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 | 0.526 |
CLV_C14_Caspase3-7 | 207 | 211 | PF00656 | 0.353 |
CLV_C14_Caspase3-7 | 246 | 250 | PF00656 | 0.684 |
CLV_C14_Caspase3-7 | 337 | 341 | PF00656 | 0.606 |
CLV_NRD_NRD_1 | 102 | 104 | PF00675 | 0.532 |
CLV_NRD_NRD_1 | 26 | 28 | PF00675 | 0.470 |
CLV_NRD_NRD_1 | 268 | 270 | PF00675 | 0.667 |
CLV_NRD_NRD_1 | 286 | 288 | PF00675 | 0.395 |
CLV_NRD_NRD_1 | 302 | 304 | PF00675 | 0.596 |
CLV_NRD_NRD_1 | 324 | 326 | PF00675 | 0.628 |
CLV_NRD_NRD_1 | 57 | 59 | PF00675 | 0.418 |
CLV_NRD_NRD_1 | 9 | 11 | PF00675 | 0.520 |
CLV_NRD_NRD_1 | 99 | 101 | PF00675 | 0.543 |
CLV_PCSK_FUR_1 | 100 | 104 | PF00082 | 0.635 |
CLV_PCSK_KEX2_1 | 101 | 103 | PF00082 | 0.477 |
CLV_PCSK_KEX2_1 | 26 | 28 | PF00082 | 0.553 |
CLV_PCSK_KEX2_1 | 286 | 288 | PF00082 | 0.544 |
CLV_PCSK_KEX2_1 | 302 | 304 | PF00082 | 0.596 |
CLV_PCSK_KEX2_1 | 323 | 325 | PF00082 | 0.634 |
CLV_PCSK_KEX2_1 | 362 | 364 | PF00082 | 0.670 |
CLV_PCSK_KEX2_1 | 369 | 371 | PF00082 | 0.659 |
CLV_PCSK_KEX2_1 | 62 | 64 | PF00082 | 0.412 |
CLV_PCSK_KEX2_1 | 9 | 11 | PF00082 | 0.520 |
CLV_PCSK_PC1ET2_1 | 101 | 103 | PF00082 | 0.490 |
CLV_PCSK_PC1ET2_1 | 323 | 325 | PF00082 | 0.669 |
CLV_PCSK_PC1ET2_1 | 362 | 364 | PF00082 | 0.670 |
CLV_PCSK_PC1ET2_1 | 369 | 371 | PF00082 | 0.659 |
CLV_PCSK_PC1ET2_1 | 62 | 64 | PF00082 | 0.423 |
CLV_PCSK_PC7_1 | 282 | 288 | PF00082 | 0.537 |
CLV_PCSK_PC7_1 | 58 | 64 | PF00082 | 0.420 |
CLV_PCSK_SKI1_1 | 112 | 116 | PF00082 | 0.481 |
CLV_PCSK_SKI1_1 | 129 | 133 | PF00082 | 0.361 |
CLV_PCSK_SKI1_1 | 26 | 30 | PF00082 | 0.448 |
CLV_PCSK_SKI1_1 | 298 | 302 | PF00082 | 0.637 |
CLV_PCSK_SKI1_1 | 349 | 353 | PF00082 | 0.619 |
CLV_PCSK_SKI1_1 | 376 | 380 | PF00082 | 0.641 |
DEG_SCF_FBW7_2 | 377 | 383 | PF00400 | 0.549 |
DOC_CKS1_1 | 31 | 36 | PF01111 | 0.428 |
DOC_CKS1_1 | 377 | 382 | PF01111 | 0.550 |
DOC_CYCLIN_RxL_1 | 112 | 125 | PF00134 | 0.458 |
DOC_MAPK_gen_1 | 116 | 122 | PF00069 | 0.456 |
DOC_PP4_FxxP_1 | 301 | 304 | PF00568 | 0.654 |
DOC_PP4_FxxP_1 | 31 | 34 | PF00568 | 0.434 |
DOC_USP7_MATH_1 | 19 | 23 | PF00917 | 0.496 |
DOC_USP7_MATH_1 | 245 | 249 | PF00917 | 0.643 |
DOC_USP7_UBL2_3 | 294 | 298 | PF12436 | 0.617 |
DOC_USP7_UBL2_3 | 345 | 349 | PF12436 | 0.704 |
DOC_WW_Pin1_4 | 30 | 35 | PF00397 | 0.435 |
DOC_WW_Pin1_4 | 309 | 314 | PF00397 | 0.740 |
DOC_WW_Pin1_4 | 317 | 322 | PF00397 | 0.508 |
DOC_WW_Pin1_4 | 376 | 381 | PF00397 | 0.551 |
DOC_WW_Pin1_4 | 385 | 390 | PF00397 | 0.696 |
LIG_14-3-3_CanoR_1 | 137 | 145 | PF00244 | 0.410 |
LIG_14-3-3_CanoR_1 | 400 | 407 | PF00244 | 0.672 |
LIG_APCC_ABBA_1 | 241 | 246 | PF00400 | 0.526 |
LIG_FHA_1 | 27 | 33 | PF00498 | 0.453 |
LIG_FHA_1 | 377 | 383 | PF00498 | 0.551 |
LIG_FHA_1 | 401 | 407 | PF00498 | 0.699 |
LIG_FHA_2 | 212 | 218 | PF00498 | 0.663 |
LIG_FHA_2 | 276 | 282 | PF00498 | 0.532 |
LIG_LIR_Apic_2 | 214 | 219 | PF02991 | 0.637 |
LIG_LIR_Apic_2 | 29 | 34 | PF02991 | 0.434 |
LIG_LIR_Apic_2 | 299 | 304 | PF02991 | 0.693 |
LIG_LIR_Gen_1 | 51 | 61 | PF02991 | 0.410 |
LIG_LIR_Nem_3 | 44 | 49 | PF02991 | 0.409 |
LIG_LIR_Nem_3 | 51 | 57 | PF02991 | 0.406 |
LIG_MYND_3 | 183 | 187 | PF01753 | 0.495 |
LIG_PDZ_Class_3 | 421 | 426 | PF00595 | 0.652 |
LIG_Pex14_1 | 65 | 69 | PF04695 | 0.408 |
LIG_SH2_CRK | 16 | 20 | PF00017 | 0.473 |
LIG_SH2_GRB2like | 15 | 18 | PF00017 | 0.483 |
LIG_SH2_NCK_1 | 135 | 139 | PF00017 | 0.400 |
LIG_SH2_NCK_1 | 16 | 20 | PF00017 | 0.457 |
LIG_SH2_NCK_1 | 216 | 220 | PF00017 | 0.674 |
LIG_SH2_SRC | 216 | 219 | PF00017 | 0.463 |
LIG_SH2_STAT3 | 150 | 153 | PF00017 | 0.485 |
LIG_SH2_STAT3 | 61 | 64 | PF00017 | 0.419 |
LIG_SH2_STAT5 | 150 | 153 | PF00017 | 0.441 |
LIG_SH2_STAT5 | 167 | 170 | PF00017 | 0.432 |
LIG_SH2_STAT5 | 289 | 292 | PF00017 | 0.518 |
LIG_SH2_STAT5 | 405 | 408 | PF00017 | 0.410 |
LIG_SH2_STAT5 | 76 | 79 | PF00017 | 0.421 |
LIG_TRAF2_1 | 155 | 158 | PF00917 | 0.586 |
LIG_TRAF2_1 | 235 | 238 | PF00917 | 0.584 |
LIG_TRAF2_1 | 274 | 277 | PF00917 | 0.633 |
LIG_TRAF2_1 | 278 | 281 | PF00917 | 0.674 |
LIG_TRAF2_1 | 334 | 337 | PF00917 | 0.608 |
LIG_WRC_WIRS_1 | 66 | 71 | PF05994 | 0.410 |
MOD_CDK_SPxK_1 | 30 | 36 | PF00069 | 0.430 |
MOD_CDK_SPxK_1 | 317 | 323 | PF00069 | 0.693 |
MOD_CDK_SPxxK_3 | 317 | 324 | PF00069 | 0.689 |
MOD_CK1_1 | 152 | 158 | PF00069 | 0.488 |
MOD_CK1_1 | 312 | 318 | PF00069 | 0.530 |
MOD_CK1_1 | 381 | 387 | PF00069 | 0.711 |
MOD_CK2_1 | 152 | 158 | PF00069 | 0.594 |
MOD_CK2_1 | 17 | 23 | PF00069 | 0.528 |
MOD_CK2_1 | 211 | 217 | PF00069 | 0.603 |
MOD_CK2_1 | 232 | 238 | PF00069 | 0.575 |
MOD_CK2_1 | 271 | 277 | PF00069 | 0.648 |
MOD_Cter_Amidation | 24 | 27 | PF01082 | 0.487 |
MOD_GlcNHglycan | 234 | 237 | PF01048 | 0.527 |
MOD_GlcNHglycan | 262 | 265 | PF01048 | 0.690 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.719 |
MOD_GlcNHglycan | 84 | 87 | PF01048 | 0.527 |
MOD_GSK3_1 | 199 | 206 | PF00069 | 0.573 |
MOD_GSK3_1 | 245 | 252 | PF00069 | 0.549 |
MOD_GSK3_1 | 26 | 33 | PF00069 | 0.440 |
MOD_GSK3_1 | 271 | 278 | PF00069 | 0.539 |
MOD_GSK3_1 | 292 | 299 | PF00069 | 0.567 |
MOD_GSK3_1 | 353 | 360 | PF00069 | 0.747 |
MOD_GSK3_1 | 381 | 388 | PF00069 | 0.708 |
MOD_LATS_1 | 24 | 30 | PF00433 | 0.480 |
MOD_N-GLC_1 | 80 | 85 | PF02516 | 0.418 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.621 |
MOD_NEK2_1 | 232 | 237 | PF00069 | 0.543 |
MOD_NEK2_2 | 211 | 216 | PF00069 | 0.631 |
MOD_NEK2_2 | 296 | 301 | PF00069 | 0.640 |
MOD_NEK2_2 | 65 | 70 | PF00069 | 0.410 |
MOD_PIKK_1 | 102 | 108 | PF00454 | 0.574 |
MOD_PIKK_1 | 149 | 155 | PF00454 | 0.508 |
MOD_PKA_1 | 102 | 108 | PF00069 | 0.574 |
MOD_PKA_1 | 26 | 32 | PF00069 | 0.455 |
MOD_PKA_1 | 324 | 330 | PF00069 | 0.696 |
MOD_PKA_2 | 102 | 108 | PF00069 | 0.574 |
MOD_PKA_2 | 136 | 142 | PF00069 | 0.404 |
MOD_PKA_2 | 2 | 8 | PF00069 | 0.551 |
MOD_PKA_2 | 26 | 32 | PF00069 | 0.567 |
MOD_PKA_2 | 324 | 330 | PF00069 | 0.696 |
MOD_PKB_1 | 100 | 108 | PF00069 | 0.636 |
MOD_Plk_4 | 211 | 217 | PF00069 | 0.608 |
MOD_Plk_4 | 296 | 302 | PF00069 | 0.677 |
MOD_ProDKin_1 | 30 | 36 | PF00069 | 0.430 |
MOD_ProDKin_1 | 309 | 315 | PF00069 | 0.743 |
MOD_ProDKin_1 | 317 | 323 | PF00069 | 0.507 |
MOD_ProDKin_1 | 376 | 382 | PF00069 | 0.551 |
MOD_ProDKin_1 | 385 | 391 | PF00069 | 0.695 |
MOD_SUMO_rev_2 | 220 | 230 | PF00179 | 0.661 |
TRG_ENDOCYTIC_2 | 15 | 18 | PF00928 | 0.483 |
TRG_ER_diArg_1 | 100 | 103 | PF00400 | 0.637 |
TRG_ER_diArg_1 | 26 | 28 | PF00400 | 0.577 |
TRG_ER_diArg_1 | 301 | 303 | PF00400 | 0.684 |
TRG_ER_diArg_1 | 370 | 373 | PF00400 | 0.656 |
TRG_NLS_Bipartite_1 | 100 | 120 | PF00514 | 0.488 |
TRG_NLS_MonoCore_2 | 322 | 327 | PF00514 | 0.678 |
TRG_NLS_MonoExtC_3 | 115 | 121 | PF00514 | 0.462 |
TRG_NLS_MonoExtC_3 | 324 | 330 | PF00514 | 0.598 |
TRG_NLS_MonoExtN_4 | 321 | 327 | PF00514 | 0.627 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P2P6 | Leptomonas seymouri | 78% | 100% |
A0A0S4IKL5 | Bodo saltans | 52% | 91% |
A0A1X0P5A6 | Trypanosomatidae | 61% | 96% |
A0A3Q8IPV2 | Leishmania donovani | 96% | 100% |
A0A3R7NKQ1 | Trypanosoma rangeli | 61% | 97% |
A4HN18 | Leishmania braziliensis | 91% | 100% |
A4IBN9 | Leishmania infantum | 96% | 100% |
C9ZYZ2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 60% | 97% |
E9AFH3 | Leishmania major | 95% | 100% |
V5BY99 | Trypanosoma cruzi | 62% | 96% |