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 | 0.489 |
CLV_C14_Caspase3-7 | 207 | 211 | PF00656 | 0.407 |
CLV_C14_Caspase3-7 | 246 | 250 | PF00656 | 0.659 |
CLV_C14_Caspase3-7 | 337 | 341 | PF00656 | 0.566 |
CLV_NRD_NRD_1 | 102 | 104 | PF00675 | 0.515 |
CLV_NRD_NRD_1 | 26 | 28 | PF00675 | 0.431 |
CLV_NRD_NRD_1 | 268 | 270 | PF00675 | 0.633 |
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 | 0.366 |
CLV_NRD_NRD_1 | 9 | 11 | PF00675 | 0.466 |
CLV_NRD_NRD_1 | 99 | 101 | PF00675 | 0.528 |
CLV_PCSK_FUR_1 | 100 | 104 | PF00082 | 0.514 |
CLV_PCSK_KEX2_1 | 101 | 103 | PF00082 | 0.437 |
CLV_PCSK_KEX2_1 | 26 | 28 | PF00082 | 0.431 |
CLV_PCSK_KEX2_1 | 286 | 288 | PF00082 | 0.499 |
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 | 0.609 |
CLV_PCSK_KEX2_1 | 62 | 64 | PF00082 | 0.373 |
CLV_PCSK_KEX2_1 | 9 | 11 | PF00082 | 0.466 |
CLV_PCSK_PC1ET2_1 | 101 | 103 | PF00082 | 0.437 |
CLV_PCSK_PC1ET2_1 | 323 | 325 | PF00082 | 0.614 |
CLV_PCSK_PC1ET2_1 | 362 | 364 | PF00082 | 0.609 |
CLV_PCSK_PC1ET2_1 | 62 | 64 | PF00082 | 0.386 |
CLV_PCSK_PC7_1 | 282 | 288 | PF00082 | 0.485 |
CLV_PCSK_PC7_1 | 58 | 64 | PF00082 | 0.367 |
CLV_PCSK_SKI1_1 | 112 | 116 | PF00082 | 0.427 |
CLV_PCSK_SKI1_1 | 129 | 133 | PF00082 | 0.317 |
CLV_PCSK_SKI1_1 | 26 | 30 | PF00082 | 0.403 |
CLV_PCSK_SKI1_1 | 298 | 302 | PF00082 | 0.587 |
CLV_PCSK_SKI1_1 | 349 | 353 | PF00082 | 0.557 |
DOC_CKS1_1 | 31 | 36 | PF01111 | 0.376 |
DOC_CYCLIN_RxL_1 | 112 | 125 | PF00134 | 0.404 |
DOC_MAPK_gen_1 | 116 | 122 | PF00069 | 0.402 |
DOC_PP4_FxxP_1 | 301 | 304 | PF00568 | 0.601 |
DOC_PP4_FxxP_1 | 31 | 34 | PF00568 | 0.382 |
DOC_USP7_MATH_1 | 152 | 156 | PF00917 | 0.346 |
DOC_USP7_MATH_1 | 19 | 23 | PF00917 | 0.444 |
DOC_USP7_MATH_1 | 245 | 249 | PF00917 | 0.651 |
DOC_USP7_UBL2_3 | 294 | 298 | PF12436 | 0.567 |
DOC_USP7_UBL2_3 | 345 | 349 | PF12436 | 0.710 |
DOC_WW_Pin1_4 | 30 | 35 | PF00397 | 0.391 |
DOC_WW_Pin1_4 | 309 | 314 | PF00397 | 0.730 |
DOC_WW_Pin1_4 | 317 | 322 | PF00397 | 0.627 |
DOC_WW_Pin1_4 | 385 | 390 | PF00397 | 0.664 |
LIG_14-3-3_CanoR_1 | 137 | 145 | PF00244 | 0.361 |
LIG_14-3-3_CanoR_1 | 400 | 407 | PF00244 | 0.631 |
LIG_FHA_1 | 27 | 33 | PF00498 | 0.402 |
LIG_FHA_1 | 401 | 407 | PF00498 | 0.673 |
LIG_FHA_2 | 212 | 218 | PF00498 | 0.576 |
LIG_FHA_2 | 272 | 278 | PF00498 | 0.612 |
LIG_LIR_Apic_2 | 214 | 219 | PF02991 | 0.597 |
LIG_LIR_Apic_2 | 29 | 34 | PF02991 | 0.382 |
LIG_LIR_Apic_2 | 299 | 304 | PF02991 | 0.645 |
LIG_LIR_Gen_1 | 51 | 61 | PF02991 | 0.369 |
LIG_LIR_Nem_3 | 44 | 49 | PF02991 | 0.364 |
LIG_LIR_Nem_3 | 51 | 57 | PF02991 | 0.371 |
LIG_MYND_3 | 183 | 187 | PF01753 | 0.440 |
LIG_MYND_3 | 379 | 383 | PF01753 | 0.652 |
LIG_PDZ_Class_3 | 421 | 426 | PF00595 | 0.610 |
LIG_Pex14_1 | 65 | 69 | PF04695 | 0.356 |
LIG_SH2_CRK | 16 | 20 | PF00017 | 0.417 |
LIG_SH2_GRB2like | 15 | 18 | PF00017 | 0.429 |
LIG_SH2_NCK_1 | 135 | 139 | PF00017 | 0.351 |
LIG_SH2_NCK_1 | 16 | 20 | PF00017 | 0.402 |
LIG_SH2_NCK_1 | 216 | 220 | PF00017 | 0.541 |
LIG_SH2_STAT3 | 150 | 153 | PF00017 | 0.437 |
LIG_SH2_STAT3 | 61 | 64 | PF00017 | 0.370 |
LIG_SH2_STAT5 | 150 | 153 | PF00017 | 0.402 |
LIG_SH2_STAT5 | 167 | 170 | PF00017 | 0.390 |
LIG_SH2_STAT5 | 289 | 292 | PF00017 | 0.512 |
LIG_SH2_STAT5 | 76 | 79 | PF00017 | 0.370 |
LIG_TRAF2_1 | 155 | 158 | PF00917 | 0.470 |
LIG_TRAF2_1 | 235 | 238 | PF00917 | 0.532 |
LIG_TRAF2_1 | 274 | 277 | PF00917 | 0.594 |
LIG_TRAF2_1 | 278 | 281 | PF00917 | 0.655 |
LIG_TRAF2_1 | 334 | 337 | PF00917 | 0.558 |
LIG_WRC_WIRS_1 | 66 | 71 | PF05994 | 0.357 |
MOD_CDK_SPxK_1 | 30 | 36 | PF00069 | 0.385 |
MOD_CDK_SPxK_1 | 317 | 323 | PF00069 | 0.639 |
MOD_CDK_SPxxK_3 | 317 | 324 | PF00069 | 0.634 |
MOD_CK1_1 | 381 | 387 | PF00069 | 0.686 |
MOD_CK2_1 | 152 | 158 | PF00069 | 0.479 |
MOD_CK2_1 | 17 | 23 | PF00069 | 0.479 |
MOD_CK2_1 | 211 | 217 | PF00069 | 0.554 |
MOD_CK2_1 | 232 | 238 | PF00069 | 0.541 |
MOD_CK2_1 | 271 | 277 | PF00069 | 0.622 |
MOD_Cter_Amidation | 24 | 27 | PF01082 | 0.451 |
MOD_GlcNHglycan | 234 | 237 | PF01048 | 0.480 |
MOD_GlcNHglycan | 262 | 265 | PF01048 | 0.687 |
MOD_GlcNHglycan | 314 | 317 | PF01048 | 0.631 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.710 |
MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.509 |
MOD_GSK3_1 | 199 | 206 | PF00069 | 0.532 |
MOD_GSK3_1 | 245 | 252 | PF00069 | 0.517 |
MOD_GSK3_1 | 26 | 33 | PF00069 | 0.392 |
MOD_GSK3_1 | 271 | 278 | PF00069 | 0.494 |
MOD_GSK3_1 | 292 | 299 | PF00069 | 0.537 |
MOD_GSK3_1 | 305 | 312 | PF00069 | 0.561 |
MOD_GSK3_1 | 381 | 388 | PF00069 | 0.664 |
MOD_LATS_1 | 24 | 30 | PF00433 | 0.428 |
MOD_N-GLC_1 | 80 | 85 | PF02516 | 0.366 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.570 |
MOD_NEK2_1 | 232 | 237 | PF00069 | 0.485 |
MOD_NEK2_2 | 211 | 216 | PF00069 | 0.595 |
MOD_NEK2_2 | 296 | 301 | PF00069 | 0.591 |
MOD_NEK2_2 | 65 | 70 | PF00069 | 0.358 |
MOD_PIKK_1 | 102 | 108 | PF00454 | 0.530 |
MOD_PKA_1 | 102 | 108 | PF00069 | 0.530 |
MOD_PKA_1 | 26 | 32 | PF00069 | 0.411 |
MOD_PKA_1 | 324 | 330 | PF00069 | 0.664 |
MOD_PKA_2 | 102 | 108 | PF00069 | 0.530 |
MOD_PKA_2 | 136 | 142 | PF00069 | 0.354 |
MOD_PKA_2 | 26 | 32 | PF00069 | 0.539 |
MOD_PKA_2 | 324 | 330 | PF00069 | 0.676 |
MOD_PKB_1 | 100 | 108 | PF00069 | 0.515 |
MOD_PKB_1 | 303 | 311 | PF00069 | 0.622 |
MOD_Plk_1 | 353 | 359 | PF00069 | 0.622 |
MOD_Plk_4 | 211 | 217 | PF00069 | 0.568 |
MOD_Plk_4 | 296 | 302 | PF00069 | 0.631 |
MOD_ProDKin_1 | 30 | 36 | PF00069 | 0.385 |
MOD_ProDKin_1 | 309 | 315 | PF00069 | 0.732 |
MOD_ProDKin_1 | 317 | 323 | PF00069 | 0.625 |
MOD_ProDKin_1 | 385 | 391 | PF00069 | 0.662 |
MOD_SUMO_for_1 | 351 | 354 | PF00179 | 0.591 |
MOD_SUMO_rev_2 | 220 | 230 | PF00179 | 0.621 |
TRG_ENDOCYTIC_2 | 15 | 18 | PF00928 | 0.429 |
TRG_ER_diArg_1 | 100 | 103 | PF00400 | 0.516 |
TRG_ER_diArg_1 | 241 | 244 | PF00400 | 0.566 |
TRG_ER_diArg_1 | 26 | 28 | PF00400 | 0.533 |
TRG_ER_diArg_1 | 301 | 303 | PF00400 | 0.670 |
TRG_ER_diArg_1 | 370 | 373 | PF00400 | 0.578 |
TRG_NLS_Bipartite_1 | 100 | 120 | PF00514 | 0.434 |
TRG_NLS_MonoCore_2 | 322 | 327 | PF00514 | 0.628 |
TRG_NLS_MonoExtC_3 | 115 | 121 | PF00514 | 0.409 |
TRG_NLS_MonoExtC_3 | 324 | 330 | PF00514 | 0.545 |
TRG_NLS_MonoExtN_4 | 321 | 327 | PF00514 | 0.574 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2P6 | Leptomonas seymouri | 78% | 100% |
A0A0S4IKL5 | Bodo saltans | 51% | 91% |
A0A1X0P5A6 | Trypanosomatidae | 61% | 96% |
A0A3Q8IPV2 | Leishmania donovani | 97% | 100% |
A0A3R7NKQ1 | Trypanosoma rangeli | 61% | 97% |
A4HN18 | Leishmania braziliensis | 92% | 100% |
A4IBN9 | Leishmania infantum | 97% | 100% |
C9ZYZ2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 60% | 97% |
E9B6M8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
V5BY99 | Trypanosoma cruzi | 60% | 96% |