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: A4HKM6
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_C14_Caspase3-7 | 258 | 262 | PF00656 | 0.537 |
CLV_NRD_NRD_1 | 403 | 405 | PF00675 | 0.437 |
CLV_PCSK_SKI1_1 | 436 | 440 | PF00082 | 0.361 |
CLV_PCSK_SKI1_1 | 446 | 450 | PF00082 | 0.396 |
CLV_PCSK_SKI1_1 | 505 | 509 | PF00082 | 0.556 |
DEG_APCC_DBOX_1 | 536 | 544 | PF00400 | 0.609 |
DEG_SCF_FBW7_1 | 107 | 113 | PF00400 | 0.536 |
DEG_SPOP_SBC_1 | 235 | 239 | PF00917 | 0.542 |
DOC_CKS1_1 | 107 | 112 | PF01111 | 0.534 |
DOC_CYCLIN_yCln2_LP_2 | 101 | 107 | PF00134 | 0.530 |
DOC_CYCLIN_yCln2_LP_2 | 177 | 183 | PF00134 | 0.691 |
DOC_MAPK_gen_1 | 404 | 412 | PF00069 | 0.437 |
DOC_MAPK_MEF2A_6 | 404 | 412 | PF00069 | 0.437 |
DOC_PP2B_LxvP_1 | 101 | 104 | PF13499 | 0.527 |
DOC_PP2B_LxvP_1 | 144 | 147 | PF13499 | 0.521 |
DOC_PP2B_LxvP_1 | 177 | 180 | PF13499 | 0.687 |
DOC_USP7_MATH_1 | 120 | 124 | PF00917 | 0.683 |
DOC_USP7_MATH_1 | 132 | 136 | PF00917 | 0.586 |
DOC_USP7_MATH_1 | 139 | 143 | PF00917 | 0.510 |
DOC_USP7_MATH_1 | 205 | 209 | PF00917 | 0.645 |
DOC_USP7_MATH_1 | 228 | 232 | PF00917 | 0.540 |
DOC_USP7_MATH_1 | 235 | 239 | PF00917 | 0.503 |
DOC_USP7_MATH_1 | 341 | 345 | PF00917 | 0.640 |
DOC_USP7_MATH_1 | 367 | 371 | PF00917 | 0.648 |
DOC_USP7_MATH_1 | 388 | 392 | PF00917 | 0.531 |
DOC_USP7_MATH_1 | 451 | 455 | PF00917 | 0.437 |
DOC_USP7_MATH_1 | 5 | 9 | PF00917 | 0.671 |
DOC_USP7_MATH_1 | 565 | 569 | PF00917 | 0.517 |
DOC_USP7_MATH_1 | 59 | 63 | PF00917 | 0.599 |
DOC_USP7_MATH_1 | 87 | 91 | PF00917 | 0.572 |
DOC_USP7_MATH_1 | 92 | 96 | PF00917 | 0.668 |
DOC_WW_Pin1_4 | 106 | 111 | PF00397 | 0.698 |
DOC_WW_Pin1_4 | 133 | 138 | PF00397 | 0.704 |
DOC_WW_Pin1_4 | 16 | 21 | PF00397 | 0.705 |
DOC_WW_Pin1_4 | 181 | 186 | PF00397 | 0.533 |
DOC_WW_Pin1_4 | 226 | 231 | PF00397 | 0.654 |
DOC_WW_Pin1_4 | 347 | 352 | PF00397 | 0.725 |
DOC_WW_Pin1_4 | 386 | 391 | PF00397 | 0.666 |
DOC_WW_Pin1_4 | 85 | 90 | PF00397 | 0.537 |
LIG_14-3-3_CanoR_1 | 505 | 510 | PF00244 | 0.554 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.672 |
LIG_BIR_III_2 | 182 | 186 | PF00653 | 0.531 |
LIG_BRCT_BRCA1_1 | 134 | 138 | PF00533 | 0.702 |
LIG_BRCT_BRCA1_1 | 195 | 199 | PF00533 | 0.597 |
LIG_BRCT_BRCA1_1 | 239 | 243 | PF00533 | 0.540 |
LIG_BRCT_BRCA1_1 | 358 | 362 | PF00533 | 0.544 |
LIG_BRCT_BRCA1_1 | 390 | 394 | PF00533 | 0.437 |
LIG_FHA_1 | 262 | 268 | PF00498 | 0.683 |
LIG_FHA_1 | 547 | 553 | PF00498 | 0.474 |
LIG_FHA_1 | 73 | 79 | PF00498 | 0.540 |
LIG_FHA_2 | 256 | 262 | PF00498 | 0.535 |
LIG_FHA_2 | 324 | 330 | PF00498 | 0.537 |
LIG_FHA_2 | 366 | 372 | PF00498 | 0.540 |
LIG_FHA_2 | 456 | 462 | PF00498 | 0.437 |
LIG_GBD_Chelix_1 | 566 | 574 | PF00786 | 0.528 |
LIG_LIR_Gen_1 | 508 | 516 | PF02991 | 0.558 |
LIG_LIR_Nem_3 | 508 | 512 | PF02991 | 0.564 |
LIG_NRBOX | 573 | 579 | PF00104 | 0.549 |
LIG_PCNA_PIPBox_1 | 466 | 475 | PF02747 | 0.437 |
LIG_PCNA_yPIPBox_3 | 463 | 473 | PF02747 | 0.437 |
LIG_SH2_CRK | 509 | 513 | PF00017 | 0.476 |
LIG_SH2_GRB2like | 509 | 512 | PF00017 | 0.547 |
LIG_SH2_SRC | 509 | 512 | PF00017 | 0.547 |
LIG_SH2_STAP1 | 509 | 513 | PF00017 | 0.546 |
LIG_SH2_STAT3 | 483 | 486 | PF00017 | 0.437 |
LIG_SH2_STAT5 | 472 | 475 | PF00017 | 0.437 |
LIG_SH3_3 | 101 | 107 | PF00018 | 0.618 |
LIG_SH3_3 | 86 | 92 | PF00018 | 0.594 |
LIG_SUMO_SIM_par_1 | 510 | 518 | PF11976 | 0.362 |
LIG_TRAF2_1 | 390 | 393 | PF00917 | 0.496 |
LIG_TYR_ITIM | 507 | 512 | PF00017 | 0.449 |
MOD_CK1_1 | 167 | 173 | PF00069 | 0.534 |
MOD_CK1_1 | 208 | 214 | PF00069 | 0.600 |
MOD_CK1_1 | 226 | 232 | PF00069 | 0.491 |
MOD_CK1_1 | 31 | 37 | PF00069 | 0.532 |
MOD_CK1_1 | 345 | 351 | PF00069 | 0.659 |
MOD_CK1_1 | 369 | 375 | PF00069 | 0.566 |
MOD_CK1_1 | 64 | 70 | PF00069 | 0.606 |
MOD_CK1_1 | 8 | 14 | PF00069 | 0.511 |
MOD_CK1_1 | 90 | 96 | PF00069 | 0.679 |
MOD_CK2_1 | 323 | 329 | PF00069 | 0.535 |
MOD_CK2_1 | 365 | 371 | PF00069 | 0.541 |
MOD_CK2_1 | 455 | 461 | PF00069 | 0.437 |
MOD_CK2_1 | 533 | 539 | PF00069 | 0.596 |
MOD_CK2_1 | 541 | 547 | PF00069 | 0.518 |
MOD_CK2_1 | 565 | 571 | PF00069 | 0.521 |
MOD_GlcNHglycan | 113 | 116 | PF01048 | 0.501 |
MOD_GlcNHglycan | 122 | 125 | PF01048 | 0.611 |
MOD_GlcNHglycan | 148 | 151 | PF01048 | 0.718 |
MOD_GlcNHglycan | 159 | 162 | PF01048 | 0.585 |
MOD_GlcNHglycan | 166 | 169 | PF01048 | 0.507 |
MOD_GlcNHglycan | 190 | 193 | PF01048 | 0.653 |
MOD_GlcNHglycan | 195 | 198 | PF01048 | 0.610 |
MOD_GlcNHglycan | 207 | 210 | PF01048 | 0.545 |
MOD_GlcNHglycan | 225 | 228 | PF01048 | 0.517 |
MOD_GlcNHglycan | 230 | 233 | PF01048 | 0.625 |
MOD_GlcNHglycan | 239 | 242 | PF01048 | 0.598 |
MOD_GlcNHglycan | 264 | 267 | PF01048 | 0.548 |
MOD_GlcNHglycan | 302 | 305 | PF01048 | 0.594 |
MOD_GlcNHglycan | 344 | 347 | PF01048 | 0.733 |
MOD_GlcNHglycan | 43 | 46 | PF01048 | 0.677 |
MOD_GlcNHglycan | 453 | 456 | PF01048 | 0.437 |
MOD_GlcNHglycan | 563 | 566 | PF01048 | 0.524 |
MOD_GlcNHglycan | 567 | 570 | PF01048 | 0.468 |
MOD_GlcNHglycan | 57 | 60 | PF01048 | 0.585 |
MOD_GlcNHglycan | 63 | 66 | PF01048 | 0.528 |
MOD_GlcNHglycan | 8 | 11 | PF01048 | 0.503 |
MOD_GlcNHglycan | 89 | 92 | PF01048 | 0.651 |
MOD_GlcNHglycan | 94 | 97 | PF01048 | 0.661 |
MOD_GSK3_1 | 106 | 113 | PF00069 | 0.528 |
MOD_GSK3_1 | 133 | 140 | PF00069 | 0.565 |
MOD_GSK3_1 | 164 | 171 | PF00069 | 0.648 |
MOD_GSK3_1 | 184 | 191 | PF00069 | 0.652 |
MOD_GSK3_1 | 222 | 229 | PF00069 | 0.545 |
MOD_GSK3_1 | 28 | 35 | PF00069 | 0.554 |
MOD_GSK3_1 | 323 | 330 | PF00069 | 0.730 |
MOD_GSK3_1 | 335 | 342 | PF00069 | 0.569 |
MOD_GSK3_1 | 353 | 360 | PF00069 | 0.600 |
MOD_GSK3_1 | 365 | 372 | PF00069 | 0.566 |
MOD_GSK3_1 | 41 | 48 | PF00069 | 0.636 |
MOD_GSK3_1 | 436 | 443 | PF00069 | 0.352 |
MOD_GSK3_1 | 447 | 454 | PF00069 | 0.391 |
MOD_GSK3_1 | 55 | 62 | PF00069 | 0.582 |
MOD_GSK3_1 | 561 | 568 | PF00069 | 0.522 |
MOD_GSK3_1 | 92 | 99 | PF00069 | 0.706 |
MOD_N-GLC_1 | 533 | 538 | PF02516 | 0.595 |
MOD_N-GLC_1 | 55 | 60 | PF02516 | 0.521 |
MOD_NEK2_1 | 111 | 116 | PF00069 | 0.732 |
MOD_NEK2_1 | 154 | 159 | PF00069 | 0.653 |
MOD_NEK2_1 | 169 | 174 | PF00069 | 0.520 |
MOD_NEK2_1 | 243 | 248 | PF00069 | 0.528 |
MOD_NEK2_1 | 294 | 299 | PF00069 | 0.700 |
MOD_NEK2_1 | 323 | 328 | PF00069 | 0.716 |
MOD_NEK2_1 | 379 | 384 | PF00069 | 0.523 |
MOD_NEK2_1 | 43 | 48 | PF00069 | 0.534 |
MOD_NEK2_1 | 55 | 60 | PF00069 | 0.488 |
MOD_NEK2_1 | 6 | 11 | PF00069 | 0.680 |
MOD_NEK2_2 | 357 | 362 | PF00069 | 0.545 |
MOD_PIKK_1 | 388 | 394 | PF00454 | 0.437 |
MOD_PKB_1 | 434 | 442 | PF00069 | 0.284 |
MOD_Plk_1 | 455 | 461 | PF00069 | 0.437 |
MOD_Plk_4 | 357 | 363 | PF00069 | 0.546 |
MOD_Plk_4 | 440 | 446 | PF00069 | 0.437 |
MOD_ProDKin_1 | 106 | 112 | PF00069 | 0.700 |
MOD_ProDKin_1 | 133 | 139 | PF00069 | 0.704 |
MOD_ProDKin_1 | 16 | 22 | PF00069 | 0.705 |
MOD_ProDKin_1 | 181 | 187 | PF00069 | 0.535 |
MOD_ProDKin_1 | 226 | 232 | PF00069 | 0.653 |
MOD_ProDKin_1 | 347 | 353 | PF00069 | 0.725 |
MOD_ProDKin_1 | 386 | 392 | PF00069 | 0.437 |
MOD_ProDKin_1 | 85 | 91 | PF00069 | 0.537 |
MOD_SUMO_rev_2 | 471 | 480 | PF00179 | 0.437 |
MOD_SUMO_rev_2 | 517 | 526 | PF00179 | 0.548 |
TRG_DiLeu_BaEn_1 | 573 | 578 | PF01217 | 0.547 |
TRG_DiLeu_BaLyEn_6 | 548 | 553 | PF01217 | 0.615 |
TRG_DiLeu_LyEn_5 | 375 | 380 | PF01217 | 0.532 |
TRG_DiLeu_LyEn_5 | 573 | 578 | PF01217 | 0.547 |
TRG_ENDOCYTIC_2 | 509 | 512 | PF00928 | 0.477 |
TRG_Pf-PMV_PEXEL_1 | 404 | 409 | PF00026 | 0.501 |
TRG_Pf-PMV_PEXEL_1 | 436 | 440 | PF00026 | 0.437 |
TRG_Pf-PMV_PEXEL_1 | 528 | 532 | PF00026 | 0.407 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7X5T9 | Leishmania donovani | 63% | 99% |
A4I861 | Leishmania infantum | 64% | 99% |
E9B314 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 65% | 99% |
Q4Q540 | Leishmania major | 63% | 98% |