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: 18 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 10 |
NetGPI | no | yes: 0, no: 10 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 205 | 209 | PF00656 | 0.687 |
CLV_C14_Caspase3-7 | 273 | 277 | PF00656 | 0.486 |
CLV_C14_Caspase3-7 | 97 | 101 | PF00656 | 0.397 |
CLV_MEL_PAP_1 | 425 | 431 | PF00089 | 0.388 |
CLV_NRD_NRD_1 | 114 | 116 | PF00675 | 0.345 |
CLV_NRD_NRD_1 | 184 | 186 | PF00675 | 0.364 |
CLV_NRD_NRD_1 | 313 | 315 | PF00675 | 0.614 |
CLV_NRD_NRD_1 | 4 | 6 | PF00675 | 0.626 |
CLV_NRD_NRD_1 | 427 | 429 | PF00675 | 0.419 |
CLV_PCSK_KEX2_1 | 114 | 116 | PF00082 | 0.345 |
CLV_PCSK_KEX2_1 | 184 | 186 | PF00082 | 0.364 |
CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.564 |
CLV_PCSK_KEX2_1 | 427 | 429 | PF00082 | 0.419 |
CLV_PCSK_SKI1_1 | 152 | 156 | PF00082 | 0.413 |
CLV_PCSK_SKI1_1 | 188 | 192 | PF00082 | 0.486 |
CLV_PCSK_SKI1_1 | 241 | 245 | PF00082 | 0.467 |
CLV_PCSK_SKI1_1 | 387 | 391 | PF00082 | 0.500 |
CLV_PCSK_SKI1_1 | 5 | 9 | PF00082 | 0.457 |
CLV_Separin_Metazoa | 111 | 115 | PF03568 | 0.330 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.554 |
DEG_SPOP_SBC_1 | 228 | 232 | PF00917 | 0.333 |
DOC_CYCLIN_RxL_1 | 339 | 350 | PF00134 | 0.283 |
DOC_CYCLIN_RxL_1 | 382 | 393 | PF00134 | 0.491 |
DOC_CYCLIN_yCln2_LP_2 | 61 | 67 | PF00134 | 0.290 |
DOC_MAPK_gen_1 | 137 | 146 | PF00069 | 0.266 |
DOC_MAPK_gen_1 | 184 | 191 | PF00069 | 0.523 |
DOC_MAPK_gen_1 | 3 | 9 | PF00069 | 0.604 |
DOC_MAPK_MEF2A_6 | 137 | 146 | PF00069 | 0.289 |
DOC_PP1_RVXF_1 | 186 | 192 | PF00149 | 0.440 |
DOC_PP2B_LxvP_1 | 195 | 198 | PF13499 | 0.532 |
DOC_PP4_FxxP_1 | 131 | 134 | PF00568 | 0.483 |
DOC_PP4_FxxP_1 | 37 | 40 | PF00568 | 0.365 |
DOC_USP7_MATH_1 | 154 | 158 | PF00917 | 0.367 |
DOC_USP7_MATH_1 | 198 | 202 | PF00917 | 0.532 |
DOC_USP7_MATH_1 | 221 | 225 | PF00917 | 0.634 |
DOC_USP7_MATH_1 | 228 | 232 | PF00917 | 0.586 |
DOC_USP7_MATH_1 | 310 | 314 | PF00917 | 0.640 |
DOC_USP7_MATH_1 | 367 | 371 | PF00917 | 0.560 |
DOC_WW_Pin1_4 | 178 | 183 | PF00397 | 0.356 |
DOC_WW_Pin1_4 | 224 | 229 | PF00397 | 0.464 |
DOC_WW_Pin1_4 | 369 | 374 | PF00397 | 0.545 |
LIG_14-3-3_CanoR_1 | 241 | 247 | PF00244 | 0.445 |
LIG_14-3-3_CanoR_1 | 4 | 10 | PF00244 | 0.494 |
LIG_14-3-3_CanoR_1 | 66 | 74 | PF00244 | 0.287 |
LIG_Actin_WH2_2 | 139 | 154 | PF00022 | 0.282 |
LIG_APCC_ABBA_1 | 345 | 350 | PF00400 | 0.507 |
LIG_deltaCOP1_diTrp_1 | 400 | 406 | PF00928 | 0.365 |
LIG_deltaCOP1_diTrp_1 | 84 | 90 | PF00928 | 0.392 |
LIG_FHA_1 | 100 | 106 | PF00498 | 0.500 |
LIG_FHA_1 | 283 | 289 | PF00498 | 0.382 |
LIG_FHA_1 | 29 | 35 | PF00498 | 0.377 |
LIG_FHA_1 | 374 | 380 | PF00498 | 0.669 |
LIG_FHA_2 | 215 | 221 | PF00498 | 0.525 |
LIG_FHA_2 | 230 | 236 | PF00498 | 0.358 |
LIG_FHA_2 | 243 | 249 | PF00498 | 0.380 |
LIG_FHA_2 | 57 | 63 | PF00498 | 0.341 |
LIG_IBAR_NPY_1 | 93 | 95 | PF08397 | 0.424 |
LIG_LIR_Apic_2 | 129 | 134 | PF02991 | 0.502 |
LIG_LIR_Apic_2 | 224 | 228 | PF02991 | 0.598 |
LIG_LIR_Gen_1 | 400 | 411 | PF02991 | 0.375 |
LIG_LIR_Nem_3 | 118 | 124 | PF02991 | 0.474 |
LIG_LIR_Nem_3 | 400 | 406 | PF02991 | 0.416 |
LIG_LIR_Nem_3 | 424 | 429 | PF02991 | 0.398 |
LIG_NRBOX | 238 | 244 | PF00104 | 0.347 |
LIG_NRBOX | 262 | 268 | PF00104 | 0.250 |
LIG_PDZ_Class_3 | 440 | 445 | PF00595 | 0.465 |
LIG_Pex14_1 | 86 | 90 | PF04695 | 0.376 |
LIG_Pex14_2 | 397 | 401 | PF04695 | 0.374 |
LIG_PTB_Apo_2 | 405 | 412 | PF02174 | 0.381 |
LIG_PTB_Phospho_1 | 405 | 411 | PF10480 | 0.385 |
LIG_SH2_PTP2 | 225 | 228 | PF00017 | 0.474 |
LIG_SH2_STAP1 | 256 | 260 | PF00017 | 0.394 |
LIG_SH2_STAP1 | 95 | 99 | PF00017 | 0.263 |
LIG_SH2_STAT3 | 74 | 77 | PF00017 | 0.508 |
LIG_SH2_STAT5 | 108 | 111 | PF00017 | 0.481 |
LIG_SH2_STAT5 | 225 | 228 | PF00017 | 0.474 |
LIG_SH2_STAT5 | 321 | 324 | PF00017 | 0.453 |
LIG_SH2_STAT5 | 33 | 36 | PF00017 | 0.375 |
LIG_SH2_STAT5 | 46 | 49 | PF00017 | 0.338 |
LIG_SH3_3 | 141 | 147 | PF00018 | 0.474 |
LIG_SH3_3 | 37 | 43 | PF00018 | 0.364 |
LIG_SH3_3 | 88 | 94 | PF00018 | 0.421 |
LIG_SUMO_SIM_anti_2 | 257 | 265 | PF11976 | 0.526 |
LIG_SUMO_SIM_par_1 | 79 | 85 | PF11976 | 0.376 |
LIG_TRAF2_1 | 329 | 332 | PF00917 | 0.461 |
LIG_TRAF2_1 | 94 | 97 | PF00917 | 0.400 |
LIG_WRC_WIRS_1 | 128 | 133 | PF05994 | 0.504 |
LIG_WRC_WIRS_1 | 243 | 248 | PF05994 | 0.377 |
LIG_WRC_WIRS_1 | 266 | 271 | PF05994 | 0.510 |
MOD_CDK_SPK_2 | 224 | 229 | PF00069 | 0.387 |
MOD_CDK_SPxK_1 | 178 | 184 | PF00069 | 0.356 |
MOD_CDK_SPxxK_3 | 178 | 185 | PF00069 | 0.345 |
MOD_CK1_1 | 123 | 129 | PF00069 | 0.545 |
MOD_CK1_1 | 201 | 207 | PF00069 | 0.450 |
MOD_CK1_1 | 224 | 230 | PF00069 | 0.558 |
MOD_CK1_1 | 258 | 264 | PF00069 | 0.447 |
MOD_CK1_1 | 265 | 271 | PF00069 | 0.413 |
MOD_CK1_1 | 281 | 287 | PF00069 | 0.369 |
MOD_CK1_1 | 313 | 319 | PF00069 | 0.593 |
MOD_CK1_1 | 369 | 375 | PF00069 | 0.636 |
MOD_CK1_1 | 393 | 399 | PF00069 | 0.461 |
MOD_CK2_1 | 156 | 162 | PF00069 | 0.300 |
MOD_CK2_1 | 214 | 220 | PF00069 | 0.542 |
MOD_CK2_1 | 230 | 236 | PF00069 | 0.409 |
MOD_CK2_1 | 242 | 248 | PF00069 | 0.297 |
MOD_CK2_1 | 415 | 421 | PF00069 | 0.414 |
MOD_CK2_1 | 56 | 62 | PF00069 | 0.331 |
MOD_GlcNHglycan | 125 | 128 | PF01048 | 0.565 |
MOD_GlcNHglycan | 156 | 159 | PF01048 | 0.300 |
MOD_GlcNHglycan | 200 | 203 | PF01048 | 0.448 |
MOD_GlcNHglycan | 257 | 260 | PF01048 | 0.406 |
MOD_GlcNHglycan | 315 | 318 | PF01048 | 0.477 |
MOD_GlcNHglycan | 362 | 365 | PF01048 | 0.531 |
MOD_GlcNHglycan | 369 | 372 | PF01048 | 0.639 |
MOD_GlcNHglycan | 392 | 395 | PF01048 | 0.443 |
MOD_GlcNHglycan | 440 | 443 | PF01048 | 0.380 |
MOD_GSK3_1 | 123 | 130 | PF00069 | 0.541 |
MOD_GSK3_1 | 173 | 180 | PF00069 | 0.454 |
MOD_GSK3_1 | 193 | 200 | PF00069 | 0.521 |
MOD_GSK3_1 | 212 | 219 | PF00069 | 0.537 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.445 |
MOD_GSK3_1 | 24 | 31 | PF00069 | 0.397 |
MOD_GSK3_1 | 258 | 265 | PF00069 | 0.387 |
MOD_GSK3_1 | 278 | 285 | PF00069 | 0.333 |
MOD_GSK3_1 | 309 | 316 | PF00069 | 0.569 |
MOD_GSK3_1 | 369 | 376 | PF00069 | 0.536 |
MOD_GSK3_1 | 434 | 441 | PF00069 | 0.434 |
MOD_LATS_1 | 22 | 28 | PF00433 | 0.409 |
MOD_N-GLC_1 | 281 | 286 | PF02516 | 0.429 |
MOD_N-GLC_1 | 5 | 10 | PF02516 | 0.390 |
MOD_NEK2_1 | 177 | 182 | PF00069 | 0.277 |
MOD_NEK2_1 | 242 | 247 | PF00069 | 0.306 |
MOD_NEK2_1 | 262 | 267 | PF00069 | 0.460 |
MOD_NEK2_1 | 323 | 328 | PF00069 | 0.435 |
MOD_NEK2_1 | 366 | 371 | PF00069 | 0.505 |
MOD_NEK2_1 | 390 | 395 | PF00069 | 0.398 |
MOD_NEK2_2 | 156 | 161 | PF00069 | 0.274 |
MOD_PKA_2 | 171 | 177 | PF00069 | 0.278 |
MOD_PKA_2 | 198 | 204 | PF00069 | 0.657 |
MOD_PKA_2 | 313 | 319 | PF00069 | 0.579 |
MOD_PKA_2 | 65 | 71 | PF00069 | 0.392 |
MOD_PKB_1 | 3 | 11 | PF00069 | 0.392 |
MOD_Plk_1 | 5 | 11 | PF00069 | 0.382 |
MOD_Plk_4 | 221 | 227 | PF00069 | 0.473 |
MOD_Plk_4 | 258 | 264 | PF00069 | 0.255 |
MOD_Plk_4 | 28 | 34 | PF00069 | 0.423 |
MOD_Plk_4 | 421 | 427 | PF00069 | 0.411 |
MOD_ProDKin_1 | 178 | 184 | PF00069 | 0.356 |
MOD_ProDKin_1 | 224 | 230 | PF00069 | 0.463 |
MOD_ProDKin_1 | 369 | 375 | PF00069 | 0.545 |
MOD_SUMO_for_1 | 136 | 139 | PF00179 | 0.416 |
MOD_SUMO_rev_2 | 230 | 240 | PF00179 | 0.376 |
TRG_DiLeu_BaLyEn_6 | 238 | 243 | PF01217 | 0.463 |
TRG_ENDOCYTIC_2 | 121 | 124 | PF00928 | 0.433 |
TRG_ENDOCYTIC_2 | 95 | 98 | PF00928 | 0.552 |
TRG_ER_diArg_1 | 113 | 115 | PF00400 | 0.449 |
TRG_ER_diArg_1 | 184 | 186 | PF00400 | 0.364 |
TRG_ER_diArg_1 | 2 | 5 | PF00400 | 0.638 |
TRG_ER_diArg_1 | 426 | 428 | PF00400 | 0.420 |
TRG_Pf-PMV_PEXEL_1 | 107 | 111 | PF00026 | 0.456 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IGW5 | Leptomonas seymouri | 69% | 100% |
A0A1X0NU50 | Trypanosomatidae | 53% | 99% |
A0A3R7M6E1 | Trypanosoma rangeli | 51% | 100% |
A0A3S7WXB0 | Leishmania donovani | 84% | 100% |
A4I006 | Leishmania infantum | 84% | 100% |
C9ZSQ8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 52% | 99% |
E9AVX9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |
Q4QBK0 | Leishmania major | 84% | 100% |
V5B8Q9 | Trypanosoma cruzi | 50% | 98% |