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: A4HQK2
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 | 204 | 206 | PF00675 | 0.370 |
CLV_NRD_NRD_1 | 304 | 306 | PF00675 | 0.665 |
CLV_NRD_NRD_1 | 307 | 309 | PF00675 | 0.644 |
CLV_NRD_NRD_1 | 430 | 432 | PF00675 | 0.466 |
CLV_NRD_NRD_1 | 585 | 587 | PF00675 | 0.482 |
CLV_PCSK_KEX2_1 | 11 | 13 | PF00082 | 0.449 |
CLV_PCSK_KEX2_1 | 204 | 206 | PF00082 | 0.415 |
CLV_PCSK_KEX2_1 | 242 | 244 | PF00082 | 0.415 |
CLV_PCSK_KEX2_1 | 585 | 587 | PF00082 | 0.483 |
CLV_PCSK_KEX2_1 | 61 | 63 | PF00082 | 0.328 |
CLV_PCSK_KEX2_1 | 652 | 654 | PF00082 | 0.543 |
CLV_PCSK_PC1ET2_1 | 11 | 13 | PF00082 | 0.449 |
CLV_PCSK_PC1ET2_1 | 242 | 244 | PF00082 | 0.475 |
CLV_PCSK_PC1ET2_1 | 61 | 63 | PF00082 | 0.449 |
CLV_PCSK_PC1ET2_1 | 652 | 654 | PF00082 | 0.543 |
CLV_PCSK_SKI1_1 | 152 | 156 | PF00082 | 0.435 |
CLV_PCSK_SKI1_1 | 420 | 424 | PF00082 | 0.535 |
CLV_Separin_Metazoa | 195 | 199 | PF03568 | 0.475 |
CLV_Separin_Metazoa | 458 | 462 | PF03568 | 0.545 |
DEG_APCC_DBOX_1 | 585 | 593 | PF00400 | 0.428 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.614 |
DOC_CDC14_PxL_1 | 352 | 360 | PF14671 | 0.586 |
DOC_CYCLIN_RxL_1 | 149 | 156 | PF00134 | 0.262 |
DOC_MAPK_gen_1 | 40 | 47 | PF00069 | 0.349 |
DOC_MAPK_gen_1 | 431 | 437 | PF00069 | 0.616 |
DOC_MAPK_gen_1 | 585 | 592 | PF00069 | 0.556 |
DOC_MAPK_gen_1 | 597 | 605 | PF00069 | 0.370 |
DOC_MAPK_gen_1 | 673 | 680 | PF00069 | 0.442 |
DOC_MAPK_MEF2A_6 | 321 | 329 | PF00069 | 0.685 |
DOC_MAPK_MEF2A_6 | 364 | 371 | PF00069 | 0.501 |
DOC_MAPK_MEF2A_6 | 40 | 47 | PF00069 | 0.413 |
DOC_MAPK_MEF2A_6 | 597 | 605 | PF00069 | 0.524 |
DOC_MAPK_NFAT4_5 | 40 | 48 | PF00069 | 0.433 |
DOC_MIT_MIM_1 | 8 | 16 | PF04212 | 0.449 |
DOC_PP1_RVXF_1 | 511 | 518 | PF00149 | 0.403 |
DOC_PP2B_LxvP_1 | 208 | 211 | PF13499 | 0.344 |
DOC_PP4_FxxP_1 | 622 | 625 | PF00568 | 0.476 |
DOC_USP7_MATH_1 | 298 | 302 | PF00917 | 0.721 |
DOC_USP7_MATH_1 | 430 | 434 | PF00917 | 0.572 |
DOC_USP7_MATH_1 | 618 | 622 | PF00917 | 0.455 |
DOC_USP7_MATH_1 | 646 | 650 | PF00917 | 0.611 |
DOC_USP7_UBL2_3 | 306 | 310 | PF12436 | 0.795 |
DOC_WW_Pin1_4 | 621 | 626 | PF00397 | 0.344 |
LIG_14-3-3_CanoR_1 | 12 | 17 | PF00244 | 0.423 |
LIG_14-3-3_CanoR_1 | 271 | 281 | PF00244 | 0.398 |
LIG_14-3-3_CanoR_1 | 455 | 463 | PF00244 | 0.476 |
LIG_14-3-3_CanoR_1 | 532 | 542 | PF00244 | 0.426 |
LIG_14-3-3_CanoR_1 | 585 | 590 | PF00244 | 0.503 |
LIG_14-3-3_CanoR_1 | 691 | 699 | PF00244 | 0.617 |
LIG_APCC_ABBA_1 | 375 | 380 | PF00400 | 0.554 |
LIG_APCC_ABBA_1 | 578 | 583 | PF00400 | 0.451 |
LIG_APCC_ABBA_1 | 601 | 606 | PF00400 | 0.440 |
LIG_BRCT_BRCA1_1 | 146 | 150 | PF00533 | 0.413 |
LIG_BRCT_BRCA1_1 | 342 | 346 | PF00533 | 0.306 |
LIG_BRCT_BRCA1_1 | 347 | 351 | PF00533 | 0.292 |
LIG_BRCT_BRCA1_2 | 146 | 152 | PF00533 | 0.475 |
LIG_CaM_IQ_9 | 10 | 26 | PF13499 | 0.383 |
LIG_eIF4E_1 | 203 | 209 | PF01652 | 0.449 |
LIG_FHA_1 | 242 | 248 | PF00498 | 0.458 |
LIG_FHA_1 | 315 | 321 | PF00498 | 0.642 |
LIG_FHA_1 | 364 | 370 | PF00498 | 0.427 |
LIG_FHA_1 | 406 | 412 | PF00498 | 0.524 |
LIG_FHA_1 | 501 | 507 | PF00498 | 0.540 |
LIG_FHA_1 | 524 | 530 | PF00498 | 0.372 |
LIG_FHA_1 | 665 | 671 | PF00498 | 0.476 |
LIG_FHA_1 | 729 | 735 | PF00498 | 0.564 |
LIG_FHA_1 | 86 | 92 | PF00498 | 0.437 |
LIG_FHA_2 | 54 | 60 | PF00498 | 0.449 |
LIG_FHA_2 | 605 | 611 | PF00498 | 0.501 |
LIG_FHA_2 | 715 | 721 | PF00498 | 0.615 |
LIG_FHA_2 | 723 | 729 | PF00498 | 0.548 |
LIG_GBD_Chelix_1 | 470 | 478 | PF00786 | 0.519 |
LIG_LIR_Apic_2 | 275 | 281 | PF02991 | 0.650 |
LIG_LIR_Apic_2 | 621 | 625 | PF02991 | 0.471 |
LIG_LIR_Gen_1 | 138 | 146 | PF02991 | 0.371 |
LIG_LIR_Gen_1 | 258 | 267 | PF02991 | 0.228 |
LIG_LIR_Gen_1 | 454 | 464 | PF02991 | 0.419 |
LIG_LIR_Gen_1 | 503 | 512 | PF02991 | 0.467 |
LIG_LIR_Gen_1 | 56 | 65 | PF02991 | 0.328 |
LIG_LIR_Gen_1 | 632 | 642 | PF02991 | 0.531 |
LIG_LIR_Nem_3 | 138 | 143 | PF02991 | 0.276 |
LIG_LIR_Nem_3 | 227 | 231 | PF02991 | 0.423 |
LIG_LIR_Nem_3 | 232 | 237 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 253 | 259 | PF02991 | 0.325 |
LIG_LIR_Nem_3 | 382 | 388 | PF02991 | 0.516 |
LIG_LIR_Nem_3 | 394 | 399 | PF02991 | 0.472 |
LIG_LIR_Nem_3 | 454 | 459 | PF02991 | 0.497 |
LIG_LIR_Nem_3 | 465 | 470 | PF02991 | 0.389 |
LIG_LIR_Nem_3 | 503 | 508 | PF02991 | 0.475 |
LIG_LIR_Nem_3 | 56 | 60 | PF02991 | 0.328 |
LIG_LIR_Nem_3 | 632 | 637 | PF02991 | 0.576 |
LIG_LYPXL_S_1 | 395 | 399 | PF13949 | 0.567 |
LIG_LYPXL_yS_3 | 396 | 399 | PF13949 | 0.570 |
LIG_NRBOX | 41 | 47 | PF00104 | 0.314 |
LIG_NRBOX | 660 | 666 | PF00104 | 0.463 |
LIG_PCNA_yPIPBox_3 | 39 | 52 | PF02747 | 0.223 |
LIG_PCNA_yPIPBox_3 | 652 | 665 | PF02747 | 0.322 |
LIG_SH2_CRK | 259 | 263 | PF00017 | 0.328 |
LIG_SH2_CRK | 634 | 638 | PF00017 | 0.339 |
LIG_SH2_NCK_1 | 278 | 282 | PF00017 | 0.647 |
LIG_SH2_PTP2 | 234 | 237 | PF00017 | 0.475 |
LIG_SH2_SRC | 117 | 120 | PF00017 | 0.328 |
LIG_SH2_STAP1 | 174 | 178 | PF00017 | 0.368 |
LIG_SH2_STAP1 | 456 | 460 | PF00017 | 0.392 |
LIG_SH2_STAT3 | 174 | 177 | PF00017 | 0.385 |
LIG_SH2_STAT5 | 117 | 120 | PF00017 | 0.328 |
LIG_SH2_STAT5 | 174 | 177 | PF00017 | 0.344 |
LIG_SH2_STAT5 | 234 | 237 | PF00017 | 0.323 |
LIG_SH2_STAT5 | 256 | 259 | PF00017 | 0.297 |
LIG_SH2_STAT5 | 273 | 276 | PF00017 | 0.541 |
LIG_SH2_STAT5 | 54 | 57 | PF00017 | 0.351 |
LIG_SH3_3 | 565 | 571 | PF00018 | 0.528 |
LIG_SH3_3 | 675 | 681 | PF00018 | 0.417 |
LIG_SH3_3 | 75 | 81 | PF00018 | 0.344 |
LIG_SUMO_SIM_par_1 | 365 | 370 | PF11976 | 0.389 |
LIG_SUMO_SIM_par_1 | 407 | 412 | PF11976 | 0.559 |
LIG_SUMO_SIM_par_1 | 614 | 621 | PF11976 | 0.548 |
LIG_SUMO_SIM_par_1 | 731 | 737 | PF11976 | 0.457 |
LIG_TRAF2_1 | 192 | 195 | PF00917 | 0.475 |
LIG_TRAF2_1 | 414 | 417 | PF00917 | 0.580 |
LIG_TRAF2_1 | 725 | 728 | PF00917 | 0.577 |
LIG_TYR_ITIM | 257 | 262 | PF00017 | 0.328 |
LIG_UBA3_1 | 589 | 597 | PF00899 | 0.569 |
LIG_WRC_WIRS_1 | 619 | 624 | PF05994 | 0.479 |
LIG_WRC_WIRS_1 | 86 | 91 | PF05994 | 0.444 |
MOD_CDC14_SPxK_1 | 624 | 627 | PF00782 | 0.357 |
MOD_CDK_SPxK_1 | 621 | 627 | PF00069 | 0.349 |
MOD_CDK_SPxxK_3 | 621 | 628 | PF00069 | 0.353 |
MOD_CK1_1 | 153 | 159 | PF00069 | 0.425 |
MOD_CK1_1 | 172 | 178 | PF00069 | 0.404 |
MOD_CK1_1 | 296 | 302 | PF00069 | 0.777 |
MOD_CK1_1 | 314 | 320 | PF00069 | 0.575 |
MOD_CK1_1 | 525 | 531 | PF00069 | 0.305 |
MOD_CK1_1 | 551 | 557 | PF00069 | 0.532 |
MOD_CK1_1 | 621 | 627 | PF00069 | 0.349 |
MOD_CK2_1 | 53 | 59 | PF00069 | 0.449 |
MOD_CK2_1 | 604 | 610 | PF00069 | 0.481 |
MOD_CK2_1 | 691 | 697 | PF00069 | 0.600 |
MOD_CK2_1 | 714 | 720 | PF00069 | 0.545 |
MOD_CK2_1 | 722 | 728 | PF00069 | 0.474 |
MOD_Cter_Amidation | 306 | 309 | PF01082 | 0.664 |
MOD_GlcNHglycan | 296 | 299 | PF01048 | 0.764 |
MOD_GlcNHglycan | 300 | 303 | PF01048 | 0.786 |
MOD_GlcNHglycan | 400 | 403 | PF01048 | 0.611 |
MOD_GlcNHglycan | 411 | 414 | PF01048 | 0.501 |
MOD_GlcNHglycan | 480 | 483 | PF01048 | 0.598 |
MOD_GlcNHglycan | 610 | 614 | PF01048 | 0.463 |
MOD_GSK3_1 | 131 | 138 | PF00069 | 0.357 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.428 |
MOD_GSK3_1 | 211 | 218 | PF00069 | 0.223 |
MOD_GSK3_1 | 289 | 296 | PF00069 | 0.697 |
MOD_GSK3_1 | 405 | 412 | PF00069 | 0.483 |
MOD_GSK3_1 | 435 | 442 | PF00069 | 0.573 |
MOD_GSK3_1 | 551 | 558 | PF00069 | 0.582 |
MOD_GSK3_1 | 581 | 588 | PF00069 | 0.490 |
MOD_GSK3_1 | 660 | 667 | PF00069 | 0.493 |
MOD_GSK3_1 | 728 | 735 | PF00069 | 0.501 |
MOD_N-GLC_1 | 548 | 553 | PF02516 | 0.424 |
MOD_NEK2_1 | 135 | 140 | PF00069 | 0.404 |
MOD_NEK2_1 | 150 | 155 | PF00069 | 0.303 |
MOD_NEK2_1 | 250 | 255 | PF00069 | 0.381 |
MOD_NEK2_1 | 436 | 441 | PF00069 | 0.440 |
MOD_NEK2_1 | 478 | 483 | PF00069 | 0.575 |
MOD_NEK2_1 | 508 | 513 | PF00069 | 0.427 |
MOD_NEK2_1 | 522 | 527 | PF00069 | 0.369 |
MOD_NEK2_1 | 581 | 586 | PF00069 | 0.547 |
MOD_NEK2_1 | 604 | 609 | PF00069 | 0.429 |
MOD_NEK2_1 | 611 | 616 | PF00069 | 0.386 |
MOD_NEK2_1 | 664 | 669 | PF00069 | 0.385 |
MOD_NEK2_2 | 618 | 623 | PF00069 | 0.478 |
MOD_PIKK_1 | 551 | 557 | PF00454 | 0.338 |
MOD_PIKK_1 | 566 | 572 | PF00454 | 0.579 |
MOD_PK_1 | 139 | 145 | PF00069 | 0.329 |
MOD_PK_1 | 597 | 603 | PF00069 | 0.580 |
MOD_PKA_1 | 585 | 591 | PF00069 | 0.508 |
MOD_PKA_2 | 314 | 320 | PF00069 | 0.728 |
MOD_PKA_2 | 363 | 369 | PF00069 | 0.362 |
MOD_PKA_2 | 430 | 436 | PF00069 | 0.443 |
MOD_PKA_2 | 454 | 460 | PF00069 | 0.534 |
MOD_PKA_2 | 585 | 591 | PF00069 | 0.510 |
MOD_Plk_1 | 548 | 554 | PF00069 | 0.431 |
MOD_Plk_2-3 | 53 | 59 | PF00069 | 0.328 |
MOD_Plk_4 | 117 | 123 | PF00069 | 0.464 |
MOD_Plk_4 | 145 | 151 | PF00069 | 0.328 |
MOD_Plk_4 | 169 | 175 | PF00069 | 0.413 |
MOD_Plk_4 | 230 | 236 | PF00069 | 0.342 |
MOD_Plk_4 | 400 | 406 | PF00069 | 0.502 |
MOD_Plk_4 | 436 | 442 | PF00069 | 0.573 |
MOD_Plk_4 | 444 | 450 | PF00069 | 0.478 |
MOD_Plk_4 | 525 | 531 | PF00069 | 0.425 |
MOD_Plk_4 | 585 | 591 | PF00069 | 0.578 |
MOD_Plk_4 | 660 | 666 | PF00069 | 0.410 |
MOD_Plk_4 | 94 | 100 | PF00069 | 0.427 |
MOD_ProDKin_1 | 621 | 627 | PF00069 | 0.349 |
MOD_SUMO_for_1 | 60 | 63 | PF00179 | 0.449 |
MOD_SUMO_for_1 | 692 | 695 | PF00179 | 0.606 |
TRG_DiLeu_BaEn_1 | 108 | 113 | PF01217 | 0.344 |
TRG_DiLeu_BaEn_1 | 400 | 405 | PF01217 | 0.566 |
TRG_DiLeu_BaEn_1 | 5 | 10 | PF01217 | 0.333 |
TRG_DiLeu_BaEn_4 | 194 | 200 | PF01217 | 0.475 |
TRG_DiLeu_BaLyEn_6 | 208 | 213 | PF01217 | 0.223 |
TRG_DiLeu_BaLyEn_6 | 383 | 388 | PF01217 | 0.487 |
TRG_DiLeu_BaLyEn_6 | 588 | 593 | PF01217 | 0.534 |
TRG_ENDOCYTIC_2 | 234 | 237 | PF00928 | 0.457 |
TRG_ENDOCYTIC_2 | 259 | 262 | PF00928 | 0.328 |
TRG_ENDOCYTIC_2 | 396 | 399 | PF00928 | 0.570 |
TRG_ENDOCYTIC_2 | 456 | 459 | PF00928 | 0.515 |
TRG_ENDOCYTIC_2 | 634 | 637 | PF00928 | 0.566 |
TRG_ER_diArg_1 | 161 | 164 | PF00400 | 0.475 |
TRG_ER_diArg_1 | 181 | 184 | PF00400 | 0.145 |
TRG_ER_diArg_1 | 203 | 205 | PF00400 | 0.417 |
TRG_NES_CRM1_1 | 365 | 380 | PF08389 | 0.527 |
TRG_NLS_MonoExtC_3 | 304 | 309 | PF00514 | 0.675 |
TRG_NLS_MonoExtN_4 | 303 | 309 | PF00514 | 0.648 |
TRG_Pf-PMV_PEXEL_1 | 461 | 465 | PF00026 | 0.525 |
TRG_Pf-PMV_PEXEL_1 | 62 | 66 | PF00026 | 0.405 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IM39 | Leptomonas seymouri | 66% | 100% |
A0A0S4JTJ6 | Bodo saltans | 34% | 95% |
A0A1X0NLV8 | Trypanosomatidae | 41% | 98% |
A0A3S7XCH5 | Leishmania donovani | 82% | 100% |
A0A422NVV8 | Trypanosoma rangeli | 42% | 99% |
A4ICC0 | Leishmania infantum | 81% | 100% |
D0A3Q3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 42% | 100% |
E9AUB5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 81% | 100% |
Q4Q075 | Leishmania major | 82% | 100% |
V5AXN4 | Trypanosoma cruzi | 40% | 99% |