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: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 4 |
GO:0043226 | organelle | 2 | 4 |
GO:0043227 | membrane-bounded organelle | 3 | 4 |
GO:0043229 | intracellular organelle | 3 | 4 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 4 |
GO:0110165 | cellular anatomical entity | 1 | 4 |
Related structures:
AlphaFold database: E9AVN3
Term | Name | Level | Count |
---|---|---|---|
GO:0006405 | RNA export from nucleus | 5 | 1 |
GO:0006406 | mRNA export from nucleus | 6 | 1 |
GO:0006810 | transport | 3 | 1 |
GO:0006913 | nucleocytoplasmic transport | 5 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0015931 | nucleobase-containing compound transport | 5 | 1 |
GO:0016973 | poly(A)+ mRNA export from nucleus | 7 | 1 |
GO:0046907 | intracellular transport | 3 | 1 |
GO:0050657 | nucleic acid transport | 6 | 1 |
GO:0050658 | RNA transport | 4 | 1 |
GO:0051028 | mRNA transport | 5 | 1 |
GO:0051168 | nuclear export | 6 | 1 |
GO:0051169 | nuclear transport | 4 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0051236 | establishment of RNA localization | 3 | 1 |
GO:0051641 | cellular localization | 2 | 1 |
GO:0051649 | establishment of localization in cell | 3 | 1 |
GO:0071702 | organic substance transport | 4 | 1 |
GO:0071705 | nitrogen compound transport | 4 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 101 | 105 | PF00656 | 0.585 |
CLV_C14_Caspase3-7 | 221 | 225 | PF00656 | 0.506 |
CLV_C14_Caspase3-7 | 234 | 238 | PF00656 | 0.551 |
CLV_C14_Caspase3-7 | 409 | 413 | PF00656 | 0.494 |
CLV_C14_Caspase3-7 | 84 | 88 | PF00656 | 0.659 |
CLV_NRD_NRD_1 | 192 | 194 | PF00675 | 0.637 |
CLV_NRD_NRD_1 | 267 | 269 | PF00675 | 0.653 |
CLV_NRD_NRD_1 | 404 | 406 | PF00675 | 0.541 |
CLV_PCSK_KEX2_1 | 142 | 144 | PF00082 | 0.460 |
CLV_PCSK_KEX2_1 | 146 | 148 | PF00082 | 0.448 |
CLV_PCSK_KEX2_1 | 150 | 152 | PF00082 | 0.410 |
CLV_PCSK_KEX2_1 | 192 | 194 | PF00082 | 0.575 |
CLV_PCSK_KEX2_1 | 404 | 406 | PF00082 | 0.580 |
CLV_PCSK_PC1ET2_1 | 142 | 144 | PF00082 | 0.459 |
CLV_PCSK_PC1ET2_1 | 146 | 148 | PF00082 | 0.435 |
CLV_PCSK_PC1ET2_1 | 150 | 152 | PF00082 | 0.389 |
CLV_PCSK_SKI1_1 | 139 | 143 | PF00082 | 0.494 |
CLV_PCSK_SKI1_1 | 248 | 252 | PF00082 | 0.559 |
CLV_PCSK_SKI1_1 | 260 | 264 | PF00082 | 0.622 |
CLV_PCSK_SKI1_1 | 311 | 315 | PF00082 | 0.434 |
DEG_APCC_DBOX_1 | 310 | 318 | PF00400 | 0.420 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.704 |
DOC_CYCLIN_yCln2_LP_2 | 229 | 235 | PF00134 | 0.629 |
DOC_MAPK_MEF2A_6 | 358 | 366 | PF00069 | 0.338 |
DOC_PP4_FxxP_1 | 472 | 475 | PF00568 | 0.615 |
DOC_USP7_MATH_1 | 115 | 119 | PF00917 | 0.582 |
DOC_USP7_MATH_1 | 313 | 317 | PF00917 | 0.528 |
DOC_USP7_MATH_1 | 74 | 78 | PF00917 | 0.809 |
DOC_USP7_UBL2_3 | 138 | 142 | PF12436 | 0.430 |
DOC_USP7_UBL2_3 | 146 | 150 | PF12436 | 0.418 |
DOC_USP7_UBL2_3 | 163 | 167 | PF12436 | 0.525 |
DOC_USP7_UBL2_3 | 171 | 175 | PF12436 | 0.580 |
DOC_USP7_UBL2_3 | 176 | 180 | PF12436 | 0.558 |
DOC_USP7_UBL2_3 | 195 | 199 | PF12436 | 0.706 |
DOC_USP7_UBL2_3 | 260 | 264 | PF12436 | 0.579 |
DOC_USP7_UBL2_3 | 443 | 447 | PF12436 | 0.655 |
DOC_USP7_UBL2_3 | 470 | 474 | PF12436 | 0.458 |
DOC_WW_Pin1_4 | 453 | 458 | PF00397 | 0.629 |
LIG_14-3-3_CanoR_1 | 268 | 278 | PF00244 | 0.513 |
LIG_14-3-3_CanoR_1 | 300 | 304 | PF00244 | 0.533 |
LIG_14-3-3_CanoR_1 | 358 | 366 | PF00244 | 0.414 |
LIG_14-3-3_CanoR_1 | 58 | 62 | PF00244 | 0.422 |
LIG_Actin_WH2_2 | 239 | 254 | PF00022 | 0.577 |
LIG_APCC_ABBA_1 | 15 | 20 | PF00400 | 0.618 |
LIG_BRCT_BRCA1_1 | 464 | 468 | PF00533 | 0.559 |
LIG_BRCT_BRCA1_2 | 464 | 470 | PF00533 | 0.508 |
LIG_eIF4E_1 | 326 | 332 | PF01652 | 0.424 |
LIG_FHA_1 | 128 | 134 | PF00498 | 0.399 |
LIG_FHA_1 | 357 | 363 | PF00498 | 0.416 |
LIG_FHA_1 | 375 | 381 | PF00498 | 0.696 |
LIG_FHA_2 | 238 | 244 | PF00498 | 0.355 |
LIG_FHA_2 | 358 | 364 | PF00498 | 0.485 |
LIG_FHA_2 | 461 | 467 | PF00498 | 0.484 |
LIG_GBD_Chelix_1 | 278 | 286 | PF00786 | 0.479 |
LIG_LIR_Apic_2 | 471 | 475 | PF02991 | 0.595 |
LIG_LIR_Gen_1 | 211 | 220 | PF02991 | 0.623 |
LIG_LIR_Gen_1 | 422 | 431 | PF02991 | 0.529 |
LIG_LIR_Gen_1 | 456 | 462 | PF02991 | 0.628 |
LIG_LIR_Nem_3 | 339 | 345 | PF02991 | 0.403 |
LIG_LIR_Nem_3 | 381 | 386 | PF02991 | 0.492 |
LIG_LIR_Nem_3 | 422 | 427 | PF02991 | 0.500 |
LIG_LIR_Nem_3 | 456 | 461 | PF02991 | 0.631 |
LIG_LIR_Nem_3 | 481 | 486 | PF02991 | 0.536 |
LIG_NRP_CendR_1 | 515 | 516 | PF00754 | 0.697 |
LIG_Pex14_2 | 468 | 472 | PF04695 | 0.571 |
LIG_SH2_CRK | 483 | 487 | PF00017 | 0.641 |
LIG_SH2_STAT5 | 506 | 509 | PF00017 | 0.594 |
LIG_SH3_1 | 474 | 480 | PF00018 | 0.528 |
LIG_SH3_3 | 363 | 369 | PF00018 | 0.435 |
LIG_SH3_3 | 451 | 457 | PF00018 | 0.509 |
LIG_SH3_3 | 474 | 480 | PF00018 | 0.504 |
LIG_SH3_3 | 485 | 491 | PF00018 | 0.528 |
LIG_SUMO_SIM_anti_2 | 2 | 12 | PF11976 | 0.537 |
LIG_SUMO_SIM_anti_2 | 359 | 367 | PF11976 | 0.370 |
LIG_SUMO_SIM_par_1 | 128 | 137 | PF11976 | 0.550 |
LIG_TYR_ITSM | 479 | 486 | PF00017 | 0.584 |
LIG_UBA3_1 | 131 | 139 | PF00899 | 0.501 |
LIG_WRC_WIRS_1 | 421 | 426 | PF05994 | 0.496 |
MOD_CK1_1 | 169 | 175 | PF00069 | 0.656 |
MOD_CK1_1 | 21 | 27 | PF00069 | 0.657 |
MOD_CK1_1 | 429 | 435 | PF00069 | 0.693 |
MOD_CK1_1 | 49 | 55 | PF00069 | 0.732 |
MOD_CK2_1 | 106 | 112 | PF00069 | 0.769 |
MOD_CK2_1 | 117 | 123 | PF00069 | 0.592 |
MOD_CK2_1 | 237 | 243 | PF00069 | 0.499 |
MOD_CK2_1 | 268 | 274 | PF00069 | 0.578 |
MOD_CK2_1 | 453 | 459 | PF00069 | 0.536 |
MOD_CK2_1 | 460 | 466 | PF00069 | 0.469 |
MOD_Cter_Amidation | 144 | 147 | PF01082 | 0.547 |
MOD_Cter_Amidation | 190 | 193 | PF01082 | 0.571 |
MOD_GlcNHglycan | 108 | 111 | PF01048 | 0.698 |
MOD_GlcNHglycan | 117 | 120 | PF01048 | 0.596 |
MOD_GlcNHglycan | 189 | 192 | PF01048 | 0.735 |
MOD_GlcNHglycan | 25 | 28 | PF01048 | 0.683 |
MOD_GlcNHglycan | 271 | 274 | PF01048 | 0.577 |
MOD_GlcNHglycan | 297 | 300 | PF01048 | 0.456 |
MOD_GlcNHglycan | 34 | 37 | PF01048 | 0.611 |
MOD_GlcNHglycan | 428 | 431 | PF01048 | 0.489 |
MOD_GlcNHglycan | 46 | 51 | PF01048 | 0.764 |
MOD_GlcNHglycan | 499 | 502 | PF01048 | 0.632 |
MOD_GlcNHglycan | 76 | 79 | PF01048 | 0.784 |
MOD_GSK3_1 | 127 | 134 | PF00069 | 0.343 |
MOD_GSK3_1 | 154 | 161 | PF00069 | 0.549 |
MOD_GSK3_1 | 165 | 172 | PF00069 | 0.584 |
MOD_GSK3_1 | 21 | 28 | PF00069 | 0.676 |
MOD_GSK3_1 | 233 | 240 | PF00069 | 0.551 |
MOD_GSK3_1 | 251 | 258 | PF00069 | 0.544 |
MOD_GSK3_1 | 263 | 270 | PF00069 | 0.584 |
MOD_GSK3_1 | 295 | 302 | PF00069 | 0.432 |
MOD_GSK3_1 | 370 | 377 | PF00069 | 0.580 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.774 |
MOD_GSK3_1 | 422 | 429 | PF00069 | 0.501 |
MOD_GSK3_1 | 57 | 64 | PF00069 | 0.479 |
MOD_N-GLC_1 | 412 | 417 | PF02516 | 0.262 |
MOD_N-GLC_1 | 497 | 502 | PF02516 | 0.639 |
MOD_N-GLC_1 | 66 | 71 | PF02516 | 0.506 |
MOD_NEK2_1 | 131 | 136 | PF00069 | 0.504 |
MOD_NEK2_1 | 155 | 160 | PF00069 | 0.470 |
MOD_NEK2_1 | 251 | 256 | PF00069 | 0.629 |
MOD_NEK2_1 | 357 | 362 | PF00069 | 0.410 |
MOD_NEK2_1 | 370 | 375 | PF00069 | 0.518 |
MOD_NEK2_1 | 420 | 425 | PF00069 | 0.479 |
MOD_NEK2_1 | 468 | 473 | PF00069 | 0.610 |
MOD_NEK2_1 | 57 | 62 | PF00069 | 0.570 |
MOD_NEK2_2 | 208 | 213 | PF00069 | 0.597 |
MOD_PIKK_1 | 263 | 269 | PF00454 | 0.587 |
MOD_PIKK_1 | 34 | 40 | PF00454 | 0.531 |
MOD_PKA_1 | 187 | 193 | PF00069 | 0.689 |
MOD_PKA_1 | 195 | 201 | PF00069 | 0.708 |
MOD_PKA_1 | 263 | 269 | PF00069 | 0.546 |
MOD_PKA_2 | 251 | 257 | PF00069 | 0.486 |
MOD_PKA_2 | 267 | 273 | PF00069 | 0.593 |
MOD_PKA_2 | 299 | 305 | PF00069 | 0.539 |
MOD_PKA_2 | 357 | 363 | PF00069 | 0.348 |
MOD_PKA_2 | 57 | 63 | PF00069 | 0.635 |
MOD_Plk_1 | 127 | 133 | PF00069 | 0.408 |
MOD_Plk_1 | 21 | 27 | PF00069 | 0.470 |
MOD_Plk_1 | 3 | 9 | PF00069 | 0.658 |
MOD_Plk_1 | 338 | 344 | PF00069 | 0.315 |
MOD_Plk_1 | 378 | 384 | PF00069 | 0.606 |
MOD_Plk_1 | 407 | 413 | PF00069 | 0.512 |
MOD_Plk_2-3 | 66 | 72 | PF00069 | 0.609 |
MOD_Plk_4 | 127 | 133 | PF00069 | 0.481 |
MOD_Plk_4 | 208 | 214 | PF00069 | 0.598 |
MOD_Plk_4 | 3 | 9 | PF00069 | 0.675 |
MOD_Plk_4 | 313 | 319 | PF00069 | 0.489 |
MOD_Plk_4 | 338 | 344 | PF00069 | 0.320 |
MOD_Plk_4 | 468 | 474 | PF00069 | 0.518 |
MOD_ProDKin_1 | 453 | 459 | PF00069 | 0.627 |
MOD_SUMO_rev_2 | 134 | 141 | PF00179 | 0.495 |
MOD_SUMO_rev_2 | 408 | 415 | PF00179 | 0.283 |
MOD_SUMO_rev_2 | 433 | 442 | PF00179 | 0.656 |
TRG_DiLeu_BaEn_2 | 208 | 214 | PF01217 | 0.598 |
TRG_DiLeu_BaEn_3 | 2 | 8 | PF01217 | 0.696 |
TRG_DiLeu_BaEn_4 | 3 | 9 | PF01217 | 0.697 |
TRG_ENDOCYTIC_2 | 483 | 486 | PF00928 | 0.547 |
TRG_ER_diArg_1 | 403 | 405 | PF00400 | 0.560 |
TRG_ER_diArg_1 | 514 | 516 | PF00400 | 0.642 |
TRG_NLS_Bipartite_1 | 138 | 154 | PF00514 | 0.461 |
TRG_NLS_Bipartite_1 | 162 | 179 | PF00514 | 0.585 |
TRG_NLS_MonoCore_2 | 192 | 197 | PF00514 | 0.601 |
TRG_NLS_MonoExtC_3 | 149 | 154 | PF00514 | 0.398 |
TRG_NLS_MonoExtN_4 | 147 | 154 | PF00514 | 0.461 |
TRG_NLS_MonoExtN_4 | 192 | 198 | PF00514 | 0.607 |
TRG_Pf-PMV_PEXEL_1 | 290 | 294 | PF00026 | 0.490 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PAB7 | Leptomonas seymouri | 58% | 100% |
A0A3Q8IAL9 | Leishmania donovani | 88% | 100% |
A0A422N2J9 | Trypanosoma rangeli | 35% | 100% |
A4HC96 | Leishmania braziliensis | 74% | 98% |
A4HZS8 | Leishmania infantum | 88% | 100% |
C9ZRL3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
Q4QBU6 | Leishmania major | 87% | 99% |
V5BLH2 | Trypanosoma cruzi | 34% | 100% |