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: 3 |
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: 8 |
NetGPI | no | yes: 0, no: 8 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005783 | endoplasmic reticulum | 5 | 2 |
GO:0005794 | Golgi apparatus | 5 | 2 |
GO:0016020 | membrane | 2 | 9 |
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 | 9 |
Related structures:
AlphaFold database: Q4QGX2
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:0006897 | endocytosis | 5 | 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:0016192 | vesicle-mediated 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 | 9 |
GO:0016409 | palmitoyltransferase activity | 5 | 9 |
GO:0016417 | S-acyltransferase activity | 5 | 9 |
GO:0016740 | transferase activity | 2 | 9 |
GO:0016746 | acyltransferase activity | 3 | 9 |
GO:0016747 | acyltransferase activity, transferring groups other than amino-acyl groups | 4 | 9 |
GO:0019706 | protein-cysteine S-palmitoyltransferase activity | 4 | 9 |
GO:0019707 | protein-cysteine S-acyltransferase activity | 3 | 9 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 9 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 213 | 217 | PF00656 | 0.630 |
CLV_C14_Caspase3-7 | 243 | 247 | PF00656 | 0.691 |
CLV_C14_Caspase3-7 | 379 | 383 | PF00656 | 0.519 |
CLV_NRD_NRD_1 | 257 | 259 | PF00675 | 0.475 |
CLV_NRD_NRD_1 | 287 | 289 | PF00675 | 0.386 |
CLV_NRD_NRD_1 | 29 | 31 | PF00675 | 0.505 |
CLV_NRD_NRD_1 | 377 | 379 | PF00675 | 0.362 |
CLV_NRD_NRD_1 | 494 | 496 | PF00675 | 0.377 |
CLV_NRD_NRD_1 | 514 | 516 | PF00675 | 0.364 |
CLV_PCSK_KEX2_1 | 287 | 289 | PF00082 | 0.396 |
CLV_PCSK_KEX2_1 | 376 | 378 | PF00082 | 0.364 |
CLV_PCSK_KEX2_1 | 494 | 496 | PF00082 | 0.443 |
CLV_PCSK_KEX2_1 | 513 | 515 | PF00082 | 0.392 |
CLV_PCSK_PC1ET2_1 | 494 | 496 | PF00082 | 0.443 |
CLV_PCSK_PC1ET2_1 | 513 | 515 | PF00082 | 0.392 |
CLV_PCSK_PC7_1 | 509 | 515 | PF00082 | 0.412 |
CLV_PCSK_SKI1_1 | 105 | 109 | PF00082 | 0.457 |
CLV_PCSK_SKI1_1 | 288 | 292 | PF00082 | 0.486 |
CLV_PCSK_SKI1_1 | 509 | 513 | PF00082 | 0.385 |
DOC_MAPK_gen_1 | 104 | 110 | PF00069 | 0.614 |
DOC_MAPK_gen_1 | 494 | 501 | PF00069 | 0.603 |
DOC_PP1_RVXF_1 | 495 | 502 | PF00149 | 0.612 |
DOC_PP4_FxxP_1 | 291 | 294 | PF00568 | 0.626 |
DOC_USP7_MATH_1 | 266 | 270 | PF00917 | 0.641 |
DOC_USP7_MATH_1 | 294 | 298 | PF00917 | 0.620 |
DOC_USP7_MATH_1 | 57 | 61 | PF00917 | 0.685 |
DOC_USP7_MATH_1 | 80 | 84 | PF00917 | 0.727 |
DOC_USP7_MATH_2 | 131 | 137 | PF00917 | 0.681 |
DOC_USP7_UBL2_3 | 31 | 35 | PF12436 | 0.660 |
DOC_USP7_UBL2_3 | 387 | 391 | PF12436 | 0.604 |
DOC_WW_Pin1_4 | 127 | 132 | PF00397 | 0.673 |
DOC_WW_Pin1_4 | 136 | 141 | PF00397 | 0.690 |
DOC_WW_Pin1_4 | 35 | 40 | PF00397 | 0.653 |
DOC_WW_Pin1_4 | 95 | 100 | PF00397 | 0.680 |
LIG_14-3-3_CanoR_1 | 12 | 20 | PF00244 | 0.698 |
LIG_14-3-3_CanoR_1 | 121 | 131 | PF00244 | 0.676 |
LIG_14-3-3_CanoR_1 | 233 | 238 | PF00244 | 0.696 |
LIG_14-3-3_CanoR_1 | 282 | 286 | PF00244 | 0.657 |
LIG_14-3-3_CanoR_1 | 293 | 299 | PF00244 | 0.528 |
LIG_14-3-3_CanoR_1 | 495 | 500 | PF00244 | 0.642 |
LIG_Actin_WH2_2 | 130 | 146 | PF00022 | 0.641 |
LIG_BRCT_BRCA1_1 | 134 | 138 | PF00533 | 0.706 |
LIG_BRCT_BRCA1_1 | 314 | 318 | PF00533 | 0.398 |
LIG_BRCT_BRCA1_1 | 448 | 452 | PF00533 | 0.319 |
LIG_deltaCOP1_diTrp_1 | 246 | 253 | PF00928 | 0.691 |
LIG_FHA_1 | 168 | 174 | PF00498 | 0.680 |
LIG_FHA_1 | 180 | 186 | PF00498 | 0.649 |
LIG_FHA_1 | 350 | 356 | PF00498 | 0.416 |
LIG_FHA_1 | 459 | 465 | PF00498 | 0.303 |
LIG_FHA_1 | 51 | 57 | PF00498 | 0.664 |
LIG_FHA_2 | 107 | 113 | PF00498 | 0.661 |
LIG_FHA_2 | 124 | 130 | PF00498 | 0.613 |
LIG_FHA_2 | 377 | 383 | PF00498 | 0.519 |
LIG_LIR_Gen_1 | 409 | 419 | PF02991 | 0.534 |
LIG_LIR_Gen_1 | 478 | 483 | PF02991 | 0.498 |
LIG_LIR_Gen_1 | 486 | 492 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 315 | 321 | PF02991 | 0.393 |
LIG_LIR_Nem_3 | 409 | 415 | PF02991 | 0.534 |
LIG_LIR_Nem_3 | 478 | 482 | PF02991 | 0.498 |
LIG_LIR_Nem_3 | 486 | 491 | PF02991 | 0.465 |
LIG_LIR_Nem_3 | 96 | 100 | PF02991 | 0.643 |
LIG_MLH1_MIPbox_1 | 448 | 452 | PF16413 | 0.319 |
LIG_PCNA_PIPBox_1 | 156 | 165 | PF02747 | 0.649 |
LIG_PCNA_yPIPBox_3 | 329 | 337 | PF02747 | 0.363 |
LIG_Pex14_1 | 314 | 318 | PF04695 | 0.398 |
LIG_SH2_CRK | 351 | 355 | PF00017 | 0.335 |
LIG_SH2_PTP2 | 321 | 324 | PF00017 | 0.357 |
LIG_SH2_SRC | 488 | 491 | PF00017 | 0.564 |
LIG_SH2_STAP1 | 351 | 355 | PF00017 | 0.303 |
LIG_SH2_STAT5 | 113 | 116 | PF00017 | 0.657 |
LIG_SH2_STAT5 | 321 | 324 | PF00017 | 0.320 |
LIG_SH2_STAT5 | 325 | 328 | PF00017 | 0.325 |
LIG_SH2_STAT5 | 351 | 354 | PF00017 | 0.343 |
LIG_SH2_STAT5 | 436 | 439 | PF00017 | 0.376 |
LIG_SH2_STAT5 | 451 | 454 | PF00017 | 0.341 |
LIG_SH2_STAT5 | 479 | 482 | PF00017 | 0.564 |
LIG_SH3_3 | 111 | 117 | PF00018 | 0.709 |
LIG_SH3_3 | 125 | 131 | PF00018 | 0.736 |
LIG_SH3_3 | 134 | 140 | PF00018 | 0.657 |
LIG_SH3_3 | 166 | 172 | PF00018 | 0.668 |
LIG_SH3_3 | 17 | 23 | PF00018 | 0.689 |
LIG_SH3_3 | 192 | 198 | PF00018 | 0.679 |
LIG_SH3_3 | 31 | 37 | PF00018 | 0.660 |
LIG_SH3_3 | 496 | 502 | PF00018 | 0.622 |
LIG_SH3_3 | 70 | 76 | PF00018 | 0.705 |
LIG_SH3_4 | 31 | 38 | PF00018 | 0.657 |
LIG_Sin3_3 | 340 | 347 | PF02671 | 0.303 |
LIG_SUMO_SIM_anti_2 | 306 | 311 | PF11976 | 0.363 |
LIG_SUMO_SIM_anti_2 | 352 | 358 | PF11976 | 0.333 |
LIG_SUMO_SIM_anti_2 | 461 | 466 | PF11976 | 0.303 |
LIG_SUMO_SIM_par_1 | 106 | 112 | PF11976 | 0.625 |
LIG_SUMO_SIM_par_1 | 352 | 358 | PF11976 | 0.440 |
LIG_TRAF2_1 | 130 | 133 | PF00917 | 0.686 |
LIG_TYR_ITSM | 484 | 491 | PF00017 | 0.541 |
LIG_UBA3_1 | 107 | 115 | PF00899 | 0.661 |
LIG_UBA3_1 | 354 | 360 | PF00899 | 0.350 |
LIG_WRC_WIRS_1 | 356 | 361 | PF05994 | 0.353 |
LIG_WRC_WIRS_1 | 415 | 420 | PF05994 | 0.395 |
MOD_CK1_1 | 106 | 112 | PF00069 | 0.658 |
MOD_CK1_1 | 136 | 142 | PF00069 | 0.693 |
MOD_CK1_1 | 417 | 423 | PF00069 | 0.469 |
MOD_CK1_1 | 50 | 56 | PF00069 | 0.636 |
MOD_CK1_1 | 503 | 509 | PF00069 | 0.649 |
MOD_CK1_1 | 83 | 89 | PF00069 | 0.691 |
MOD_CK2_1 | 106 | 112 | PF00069 | 0.667 |
MOD_CK2_1 | 123 | 129 | PF00069 | 0.638 |
MOD_CK2_1 | 139 | 145 | PF00069 | 0.693 |
MOD_CK2_1 | 173 | 179 | PF00069 | 0.688 |
MOD_CK2_1 | 233 | 239 | PF00069 | 0.651 |
MOD_CK2_1 | 57 | 63 | PF00069 | 0.680 |
MOD_GlcNHglycan | 100 | 103 | PF01048 | 0.447 |
MOD_GlcNHglycan | 14 | 17 | PF01048 | 0.547 |
MOD_GlcNHglycan | 164 | 167 | PF01048 | 0.447 |
MOD_GlcNHglycan | 262 | 265 | PF01048 | 0.437 |
MOD_GlcNHglycan | 367 | 370 | PF01048 | 0.411 |
MOD_GlcNHglycan | 419 | 422 | PF01048 | 0.398 |
MOD_GlcNHglycan | 448 | 451 | PF01048 | 0.541 |
MOD_GlcNHglycan | 502 | 505 | PF01048 | 0.496 |
MOD_GSK3_1 | 123 | 130 | PF00069 | 0.679 |
MOD_GSK3_1 | 132 | 139 | PF00069 | 0.695 |
MOD_GSK3_1 | 22 | 29 | PF00069 | 0.688 |
MOD_GSK3_1 | 277 | 284 | PF00069 | 0.656 |
MOD_GSK3_1 | 376 | 383 | PF00069 | 0.617 |
MOD_GSK3_1 | 48 | 55 | PF00069 | 0.662 |
MOD_N-GLC_1 | 272 | 277 | PF02516 | 0.408 |
MOD_N-GLC_2 | 390 | 392 | PF02516 | 0.348 |
MOD_N-GLC_2 | 404 | 406 | PF02516 | 0.265 |
MOD_NEK2_1 | 103 | 108 | PF00069 | 0.683 |
MOD_NEK2_1 | 312 | 317 | PF00069 | 0.408 |
MOD_NEK2_1 | 350 | 355 | PF00069 | 0.486 |
MOD_NEK2_1 | 414 | 419 | PF00069 | 0.366 |
MOD_NEK2_1 | 475 | 480 | PF00069 | 0.420 |
MOD_PIKK_1 | 281 | 287 | PF00454 | 0.622 |
MOD_PIKK_1 | 323 | 329 | PF00454 | 0.383 |
MOD_PK_1 | 30 | 36 | PF00069 | 0.661 |
MOD_PKA_1 | 30 | 36 | PF00069 | 0.695 |
MOD_PKA_1 | 376 | 382 | PF00069 | 0.541 |
MOD_PKA_1 | 495 | 501 | PF00069 | 0.588 |
MOD_PKA_2 | 281 | 287 | PF00069 | 0.679 |
MOD_PKA_2 | 376 | 382 | PF00069 | 0.571 |
MOD_PKA_2 | 446 | 452 | PF00069 | 0.328 |
MOD_PKA_2 | 80 | 86 | PF00069 | 0.696 |
MOD_PKA_2 | 90 | 96 | PF00069 | 0.654 |
MOD_PKB_1 | 10 | 18 | PF00069 | 0.705 |
MOD_PKB_1 | 231 | 239 | PF00069 | 0.692 |
MOD_Plk_1 | 132 | 138 | PF00069 | 0.649 |
MOD_Plk_1 | 83 | 89 | PF00069 | 0.693 |
MOD_Plk_4 | 103 | 109 | PF00069 | 0.651 |
MOD_Plk_4 | 133 | 139 | PF00069 | 0.690 |
MOD_Plk_4 | 313 | 319 | PF00069 | 0.420 |
MOD_Plk_4 | 350 | 356 | PF00069 | 0.465 |
MOD_Plk_4 | 423 | 429 | PF00069 | 0.358 |
MOD_Plk_4 | 432 | 438 | PF00069 | 0.325 |
MOD_Plk_4 | 458 | 464 | PF00069 | 0.354 |
MOD_Plk_4 | 475 | 481 | PF00069 | 0.319 |
MOD_ProDKin_1 | 127 | 133 | PF00069 | 0.674 |
MOD_ProDKin_1 | 136 | 142 | PF00069 | 0.689 |
MOD_ProDKin_1 | 35 | 41 | PF00069 | 0.655 |
MOD_ProDKin_1 | 95 | 101 | PF00069 | 0.678 |
MOD_SUMO_rev_2 | 251 | 261 | PF00179 | 0.656 |
TRG_ENDOCYTIC_2 | 321 | 324 | PF00928 | 0.320 |
TRG_ENDOCYTIC_2 | 351 | 354 | PF00928 | 0.398 |
TRG_ENDOCYTIC_2 | 412 | 415 | PF00928 | 0.564 |
TRG_ENDOCYTIC_2 | 479 | 482 | PF00928 | 0.627 |
TRG_ENDOCYTIC_2 | 488 | 491 | PF00928 | 0.564 |
TRG_ER_diArg_1 | 10 | 13 | PF00400 | 0.707 |
TRG_ER_diArg_1 | 286 | 288 | PF00400 | 0.604 |
TRG_ER_diArg_1 | 376 | 378 | PF00400 | 0.541 |
TRG_ER_diArg_1 | 514 | 516 | PF00400 | 0.638 |
TRG_NLS_Bipartite_1 | 494 | 516 | PF00514 | 0.631 |
TRG_NLS_MonoCore_2 | 511 | 516 | PF00514 | 0.623 |
TRG_NLS_MonoExtC_3 | 512 | 517 | PF00514 | 0.598 |
TRG_NLS_MonoExtN_4 | 494 | 499 | PF00514 | 0.567 |
TRG_NLS_MonoExtN_4 | 509 | 516 | PF00514 | 0.581 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7WRS6 | Leishmania donovani | 88% | 100% |
A4H6N2 | Leishmania braziliensis | 63% | 100% |
A4HCH5 | Leishmania braziliensis | 32% | 100% |
A4HV16 | Leishmania infantum | 88% | 100% |
A4HV17 | Leishmania infantum | 52% | 100% |
E9ANQ1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 83% |
E9ANQ2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 46% | 100% |