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. | yes | yes: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 10 |
NetGPI | no | yes: 0, no: 10 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005730 | nucleolus | 5 | 11 |
GO:0043226 | organelle | 2 | 11 |
GO:0043228 | non-membrane-bounded organelle | 3 | 11 |
GO:0043229 | intracellular organelle | 3 | 11 |
GO:0043232 | intracellular non-membrane-bounded organelle | 4 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 11 |
GO:0030684 | preribosome | 3 | 1 |
GO:0030688 | preribosome, small subunit precursor | 4 | 1 |
GO:0032991 | protein-containing complex | 1 | 1 |
GO:1990904 | ribonucleoprotein complex | 2 | 1 |
Related structures:
AlphaFold database: A0A3S5H5Y1
Term | Name | Level | Count |
---|---|---|---|
GO:0009987 | cellular process | 1 | 11 |
GO:0022613 | ribonucleoprotein complex biogenesis | 4 | 10 |
GO:0042254 | ribosome biogenesis | 5 | 10 |
GO:0044085 | cellular component biogenesis | 3 | 10 |
GO:0071840 | cellular component organization or biogenesis | 2 | 10 |
GO:0000462 | maturation of SSU-rRNA from tricistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, LSU-rRNA) | 10 | 1 |
GO:0000469 | cleavage involved in rRNA processing | 7 | 1 |
GO:0000478 | endonucleolytic cleavage involved in rRNA processing | 8 | 1 |
GO:0000479 | endonucleolytic cleavage of tricistronic rRNA transcript (SSU-rRNA, 5.8S rRNA, LSU-rRNA) | 9 | 1 |
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:0016070 | RNA metabolic process | 5 | 1 |
GO:0016072 | rRNA metabolic process | 7 | 1 |
GO:0030490 | maturation of SSU-rRNA | 9 | 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:0090305 | nucleic acid phosphodiester bond hydrolysis | 5 | 1 |
GO:0090501 | RNA phosphodiester bond hydrolysis | 6 | 1 |
GO:0090502 | RNA phosphodiester bond hydrolysis, endonucleolytic | 7 | 1 |
GO:1901360 | organic cyclic compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0000166 | nucleotide binding | 3 | 1 |
GO:0003676 | nucleic acid binding | 3 | 1 |
GO:0003723 | RNA binding | 4 | 1 |
GO:0003824 | catalytic activity | 1 | 1 |
GO:0003924 | GTPase activity | 7 | 1 |
GO:0005488 | binding | 1 | 1 |
GO:0005525 | GTP binding | 5 | 1 |
GO:0016462 | pyrophosphatase activity | 5 | 1 |
GO:0016787 | hydrolase activity | 2 | 1 |
GO:0016817 | hydrolase activity, acting on acid anhydrides | 3 | 1 |
GO:0016818 | hydrolase activity, acting on acid anhydrides, in phosphorus-containing anhydrides | 4 | 1 |
GO:0017076 | purine nucleotide binding | 4 | 1 |
GO:0017111 | ribonucleoside triphosphate phosphatase activity | 6 | 1 |
GO:0019001 | guanyl nucleotide binding | 5 | 1 |
GO:0030515 | snoRNA binding | 5 | 1 |
GO:0032553 | ribonucleotide binding | 3 | 1 |
GO:0032555 | purine ribonucleotide binding | 4 | 1 |
GO:0032561 | guanyl ribonucleotide binding | 5 | 1 |
GO:0034511 | U3 snoRNA binding | 6 | 1 |
GO:0035639 | purine ribonucleoside triphosphate binding | 4 | 1 |
GO:0036094 | small molecule binding | 2 | 1 |
GO:0043167 | ion binding | 2 | 1 |
GO:0043168 | anion binding | 3 | 1 |
GO:0097159 | organic cyclic compound binding | 2 | 1 |
GO:0097367 | carbohydrate derivative binding | 2 | 1 |
GO:1901265 | nucleoside phosphate binding | 3 | 1 |
GO:1901363 | heterocyclic compound binding | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 518 | 522 | PF00656 | 0.420 |
CLV_NRD_NRD_1 | 115 | 117 | PF00675 | 0.551 |
CLV_NRD_NRD_1 | 322 | 324 | PF00675 | 0.593 |
CLV_NRD_NRD_1 | 595 | 597 | PF00675 | 0.296 |
CLV_NRD_NRD_1 | 64 | 66 | PF00675 | 0.535 |
CLV_NRD_NRD_1 | 719 | 721 | PF00675 | 0.296 |
CLV_PCSK_FUR_1 | 53 | 57 | PF00082 | 0.572 |
CLV_PCSK_KEX2_1 | 55 | 57 | PF00082 | 0.465 |
CLV_PCSK_KEX2_1 | 64 | 66 | PF00082 | 0.443 |
CLV_PCSK_KEX2_1 | 677 | 679 | PF00082 | 0.292 |
CLV_PCSK_KEX2_1 | 719 | 721 | PF00082 | 0.296 |
CLV_PCSK_KEX2_1 | 753 | 755 | PF00082 | 0.283 |
CLV_PCSK_PC1ET2_1 | 55 | 57 | PF00082 | 0.477 |
CLV_PCSK_PC1ET2_1 | 677 | 679 | PF00082 | 0.292 |
CLV_PCSK_PC1ET2_1 | 753 | 755 | PF00082 | 0.283 |
CLV_PCSK_SKI1_1 | 117 | 121 | PF00082 | 0.421 |
CLV_PCSK_SKI1_1 | 14 | 18 | PF00082 | 0.547 |
CLV_PCSK_SKI1_1 | 164 | 168 | PF00082 | 0.668 |
CLV_PCSK_SKI1_1 | 223 | 227 | PF00082 | 0.379 |
CLV_PCSK_SKI1_1 | 264 | 268 | PF00082 | 0.331 |
CLV_PCSK_SKI1_1 | 478 | 482 | PF00082 | 0.294 |
CLV_PCSK_SKI1_1 | 483 | 487 | PF00082 | 0.288 |
CLV_PCSK_SKI1_1 | 551 | 555 | PF00082 | 0.442 |
CLV_PCSK_SKI1_1 | 58 | 62 | PF00082 | 0.526 |
CLV_PCSK_SKI1_1 | 626 | 630 | PF00082 | 0.442 |
CLV_PCSK_SKI1_1 | 678 | 682 | PF00082 | 0.296 |
CLV_PCSK_SKI1_1 | 696 | 700 | PF00082 | 0.296 |
CLV_PCSK_SKI1_1 | 734 | 738 | PF00082 | 0.373 |
CLV_PCSK_SKI1_1 | 753 | 757 | PF00082 | 0.147 |
DEG_APCC_DBOX_1 | 338 | 346 | PF00400 | 0.497 |
DOC_CDC14_PxL_1 | 643 | 651 | PF14671 | 0.296 |
DOC_CKS1_1 | 201 | 206 | PF01111 | 0.406 |
DOC_CKS1_1 | 467 | 472 | PF01111 | 0.296 |
DOC_CYCLIN_RxL_1 | 548 | 557 | PF00134 | 0.398 |
DOC_MAPK_gen_1 | 219 | 227 | PF00069 | 0.376 |
DOC_MAPK_gen_1 | 323 | 331 | PF00069 | 0.624 |
DOC_MAPK_MEF2A_6 | 138 | 147 | PF00069 | 0.341 |
DOC_PP1_RVXF_1 | 114 | 121 | PF00149 | 0.297 |
DOC_PP1_RVXF_1 | 262 | 269 | PF00149 | 0.296 |
DOC_PP4_FxxP_1 | 630 | 633 | PF00568 | 0.327 |
DOC_PP4_FxxP_1 | 644 | 647 | PF00568 | 0.296 |
DOC_USP7_MATH_1 | 137 | 141 | PF00917 | 0.418 |
DOC_USP7_MATH_1 | 18 | 22 | PF00917 | 0.652 |
DOC_USP7_MATH_1 | 197 | 201 | PF00917 | 0.482 |
DOC_USP7_MATH_1 | 244 | 248 | PF00917 | 0.517 |
DOC_USP7_MATH_1 | 35 | 39 | PF00917 | 0.469 |
DOC_USP7_MATH_1 | 378 | 382 | PF00917 | 0.542 |
DOC_USP7_MATH_1 | 582 | 586 | PF00917 | 0.296 |
DOC_USP7_MATH_1 | 81 | 85 | PF00917 | 0.419 |
DOC_USP7_UBL2_3 | 42 | 46 | PF12436 | 0.617 |
DOC_WW_Pin1_4 | 200 | 205 | PF00397 | 0.411 |
DOC_WW_Pin1_4 | 466 | 471 | PF00397 | 0.296 |
DOC_WW_Pin1_4 | 584 | 589 | PF00397 | 0.302 |
DOC_WW_Pin1_4 | 598 | 603 | PF00397 | 0.239 |
LIG_14-3-3_CanoR_1 | 230 | 236 | PF00244 | 0.406 |
LIG_14-3-3_CanoR_1 | 421 | 430 | PF00244 | 0.602 |
LIG_14-3-3_CanoR_1 | 440 | 448 | PF00244 | 0.465 |
LIG_14-3-3_CanoR_1 | 483 | 489 | PF00244 | 0.290 |
LIG_14-3-3_CanoR_1 | 533 | 539 | PF00244 | 0.428 |
LIG_14-3-3_CanoR_1 | 575 | 583 | PF00244 | 0.334 |
LIG_14-3-3_CanoR_1 | 626 | 631 | PF00244 | 0.322 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.624 |
LIG_BRCT_BRCA1_1 | 600 | 604 | PF00533 | 0.296 |
LIG_BRCT_BRCA1_1 | 615 | 619 | PF00533 | 0.296 |
LIG_deltaCOP1_diTrp_1 | 563 | 571 | PF00928 | 0.296 |
LIG_Dynein_DLC8_1 | 419 | 425 | PF01221 | 0.670 |
LIG_eIF4E_1 | 636 | 642 | PF01652 | 0.442 |
LIG_FHA_1 | 189 | 195 | PF00498 | 0.401 |
LIG_FHA_1 | 201 | 207 | PF00498 | 0.382 |
LIG_FHA_1 | 237 | 243 | PF00498 | 0.436 |
LIG_FHA_1 | 250 | 256 | PF00498 | 0.305 |
LIG_FHA_1 | 284 | 290 | PF00498 | 0.411 |
LIG_FHA_1 | 301 | 307 | PF00498 | 0.275 |
LIG_FHA_1 | 311 | 317 | PF00498 | 0.283 |
LIG_FHA_1 | 369 | 375 | PF00498 | 0.571 |
LIG_FHA_1 | 585 | 591 | PF00498 | 0.314 |
LIG_FHA_1 | 671 | 677 | PF00498 | 0.409 |
LIG_FHA_1 | 722 | 728 | PF00498 | 0.308 |
LIG_FHA_1 | 85 | 91 | PF00498 | 0.406 |
LIG_FHA_2 | 154 | 160 | PF00498 | 0.457 |
LIG_FHA_2 | 165 | 171 | PF00498 | 0.565 |
LIG_FHA_2 | 213 | 219 | PF00498 | 0.408 |
LIG_FHA_2 | 348 | 354 | PF00498 | 0.546 |
LIG_FHA_2 | 356 | 362 | PF00498 | 0.506 |
LIG_FHA_2 | 404 | 410 | PF00498 | 0.698 |
LIG_FHA_2 | 421 | 427 | PF00498 | 0.439 |
LIG_FHA_2 | 440 | 446 | PF00498 | 0.417 |
LIG_FHA_2 | 772 | 778 | PF00498 | 0.636 |
LIG_FXI_DFP_1 | 99 | 103 | PF00024 | 0.497 |
LIG_LIR_Apic_2 | 629 | 633 | PF02991 | 0.296 |
LIG_LIR_Apic_2 | 704 | 710 | PF02991 | 0.312 |
LIG_LIR_Gen_1 | 106 | 115 | PF02991 | 0.533 |
LIG_LIR_Gen_1 | 140 | 147 | PF02991 | 0.363 |
LIG_LIR_Gen_1 | 177 | 187 | PF02991 | 0.534 |
LIG_LIR_Gen_1 | 249 | 258 | PF02991 | 0.341 |
LIG_LIR_Gen_1 | 563 | 573 | PF02991 | 0.292 |
LIG_LIR_Gen_1 | 601 | 611 | PF02991 | 0.306 |
LIG_LIR_Gen_1 | 613 | 619 | PF02991 | 0.273 |
LIG_LIR_Nem_3 | 106 | 112 | PF02991 | 0.544 |
LIG_LIR_Nem_3 | 140 | 145 | PF02991 | 0.362 |
LIG_LIR_Nem_3 | 177 | 183 | PF02991 | 0.482 |
LIG_LIR_Nem_3 | 249 | 254 | PF02991 | 0.336 |
LIG_LIR_Nem_3 | 563 | 569 | PF02991 | 0.292 |
LIG_LIR_Nem_3 | 601 | 607 | PF02991 | 0.306 |
LIG_LIR_Nem_3 | 613 | 618 | PF02991 | 0.267 |
LIG_LIR_Nem_3 | 629 | 634 | PF02991 | 0.244 |
LIG_LIR_Nem_3 | 712 | 717 | PF02991 | 0.382 |
LIG_LIR_Nem_3 | 750 | 755 | PF02991 | 0.283 |
LIG_LRP6_Inhibitor_1 | 152 | 158 | PF00058 | 0.538 |
LIG_MLH1_MIPbox_1 | 615 | 619 | PF16413 | 0.201 |
LIG_MYND_3 | 646 | 650 | PF01753 | 0.296 |
LIG_PDZ_Class_3 | 775 | 780 | PF00595 | 0.628 |
LIG_Pex14_2 | 615 | 619 | PF04695 | 0.296 |
LIG_Pex14_2 | 752 | 756 | PF04695 | 0.417 |
LIG_SH2_CRK | 251 | 255 | PF00017 | 0.331 |
LIG_SH2_CRK | 503 | 507 | PF00017 | 0.303 |
LIG_SH2_CRK | 512 | 516 | PF00017 | 0.285 |
LIG_SH2_GRB2like | 231 | 234 | PF00017 | 0.446 |
LIG_SH2_GRB2like | 251 | 254 | PF00017 | 0.201 |
LIG_SH2_PTP2 | 599 | 602 | PF00017 | 0.296 |
LIG_SH2_SRC | 503 | 506 | PF00017 | 0.296 |
LIG_SH2_STAP1 | 190 | 194 | PF00017 | 0.482 |
LIG_SH2_STAP1 | 251 | 255 | PF00017 | 0.382 |
LIG_SH2_STAP1 | 503 | 507 | PF00017 | 0.298 |
LIG_SH2_STAT3 | 507 | 510 | PF00017 | 0.312 |
LIG_SH2_STAT5 | 190 | 193 | PF00017 | 0.486 |
LIG_SH2_STAT5 | 231 | 234 | PF00017 | 0.388 |
LIG_SH2_STAT5 | 251 | 254 | PF00017 | 0.114 |
LIG_SH2_STAT5 | 505 | 508 | PF00017 | 0.298 |
LIG_SH2_STAT5 | 599 | 602 | PF00017 | 0.296 |
LIG_SH2_STAT5 | 714 | 717 | PF00017 | 0.382 |
LIG_SH3_3 | 464 | 470 | PF00018 | 0.296 |
LIG_SH3_3 | 536 | 542 | PF00018 | 0.305 |
LIG_SH3_3 | 665 | 671 | PF00018 | 0.298 |
LIG_SUMO_SIM_anti_2 | 205 | 211 | PF11976 | 0.342 |
LIG_SUMO_SIM_par_1 | 143 | 148 | PF11976 | 0.349 |
LIG_SUMO_SIM_par_1 | 709 | 715 | PF11976 | 0.312 |
LIG_TRAF2_1 | 276 | 279 | PF00917 | 0.354 |
LIG_TRAF2_1 | 442 | 445 | PF00917 | 0.502 |
LIG_TRAF2_1 | 457 | 460 | PF00917 | 0.542 |
LIG_TRAF2_1 | 648 | 651 | PF00917 | 0.296 |
LIG_UBA3_1 | 254 | 262 | PF00899 | 0.331 |
LIG_UBA3_1 | 447 | 454 | PF00899 | 0.597 |
LIG_UBA3_1 | 589 | 597 | PF00899 | 0.312 |
LIG_WRC_WIRS_1 | 213 | 218 | PF05994 | 0.401 |
LIG_WRC_WIRS_1 | 485 | 490 | PF05994 | 0.312 |
LIG_WRC_WIRS_1 | 627 | 632 | PF05994 | 0.296 |
LIG_WW_1 | 500 | 503 | PF00397 | 0.354 |
MOD_CK1_1 | 110 | 116 | PF00069 | 0.463 |
MOD_CK1_1 | 200 | 206 | PF00069 | 0.435 |
MOD_CK1_1 | 234 | 240 | PF00069 | 0.537 |
MOD_CK1_1 | 419 | 425 | PF00069 | 0.584 |
MOD_CK1_1 | 487 | 493 | PF00069 | 0.296 |
MOD_CK1_1 | 605 | 611 | PF00069 | 0.300 |
MOD_CK1_1 | 613 | 619 | PF00069 | 0.290 |
MOD_CK1_1 | 84 | 90 | PF00069 | 0.398 |
MOD_CK2_1 | 153 | 159 | PF00069 | 0.429 |
MOD_CK2_1 | 331 | 337 | PF00069 | 0.514 |
MOD_CK2_1 | 346 | 352 | PF00069 | 0.607 |
MOD_CK2_1 | 439 | 445 | PF00069 | 0.502 |
MOD_CK2_1 | 454 | 460 | PF00069 | 0.533 |
MOD_CK2_1 | 645 | 651 | PF00069 | 0.296 |
MOD_CK2_1 | 771 | 777 | PF00069 | 0.579 |
MOD_Cter_Amidation | 717 | 720 | PF01082 | 0.296 |
MOD_GlcNHglycan | 300 | 303 | PF01048 | 0.341 |
MOD_GlcNHglycan | 37 | 40 | PF01048 | 0.650 |
MOD_GlcNHglycan | 517 | 520 | PF01048 | 0.408 |
MOD_GlcNHglycan | 556 | 559 | PF01048 | 0.286 |
MOD_GlcNHglycan | 608 | 611 | PF01048 | 0.404 |
MOD_GlcNHglycan | 67 | 70 | PF01048 | 0.488 |
MOD_GlcNHglycan | 681 | 684 | PF01048 | 0.358 |
MOD_GlcNHglycan | 83 | 86 | PF01048 | 0.384 |
MOD_GSK3_1 | 143 | 150 | PF00069 | 0.375 |
MOD_GSK3_1 | 160 | 167 | PF00069 | 0.473 |
MOD_GSK3_1 | 171 | 178 | PF00069 | 0.576 |
MOD_GSK3_1 | 258 | 265 | PF00069 | 0.335 |
MOD_GSK3_1 | 283 | 290 | PF00069 | 0.442 |
MOD_GSK3_1 | 306 | 313 | PF00069 | 0.283 |
MOD_GSK3_1 | 416 | 423 | PF00069 | 0.595 |
MOD_GSK3_1 | 598 | 605 | PF00069 | 0.296 |
MOD_GSK3_1 | 606 | 613 | PF00069 | 0.296 |
MOD_GSK3_1 | 758 | 765 | PF00069 | 0.491 |
MOD_LATS_1 | 40 | 46 | PF00433 | 0.540 |
MOD_N-GLC_1 | 347 | 352 | PF02516 | 0.582 |
MOD_N-GLC_1 | 81 | 86 | PF02516 | 0.412 |
MOD_N-GLC_2 | 547 | 549 | PF02516 | 0.405 |
MOD_NEK2_1 | 147 | 152 | PF00069 | 0.372 |
MOD_NEK2_1 | 160 | 165 | PF00069 | 0.492 |
MOD_NEK2_1 | 236 | 241 | PF00069 | 0.481 |
MOD_NEK2_1 | 258 | 263 | PF00069 | 0.314 |
MOD_NEK2_1 | 289 | 294 | PF00069 | 0.382 |
MOD_NEK2_1 | 300 | 305 | PF00069 | 0.405 |
MOD_NEK2_1 | 554 | 559 | PF00069 | 0.382 |
MOD_NEK2_1 | 663 | 668 | PF00069 | 0.396 |
MOD_NEK2_1 | 94 | 99 | PF00069 | 0.468 |
MOD_NEK2_2 | 484 | 489 | PF00069 | 0.442 |
MOD_PIKK_1 | 147 | 153 | PF00454 | 0.388 |
MOD_PIKK_1 | 197 | 203 | PF00454 | 0.482 |
MOD_PIKK_1 | 244 | 250 | PF00454 | 0.562 |
MOD_PIKK_1 | 283 | 289 | PF00454 | 0.411 |
MOD_PIKK_1 | 300 | 306 | PF00454 | 0.275 |
MOD_PIKK_1 | 420 | 426 | PF00454 | 0.625 |
MOD_PKA_2 | 338 | 344 | PF00069 | 0.554 |
MOD_PKA_2 | 420 | 426 | PF00069 | 0.617 |
MOD_PKA_2 | 439 | 445 | PF00069 | 0.346 |
MOD_PKA_2 | 515 | 521 | PF00069 | 0.390 |
MOD_PKA_2 | 574 | 580 | PF00069 | 0.331 |
MOD_PKB_1 | 624 | 632 | PF00069 | 0.442 |
MOD_Plk_1 | 287 | 293 | PF00069 | 0.433 |
MOD_Plk_1 | 347 | 353 | PF00069 | 0.599 |
MOD_Plk_2-3 | 439 | 445 | PF00069 | 0.502 |
MOD_Plk_4 | 175 | 181 | PF00069 | 0.521 |
MOD_Plk_4 | 202 | 208 | PF00069 | 0.385 |
MOD_Plk_4 | 231 | 237 | PF00069 | 0.363 |
MOD_Plk_4 | 541 | 547 | PF00069 | 0.338 |
MOD_Plk_4 | 626 | 632 | PF00069 | 0.296 |
MOD_Plk_4 | 670 | 676 | PF00069 | 0.404 |
MOD_ProDKin_1 | 200 | 206 | PF00069 | 0.409 |
MOD_ProDKin_1 | 466 | 472 | PF00069 | 0.296 |
MOD_ProDKin_1 | 584 | 590 | PF00069 | 0.302 |
MOD_ProDKin_1 | 598 | 604 | PF00069 | 0.239 |
MOD_SUMO_for_1 | 430 | 433 | PF00179 | 0.549 |
MOD_SUMO_rev_2 | 110 | 119 | PF00179 | 0.442 |
MOD_SUMO_rev_2 | 557 | 567 | PF00179 | 0.296 |
MOD_SUMO_rev_2 | 702 | 708 | PF00179 | 0.417 |
TRG_DiLeu_BaEn_1 | 550 | 555 | PF01217 | 0.442 |
TRG_DiLeu_BaLyEn_6 | 637 | 642 | PF01217 | 0.417 |
TRG_ENDOCYTIC_2 | 251 | 254 | PF00928 | 0.312 |
TRG_ENDOCYTIC_2 | 274 | 277 | PF00928 | 0.296 |
TRG_ENDOCYTIC_2 | 482 | 485 | PF00928 | 0.296 |
TRG_ENDOCYTIC_2 | 503 | 506 | PF00928 | 0.296 |
TRG_ENDOCYTIC_2 | 512 | 515 | PF00928 | 0.296 |
TRG_ENDOCYTIC_2 | 697 | 700 | PF00928 | 0.296 |
TRG_ENDOCYTIC_2 | 714 | 717 | PF00928 | 0.296 |
TRG_ER_diArg_1 | 476 | 479 | PF00400 | 0.312 |
TRG_ER_diArg_1 | 64 | 66 | PF00400 | 0.520 |
TRG_Pf-PMV_PEXEL_1 | 158 | 162 | PF00026 | 0.594 |
TRG_Pf-PMV_PEXEL_1 | 328 | 332 | PF00026 | 0.584 |
TRG_Pf-PMV_PEXEL_1 | 446 | 451 | PF00026 | 0.605 |
TRG_Pf-PMV_PEXEL_1 | 454 | 458 | PF00026 | 0.599 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PD92 | Leptomonas seymouri | 83% | 100% |
A0A0S4JNZ2 | Bodo saltans | 54% | 100% |
A0A1X0NPB7 | Trypanosomatidae | 62% | 100% |
A0A422NAK8 | Trypanosoma rangeli | 61% | 100% |
A4H4Z3 | Leishmania braziliensis | 89% | 100% |
C9ZUQ9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 59% | 100% |
E9AL58 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 96% | 100% |
O13956 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 28% | 100% |
Q07381 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 26% | 99% |
Q19329 | Caenorhabditis elegans | 31% | 99% |
Q2NL82 | Homo sapiens | 29% | 97% |
Q4QIP6 | Leishmania major | 97% | 100% |
Q5R434 | Pongo abelii | 29% | 97% |
Q5SWD9 | Mus musculus | 30% | 97% |
Q5XGY1 | Xenopus laevis | 29% | 96% |
Q61WR2 | Caenorhabditis briggsae | 31% | 99% |
Q9VP47 | Drosophila melanogaster | 29% | 96% |
V5BHC1 | Trypanosoma cruzi | 59% | 100% |