Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 4 |
Forrest at al. (procyclic) | no | yes: 4 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 3 |
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: 12 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 2 |
GO:0005730 | nucleolus | 5 | 2 |
GO:0005737 | cytoplasm | 2 | 12 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043228 | non-membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
Related structures:
AlphaFold database: Q4Q7J1
Term | Name | Level | Count |
---|---|---|---|
GO:0006606 | protein import into nucleus | 5 | 12 |
GO:0006607 | NLS-bearing protein import into nucleus | 6 | 2 |
GO:0006810 | transport | 3 | 12 |
GO:0006886 | intracellular protein transport | 4 | 12 |
GO:0006913 | nucleocytoplasmic transport | 5 | 12 |
GO:0008104 | protein localization | 4 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0015031 | protein transport | 4 | 12 |
GO:0033036 | macromolecule localization | 2 | 12 |
GO:0033365 | protein localization to organelle | 5 | 12 |
GO:0034504 | protein localization to nucleus | 6 | 12 |
GO:0045184 | establishment of protein localization | 3 | 12 |
GO:0046907 | intracellular transport | 3 | 12 |
GO:0051169 | nuclear transport | 4 | 12 |
GO:0051170 | import into nucleus | 6 | 12 |
GO:0051179 | localization | 1 | 12 |
GO:0051234 | establishment of localization | 2 | 12 |
GO:0051641 | cellular localization | 2 | 12 |
GO:0051649 | establishment of localization in cell | 3 | 12 |
GO:0070727 | cellular macromolecule localization | 3 | 12 |
GO:0071702 | organic substance transport | 4 | 12 |
GO:0071705 | nitrogen compound transport | 4 | 12 |
GO:0072594 | establishment of protein localization to organelle | 4 | 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005048 | signal sequence binding | 4 | 2 |
GO:0005488 | binding | 1 | 2 |
GO:0008139 | nuclear localization sequence binding | 5 | 2 |
GO:0033218 | amide binding | 2 | 2 |
GO:0042277 | peptide binding | 3 | 2 |
GO:0061608 | nuclear import signal receptor activity | 3 | 12 |
GO:0140104 | molecular carrier activity | 1 | 12 |
GO:0140142 | nucleocytoplasmic carrier activity | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 108 | 110 | PF00675 | 0.346 |
CLV_NRD_NRD_1 | 22 | 24 | PF00675 | 0.491 |
CLV_NRD_NRD_1 | 355 | 357 | PF00675 | 0.320 |
CLV_NRD_NRD_1 | 397 | 399 | PF00675 | 0.413 |
CLV_PCSK_KEX2_1 | 22 | 24 | PF00082 | 0.491 |
CLV_PCSK_KEX2_1 | 352 | 354 | PF00082 | 0.291 |
CLV_PCSK_PC1ET2_1 | 352 | 354 | PF00082 | 0.305 |
CLV_PCSK_SKI1_1 | 109 | 113 | PF00082 | 0.304 |
CLV_PCSK_SKI1_1 | 232 | 236 | PF00082 | 0.339 |
CLV_PCSK_SKI1_1 | 352 | 356 | PF00082 | 0.425 |
CLV_PCSK_SKI1_1 | 439 | 443 | PF00082 | 0.361 |
CLV_PCSK_SKI1_1 | 8 | 12 | PF00082 | 0.623 |
CLV_PCSK_SKI1_1 | 99 | 103 | PF00082 | 0.412 |
CLV_Separin_Metazoa | 346 | 350 | PF03568 | 0.425 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.628 |
DEG_SPOP_SBC_1 | 122 | 126 | PF00917 | 0.425 |
DOC_CDC14_PxL_1 | 423 | 431 | PF14671 | 0.464 |
DOC_CDC14_PxL_1 | 82 | 90 | PF14671 | 0.514 |
DOC_MAPK_gen_1 | 22 | 30 | PF00069 | 0.520 |
DOC_MAPK_MEF2A_6 | 138 | 146 | PF00069 | 0.320 |
DOC_MAPK_MEF2A_6 | 418 | 425 | PF00069 | 0.406 |
DOC_MAPK_MEF2A_6 | 491 | 500 | PF00069 | 0.538 |
DOC_MAPK_RevD_3 | 385 | 399 | PF00069 | 0.339 |
DOC_PP2B_LxvP_1 | 306 | 309 | PF13499 | 0.389 |
DOC_PP2B_LxvP_1 | 390 | 393 | PF13499 | 0.425 |
DOC_PP2B_PxIxI_1 | 315 | 321 | PF00149 | 0.425 |
DOC_USP7_MATH_1 | 157 | 161 | PF00917 | 0.320 |
DOC_USP7_MATH_1 | 60 | 64 | PF00917 | 0.665 |
DOC_USP7_UBL2_3 | 7 | 11 | PF12436 | 0.724 |
DOC_WW_Pin1_4 | 178 | 183 | PF00397 | 0.348 |
DOC_WW_Pin1_4 | 73 | 78 | PF00397 | 0.539 |
LIG_14-3-3_CanoR_1 | 109 | 115 | PF00244 | 0.387 |
LIG_14-3-3_CanoR_1 | 232 | 237 | PF00244 | 0.328 |
LIG_14-3-3_CanoR_1 | 25 | 31 | PF00244 | 0.555 |
LIG_14-3-3_CanoR_1 | 289 | 294 | PF00244 | 0.218 |
LIG_Actin_WH2_2 | 216 | 234 | PF00022 | 0.389 |
LIG_APCC_ABBAyCdc20_2 | 31 | 37 | PF00400 | 0.675 |
LIG_BIR_III_4 | 516 | 520 | PF00653 | 0.554 |
LIG_BRCT_BRCA1_1 | 533 | 537 | PF00533 | 0.655 |
LIG_deltaCOP1_diTrp_1 | 400 | 410 | PF00928 | 0.425 |
LIG_EH1_1 | 371 | 379 | PF00400 | 0.425 |
LIG_eIF4E_1 | 372 | 378 | PF01652 | 0.391 |
LIG_FHA_1 | 103 | 109 | PF00498 | 0.378 |
LIG_FHA_1 | 161 | 167 | PF00498 | 0.339 |
LIG_FHA_1 | 233 | 239 | PF00498 | 0.329 |
LIG_FHA_1 | 330 | 336 | PF00498 | 0.304 |
LIG_FHA_1 | 440 | 446 | PF00498 | 0.344 |
LIG_FHA_2 | 257 | 263 | PF00498 | 0.425 |
LIG_FHA_2 | 485 | 491 | PF00498 | 0.547 |
LIG_FHA_2 | 504 | 510 | PF00498 | 0.381 |
LIG_FHA_2 | 95 | 101 | PF00498 | 0.459 |
LIG_LIR_Gen_1 | 117 | 128 | PF02991 | 0.425 |
LIG_LIR_Nem_3 | 117 | 123 | PF02991 | 0.421 |
LIG_LIR_Nem_3 | 139 | 144 | PF02991 | 0.391 |
LIG_LIR_Nem_3 | 48 | 53 | PF02991 | 0.509 |
LIG_LYPXL_yS_3 | 141 | 144 | PF13949 | 0.389 |
LIG_MAD2 | 110 | 118 | PF02301 | 0.480 |
LIG_MAD2 | 301 | 309 | PF02301 | 0.425 |
LIG_MYND_3 | 247 | 251 | PF01753 | 0.483 |
LIG_NRBOX | 131 | 137 | PF00104 | 0.389 |
LIG_NRBOX | 259 | 265 | PF00104 | 0.320 |
LIG_PDZ_Class_2 | 534 | 539 | PF00595 | 0.622 |
LIG_Pex14_1 | 277 | 281 | PF04695 | 0.304 |
LIG_Pex14_2 | 146 | 150 | PF04695 | 0.304 |
LIG_PTB_Apo_2 | 404 | 411 | PF02174 | 0.423 |
LIG_SH2_CRK | 120 | 124 | PF00017 | 0.421 |
LIG_SH2_NCK_1 | 120 | 124 | PF00017 | 0.425 |
LIG_SH2_STAP1 | 494 | 498 | PF00017 | 0.478 |
LIG_SH2_STAT5 | 281 | 284 | PF00017 | 0.320 |
LIG_SH2_STAT5 | 419 | 422 | PF00017 | 0.337 |
LIG_SH3_1 | 243 | 249 | PF00018 | 0.390 |
LIG_SH3_3 | 243 | 249 | PF00018 | 0.380 |
LIG_SH3_3 | 310 | 316 | PF00018 | 0.382 |
LIG_SH3_3 | 379 | 385 | PF00018 | 0.425 |
LIG_SH3_3 | 422 | 428 | PF00018 | 0.368 |
LIG_SUMO_SIM_anti_2 | 259 | 269 | PF11976 | 0.425 |
LIG_SUMO_SIM_par_1 | 110 | 115 | PF11976 | 0.375 |
LIG_SUMO_SIM_par_1 | 219 | 225 | PF11976 | 0.425 |
LIG_SUMO_SIM_par_1 | 304 | 311 | PF11976 | 0.399 |
LIG_SUMO_SIM_par_1 | 441 | 446 | PF11976 | 0.350 |
LIG_UBA3_1 | 107 | 116 | PF00899 | 0.521 |
LIG_UBA3_1 | 217 | 224 | PF00899 | 0.451 |
LIG_WRC_WIRS_1 | 501 | 506 | PF05994 | 0.538 |
MOD_CK1_1 | 160 | 166 | PF00069 | 0.358 |
MOD_CK1_1 | 280 | 286 | PF00069 | 0.291 |
MOD_CK1_1 | 307 | 313 | PF00069 | 0.364 |
MOD_CK1_1 | 461 | 467 | PF00069 | 0.544 |
MOD_CK2_1 | 219 | 225 | PF00069 | 0.425 |
MOD_CK2_1 | 289 | 295 | PF00069 | 0.218 |
MOD_CK2_1 | 388 | 394 | PF00069 | 0.425 |
MOD_CK2_1 | 504 | 510 | PF00069 | 0.496 |
MOD_CK2_1 | 60 | 66 | PF00069 | 0.620 |
MOD_CK2_1 | 94 | 100 | PF00069 | 0.428 |
MOD_GlcNHglycan | 125 | 128 | PF01048 | 0.320 |
MOD_GlcNHglycan | 147 | 150 | PF01048 | 0.385 |
MOD_GlcNHglycan | 188 | 192 | PF01048 | 0.401 |
MOD_GlcNHglycan | 197 | 200 | PF01048 | 0.490 |
MOD_GlcNHglycan | 337 | 340 | PF01048 | 0.385 |
MOD_GlcNHglycan | 390 | 393 | PF01048 | 0.423 |
MOD_GlcNHglycan | 460 | 463 | PF01048 | 0.575 |
MOD_GlcNHglycan | 533 | 536 | PF01048 | 0.675 |
MOD_GSK3_1 | 156 | 163 | PF00069 | 0.326 |
MOD_GSK3_1 | 232 | 239 | PF00069 | 0.320 |
MOD_GSK3_1 | 304 | 311 | PF00069 | 0.337 |
MOD_GSK3_1 | 325 | 332 | PF00069 | 0.369 |
MOD_GSK3_1 | 406 | 413 | PF00069 | 0.474 |
MOD_GSK3_1 | 457 | 464 | PF00069 | 0.504 |
MOD_GSK3_1 | 500 | 507 | PF00069 | 0.474 |
MOD_GSK3_1 | 72 | 79 | PF00069 | 0.515 |
MOD_N-GLC_1 | 195 | 200 | PF02516 | 0.425 |
MOD_N-GLC_1 | 232 | 237 | PF02516 | 0.339 |
MOD_N-GLC_1 | 264 | 269 | PF02516 | 0.451 |
MOD_N-GLC_1 | 406 | 411 | PF02516 | 0.339 |
MOD_N-GLC_1 | 55 | 60 | PF02516 | 0.696 |
MOD_N-GLC_2 | 240 | 242 | PF02516 | 0.339 |
MOD_N-GLC_2 | 381 | 383 | PF02516 | 0.425 |
MOD_N-GLC_2 | 90 | 92 | PF02516 | 0.499 |
MOD_NEK2_1 | 102 | 107 | PF00069 | 0.404 |
MOD_NEK2_1 | 377 | 382 | PF00069 | 0.446 |
MOD_NEK2_1 | 410 | 415 | PF00069 | 0.501 |
MOD_NEK2_1 | 429 | 434 | PF00069 | 0.225 |
MOD_PIKK_1 | 329 | 335 | PF00454 | 0.293 |
MOD_PK_1 | 110 | 116 | PF00069 | 0.403 |
MOD_PK_1 | 289 | 295 | PF00069 | 0.218 |
MOD_PKA_1 | 356 | 362 | PF00069 | 0.320 |
MOD_Plk_1 | 160 | 166 | PF00069 | 0.363 |
MOD_Plk_1 | 187 | 193 | PF00069 | 0.425 |
MOD_Plk_1 | 232 | 238 | PF00069 | 0.339 |
MOD_Plk_1 | 329 | 335 | PF00069 | 0.425 |
MOD_Plk_1 | 406 | 412 | PF00069 | 0.339 |
MOD_Plk_2-3 | 67 | 73 | PF00069 | 0.516 |
MOD_Plk_4 | 102 | 108 | PF00069 | 0.381 |
MOD_Plk_4 | 160 | 166 | PF00069 | 0.380 |
MOD_Plk_4 | 256 | 262 | PF00069 | 0.369 |
MOD_Plk_4 | 289 | 295 | PF00069 | 0.218 |
MOD_Plk_4 | 500 | 506 | PF00069 | 0.479 |
MOD_Plk_4 | 84 | 90 | PF00069 | 0.505 |
MOD_ProDKin_1 | 178 | 184 | PF00069 | 0.348 |
MOD_ProDKin_1 | 73 | 79 | PF00069 | 0.536 |
MOD_SUMO_rev_2 | 431 | 441 | PF00179 | 0.388 |
MOD_SUMO_rev_2 | 456 | 461 | PF00179 | 0.458 |
TRG_DiLeu_BaEn_1 | 37 | 42 | PF01217 | 0.617 |
TRG_ENDOCYTIC_2 | 120 | 123 | PF00928 | 0.411 |
TRG_ENDOCYTIC_2 | 141 | 144 | PF00928 | 0.399 |
TRG_ER_diArg_1 | 22 | 25 | PF00400 | 0.510 |
TRG_ER_diArg_1 | 30 | 33 | PF00400 | 0.516 |
TRG_NES_CRM1_1 | 373 | 388 | PF08389 | 0.425 |
TRG_Pf-PMV_PEXEL_1 | 353 | 358 | PF00026 | 0.425 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PFK7 | Leptomonas seymouri | 84% | 100% |
A0A0S4KNG1 | Bodo saltans | 50% | 100% |
A0A1X0P216 | Trypanosomatidae | 56% | 100% |
A0A3R7LEH1 | Trypanosoma rangeli | 54% | 100% |
A0A3S7X3A8 | Leishmania donovani | 99% | 100% |
A2VE08 | Bos taurus | 43% | 100% |
A4HI66 | Leishmania braziliensis | 94% | 100% |
A4I5E3 | Leishmania infantum | 99% | 100% |
A9QM74 | Homo sapiens | 41% | 100% |
B6HJ92 | Penicillium rubens (strain ATCC 28089 / DSM 1075 / NRRL 1951 / Wisconsin 54-1255) | 39% | 98% |
C0LLJ0 | Mus musculus | 38% | 100% |
C1JZ66 | Bos taurus | 41% | 100% |
C6K7I2 | Sus scrofa | 40% | 100% |
C9ZQT2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 55% | 100% |
E9B0P1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 99% | 100% |
F4JL11 | Arabidopsis thaliana | 43% | 100% |
F4KF65 | Arabidopsis thaliana | 26% | 100% |
G5EB89 | Emericella nidulans (strain FGSC A4 / ATCC 38163 / CBS 112.46 / NRRL 194 / M139) | 40% | 97% |
O00505 | Homo sapiens | 38% | 100% |
O00629 | Homo sapiens | 43% | 100% |
O04294 | Arabidopsis thaliana | 40% | 100% |
O14063 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 40% | 99% |
O15131 | Homo sapiens | 41% | 100% |
O22478 | Solanum lycopersicum | 40% | 100% |
O35343 | Mus musculus | 42% | 100% |
O35344 | Mus musculus | 38% | 100% |
O35345 | Mus musculus | 41% | 100% |
O60684 | Homo sapiens | 41% | 100% |
O80480 | Arabidopsis thaliana | 40% | 100% |
O94374 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 46% | 100% |
P52170 | Xenopus laevis | 39% | 100% |
P52171 | Xenopus laevis | 38% | 100% |
P52292 | Homo sapiens | 45% | 100% |
P52293 | Mus musculus | 43% | 100% |
P52294 | Homo sapiens | 43% | 100% |
P52295 | Drosophila melanogaster | 37% | 100% |
P83953 | Rattus norvegicus | 42% | 100% |
P91276 | Caenorhabditis elegans | 31% | 100% |
Q02821 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 41% | 99% |
Q0V7M0 | Bos taurus | 41% | 100% |
Q19969 | Caenorhabditis elegans | 40% | 100% |
Q4WVW4 | Neosartorya fumigata (strain ATCC MYA-4609 / Af293 / CBS 101355 / FGSC A1100) | 24% | 93% |
Q503E9 | Danio rerio | 42% | 100% |
Q557F4 | Dictyostelium discoideum | 32% | 98% |
Q56R16 | Rattus norvegicus | 42% | 100% |
Q5R909 | Pongo abelii | 43% | 100% |
Q5RBV0 | Pongo abelii | 41% | 100% |
Q5ZML1 | Gallus gallus | 42% | 100% |
Q60960 | Mus musculus | 42% | 100% |
Q71VM4 | Oryza sativa subsp. japonica | 41% | 100% |
Q76P29 | Dictyostelium discoideum | 38% | 100% |
Q96321 | Arabidopsis thaliana | 42% | 100% |
Q9FJ09 | Arabidopsis thaliana | 41% | 100% |
Q9FJ92 | Arabidopsis thaliana | 37% | 100% |
Q9FWY7 | Arabidopsis thaliana | 41% | 100% |
Q9FYP9 | Oryza sativa subsp. japonica | 26% | 100% |
Q9M9X7 | Arabidopsis thaliana | 38% | 100% |
Q9SLX0 | Oryza sativa subsp. japonica | 42% | 100% |
V5B924 | Trypanosoma cruzi | 52% | 100% |