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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 187 | 191 | PF00656 | 0.495 |
CLV_C14_Caspase3-7 | 207 | 211 | PF00656 | 0.410 |
CLV_C14_Caspase3-7 | 246 | 250 | PF00656 | 0.672 |
CLV_C14_Caspase3-7 | 337 | 341 | PF00656 | 0.572 |
CLV_NRD_NRD_1 | 102 | 104 | PF00675 | 0.515 |
CLV_NRD_NRD_1 | 26 | 28 | PF00675 | 0.432 |
CLV_NRD_NRD_1 | 268 | 270 | PF00675 | 0.643 |
CLV_NRD_NRD_1 | 286 | 288 | PF00675 | 0.400 |
CLV_NRD_NRD_1 | 302 | 304 | PF00675 | 0.657 |
CLV_NRD_NRD_1 | 324 | 326 | PF00675 | 0.615 |
CLV_NRD_NRD_1 | 57 | 59 | PF00675 | 0.367 |
CLV_NRD_NRD_1 | 9 | 11 | PF00675 | 0.462 |
CLV_NRD_NRD_1 | 99 | 101 | PF00675 | 0.522 |
CLV_PCSK_FUR_1 | 100 | 104 | PF00082 | 0.511 |
CLV_PCSK_KEX2_1 | 101 | 103 | PF00082 | 0.432 |
CLV_PCSK_KEX2_1 | 26 | 28 | PF00082 | 0.432 |
CLV_PCSK_KEX2_1 | 286 | 288 | PF00082 | 0.500 |
CLV_PCSK_KEX2_1 | 302 | 304 | PF00082 | 0.657 |
CLV_PCSK_KEX2_1 | 323 | 325 | PF00082 | 0.617 |
CLV_PCSK_KEX2_1 | 362 | 364 | PF00082 | 0.625 |
CLV_PCSK_KEX2_1 | 62 | 64 | PF00082 | 0.375 |
CLV_PCSK_KEX2_1 | 9 | 11 | PF00082 | 0.462 |
CLV_PCSK_PC1ET2_1 | 101 | 103 | PF00082 | 0.432 |
CLV_PCSK_PC1ET2_1 | 323 | 325 | PF00082 | 0.614 |
CLV_PCSK_PC1ET2_1 | 362 | 364 | PF00082 | 0.625 |
CLV_PCSK_PC1ET2_1 | 62 | 64 | PF00082 | 0.388 |
CLV_PCSK_PC7_1 | 282 | 288 | PF00082 | 0.488 |
CLV_PCSK_PC7_1 | 58 | 64 | PF00082 | 0.368 |
CLV_PCSK_SKI1_1 | 112 | 116 | PF00082 | 0.425 |
CLV_PCSK_SKI1_1 | 129 | 133 | PF00082 | 0.316 |
CLV_PCSK_SKI1_1 | 26 | 30 | PF00082 | 0.404 |
CLV_PCSK_SKI1_1 | 298 | 302 | PF00082 | 0.585 |
CLV_PCSK_SKI1_1 | 349 | 353 | PF00082 | 0.599 |
CLV_PCSK_SKI1_1 | 376 | 380 | PF00082 | 0.573 |
DEG_SCF_FBW7_2 | 377 | 383 | PF00400 | 0.494 |
DOC_ANK_TNKS_1 | 304 | 311 | PF00023 | 0.517 |
DOC_CKS1_1 | 31 | 36 | PF01111 | 0.376 |
DOC_CKS1_1 | 377 | 382 | PF01111 | 0.493 |
DOC_CYCLIN_RxL_1 | 112 | 125 | PF00134 | 0.403 |
DOC_MAPK_gen_1 | 116 | 122 | PF00069 | 0.401 |
DOC_PP4_FxxP_1 | 301 | 304 | PF00568 | 0.601 |
DOC_PP4_FxxP_1 | 31 | 34 | PF00568 | 0.382 |
DOC_USP7_MATH_1 | 19 | 23 | PF00917 | 0.444 |
DOC_USP7_UBL2_3 | 294 | 298 | PF12436 | 0.560 |
DOC_USP7_UBL2_3 | 345 | 349 | PF12436 | 0.721 |
DOC_WW_Pin1_4 | 30 | 35 | PF00397 | 0.392 |
DOC_WW_Pin1_4 | 310 | 315 | PF00397 | 0.724 |
DOC_WW_Pin1_4 | 317 | 322 | PF00397 | 0.624 |
DOC_WW_Pin1_4 | 376 | 381 | PF00397 | 0.709 |
DOC_WW_Pin1_4 | 385 | 390 | PF00397 | 0.658 |
LIG_14-3-3_CanoR_1 | 137 | 145 | PF00244 | 0.356 |
LIG_14-3-3_CanoR_1 | 147 | 151 | PF00244 | 0.397 |
LIG_14-3-3_CanoR_1 | 325 | 335 | PF00244 | 0.691 |
LIG_14-3-3_CanoR_1 | 400 | 407 | PF00244 | 0.621 |
LIG_Actin_WH2_2 | 42 | 60 | PF00022 | 0.286 |
LIG_BRCT_BRCA1_1 | 262 | 266 | PF00533 | 0.430 |
LIG_FHA_1 | 2 | 8 | PF00498 | 0.577 |
LIG_FHA_1 | 27 | 33 | PF00498 | 0.403 |
LIG_FHA_1 | 377 | 383 | PF00498 | 0.546 |
LIG_FHA_1 | 401 | 407 | PF00498 | 0.661 |
LIG_FHA_2 | 212 | 218 | PF00498 | 0.582 |
LIG_FHA_2 | 254 | 260 | PF00498 | 0.413 |
LIG_FHA_2 | 276 | 282 | PF00498 | 0.508 |
LIG_LIR_Apic_2 | 214 | 219 | PF02991 | 0.606 |
LIG_LIR_Apic_2 | 29 | 34 | PF02991 | 0.384 |
LIG_LIR_Gen_1 | 51 | 61 | PF02991 | 0.369 |
LIG_LIR_Nem_3 | 44 | 49 | PF02991 | 0.362 |
LIG_LIR_Nem_3 | 51 | 57 | PF02991 | 0.372 |
LIG_MYND_3 | 183 | 187 | PF01753 | 0.447 |
LIG_PDZ_Class_3 | 421 | 426 | PF00595 | 0.614 |
LIG_Pex14_1 | 65 | 69 | PF04695 | 0.356 |
LIG_SH2_CRK | 16 | 20 | PF00017 | 0.416 |
LIG_SH2_GRB2like | 15 | 18 | PF00017 | 0.426 |
LIG_SH2_NCK_1 | 135 | 139 | PF00017 | 0.348 |
LIG_SH2_NCK_1 | 16 | 20 | PF00017 | 0.400 |
LIG_SH2_NCK_1 | 216 | 220 | PF00017 | 0.550 |
LIG_SH2_SRC | 216 | 219 | PF00017 | 0.413 |
LIG_SH2_STAT3 | 150 | 153 | PF00017 | 0.427 |
LIG_SH2_STAT3 | 61 | 64 | PF00017 | 0.372 |
LIG_SH2_STAT5 | 150 | 153 | PF00017 | 0.393 |
LIG_SH2_STAT5 | 167 | 170 | PF00017 | 0.392 |
LIG_SH2_STAT5 | 289 | 292 | PF00017 | 0.511 |
LIG_SH2_STAT5 | 76 | 79 | PF00017 | 0.369 |
LIG_TRAF2_1 | 155 | 158 | PF00917 | 0.465 |
LIG_TRAF2_1 | 235 | 238 | PF00917 | 0.550 |
LIG_TRAF2_1 | 274 | 277 | PF00917 | 0.598 |
LIG_TRAF2_1 | 278 | 281 | PF00917 | 0.662 |
LIG_TRAF2_1 | 334 | 337 | PF00917 | 0.564 |
LIG_WRC_WIRS_1 | 66 | 71 | PF05994 | 0.357 |
MOD_CDK_SPxK_1 | 30 | 36 | PF00069 | 0.386 |
MOD_CDK_SPxK_1 | 317 | 323 | PF00069 | 0.637 |
MOD_CDK_SPxxK_3 | 317 | 324 | PF00069 | 0.633 |
MOD_CK1_1 | 149 | 155 | PF00069 | 0.506 |
MOD_CK1_1 | 381 | 387 | PF00069 | 0.690 |
MOD_CK2_1 | 152 | 158 | PF00069 | 0.471 |
MOD_CK2_1 | 17 | 23 | PF00069 | 0.478 |
MOD_CK2_1 | 211 | 217 | PF00069 | 0.560 |
MOD_CK2_1 | 232 | 238 | PF00069 | 0.560 |
MOD_CK2_1 | 271 | 277 | PF00069 | 0.629 |
MOD_Cter_Amidation | 24 | 27 | PF01082 | 0.452 |
MOD_GlcNHglycan | 234 | 237 | PF01048 | 0.497 |
MOD_GlcNHglycan | 262 | 265 | PF01048 | 0.696 |
MOD_GlcNHglycan | 314 | 317 | PF01048 | 0.630 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.703 |
MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.506 |
MOD_GSK3_1 | 199 | 206 | PF00069 | 0.530 |
MOD_GSK3_1 | 249 | 256 | PF00069 | 0.500 |
MOD_GSK3_1 | 26 | 33 | PF00069 | 0.393 |
MOD_GSK3_1 | 271 | 278 | PF00069 | 0.501 |
MOD_GSK3_1 | 312 | 319 | PF00069 | 0.584 |
MOD_GSK3_1 | 354 | 361 | PF00069 | 0.554 |
MOD_GSK3_1 | 381 | 388 | PF00069 | 0.665 |
MOD_LATS_1 | 24 | 30 | PF00433 | 0.430 |
MOD_N-GLC_1 | 80 | 85 | PF02516 | 0.364 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.562 |
MOD_NEK2_1 | 232 | 237 | PF00069 | 0.503 |
MOD_NEK2_2 | 211 | 216 | PF00069 | 0.600 |
MOD_NEK2_2 | 65 | 70 | PF00069 | 0.358 |
MOD_PIKK_1 | 102 | 108 | PF00454 | 0.528 |
MOD_PIKK_1 | 149 | 155 | PF00454 | 0.415 |
MOD_PKA_1 | 102 | 108 | PF00069 | 0.528 |
MOD_PKA_1 | 26 | 32 | PF00069 | 0.413 |
MOD_PKA_1 | 324 | 330 | PF00069 | 0.667 |
MOD_PKA_2 | 102 | 108 | PF00069 | 0.528 |
MOD_PKA_2 | 136 | 142 | PF00069 | 0.351 |
MOD_PKA_2 | 146 | 152 | PF00069 | 0.393 |
MOD_PKA_2 | 26 | 32 | PF00069 | 0.540 |
MOD_PKA_2 | 324 | 330 | PF00069 | 0.679 |
MOD_PKB_1 | 100 | 108 | PF00069 | 0.512 |
MOD_Plk_2-3 | 253 | 259 | PF00069 | 0.406 |
MOD_Plk_4 | 211 | 217 | PF00069 | 0.574 |
MOD_ProDKin_1 | 30 | 36 | PF00069 | 0.386 |
MOD_ProDKin_1 | 310 | 316 | PF00069 | 0.725 |
MOD_ProDKin_1 | 317 | 323 | PF00069 | 0.623 |
MOD_ProDKin_1 | 376 | 382 | PF00069 | 0.711 |
MOD_ProDKin_1 | 385 | 391 | PF00069 | 0.656 |
MOD_SUMO_for_1 | 351 | 354 | PF00179 | 0.630 |
MOD_SUMO_rev_2 | 220 | 230 | PF00179 | 0.636 |
TRG_ENDOCYTIC_2 | 15 | 18 | PF00928 | 0.426 |
TRG_ER_diArg_1 | 100 | 103 | PF00400 | 0.510 |
TRG_ER_diArg_1 | 241 | 244 | PF00400 | 0.587 |
TRG_ER_diArg_1 | 26 | 28 | PF00400 | 0.534 |
TRG_ER_diArg_1 | 301 | 303 | PF00400 | 0.673 |
TRG_ER_diArg_1 | 370 | 373 | PF00400 | 0.582 |
TRG_ER_diArg_1 | 8 | 10 | PF00400 | 0.489 |
TRG_NLS_Bipartite_1 | 100 | 120 | PF00514 | 0.432 |
TRG_NLS_MonoCore_2 | 322 | 327 | PF00514 | 0.628 |
TRG_NLS_MonoExtC_3 | 115 | 121 | PF00514 | 0.407 |
TRG_NLS_MonoExtC_3 | 324 | 330 | PF00514 | 0.548 |
TRG_NLS_MonoExtN_4 | 321 | 327 | PF00514 | 0.574 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2P6 | Leptomonas seymouri | 78% | 100% |
A0A0S4IKL5 | Bodo saltans | 52% | 91% |
A0A1X0P5A6 | Trypanosomatidae | 62% | 96% |
A0A3Q8IPV2 | Leishmania donovani | 93% | 100% |
A0A3R7NKQ1 | Trypanosoma rangeli | 62% | 97% |
A4IBN9 | Leishmania infantum | 93% | 100% |
C9ZYZ2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 60% | 97% |
E9AFH3 | Leishmania major | 92% | 100% |
E9B6M8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
V5BY99 | Trypanosoma cruzi | 62% | 96% |