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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005643 | nuclear pore | 3 | 7 |
GO:0032991 | protein-containing complex | 1 | 7 |
GO:0140513 | nuclear protein-containing complex | 2 | 7 |
GO:0044613 | nuclear pore central transport channel | 3 | 1 |
Related structures:
AlphaFold database: A4HJS8
Term | Name | Level | Count |
---|---|---|---|
GO:0006606 | protein import into nucleus | 5 | 1 |
GO:0006607 | NLS-bearing protein import into nucleus | 6 | 1 |
GO:0006810 | transport | 3 | 1 |
GO:0006886 | intracellular protein transport | 4 | 1 |
GO:0006913 | nucleocytoplasmic transport | 5 | 1 |
GO:0006996 | organelle organization | 4 | 1 |
GO:0006997 | nucleus organization | 5 | 1 |
GO:0006999 | nuclear pore organization | 5 | 1 |
GO:0008104 | protein localization | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0015031 | protein transport | 4 | 1 |
GO:0016043 | cellular component organization | 3 | 1 |
GO:0033036 | macromolecule localization | 2 | 1 |
GO:0033365 | protein localization to organelle | 5 | 1 |
GO:0034504 | protein localization to nucleus | 6 | 1 |
GO:0036228 | protein localization to nuclear inner membrane | 5 | 1 |
GO:0043933 | protein-containing complex organization | 4 | 1 |
GO:0045184 | establishment of protein localization | 3 | 1 |
GO:0046907 | intracellular transport | 3 | 1 |
GO:0051169 | nuclear transport | 4 | 1 |
GO:0051170 | import into nucleus | 6 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0051641 | cellular localization | 2 | 1 |
GO:0051649 | establishment of localization in cell | 3 | 1 |
GO:0051668 | localization within membrane | 3 | 1 |
GO:0070727 | cellular macromolecule localization | 3 | 1 |
GO:0071702 | organic substance transport | 4 | 1 |
GO:0071705 | nitrogen compound transport | 4 | 1 |
GO:0071840 | cellular component organization or biogenesis | 2 | 1 |
GO:0072594 | establishment of protein localization to organelle | 4 | 1 |
GO:0072657 | protein localization to membrane | 4 | 1 |
GO:0090435 | protein localization to nuclear envelope | 7 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005198 | structural molecule activity | 1 | 1 |
GO:0017056 | structural constituent of nuclear pore | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 269 | 271 | PF00675 | 0.391 |
CLV_NRD_NRD_1 | 282 | 284 | PF00675 | 0.245 |
CLV_NRD_NRD_1 | 304 | 306 | PF00675 | 0.414 |
CLV_NRD_NRD_1 | 331 | 333 | PF00675 | 0.402 |
CLV_PCSK_KEX2_1 | 268 | 270 | PF00082 | 0.380 |
CLV_PCSK_KEX2_1 | 304 | 306 | PF00082 | 0.414 |
CLV_PCSK_KEX2_1 | 331 | 333 | PF00082 | 0.402 |
CLV_PCSK_SKI1_1 | 351 | 355 | PF00082 | 0.326 |
CLV_PCSK_SKI1_1 | 368 | 372 | PF00082 | 0.331 |
CLV_Separin_Metazoa | 328 | 332 | PF03568 | 0.388 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.720 |
DOC_MAPK_DCC_7 | 255 | 263 | PF00069 | 0.302 |
DOC_MAPK_gen_1 | 268 | 280 | PF00069 | 0.380 |
DOC_PP2B_LxvP_1 | 354 | 357 | PF13499 | 0.312 |
DOC_PP4_FxxP_1 | 125 | 128 | PF00568 | 0.662 |
DOC_PP4_FxxP_1 | 59 | 62 | PF00568 | 0.673 |
DOC_USP7_MATH_1 | 186 | 190 | PF00917 | 0.605 |
DOC_USP7_MATH_1 | 382 | 386 | PF00917 | 0.433 |
DOC_USP7_MATH_1 | 454 | 458 | PF00917 | 0.594 |
DOC_USP7_MATH_1 | 62 | 66 | PF00917 | 0.663 |
DOC_USP7_UBL2_3 | 446 | 450 | PF12436 | 0.495 |
DOC_WW_Pin1_4 | 247 | 252 | PF00397 | 0.327 |
DOC_WW_Pin1_4 | 256 | 261 | PF00397 | 0.303 |
DOC_WW_Pin1_4 | 49 | 54 | PF00397 | 0.673 |
DOC_WW_Pin1_4 | 70 | 75 | PF00397 | 0.625 |
LIG_14-3-3_CanoR_1 | 183 | 191 | PF00244 | 0.527 |
LIG_14-3-3_CanoR_1 | 319 | 324 | PF00244 | 0.316 |
LIG_14-3-3_CanoR_1 | 332 | 338 | PF00244 | 0.325 |
LIG_14-3-3_CanoR_1 | 359 | 367 | PF00244 | 0.377 |
LIG_14-3-3_CanoR_1 | 368 | 378 | PF00244 | 0.429 |
LIG_Clathr_ClatBox_1 | 191 | 195 | PF01394 | 0.433 |
LIG_deltaCOP1_diTrp_1 | 426 | 430 | PF00928 | 0.434 |
LIG_eIF4E_1 | 337 | 343 | PF01652 | 0.231 |
LIG_FHA_1 | 128 | 134 | PF00498 | 0.515 |
LIG_FHA_1 | 166 | 172 | PF00498 | 0.580 |
LIG_FHA_1 | 173 | 179 | PF00498 | 0.582 |
LIG_FHA_1 | 228 | 234 | PF00498 | 0.541 |
LIG_FHA_1 | 25 | 31 | PF00498 | 0.687 |
LIG_FHA_2 | 175 | 181 | PF00498 | 0.590 |
LIG_LIR_Apic_2 | 122 | 128 | PF02991 | 0.663 |
LIG_LIR_Apic_2 | 57 | 62 | PF02991 | 0.614 |
LIG_LIR_Gen_1 | 195 | 203 | PF02991 | 0.423 |
LIG_LIR_Gen_1 | 426 | 434 | PF02991 | 0.429 |
LIG_LIR_Nem_3 | 195 | 201 | PF02991 | 0.424 |
LIG_LIR_Nem_3 | 227 | 232 | PF02991 | 0.454 |
LIG_LIR_Nem_3 | 426 | 430 | PF02991 | 0.434 |
LIG_NRBOX | 349 | 355 | PF00104 | 0.388 |
LIG_NRBOX | 440 | 446 | PF00104 | 0.429 |
LIG_PCNA_PIPBox_1 | 184 | 193 | PF02747 | 0.439 |
LIG_PCNA_yPIPBox_3 | 183 | 191 | PF02747 | 0.527 |
LIG_Pex14_2 | 55 | 59 | PF04695 | 0.684 |
LIG_SH2_CRK | 198 | 202 | PF00017 | 0.426 |
LIG_SH2_CRK | 321 | 325 | PF00017 | 0.312 |
LIG_SH2_CRK | 360 | 364 | PF00017 | 0.231 |
LIG_SH2_GRB2like | 232 | 235 | PF00017 | 0.533 |
LIG_SH2_SRC | 232 | 235 | PF00017 | 0.485 |
LIG_SH2_STAP1 | 229 | 233 | PF00017 | 0.560 |
LIG_SH2_STAP1 | 360 | 364 | PF00017 | 0.231 |
LIG_SH2_STAT5 | 190 | 193 | PF00017 | 0.433 |
LIG_SH2_STAT5 | 229 | 232 | PF00017 | 0.547 |
LIG_SH3_3 | 156 | 162 | PF00018 | 0.704 |
LIG_SUMO_SIM_anti_2 | 313 | 318 | PF11976 | 0.334 |
LIG_SUMO_SIM_par_1 | 174 | 180 | PF11976 | 0.600 |
MOD_CK1_1 | 87 | 93 | PF00069 | 0.700 |
MOD_CK2_1 | 333 | 339 | PF00069 | 0.388 |
MOD_CK2_1 | 342 | 348 | PF00069 | 0.296 |
MOD_CK2_1 | 454 | 460 | PF00069 | 0.392 |
MOD_GlcNHglycan | 112 | 115 | PF01048 | 0.727 |
MOD_GlcNHglycan | 122 | 125 | PF01048 | 0.595 |
MOD_GlcNHglycan | 136 | 139 | PF01048 | 0.529 |
MOD_GlcNHglycan | 184 | 187 | PF01048 | 0.585 |
MOD_GlcNHglycan | 384 | 387 | PF01048 | 0.583 |
MOD_GlcNHglycan | 407 | 410 | PF01048 | 0.528 |
MOD_GlcNHglycan | 64 | 67 | PF01048 | 0.626 |
MOD_GlcNHglycan | 70 | 73 | PF01048 | 0.608 |
MOD_GlcNHglycan | 82 | 85 | PF01048 | 0.552 |
MOD_GlcNHglycan | 86 | 89 | PF01048 | 0.609 |
MOD_GSK3_1 | 116 | 123 | PF00069 | 0.664 |
MOD_GSK3_1 | 182 | 189 | PF00069 | 0.560 |
MOD_GSK3_1 | 2 | 9 | PF00069 | 0.527 |
MOD_GSK3_1 | 21 | 28 | PF00069 | 0.592 |
MOD_GSK3_1 | 32 | 39 | PF00069 | 0.656 |
MOD_GSK3_1 | 338 | 345 | PF00069 | 0.234 |
MOD_GSK3_1 | 369 | 376 | PF00069 | 0.432 |
MOD_GSK3_1 | 382 | 389 | PF00069 | 0.460 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.620 |
MOD_GSK3_1 | 80 | 87 | PF00069 | 0.612 |
MOD_N-GLC_1 | 33 | 38 | PF02516 | 0.694 |
MOD_N-GLC_1 | 386 | 391 | PF02516 | 0.609 |
MOD_N-GLC_2 | 213 | 215 | PF02516 | 0.406 |
MOD_NEK2_1 | 194 | 199 | PF00069 | 0.495 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.593 |
MOD_NEK2_1 | 25 | 30 | PF00069 | 0.686 |
MOD_NEK2_1 | 342 | 347 | PF00069 | 0.388 |
MOD_PIKK_1 | 261 | 267 | PF00454 | 0.418 |
MOD_PIKK_1 | 358 | 364 | PF00454 | 0.378 |
MOD_PKA_1 | 268 | 274 | PF00069 | 0.270 |
MOD_PKA_2 | 182 | 188 | PF00069 | 0.537 |
MOD_PKA_2 | 227 | 233 | PF00069 | 0.517 |
MOD_PKA_2 | 268 | 274 | PF00069 | 0.388 |
MOD_PKA_2 | 358 | 364 | PF00069 | 0.364 |
MOD_Plk_1 | 194 | 200 | PF00069 | 0.496 |
MOD_Plk_1 | 338 | 344 | PF00069 | 0.231 |
MOD_Plk_1 | 373 | 379 | PF00069 | 0.571 |
MOD_Plk_4 | 186 | 192 | PF00069 | 0.507 |
MOD_Plk_4 | 319 | 325 | PF00069 | 0.312 |
MOD_Plk_4 | 338 | 344 | PF00069 | 0.312 |
MOD_Plk_4 | 6 | 12 | PF00069 | 0.502 |
MOD_ProDKin_1 | 247 | 253 | PF00069 | 0.327 |
MOD_ProDKin_1 | 256 | 262 | PF00069 | 0.303 |
MOD_ProDKin_1 | 49 | 55 | PF00069 | 0.677 |
MOD_ProDKin_1 | 70 | 76 | PF00069 | 0.625 |
MOD_SUMO_rev_2 | 442 | 452 | PF00179 | 0.494 |
TRG_DiLeu_BaEn_2 | 365 | 371 | PF01217 | 0.435 |
TRG_DiLeu_BaLyEn_6 | 410 | 415 | PF01217 | 0.587 |
TRG_ENDOCYTIC_2 | 198 | 201 | PF00928 | 0.432 |
TRG_ENDOCYTIC_2 | 321 | 324 | PF00928 | 0.312 |
TRG_ENDOCYTIC_2 | 360 | 363 | PF00928 | 0.231 |
TRG_ER_diArg_1 | 267 | 270 | PF00400 | 0.471 |
TRG_ER_diArg_1 | 303 | 305 | PF00400 | 0.428 |
TRG_ER_diArg_1 | 330 | 332 | PF00400 | 0.391 |
TRG_ER_diArg_1 | 455 | 458 | PF00400 | 0.452 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8ICT1 | Leishmania donovani | 79% | 100% |
A0A3R7KYW1 | Trypanosoma rangeli | 40% | 100% |
A4I794 | Leishmania infantum | 79% | 100% |
E9B289 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 75% | 100% |
Q4Q5W9 | Leishmania major | 74% | 99% |