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: 18 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 1, no: 14 |
NetGPI | no | yes: 0, no: 15 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005634 | nucleus | 5 | 2 |
GO:0043226 | organelle | 2 | 2 |
GO:0043227 | membrane-bounded organelle | 3 | 2 |
GO:0043229 | intracellular organelle | 3 | 2 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 2 |
GO:0110165 | cellular anatomical entity | 1 | 2 |
Related structures:
AlphaFold database: A4HKP4
Term | Name | Level | Count |
---|---|---|---|
GO:0006139 | nucleobase-containing compound metabolic process | 3 | 2 |
GO:0006163 | purine nucleotide metabolic process | 5 | 2 |
GO:0006195 | purine nucleotide catabolic process | 6 | 2 |
GO:0006203 | dGTP catabolic process | 7 | 2 |
GO:0006725 | cellular aromatic compound metabolic process | 3 | 2 |
GO:0006753 | nucleoside phosphate metabolic process | 4 | 2 |
GO:0006793 | phosphorus metabolic process | 3 | 2 |
GO:0006796 | phosphate-containing compound metabolic process | 4 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009056 | catabolic process | 2 | 2 |
GO:0009117 | nucleotide metabolic process | 5 | 2 |
GO:0009141 | nucleoside triphosphate metabolic process | 5 | 2 |
GO:0009143 | nucleoside triphosphate catabolic process | 6 | 2 |
GO:0009144 | purine nucleoside triphosphate metabolic process | 6 | 2 |
GO:0009146 | purine nucleoside triphosphate catabolic process | 7 | 2 |
GO:0009151 | purine deoxyribonucleotide metabolic process | 6 | 2 |
GO:0009155 | purine deoxyribonucleotide catabolic process | 6 | 2 |
GO:0009166 | nucleotide catabolic process | 6 | 2 |
GO:0009200 | deoxyribonucleoside triphosphate metabolic process | 6 | 2 |
GO:0009204 | deoxyribonucleoside triphosphate catabolic process | 7 | 2 |
GO:0009215 | purine deoxyribonucleoside triphosphate metabolic process | 7 | 2 |
GO:0009217 | purine deoxyribonucleoside triphosphate catabolic process | 8 | 2 |
GO:0009262 | deoxyribonucleotide metabolic process | 4 | 2 |
GO:0009264 | deoxyribonucleotide catabolic process | 5 | 2 |
GO:0009394 | 2'-deoxyribonucleotide metabolic process | 5 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0019439 | aromatic compound catabolic process | 4 | 2 |
GO:0019637 | organophosphate metabolic process | 3 | 2 |
GO:0019692 | deoxyribose phosphate metabolic process | 4 | 2 |
GO:0034641 | cellular nitrogen compound metabolic process | 3 | 2 |
GO:0034655 | nucleobase-containing compound catabolic process | 4 | 2 |
GO:0044237 | cellular metabolic process | 2 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0044248 | cellular catabolic process | 3 | 2 |
GO:0044270 | cellular nitrogen compound catabolic process | 4 | 2 |
GO:0044281 | small molecule metabolic process | 2 | 2 |
GO:0046070 | dGTP metabolic process | 7 | 2 |
GO:0046386 | deoxyribose phosphate catabolic process | 5 | 2 |
GO:0046434 | organophosphate catabolic process | 4 | 2 |
GO:0046483 | heterocycle metabolic process | 3 | 2 |
GO:0046700 | heterocycle catabolic process | 4 | 2 |
GO:0055086 | nucleobase-containing small molecule metabolic process | 3 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:0072521 | purine-containing compound metabolic process | 4 | 2 |
GO:0072523 | purine-containing compound catabolic process | 5 | 2 |
GO:1901135 | carbohydrate derivative metabolic process | 3 | 2 |
GO:1901136 | carbohydrate derivative catabolic process | 4 | 2 |
GO:1901292 | nucleoside phosphate catabolic process | 5 | 2 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 2 |
GO:1901361 | organic cyclic compound catabolic process | 4 | 2 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 2 |
GO:1901565 | organonitrogen compound catabolic process | 4 | 2 |
GO:1901575 | organic substance catabolic process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 2 |
GO:0008832 | dGTPase activity | 6 | 2 |
GO:0016787 | hydrolase activity | 2 | 2 |
GO:0016788 | hydrolase activity, acting on ester bonds | 3 | 2 |
GO:0016793 | triphosphoric monoester hydrolase activity | 5 | 2 |
GO:0042578 | phosphoric ester hydrolase activity | 4 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 278 | 282 | PF00656 | 0.489 |
CLV_C14_Caspase3-7 | 92 | 96 | PF00656 | 0.398 |
CLV_NRD_NRD_1 | 13 | 15 | PF00675 | 0.705 |
CLV_NRD_NRD_1 | 157 | 159 | PF00675 | 0.368 |
CLV_NRD_NRD_1 | 170 | 172 | PF00675 | 0.335 |
CLV_NRD_NRD_1 | 256 | 258 | PF00675 | 0.363 |
CLV_NRD_NRD_1 | 360 | 362 | PF00675 | 0.399 |
CLV_NRD_NRD_1 | 376 | 378 | PF00675 | 0.393 |
CLV_NRD_NRD_1 | 384 | 386 | PF00675 | 0.332 |
CLV_PCSK_KEX2_1 | 13 | 15 | PF00082 | 0.638 |
CLV_PCSK_KEX2_1 | 227 | 229 | PF00082 | 0.438 |
CLV_PCSK_KEX2_1 | 24 | 26 | PF00082 | 0.531 |
CLV_PCSK_KEX2_1 | 256 | 258 | PF00082 | 0.363 |
CLV_PCSK_KEX2_1 | 376 | 378 | PF00082 | 0.559 |
CLV_PCSK_KEX2_1 | 384 | 386 | PF00082 | 0.466 |
CLV_PCSK_KEX2_1 | 426 | 428 | PF00082 | 0.567 |
CLV_PCSK_KEX2_1 | 478 | 480 | PF00082 | 0.420 |
CLV_PCSK_KEX2_1 | 608 | 610 | PF00082 | 0.694 |
CLV_PCSK_PC1ET2_1 | 227 | 229 | PF00082 | 0.438 |
CLV_PCSK_PC1ET2_1 | 24 | 26 | PF00082 | 0.567 |
CLV_PCSK_PC1ET2_1 | 426 | 428 | PF00082 | 0.460 |
CLV_PCSK_PC1ET2_1 | 478 | 480 | PF00082 | 0.420 |
CLV_PCSK_PC1ET2_1 | 608 | 610 | PF00082 | 0.694 |
CLV_PCSK_SKI1_1 | 256 | 260 | PF00082 | 0.299 |
CLV_PCSK_SKI1_1 | 384 | 388 | PF00082 | 0.369 |
CLV_PCSK_SKI1_1 | 44 | 48 | PF00082 | 0.425 |
CLV_PCSK_SKI1_1 | 608 | 612 | PF00082 | 0.692 |
DEG_APCC_DBOX_1 | 290 | 298 | PF00400 | 0.467 |
DEG_APCC_DBOX_1 | 383 | 391 | PF00400 | 0.440 |
DEG_COP1_1 | 99 | 109 | PF00400 | 0.305 |
DEG_SCF_FBW7_1 | 583 | 589 | PF00400 | 0.494 |
DOC_ANK_TNKS_1 | 90 | 97 | PF00023 | 0.305 |
DOC_CKS1_1 | 247 | 252 | PF01111 | 0.490 |
DOC_CKS1_1 | 583 | 588 | PF01111 | 0.496 |
DOC_CYCLIN_RxL_1 | 605 | 615 | PF00134 | 0.591 |
DOC_CYCLIN_RxL_1 | 638 | 648 | PF00134 | 0.497 |
DOC_MAPK_gen_1 | 227 | 233 | PF00069 | 0.422 |
DOC_MAPK_gen_1 | 302 | 312 | PF00069 | 0.426 |
DOC_MAPK_gen_1 | 608 | 614 | PF00069 | 0.595 |
DOC_MAPK_MEF2A_6 | 534 | 541 | PF00069 | 0.565 |
DOC_PP1_RVXF_1 | 536 | 542 | PF00149 | 0.418 |
DOC_PP2B_PxIxI_1 | 40 | 46 | PF00149 | 0.398 |
DOC_PP4_FxxP_1 | 104 | 107 | PF00568 | 0.398 |
DOC_PP4_FxxP_1 | 488 | 491 | PF00568 | 0.463 |
DOC_PP4_MxPP_1 | 1 | 4 | PF00568 | 0.583 |
DOC_USP7_MATH_1 | 23 | 27 | PF00917 | 0.411 |
DOC_USP7_MATH_1 | 333 | 337 | PF00917 | 0.466 |
DOC_USP7_MATH_1 | 491 | 495 | PF00917 | 0.596 |
DOC_USP7_MATH_1 | 517 | 521 | PF00917 | 0.512 |
DOC_USP7_MATH_1 | 567 | 571 | PF00917 | 0.807 |
DOC_USP7_MATH_1 | 573 | 577 | PF00917 | 0.758 |
DOC_USP7_MATH_1 | 586 | 590 | PF00917 | 0.492 |
DOC_USP7_MATH_1 | 71 | 75 | PF00917 | 0.445 |
DOC_USP7_MATH_2 | 531 | 537 | PF00917 | 0.420 |
DOC_WW_Pin1_4 | 246 | 251 | PF00397 | 0.488 |
DOC_WW_Pin1_4 | 46 | 51 | PF00397 | 0.428 |
DOC_WW_Pin1_4 | 527 | 532 | PF00397 | 0.471 |
DOC_WW_Pin1_4 | 556 | 561 | PF00397 | 0.574 |
DOC_WW_Pin1_4 | 582 | 587 | PF00397 | 0.775 |
LIG_14-3-3_CanoR_1 | 158 | 167 | PF00244 | 0.376 |
LIG_14-3-3_CanoR_1 | 171 | 181 | PF00244 | 0.374 |
LIG_14-3-3_CanoR_1 | 218 | 224 | PF00244 | 0.432 |
LIG_14-3-3_CanoR_1 | 25 | 30 | PF00244 | 0.563 |
LIG_14-3-3_CanoR_1 | 393 | 402 | PF00244 | 0.508 |
LIG_14-3-3_CanoR_1 | 403 | 410 | PF00244 | 0.483 |
LIG_14-3-3_CanoR_1 | 414 | 419 | PF00244 | 0.664 |
LIG_14-3-3_CanoR_1 | 44 | 52 | PF00244 | 0.349 |
LIG_14-3-3_CanoR_1 | 492 | 501 | PF00244 | 0.595 |
LIG_14-3-3_CanoR_1 | 526 | 530 | PF00244 | 0.524 |
LIG_14-3-3_CanoR_1 | 538 | 548 | PF00244 | 0.496 |
LIG_Actin_WH2_2 | 177 | 194 | PF00022 | 0.441 |
LIG_Actin_WH2_2 | 300 | 318 | PF00022 | 0.440 |
LIG_BRCT_BRCA1_1 | 138 | 142 | PF00533 | 0.326 |
LIG_Clathr_ClatBox_1 | 309 | 313 | PF01394 | 0.424 |
LIG_EVH1_2 | 3 | 7 | PF00568 | 0.459 |
LIG_FHA_1 | 218 | 224 | PF00498 | 0.432 |
LIG_FHA_1 | 302 | 308 | PF00498 | 0.481 |
LIG_FHA_1 | 506 | 512 | PF00498 | 0.627 |
LIG_FHA_1 | 591 | 597 | PF00498 | 0.755 |
LIG_FHA_1 | 665 | 671 | PF00498 | 0.627 |
LIG_FHA_2 | 185 | 191 | PF00498 | 0.415 |
LIG_FHA_2 | 439 | 445 | PF00498 | 0.415 |
LIG_FHA_2 | 470 | 476 | PF00498 | 0.487 |
LIG_FHA_2 | 528 | 534 | PF00498 | 0.458 |
LIG_LIR_Apic_2 | 103 | 107 | PF02991 | 0.305 |
LIG_LIR_Apic_2 | 486 | 491 | PF02991 | 0.473 |
LIG_LIR_Apic_2 | 64 | 69 | PF02991 | 0.405 |
LIG_LIR_Gen_1 | 139 | 150 | PF02991 | 0.326 |
LIG_LIR_Gen_1 | 183 | 194 | PF02991 | 0.331 |
LIG_LIR_Gen_1 | 249 | 259 | PF02991 | 0.488 |
LIG_LIR_Gen_1 | 348 | 356 | PF02991 | 0.378 |
LIG_LIR_Gen_1 | 509 | 518 | PF02991 | 0.652 |
LIG_LIR_Gen_1 | 540 | 548 | PF02991 | 0.542 |
LIG_LIR_LC3C_4 | 519 | 523 | PF02991 | 0.393 |
LIG_LIR_Nem_3 | 139 | 145 | PF02991 | 0.326 |
LIG_LIR_Nem_3 | 183 | 189 | PF02991 | 0.357 |
LIG_LIR_Nem_3 | 190 | 196 | PF02991 | 0.283 |
LIG_LIR_Nem_3 | 31 | 37 | PF02991 | 0.438 |
LIG_LIR_Nem_3 | 348 | 353 | PF02991 | 0.372 |
LIG_LIR_Nem_3 | 38 | 42 | PF02991 | 0.369 |
LIG_LIR_Nem_3 | 540 | 544 | PF02991 | 0.530 |
LIG_LIR_Nem_3 | 64 | 68 | PF02991 | 0.401 |
LIG_LIR_Nem_3 | 88 | 93 | PF02991 | 0.392 |
LIG_PCNA_yPIPBox_3 | 296 | 307 | PF02747 | 0.365 |
LIG_PTB_Apo_2 | 60 | 67 | PF02174 | 0.453 |
LIG_PTB_Phospho_1 | 60 | 66 | PF10480 | 0.450 |
LIG_SH2_CRK | 396 | 400 | PF00017 | 0.362 |
LIG_SH2_CRK | 90 | 94 | PF00017 | 0.398 |
LIG_SH2_NCK_1 | 396 | 400 | PF00017 | 0.387 |
LIG_SH2_NCK_1 | 619 | 623 | PF00017 | 0.467 |
LIG_SH2_PTP2 | 193 | 196 | PF00017 | 0.419 |
LIG_SH2_PTP2 | 66 | 69 | PF00017 | 0.484 |
LIG_SH2_SRC | 344 | 347 | PF00017 | 0.333 |
LIG_SH2_SRC | 66 | 69 | PF00017 | 0.395 |
LIG_SH2_STAT5 | 193 | 196 | PF00017 | 0.419 |
LIG_SH2_STAT5 | 238 | 241 | PF00017 | 0.377 |
LIG_SH2_STAT5 | 344 | 347 | PF00017 | 0.373 |
LIG_SH2_STAT5 | 396 | 399 | PF00017 | 0.421 |
LIG_SH2_STAT5 | 487 | 490 | PF00017 | 0.506 |
LIG_SH2_STAT5 | 66 | 69 | PF00017 | 0.370 |
LIG_SH2_STAT5 | 84 | 87 | PF00017 | 0.285 |
LIG_SH3_3 | 17 | 23 | PF00018 | 0.615 |
LIG_SH3_3 | 335 | 341 | PF00018 | 0.448 |
LIG_SH3_3 | 580 | 586 | PF00018 | 0.502 |
LIG_SUMO_SIM_anti_2 | 166 | 171 | PF11976 | 0.407 |
LIG_SUMO_SIM_anti_2 | 519 | 525 | PF11976 | 0.375 |
LIG_SUMO_SIM_par_1 | 304 | 311 | PF11976 | 0.336 |
LIG_TRAF2_1 | 421 | 424 | PF00917 | 0.606 |
LIG_TRAF2_1 | 530 | 533 | PF00917 | 0.425 |
LIG_TYR_ITIM | 191 | 196 | PF00017 | 0.423 |
LIG_UBA3_1 | 167 | 172 | PF00899 | 0.305 |
LIG_UBA3_1 | 197 | 205 | PF00899 | 0.383 |
LIG_WRC_WIRS_1 | 142 | 147 | PF05994 | 0.398 |
MOD_CDK_SPxxK_3 | 527 | 534 | PF00069 | 0.491 |
MOD_CK1_1 | 369 | 375 | PF00069 | 0.414 |
MOD_CK1_1 | 405 | 411 | PF00069 | 0.496 |
MOD_CK1_1 | 540 | 546 | PF00069 | 0.511 |
MOD_CK1_1 | 554 | 560 | PF00069 | 0.686 |
MOD_CK1_1 | 582 | 588 | PF00069 | 0.624 |
MOD_CK1_1 | 599 | 605 | PF00069 | 0.517 |
MOD_CK1_1 | 636 | 642 | PF00069 | 0.741 |
MOD_CK2_1 | 172 | 178 | PF00069 | 0.251 |
MOD_CK2_1 | 418 | 424 | PF00069 | 0.570 |
MOD_CK2_1 | 433 | 439 | PF00069 | 0.438 |
MOD_CK2_1 | 527 | 533 | PF00069 | 0.452 |
MOD_CK2_1 | 586 | 592 | PF00069 | 0.534 |
MOD_CK2_1 | 71 | 77 | PF00069 | 0.371 |
MOD_GlcNHglycan | 228 | 231 | PF01048 | 0.448 |
MOD_GlcNHglycan | 369 | 372 | PF01048 | 0.640 |
MOD_GlcNHglycan | 483 | 486 | PF01048 | 0.541 |
MOD_GlcNHglycan | 575 | 578 | PF01048 | 0.637 |
MOD_GlcNHglycan | 635 | 638 | PF01048 | 0.642 |
MOD_GlcNHglycan | 647 | 650 | PF01048 | 0.467 |
MOD_GSK3_1 | 141 | 148 | PF00069 | 0.398 |
MOD_GSK3_1 | 172 | 179 | PF00069 | 0.403 |
MOD_GSK3_1 | 25 | 32 | PF00069 | 0.570 |
MOD_GSK3_1 | 363 | 370 | PF00069 | 0.448 |
MOD_GSK3_1 | 394 | 401 | PF00069 | 0.429 |
MOD_GSK3_1 | 414 | 421 | PF00069 | 0.549 |
MOD_GSK3_1 | 501 | 508 | PF00069 | 0.572 |
MOD_GSK3_1 | 533 | 540 | PF00069 | 0.416 |
MOD_GSK3_1 | 548 | 555 | PF00069 | 0.630 |
MOD_GSK3_1 | 582 | 589 | PF00069 | 0.729 |
MOD_GSK3_1 | 590 | 597 | PF00069 | 0.708 |
MOD_GSK3_1 | 664 | 671 | PF00069 | 0.627 |
MOD_N-GLC_1 | 110 | 115 | PF02516 | 0.363 |
MOD_N-GLC_1 | 176 | 181 | PF02516 | 0.498 |
MOD_N-GLC_1 | 505 | 510 | PF02516 | 0.647 |
MOD_N-GLC_1 | 586 | 591 | PF02516 | 0.551 |
MOD_NEK2_1 | 141 | 146 | PF00069 | 0.374 |
MOD_NEK2_1 | 289 | 294 | PF00069 | 0.418 |
MOD_NEK2_1 | 322 | 327 | PF00069 | 0.462 |
MOD_NEK2_1 | 356 | 361 | PF00069 | 0.430 |
MOD_NEK2_1 | 367 | 372 | PF00069 | 0.433 |
MOD_NEK2_1 | 395 | 400 | PF00069 | 0.481 |
MOD_NEK2_1 | 443 | 448 | PF00069 | 0.408 |
MOD_NEK2_1 | 537 | 542 | PF00069 | 0.521 |
MOD_NEK2_1 | 590 | 595 | PF00069 | 0.757 |
MOD_NEK2_1 | 596 | 601 | PF00069 | 0.728 |
MOD_NEK2_1 | 61 | 66 | PF00069 | 0.378 |
MOD_NEK2_1 | 645 | 650 | PF00069 | 0.740 |
MOD_NEK2_1 | 76 | 81 | PF00069 | 0.282 |
MOD_NEK2_1 | 89 | 94 | PF00069 | 0.345 |
MOD_NEK2_2 | 586 | 591 | PF00069 | 0.483 |
MOD_OFUCOSY | 330 | 337 | PF10250 | 0.239 |
MOD_PIKK_1 | 419 | 425 | PF00454 | 0.615 |
MOD_PIKK_1 | 467 | 473 | PF00454 | 0.672 |
MOD_PIKK_1 | 559 | 565 | PF00454 | 0.699 |
MOD_PIKK_1 | 568 | 574 | PF00454 | 0.677 |
MOD_PIKK_1 | 655 | 661 | PF00454 | 0.676 |
MOD_PK_1 | 25 | 31 | PF00069 | 0.515 |
MOD_PK_1 | 414 | 420 | PF00069 | 0.542 |
MOD_PK_1 | 8 | 14 | PF00069 | 0.681 |
MOD_PKA_1 | 158 | 164 | PF00069 | 0.305 |
MOD_PKA_2 | 217 | 223 | PF00069 | 0.451 |
MOD_PKA_2 | 240 | 246 | PF00069 | 0.364 |
MOD_PKA_2 | 29 | 35 | PF00069 | 0.570 |
MOD_PKA_2 | 301 | 307 | PF00069 | 0.397 |
MOD_PKA_2 | 402 | 408 | PF00069 | 0.502 |
MOD_PKA_2 | 491 | 497 | PF00069 | 0.599 |
MOD_PKA_2 | 525 | 531 | PF00069 | 0.560 |
MOD_PKA_2 | 537 | 543 | PF00069 | 0.500 |
MOD_PKA_2 | 590 | 596 | PF00069 | 0.721 |
MOD_Plk_1 | 269 | 275 | PF00069 | 0.483 |
MOD_Plk_1 | 405 | 411 | PF00069 | 0.627 |
MOD_Plk_1 | 443 | 449 | PF00069 | 0.427 |
MOD_Plk_1 | 551 | 557 | PF00069 | 0.560 |
MOD_Plk_1 | 579 | 585 | PF00069 | 0.555 |
MOD_Plk_1 | 586 | 592 | PF00069 | 0.536 |
MOD_Plk_1 | 76 | 82 | PF00069 | 0.345 |
MOD_Plk_2-3 | 308 | 314 | PF00069 | 0.333 |
MOD_Plk_2-3 | 433 | 439 | PF00069 | 0.398 |
MOD_Plk_2-3 | 627 | 633 | PF00069 | 0.749 |
MOD_Plk_4 | 141 | 147 | PF00069 | 0.398 |
MOD_Plk_4 | 163 | 169 | PF00069 | 0.398 |
MOD_Plk_4 | 248 | 254 | PF00069 | 0.504 |
MOD_Plk_4 | 29 | 35 | PF00069 | 0.562 |
MOD_Plk_4 | 405 | 411 | PF00069 | 0.532 |
MOD_Plk_4 | 483 | 489 | PF00069 | 0.448 |
MOD_Plk_4 | 507 | 513 | PF00069 | 0.616 |
MOD_Plk_4 | 517 | 523 | PF00069 | 0.403 |
MOD_Plk_4 | 61 | 67 | PF00069 | 0.400 |
MOD_ProDKin_1 | 246 | 252 | PF00069 | 0.483 |
MOD_ProDKin_1 | 46 | 52 | PF00069 | 0.424 |
MOD_ProDKin_1 | 527 | 533 | PF00069 | 0.464 |
MOD_ProDKin_1 | 556 | 562 | PF00069 | 0.573 |
MOD_ProDKin_1 | 582 | 588 | PF00069 | 0.775 |
MOD_SUMO_for_1 | 425 | 428 | PF00179 | 0.565 |
MOD_SUMO_for_1 | 7 | 10 | PF00179 | 0.463 |
MOD_SUMO_rev_2 | 16 | 26 | PF00179 | 0.644 |
TRG_DiLeu_BaEn_4 | 665 | 671 | PF01217 | 0.627 |
TRG_ENDOCYTIC_2 | 193 | 196 | PF00928 | 0.419 |
TRG_ENDOCYTIC_2 | 34 | 37 | PF00928 | 0.411 |
TRG_ENDOCYTIC_2 | 396 | 399 | PF00928 | 0.342 |
TRG_ENDOCYTIC_2 | 84 | 87 | PF00928 | 0.398 |
TRG_ENDOCYTIC_2 | 90 | 93 | PF00928 | 0.398 |
TRG_ER_diArg_1 | 12 | 14 | PF00400 | 0.711 |
TRG_ER_diArg_1 | 255 | 257 | PF00400 | 0.326 |
TRG_ER_diArg_1 | 375 | 377 | PF00400 | 0.375 |
TRG_ER_diArg_1 | 384 | 386 | PF00400 | 0.435 |
TRG_NLS_MonoExtC_3 | 607 | 613 | PF00514 | 0.687 |
TRG_NLS_MonoExtN_4 | 605 | 612 | PF00514 | 0.685 |
TRG_Pf-PMV_PEXEL_1 | 256 | 260 | PF00026 | 0.305 |
TRG_Pf-PMV_PEXEL_1 | 361 | 365 | PF00026 | 0.399 |
TRG_Pf-PMV_PEXEL_1 | 384 | 388 | PF00026 | 0.447 |
TRG_Pf-PMV_PEXEL_1 | 44 | 48 | PF00026 | 0.401 |
TRG_Pf-PMV_PEXEL_1 | 56 | 60 | PF00026 | 0.387 |
TRG_Pf-PMV_PEXEL_1 | 91 | 95 | PF00026 | 0.398 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PD02 | Leptomonas seymouri | 66% | 100% |
A0A0S4J2F4 | Bodo saltans | 30% | 100% |
A0A0S4J714 | Bodo saltans | 34% | 95% |
A0A1X0P1Y8 | Trypanosomatidae | 34% | 87% |
A0A3Q8IGB9 | Leishmania donovani | 89% | 100% |
A0A3R7LQB8 | Trypanosoma rangeli | 33% | 89% |
A0A3R7NIH1 | Trypanosoma rangeli | 29% | 100% |
A0A3S7WPC5 | Leishmania donovani | 34% | 100% |
A4H4I2 | Leishmania braziliensis | 35% | 100% |
A4HSQ7 | Leishmania infantum | 34% | 100% |
A4I875 | Leishmania infantum | 89% | 100% |
C9ZTA3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 28% | 100% |
E9AKP4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 100% |
E9B333 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
Q09374 | Caenorhabditis elegans | 26% | 100% |
Q4Q521 | Leishmania major | 88% | 100% |
Q4QJ63 | Leishmania major | 34% | 100% |
Q60710 | Mus musculus | 30% | 100% |
V5BPJ7 | Trypanosoma cruzi | 34% | 83% |