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: 18 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 9 |
NetGPI | no | yes: 0, no: 9 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
GO:0005783 | endoplasmic reticulum | 5 | 1 |
GO:0005794 | Golgi apparatus | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
Related structures:
AlphaFold database: A4H754
Term | Name | Level | Count |
---|---|---|---|
GO:0006497 | protein lipidation | 5 | 1 |
GO:0006605 | protein targeting | 5 | 1 |
GO:0006612 | protein targeting to membrane | 5 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0006810 | transport | 3 | 1 |
GO:0006886 | intracellular protein transport | 4 | 1 |
GO:0008104 | protein localization | 4 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0015031 | protein transport | 4 | 1 |
GO:0018193 | peptidyl-amino acid modification | 5 | 1 |
GO:0018198 | peptidyl-cysteine modification | 6 | 1 |
GO:0018230 | peptidyl-L-cysteine S-palmitoylation | 7 | 1 |
GO:0018231 | peptidyl-S-diacylglycerol-L-cysteine biosynthetic process from peptidyl-cysteine | 7 | 1 |
GO:0018345 | protein palmitoylation | 6 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0033036 | macromolecule localization | 2 | 1 |
GO:0036211 | protein modification process | 4 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0043543 | protein acylation | 5 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0045184 | establishment of protein localization | 3 | 1 |
GO:0046907 | intracellular transport | 3 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0051641 | cellular localization | 2 | 1 |
GO:0051649 | establishment of localization in cell | 3 | 1 |
GO:0051668 | localization within membrane | 3 | 1 |
GO:0070727 | cellular macromolecule localization | 3 | 1 |
GO:0071702 | organic substance transport | 4 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0071705 | nitrogen compound transport | 4 | 1 |
GO:0072657 | protein localization to membrane | 4 | 1 |
GO:0090150 | establishment of protein localization to membrane | 4 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 10 |
GO:0016409 | palmitoyltransferase activity | 5 | 10 |
GO:0016417 | S-acyltransferase activity | 5 | 10 |
GO:0016740 | transferase activity | 2 | 10 |
GO:0016746 | acyltransferase activity | 3 | 10 |
GO:0016747 | acyltransferase activity, transferring groups other than amino-acyl groups | 4 | 10 |
GO:0019706 | protein-cysteine S-palmitoyltransferase activity | 4 | 10 |
GO:0019707 | protein-cysteine S-acyltransferase activity | 3 | 10 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 10 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 149 | 153 | PF00656 | 0.703 |
CLV_C14_Caspase3-7 | 192 | 196 | PF00656 | 0.603 |
CLV_C14_Caspase3-7 | 268 | 272 | PF00656 | 0.530 |
CLV_C14_Caspase3-7 | 525 | 529 | PF00656 | 0.616 |
CLV_MEL_PAP_1 | 80 | 86 | PF00089 | 0.448 |
CLV_NRD_NRD_1 | 142 | 144 | PF00675 | 0.415 |
CLV_NRD_NRD_1 | 245 | 247 | PF00675 | 0.504 |
CLV_NRD_NRD_1 | 251 | 253 | PF00675 | 0.508 |
CLV_NRD_NRD_1 | 276 | 278 | PF00675 | 0.445 |
CLV_PCSK_KEX2_1 | 245 | 247 | PF00082 | 0.504 |
CLV_PCSK_KEX2_1 | 251 | 253 | PF00082 | 0.508 |
CLV_PCSK_SKI1_1 | 112 | 116 | PF00082 | 0.526 |
CLV_PCSK_SKI1_1 | 137 | 141 | PF00082 | 0.408 |
CLV_PCSK_SKI1_1 | 20 | 24 | PF00082 | 0.314 |
DEG_APCC_DBOX_1 | 250 | 258 | PF00400 | 0.652 |
DEG_APCC_DBOX_1 | 314 | 322 | PF00400 | 0.502 |
DEG_APCC_DBOX_1 | 501 | 509 | PF00400 | 0.621 |
DOC_CKS1_1 | 476 | 481 | PF01111 | 0.582 |
DOC_MAPK_gen_1 | 245 | 256 | PF00069 | 0.674 |
DOC_MAPK_gen_1 | 277 | 284 | PF00069 | 0.583 |
DOC_MAPK_MEF2A_6 | 249 | 258 | PF00069 | 0.632 |
DOC_MAPK_MEF2A_6 | 498 | 505 | PF00069 | 0.583 |
DOC_MAPK_NFAT4_5 | 498 | 506 | PF00069 | 0.586 |
DOC_PP1_RVXF_1 | 400 | 407 | PF00149 | 0.444 |
DOC_PP4_FxxP_1 | 284 | 287 | PF00568 | 0.565 |
DOC_PP4_FxxP_1 | 364 | 367 | PF00568 | 0.247 |
DOC_USP7_MATH_1 | 191 | 195 | PF00917 | 0.597 |
DOC_USP7_MATH_1 | 532 | 536 | PF00917 | 0.765 |
DOC_USP7_MATH_1 | 7 | 11 | PF00917 | 0.670 |
DOC_USP7_MATH_2 | 77 | 83 | PF00917 | 0.591 |
DOC_USP7_UBL2_3 | 137 | 141 | PF12436 | 0.704 |
DOC_WW_Pin1_4 | 445 | 450 | PF00397 | 0.697 |
DOC_WW_Pin1_4 | 451 | 456 | PF00397 | 0.675 |
DOC_WW_Pin1_4 | 475 | 480 | PF00397 | 0.623 |
DOC_WW_Pin1_4 | 528 | 533 | PF00397 | 0.709 |
DOC_WW_Pin1_4 | 545 | 550 | PF00397 | 0.730 |
LIG_14-3-3_CanoR_1 | 504 | 509 | PF00244 | 0.598 |
LIG_14-3-3_CanoR_1 | 577 | 581 | PF00244 | 0.597 |
LIG_14-3-3_CanoR_1 | 83 | 89 | PF00244 | 0.598 |
LIG_AP2alpha_1 | 493 | 497 | PF02296 | 0.572 |
LIG_APCC_ABBA_1 | 187 | 192 | PF00400 | 0.742 |
LIG_APCC_ABBAyCdc20_2 | 186 | 192 | PF00400 | 0.741 |
LIG_BRCT_BRCA1_1 | 381 | 385 | PF00533 | 0.371 |
LIG_eIF4E_1 | 17 | 23 | PF01652 | 0.579 |
LIG_eIF4E_1 | 334 | 340 | PF01652 | 0.569 |
LIG_eIF4E_1 | 341 | 347 | PF01652 | 0.324 |
LIG_eIF4E_1 | 41 | 47 | PF01652 | 0.505 |
LIG_FHA_1 | 17 | 23 | PF00498 | 0.501 |
LIG_FHA_1 | 406 | 412 | PF00498 | 0.574 |
LIG_FHA_1 | 41 | 47 | PF00498 | 0.358 |
LIG_FHA_1 | 476 | 482 | PF00498 | 0.627 |
LIG_FHA_1 | 537 | 543 | PF00498 | 0.597 |
LIG_FHA_1 | 570 | 576 | PF00498 | 0.740 |
LIG_FHA_1 | 597 | 603 | PF00498 | 0.610 |
LIG_FHA_2 | 203 | 209 | PF00498 | 0.620 |
LIG_FHA_2 | 271 | 277 | PF00498 | 0.603 |
LIG_FHA_2 | 458 | 464 | PF00498 | 0.617 |
LIG_GBD_Chelix_1 | 49 | 57 | PF00786 | 0.272 |
LIG_IRF3_LxIS_1 | 62 | 67 | PF10401 | 0.203 |
LIG_LIR_Apic_2 | 281 | 287 | PF02991 | 0.569 |
LIG_LIR_Apic_2 | 362 | 367 | PF02991 | 0.244 |
LIG_LIR_Gen_1 | 142 | 151 | PF02991 | 0.748 |
LIG_LIR_Gen_1 | 32 | 41 | PF02991 | 0.412 |
LIG_LIR_Gen_1 | 332 | 342 | PF02991 | 0.552 |
LIG_LIR_Gen_1 | 358 | 367 | PF02991 | 0.353 |
LIG_LIR_Gen_1 | 373 | 383 | PF02991 | 0.216 |
LIG_LIR_Gen_1 | 384 | 393 | PF02991 | 0.289 |
LIG_LIR_Nem_3 | 142 | 148 | PF02991 | 0.755 |
LIG_LIR_Nem_3 | 32 | 36 | PF02991 | 0.386 |
LIG_LIR_Nem_3 | 332 | 338 | PF02991 | 0.552 |
LIG_LIR_Nem_3 | 358 | 364 | PF02991 | 0.334 |
LIG_LIR_Nem_3 | 373 | 379 | PF02991 | 0.201 |
LIG_LIR_Nem_3 | 382 | 388 | PF02991 | 0.274 |
LIG_LIR_Nem_3 | 428 | 433 | PF02991 | 0.659 |
LIG_NRBOX | 48 | 54 | PF00104 | 0.233 |
LIG_PCNA_PIPBox_1 | 348 | 357 | PF02747 | 0.360 |
LIG_PCNA_yPIPBox_3 | 11 | 20 | PF02747 | 0.630 |
LIG_Pex14_1 | 359 | 363 | PF04695 | 0.258 |
LIG_Pex14_2 | 29 | 33 | PF04695 | 0.268 |
LIG_Pex14_2 | 375 | 379 | PF04695 | 0.360 |
LIG_Pex14_2 | 493 | 497 | PF04695 | 0.589 |
LIG_Pex14_2 | 58 | 62 | PF04695 | 0.325 |
LIG_PTB_Apo_2 | 328 | 335 | PF02174 | 0.530 |
LIG_PTB_Phospho_1 | 328 | 334 | PF10480 | 0.530 |
LIG_REV1ctd_RIR_1 | 362 | 366 | PF16727 | 0.296 |
LIG_SH2_CRK | 430 | 434 | PF00017 | 0.631 |
LIG_SH2_GRB2like | 329 | 332 | PF00017 | 0.523 |
LIG_SH2_GRB2like | 591 | 594 | PF00017 | 0.657 |
LIG_SH2_NCK_1 | 41 | 45 | PF00017 | 0.447 |
LIG_SH2_PTP2 | 591 | 594 | PF00017 | 0.614 |
LIG_SH2_SRC | 329 | 332 | PF00017 | 0.590 |
LIG_SH2_SRC | 396 | 399 | PF00017 | 0.530 |
LIG_SH2_SRC | 430 | 433 | PF00017 | 0.680 |
LIG_SH2_SRC | 591 | 594 | PF00017 | 0.614 |
LIG_SH2_STAP1 | 361 | 365 | PF00017 | 0.330 |
LIG_SH2_STAP1 | 381 | 385 | PF00017 | 0.155 |
LIG_SH2_STAP1 | 41 | 45 | PF00017 | 0.487 |
LIG_SH2_STAT5 | 335 | 338 | PF00017 | 0.353 |
LIG_SH2_STAT5 | 341 | 344 | PF00017 | 0.285 |
LIG_SH2_STAT5 | 355 | 358 | PF00017 | 0.284 |
LIG_SH2_STAT5 | 361 | 364 | PF00017 | 0.159 |
LIG_SH2_STAT5 | 376 | 379 | PF00017 | 0.328 |
LIG_SH2_STAT5 | 396 | 399 | PF00017 | 0.355 |
LIG_SH2_STAT5 | 472 | 475 | PF00017 | 0.459 |
LIG_SH2_STAT5 | 591 | 594 | PF00017 | 0.657 |
LIG_SH3_1 | 591 | 597 | PF00018 | 0.611 |
LIG_SH3_3 | 476 | 482 | PF00018 | 0.542 |
LIG_SH3_3 | 551 | 557 | PF00018 | 0.690 |
LIG_SH3_3 | 578 | 584 | PF00018 | 0.734 |
LIG_SH3_3 | 591 | 597 | PF00018 | 0.718 |
LIG_SUMO_SIM_anti_2 | 255 | 260 | PF11976 | 0.600 |
LIG_SUMO_SIM_anti_2 | 32 | 38 | PF11976 | 0.277 |
LIG_SUMO_SIM_anti_2 | 48 | 54 | PF11976 | 0.283 |
LIG_SUMO_SIM_par_1 | 255 | 260 | PF11976 | 0.600 |
LIG_SUMO_SIM_par_1 | 67 | 73 | PF11976 | 0.208 |
LIG_TRAF2_1 | 173 | 176 | PF00917 | 0.737 |
LIG_TRAF2_1 | 206 | 209 | PF00917 | 0.638 |
LIG_TRAF2_1 | 449 | 452 | PF00917 | 0.630 |
LIG_TYR_ITIM | 339 | 344 | PF00017 | 0.308 |
LIG_Vh1_VBS_1 | 379 | 397 | PF01044 | 0.203 |
LIG_WRC_WIRS_1 | 30 | 35 | PF05994 | 0.387 |
LIG_WRC_WIRS_1 | 59 | 64 | PF05994 | 0.426 |
LIG_WRC_WIRS_1 | 89 | 94 | PF05994 | 0.381 |
MOD_CK1_1 | 198 | 204 | PF00069 | 0.709 |
MOD_CK1_1 | 454 | 460 | PF00069 | 0.529 |
MOD_CK1_1 | 535 | 541 | PF00069 | 0.647 |
MOD_CK1_1 | 65 | 71 | PF00069 | 0.483 |
MOD_CK1_1 | 82 | 88 | PF00069 | 0.379 |
MOD_CK2_1 | 202 | 208 | PF00069 | 0.672 |
MOD_CK2_1 | 445 | 451 | PF00069 | 0.673 |
MOD_CK2_1 | 457 | 463 | PF00069 | 0.516 |
MOD_GlcNHglycan | 105 | 108 | PF01048 | 0.428 |
MOD_GlcNHglycan | 195 | 198 | PF01048 | 0.571 |
MOD_GlcNHglycan | 367 | 370 | PF01048 | 0.412 |
MOD_GlcNHglycan | 381 | 384 | PF01048 | 0.299 |
MOD_GlcNHglycan | 443 | 448 | PF01048 | 0.592 |
MOD_GlcNHglycan | 532 | 535 | PF01048 | 0.732 |
MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.481 |
MOD_GSK3_1 | 191 | 198 | PF00069 | 0.705 |
MOD_GSK3_1 | 355 | 362 | PF00069 | 0.426 |
MOD_GSK3_1 | 457 | 464 | PF00069 | 0.560 |
MOD_GSK3_1 | 528 | 535 | PF00069 | 0.639 |
MOD_GSK3_1 | 58 | 65 | PF00069 | 0.453 |
MOD_GSK3_1 | 592 | 599 | PF00069 | 0.708 |
MOD_N-GLC_1 | 300 | 305 | PF02516 | 0.360 |
MOD_N-GLC_2 | 126 | 128 | PF02516 | 0.513 |
MOD_N-GLC_2 | 290 | 292 | PF02516 | 0.360 |
MOD_NEK2_1 | 166 | 171 | PF00069 | 0.636 |
MOD_NEK2_1 | 29 | 34 | PF00069 | 0.249 |
MOD_NEK2_1 | 300 | 305 | PF00069 | 0.308 |
MOD_NEK2_1 | 342 | 347 | PF00069 | 0.383 |
MOD_NEK2_1 | 379 | 384 | PF00069 | 0.355 |
MOD_NEK2_1 | 418 | 423 | PF00069 | 0.392 |
MOD_NEK2_1 | 576 | 581 | PF00069 | 0.496 |
MOD_NEK2_1 | 58 | 63 | PF00069 | 0.317 |
MOD_NEK2_1 | 64 | 69 | PF00069 | 0.294 |
MOD_PIKK_1 | 150 | 156 | PF00454 | 0.694 |
MOD_PIKK_1 | 257 | 263 | PF00454 | 0.301 |
MOD_PK_1 | 504 | 510 | PF00069 | 0.506 |
MOD_PK_1 | 601 | 607 | PF00069 | 0.504 |
MOD_PKA_1 | 143 | 149 | PF00069 | 0.483 |
MOD_PKA_2 | 167 | 173 | PF00069 | 0.736 |
MOD_PKA_2 | 576 | 582 | PF00069 | 0.497 |
MOD_PKA_2 | 82 | 88 | PF00069 | 0.534 |
MOD_PKB_1 | 502 | 510 | PF00069 | 0.502 |
MOD_Plk_1 | 280 | 286 | PF00069 | 0.306 |
MOD_Plk_2-3 | 220 | 226 | PF00069 | 0.532 |
MOD_Plk_2-3 | 513 | 519 | PF00069 | 0.669 |
MOD_Plk_4 | 280 | 286 | PF00069 | 0.306 |
MOD_Plk_4 | 29 | 35 | PF00069 | 0.241 |
MOD_Plk_4 | 342 | 348 | PF00069 | 0.404 |
MOD_Plk_4 | 359 | 365 | PF00069 | 0.227 |
MOD_Plk_4 | 370 | 376 | PF00069 | 0.302 |
MOD_Plk_4 | 381 | 387 | PF00069 | 0.287 |
MOD_Plk_4 | 65 | 71 | PF00069 | 0.405 |
MOD_Plk_4 | 88 | 94 | PF00069 | 0.495 |
MOD_ProDKin_1 | 445 | 451 | PF00069 | 0.631 |
MOD_ProDKin_1 | 475 | 481 | PF00069 | 0.536 |
MOD_ProDKin_1 | 528 | 534 | PF00069 | 0.650 |
MOD_ProDKin_1 | 545 | 551 | PF00069 | 0.681 |
MOD_SUMO_rev_2 | 136 | 146 | PF00179 | 0.506 |
TRG_DiLeu_BaEn_1 | 281 | 286 | PF01217 | 0.394 |
TRG_DiLeu_BaEn_2 | 279 | 285 | PF01217 | 0.466 |
TRG_ENDOCYTIC_2 | 334 | 337 | PF00928 | 0.340 |
TRG_ENDOCYTIC_2 | 341 | 344 | PF00928 | 0.247 |
TRG_ENDOCYTIC_2 | 361 | 364 | PF00928 | 0.160 |
TRG_ENDOCYTIC_2 | 376 | 379 | PF00928 | 0.400 |
TRG_ENDOCYTIC_2 | 430 | 433 | PF00928 | 0.544 |
TRG_ENDOCYTIC_2 | 472 | 475 | PF00928 | 0.381 |
TRG_ER_diArg_1 | 186 | 189 | PF00400 | 0.590 |
TRG_ER_diArg_1 | 244 | 246 | PF00400 | 0.651 |
TRG_ER_diArg_1 | 250 | 252 | PF00400 | 0.649 |
TRG_ER_diArg_1 | 501 | 504 | PF00400 | 0.538 |
TRG_NES_CRM1_1 | 233 | 247 | PF08389 | 0.592 |
TRG_NLS_MonoExtC_3 | 247 | 252 | PF00514 | 0.604 |
TRG_NLS_MonoExtN_4 | 245 | 252 | PF00514 | 0.608 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P7C7 | Leptomonas seymouri | 50% | 96% |
A0A1X0NNR1 | Trypanosomatidae | 25% | 100% |
A0A3Q8ICU7 | Leishmania donovani | 74% | 100% |
A4HVJ3 | Leishmania infantum | 74% | 100% |
D0A6R2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 26% | 100% |
E9AP89 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 72% | 100% |
Q4QG89 | Leishmania major | 71% | 99% |
V5AVF5 | Trypanosoma cruzi | 26% | 100% |