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: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: Q4Q4Q8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 249 | 253 | PF00656 | 0.537 |
CLV_C14_Caspase3-7 | 264 | 268 | PF00656 | 0.376 |
CLV_C14_Caspase3-7 | 45 | 49 | PF00656 | 0.333 |
CLV_NRD_NRD_1 | 228 | 230 | PF00675 | 0.362 |
CLV_NRD_NRD_1 | 275 | 277 | PF00675 | 0.335 |
CLV_NRD_NRD_1 | 41 | 43 | PF00675 | 0.323 |
CLV_NRD_NRD_1 | 412 | 414 | PF00675 | 0.635 |
CLV_PCSK_KEX2_1 | 192 | 194 | PF00082 | 0.430 |
CLV_PCSK_KEX2_1 | 230 | 232 | PF00082 | 0.367 |
CLV_PCSK_KEX2_1 | 241 | 243 | PF00082 | 0.288 |
CLV_PCSK_KEX2_1 | 41 | 43 | PF00082 | 0.330 |
CLV_PCSK_KEX2_1 | 412 | 414 | PF00082 | 0.581 |
CLV_PCSK_PC1ET2_1 | 192 | 194 | PF00082 | 0.387 |
CLV_PCSK_PC1ET2_1 | 230 | 232 | PF00082 | 0.367 |
CLV_PCSK_PC1ET2_1 | 241 | 243 | PF00082 | 0.288 |
DEG_COP1_1 | 56 | 65 | PF00400 | 0.401 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.480 |
DEG_SCF_FBW7_1 | 19 | 26 | PF00400 | 0.524 |
DEG_SPOP_SBC_1 | 47 | 51 | PF00917 | 0.376 |
DOC_CKS1_1 | 20 | 25 | PF01111 | 0.522 |
DOC_MAPK_gen_1 | 382 | 390 | PF00069 | 0.511 |
DOC_MAPK_MEF2A_6 | 384 | 392 | PF00069 | 0.517 |
DOC_PP2B_LxvP_1 | 388 | 391 | PF13499 | 0.523 |
DOC_PP4_FxxP_1 | 151 | 154 | PF00568 | 0.343 |
DOC_USP7_MATH_1 | 113 | 117 | PF00917 | 0.318 |
DOC_USP7_MATH_1 | 180 | 184 | PF00917 | 0.469 |
DOC_USP7_MATH_1 | 23 | 27 | PF00917 | 0.510 |
DOC_USP7_MATH_1 | 261 | 265 | PF00917 | 0.314 |
DOC_USP7_MATH_1 | 305 | 309 | PF00917 | 0.646 |
DOC_USP7_MATH_1 | 378 | 382 | PF00917 | 0.469 |
DOC_USP7_MATH_2 | 335 | 341 | PF00917 | 0.327 |
DOC_WW_Pin1_4 | 19 | 24 | PF00397 | 0.526 |
DOC_WW_Pin1_4 | 413 | 418 | PF00397 | 0.642 |
LIG_14-3-3_CanoR_1 | 130 | 134 | PF00244 | 0.387 |
LIG_14-3-3_CanoR_1 | 384 | 389 | PF00244 | 0.733 |
LIG_14-3-3_CanoR_1 | 41 | 47 | PF00244 | 0.442 |
LIG_Actin_WH2_2 | 117 | 132 | PF00022 | 0.354 |
LIG_deltaCOP1_diTrp_1 | 95 | 101 | PF00928 | 0.283 |
LIG_FHA_1 | 207 | 213 | PF00498 | 0.573 |
LIG_FHA_1 | 289 | 295 | PF00498 | 0.418 |
LIG_FHA_1 | 323 | 329 | PF00498 | 0.528 |
LIG_FHA_1 | 352 | 358 | PF00498 | 0.308 |
LIG_FHA_1 | 362 | 368 | PF00498 | 0.319 |
LIG_FHA_1 | 371 | 377 | PF00498 | 0.482 |
LIG_FHA_1 | 385 | 391 | PF00498 | 0.472 |
LIG_FHA_1 | 48 | 54 | PF00498 | 0.526 |
LIG_FHA_2 | 11 | 17 | PF00498 | 0.488 |
LIG_FHA_2 | 433 | 439 | PF00498 | 0.713 |
LIG_LIR_Apic_2 | 217 | 221 | PF02991 | 0.306 |
LIG_LIR_LC3C_4 | 211 | 215 | PF02991 | 0.208 |
LIG_LIR_Nem_3 | 254 | 260 | PF02991 | 0.360 |
LIG_LIR_Nem_3 | 95 | 101 | PF02991 | 0.326 |
LIG_MYND_1 | 19 | 23 | PF01753 | 0.466 |
LIG_SH2_CRK | 218 | 222 | PF00017 | 0.335 |
LIG_SH2_NCK_1 | 218 | 222 | PF00017 | 0.335 |
LIG_SH2_NCK_1 | 44 | 48 | PF00017 | 0.359 |
LIG_SH2_SRC | 61 | 64 | PF00017 | 0.288 |
LIG_SH2_STAT5 | 133 | 136 | PF00017 | 0.304 |
LIG_SH2_STAT5 | 257 | 260 | PF00017 | 0.334 |
LIG_SH2_STAT5 | 61 | 64 | PF00017 | 0.417 |
LIG_SH2_STAT5 | 67 | 70 | PF00017 | 0.466 |
LIG_SH3_3 | 25 | 31 | PF00018 | 0.474 |
LIG_SH3_3 | 272 | 278 | PF00018 | 0.450 |
LIG_SH3_3 | 356 | 362 | PF00018 | 0.327 |
LIG_SH3_3 | 403 | 409 | PF00018 | 0.665 |
LIG_SH3_3 | 84 | 90 | PF00018 | 0.348 |
LIG_SUMO_SIM_anti_2 | 209 | 214 | PF11976 | 0.306 |
LIG_SUMO_SIM_anti_2 | 354 | 361 | PF11976 | 0.383 |
LIG_SUMO_SIM_anti_2 | 440 | 446 | PF11976 | 0.465 |
LIG_SUMO_SIM_par_1 | 211 | 217 | PF11976 | 0.270 |
LIG_SUMO_SIM_par_1 | 363 | 369 | PF11976 | 0.329 |
LIG_SUMO_SIM_par_1 | 443 | 448 | PF11976 | 0.344 |
LIG_TRAF2_1 | 422 | 425 | PF00917 | 0.585 |
LIG_TRAF2_2 | 118 | 123 | PF00917 | 0.281 |
LIG_WRC_WIRS_1 | 30 | 35 | PF05994 | 0.478 |
MOD_CK1_1 | 313 | 319 | PF00069 | 0.531 |
MOD_CK1_1 | 321 | 327 | PF00069 | 0.518 |
MOD_CK1_1 | 340 | 346 | PF00069 | 0.531 |
MOD_CK1_1 | 368 | 374 | PF00069 | 0.490 |
MOD_CK1_1 | 70 | 76 | PF00069 | 0.443 |
MOD_CK2_1 | 419 | 425 | PF00069 | 0.572 |
MOD_CK2_1 | 432 | 438 | PF00069 | 0.698 |
MOD_CK2_1 | 46 | 52 | PF00069 | 0.466 |
MOD_GlcNHglycan | 198 | 201 | PF01048 | 0.298 |
MOD_GlcNHglycan | 248 | 251 | PF01048 | 0.369 |
MOD_GlcNHglycan | 25 | 28 | PF01048 | 0.605 |
MOD_GlcNHglycan | 312 | 315 | PF01048 | 0.520 |
MOD_GlcNHglycan | 354 | 357 | PF01048 | 0.403 |
MOD_GlcNHglycan | 427 | 430 | PF01048 | 0.589 |
MOD_GlcNHglycan | 44 | 47 | PF01048 | 0.500 |
MOD_GlcNHglycan | 72 | 75 | PF01048 | 0.463 |
MOD_GSK3_1 | 109 | 116 | PF00069 | 0.298 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.223 |
MOD_GSK3_1 | 19 | 26 | PF00069 | 0.453 |
MOD_GSK3_1 | 261 | 268 | PF00069 | 0.503 |
MOD_GSK3_1 | 318 | 325 | PF00069 | 0.355 |
MOD_GSK3_1 | 347 | 354 | PF00069 | 0.373 |
MOD_GSK3_1 | 361 | 368 | PF00069 | 0.298 |
MOD_GSK3_1 | 4 | 11 | PF00069 | 0.644 |
MOD_GSK3_1 | 419 | 426 | PF00069 | 0.609 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.578 |
MOD_GSK3_1 | 433 | 440 | PF00069 | 0.469 |
MOD_GSK3_1 | 61 | 68 | PF00069 | 0.454 |
MOD_N-GLC_1 | 136 | 141 | PF02516 | 0.474 |
MOD_NEK2_1 | 129 | 134 | PF00069 | 0.347 |
MOD_NEK2_1 | 283 | 288 | PF00069 | 0.371 |
MOD_NEK2_1 | 319 | 324 | PF00069 | 0.440 |
MOD_NEK2_1 | 65 | 70 | PF00069 | 0.409 |
MOD_PIKK_1 | 113 | 119 | PF00454 | 0.331 |
MOD_PIKK_1 | 168 | 174 | PF00454 | 0.453 |
MOD_PIKK_1 | 180 | 186 | PF00454 | 0.363 |
MOD_PIKK_1 | 261 | 267 | PF00454 | 0.416 |
MOD_PKA_1 | 102 | 108 | PF00069 | 0.366 |
MOD_PKA_2 | 129 | 135 | PF00069 | 0.389 |
MOD_Plk_1 | 168 | 174 | PF00069 | 0.383 |
MOD_Plk_1 | 400 | 406 | PF00069 | 0.719 |
MOD_Plk_1 | 423 | 429 | PF00069 | 0.511 |
MOD_Plk_1 | 94 | 100 | PF00069 | 0.351 |
MOD_Plk_4 | 208 | 214 | PF00069 | 0.336 |
MOD_Plk_4 | 29 | 35 | PF00069 | 0.497 |
MOD_Plk_4 | 361 | 367 | PF00069 | 0.341 |
MOD_ProDKin_1 | 19 | 25 | PF00069 | 0.523 |
MOD_ProDKin_1 | 413 | 419 | PF00069 | 0.642 |
TRG_DiLeu_BaLyEn_6 | 16 | 21 | PF01217 | 0.482 |
TRG_ENDOCYTIC_2 | 164 | 167 | PF00928 | 0.322 |
TRG_ER_diArg_1 | 40 | 42 | PF00400 | 0.329 |
TRG_ER_diArg_1 | 412 | 415 | PF00400 | 0.610 |
TRG_NLS_MonoExtC_3 | 228 | 233 | PF00514 | 0.362 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I5I9 | Leptomonas seymouri | 54% | 100% |
A0A1X0NRZ3 | Trypanosomatidae | 33% | 100% |
A0A3Q8IGJ4 | Leishmania donovani | 95% | 100% |
A0A422P320 | Trypanosoma rangeli | 39% | 100% |
A4HL03 | Leishmania braziliensis | 78% | 100% |
A4I8I3 | Leishmania infantum | 95% | 100% |
D0AAN3 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 100% |
E9B3E4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
V5DMD9 | Trypanosoma cruzi | 35% | 100% |