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: 9 |
NetGPI | no | yes: 0, no: 9 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 465 | 469 | PF00656 | 0.572 |
CLV_NRD_NRD_1 | 108 | 110 | PF00675 | 0.623 |
CLV_NRD_NRD_1 | 116 | 118 | PF00675 | 0.615 |
CLV_NRD_NRD_1 | 317 | 319 | PF00675 | 0.610 |
CLV_NRD_NRD_1 | 378 | 380 | PF00675 | 0.342 |
CLV_PCSK_FUR_1 | 112 | 116 | PF00082 | 0.454 |
CLV_PCSK_KEX2_1 | 114 | 116 | PF00082 | 0.685 |
CLV_PCSK_KEX2_1 | 377 | 379 | PF00082 | 0.329 |
CLV_PCSK_KEX2_1 | 48 | 50 | PF00082 | 0.440 |
CLV_PCSK_PC1ET2_1 | 48 | 50 | PF00082 | 0.491 |
CLV_PCSK_PC7_1 | 112 | 118 | PF00082 | 0.655 |
CLV_PCSK_SKI1_1 | 121 | 125 | PF00082 | 0.475 |
CLV_PCSK_SKI1_1 | 401 | 405 | PF00082 | 0.327 |
CLV_PCSK_SKI1_1 | 66 | 70 | PF00082 | 0.445 |
DEG_COP1_1 | 134 | 145 | PF00400 | 0.480 |
DEG_SCF_FBW7_1 | 22 | 28 | PF00400 | 0.427 |
DEG_SCF_TRCP1_1 | 157 | 162 | PF00400 | 0.421 |
DEG_SPOP_SBC_1 | 132 | 136 | PF00917 | 0.535 |
DOC_CKS1_1 | 22 | 27 | PF01111 | 0.425 |
DOC_MAPK_gen_1 | 191 | 200 | PF00069 | 0.417 |
DOC_MAPK_gen_1 | 205 | 215 | PF00069 | 0.316 |
DOC_MAPK_gen_1 | 86 | 93 | PF00069 | 0.461 |
DOC_MAPK_MEF2A_6 | 193 | 202 | PF00069 | 0.435 |
DOC_PP1_RVXF_1 | 182 | 189 | PF00149 | 0.356 |
DOC_PP2B_LxvP_1 | 91 | 94 | PF13499 | 0.553 |
DOC_PP4_FxxP_1 | 304 | 307 | PF00568 | 0.473 |
DOC_USP7_MATH_1 | 13 | 17 | PF00917 | 0.667 |
DOC_USP7_MATH_1 | 132 | 136 | PF00917 | 0.535 |
DOC_USP7_MATH_1 | 307 | 311 | PF00917 | 0.482 |
DOC_USP7_MATH_1 | 326 | 330 | PF00917 | 0.344 |
DOC_USP7_MATH_1 | 372 | 376 | PF00917 | 0.365 |
DOC_USP7_UBL2_3 | 124 | 128 | PF12436 | 0.510 |
DOC_USP7_UBL2_3 | 474 | 478 | PF12436 | 0.641 |
DOC_WW_Pin1_4 | 1 | 6 | PF00397 | 0.629 |
DOC_WW_Pin1_4 | 133 | 138 | PF00397 | 0.494 |
DOC_WW_Pin1_4 | 147 | 152 | PF00397 | 0.444 |
DOC_WW_Pin1_4 | 15 | 20 | PF00397 | 0.610 |
DOC_WW_Pin1_4 | 21 | 26 | PF00397 | 0.641 |
DOC_WW_Pin1_4 | 233 | 238 | PF00397 | 0.382 |
DOC_WW_Pin1_4 | 347 | 352 | PF00397 | 0.554 |
DOC_WW_Pin1_4 | 405 | 410 | PF00397 | 0.276 |
DOC_WW_Pin1_4 | 438 | 443 | PF00397 | 0.276 |
LIG_14-3-3_CanoR_1 | 193 | 200 | PF00244 | 0.468 |
LIG_14-3-3_CanoR_1 | 232 | 236 | PF00244 | 0.455 |
LIG_14-3-3_CanoR_1 | 488 | 492 | PF00244 | 0.557 |
LIG_APCC_ABBA_1 | 213 | 218 | PF00400 | 0.408 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.537 |
LIG_BIR_III_4 | 468 | 472 | PF00653 | 0.482 |
LIG_deltaCOP1_diTrp_1 | 294 | 304 | PF00928 | 0.300 |
LIG_deltaCOP1_diTrp_1 | 397 | 404 | PF00928 | 0.393 |
LIG_EH1_1 | 56 | 64 | PF00400 | 0.434 |
LIG_FHA_1 | 193 | 199 | PF00498 | 0.483 |
LIG_FHA_1 | 219 | 225 | PF00498 | 0.427 |
LIG_FHA_1 | 272 | 278 | PF00498 | 0.453 |
LIG_FHA_1 | 388 | 394 | PF00498 | 0.256 |
LIG_FHA_1 | 439 | 445 | PF00498 | 0.324 |
LIG_FHA_1 | 481 | 487 | PF00498 | 0.460 |
LIG_FHA_2 | 136 | 142 | PF00498 | 0.608 |
LIG_FHA_2 | 192 | 198 | PF00498 | 0.337 |
LIG_FHA_2 | 22 | 28 | PF00498 | 0.657 |
LIG_FHA_2 | 279 | 285 | PF00498 | 0.434 |
LIG_HCF-1_HBM_1 | 476 | 479 | PF13415 | 0.497 |
LIG_LIR_Apic_2 | 303 | 307 | PF02991 | 0.412 |
LIG_LIR_Apic_2 | 61 | 67 | PF02991 | 0.316 |
LIG_LIR_Gen_1 | 294 | 302 | PF02991 | 0.340 |
LIG_LIR_Nem_3 | 294 | 298 | PF02991 | 0.338 |
LIG_LIR_Nem_3 | 397 | 403 | PF02991 | 0.393 |
LIG_NBox_RRM_1 | 220 | 230 | PF00076 | 0.377 |
LIG_Pex14_1 | 400 | 404 | PF04695 | 0.393 |
LIG_Pex14_2 | 293 | 297 | PF04695 | 0.297 |
LIG_REV1ctd_RIR_1 | 186 | 195 | PF16727 | 0.351 |
LIG_SH2_NCK_1 | 216 | 220 | PF00017 | 0.435 |
LIG_SH2_SRC | 216 | 219 | PF00017 | 0.544 |
LIG_SH2_STAP1 | 216 | 220 | PF00017 | 0.376 |
LIG_SH2_STAP1 | 243 | 247 | PF00017 | 0.455 |
LIG_SH2_STAT3 | 479 | 482 | PF00017 | 0.489 |
LIG_SH2_STAT5 | 187 | 190 | PF00017 | 0.425 |
LIG_SH2_STAT5 | 449 | 452 | PF00017 | 0.276 |
LIG_SH2_STAT5 | 56 | 59 | PF00017 | 0.321 |
LIG_SH3_3 | 166 | 172 | PF00018 | 0.606 |
LIG_SH3_3 | 2 | 8 | PF00018 | 0.537 |
LIG_SH3_3 | 259 | 265 | PF00018 | 0.539 |
LIG_SH3_3 | 406 | 412 | PF00018 | 0.276 |
LIG_SH3_3 | 445 | 451 | PF00018 | 0.276 |
LIG_SH3_3 | 68 | 74 | PF00018 | 0.355 |
LIG_SH3_3 | 90 | 96 | PF00018 | 0.449 |
LIG_TRAF2_1 | 194 | 197 | PF00917 | 0.356 |
LIG_UBA3_1 | 122 | 128 | PF00899 | 0.478 |
LIG_WRC_WIRS_1 | 373 | 378 | PF05994 | 0.380 |
LIG_WW_3 | 393 | 397 | PF00397 | 0.276 |
MOD_CDC14_SPxK_1 | 236 | 239 | PF00782 | 0.367 |
MOD_CDC14_SPxK_1 | 408 | 411 | PF00782 | 0.276 |
MOD_CDK_SPxK_1 | 233 | 239 | PF00069 | 0.378 |
MOD_CDK_SPxK_1 | 405 | 411 | PF00069 | 0.276 |
MOD_CK1_1 | 135 | 141 | PF00069 | 0.562 |
MOD_CK1_1 | 18 | 24 | PF00069 | 0.599 |
MOD_CK1_1 | 9 | 15 | PF00069 | 0.663 |
MOD_CK2_1 | 135 | 141 | PF00069 | 0.719 |
MOD_CK2_1 | 191 | 197 | PF00069 | 0.358 |
MOD_CK2_1 | 278 | 284 | PF00069 | 0.446 |
MOD_CK2_1 | 360 | 366 | PF00069 | 0.629 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.473 |
MOD_GlcNHglycan | 157 | 160 | PF01048 | 0.434 |
MOD_GlcNHglycan | 161 | 164 | PF01048 | 0.433 |
MOD_GlcNHglycan | 309 | 312 | PF01048 | 0.537 |
MOD_GlcNHglycan | 325 | 329 | PF01048 | 0.580 |
MOD_GlcNHglycan | 335 | 338 | PF01048 | 0.659 |
MOD_GlcNHglycan | 368 | 371 | PF01048 | 0.521 |
MOD_GlcNHglycan | 468 | 472 | PF01048 | 0.472 |
MOD_GSK3_1 | 131 | 138 | PF00069 | 0.621 |
MOD_GSK3_1 | 155 | 162 | PF00069 | 0.488 |
MOD_GSK3_1 | 17 | 24 | PF00069 | 0.560 |
MOD_GSK3_1 | 173 | 180 | PF00069 | 0.383 |
MOD_GSK3_1 | 324 | 331 | PF00069 | 0.618 |
MOD_GSK3_1 | 338 | 345 | PF00069 | 0.489 |
MOD_GSK3_1 | 9 | 16 | PF00069 | 0.608 |
MOD_NEK2_1 | 161 | 166 | PF00069 | 0.472 |
MOD_NEK2_1 | 467 | 472 | PF00069 | 0.488 |
MOD_NEK2_2 | 313 | 318 | PF00069 | 0.569 |
MOD_NEK2_2 | 372 | 377 | PF00069 | 0.310 |
MOD_PIKK_1 | 218 | 224 | PF00454 | 0.417 |
MOD_PIKK_1 | 478 | 484 | PF00454 | 0.492 |
MOD_PKA_2 | 192 | 198 | PF00069 | 0.426 |
MOD_PKA_2 | 231 | 237 | PF00069 | 0.447 |
MOD_Plk_1 | 211 | 217 | PF00069 | 0.420 |
MOD_Plk_4 | 211 | 217 | PF00069 | 0.405 |
MOD_Plk_4 | 250 | 256 | PF00069 | 0.361 |
MOD_Plk_4 | 387 | 393 | PF00069 | 0.260 |
MOD_ProDKin_1 | 1 | 7 | PF00069 | 0.628 |
MOD_ProDKin_1 | 133 | 139 | PF00069 | 0.497 |
MOD_ProDKin_1 | 147 | 153 | PF00069 | 0.440 |
MOD_ProDKin_1 | 15 | 21 | PF00069 | 0.610 |
MOD_ProDKin_1 | 233 | 239 | PF00069 | 0.378 |
MOD_ProDKin_1 | 347 | 353 | PF00069 | 0.554 |
MOD_ProDKin_1 | 405 | 411 | PF00069 | 0.276 |
MOD_ProDKin_1 | 438 | 444 | PF00069 | 0.276 |
TRG_DiLeu_BaLyEn_6 | 87 | 92 | PF01217 | 0.463 |
TRG_ENDOCYTIC_2 | 449 | 452 | PF00928 | 0.272 |
TRG_ENDOCYTIC_2 | 56 | 59 | PF00928 | 0.438 |
TRG_ER_diArg_1 | 114 | 117 | PF00400 | 0.517 |
TRG_ER_diArg_1 | 277 | 280 | PF00400 | 0.485 |
TRG_ER_diArg_1 | 376 | 379 | PF00400 | 0.348 |
TRG_ER_diArg_1 | 50 | 53 | PF00400 | 0.369 |
TRG_ER_diArg_1 | 87 | 90 | PF00400 | 0.490 |
TRG_NLS_MonoExtC_3 | 46 | 51 | PF00514 | 0.469 |
TRG_NLS_MonoExtN_4 | 47 | 52 | PF00514 | 0.459 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PB52 | Leptomonas seymouri | 67% | 100% |
A0A3R7K8Q3 | Trypanosoma rangeli | 49% | 100% |
A0A3S7WX66 | Leishmania donovani | 100% | 100% |
A4HCA4 | Leishmania braziliensis | 78% | 100% |
C9ZRM2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 48% | 100% |
E9AVP1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 90% | 100% |
Q4QBT8 | Leishmania major | 91% | 99% |
V5DMI0 | Trypanosoma cruzi | 47% | 100% |