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: 6 |
NetGPI | no | yes: 0, no: 6 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Related structures:
AlphaFold database: A0A3S7XAY5
Term | Name | Level | Count |
---|---|---|---|
GO:0006508 | proteolysis | 4 | 1 |
GO:0006511 | ubiquitin-dependent protein catabolic process | 7 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009056 | catabolic process | 2 | 1 |
GO:0009057 | macromolecule catabolic process | 4 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0016567 | protein ubiquitination | 7 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0019941 | modification-dependent protein catabolic process | 6 | 1 |
GO:0032446 | protein modification by small protein conjugation | 6 | 1 |
GO:0036211 | protein modification process | 4 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0043632 | modification-dependent macromolecule catabolic process | 5 | 1 |
GO:0044237 | cellular metabolic process | 2 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0044248 | cellular catabolic process | 3 | 1 |
GO:0044260 | obsolete cellular macromolecule metabolic process | 3 | 1 |
GO:0044265 | obsolete cellular macromolecule catabolic process | 4 | 1 |
GO:0051603 | proteolysis involved in protein catabolic process | 5 | 1 |
GO:0070647 | protein modification by small protein conjugation or removal | 5 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
GO:1901575 | organic substance catabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 1 |
GO:0004842 | ubiquitin-protein transferase activity | 4 | 1 |
GO:0016740 | transferase activity | 2 | 1 |
GO:0019787 | ubiquitin-like protein transferase activity | 3 | 1 |
GO:0061630 | ubiquitin protein ligase activity | 5 | 1 |
GO:0061659 | ubiquitin-like protein ligase activity | 4 | 1 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 136 | 140 | PF00656 | 0.684 |
CLV_C14_Caspase3-7 | 19 | 23 | PF00656 | 0.642 |
CLV_C14_Caspase3-7 | 224 | 228 | PF00656 | 0.690 |
CLV_C14_Caspase3-7 | 408 | 412 | PF00656 | 0.725 |
CLV_NRD_NRD_1 | 162 | 164 | PF00675 | 0.608 |
CLV_PCSK_KEX2_1 | 162 | 164 | PF00082 | 0.506 |
CLV_PCSK_SKI1_1 | 214 | 218 | PF00082 | 0.588 |
CLV_PCSK_SKI1_1 | 241 | 245 | PF00082 | 0.468 |
CLV_PCSK_SKI1_1 | 278 | 282 | PF00082 | 0.551 |
CLV_PCSK_SKI1_1 | 287 | 291 | PF00082 | 0.493 |
CLV_PCSK_SKI1_1 | 32 | 36 | PF00082 | 0.665 |
CLV_PCSK_SKI1_1 | 489 | 493 | PF00082 | 0.626 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.661 |
DEG_SCF_TRCP1_1 | 411 | 417 | PF00400 | 0.676 |
DEG_SPOP_SBC_1 | 204 | 208 | PF00917 | 0.580 |
DEG_SPOP_SBC_1 | 220 | 224 | PF00917 | 0.595 |
DEG_SPOP_SBC_1 | 669 | 673 | PF00917 | 0.680 |
DOC_CYCLIN_RxL_1 | 287 | 296 | PF00134 | 0.475 |
DOC_MAPK_gen_1 | 194 | 202 | PF00069 | 0.711 |
DOC_MAPK_MEF2A_6 | 194 | 202 | PF00069 | 0.711 |
DOC_MAPK_MEF2A_6 | 66 | 74 | PF00069 | 0.580 |
DOC_PP1_RVXF_1 | 288 | 294 | PF00149 | 0.473 |
DOC_PP2B_LxvP_1 | 158 | 161 | PF13499 | 0.515 |
DOC_PP2B_LxvP_1 | 376 | 379 | PF13499 | 0.644 |
DOC_PP2B_LxvP_1 | 390 | 393 | PF13499 | 0.372 |
DOC_PP2B_LxvP_1 | 524 | 527 | PF13499 | 0.724 |
DOC_PP2B_LxvP_1 | 554 | 557 | PF13499 | 0.714 |
DOC_PP4_FxxP_1 | 606 | 609 | PF00568 | 0.606 |
DOC_USP7_MATH_1 | 103 | 107 | PF00917 | 0.497 |
DOC_USP7_MATH_1 | 140 | 144 | PF00917 | 0.551 |
DOC_USP7_MATH_1 | 16 | 20 | PF00917 | 0.511 |
DOC_USP7_MATH_1 | 189 | 193 | PF00917 | 0.672 |
DOC_USP7_MATH_1 | 204 | 208 | PF00917 | 0.635 |
DOC_USP7_MATH_1 | 219 | 223 | PF00917 | 0.576 |
DOC_USP7_MATH_1 | 37 | 41 | PF00917 | 0.611 |
DOC_USP7_MATH_1 | 379 | 383 | PF00917 | 0.633 |
DOC_USP7_MATH_1 | 431 | 435 | PF00917 | 0.641 |
DOC_USP7_MATH_1 | 540 | 544 | PF00917 | 0.756 |
DOC_USP7_MATH_1 | 635 | 639 | PF00917 | 0.658 |
DOC_USP7_MATH_1 | 649 | 653 | PF00917 | 0.572 |
DOC_USP7_MATH_1 | 669 | 673 | PF00917 | 0.602 |
DOC_USP7_MATH_1 | 692 | 696 | PF00917 | 0.765 |
DOC_USP7_MATH_1 | 711 | 715 | PF00917 | 0.481 |
DOC_USP7_MATH_1 | 82 | 86 | PF00917 | 0.621 |
DOC_WW_Pin1_4 | 185 | 190 | PF00397 | 0.731 |
DOC_WW_Pin1_4 | 35 | 40 | PF00397 | 0.685 |
DOC_WW_Pin1_4 | 562 | 567 | PF00397 | 0.696 |
DOC_WW_Pin1_4 | 576 | 581 | PF00397 | 0.646 |
DOC_WW_Pin1_4 | 590 | 595 | PF00397 | 0.574 |
DOC_WW_Pin1_4 | 656 | 661 | PF00397 | 0.685 |
DOC_WW_Pin1_4 | 677 | 682 | PF00397 | 0.699 |
LIG_14-3-3_CanoR_1 | 337 | 342 | PF00244 | 0.534 |
LIG_14-3-3_CanoR_1 | 597 | 606 | PF00244 | 0.720 |
LIG_14-3-3_CanoR_1 | 619 | 625 | PF00244 | 0.687 |
LIG_APCC_ABBA_1 | 31 | 36 | PF00400 | 0.661 |
LIG_Clathr_ClatBox_1 | 292 | 296 | PF01394 | 0.511 |
LIG_eIF4E_1 | 628 | 634 | PF01652 | 0.625 |
LIG_FHA_1 | 211 | 217 | PF00498 | 0.604 |
LIG_FHA_1 | 251 | 257 | PF00498 | 0.355 |
LIG_FHA_1 | 330 | 336 | PF00498 | 0.545 |
LIG_FHA_1 | 338 | 344 | PF00498 | 0.543 |
LIG_FHA_1 | 40 | 46 | PF00498 | 0.611 |
LIG_FHA_1 | 415 | 421 | PF00498 | 0.579 |
LIG_FHA_1 | 464 | 470 | PF00498 | 0.700 |
LIG_FHA_1 | 519 | 525 | PF00498 | 0.704 |
LIG_FHA_1 | 577 | 583 | PF00498 | 0.744 |
LIG_FHA_1 | 628 | 634 | PF00498 | 0.603 |
LIG_FHA_1 | 649 | 655 | PF00498 | 0.668 |
LIG_FHA_1 | 695 | 701 | PF00498 | 0.811 |
LIG_FHA_2 | 342 | 348 | PF00498 | 0.565 |
LIG_FHA_2 | 403 | 409 | PF00498 | 0.746 |
LIG_FHA_2 | 446 | 452 | PF00498 | 0.511 |
LIG_LIR_Apic_2 | 676 | 681 | PF02991 | 0.612 |
LIG_LIR_Gen_1 | 307 | 316 | PF02991 | 0.411 |
LIG_LIR_Gen_1 | 446 | 455 | PF02991 | 0.526 |
LIG_LIR_Gen_1 | 714 | 719 | PF02991 | 0.661 |
LIG_LIR_Nem_3 | 123 | 129 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 231 | 235 | PF02991 | 0.811 |
LIG_LIR_Nem_3 | 284 | 289 | PF02991 | 0.479 |
LIG_LIR_Nem_3 | 307 | 311 | PF02991 | 0.411 |
LIG_LIR_Nem_3 | 384 | 390 | PF02991 | 0.558 |
LIG_LIR_Nem_3 | 434 | 439 | PF02991 | 0.577 |
LIG_LIR_Nem_3 | 446 | 450 | PF02991 | 0.497 |
LIG_LIR_Nem_3 | 714 | 718 | PF02991 | 0.658 |
LIG_PDZ_Class_2 | 714 | 719 | PF00595 | 0.572 |
LIG_SH2_CRK | 110 | 114 | PF00017 | 0.492 |
LIG_SH2_CRK | 126 | 130 | PF00017 | 0.331 |
LIG_SH2_CRK | 373 | 377 | PF00017 | 0.737 |
LIG_SH2_CRK | 442 | 446 | PF00017 | 0.633 |
LIG_SH2_CRK | 61 | 65 | PF00017 | 0.473 |
LIG_SH2_GRB2like | 122 | 125 | PF00017 | 0.411 |
LIG_SH2_PTP2 | 715 | 718 | PF00017 | 0.761 |
LIG_SH2_STAP1 | 122 | 126 | PF00017 | 0.411 |
LIG_SH2_STAP1 | 349 | 353 | PF00017 | 0.611 |
LIG_SH2_STAP1 | 61 | 65 | PF00017 | 0.473 |
LIG_SH2_STAT3 | 499 | 502 | PF00017 | 0.769 |
LIG_SH2_STAT5 | 110 | 113 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 442 | 445 | PF00017 | 0.628 |
LIG_SH2_STAT5 | 49 | 52 | PF00017 | 0.485 |
LIG_SH2_STAT5 | 499 | 502 | PF00017 | 0.675 |
LIG_SH2_STAT5 | 715 | 718 | PF00017 | 0.761 |
LIG_SH3_3 | 232 | 238 | PF00018 | 0.702 |
LIG_SH3_3 | 332 | 338 | PF00018 | 0.455 |
LIG_SH3_3 | 497 | 503 | PF00018 | 0.737 |
LIG_SUMO_SIM_anti_2 | 67 | 75 | PF11976 | 0.495 |
LIG_SUMO_SIM_par_1 | 252 | 257 | PF11976 | 0.411 |
LIG_SUMO_SIM_par_1 | 277 | 285 | PF11976 | 0.514 |
LIG_SUMO_SIM_par_1 | 661 | 666 | PF11976 | 0.680 |
LIG_SUMO_SIM_par_1 | 67 | 75 | PF11976 | 0.483 |
LIG_TYR_ITIM | 108 | 113 | PF00017 | 0.436 |
LIG_UBA3_1 | 45 | 53 | PF00899 | 0.545 |
MOD_CDK_SPxxK_3 | 590 | 597 | PF00069 | 0.614 |
MOD_CK1_1 | 133 | 139 | PF00069 | 0.547 |
MOD_CK1_1 | 207 | 213 | PF00069 | 0.599 |
MOD_CK1_1 | 222 | 228 | PF00069 | 0.639 |
MOD_CK1_1 | 336 | 342 | PF00069 | 0.472 |
MOD_CK1_1 | 382 | 388 | PF00069 | 0.566 |
MOD_CK1_1 | 432 | 438 | PF00069 | 0.593 |
MOD_CK1_1 | 576 | 582 | PF00069 | 0.705 |
MOD_CK1_1 | 596 | 602 | PF00069 | 0.717 |
MOD_CK1_1 | 694 | 700 | PF00069 | 0.713 |
MOD_CK2_1 | 341 | 347 | PF00069 | 0.656 |
MOD_CK2_1 | 445 | 451 | PF00069 | 0.524 |
MOD_CK2_1 | 670 | 676 | PF00069 | 0.607 |
MOD_CK2_1 | 86 | 92 | PF00069 | 0.632 |
MOD_GlcNHglycan | 113 | 116 | PF01048 | 0.411 |
MOD_GlcNHglycan | 158 | 161 | PF01048 | 0.542 |
MOD_GlcNHglycan | 22 | 25 | PF01048 | 0.669 |
MOD_GlcNHglycan | 227 | 230 | PF01048 | 0.791 |
MOD_GlcNHglycan | 258 | 261 | PF01048 | 0.513 |
MOD_GlcNHglycan | 39 | 42 | PF01048 | 0.605 |
MOD_GlcNHglycan | 411 | 414 | PF01048 | 0.770 |
MOD_GlcNHglycan | 538 | 541 | PF01048 | 0.724 |
MOD_GlcNHglycan | 569 | 572 | PF01048 | 0.669 |
MOD_GlcNHglycan | 61 | 64 | PF01048 | 0.464 |
MOD_GlcNHglycan | 625 | 628 | PF01048 | 0.711 |
MOD_GlcNHglycan | 637 | 640 | PF01048 | 0.558 |
MOD_GlcNHglycan | 656 | 659 | PF01048 | 0.686 |
MOD_GlcNHglycan | 693 | 697 | PF01048 | 0.714 |
MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.629 |
MOD_GlcNHglycan | 92 | 95 | PF01048 | 0.505 |
MOD_GSK3_1 | 130 | 137 | PF00069 | 0.489 |
MOD_GSK3_1 | 16 | 23 | PF00069 | 0.609 |
MOD_GSK3_1 | 179 | 186 | PF00069 | 0.790 |
MOD_GSK3_1 | 203 | 210 | PF00069 | 0.702 |
MOD_GSK3_1 | 221 | 228 | PF00069 | 0.612 |
MOD_GSK3_1 | 250 | 257 | PF00069 | 0.360 |
MOD_GSK3_1 | 329 | 336 | PF00069 | 0.518 |
MOD_GSK3_1 | 337 | 344 | PF00069 | 0.525 |
MOD_GSK3_1 | 35 | 42 | PF00069 | 0.451 |
MOD_GSK3_1 | 379 | 386 | PF00069 | 0.579 |
MOD_GSK3_1 | 445 | 452 | PF00069 | 0.510 |
MOD_GSK3_1 | 536 | 543 | PF00069 | 0.705 |
MOD_GSK3_1 | 572 | 579 | PF00069 | 0.695 |
MOD_GSK3_1 | 593 | 600 | PF00069 | 0.744 |
MOD_GSK3_1 | 623 | 630 | PF00069 | 0.679 |
MOD_GSK3_1 | 688 | 695 | PF00069 | 0.721 |
MOD_GSK3_1 | 82 | 89 | PF00069 | 0.616 |
MOD_LATS_1 | 331 | 337 | PF00433 | 0.525 |
MOD_N-GLC_1 | 432 | 437 | PF02516 | 0.622 |
MOD_N-GLC_1 | 702 | 707 | PF02516 | 0.715 |
MOD_N-GLC_2 | 322 | 324 | PF02516 | 0.411 |
MOD_NEK2_1 | 156 | 161 | PF00069 | 0.490 |
MOD_NEK2_1 | 20 | 25 | PF00069 | 0.601 |
MOD_NEK2_1 | 205 | 210 | PF00069 | 0.564 |
MOD_NEK2_1 | 254 | 259 | PF00069 | 0.411 |
MOD_NEK2_1 | 274 | 279 | PF00069 | 0.307 |
MOD_NEK2_1 | 281 | 286 | PF00069 | 0.426 |
MOD_NEK2_1 | 329 | 334 | PF00069 | 0.528 |
MOD_NEK2_1 | 429 | 434 | PF00069 | 0.686 |
MOD_NEK2_1 | 449 | 454 | PF00069 | 0.388 |
MOD_NEK2_1 | 654 | 659 | PF00069 | 0.660 |
MOD_NEK2_1 | 72 | 77 | PF00069 | 0.503 |
MOD_NEK2_2 | 189 | 194 | PF00069 | 0.713 |
MOD_NEK2_2 | 372 | 377 | PF00069 | 0.650 |
MOD_NEK2_2 | 47 | 52 | PF00069 | 0.400 |
MOD_NEK2_2 | 506 | 511 | PF00069 | 0.628 |
MOD_PKA_2 | 336 | 342 | PF00069 | 0.489 |
MOD_PKA_2 | 409 | 415 | PF00069 | 0.717 |
MOD_PKA_2 | 596 | 602 | PF00069 | 0.822 |
MOD_PKA_2 | 604 | 610 | PF00069 | 0.698 |
MOD_PKA_2 | 618 | 624 | PF00069 | 0.570 |
MOD_Plk_1 | 122 | 128 | PF00069 | 0.402 |
MOD_Plk_1 | 349 | 355 | PF00069 | 0.615 |
MOD_Plk_1 | 383 | 389 | PF00069 | 0.570 |
MOD_Plk_1 | 432 | 438 | PF00069 | 0.605 |
MOD_Plk_1 | 669 | 675 | PF00069 | 0.616 |
MOD_Plk_2-3 | 670 | 676 | PF00069 | 0.593 |
MOD_Plk_4 | 130 | 136 | PF00069 | 0.490 |
MOD_Plk_4 | 250 | 256 | PF00069 | 0.411 |
MOD_Plk_4 | 304 | 310 | PF00069 | 0.513 |
MOD_Plk_4 | 383 | 389 | PF00069 | 0.591 |
MOD_Plk_4 | 41 | 47 | PF00069 | 0.660 |
MOD_Plk_4 | 415 | 421 | PF00069 | 0.540 |
MOD_Plk_4 | 506 | 512 | PF00069 | 0.625 |
MOD_Plk_4 | 526 | 532 | PF00069 | 0.632 |
MOD_Plk_4 | 620 | 626 | PF00069 | 0.764 |
MOD_Plk_4 | 628 | 634 | PF00069 | 0.594 |
MOD_Plk_4 | 649 | 655 | PF00069 | 0.700 |
MOD_Plk_4 | 695 | 701 | PF00069 | 0.716 |
MOD_Plk_4 | 711 | 717 | PF00069 | 0.659 |
MOD_Plk_4 | 86 | 92 | PF00069 | 0.544 |
MOD_ProDKin_1 | 185 | 191 | PF00069 | 0.729 |
MOD_ProDKin_1 | 35 | 41 | PF00069 | 0.691 |
MOD_ProDKin_1 | 562 | 568 | PF00069 | 0.697 |
MOD_ProDKin_1 | 576 | 582 | PF00069 | 0.647 |
MOD_ProDKin_1 | 590 | 596 | PF00069 | 0.572 |
MOD_ProDKin_1 | 656 | 662 | PF00069 | 0.683 |
MOD_ProDKin_1 | 677 | 683 | PF00069 | 0.699 |
TRG_DiLeu_BaLyEn_6 | 487 | 492 | PF01217 | 0.661 |
TRG_ENDOCYTIC_2 | 110 | 113 | PF00928 | 0.492 |
TRG_ENDOCYTIC_2 | 126 | 129 | PF00928 | 0.331 |
TRG_ENDOCYTIC_2 | 373 | 376 | PF00928 | 0.650 |
TRG_ENDOCYTIC_2 | 387 | 390 | PF00928 | 0.353 |
TRG_ENDOCYTIC_2 | 442 | 445 | PF00928 | 0.576 |
TRG_ENDOCYTIC_2 | 61 | 64 | PF00928 | 0.474 |
TRG_ENDOCYTIC_2 | 715 | 718 | PF00928 | 0.660 |
TRG_ER_diArg_1 | 161 | 163 | PF00400 | 0.619 |
TRG_Pf-PMV_PEXEL_1 | 241 | 245 | PF00026 | 0.513 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDB4 | Leptomonas seymouri | 43% | 100% |
A4HPC6 | Leishmania braziliensis | 71% | 100% |
A4ICG6 | Leishmania infantum | 99% | 100% |
E9AT37 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
Q4Q1G1 | Leishmania major | 92% | 100% |