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: 12 |
NetGPI | no | yes: 0, no: 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 1 |
GO:0005730 | nucleolus | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043228 | non-membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A4H481
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 1 |
GO:0006364 | rRNA processing | 8 | 1 |
GO:0006396 | RNA processing | 6 | 1 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016070 | RNA metabolic process | 5 | 1 |
GO:0016072 | rRNA metabolic process | 7 | 1 |
GO:0034470 | ncRNA processing | 7 | 1 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 1 |
GO:0034660 | ncRNA metabolic process | 6 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0046483 | heterocycle metabolic process | 3 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0090304 | nucleic acid metabolic process | 4 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 13 |
GO:0003676 | nucleic acid binding | 3 | 13 |
GO:0003724 | RNA helicase activity | 3 | 13 |
GO:0003743 | translation initiation factor activity | 4 | 13 |
GO:0003824 | catalytic activity | 1 | 13 |
GO:0004386 | helicase activity | 2 | 13 |
GO:0005488 | binding | 1 | 13 |
GO:0005524 | ATP binding | 5 | 13 |
GO:0008135 | translation factor activity, RNA binding | 3 | 13 |
GO:0008186 | ATP-dependent activity, acting on RNA | 2 | 13 |
GO:0016787 | hydrolase activity | 2 | 13 |
GO:0017076 | purine nucleotide binding | 4 | 13 |
GO:0030554 | adenyl nucleotide binding | 5 | 13 |
GO:0032553 | ribonucleotide binding | 3 | 13 |
GO:0032555 | purine ribonucleotide binding | 4 | 13 |
GO:0032559 | adenyl ribonucleotide binding | 5 | 13 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 13 |
GO:0036094 | small molecule binding | 2 | 13 |
GO:0043167 | ion binding | 2 | 13 |
GO:0043168 | anion binding | 3 | 13 |
GO:0045182 | translation regulator activity | 1 | 13 |
GO:0090079 | translation regulator activity, nucleic acid binding | 2 | 13 |
GO:0097159 | organic cyclic compound binding | 2 | 13 |
GO:0097367 | carbohydrate derivative binding | 2 | 13 |
GO:0140098 | catalytic activity, acting on RNA | 3 | 13 |
GO:0140640 | catalytic activity, acting on a nucleic acid | 2 | 13 |
GO:0140657 | ATP-dependent activity | 1 | 13 |
GO:1901265 | nucleoside phosphate binding | 3 | 13 |
GO:1901363 | heterocyclic compound binding | 2 | 13 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 112 | 116 | PF00656 | 0.476 |
CLV_NRD_NRD_1 | 182 | 184 | PF00675 | 0.187 |
CLV_NRD_NRD_1 | 205 | 207 | PF00675 | 0.689 |
CLV_NRD_NRD_1 | 29 | 31 | PF00675 | 0.167 |
CLV_NRD_NRD_1 | 505 | 507 | PF00675 | 0.535 |
CLV_NRD_NRD_1 | 533 | 535 | PF00675 | 0.595 |
CLV_NRD_NRD_1 | 600 | 602 | PF00675 | 0.606 |
CLV_NRD_NRD_1 | 622 | 624 | PF00675 | 0.716 |
CLV_PCSK_FUR_1 | 531 | 535 | PF00082 | 0.718 |
CLV_PCSK_FUR_1 | 558 | 562 | PF00082 | 0.606 |
CLV_PCSK_KEX2_1 | 182 | 184 | PF00082 | 0.182 |
CLV_PCSK_KEX2_1 | 205 | 207 | PF00082 | 0.689 |
CLV_PCSK_KEX2_1 | 448 | 450 | PF00082 | 0.257 |
CLV_PCSK_KEX2_1 | 533 | 535 | PF00082 | 0.574 |
CLV_PCSK_KEX2_1 | 560 | 562 | PF00082 | 0.745 |
CLV_PCSK_KEX2_1 | 600 | 602 | PF00082 | 0.579 |
CLV_PCSK_KEX2_1 | 624 | 626 | PF00082 | 0.760 |
CLV_PCSK_PC1ET2_1 | 448 | 450 | PF00082 | 0.294 |
CLV_PCSK_PC1ET2_1 | 560 | 562 | PF00082 | 0.693 |
CLV_PCSK_PC1ET2_1 | 624 | 626 | PF00082 | 0.760 |
CLV_PCSK_PC7_1 | 556 | 562 | PF00082 | 0.493 |
CLV_PCSK_SKI1_1 | 100 | 104 | PF00082 | 0.260 |
CLV_PCSK_SKI1_1 | 132 | 136 | PF00082 | 0.236 |
CLV_PCSK_SKI1_1 | 170 | 174 | PF00082 | 0.267 |
CLV_PCSK_SKI1_1 | 182 | 186 | PF00082 | 0.199 |
CLV_PCSK_SKI1_1 | 624 | 628 | PF00082 | 0.667 |
CLV_Separin_Metazoa | 349 | 353 | PF03568 | 0.428 |
DEG_APCC_DBOX_1 | 169 | 177 | PF00400 | 0.350 |
DEG_APCC_DBOX_1 | 346 | 354 | PF00400 | 0.431 |
DEG_SCF_FBW7_2 | 74 | 81 | PF00400 | 0.417 |
DEG_SPOP_SBC_1 | 297 | 301 | PF00917 | 0.606 |
DOC_CDC14_PxL_1 | 319 | 327 | PF14671 | 0.397 |
DOC_CKS1_1 | 22 | 27 | PF01111 | 0.493 |
DOC_CKS1_1 | 75 | 80 | PF01111 | 0.417 |
DOC_CYCLIN_RxL_1 | 129 | 137 | PF00134 | 0.448 |
DOC_CYCLIN_RxL_1 | 144 | 158 | PF00134 | 0.407 |
DOC_CYCLIN_RxL_1 | 179 | 190 | PF00134 | 0.423 |
DOC_CYCLIN_yCln2_LP_2 | 175 | 178 | PF00134 | 0.483 |
DOC_MAPK_DCC_7 | 397 | 406 | PF00069 | 0.428 |
DOC_MAPK_gen_1 | 179 | 187 | PF00069 | 0.450 |
DOC_MAPK_gen_1 | 428 | 438 | PF00069 | 0.495 |
DOC_MAPK_HePTP_8 | 394 | 406 | PF00069 | 0.428 |
DOC_MAPK_MEF2A_6 | 347 | 355 | PF00069 | 0.417 |
DOC_MAPK_MEF2A_6 | 397 | 406 | PF00069 | 0.428 |
DOC_MAPK_MEF2A_6 | 486 | 493 | PF00069 | 0.308 |
DOC_PP1_RVXF_1 | 181 | 188 | PF00149 | 0.391 |
DOC_PP2B_LxvP_1 | 175 | 178 | PF13499 | 0.461 |
DOC_PP2B_LxvP_1 | 198 | 201 | PF13499 | 0.587 |
DOC_PP2B_LxvP_1 | 314 | 317 | PF13499 | 0.333 |
DOC_PP2B_LxvP_1 | 399 | 402 | PF13499 | 0.417 |
DOC_PP4_FxxP_1 | 226 | 229 | PF00568 | 0.480 |
DOC_PP4_FxxP_1 | 303 | 306 | PF00568 | 0.551 |
DOC_PP4_FxxP_1 | 56 | 59 | PF00568 | 0.433 |
DOC_PP4_FxxP_1 | 93 | 96 | PF00568 | 0.483 |
DOC_USP7_MATH_1 | 140 | 144 | PF00917 | 0.350 |
DOC_USP7_MATH_1 | 208 | 212 | PF00917 | 0.606 |
DOC_USP7_MATH_1 | 222 | 226 | PF00917 | 0.507 |
DOC_USP7_MATH_1 | 233 | 237 | PF00917 | 0.455 |
DOC_USP7_MATH_1 | 275 | 279 | PF00917 | 0.663 |
DOC_USP7_MATH_1 | 297 | 301 | PF00917 | 0.643 |
DOC_USP7_MATH_1 | 361 | 365 | PF00917 | 0.417 |
DOC_USP7_MATH_1 | 402 | 406 | PF00917 | 0.558 |
DOC_USP7_MATH_1 | 466 | 470 | PF00917 | 0.438 |
DOC_USP7_MATH_1 | 47 | 51 | PF00917 | 0.428 |
DOC_USP7_MATH_1 | 520 | 524 | PF00917 | 0.506 |
DOC_USP7_MATH_1 | 538 | 542 | PF00917 | 0.724 |
DOC_USP7_MATH_1 | 596 | 600 | PF00917 | 0.614 |
DOC_USP7_UBL2_3 | 482 | 486 | PF12436 | 0.280 |
DOC_USP7_UBL2_3 | 624 | 628 | PF12436 | 0.627 |
DOC_WW_Pin1_4 | 124 | 129 | PF00397 | 0.416 |
DOC_WW_Pin1_4 | 21 | 26 | PF00397 | 0.365 |
DOC_WW_Pin1_4 | 218 | 223 | PF00397 | 0.584 |
DOC_WW_Pin1_4 | 224 | 229 | PF00397 | 0.620 |
DOC_WW_Pin1_4 | 460 | 465 | PF00397 | 0.503 |
DOC_WW_Pin1_4 | 571 | 576 | PF00397 | 0.487 |
DOC_WW_Pin1_4 | 609 | 614 | PF00397 | 0.735 |
DOC_WW_Pin1_4 | 617 | 622 | PF00397 | 0.769 |
DOC_WW_Pin1_4 | 74 | 79 | PF00397 | 0.417 |
LIG_14-3-3_CanoR_1 | 159 | 166 | PF00244 | 0.451 |
LIG_14-3-3_CanoR_1 | 194 | 199 | PF00244 | 0.536 |
LIG_14-3-3_CanoR_1 | 352 | 356 | PF00244 | 0.422 |
LIG_14-3-3_CanoR_1 | 457 | 461 | PF00244 | 0.415 |
LIG_14-3-3_CanoR_1 | 519 | 527 | PF00244 | 0.660 |
LIG_14-3-3_CanoR_1 | 558 | 566 | PF00244 | 0.661 |
LIG_APCC_ABBA_1 | 406 | 411 | PF00400 | 0.428 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.339 |
LIG_BIR_III_4 | 282 | 286 | PF00653 | 0.465 |
LIG_BIR_III_4 | 67 | 71 | PF00653 | 0.462 |
LIG_BRCT_BRCA1_1 | 142 | 146 | PF00533 | 0.350 |
LIG_BRCT_BRCA1_1 | 299 | 303 | PF00533 | 0.427 |
LIG_EH1_1 | 166 | 174 | PF00400 | 0.350 |
LIG_eIF4E_1 | 69 | 75 | PF01652 | 0.417 |
LIG_FHA_1 | 186 | 192 | PF00498 | 0.422 |
LIG_FHA_1 | 219 | 225 | PF00498 | 0.472 |
LIG_FHA_1 | 256 | 262 | PF00498 | 0.425 |
LIG_FHA_1 | 352 | 358 | PF00498 | 0.442 |
LIG_FHA_2 | 110 | 116 | PF00498 | 0.476 |
LIG_FHA_2 | 159 | 165 | PF00498 | 0.414 |
LIG_FHA_2 | 194 | 200 | PF00498 | 0.483 |
LIG_FHA_2 | 438 | 444 | PF00498 | 0.326 |
LIG_FHA_2 | 544 | 550 | PF00498 | 0.616 |
LIG_IRF3_LxIS_1 | 381 | 386 | PF10401 | 0.472 |
LIG_LIR_Apic_2 | 223 | 229 | PF02991 | 0.478 |
LIG_LIR_Apic_2 | 300 | 306 | PF02991 | 0.600 |
LIG_LIR_Apic_2 | 459 | 464 | PF02991 | 0.436 |
LIG_LIR_Apic_2 | 53 | 59 | PF02991 | 0.432 |
LIG_LIR_Gen_1 | 143 | 154 | PF02991 | 0.376 |
LIG_LIR_Gen_1 | 18 | 27 | PF02991 | 0.413 |
LIG_LIR_Gen_1 | 243 | 253 | PF02991 | 0.562 |
LIG_LIR_Gen_1 | 3 | 11 | PF02991 | 0.361 |
LIG_LIR_Gen_1 | 310 | 320 | PF02991 | 0.456 |
LIG_LIR_Gen_1 | 81 | 92 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 143 | 149 | PF02991 | 0.500 |
LIG_LIR_Nem_3 | 18 | 22 | PF02991 | 0.410 |
LIG_LIR_Nem_3 | 243 | 248 | PF02991 | 0.611 |
LIG_LIR_Nem_3 | 3 | 7 | PF02991 | 0.340 |
LIG_LIR_Nem_3 | 310 | 316 | PF02991 | 0.443 |
LIG_LIR_Nem_3 | 67 | 72 | PF02991 | 0.421 |
LIG_LIR_Nem_3 | 81 | 87 | PF02991 | 0.417 |
LIG_LIR_Nem_3 | 88 | 93 | PF02991 | 0.417 |
LIG_LYPXL_SIV_4 | 323 | 331 | PF13949 | 0.462 |
LIG_MYND_1 | 229 | 233 | PF01753 | 0.483 |
LIG_NRBOX | 130 | 136 | PF00104 | 0.484 |
LIG_NRBOX | 364 | 370 | PF00104 | 0.516 |
LIG_RPA_C_Plants | 496 | 507 | PF08784 | 0.512 |
LIG_SH2_CRK | 410 | 414 | PF00017 | 0.417 |
LIG_SH2_GRB2like | 341 | 344 | PF00017 | 0.516 |
LIG_SH2_SRC | 341 | 344 | PF00017 | 0.516 |
LIG_SH2_SRC | 84 | 87 | PF00017 | 0.442 |
LIG_SH2_STAP1 | 442 | 446 | PF00017 | 0.375 |
LIG_SH2_STAT5 | 151 | 154 | PF00017 | 0.517 |
LIG_SH2_STAT5 | 313 | 316 | PF00017 | 0.317 |
LIG_SH2_STAT5 | 324 | 327 | PF00017 | 0.418 |
LIG_SH2_STAT5 | 341 | 344 | PF00017 | 0.508 |
LIG_SH2_STAT5 | 419 | 422 | PF00017 | 0.408 |
LIG_SH3_3 | 317 | 323 | PF00018 | 0.457 |
LIG_SH3_3 | 563 | 569 | PF00018 | 0.606 |
LIG_SH3_3 | 72 | 78 | PF00018 | 0.408 |
LIG_SUMO_SIM_anti_2 | 434 | 441 | PF11976 | 0.339 |
LIG_SUMO_SIM_anti_2 | 443 | 448 | PF11976 | 0.330 |
LIG_TYR_ITIM | 149 | 154 | PF00017 | 0.516 |
LIG_TYR_ITIM | 82 | 87 | PF00017 | 0.417 |
LIG_WRC_WIRS_1 | 135 | 140 | PF05994 | 0.438 |
LIG_WRC_WIRS_1 | 378 | 383 | PF05994 | 0.428 |
LIG_WW_3 | 176 | 180 | PF00397 | 0.441 |
LIG_WW_3 | 525 | 529 | PF00397 | 0.461 |
MOD_CDC14_SPxK_1 | 620 | 623 | PF00782 | 0.637 |
MOD_CDK_SPxK_1 | 124 | 130 | PF00069 | 0.408 |
MOD_CDK_SPxK_1 | 617 | 623 | PF00069 | 0.643 |
MOD_CDK_SPxK_1 | 74 | 80 | PF00069 | 0.417 |
MOD_CDK_SPxxK_3 | 23 | 30 | PF00069 | 0.229 |
MOD_CDK_SPxxK_3 | 460 | 467 | PF00069 | 0.503 |
MOD_CDK_SPxxK_3 | 617 | 624 | PF00069 | 0.618 |
MOD_CK1_1 | 211 | 217 | PF00069 | 0.777 |
MOD_CK1_1 | 278 | 284 | PF00069 | 0.658 |
MOD_CK1_1 | 287 | 293 | PF00069 | 0.652 |
MOD_CK1_1 | 299 | 305 | PF00069 | 0.604 |
MOD_CK1_1 | 364 | 370 | PF00069 | 0.417 |
MOD_CK1_1 | 50 | 56 | PF00069 | 0.430 |
MOD_CK1_1 | 562 | 568 | PF00069 | 0.700 |
MOD_CK1_1 | 617 | 623 | PF00069 | 0.676 |
MOD_CK2_1 | 193 | 199 | PF00069 | 0.578 |
MOD_GlcNHglycan | 210 | 213 | PF01048 | 0.636 |
MOD_GlcNHglycan | 277 | 280 | PF01048 | 0.635 |
MOD_GlcNHglycan | 289 | 292 | PF01048 | 0.702 |
MOD_GlcNHglycan | 468 | 471 | PF01048 | 0.455 |
MOD_GlcNHglycan | 479 | 482 | PF01048 | 0.259 |
MOD_GlcNHglycan | 49 | 52 | PF01048 | 0.226 |
MOD_GlcNHglycan | 536 | 539 | PF01048 | 0.745 |
MOD_GlcNHglycan | 540 | 543 | PF01048 | 0.700 |
MOD_GlcNHglycan | 552 | 555 | PF01048 | 0.477 |
MOD_GlcNHglycan | 576 | 579 | PF01048 | 0.693 |
MOD_GlcNHglycan | 585 | 588 | PF01048 | 0.712 |
MOD_GSK3_1 | 11 | 18 | PF00069 | 0.499 |
MOD_GSK3_1 | 207 | 214 | PF00069 | 0.774 |
MOD_GSK3_1 | 218 | 225 | PF00069 | 0.766 |
MOD_GSK3_1 | 251 | 258 | PF00069 | 0.459 |
MOD_GSK3_1 | 285 | 292 | PF00069 | 0.696 |
MOD_GSK3_1 | 456 | 463 | PF00069 | 0.480 |
MOD_GSK3_1 | 534 | 541 | PF00069 | 0.592 |
MOD_GSK3_1 | 543 | 550 | PF00069 | 0.651 |
MOD_LATS_1 | 192 | 198 | PF00433 | 0.642 |
MOD_LATS_1 | 332 | 338 | PF00433 | 0.350 |
MOD_N-GLC_2 | 343 | 345 | PF02516 | 0.217 |
MOD_NEK2_1 | 134 | 139 | PF00069 | 0.397 |
MOD_NEK2_1 | 185 | 190 | PF00069 | 0.409 |
MOD_NEK2_1 | 383 | 388 | PF00069 | 0.505 |
MOD_NEK2_1 | 559 | 564 | PF00069 | 0.720 |
MOD_PIKK_1 | 109 | 115 | PF00454 | 0.452 |
MOD_PIKK_1 | 292 | 298 | PF00454 | 0.495 |
MOD_PIKK_1 | 307 | 313 | PF00454 | 0.368 |
MOD_PIKK_1 | 332 | 338 | PF00454 | 0.438 |
MOD_PIKK_1 | 367 | 373 | PF00454 | 0.428 |
MOD_PIKK_1 | 526 | 532 | PF00454 | 0.465 |
MOD_PKA_2 | 158 | 164 | PF00069 | 0.417 |
MOD_PKA_2 | 193 | 199 | PF00069 | 0.576 |
MOD_PKA_2 | 351 | 357 | PF00069 | 0.420 |
MOD_PKA_2 | 456 | 462 | PF00069 | 0.355 |
MOD_PKA_2 | 521 | 527 | PF00069 | 0.696 |
MOD_Plk_1 | 254 | 260 | PF00069 | 0.551 |
MOD_Plk_1 | 442 | 448 | PF00069 | 0.416 |
MOD_Plk_2-3 | 158 | 164 | PF00069 | 0.486 |
MOD_Plk_4 | 15 | 21 | PF00069 | 0.433 |
MOD_Plk_4 | 255 | 261 | PF00069 | 0.422 |
MOD_Plk_4 | 335 | 341 | PF00069 | 0.419 |
MOD_Plk_4 | 364 | 370 | PF00069 | 0.424 |
MOD_Plk_4 | 402 | 408 | PF00069 | 0.525 |
MOD_Plk_4 | 415 | 421 | PF00069 | 0.327 |
MOD_Plk_4 | 442 | 448 | PF00069 | 0.385 |
MOD_Plk_4 | 456 | 462 | PF00069 | 0.317 |
MOD_ProDKin_1 | 124 | 130 | PF00069 | 0.416 |
MOD_ProDKin_1 | 21 | 27 | PF00069 | 0.366 |
MOD_ProDKin_1 | 218 | 224 | PF00069 | 0.583 |
MOD_ProDKin_1 | 460 | 466 | PF00069 | 0.500 |
MOD_ProDKin_1 | 571 | 577 | PF00069 | 0.488 |
MOD_ProDKin_1 | 609 | 615 | PF00069 | 0.737 |
MOD_ProDKin_1 | 617 | 623 | PF00069 | 0.770 |
MOD_ProDKin_1 | 74 | 80 | PF00069 | 0.417 |
TRG_DiLeu_BaEn_1 | 243 | 248 | PF01217 | 0.497 |
TRG_DiLeu_BaLyEn_6 | 171 | 176 | PF01217 | 0.514 |
TRG_DiLeu_BaLyEn_6 | 226 | 231 | PF01217 | 0.482 |
TRG_DiLeu_BaLyEn_6 | 470 | 475 | PF01217 | 0.482 |
TRG_ENDOCYTIC_2 | 151 | 154 | PF00928 | 0.520 |
TRG_ENDOCYTIC_2 | 19 | 22 | PF00928 | 0.394 |
TRG_ENDOCYTIC_2 | 313 | 316 | PF00928 | 0.352 |
TRG_ENDOCYTIC_2 | 69 | 72 | PF00928 | 0.418 |
TRG_ENDOCYTIC_2 | 84 | 87 | PF00928 | 0.411 |
TRG_ER_diArg_1 | 182 | 184 | PF00400 | 0.408 |
TRG_ER_diArg_1 | 205 | 207 | PF00400 | 0.689 |
TRG_ER_diArg_1 | 531 | 534 | PF00400 | 0.665 |
TRG_ER_diArg_1 | 555 | 558 | PF00400 | 0.561 |
TRG_ER_diArg_1 | 623 | 626 | PF00400 | 0.772 |
TRG_ER_diLys_1 | 627 | 630 | PF00400 | 0.508 |
TRG_NLS_Bipartite_1 | 610 | 628 | PF00514 | 0.624 |
TRG_NLS_MonoExtC_3 | 622 | 627 | PF00514 | 0.616 |
TRG_NLS_MonoExtN_4 | 621 | 628 | PF00514 | 0.736 |
TRG_Pf-PMV_PEXEL_1 | 132 | 136 | PF00026 | 0.287 |
TRG_Pf-PMV_PEXEL_1 | 150 | 155 | PF00026 | 0.175 |
TRG_Pf-PMV_PEXEL_1 | 80 | 85 | PF00026 | 0.208 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I1U1 | Leptomonas seymouri | 26% | 81% |
A0A0N1I2T9 | Leptomonas seymouri | 70% | 100% |
A0A0S4ISP4 | Bodo saltans | 27% | 85% |
A0A0S4J5D6 | Bodo saltans | 49% | 100% |
A0A0S4KKU4 | Bodo saltans | 29% | 91% |
A0A1X0NVK0 | Trypanosomatidae | 27% | 88% |
A0A1X0P0F9 | Trypanosomatidae | 55% | 100% |
A0A3Q8IE53 | Leishmania donovani | 27% | 80% |
A0A3R7M1K3 | Trypanosoma rangeli | 27% | 88% |
A0A3R7N587 | Trypanosoma rangeli | 26% | 76% |
A0A3S5H5H4 | Leishmania donovani | 79% | 100% |
A0A3S5H6T7 | Leishmania donovani | 31% | 100% |
A0A3S7X5R1 | Leishmania donovani | 26% | 82% |
A0A422NDK5 | Trypanosoma rangeli | 57% | 100% |
A2XVF7 | Oryza sativa subsp. indica | 31% | 76% |
A3AVH5 | Oryza sativa subsp. japonica | 31% | 76% |
A4HFC4 | Leishmania braziliensis | 27% | 91% |
A4HKL3 | Leishmania braziliensis | 27% | 82% |
A4HSF8 | Leishmania infantum | 80% | 100% |
A4I2K1 | Leishmania infantum | 27% | 80% |
A4I846 | Leishmania infantum | 26% | 82% |
A6ZL85 | Saccharomyces cerevisiae (strain YJM789) | 28% | 82% |
A7TJ71 | Vanderwaltozyma polyspora (strain ATCC 22028 / DSM 70294 / BCRC 21397 / CBS 2163 / NBRC 10782 / NRRL Y-8283 / UCD 57-17) | 28% | 82% |
C9ZNU6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 31% | 98% |
D0A4H6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 53% | 100% |
D0A6Z3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 100% |
D0AAB3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 87% |
E9ACY2 | Leishmania major | 27% | 80% |
E9AKE2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 80% | 100% |
E9AYQ7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 28% | 80% |
E9B304 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 81% |
O60173 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 29% | 89% |
P26802 | Drosophila melanogaster | 30% | 92% |
P38112 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 28% | 82% |
Q0CF43 | Aspergillus terreus (strain NIH 2624 / FGSC A1156) | 27% | 82% |
Q0UHM7 | Phaeosphaeria nodorum (strain SN15 / ATCC MYA-4574 / FGSC 10173) | 28% | 76% |
Q4IJH1 | Gibberella zeae (strain ATCC MYA-4620 / CBS 123657 / FGSC 9075 / NRRL 31084 / PH-1) | 28% | 100% |
Q4Q552 | Leishmania major | 27% | 82% |
Q4QFH1 | Leishmania major | 31% | 100% |
Q4QJG6 | Leishmania major | 79% | 99% |
Q6C835 | Yarrowia lipolytica (strain CLIB 122 / E 150) | 29% | 79% |
Q6CRF4 | Kluyveromyces lactis (strain ATCC 8585 / CBS 2359 / DSM 70799 / NBRC 1267 / NRRL Y-1140 / WM37) | 29% | 82% |
Q6NZQ2 | Mus musculus | 26% | 92% |
Q7XJN0 | Arabidopsis thaliana | 26% | 100% |
Q93Y39 | Arabidopsis thaliana | 31% | 76% |
V5CZW7 | Trypanosoma cruzi | 57% | 100% |
V5DCA1 | Trypanosoma cruzi | 26% | 88% |