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: E9B314
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 | 447 | 449 | PF00675 | 0.385 |
CLV_PCSK_KEX2_1 | 416 | 418 | PF00082 | 0.638 |
CLV_PCSK_PC1ET2_1 | 416 | 418 | PF00082 | 0.638 |
CLV_PCSK_SKI1_1 | 480 | 484 | PF00082 | 0.368 |
CLV_PCSK_SKI1_1 | 490 | 494 | PF00082 | 0.352 |
CLV_PCSK_SKI1_1 | 552 | 556 | PF00082 | 0.492 |
DEG_APCC_DBOX_1 | 583 | 591 | PF00400 | 0.552 |
DEG_SPOP_SBC_1 | 101 | 105 | PF00917 | 0.515 |
DEG_SPOP_SBC_1 | 325 | 329 | PF00917 | 0.560 |
DEG_SPOP_SBC_1 | 357 | 361 | PF00917 | 0.572 |
DEG_SPOP_SBC_1 | 411 | 415 | PF00917 | 0.542 |
DEG_SPOP_SBC_1 | 84 | 88 | PF00917 | 0.608 |
DOC_CKS1_1 | 142 | 147 | PF01111 | 0.489 |
DOC_CKS1_1 | 346 | 351 | PF01111 | 0.488 |
DOC_MAPK_gen_1 | 448 | 456 | PF00069 | 0.385 |
DOC_MAPK_MEF2A_6 | 448 | 456 | PF00069 | 0.385 |
DOC_USP7_MATH_1 | 101 | 105 | PF00917 | 0.531 |
DOC_USP7_MATH_1 | 122 | 126 | PF00917 | 0.647 |
DOC_USP7_MATH_1 | 130 | 134 | PF00917 | 0.553 |
DOC_USP7_MATH_1 | 188 | 192 | PF00917 | 0.553 |
DOC_USP7_MATH_1 | 203 | 207 | PF00917 | 0.602 |
DOC_USP7_MATH_1 | 266 | 270 | PF00917 | 0.593 |
DOC_USP7_MATH_1 | 325 | 329 | PF00917 | 0.554 |
DOC_USP7_MATH_1 | 356 | 360 | PF00917 | 0.628 |
DOC_USP7_MATH_1 | 373 | 377 | PF00917 | 0.520 |
DOC_USP7_MATH_1 | 411 | 415 | PF00917 | 0.651 |
DOC_USP7_MATH_1 | 432 | 436 | PF00917 | 0.385 |
DOC_USP7_MATH_1 | 495 | 499 | PF00917 | 0.385 |
DOC_USP7_MATH_1 | 5 | 9 | PF00917 | 0.636 |
DOC_USP7_MATH_1 | 612 | 616 | PF00917 | 0.503 |
DOC_USP7_MATH_1 | 69 | 73 | PF00917 | 0.639 |
DOC_USP7_MATH_1 | 85 | 89 | PF00917 | 0.542 |
DOC_USP7_MATH_1 | 90 | 94 | PF00917 | 0.620 |
DOC_WW_Pin1_4 | 102 | 107 | PF00397 | 0.644 |
DOC_WW_Pin1_4 | 131 | 136 | PF00397 | 0.652 |
DOC_WW_Pin1_4 | 141 | 146 | PF00397 | 0.561 |
DOC_WW_Pin1_4 | 159 | 164 | PF00397 | 0.594 |
DOC_WW_Pin1_4 | 16 | 21 | PF00397 | 0.649 |
DOC_WW_Pin1_4 | 171 | 176 | PF00397 | 0.566 |
DOC_WW_Pin1_4 | 224 | 229 | PF00397 | 0.602 |
DOC_WW_Pin1_4 | 345 | 350 | PF00397 | 0.556 |
DOC_WW_Pin1_4 | 391 | 396 | PF00397 | 0.730 |
DOC_WW_Pin1_4 | 402 | 407 | PF00397 | 0.737 |
DOC_WW_Pin1_4 | 430 | 435 | PF00397 | 0.385 |
DOC_WW_Pin1_4 | 65 | 70 | PF00397 | 0.627 |
LIG_14-3-3_CanoR_1 | 509 | 514 | PF00244 | 0.342 |
LIG_14-3-3_CanoR_1 | 552 | 557 | PF00244 | 0.492 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.634 |
LIG_BRCT_BRCA1_1 | 132 | 136 | PF00533 | 0.651 |
LIG_BRCT_BRCA1_1 | 361 | 365 | PF00533 | 0.612 |
LIG_BRCT_BRCA1_1 | 434 | 438 | PF00533 | 0.385 |
LIG_FHA_1 | 136 | 142 | PF00498 | 0.505 |
LIG_FHA_1 | 594 | 600 | PF00498 | 0.428 |
LIG_FHA_2 | 500 | 506 | PF00498 | 0.385 |
LIG_FHA_2 | 510 | 516 | PF00498 | 0.292 |
LIG_GBD_Chelix_1 | 613 | 621 | PF00786 | 0.468 |
LIG_LIR_Gen_1 | 555 | 563 | PF02991 | 0.439 |
LIG_LIR_Nem_3 | 162 | 167 | PF02991 | 0.610 |
LIG_LIR_Nem_3 | 555 | 559 | PF02991 | 0.439 |
LIG_LIR_Nem_3 | 73 | 79 | PF02991 | 0.626 |
LIG_NRBOX | 620 | 626 | PF00104 | 0.485 |
LIG_PCNA_PIPBox_1 | 510 | 519 | PF02747 | 0.385 |
LIG_PCNA_yPIPBox_3 | 507 | 517 | PF02747 | 0.385 |
LIG_SH2_CRK | 556 | 560 | PF00017 | 0.441 |
LIG_SH2_GRB2like | 556 | 559 | PF00017 | 0.496 |
LIG_SH2_SRC | 556 | 559 | PF00017 | 0.496 |
LIG_SH2_STAP1 | 556 | 560 | PF00017 | 0.496 |
LIG_SH2_STAT3 | 527 | 530 | PF00017 | 0.385 |
LIG_SH2_STAT5 | 516 | 519 | PF00017 | 0.399 |
LIG_SH3_3 | 139 | 145 | PF00018 | 0.614 |
LIG_SH3_3 | 172 | 178 | PF00018 | 0.499 |
LIG_SH3_3 | 343 | 349 | PF00018 | 0.598 |
LIG_SUMO_SIM_par_1 | 229 | 234 | PF11976 | 0.621 |
LIG_TRAF2_1 | 434 | 437 | PF00917 | 0.385 |
LIG_TRAF2_2 | 434 | 439 | PF00917 | 0.342 |
MOD_CK1_1 | 104 | 110 | PF00069 | 0.566 |
MOD_CK1_1 | 125 | 131 | PF00069 | 0.490 |
MOD_CK1_1 | 191 | 197 | PF00069 | 0.584 |
MOD_CK1_1 | 252 | 258 | PF00069 | 0.622 |
MOD_CK1_1 | 296 | 302 | PF00069 | 0.607 |
MOD_CK1_1 | 359 | 365 | PF00069 | 0.502 |
MOD_CK1_1 | 377 | 383 | PF00069 | 0.582 |
MOD_CK1_1 | 389 | 395 | PF00069 | 0.615 |
MOD_CK1_1 | 53 | 59 | PF00069 | 0.634 |
MOD_CK1_1 | 93 | 99 | PF00069 | 0.676 |
MOD_CK2_1 | 499 | 505 | PF00069 | 0.385 |
MOD_CK2_1 | 509 | 515 | PF00069 | 0.292 |
MOD_CK2_1 | 580 | 586 | PF00069 | 0.566 |
MOD_CK2_1 | 588 | 594 | PF00069 | 0.483 |
MOD_CK2_1 | 612 | 618 | PF00069 | 0.506 |
MOD_GlcNHglycan | 111 | 114 | PF01048 | 0.503 |
MOD_GlcNHglycan | 119 | 122 | PF01048 | 0.588 |
MOD_GlcNHglycan | 124 | 127 | PF01048 | 0.537 |
MOD_GlcNHglycan | 146 | 149 | PF01048 | 0.671 |
MOD_GlcNHglycan | 157 | 160 | PF01048 | 0.563 |
MOD_GlcNHglycan | 164 | 167 | PF01048 | 0.495 |
MOD_GlcNHglycan | 188 | 191 | PF01048 | 0.609 |
MOD_GlcNHglycan | 193 | 196 | PF01048 | 0.582 |
MOD_GlcNHglycan | 205 | 208 | PF01048 | 0.532 |
MOD_GlcNHglycan | 251 | 254 | PF01048 | 0.568 |
MOD_GlcNHglycan | 268 | 271 | PF01048 | 0.564 |
MOD_GlcNHglycan | 295 | 298 | PF01048 | 0.601 |
MOD_GlcNHglycan | 328 | 331 | PF01048 | 0.666 |
MOD_GlcNHglycan | 361 | 364 | PF01048 | 0.546 |
MOD_GlcNHglycan | 388 | 391 | PF01048 | 0.721 |
MOD_GlcNHglycan | 48 | 51 | PF01048 | 0.644 |
MOD_GlcNHglycan | 497 | 500 | PF01048 | 0.392 |
MOD_GlcNHglycan | 52 | 55 | PF01048 | 0.614 |
MOD_GlcNHglycan | 541 | 544 | PF01048 | 0.493 |
MOD_GlcNHglycan | 58 | 61 | PF01048 | 0.567 |
MOD_GlcNHglycan | 610 | 613 | PF01048 | 0.484 |
MOD_GlcNHglycan | 614 | 617 | PF01048 | 0.425 |
MOD_GlcNHglycan | 79 | 82 | PF01048 | 0.584 |
MOD_GlcNHglycan | 92 | 95 | PF01048 | 0.625 |
MOD_GSK3_1 | 100 | 107 | PF00069 | 0.565 |
MOD_GSK3_1 | 131 | 138 | PF00069 | 0.547 |
MOD_GSK3_1 | 155 | 162 | PF00069 | 0.649 |
MOD_GSK3_1 | 182 | 189 | PF00069 | 0.612 |
MOD_GSK3_1 | 281 | 288 | PF00069 | 0.541 |
MOD_GSK3_1 | 359 | 366 | PF00069 | 0.639 |
MOD_GSK3_1 | 373 | 380 | PF00069 | 0.547 |
MOD_GSK3_1 | 405 | 412 | PF00069 | 0.723 |
MOD_GSK3_1 | 423 | 430 | PF00069 | 0.571 |
MOD_GSK3_1 | 46 | 53 | PF00069 | 0.614 |
MOD_GSK3_1 | 480 | 487 | PF00069 | 0.393 |
MOD_GSK3_1 | 491 | 498 | PF00069 | 0.369 |
MOD_GSK3_1 | 608 | 615 | PF00069 | 0.511 |
MOD_GSK3_1 | 65 | 72 | PF00069 | 0.512 |
MOD_GSK3_1 | 90 | 97 | PF00069 | 0.653 |
MOD_N-GLC_1 | 402 | 407 | PF02516 | 0.533 |
MOD_N-GLC_1 | 580 | 585 | PF02516 | 0.535 |
MOD_NEK2_1 | 109 | 114 | PF00069 | 0.685 |
MOD_NEK2_1 | 152 | 157 | PF00069 | 0.619 |
MOD_NEK2_1 | 301 | 306 | PF00069 | 0.490 |
MOD_NEK2_1 | 367 | 372 | PF00069 | 0.658 |
MOD_NEK2_1 | 6 | 11 | PF00069 | 0.637 |
MOD_PIKK_1 | 432 | 438 | PF00454 | 0.385 |
MOD_PKA_2 | 508 | 514 | PF00069 | 0.342 |
MOD_PKB_1 | 478 | 486 | PF00069 | 0.265 |
MOD_Plk_1 | 452 | 458 | PF00069 | 0.342 |
MOD_Plk_1 | 499 | 505 | PF00069 | 0.390 |
MOD_Plk_4 | 484 | 490 | PF00069 | 0.385 |
MOD_ProDKin_1 | 102 | 108 | PF00069 | 0.637 |
MOD_ProDKin_1 | 131 | 137 | PF00069 | 0.653 |
MOD_ProDKin_1 | 141 | 147 | PF00069 | 0.563 |
MOD_ProDKin_1 | 159 | 165 | PF00069 | 0.595 |
MOD_ProDKin_1 | 16 | 22 | PF00069 | 0.649 |
MOD_ProDKin_1 | 171 | 177 | PF00069 | 0.565 |
MOD_ProDKin_1 | 224 | 230 | PF00069 | 0.599 |
MOD_ProDKin_1 | 345 | 351 | PF00069 | 0.555 |
MOD_ProDKin_1 | 391 | 397 | PF00069 | 0.735 |
MOD_ProDKin_1 | 402 | 408 | PF00069 | 0.737 |
MOD_ProDKin_1 | 430 | 436 | PF00069 | 0.385 |
MOD_ProDKin_1 | 65 | 71 | PF00069 | 0.625 |
MOD_SUMO_rev_2 | 433 | 443 | PF00179 | 0.342 |
MOD_SUMO_rev_2 | 515 | 524 | PF00179 | 0.385 |
MOD_SUMO_rev_2 | 564 | 573 | PF00179 | 0.500 |
TRG_DiLeu_BaEn_1 | 620 | 625 | PF01217 | 0.485 |
TRG_DiLeu_BaLyEn_6 | 595 | 600 | PF01217 | 0.493 |
TRG_DiLeu_LyEn_5 | 620 | 625 | PF01217 | 0.485 |
TRG_ENDOCYTIC_2 | 556 | 559 | PF00928 | 0.441 |
TRG_Pf-PMV_PEXEL_1 | 448 | 453 | PF00026 | 0.385 |
TRG_Pf-PMV_PEXEL_1 | 480 | 484 | PF00026 | 0.385 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7X5T9 | Leishmania donovani | 82% | 97% |
A4HKM6 | Leishmania braziliensis | 65% | 100% |
A4I861 | Leishmania infantum | 82% | 97% |
Q4Q540 | Leishmania major | 81% | 99% |