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: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005737 | cytoplasm | 2 | 1 |
GO:0110165 | cellular anatomical entity | 1 | 1 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 171 | 175 | PF00656 | 0.515 |
CLV_NRD_NRD_1 | 264 | 266 | PF00675 | 0.392 |
CLV_NRD_NRD_1 | 3 | 5 | PF00675 | 0.600 |
CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.600 |
CLV_PCSK_KEX2_1 | 389 | 391 | PF00082 | 0.616 |
CLV_PCSK_PC1ET2_1 | 389 | 391 | PF00082 | 0.622 |
CLV_PCSK_SKI1_1 | 179 | 183 | PF00082 | 0.450 |
CLV_PCSK_SKI1_1 | 184 | 188 | PF00082 | 0.490 |
CLV_PCSK_SKI1_1 | 218 | 222 | PF00082 | 0.412 |
CLV_PCSK_SKI1_1 | 257 | 261 | PF00082 | 0.383 |
CLV_PCSK_SKI1_1 | 265 | 269 | PF00082 | 0.370 |
CLV_PCSK_SKI1_1 | 384 | 388 | PF00082 | 0.522 |
DEG_APCC_DBOX_1 | 217 | 225 | PF00400 | 0.441 |
DEG_APCC_KENBOX_2 | 289 | 293 | PF00400 | 0.445 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.614 |
DEG_SCF_FBW7_2 | 92 | 99 | PF00400 | 0.468 |
DOC_CKS1_1 | 196 | 201 | PF01111 | 0.491 |
DOC_CKS1_1 | 93 | 98 | PF01111 | 0.467 |
DOC_CYCLIN_RxL_1 | 254 | 264 | PF00134 | 0.374 |
DOC_CYCLIN_yCln2_LP_2 | 48 | 54 | PF00134 | 0.631 |
DOC_MAPK_gen_1 | 265 | 272 | PF00069 | 0.407 |
DOC_PP1_RVXF_1 | 263 | 270 | PF00149 | 0.390 |
DOC_PP1_RVXF_1 | 312 | 319 | PF00149 | 0.465 |
DOC_PP2B_LxvP_1 | 285 | 288 | PF13499 | 0.456 |
DOC_PP2B_LxvP_1 | 48 | 51 | PF13499 | 0.615 |
DOC_PP4_FxxP_1 | 196 | 199 | PF00568 | 0.502 |
DOC_USP7_MATH_1 | 369 | 373 | PF00917 | 0.707 |
DOC_USP7_MATH_1 | 54 | 58 | PF00917 | 0.504 |
DOC_WW_Pin1_4 | 10 | 15 | PF00397 | 0.524 |
DOC_WW_Pin1_4 | 105 | 110 | PF00397 | 0.461 |
DOC_WW_Pin1_4 | 17 | 22 | PF00397 | 0.459 |
DOC_WW_Pin1_4 | 190 | 195 | PF00397 | 0.401 |
DOC_WW_Pin1_4 | 309 | 314 | PF00397 | 0.434 |
DOC_WW_Pin1_4 | 318 | 323 | PF00397 | 0.455 |
DOC_WW_Pin1_4 | 92 | 97 | PF00397 | 0.466 |
LIG_14-3-3_CanoR_1 | 271 | 275 | PF00244 | 0.405 |
LIG_14-3-3_CanoR_1 | 3 | 12 | PF00244 | 0.542 |
LIG_14-3-3_CanoR_1 | 40 | 45 | PF00244 | 0.514 |
LIG_BRCT_BRCA1_1 | 387 | 391 | PF00533 | 0.707 |
LIG_Clathr_ClatBox_1 | 76 | 80 | PF01394 | 0.539 |
LIG_deltaCOP1_diTrp_1 | 118 | 125 | PF00928 | 0.439 |
LIG_deltaCOP1_diTrp_1 | 177 | 182 | PF00928 | 0.448 |
LIG_deltaCOP1_diTrp_1 | 188 | 196 | PF00928 | 0.355 |
LIG_eIF4E_1 | 254 | 260 | PF01652 | 0.386 |
LIG_FHA_1 | 181 | 187 | PF00498 | 0.530 |
LIG_FHA_2 | 271 | 277 | PF00498 | 0.441 |
LIG_LIR_Apic_2 | 193 | 199 | PF02991 | 0.506 |
LIG_LIR_Gen_1 | 102 | 111 | PF02991 | 0.501 |
LIG_LIR_Gen_1 | 198 | 208 | PF02991 | 0.367 |
LIG_LIR_Gen_1 | 273 | 282 | PF02991 | 0.432 |
LIG_LIR_Nem_3 | 102 | 107 | PF02991 | 0.473 |
LIG_LIR_Nem_3 | 176 | 181 | PF02991 | 0.423 |
LIG_LIR_Nem_3 | 198 | 204 | PF02991 | 0.391 |
LIG_LIR_Nem_3 | 273 | 277 | PF02991 | 0.392 |
LIG_LIR_Nem_3 | 293 | 299 | PF02991 | 0.200 |
LIG_LIR_Nem_3 | 367 | 373 | PF02991 | 0.616 |
LIG_LIR_Nem_3 | 377 | 382 | PF02991 | 0.603 |
LIG_Pex14_1 | 178 | 182 | PF04695 | 0.380 |
LIG_SH2_CRK | 12 | 16 | PF00017 | 0.503 |
LIG_SH2_CRK | 252 | 256 | PF00017 | 0.455 |
LIG_SH2_CRK | 32 | 36 | PF00017 | 0.267 |
LIG_SH2_NCK_1 | 12 | 16 | PF00017 | 0.503 |
LIG_SH2_NCK_1 | 32 | 36 | PF00017 | 0.267 |
LIG_SH2_SRC | 52 | 55 | PF00017 | 0.618 |
LIG_SH2_STAP1 | 241 | 245 | PF00017 | 0.469 |
LIG_SH2_STAP1 | 364 | 368 | PF00017 | 0.621 |
LIG_SH2_STAT5 | 12 | 15 | PF00017 | 0.512 |
LIG_SH2_STAT5 | 192 | 195 | PF00017 | 0.403 |
LIG_SH2_STAT5 | 203 | 206 | PF00017 | 0.386 |
LIG_SH2_STAT5 | 254 | 257 | PF00017 | 0.382 |
LIG_SH2_STAT5 | 258 | 261 | PF00017 | 0.369 |
LIG_SH2_STAT5 | 317 | 320 | PF00017 | 0.452 |
LIG_SH2_STAT5 | 357 | 360 | PF00017 | 0.522 |
LIG_SH3_1 | 90 | 96 | PF00018 | 0.483 |
LIG_SH3_3 | 11 | 17 | PF00018 | 0.501 |
LIG_SH3_3 | 155 | 161 | PF00018 | 0.474 |
LIG_SH3_3 | 48 | 54 | PF00018 | 0.631 |
LIG_SH3_3 | 90 | 96 | PF00018 | 0.483 |
LIG_TRAF2_1 | 374 | 377 | PF00917 | 0.592 |
LIG_TYR_ITIM | 10 | 15 | PF00017 | 0.524 |
LIG_TYR_ITIM | 272 | 277 | PF00017 | 0.415 |
LIG_WW_2 | 158 | 161 | PF00397 | 0.462 |
MOD_CDK_SPK_2 | 309 | 314 | PF00069 | 0.446 |
MOD_CK1_1 | 173 | 179 | PF00069 | 0.366 |
MOD_CK1_1 | 195 | 201 | PF00069 | 0.540 |
MOD_CK1_1 | 328 | 334 | PF00069 | 0.690 |
MOD_CK2_1 | 130 | 136 | PF00069 | 0.496 |
MOD_GlcNHglycan | 132 | 135 | PF01048 | 0.483 |
MOD_GlcNHglycan | 155 | 158 | PF01048 | 0.587 |
MOD_GlcNHglycan | 327 | 330 | PF01048 | 0.651 |
MOD_GlcNHglycan | 393 | 396 | PF01048 | 0.729 |
MOD_GSK3_1 | 195 | 202 | PF00069 | 0.459 |
MOD_GSK3_1 | 325 | 332 | PF00069 | 0.605 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.558 |
MOD_N-GLC_1 | 190 | 195 | PF02516 | 0.406 |
MOD_N-GLC_1 | 291 | 296 | PF02516 | 0.537 |
MOD_N-GLC_1 | 44 | 49 | PF02516 | 0.516 |
MOD_NEK2_1 | 130 | 135 | PF00069 | 0.516 |
MOD_NEK2_1 | 168 | 173 | PF00069 | 0.375 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.610 |
MOD_NEK2_1 | 204 | 209 | PF00069 | 0.397 |
MOD_NEK2_1 | 23 | 28 | PF00069 | 0.518 |
MOD_NEK2_1 | 270 | 275 | PF00069 | 0.417 |
MOD_NEK2_1 | 325 | 330 | PF00069 | 0.568 |
MOD_NEK2_2 | 301 | 306 | PF00069 | 0.387 |
MOD_PIKK_1 | 23 | 29 | PF00454 | 0.449 |
MOD_PK_1 | 40 | 46 | PF00069 | 0.572 |
MOD_PKA_1 | 3 | 9 | PF00069 | 0.575 |
MOD_PKA_2 | 2 | 8 | PF00069 | 0.571 |
MOD_PKA_2 | 270 | 276 | PF00069 | 0.417 |
MOD_PKA_2 | 39 | 45 | PF00069 | 0.589 |
MOD_Plk_1 | 291 | 297 | PF00069 | 0.543 |
MOD_Plk_1 | 44 | 50 | PF00069 | 0.515 |
MOD_Plk_4 | 291 | 297 | PF00069 | 0.543 |
MOD_ProDKin_1 | 10 | 16 | PF00069 | 0.516 |
MOD_ProDKin_1 | 105 | 111 | PF00069 | 0.453 |
MOD_ProDKin_1 | 17 | 23 | PF00069 | 0.455 |
MOD_ProDKin_1 | 190 | 196 | PF00069 | 0.395 |
MOD_ProDKin_1 | 309 | 315 | PF00069 | 0.437 |
MOD_ProDKin_1 | 318 | 324 | PF00069 | 0.461 |
MOD_ProDKin_1 | 92 | 98 | PF00069 | 0.469 |
TRG_DiLeu_BaEn_1 | 235 | 240 | PF01217 | 0.480 |
TRG_DiLeu_BaLyEn_6 | 106 | 111 | PF01217 | 0.475 |
TRG_DiLeu_BaLyEn_6 | 5 | 10 | PF01217 | 0.711 |
TRG_ENDOCYTIC_2 | 12 | 15 | PF00928 | 0.512 |
TRG_ENDOCYTIC_2 | 252 | 255 | PF00928 | 0.366 |
TRG_ENDOCYTIC_2 | 274 | 277 | PF00928 | 0.374 |
TRG_ENDOCYTIC_2 | 62 | 65 | PF00928 | 0.413 |
TRG_ER_diArg_1 | 2 | 4 | PF00400 | 0.612 |
TRG_Pf-PMV_PEXEL_1 | 314 | 319 | PF00026 | 0.473 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I176 | Leptomonas seymouri | 84% | 100% |
A0A0S4KKK6 | Bodo saltans | 50% | 100% |
A0A1X0P238 | Trypanosomatidae | 74% | 100% |
A0A3S7X327 | Leishmania donovani | 95% | 100% |
A0A422NIE7 | Trypanosoma rangeli | 73% | 100% |
A4I593 | Leishmania infantum | 95% | 100% |
C9ZQM4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 71% | 100% |
E9B0J0 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 94% | 100% |
Q4Q7Q8 | Leishmania major | 95% | 100% |
V5D870 | Trypanosoma cruzi | 73% | 100% |