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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0005789 | endoplasmic reticulum membrane | 4 | 1 |
GO:0016020 | membrane | 2 | 1 |
GO:0031090 | organelle membrane | 3 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: E9AUB5
Term | Name | Level | Count |
---|---|---|---|
GO:0006807 | nitrogen compound metabolic process | 2 | 12 |
GO:0008152 | metabolic process | 1 | 12 |
GO:0019538 | protein metabolic process | 3 | 12 |
GO:0032446 | protein modification by small protein conjugation | 6 | 12 |
GO:0036211 | protein modification process | 4 | 12 |
GO:0043170 | macromolecule metabolic process | 3 | 12 |
GO:0043412 | macromolecule modification | 4 | 12 |
GO:0044238 | primary metabolic process | 2 | 12 |
GO:0070647 | protein modification by small protein conjugation or removal | 5 | 12 |
GO:0071569 | protein ufmylation | 7 | 12 |
GO:0071704 | organic substance metabolic process | 2 | 12 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 12 |
GO:0006950 | response to stress | 2 | 1 |
GO:0009894 | regulation of catabolic process | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0019222 | regulation of metabolic process | 3 | 1 |
GO:0030162 | regulation of proteolysis | 6 | 1 |
GO:0031323 | regulation of cellular metabolic process | 4 | 1 |
GO:0031329 | regulation of cellular catabolic process | 5 | 1 |
GO:0032434 | regulation of proteasomal ubiquitin-dependent protein catabolic process | 7 | 1 |
GO:0033554 | cellular response to stress | 3 | 1 |
GO:0034976 | response to endoplasmic reticulum stress | 4 | 1 |
GO:0042176 | regulation of protein catabolic process | 5 | 1 |
GO:0050789 | regulation of biological process | 2 | 1 |
GO:0050794 | regulation of cellular process | 3 | 1 |
GO:0050896 | response to stimulus | 1 | 1 |
GO:0051171 | regulation of nitrogen compound metabolic process | 4 | 1 |
GO:0051246 | regulation of protein metabolic process | 5 | 1 |
GO:0051716 | cellular response to stimulus | 2 | 1 |
GO:0060255 | regulation of macromolecule metabolic process | 4 | 1 |
GO:0061136 | regulation of proteasomal protein catabolic process | 6 | 1 |
GO:0065007 | biological regulation | 1 | 1 |
GO:0080090 | regulation of primary metabolic process | 4 | 1 |
GO:1903050 | regulation of proteolysis involved in protein catabolic process | 7 | 1 |
GO:1990564 | protein polyufmylation | 8 | 1 |
GO:1990592 | protein K69-linked ufmylation | 9 | 1 |
GO:2000058 | regulation of ubiquitin-dependent protein catabolic process | 6 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 12 |
GO:0016740 | transferase activity | 2 | 12 |
GO:0019787 | ubiquitin-like protein transferase activity | 3 | 12 |
GO:0061659 | ubiquitin-like protein ligase activity | 4 | 12 |
GO:0061666 | UFM1 ligase activity | 5 | 12 |
GO:0071568 | UFM1 transferase activity | 4 | 12 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 300 | 302 | PF00675 | 0.611 |
CLV_NRD_NRD_1 | 303 | 305 | PF00675 | 0.595 |
CLV_NRD_NRD_1 | 581 | 583 | PF00675 | 0.424 |
CLV_PCSK_KEX2_1 | 11 | 13 | PF00082 | 0.437 |
CLV_PCSK_KEX2_1 | 204 | 206 | PF00082 | 0.362 |
CLV_PCSK_KEX2_1 | 242 | 244 | PF00082 | 0.362 |
CLV_PCSK_KEX2_1 | 581 | 583 | PF00082 | 0.426 |
CLV_PCSK_KEX2_1 | 61 | 63 | PF00082 | 0.266 |
CLV_PCSK_PC1ET2_1 | 11 | 13 | PF00082 | 0.420 |
CLV_PCSK_PC1ET2_1 | 204 | 206 | PF00082 | 0.232 |
CLV_PCSK_PC1ET2_1 | 242 | 244 | PF00082 | 0.331 |
CLV_PCSK_PC1ET2_1 | 61 | 63 | PF00082 | 0.411 |
CLV_PCSK_SKI1_1 | 152 | 156 | PF00082 | 0.391 |
CLV_PCSK_SKI1_1 | 360 | 364 | PF00082 | 0.386 |
CLV_PCSK_SKI1_1 | 416 | 420 | PF00082 | 0.512 |
CLV_PCSK_SKI1_1 | 490 | 494 | PF00082 | 0.571 |
CLV_PCSK_SKI1_1 | 572 | 576 | PF00082 | 0.427 |
CLV_PCSK_SKI1_1 | 726 | 730 | PF00082 | 0.464 |
CLV_Separin_Metazoa | 195 | 199 | PF03568 | 0.331 |
DEG_APCC_DBOX_1 | 581 | 589 | PF00400 | 0.419 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.557 |
DOC_CDC14_PxL_1 | 348 | 356 | PF14671 | 0.462 |
DOC_CYCLIN_RxL_1 | 149 | 157 | PF00134 | 0.210 |
DOC_CYCLIN_RxL_1 | 569 | 579 | PF00134 | 0.497 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 37 | 46 | PF00134 | 0.287 |
DOC_MAPK_gen_1 | 39 | 47 | PF00069 | 0.285 |
DOC_MAPK_gen_1 | 427 | 433 | PF00069 | 0.623 |
DOC_MAPK_gen_1 | 581 | 588 | PF00069 | 0.510 |
DOC_MAPK_gen_1 | 623 | 633 | PF00069 | 0.406 |
DOC_MAPK_MEF2A_6 | 227 | 235 | PF00069 | 0.167 |
DOC_MAPK_MEF2A_6 | 317 | 325 | PF00069 | 0.664 |
DOC_MAPK_MEF2A_6 | 360 | 367 | PF00069 | 0.406 |
DOC_MAPK_MEF2A_6 | 39 | 47 | PF00069 | 0.361 |
DOC_MAPK_MEF2A_6 | 624 | 633 | PF00069 | 0.404 |
DOC_MAPK_NFAT4_5 | 40 | 48 | PF00069 | 0.387 |
DOC_MIT_MIM_1 | 8 | 16 | PF04212 | 0.411 |
DOC_PP1_RVXF_1 | 507 | 514 | PF00149 | 0.339 |
DOC_PP2B_LxvP_1 | 208 | 211 | PF13499 | 0.281 |
DOC_PP2B_LxvP_1 | 445 | 448 | PF13499 | 0.507 |
DOC_PP4_FxxP_1 | 618 | 621 | PF00568 | 0.457 |
DOC_USP7_MATH_1 | 211 | 215 | PF00917 | 0.438 |
DOC_USP7_MATH_1 | 353 | 357 | PF00917 | 0.487 |
DOC_USP7_MATH_1 | 422 | 426 | PF00917 | 0.532 |
DOC_USP7_MATH_1 | 644 | 648 | PF00917 | 0.592 |
DOC_USP7_UBL2_3 | 176 | 180 | PF12436 | 0.167 |
DOC_USP7_UBL2_3 | 302 | 306 | PF12436 | 0.660 |
LIG_14-3-3_CanoR_1 | 12 | 17 | PF00244 | 0.383 |
LIG_14-3-3_CanoR_1 | 322 | 326 | PF00244 | 0.636 |
LIG_14-3-3_CanoR_1 | 528 | 538 | PF00244 | 0.371 |
LIG_14-3-3_CanoR_1 | 581 | 586 | PF00244 | 0.457 |
LIG_14-3-3_CanoR_1 | 687 | 695 | PF00244 | 0.468 |
LIG_14-3-3_CanoR_1 | 726 | 731 | PF00244 | 0.421 |
LIG_APCC_ABBA_1 | 371 | 376 | PF00400 | 0.530 |
LIG_APCC_ABBA_1 | 574 | 579 | PF00400 | 0.392 |
LIG_BRCT_BRCA1_1 | 146 | 150 | PF00533 | 0.360 |
LIG_BRCT_BRCA1_2 | 146 | 152 | PF00533 | 0.331 |
LIG_CaM_IQ_9 | 10 | 26 | PF13499 | 0.322 |
LIG_eIF4E_1 | 203 | 209 | PF01652 | 0.411 |
LIG_FHA_1 | 102 | 108 | PF00498 | 0.298 |
LIG_FHA_1 | 242 | 248 | PF00498 | 0.426 |
LIG_FHA_1 | 400 | 406 | PF00498 | 0.557 |
LIG_FHA_1 | 497 | 503 | PF00498 | 0.525 |
LIG_FHA_1 | 661 | 667 | PF00498 | 0.438 |
LIG_FHA_1 | 727 | 733 | PF00498 | 0.619 |
LIG_FHA_2 | 155 | 161 | PF00498 | 0.167 |
LIG_FHA_2 | 408 | 414 | PF00498 | 0.372 |
LIG_FHA_2 | 54 | 60 | PF00498 | 0.411 |
LIG_FHA_2 | 601 | 607 | PF00498 | 0.495 |
LIG_FHA_2 | 719 | 725 | PF00498 | 0.521 |
LIG_GBD_Chelix_1 | 466 | 474 | PF00786 | 0.470 |
LIG_LIR_Apic_2 | 276 | 281 | PF02991 | 0.521 |
LIG_LIR_Gen_1 | 138 | 146 | PF02991 | 0.309 |
LIG_LIR_Gen_1 | 175 | 186 | PF02991 | 0.393 |
LIG_LIR_Gen_1 | 499 | 508 | PF02991 | 0.428 |
LIG_LIR_Gen_1 | 56 | 65 | PF02991 | 0.266 |
LIG_LIR_Gen_1 | 628 | 638 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 175 | 181 | PF02991 | 0.346 |
LIG_LIR_Nem_3 | 207 | 212 | PF02991 | 0.421 |
LIG_LIR_Nem_3 | 253 | 259 | PF02991 | 0.264 |
LIG_LIR_Nem_3 | 378 | 384 | PF02991 | 0.490 |
LIG_LIR_Nem_3 | 390 | 395 | PF02991 | 0.438 |
LIG_LIR_Nem_3 | 450 | 455 | PF02991 | 0.452 |
LIG_LIR_Nem_3 | 461 | 466 | PF02991 | 0.357 |
LIG_LIR_Nem_3 | 499 | 504 | PF02991 | 0.435 |
LIG_LIR_Nem_3 | 56 | 60 | PF02991 | 0.266 |
LIG_LIR_Nem_3 | 628 | 633 | PF02991 | 0.533 |
LIG_LYPXL_S_1 | 391 | 395 | PF13949 | 0.559 |
LIG_LYPXL_yS_3 | 392 | 395 | PF13949 | 0.558 |
LIG_NRBOX | 41 | 47 | PF00104 | 0.253 |
LIG_PCNA_PIPBox_1 | 143 | 152 | PF02747 | 0.287 |
LIG_SH2_CRK | 259 | 263 | PF00017 | 0.266 |
LIG_SH2_NCK_1 | 278 | 282 | PF00017 | 0.607 |
LIG_SH2_PTP2 | 234 | 237 | PF00017 | 0.331 |
LIG_SH2_PTP2 | 630 | 633 | PF00017 | 0.395 |
LIG_SH2_SRC | 117 | 120 | PF00017 | 0.266 |
LIG_SH2_STAP1 | 174 | 178 | PF00017 | 0.325 |
LIG_SH2_STAT3 | 174 | 177 | PF00017 | 0.325 |
LIG_SH2_STAT5 | 117 | 120 | PF00017 | 0.266 |
LIG_SH2_STAT5 | 174 | 177 | PF00017 | 0.281 |
LIG_SH2_STAT5 | 234 | 237 | PF00017 | 0.304 |
LIG_SH2_STAT5 | 256 | 259 | PF00017 | 0.271 |
LIG_SH2_STAT5 | 273 | 276 | PF00017 | 0.510 |
LIG_SH2_STAT5 | 347 | 350 | PF00017 | 0.422 |
LIG_SH2_STAT5 | 54 | 57 | PF00017 | 0.288 |
LIG_SH2_STAT5 | 630 | 633 | PF00017 | 0.501 |
LIG_SH3_3 | 561 | 567 | PF00018 | 0.543 |
LIG_SH3_3 | 671 | 677 | PF00018 | 0.395 |
LIG_SH3_3 | 75 | 81 | PF00018 | 0.281 |
LIG_SUMO_SIM_par_1 | 103 | 108 | PF11976 | 0.393 |
LIG_SUMO_SIM_par_1 | 243 | 248 | PF11976 | 0.167 |
LIG_SUMO_SIM_par_1 | 402 | 408 | PF11976 | 0.572 |
LIG_TRAF2_1 | 192 | 195 | PF00917 | 0.331 |
LIG_TRAF2_1 | 410 | 413 | PF00917 | 0.473 |
LIG_TRAF2_1 | 492 | 495 | PF00917 | 0.389 |
LIG_TRAF2_1 | 721 | 724 | PF00917 | 0.444 |
LIG_TYR_ITIM | 257 | 262 | PF00017 | 0.266 |
LIG_UBA3_1 | 373 | 379 | PF00899 | 0.585 |
LIG_UBA3_1 | 585 | 593 | PF00899 | 0.416 |
MOD_CK1_1 | 172 | 178 | PF00069 | 0.347 |
MOD_CK1_1 | 292 | 298 | PF00069 | 0.740 |
MOD_CK1_1 | 660 | 666 | PF00069 | 0.381 |
MOD_CK2_1 | 154 | 160 | PF00069 | 0.167 |
MOD_CK2_1 | 407 | 413 | PF00069 | 0.303 |
MOD_CK2_1 | 53 | 59 | PF00069 | 0.411 |
MOD_CK2_1 | 600 | 606 | PF00069 | 0.457 |
MOD_CK2_1 | 633 | 639 | PF00069 | 0.470 |
MOD_CK2_1 | 693 | 699 | PF00069 | 0.588 |
MOD_CK2_1 | 710 | 716 | PF00069 | 0.483 |
MOD_CK2_1 | 718 | 724 | PF00069 | 0.420 |
MOD_CK2_1 | 94 | 100 | PF00069 | 0.296 |
MOD_Cter_Amidation | 302 | 305 | PF01082 | 0.613 |
MOD_GlcNHglycan | 294 | 297 | PF01048 | 0.743 |
MOD_GlcNHglycan | 327 | 330 | PF01048 | 0.586 |
MOD_GlcNHglycan | 396 | 399 | PF01048 | 0.624 |
MOD_GlcNHglycan | 407 | 410 | PF01048 | 0.490 |
MOD_GlcNHglycan | 424 | 427 | PF01048 | 0.458 |
MOD_GlcNHglycan | 476 | 479 | PF01048 | 0.559 |
MOD_GlcNHglycan | 522 | 525 | PF01048 | 0.503 |
MOD_GlcNHglycan | 557 | 560 | PF01048 | 0.315 |
MOD_GlcNHglycan | 606 | 610 | PF01048 | 0.442 |
MOD_GSK3_1 | 131 | 138 | PF00069 | 0.308 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.176 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.429 |
MOD_GSK3_1 | 288 | 295 | PF00069 | 0.631 |
MOD_GSK3_1 | 321 | 328 | PF00069 | 0.561 |
MOD_GSK3_1 | 401 | 408 | PF00069 | 0.459 |
MOD_GSK3_1 | 422 | 429 | PF00069 | 0.514 |
MOD_GSK3_1 | 551 | 558 | PF00069 | 0.491 |
MOD_GSK3_1 | 577 | 584 | PF00069 | 0.466 |
MOD_GSK3_1 | 656 | 663 | PF00069 | 0.455 |
MOD_GSK3_1 | 726 | 733 | PF00069 | 0.567 |
MOD_N-GLC_1 | 544 | 549 | PF02516 | 0.393 |
MOD_N-GLC_1 | 555 | 560 | PF02516 | 0.420 |
MOD_NEK2_1 | 135 | 140 | PF00069 | 0.348 |
MOD_NEK2_1 | 150 | 155 | PF00069 | 0.244 |
MOD_NEK2_1 | 212 | 217 | PF00069 | 0.337 |
MOD_NEK2_1 | 250 | 255 | PF00069 | 0.323 |
MOD_NEK2_1 | 474 | 479 | PF00069 | 0.517 |
MOD_NEK2_1 | 486 | 491 | PF00069 | 0.376 |
MOD_NEK2_1 | 504 | 509 | PF00069 | 0.435 |
MOD_NEK2_1 | 577 | 582 | PF00069 | 0.531 |
MOD_NEK2_1 | 600 | 605 | PF00069 | 0.386 |
MOD_NEK2_1 | 607 | 612 | PF00069 | 0.350 |
MOD_NEK2_1 | 657 | 662 | PF00069 | 0.349 |
MOD_NEK2_2 | 82 | 87 | PF00069 | 0.337 |
MOD_PIKK_1 | 135 | 141 | PF00454 | 0.393 |
MOD_PIKK_1 | 562 | 568 | PF00454 | 0.575 |
MOD_PK_1 | 593 | 599 | PF00069 | 0.442 |
MOD_PK_1 | 642 | 648 | PF00069 | 0.445 |
MOD_PKA_1 | 581 | 587 | PF00069 | 0.459 |
MOD_PKA_2 | 321 | 327 | PF00069 | 0.654 |
MOD_PKA_2 | 581 | 587 | PF00069 | 0.467 |
MOD_PKA_2 | 633 | 639 | PF00069 | 0.284 |
MOD_Plk_1 | 169 | 175 | PF00069 | 0.397 |
MOD_Plk_1 | 544 | 550 | PF00069 | 0.400 |
MOD_Plk_1 | 593 | 599 | PF00069 | 0.516 |
MOD_Plk_2-3 | 53 | 59 | PF00069 | 0.266 |
MOD_Plk_4 | 145 | 151 | PF00069 | 0.266 |
MOD_Plk_4 | 169 | 175 | PF00069 | 0.411 |
MOD_Plk_4 | 212 | 218 | PF00069 | 0.335 |
MOD_Plk_4 | 353 | 359 | PF00069 | 0.468 |
MOD_Plk_4 | 396 | 402 | PF00069 | 0.472 |
MOD_Plk_4 | 581 | 587 | PF00069 | 0.427 |
MOD_Plk_4 | 633 | 639 | PF00069 | 0.311 |
MOD_Plk_4 | 660 | 666 | PF00069 | 0.346 |
MOD_Plk_4 | 94 | 100 | PF00069 | 0.378 |
MOD_SUMO_for_1 | 60 | 63 | PF00179 | 0.411 |
MOD_SUMO_for_1 | 688 | 691 | PF00179 | 0.459 |
MOD_SUMO_rev_2 | 2 | 7 | PF00179 | 0.322 |
MOD_SUMO_rev_2 | 408 | 418 | PF00179 | 0.430 |
MOD_SUMO_rev_2 | 635 | 644 | PF00179 | 0.510 |
TRG_DiLeu_BaEn_1 | 108 | 113 | PF01217 | 0.281 |
TRG_DiLeu_BaEn_1 | 396 | 401 | PF01217 | 0.557 |
TRG_DiLeu_BaEn_4 | 100 | 106 | PF01217 | 0.287 |
TRG_DiLeu_BaEn_4 | 194 | 200 | PF01217 | 0.331 |
TRG_DiLeu_BaLyEn_6 | 379 | 384 | PF01217 | 0.410 |
TRG_DiLeu_BaLyEn_6 | 584 | 589 | PF01217 | 0.506 |
TRG_ENDOCYTIC_2 | 234 | 237 | PF00928 | 0.425 |
TRG_ENDOCYTIC_2 | 259 | 262 | PF00928 | 0.266 |
TRG_ENDOCYTIC_2 | 392 | 395 | PF00928 | 0.558 |
TRG_ENDOCYTIC_2 | 452 | 455 | PF00928 | 0.466 |
TRG_ENDOCYTIC_2 | 630 | 633 | PF00928 | 0.519 |
TRG_ER_diArg_1 | 161 | 164 | PF00400 | 0.331 |
TRG_NES_CRM1_1 | 361 | 376 | PF08389 | 0.483 |
TRG_NLS_MonoExtC_3 | 300 | 305 | PF00514 | 0.622 |
TRG_NLS_MonoExtN_4 | 301 | 308 | PF00514 | 0.597 |
TRG_Pf-PMV_PEXEL_1 | 457 | 461 | PF00026 | 0.486 |
TRG_Pf-PMV_PEXEL_1 | 62 | 66 | PF00026 | 0.349 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IM39 | Leptomonas seymouri | 66% | 99% |
A0A0S4JTJ6 | Bodo saltans | 35% | 94% |
A0A1X0NLV8 | Trypanosomatidae | 42% | 98% |
A0A3S7XCH5 | Leishmania donovani | 90% | 99% |
A0A422NVV8 | Trypanosoma rangeli | 42% | 99% |
A4HQK2 | Leishmania braziliensis | 81% | 100% |
A4ICC0 | Leishmania infantum | 89% | 99% |
D0A3Q3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 43% | 99% |
Q4Q075 | Leishmania major | 90% | 100% |
V5AXN4 | Trypanosoma cruzi | 40% | 99% |