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: 7 |
NetGPI | no | yes: 0, no: 7 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005643 | nuclear pore | 3 | 8 |
GO:0032991 | protein-containing complex | 1 | 8 |
GO:0044613 | nuclear pore central transport channel | 3 | 2 |
GO:0140513 | nuclear protein-containing complex | 2 | 8 |
Related structures:
AlphaFold database: Q4Q5W9
Term | Name | Level | Count |
---|---|---|---|
GO:0006606 | protein import into nucleus | 5 | 2 |
GO:0006607 | NLS-bearing protein import into nucleus | 6 | 2 |
GO:0006810 | transport | 3 | 2 |
GO:0006886 | intracellular protein transport | 4 | 2 |
GO:0006913 | nucleocytoplasmic transport | 5 | 2 |
GO:0006996 | organelle organization | 4 | 2 |
GO:0006997 | nucleus organization | 5 | 2 |
GO:0006999 | nuclear pore organization | 5 | 2 |
GO:0008104 | protein localization | 4 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0015031 | protein transport | 4 | 2 |
GO:0016043 | cellular component organization | 3 | 2 |
GO:0033036 | macromolecule localization | 2 | 2 |
GO:0033365 | protein localization to organelle | 5 | 2 |
GO:0034504 | protein localization to nucleus | 6 | 2 |
GO:0036228 | protein localization to nuclear inner membrane | 5 | 2 |
GO:0043933 | protein-containing complex organization | 4 | 2 |
GO:0045184 | establishment of protein localization | 3 | 2 |
GO:0046907 | intracellular transport | 3 | 2 |
GO:0051169 | nuclear transport | 4 | 2 |
GO:0051170 | import into nucleus | 6 | 2 |
GO:0051179 | localization | 1 | 2 |
GO:0051234 | establishment of localization | 2 | 2 |
GO:0051641 | cellular localization | 2 | 2 |
GO:0051649 | establishment of localization in cell | 3 | 2 |
GO:0051668 | localization within membrane | 3 | 2 |
GO:0070727 | cellular macromolecule localization | 3 | 2 |
GO:0071702 | organic substance transport | 4 | 2 |
GO:0071705 | nitrogen compound transport | 4 | 2 |
GO:0071840 | cellular component organization or biogenesis | 2 | 2 |
GO:0072594 | establishment of protein localization to organelle | 4 | 2 |
GO:0072657 | protein localization to membrane | 4 | 2 |
GO:0090435 | protein localization to nuclear envelope | 7 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005198 | structural molecule activity | 1 | 2 |
GO:0017056 | structural constituent of nuclear pore | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 279 | 281 | PF00675 | 0.414 |
CLV_NRD_NRD_1 | 314 | 316 | PF00675 | 0.382 |
CLV_NRD_NRD_1 | 341 | 343 | PF00675 | 0.370 |
CLV_NRD_NRD_1 | 360 | 362 | PF00675 | 0.148 |
CLV_PCSK_KEX2_1 | 279 | 281 | PF00082 | 0.367 |
CLV_PCSK_KEX2_1 | 314 | 316 | PF00082 | 0.382 |
CLV_PCSK_KEX2_1 | 341 | 343 | PF00082 | 0.370 |
CLV_PCSK_SKI1_1 | 293 | 297 | PF00082 | 0.316 |
CLV_PCSK_SKI1_1 | 361 | 365 | PF00082 | 0.354 |
CLV_PCSK_SKI1_1 | 378 | 382 | PF00082 | 0.298 |
CLV_Separin_Metazoa | 276 | 280 | PF03568 | 0.310 |
CLV_Separin_Metazoa | 338 | 342 | PF03568 | 0.361 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.662 |
DEG_SPOP_SBC_1 | 61 | 65 | PF00917 | 0.498 |
DOC_MAPK_DCC_7 | 265 | 273 | PF00069 | 0.329 |
DOC_MAPK_gen_1 | 279 | 290 | PF00069 | 0.380 |
DOC_PP2B_LxvP_1 | 364 | 367 | PF13499 | 0.340 |
DOC_PP4_FxxP_1 | 142 | 145 | PF00568 | 0.753 |
DOC_PP4_FxxP_1 | 18 | 21 | PF00568 | 0.500 |
DOC_PP4_FxxP_1 | 59 | 62 | PF00568 | 0.632 |
DOC_USP7_MATH_1 | 192 | 196 | PF00917 | 0.502 |
DOC_USP7_MATH_1 | 466 | 470 | PF00917 | 0.491 |
DOC_USP7_MATH_1 | 60 | 64 | PF00917 | 0.566 |
DOC_USP7_UBL2_3 | 289 | 293 | PF12436 | 0.310 |
DOC_USP7_UBL2_3 | 458 | 462 | PF12436 | 0.468 |
DOC_WW_Pin1_4 | 266 | 271 | PF00397 | 0.330 |
DOC_WW_Pin1_4 | 49 | 54 | PF00397 | 0.616 |
LIG_14-3-3_CanoR_1 | 193 | 201 | PF00244 | 0.472 |
LIG_14-3-3_CanoR_1 | 329 | 334 | PF00244 | 0.360 |
LIG_14-3-3_CanoR_1 | 342 | 352 | PF00244 | 0.419 |
LIG_14-3-3_CanoR_1 | 369 | 377 | PF00244 | 0.349 |
LIG_14-3-3_CanoR_1 | 378 | 388 | PF00244 | 0.398 |
LIG_Clathr_ClatBox_1 | 201 | 205 | PF01394 | 0.396 |
LIG_deltaCOP1_diTrp_1 | 438 | 442 | PF00928 | 0.415 |
LIG_EVH1_2 | 21 | 25 | PF00568 | 0.483 |
LIG_FHA_1 | 183 | 189 | PF00498 | 0.605 |
LIG_FHA_1 | 238 | 244 | PF00498 | 0.501 |
LIG_FHA_1 | 25 | 31 | PF00498 | 0.650 |
LIG_FHA_1 | 294 | 300 | PF00498 | 0.384 |
LIG_FHA_2 | 185 | 191 | PF00498 | 0.594 |
LIG_FHA_2 | 427 | 433 | PF00498 | 0.394 |
LIG_FHA_2 | 450 | 456 | PF00498 | 0.429 |
LIG_LIR_Apic_2 | 139 | 145 | PF02991 | 0.632 |
LIG_LIR_Gen_1 | 205 | 213 | PF02991 | 0.388 |
LIG_LIR_Gen_1 | 438 | 446 | PF02991 | 0.395 |
LIG_LIR_Nem_3 | 205 | 211 | PF02991 | 0.389 |
LIG_LIR_Nem_3 | 438 | 442 | PF02991 | 0.415 |
LIG_NRBOX | 359 | 365 | PF00104 | 0.460 |
LIG_NRBOX | 452 | 458 | PF00104 | 0.457 |
LIG_PCNA_PIPBox_1 | 194 | 203 | PF02747 | 0.400 |
LIG_PCNA_yPIPBox_3 | 193 | 201 | PF02747 | 0.472 |
LIG_PCNA_yPIPBox_3 | 285 | 299 | PF02747 | 0.310 |
LIG_Pex14_2 | 55 | 59 | PF04695 | 0.632 |
LIG_SH2_CRK | 208 | 212 | PF00017 | 0.393 |
LIG_SH2_CRK | 331 | 335 | PF00017 | 0.340 |
LIG_SH2_STAP1 | 239 | 243 | PF00017 | 0.507 |
LIG_SH2_STAT5 | 200 | 203 | PF00017 | 0.397 |
LIG_SH2_STAT5 | 239 | 242 | PF00017 | 0.504 |
LIG_SH2_STAT5 | 434 | 437 | PF00017 | 0.356 |
LIG_SH3_3 | 173 | 179 | PF00018 | 0.803 |
LIG_SUMO_SIM_par_1 | 184 | 190 | PF11976 | 0.656 |
MOD_CK1_1 | 112 | 118 | PF00069 | 0.428 |
MOD_CK1_1 | 137 | 143 | PF00069 | 0.604 |
MOD_CK1_1 | 28 | 34 | PF00069 | 0.574 |
MOD_CK1_1 | 63 | 69 | PF00069 | 0.587 |
MOD_CK1_1 | 78 | 84 | PF00069 | 0.667 |
MOD_CK1_1 | 95 | 101 | PF00069 | 0.591 |
MOD_CK2_1 | 343 | 349 | PF00069 | 0.361 |
MOD_CK2_1 | 352 | 358 | PF00069 | 0.265 |
MOD_CK2_1 | 449 | 455 | PF00069 | 0.433 |
MOD_CK2_1 | 466 | 472 | PF00069 | 0.356 |
MOD_GlcNHglycan | 111 | 114 | PF01048 | 0.438 |
MOD_GlcNHglycan | 131 | 134 | PF01048 | 0.537 |
MOD_GlcNHglycan | 136 | 139 | PF01048 | 0.606 |
MOD_GlcNHglycan | 194 | 197 | PF01048 | 0.500 |
MOD_GlcNHglycan | 27 | 30 | PF01048 | 0.507 |
MOD_GlcNHglycan | 394 | 397 | PF01048 | 0.498 |
MOD_GlcNHglycan | 412 | 415 | PF01048 | 0.525 |
MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.522 |
MOD_GlcNHglycan | 72 | 75 | PF01048 | 0.538 |
MOD_GlcNHglycan | 77 | 80 | PF01048 | 0.484 |
MOD_GlcNHglycan | 94 | 97 | PF01048 | 0.457 |
MOD_GSK3_1 | 108 | 115 | PF00069 | 0.642 |
MOD_GSK3_1 | 192 | 199 | PF00069 | 0.489 |
MOD_GSK3_1 | 21 | 28 | PF00069 | 0.601 |
MOD_GSK3_1 | 368 | 375 | PF00069 | 0.427 |
MOD_GSK3_1 | 379 | 386 | PF00069 | 0.400 |
MOD_GSK3_1 | 392 | 399 | PF00069 | 0.414 |
MOD_GSK3_1 | 70 | 77 | PF00069 | 0.637 |
MOD_GSK3_1 | 91 | 98 | PF00069 | 0.684 |
MOD_N-GLC_1 | 33 | 38 | PF02516 | 0.639 |
MOD_N-GLC_1 | 396 | 401 | PF02516 | 0.562 |
MOD_N-GLC_2 | 223 | 225 | PF02516 | 0.362 |
MOD_NEK2_1 | 109 | 114 | PF00069 | 0.436 |
MOD_NEK2_1 | 134 | 139 | PF00069 | 0.587 |
MOD_NEK2_1 | 204 | 209 | PF00069 | 0.466 |
MOD_NEK2_1 | 25 | 30 | PF00069 | 0.649 |
MOD_NEK2_1 | 352 | 357 | PF00069 | 0.382 |
MOD_NEK2_1 | 410 | 415 | PF00069 | 0.746 |
MOD_NEK2_1 | 75 | 80 | PF00069 | 0.593 |
MOD_NEK2_1 | 92 | 97 | PF00069 | 0.455 |
MOD_PIKK_1 | 271 | 277 | PF00454 | 0.361 |
MOD_PIKK_1 | 368 | 374 | PF00454 | 0.468 |
MOD_PIKK_1 | 389 | 395 | PF00454 | 0.494 |
MOD_PIKK_1 | 420 | 426 | PF00454 | 0.465 |
MOD_PKA_1 | 293 | 299 | PF00069 | 0.323 |
MOD_PKA_2 | 192 | 198 | PF00069 | 0.482 |
MOD_PKA_2 | 237 | 243 | PF00069 | 0.499 |
MOD_PKA_2 | 278 | 284 | PF00069 | 0.361 |
MOD_PKA_2 | 368 | 374 | PF00069 | 0.335 |
MOD_Plk_1 | 204 | 210 | PF00069 | 0.467 |
MOD_Plk_1 | 383 | 389 | PF00069 | 0.466 |
MOD_Plk_4 | 196 | 202 | PF00069 | 0.467 |
MOD_Plk_4 | 329 | 335 | PF00069 | 0.299 |
MOD_ProDKin_1 | 266 | 272 | PF00069 | 0.330 |
MOD_ProDKin_1 | 49 | 55 | PF00069 | 0.619 |
MOD_SUMO_rev_2 | 455 | 464 | PF00179 | 0.467 |
TRG_DiLeu_BaEn_2 | 375 | 381 | PF01217 | 0.340 |
TRG_DiLeu_BaLyEn_6 | 422 | 427 | PF01217 | 0.589 |
TRG_ENDOCYTIC_2 | 208 | 211 | PF00928 | 0.398 |
TRG_ENDOCYTIC_2 | 331 | 334 | PF00928 | 0.320 |
TRG_ER_diArg_1 | 278 | 280 | PF00400 | 0.400 |
TRG_ER_diArg_1 | 313 | 315 | PF00400 | 0.396 |
TRG_ER_diArg_1 | 340 | 342 | PF00400 | 0.392 |
TRG_ER_diArg_1 | 467 | 470 | PF00400 | 0.476 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0S4JWT3 | Bodo saltans | 34% | 100% |
A0A3Q8ICT1 | Leishmania donovani | 86% | 100% |
A0A3R7KYW1 | Trypanosoma rangeli | 42% | 100% |
A4HJS8 | Leishmania braziliensis | 74% | 100% |
A4I794 | Leishmania infantum | 94% | 100% |
E9B289 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 100% |
P48837 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 23% | 88% |