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: 18 |
NetGPI | no | yes: 0, no: 18 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 16 |
GO:0110165 | cellular anatomical entity | 1 | 17 |
GO:0005737 | cytoplasm | 2 | 2 |
Related structures:
AlphaFold database: E9B4C6
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 2 |
GO:0016874 | ligase activity | 2 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 187 | 191 | PF00656 | 0.459 |
CLV_C14_Caspase3-7 | 243 | 247 | PF00656 | 0.318 |
CLV_NRD_NRD_1 | 212 | 214 | PF00675 | 0.453 |
CLV_NRD_NRD_1 | 4 | 6 | PF00675 | 0.434 |
CLV_NRD_NRD_1 | 47 | 49 | PF00675 | 0.528 |
CLV_PCSK_FUR_1 | 2 | 6 | PF00082 | 0.442 |
CLV_PCSK_KEX2_1 | 212 | 214 | PF00082 | 0.459 |
CLV_PCSK_KEX2_1 | 4 | 6 | PF00082 | 0.434 |
CLV_PCSK_SKI1_1 | 186 | 190 | PF00082 | 0.665 |
CLV_PCSK_SKI1_1 | 197 | 201 | PF00082 | 0.622 |
DEG_APCC_DBOX_1 | 320 | 328 | PF00400 | 0.287 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.721 |
DEG_SPOP_SBC_1 | 118 | 122 | PF00917 | 0.417 |
DEG_SPOP_SBC_1 | 25 | 29 | PF00917 | 0.687 |
DEG_SPOP_SBC_1 | 33 | 37 | PF00917 | 0.710 |
DOC_CKS1_1 | 123 | 128 | PF01111 | 0.387 |
DOC_CYCLIN_RxL_1 | 342 | 354 | PF00134 | 0.341 |
DOC_MAPK_gen_1 | 319 | 327 | PF00069 | 0.350 |
DOC_MAPK_gen_1 | 82 | 91 | PF00069 | 0.658 |
DOC_MAPK_MEF2A_6 | 346 | 353 | PF00069 | 0.304 |
DOC_MAPK_MEF2A_6 | 82 | 91 | PF00069 | 0.658 |
DOC_PP2B_LxvP_1 | 189 | 192 | PF13499 | 0.465 |
DOC_PP2B_PxIxI_1 | 86 | 92 | PF00149 | 0.462 |
DOC_USP7_MATH_1 | 119 | 123 | PF00917 | 0.517 |
DOC_USP7_MATH_1 | 25 | 29 | PF00917 | 0.680 |
DOC_USP7_MATH_1 | 278 | 282 | PF00917 | 0.192 |
DOC_USP7_MATH_1 | 304 | 308 | PF00917 | 0.522 |
DOC_USP7_MATH_1 | 33 | 37 | PF00917 | 0.723 |
DOC_USP7_UBL2_3 | 200 | 204 | PF12436 | 0.196 |
DOC_WW_Pin1_4 | 122 | 127 | PF00397 | 0.507 |
DOC_WW_Pin1_4 | 312 | 317 | PF00397 | 0.348 |
DOC_WW_Pin1_4 | 83 | 88 | PF00397 | 0.637 |
LIG_14-3-3_CanoR_1 | 24 | 33 | PF00244 | 0.560 |
LIG_Actin_WH2_2 | 98 | 115 | PF00022 | 0.454 |
LIG_Clathr_ClatBox_1 | 350 | 354 | PF01394 | 0.297 |
LIG_deltaCOP1_diTrp_1 | 329 | 337 | PF00928 | 0.329 |
LIG_FHA_1 | 118 | 124 | PF00498 | 0.539 |
LIG_FHA_1 | 248 | 254 | PF00498 | 0.301 |
LIG_FHA_1 | 297 | 303 | PF00498 | 0.340 |
LIG_FHA_1 | 96 | 102 | PF00498 | 0.460 |
LIG_FHA_2 | 119 | 125 | PF00498 | 0.528 |
LIG_FHA_2 | 185 | 191 | PF00498 | 0.440 |
LIG_FHA_2 | 241 | 247 | PF00498 | 0.305 |
LIG_FHA_2 | 334 | 340 | PF00498 | 0.346 |
LIG_FHA_2 | 362 | 368 | PF00498 | 0.374 |
LIG_FHA_2 | 69 | 75 | PF00498 | 0.553 |
LIG_HP1_1 | 349 | 353 | PF01393 | 0.303 |
LIG_LIR_Apic_2 | 334 | 340 | PF02991 | 0.426 |
LIG_LIR_Gen_1 | 234 | 244 | PF02991 | 0.272 |
LIG_LIR_Gen_1 | 329 | 340 | PF02991 | 0.364 |
LIG_LIR_LC3C_4 | 347 | 352 | PF02991 | 0.303 |
LIG_LIR_LC3C_4 | 98 | 103 | PF02991 | 0.302 |
LIG_LIR_Nem_3 | 146 | 151 | PF02991 | 0.379 |
LIG_LIR_Nem_3 | 234 | 239 | PF02991 | 0.266 |
LIG_LIR_Nem_3 | 329 | 335 | PF02991 | 0.339 |
LIG_LIR_Nem_3 | 339 | 344 | PF02991 | 0.370 |
LIG_LIR_Nem_3 | 366 | 372 | PF02991 | 0.296 |
LIG_NBox_RRM_1 | 225 | 235 | PF00076 | 0.202 |
LIG_NRBOX | 89 | 95 | PF00104 | 0.495 |
LIG_Pex14_1 | 337 | 341 | PF04695 | 0.374 |
LIG_SH2_GRB2like | 161 | 164 | PF00017 | 0.359 |
LIG_SH2_GRB2like | 341 | 344 | PF00017 | 0.380 |
LIG_SH2_STAP1 | 210 | 214 | PF00017 | 0.237 |
LIG_SH2_STAP1 | 344 | 348 | PF00017 | 0.332 |
LIG_SH2_STAP1 | 62 | 66 | PF00017 | 0.648 |
LIG_SH2_STAT5 | 326 | 329 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 363 | 366 | PF00017 | 0.401 |
LIG_SH3_3 | 120 | 126 | PF00018 | 0.575 |
LIG_SH3_3 | 177 | 183 | PF00018 | 0.392 |
LIG_SH3_3 | 19 | 25 | PF00018 | 0.646 |
LIG_SH3_3 | 332 | 338 | PF00018 | 0.279 |
LIG_SUMO_SIM_par_1 | 291 | 297 | PF11976 | 0.184 |
LIG_SUMO_SIM_par_1 | 347 | 355 | PF11976 | 0.314 |
LIG_TYR_ITIM | 102 | 107 | PF00017 | 0.619 |
MOD_CDK_SPK_2 | 312 | 317 | PF00069 | 0.348 |
MOD_CDK_SPxxK_3 | 312 | 319 | PF00069 | 0.335 |
MOD_CK1_1 | 122 | 128 | PF00069 | 0.474 |
MOD_CK1_1 | 26 | 32 | PF00069 | 0.727 |
MOD_CK1_1 | 51 | 57 | PF00069 | 0.671 |
MOD_CK2_1 | 118 | 124 | PF00069 | 0.501 |
MOD_CK2_1 | 44 | 50 | PF00069 | 0.798 |
MOD_CK2_1 | 68 | 74 | PF00069 | 0.675 |
MOD_GlcNHglycan | 280 | 283 | PF01048 | 0.505 |
MOD_GlcNHglycan | 30 | 33 | PF01048 | 0.576 |
MOD_GlcNHglycan | 354 | 357 | PF01048 | 0.519 |
MOD_GlcNHglycan | 50 | 53 | PF01048 | 0.395 |
MOD_GlcNHglycan | 7 | 10 | PF01048 | 0.588 |
MOD_GSK3_1 | 118 | 125 | PF00069 | 0.495 |
MOD_GSK3_1 | 159 | 166 | PF00069 | 0.346 |
MOD_GSK3_1 | 23 | 30 | PF00069 | 0.677 |
MOD_GSK3_1 | 361 | 368 | PF00069 | 0.408 |
MOD_GSK3_1 | 44 | 51 | PF00069 | 0.658 |
MOD_N-GLC_1 | 246 | 251 | PF02516 | 0.519 |
MOD_N-GLC_1 | 342 | 347 | PF02516 | 0.567 |
MOD_NEK2_1 | 107 | 112 | PF00069 | 0.418 |
MOD_NEK2_1 | 159 | 164 | PF00069 | 0.341 |
MOD_NEK2_1 | 198 | 203 | PF00069 | 0.299 |
MOD_NEK2_1 | 309 | 314 | PF00069 | 0.344 |
MOD_OFUCOSY | 164 | 169 | PF10250 | 0.541 |
MOD_PIKK_1 | 125 | 131 | PF00454 | 0.483 |
MOD_PKA_1 | 48 | 54 | PF00069 | 0.657 |
MOD_PKA_2 | 23 | 29 | PF00069 | 0.596 |
MOD_PKA_2 | 278 | 284 | PF00069 | 0.394 |
MOD_PKB_1 | 46 | 54 | PF00069 | 0.647 |
MOD_Plk_1 | 107 | 113 | PF00069 | 0.380 |
MOD_Plk_1 | 304 | 310 | PF00069 | 0.481 |
MOD_Plk_1 | 365 | 371 | PF00069 | 0.392 |
MOD_Plk_2-3 | 333 | 339 | PF00069 | 0.233 |
MOD_Plk_4 | 18 | 24 | PF00069 | 0.635 |
MOD_Plk_4 | 240 | 246 | PF00069 | 0.284 |
MOD_Plk_4 | 288 | 294 | PF00069 | 0.229 |
MOD_Plk_4 | 304 | 310 | PF00069 | 0.447 |
MOD_Plk_4 | 34 | 40 | PF00069 | 0.597 |
MOD_Plk_4 | 85 | 91 | PF00069 | 0.537 |
MOD_ProDKin_1 | 122 | 128 | PF00069 | 0.498 |
MOD_ProDKin_1 | 312 | 318 | PF00069 | 0.341 |
MOD_ProDKin_1 | 83 | 89 | PF00069 | 0.632 |
TRG_DiLeu_BaLyEn_6 | 249 | 254 | PF01217 | 0.303 |
TRG_ENDOCYTIC_2 | 104 | 107 | PF00928 | 0.497 |
TRG_ENDOCYTIC_2 | 214 | 217 | PF00928 | 0.289 |
TRG_ENDOCYTIC_2 | 287 | 290 | PF00928 | 0.297 |
TRG_ER_diArg_1 | 1 | 4 | PF00400 | 0.778 |
TRG_ER_diArg_1 | 212 | 214 | PF00400 | 0.259 |
TRG_ER_diArg_1 | 318 | 321 | PF00400 | 0.416 |
TRG_ER_diArg_1 | 45 | 48 | PF00400 | 0.738 |
TRG_ER_diArg_1 | 81 | 84 | PF00400 | 0.690 |
TRG_Pf-PMV_PEXEL_1 | 65 | 69 | PF00026 | 0.451 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PB04 | Leptomonas seymouri | 57% | 100% |
A0A0S4ITA7 | Bodo saltans | 36% | 100% |
A0A1X0NR96 | Trypanosomatidae | 44% | 100% |
A0A3S5IRC8 | Trypanosoma rangeli | 42% | 100% |
A0A3S7WZA9 | Leishmania donovani | 29% | 100% |
A0A3S7X774 | Leishmania donovani | 84% | 95% |
A0A422NKH5 | Trypanosoma rangeli | 29% | 100% |
A4HLZ4 | Leishmania braziliensis | 38% | 100% |
A4HLZ6 | Leishmania braziliensis | 70% | 100% |
A4I1M7 | Leishmania infantum | 29% | 100% |
A4I9C4 | Leishmania infantum | 37% | 100% |
A4I9C6 | Leishmania infantum | 84% | 95% |
C9ZJ94 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
E9AXR1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 29% | 100% |
Q4Q3Q0 | Leishmania major | 87% | 100% |
Q4Q9R0 | Leishmania major | 30% | 100% |
V5BF57 | Trypanosoma cruzi | 29% | 100% |