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 |
Related structures:
AlphaFold database: Q4Q7R9
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 3 |
GO:0016787 | hydrolase activity | 2 | 3 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 148 | 152 | PF00656 | 0.413 |
CLV_C14_Caspase3-7 | 16 | 20 | PF00656 | 0.554 |
CLV_C14_Caspase3-7 | 231 | 235 | PF00656 | 0.434 |
CLV_C14_Caspase3-7 | 3 | 7 | PF00656 | 0.650 |
CLV_NRD_NRD_1 | 218 | 220 | PF00675 | 0.390 |
CLV_NRD_NRD_1 | 79 | 81 | PF00675 | 0.419 |
CLV_PCSK_KEX2_1 | 220 | 222 | PF00082 | 0.479 |
CLV_PCSK_KEX2_1 | 224 | 226 | PF00082 | 0.411 |
CLV_PCSK_KEX2_1 | 79 | 81 | PF00082 | 0.419 |
CLV_PCSK_PC1ET2_1 | 220 | 222 | PF00082 | 0.479 |
CLV_PCSK_PC1ET2_1 | 224 | 226 | PF00082 | 0.411 |
CLV_PCSK_SKI1_1 | 221 | 225 | PF00082 | 0.417 |
CLV_PCSK_SKI1_1 | 237 | 241 | PF00082 | 0.418 |
CLV_PCSK_SKI1_1 | 266 | 270 | PF00082 | 0.509 |
CLV_PCSK_SKI1_1 | 295 | 299 | PF00082 | 0.469 |
CLV_PCSK_SKI1_1 | 339 | 343 | PF00082 | 0.647 |
DEG_APCC_DBOX_1 | 132 | 140 | PF00400 | 0.328 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.610 |
DEG_SPOP_SBC_1 | 392 | 396 | PF00917 | 0.711 |
DOC_CKS1_1 | 276 | 281 | PF01111 | 0.552 |
DOC_CYCLIN_RxL_1 | 310 | 323 | PF00134 | 0.621 |
DOC_CYCLIN_yCln2_LP_2 | 356 | 359 | PF00134 | 0.620 |
DOC_CYCLIN_yCln2_LP_2 | 402 | 408 | PF00134 | 0.745 |
DOC_MAPK_DCC_7 | 201 | 211 | PF00069 | 0.398 |
DOC_MAPK_DCC_7 | 240 | 249 | PF00069 | 0.488 |
DOC_MAPK_gen_1 | 201 | 211 | PF00069 | 0.449 |
DOC_MAPK_MEF2A_6 | 204 | 211 | PF00069 | 0.398 |
DOC_MAPK_MEF2A_6 | 240 | 249 | PF00069 | 0.488 |
DOC_MAPK_MEF2A_6 | 286 | 294 | PF00069 | 0.527 |
DOC_MAPK_MEF2A_6 | 295 | 302 | PF00069 | 0.454 |
DOC_MAPK_NFAT4_5 | 295 | 303 | PF00069 | 0.443 |
DOC_PP1_RVXF_1 | 62 | 69 | PF00149 | 0.496 |
DOC_PP2B_LxvP_1 | 356 | 359 | PF13499 | 0.620 |
DOC_PP2B_LxvP_1 | 408 | 411 | PF13499 | 0.580 |
DOC_PP2B_PxIxI_1 | 206 | 212 | PF00149 | 0.398 |
DOC_PP4_FxxP_1 | 256 | 259 | PF00568 | 0.395 |
DOC_PP4_FxxP_1 | 269 | 272 | PF00568 | 0.426 |
DOC_USP7_MATH_1 | 183 | 187 | PF00917 | 0.449 |
DOC_USP7_MATH_1 | 327 | 331 | PF00917 | 0.675 |
DOC_USP7_MATH_1 | 343 | 347 | PF00917 | 0.647 |
DOC_USP7_MATH_1 | 379 | 383 | PF00917 | 0.762 |
DOC_USP7_MATH_1 | 384 | 388 | PF00917 | 0.706 |
DOC_USP7_MATH_1 | 392 | 396 | PF00917 | 0.784 |
DOC_USP7_UBL2_3 | 220 | 224 | PF12436 | 0.404 |
DOC_WW_Pin1_4 | 179 | 184 | PF00397 | 0.344 |
DOC_WW_Pin1_4 | 255 | 260 | PF00397 | 0.544 |
DOC_WW_Pin1_4 | 275 | 280 | PF00397 | 0.230 |
DOC_WW_Pin1_4 | 322 | 327 | PF00397 | 0.621 |
DOC_WW_Pin1_4 | 339 | 344 | PF00397 | 0.471 |
DOC_WW_Pin1_4 | 380 | 385 | PF00397 | 0.756 |
DOC_WW_Pin1_4 | 401 | 406 | PF00397 | 0.689 |
DOC_WW_Pin1_4 | 410 | 415 | PF00397 | 0.568 |
LIG_14-3-3_CanoR_1 | 27 | 35 | PF00244 | 0.549 |
LIG_14-3-3_CanoR_1 | 67 | 73 | PF00244 | 0.414 |
LIG_AP2alpha_2 | 172 | 174 | PF02296 | 0.437 |
LIG_BIR_III_2 | 267 | 271 | PF00653 | 0.540 |
LIG_BRCT_BRCA1_1 | 126 | 130 | PF00533 | 0.328 |
LIG_BRCT_BRCA1_1 | 245 | 249 | PF00533 | 0.427 |
LIG_BRCT_BRCA1_1 | 394 | 398 | PF00533 | 0.699 |
LIG_Clathr_ClatBox_1 | 110 | 114 | PF01394 | 0.344 |
LIG_eIF4E_1 | 131 | 137 | PF01652 | 0.475 |
LIG_FHA_1 | 200 | 206 | PF00498 | 0.463 |
LIG_FHA_1 | 30 | 36 | PF00498 | 0.486 |
LIG_FHA_1 | 367 | 373 | PF00498 | 0.696 |
LIG_FHA_1 | 383 | 389 | PF00498 | 0.759 |
LIG_FHA_2 | 394 | 400 | PF00498 | 0.696 |
LIG_LIR_Apic_2 | 253 | 259 | PF02991 | 0.408 |
LIG_LIR_Apic_2 | 267 | 272 | PF02991 | 0.417 |
LIG_LIR_Apic_2 | 71 | 75 | PF02991 | 0.320 |
LIG_LIR_Gen_1 | 106 | 115 | PF02991 | 0.407 |
LIG_LIR_Gen_1 | 122 | 131 | PF02991 | 0.273 |
LIG_LIR_Gen_1 | 141 | 150 | PF02991 | 0.449 |
LIG_LIR_Gen_1 | 181 | 191 | PF02991 | 0.328 |
LIG_LIR_Nem_3 | 106 | 111 | PF02991 | 0.412 |
LIG_LIR_Nem_3 | 122 | 128 | PF02991 | 0.273 |
LIG_LIR_Nem_3 | 141 | 145 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 181 | 187 | PF02991 | 0.328 |
LIG_LIR_Nem_3 | 71 | 76 | PF02991 | 0.406 |
LIG_Pex14_1 | 72 | 76 | PF04695 | 0.473 |
LIG_Pex14_2 | 111 | 115 | PF04695 | 0.449 |
LIG_Pex14_2 | 68 | 72 | PF04695 | 0.462 |
LIG_SH2_PTP2 | 125 | 128 | PF00017 | 0.385 |
LIG_SH2_STAT3 | 131 | 134 | PF00017 | 0.328 |
LIG_SH2_STAT5 | 125 | 128 | PF00017 | 0.385 |
LIG_SH2_STAT5 | 301 | 304 | PF00017 | 0.381 |
LIG_SH2_STAT5 | 86 | 89 | PF00017 | 0.340 |
LIG_SH3_3 | 342 | 348 | PF00018 | 0.734 |
LIG_SH3_3 | 408 | 414 | PF00018 | 0.581 |
LIG_SUMO_SIM_anti_2 | 135 | 141 | PF11976 | 0.475 |
LIG_SUMO_SIM_par_1 | 135 | 141 | PF11976 | 0.475 |
LIG_WRPW_2 | 73 | 76 | PF00400 | 0.386 |
LIG_WW_3 | 27 | 31 | PF00397 | 0.470 |
MOD_CDK_SPK_2 | 339 | 344 | PF00069 | 0.533 |
MOD_CDK_SPxxK_3 | 410 | 417 | PF00069 | 0.551 |
MOD_CK1_1 | 118 | 124 | PF00069 | 0.323 |
MOD_CK1_1 | 13 | 19 | PF00069 | 0.537 |
MOD_CK1_1 | 144 | 150 | PF00069 | 0.242 |
MOD_CK1_1 | 373 | 379 | PF00069 | 0.701 |
MOD_CK1_1 | 382 | 388 | PF00069 | 0.690 |
MOD_CK1_1 | 391 | 397 | PF00069 | 0.599 |
MOD_CK1_1 | 401 | 407 | PF00069 | 0.592 |
MOD_CK2_1 | 118 | 124 | PF00069 | 0.320 |
MOD_CK2_1 | 28 | 34 | PF00069 | 0.540 |
MOD_GlcNHglycan | 117 | 120 | PF01048 | 0.330 |
MOD_GlcNHglycan | 12 | 15 | PF01048 | 0.509 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.577 |
MOD_GlcNHglycan | 330 | 333 | PF01048 | 0.594 |
MOD_GlcNHglycan | 377 | 380 | PF01048 | 0.753 |
MOD_GlcNHglycan | 390 | 393 | PF01048 | 0.665 |
MOD_GSK3_1 | 179 | 186 | PF00069 | 0.377 |
MOD_GSK3_1 | 335 | 342 | PF00069 | 0.581 |
MOD_GSK3_1 | 366 | 373 | PF00069 | 0.688 |
MOD_GSK3_1 | 375 | 382 | PF00069 | 0.648 |
MOD_GSK3_1 | 383 | 390 | PF00069 | 0.613 |
MOD_GSK3_1 | 393 | 400 | PF00069 | 0.494 |
MOD_GSK3_1 | 406 | 413 | PF00069 | 0.548 |
MOD_GSK3_1 | 9 | 16 | PF00069 | 0.590 |
MOD_NEK2_1 | 115 | 120 | PF00069 | 0.369 |
MOD_NEK2_1 | 17 | 22 | PF00069 | 0.417 |
MOD_NEK2_1 | 320 | 325 | PF00069 | 0.604 |
MOD_NEK2_1 | 371 | 376 | PF00069 | 0.727 |
MOD_NEK2_1 | 388 | 393 | PF00069 | 0.685 |
MOD_NEK2_1 | 398 | 403 | PF00069 | 0.741 |
MOD_NEK2_1 | 68 | 73 | PF00069 | 0.410 |
MOD_NEK2_1 | 9 | 14 | PF00069 | 0.678 |
MOD_NEK2_2 | 183 | 188 | PF00069 | 0.344 |
MOD_PKA_2 | 29 | 35 | PF00069 | 0.528 |
MOD_PKA_2 | 343 | 349 | PF00069 | 0.662 |
MOD_Plk_1 | 398 | 404 | PF00069 | 0.706 |
MOD_Plk_4 | 13 | 19 | PF00069 | 0.627 |
MOD_Plk_4 | 162 | 168 | PF00069 | 0.243 |
MOD_Plk_4 | 243 | 249 | PF00069 | 0.369 |
MOD_Plk_4 | 68 | 74 | PF00069 | 0.351 |
MOD_ProDKin_1 | 179 | 185 | PF00069 | 0.344 |
MOD_ProDKin_1 | 255 | 261 | PF00069 | 0.538 |
MOD_ProDKin_1 | 275 | 281 | PF00069 | 0.230 |
MOD_ProDKin_1 | 322 | 328 | PF00069 | 0.625 |
MOD_ProDKin_1 | 339 | 345 | PF00069 | 0.474 |
MOD_ProDKin_1 | 380 | 386 | PF00069 | 0.757 |
MOD_ProDKin_1 | 401 | 407 | PF00069 | 0.686 |
MOD_ProDKin_1 | 410 | 416 | PF00069 | 0.554 |
TRG_DiLeu_BaEn_1 | 132 | 137 | PF01217 | 0.475 |
TRG_DiLeu_BaEn_1 | 99 | 104 | PF01217 | 0.340 |
TRG_DiLeu_BaLyEn_6 | 185 | 190 | PF01217 | 0.363 |
TRG_ENDOCYTIC_2 | 125 | 128 | PF00928 | 0.409 |
TRG_ENDOCYTIC_2 | 95 | 98 | PF00928 | 0.363 |
TRG_ER_diArg_1 | 218 | 221 | PF00400 | 0.394 |
TRG_ER_diArg_1 | 79 | 81 | PF00400 | 0.425 |
TRG_NES_CRM1_1 | 134 | 149 | PF08389 | 0.449 |
TRG_NES_CRM1_1 | 288 | 304 | PF08389 | 0.469 |
TRG_NES_CRM1_1 | 99 | 114 | PF08389 | 0.344 |
TRG_NLS_MonoExtN_4 | 217 | 223 | PF00514 | 0.395 |
TRG_Pf-PMV_PEXEL_1 | 188 | 192 | PF00026 | 0.331 |
TRG_Pf-PMV_PEXEL_1 | 64 | 69 | PF00026 | 0.434 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HRJ3 | Leptomonas seymouri | 75% | 100% |
A0A0S4JBE5 | Bodo saltans | 47% | 97% |
A0A1X0P2B9 | Trypanosomatidae | 61% | 100% |
A0A3S5H7M3 | Leishmania donovani | 92% | 85% |
A0A422NMM6 | Trypanosoma rangeli | 58% | 100% |
A4HHZ0 | Leishmania braziliensis | 78% | 100% |
A4I567 | Leishmania infantum | 93% | 85% |
C9ZQJ3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 55% | 100% |
E9B0G4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 88% |
V5BCE0 | Trypanosoma cruzi | 54% | 100% |