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:0005783 | endoplasmic reticulum | 5 | 2 |
GO:0005794 | Golgi apparatus | 5 | 2 |
GO:0016020 | membrane | 2 | 7 |
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 | 7 |
Related structures:
AlphaFold database: Q4Q7I6
Term | Name | Level | Count |
---|---|---|---|
GO:0006497 | protein lipidation | 5 | 2 |
GO:0006605 | protein targeting | 5 | 2 |
GO:0006612 | protein targeting to membrane | 5 | 2 |
GO:0006807 | nitrogen compound metabolic process | 2 | 2 |
GO:0006810 | transport | 3 | 2 |
GO:0006886 | intracellular protein transport | 4 | 2 |
GO:0008104 | protein localization | 4 | 2 |
GO:0008152 | metabolic process | 1 | 2 |
GO:0009987 | cellular process | 1 | 2 |
GO:0015031 | protein transport | 4 | 2 |
GO:0018193 | peptidyl-amino acid modification | 5 | 2 |
GO:0018198 | peptidyl-cysteine modification | 6 | 2 |
GO:0018230 | peptidyl-L-cysteine S-palmitoylation | 7 | 2 |
GO:0018231 | peptidyl-S-diacylglycerol-L-cysteine biosynthetic process from peptidyl-cysteine | 7 | 2 |
GO:0018345 | protein palmitoylation | 6 | 2 |
GO:0019538 | protein metabolic process | 3 | 2 |
GO:0033036 | macromolecule localization | 2 | 2 |
GO:0036211 | protein modification process | 4 | 2 |
GO:0043170 | macromolecule metabolic process | 3 | 2 |
GO:0043412 | macromolecule modification | 4 | 2 |
GO:0043543 | protein acylation | 5 | 2 |
GO:0044238 | primary metabolic process | 2 | 2 |
GO:0045184 | establishment of protein localization | 3 | 2 |
GO:0046907 | intracellular transport | 3 | 2 |
GO:0051179 | localization | 1 | 2 |
GO:0051234 | establishment of localization | 2 | 2 |
GO:0051641 | cellular localization | 2 | 2 |
GO:0051649 | establishment of localization in cell | 3 | 2 |
GO:0051668 | localization within membrane | 3 | 2 |
GO:0070727 | cellular macromolecule localization | 3 | 2 |
GO:0071702 | organic substance transport | 4 | 2 |
GO:0071704 | organic substance metabolic process | 2 | 2 |
GO:0071705 | nitrogen compound transport | 4 | 2 |
GO:0072657 | protein localization to membrane | 4 | 2 |
GO:0090150 | establishment of protein localization to membrane | 4 | 2 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 2 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 7 |
GO:0016409 | palmitoyltransferase activity | 5 | 7 |
GO:0016417 | S-acyltransferase activity | 5 | 7 |
GO:0016740 | transferase activity | 2 | 7 |
GO:0016746 | acyltransferase activity | 3 | 7 |
GO:0016747 | acyltransferase activity, transferring groups other than amino-acyl groups | 4 | 7 |
GO:0019706 | protein-cysteine S-palmitoyltransferase activity | 4 | 7 |
GO:0019707 | protein-cysteine S-acyltransferase activity | 3 | 7 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 7 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 128 | 132 | PF00656 | 0.757 |
CLV_NRD_NRD_1 | 112 | 114 | PF00675 | 0.580 |
CLV_NRD_NRD_1 | 236 | 238 | PF00675 | 0.517 |
CLV_NRD_NRD_1 | 326 | 328 | PF00675 | 0.502 |
CLV_NRD_NRD_1 | 643 | 645 | PF00675 | 0.434 |
CLV_PCSK_KEX2_1 | 20 | 22 | PF00082 | 0.594 |
CLV_PCSK_KEX2_1 | 236 | 238 | PF00082 | 0.442 |
CLV_PCSK_KEX2_1 | 325 | 327 | PF00082 | 0.478 |
CLV_PCSK_KEX2_1 | 405 | 407 | PF00082 | 0.508 |
CLV_PCSK_KEX2_1 | 575 | 577 | PF00082 | 0.447 |
CLV_PCSK_KEX2_1 | 63 | 65 | PF00082 | 0.591 |
CLV_PCSK_KEX2_1 | 676 | 678 | PF00082 | 0.436 |
CLV_PCSK_PC1ET2_1 | 20 | 22 | PF00082 | 0.594 |
CLV_PCSK_PC1ET2_1 | 405 | 407 | PF00082 | 0.480 |
CLV_PCSK_PC1ET2_1 | 575 | 577 | PF00082 | 0.447 |
CLV_PCSK_PC1ET2_1 | 63 | 65 | PF00082 | 0.525 |
CLV_PCSK_PC1ET2_1 | 676 | 678 | PF00082 | 0.436 |
CLV_PCSK_SKI1_1 | 185 | 189 | PF00082 | 0.530 |
CLV_PCSK_SKI1_1 | 326 | 330 | PF00082 | 0.502 |
CLV_PCSK_SKI1_1 | 422 | 426 | PF00082 | 0.529 |
CLV_PCSK_SKI1_1 | 562 | 566 | PF00082 | 0.359 |
CLV_Separin_Metazoa | 668 | 672 | PF03568 | 0.739 |
DEG_APCC_DBOX_1 | 324 | 332 | PF00400 | 0.695 |
DEG_APCC_KENBOX_2 | 180 | 184 | PF00400 | 0.813 |
DEG_COP1_1 | 431 | 440 | PF00400 | 0.685 |
DEG_SCF_FBW7_1 | 41 | 48 | PF00400 | 0.705 |
DOC_CKS1_1 | 170 | 175 | PF01111 | 0.675 |
DOC_CKS1_1 | 42 | 47 | PF01111 | 0.839 |
DOC_CYCLIN_yCln2_LP_2 | 440 | 446 | PF00134 | 0.610 |
DOC_MAPK_FxFP_2 | 548 | 551 | PF00069 | 0.411 |
DOC_MAPK_gen_1 | 526 | 536 | PF00069 | 0.414 |
DOC_MAPK_MEF2A_6 | 334 | 342 | PF00069 | 0.737 |
DOC_MAPK_MEF2A_6 | 529 | 538 | PF00069 | 0.346 |
DOC_PP1_RVXF_1 | 630 | 636 | PF00149 | 0.650 |
DOC_PP2B_LxvP_1 | 435 | 438 | PF13499 | 0.658 |
DOC_PP2B_LxvP_1 | 637 | 640 | PF13499 | 0.667 |
DOC_PP4_FxxP_1 | 317 | 320 | PF00568 | 0.592 |
DOC_PP4_FxxP_1 | 548 | 551 | PF00568 | 0.411 |
DOC_USP7_MATH_1 | 159 | 163 | PF00917 | 0.741 |
DOC_USP7_MATH_1 | 378 | 382 | PF00917 | 0.734 |
DOC_USP7_MATH_1 | 387 | 391 | PF00917 | 0.645 |
DOC_USP7_MATH_1 | 45 | 49 | PF00917 | 0.822 |
DOC_USP7_MATH_1 | 65 | 69 | PF00917 | 0.626 |
DOC_USP7_MATH_1 | 72 | 76 | PF00917 | 0.790 |
DOC_USP7_MATH_1 | 82 | 86 | PF00917 | 0.711 |
DOC_USP7_MATH_2 | 13 | 19 | PF00917 | 0.706 |
DOC_USP7_UBL2_3 | 181 | 185 | PF12436 | 0.752 |
DOC_USP7_UBL2_3 | 571 | 575 | PF12436 | 0.546 |
DOC_WW_Pin1_4 | 169 | 174 | PF00397 | 0.729 |
DOC_WW_Pin1_4 | 32 | 37 | PF00397 | 0.765 |
DOC_WW_Pin1_4 | 41 | 46 | PF00397 | 0.771 |
DOC_WW_Pin1_4 | 52 | 57 | PF00397 | 0.672 |
DOC_WW_Pin1_4 | 9 | 14 | PF00397 | 0.755 |
LIG_14-3-3_CanoR_1 | 21 | 29 | PF00244 | 0.834 |
LIG_14-3-3_CanoR_1 | 267 | 272 | PF00244 | 0.515 |
LIG_14-3-3_CanoR_1 | 409 | 413 | PF00244 | 0.679 |
LIG_14-3-3_CanoR_1 | 429 | 437 | PF00244 | 0.773 |
LIG_14-3-3_CanoR_1 | 514 | 518 | PF00244 | 0.378 |
LIG_14-3-3_CanoR_1 | 54 | 60 | PF00244 | 0.816 |
LIG_14-3-3_CanoR_1 | 562 | 570 | PF00244 | 0.602 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.826 |
LIG_BRCT_BRCA1_1 | 240 | 244 | PF00533 | 0.690 |
LIG_BRCT_BRCA1_1 | 47 | 51 | PF00533 | 0.737 |
LIG_BRCT_BRCA1_1 | 492 | 496 | PF00533 | 0.512 |
LIG_BRCT_BRCA1_1 | 576 | 580 | PF00533 | 0.667 |
LIG_deltaCOP1_diTrp_1 | 292 | 302 | PF00928 | 0.418 |
LIG_EH_1 | 134 | 138 | PF12763 | 0.672 |
LIG_eIF4E_1 | 489 | 495 | PF01652 | 0.411 |
LIG_FHA_1 | 169 | 175 | PF00498 | 0.795 |
LIG_FHA_1 | 418 | 424 | PF00498 | 0.704 |
LIG_FHA_1 | 447 | 453 | PF00498 | 0.529 |
LIG_FHA_1 | 5 | 11 | PF00498 | 0.682 |
LIG_FHA_2 | 195 | 201 | PF00498 | 0.642 |
LIG_FHA_2 | 563 | 569 | PF00498 | 0.546 |
LIG_GBD_Chelix_1 | 299 | 307 | PF00786 | 0.430 |
LIG_Integrin_RGD_1 | 334 | 336 | PF01839 | 0.568 |
LIG_LIR_Apic_2 | 516 | 520 | PF02991 | 0.359 |
LIG_LIR_Gen_1 | 200 | 209 | PF02991 | 0.634 |
LIG_LIR_Gen_1 | 292 | 303 | PF02991 | 0.403 |
LIG_LIR_Gen_1 | 308 | 317 | PF02991 | 0.333 |
LIG_LIR_Gen_1 | 493 | 504 | PF02991 | 0.512 |
LIG_LIR_Nem_3 | 200 | 206 | PF02991 | 0.615 |
LIG_LIR_Nem_3 | 292 | 298 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 308 | 314 | PF02991 | 0.278 |
LIG_LIR_Nem_3 | 439 | 445 | PF02991 | 0.658 |
LIG_LIR_Nem_3 | 493 | 499 | PF02991 | 0.479 |
LIG_LIR_Nem_3 | 541 | 545 | PF02991 | 0.388 |
LIG_LIR_Nem_3 | 577 | 583 | PF02991 | 0.664 |
LIG_LIR_Nem_3 | 616 | 622 | PF02991 | 0.681 |
LIG_LIR_Nem_3 | 8 | 14 | PF02991 | 0.786 |
LIG_LYPXL_S_1 | 280 | 284 | PF13949 | 0.411 |
LIG_MLH1_MIPbox_1 | 492 | 496 | PF16413 | 0.512 |
LIG_MLH1_MIPbox_1 | 576 | 580 | PF16413 | 0.667 |
LIG_MYND_3 | 437 | 441 | PF01753 | 0.666 |
LIG_PCNA_TLS_4 | 409 | 416 | PF02747 | 0.633 |
LIG_Pex14_1 | 269 | 273 | PF04695 | 0.411 |
LIG_Pex14_2 | 442 | 446 | PF04695 | 0.652 |
LIG_Pex14_2 | 491 | 495 | PF04695 | 0.512 |
LIG_SH2_CRK | 203 | 207 | PF00017 | 0.688 |
LIG_SH2_CRK | 275 | 279 | PF00017 | 0.411 |
LIG_SH2_CRK | 503 | 507 | PF00017 | 0.411 |
LIG_SH2_CRK | 53 | 57 | PF00017 | 0.674 |
LIG_SH2_CRK | 532 | 536 | PF00017 | 0.346 |
LIG_SH2_CRK | 592 | 596 | PF00017 | 0.619 |
LIG_SH2_GRB2like | 592 | 595 | PF00017 | 0.674 |
LIG_SH2_NCK_1 | 11 | 15 | PF00017 | 0.782 |
LIG_SH2_NCK_1 | 203 | 207 | PF00017 | 0.638 |
LIG_SH2_SRC | 517 | 520 | PF00017 | 0.394 |
LIG_SH2_SRC | 530 | 533 | PF00017 | 0.282 |
LIG_SH2_SRC | 592 | 595 | PF00017 | 0.674 |
LIG_SH2_STAP1 | 203 | 207 | PF00017 | 0.638 |
LIG_SH2_STAP1 | 383 | 387 | PF00017 | 0.748 |
LIG_SH2_STAP1 | 503 | 507 | PF00017 | 0.512 |
LIG_SH2_STAP1 | 596 | 600 | PF00017 | 0.611 |
LIG_SH2_STAP1 | 91 | 95 | PF00017 | 0.777 |
LIG_SH2_STAT5 | 179 | 182 | PF00017 | 0.717 |
LIG_SH2_STAT5 | 383 | 386 | PF00017 | 0.753 |
LIG_SH2_STAT5 | 415 | 418 | PF00017 | 0.708 |
LIG_SH2_STAT5 | 489 | 492 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 517 | 520 | PF00017 | 0.394 |
LIG_SH2_STAT5 | 530 | 533 | PF00017 | 0.257 |
LIG_SH2_STAT5 | 539 | 542 | PF00017 | 0.339 |
LIG_SH2_STAT5 | 579 | 582 | PF00017 | 0.661 |
LIG_SH3_3 | 130 | 136 | PF00018 | 0.760 |
LIG_SH3_3 | 227 | 233 | PF00018 | 0.680 |
LIG_SH3_3 | 260 | 266 | PF00018 | 0.656 |
LIG_SH3_3 | 337 | 343 | PF00018 | 0.694 |
LIG_SH3_3 | 39 | 45 | PF00018 | 0.846 |
LIG_SUMO_SIM_anti_2 | 305 | 311 | PF11976 | 0.512 |
LIG_SUMO_SIM_anti_2 | 336 | 341 | PF11976 | 0.689 |
LIG_SUMO_SIM_par_1 | 55 | 60 | PF11976 | 0.675 |
LIG_SxIP_EBH_1 | 185 | 199 | PF03271 | 0.753 |
LIG_TRAF2_1 | 125 | 128 | PF00917 | 0.684 |
LIG_TRAF2_1 | 198 | 201 | PF00917 | 0.633 |
LIG_TRAF2_1 | 605 | 608 | PF00917 | 0.718 |
LIG_TRAF2_1 | 640 | 643 | PF00917 | 0.637 |
LIG_TRAF2_1 | 95 | 98 | PF00917 | 0.706 |
LIG_TYR_ITIM | 501 | 506 | PF00017 | 0.411 |
LIG_WRC_WIRS_1 | 539 | 544 | PF05994 | 0.411 |
MOD_CDK_SPxK_1 | 32 | 38 | PF00069 | 0.642 |
MOD_CK1_1 | 145 | 151 | PF00069 | 0.668 |
MOD_CK1_1 | 23 | 29 | PF00069 | 0.790 |
MOD_CK1_1 | 305 | 311 | PF00069 | 0.400 |
MOD_CK1_1 | 381 | 387 | PF00069 | 0.682 |
MOD_CK1_1 | 55 | 61 | PF00069 | 0.686 |
MOD_CK2_1 | 172 | 178 | PF00069 | 0.831 |
MOD_CK2_1 | 194 | 200 | PF00069 | 0.555 |
MOD_CK2_1 | 562 | 568 | PF00069 | 0.411 |
MOD_CK2_1 | 82 | 88 | PF00069 | 0.784 |
MOD_CK2_1 | 9 | 15 | PF00069 | 0.649 |
MOD_GlcNHglycan | 108 | 111 | PF01048 | 0.484 |
MOD_GlcNHglycan | 144 | 147 | PF01048 | 0.768 |
MOD_GlcNHglycan | 150 | 153 | PF01048 | 0.594 |
MOD_GlcNHglycan | 161 | 164 | PF01048 | 0.622 |
MOD_GlcNHglycan | 174 | 177 | PF01048 | 0.730 |
MOD_GlcNHglycan | 26 | 29 | PF01048 | 0.769 |
MOD_GlcNHglycan | 304 | 307 | PF01048 | 0.386 |
MOD_GlcNHglycan | 373 | 376 | PF01048 | 0.732 |
MOD_GlcNHglycan | 380 | 383 | PF01048 | 0.578 |
MOD_GlcNHglycan | 389 | 392 | PF01048 | 0.576 |
MOD_GlcNHglycan | 47 | 50 | PF01048 | 0.798 |
MOD_GlcNHglycan | 88 | 91 | PF01048 | 0.758 |
MOD_GSK3_1 | 140 | 147 | PF00069 | 0.632 |
MOD_GSK3_1 | 168 | 175 | PF00069 | 0.754 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.843 |
MOD_GSK3_1 | 228 | 235 | PF00069 | 0.573 |
MOD_GSK3_1 | 404 | 411 | PF00069 | 0.658 |
MOD_GSK3_1 | 41 | 48 | PF00069 | 0.754 |
MOD_GSK3_1 | 82 | 89 | PF00069 | 0.730 |
MOD_N-GLC_1 | 329 | 334 | PF02516 | 0.637 |
MOD_N-GLC_1 | 378 | 383 | PF02516 | 0.628 |
MOD_N-GLC_1 | 45 | 50 | PF02516 | 0.739 |
MOD_N-GLC_2 | 479 | 481 | PF02516 | 0.411 |
MOD_NEK2_1 | 188 | 193 | PF00069 | 0.587 |
MOD_NEK2_1 | 238 | 243 | PF00069 | 0.586 |
MOD_NEK2_1 | 446 | 451 | PF00069 | 0.392 |
MOD_NEK2_1 | 490 | 495 | PF00069 | 0.355 |
MOD_NEK2_1 | 57 | 62 | PF00069 | 0.660 |
MOD_NEK2_1 | 86 | 91 | PF00069 | 0.809 |
MOD_NEK2_2 | 82 | 87 | PF00069 | 0.647 |
MOD_PIKK_1 | 584 | 590 | PF00454 | 0.628 |
MOD_PIKK_1 | 65 | 71 | PF00454 | 0.664 |
MOD_PKA_1 | 20 | 26 | PF00069 | 0.756 |
MOD_PKA_1 | 405 | 411 | PF00069 | 0.657 |
MOD_PKA_2 | 20 | 26 | PF00069 | 0.839 |
MOD_PKA_2 | 405 | 411 | PF00069 | 0.604 |
MOD_PKA_2 | 428 | 434 | PF00069 | 0.734 |
MOD_PKA_2 | 513 | 519 | PF00069 | 0.499 |
MOD_PKA_2 | 86 | 92 | PF00069 | 0.796 |
MOD_Plk_1 | 378 | 384 | PF00069 | 0.684 |
MOD_Plk_4 | 305 | 311 | PF00069 | 0.415 |
MOD_Plk_4 | 397 | 403 | PF00069 | 0.567 |
MOD_Plk_4 | 490 | 496 | PF00069 | 0.355 |
MOD_Plk_4 | 513 | 519 | PF00069 | 0.430 |
MOD_ProDKin_1 | 169 | 175 | PF00069 | 0.667 |
MOD_ProDKin_1 | 32 | 38 | PF00069 | 0.717 |
MOD_ProDKin_1 | 41 | 47 | PF00069 | 0.728 |
MOD_ProDKin_1 | 52 | 58 | PF00069 | 0.587 |
MOD_ProDKin_1 | 9 | 15 | PF00069 | 0.704 |
MOD_SUMO_rev_2 | 219 | 227 | PF00179 | 0.599 |
MOD_SUMO_rev_2 | 629 | 633 | PF00179 | 0.559 |
MOD_SUMO_rev_2 | 642 | 647 | PF00179 | 0.541 |
TRG_DiLeu_BaLyEn_6 | 595 | 600 | PF01217 | 0.459 |
TRG_ENDOCYTIC_2 | 11 | 14 | PF00928 | 0.741 |
TRG_ENDOCYTIC_2 | 203 | 206 | PF00928 | 0.533 |
TRG_ENDOCYTIC_2 | 275 | 278 | PF00928 | 0.411 |
TRG_ENDOCYTIC_2 | 281 | 284 | PF00928 | 0.411 |
TRG_ENDOCYTIC_2 | 487 | 490 | PF00928 | 0.411 |
TRG_ENDOCYTIC_2 | 503 | 506 | PF00928 | 0.411 |
TRG_ENDOCYTIC_2 | 539 | 542 | PF00928 | 0.411 |
TRG_ENDOCYTIC_2 | 592 | 595 | PF00928 | 0.506 |
TRG_ENDOCYTIC_2 | 596 | 599 | PF00928 | 0.475 |
TRG_ENDOCYTIC_2 | 619 | 622 | PF00928 | 0.582 |
TRG_ER_diArg_1 | 236 | 238 | PF00400 | 0.651 |
TRG_ER_diArg_1 | 324 | 327 | PF00400 | 0.601 |
TRG_ER_diArg_1 | 456 | 459 | PF00400 | 0.513 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P984 | Leptomonas seymouri | 62% | 96% |
A0A3Q8IHU7 | Leishmania donovani | 92% | 100% |
A4HI71 | Leishmania braziliensis | 79% | 90% |
A4I5E8 | Leishmania infantum | 93% | 100% |
E9B0P6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |