHglycan | 264 | 267 | PF01048 | 0.574 |
MOD_GlcNHglycan | 276 | 280 | PF01048 | 0.608 |
MOD_GlcNHglycan | 307 | 310 | PF01048 | 0.721 |
MOD_GlcNHglycan | 348 | 351 | PF01048 | 0.594 |
MOD_GlcNHglycan | 357 | 360 | PF01048 | 0.673 |
MOD_GlcNHglycan | 373 | 376 | PF01048 | 0.530 |
MOD_GlcNHglycan | 400 | 403 | PF01048 | 0.833 |
MOD_GlcNHglycan | 414 | 417 | PF01048 | 0.537 |
MOD_GlcNHglycan | 425 | 428 | PF01048 | 0.653 |
MOD_GlcNHglycan | 436 | 439 | PF01048 | 0.594 |
MOD_GlcNHglycan | 48 | 51 | PF01048 | 0.783 |
MOD_GlcNHglycan | 509 | 512 | PF01048 | 0.379 |
MOD_GlcNHglycan | 52 | 55 | PF01048 | 0.714 |
MOD_GlcNHglycan | 58 | 61 | PF01048 | 0.640 |
MOD_GlcNHglycan | 625 | 628 | PF01048 | 0.617 |
MOD_GlcNHglycan | 629 | 632 | PF01048 | 0.540 |
MOD_GlcNHglycan | 79 | 82 | PF01048 | 0.667 |
MOD_GlcNHglycan | 92 | 95 | PF01048 | 0.729 |
MOD_GSK3_1 | 151 | 158 | PF00069 | 0.792 |
MOD_GSK3_1 | 178 | 185 | PF00069 | 0.716 |
MOD_GSK3_1 | 247 | 254 | PF00069 | 0.581 |
MOD_GSK3_1 | 293 | 300 | PF00069 | 0.606 |
MOD_GSK3_1 | 371 | 378 | PF00069 | 0.765 |
MOD_GSK3_1 | 386 | 393 | PF00069 | 0.592 |
MOD_GSK3_1 | 46 | 53 | PF00069 | 0.733 |
MOD_GSK3_1 | 503 | 510 | PF00069 | 0.360 |
MOD_GSK3_1 | 623 | 630 | PF00069 | 0.496 |
MOD_GSK3_1 | 65 | 72 | PF00069 | 0.537 |
MOD_GSK3_1 | 90 | 97 | PF00069 | 0.786 |
MOD_N-GLC_1 | 318 | 323 | PF02516 | 0.689 |
MOD_N-GLC_1 | 595 | 600 | PF02516 | 0.681 |
MOD_NEK2_1 | 109 | 114 | PF00069 | 0.840 |
MOD_NEK2_1 | 354 | 359 | PF00069 | 0.769 |
MOD_NEK2_1 | 379 | 384 | PF00069 | 0.799 |
MOD_NEK2_1 | 6 | 11 | PF00069 | 0.785 |
MOD_PIKK_1 | 444 | 450 | PF00454 | 0.530 |
MOD_PKA_2 | 520 | 526 | PF00069 | 0.452 |
MOD_Plk_1 | 464 | 470 | PF00069 | 0.452 |
MOD_Plk_1 | 511 | 517 | PF00069 | 0.379 |
MOD_Plk_4 | 496 | 502 | PF00069 | 0.530 |
MOD_ProDKin_1 | 102 | 108 | PF00069 | 0.743 |
MOD_ProDKin_1 | 127 | 133 | PF00069 | 0.796 |
MOD_ProDKin_1 | 155 | 161 | PF00069 | 0.695 |
MOD_ProDKin_1 | 16 | 22 | PF00069 | 0.802 |
MOD_ProDKin_1 | 184 | 190 | PF00069 | 0.721 |
MOD_ProDKin_1 | 318 | 324 | PF00069 | 0.684 |
MOD_ProDKin_1 | 337 | 343 | PF00069 | 0.472 |
MOD_ProDKin_1 | 357 | 363 | PF00069 | 0.632 |
MOD_ProDKin_1 | 403 | 409 | PF00069 | 0.670 |
MOD_ProDKin_1 | 442 | 448 | PF00069 | 0.530 |
MOD_ProDKin_1 | 65 | 71 | PF00069 | 0.739 |
MOD_SUMO_rev_2 | 445 | 455 | PF00179 | 0.452 |
MOD_SUMO_rev_2 | 527 | 536 | PF00179 | 0.530 |
MOD_SUMO_rev_2 | 579 | 588 | PF00179 | 0.649 |
TRG_DiLeu_BaEn_1 | 635 | 640 | PF01217 | 0.643 |
TRG_DiLeu_BaLyEn_6 | 610 | 615 | PF01217 | 0.644 |
TRG_DiLeu_LyEn_5 | 635 | 640 | PF01217 | 0.643 |
TRG_Pf-PMV_PEXEL_1 | 460 | 465 | PF00026 | 0.530 |
TRG_Pf-PMV_PEXEL_1 | 492 | 496 | PF00026 | 0.530 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7X5T9 | Leishmania donovani | 84% | 99% |
A4HKM6 | Leishmania braziliensis | 63% | 100% |
A4I861 | Leishmania infantum | 84% | 99% |
E9B314 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 100% |