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: 13 |
NetGPI | no | yes: 0, no: 13 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 11 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
GO:0005737 | cytoplasm | 2 | 2 |
Related structures:
AlphaFold database: A0A3S7X774
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 | 209 | 213 | PF00656 | 0.433 |
CLV_C14_Caspase3-7 | 265 | 269 | PF00656 | 0.316 |
CLV_C14_Caspase3-7 | 329 | 333 | PF00656 | 0.446 |
CLV_NRD_NRD_1 | 234 | 236 | PF00675 | 0.462 |
CLV_NRD_NRD_1 | 69 | 71 | PF00675 | 0.491 |
CLV_NRD_NRD_1 | 98 | 100 | PF00675 | 0.473 |
CLV_PCSK_KEX2_1 | 234 | 236 | PF00082 | 0.462 |
CLV_PCSK_KEX2_1 | 97 | 99 | PF00082 | 0.475 |
CLV_PCSK_SKI1_1 | 208 | 212 | PF00082 | 0.596 |
CLV_PCSK_SKI1_1 | 219 | 223 | PF00082 | 0.522 |
DEG_APCC_DBOX_1 | 342 | 350 | PF00400 | 0.304 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.619 |
DEG_SPOP_SBC_1 | 140 | 144 | PF00917 | 0.451 |
DEG_SPOP_SBC_1 | 334 | 338 | PF00917 | 0.375 |
DEG_SPOP_SBC_1 | 49 | 53 | PF00917 | 0.660 |
DOC_CKS1_1 | 145 | 150 | PF01111 | 0.418 |
DOC_CYCLIN_RxL_1 | 364 | 376 | PF00134 | 0.323 |
DOC_MAPK_gen_1 | 104 | 113 | PF00069 | 0.458 |
DOC_MAPK_gen_1 | 341 | 349 | PF00069 | 0.349 |
DOC_MAPK_MEF2A_6 | 104 | 113 | PF00069 | 0.515 |
DOC_MAPK_MEF2A_6 | 196 | 203 | PF00069 | 0.303 |
DOC_MAPK_MEF2A_6 | 368 | 375 | PF00069 | 0.323 |
DOC_PP2B_LxvP_1 | 211 | 214 | PF13499 | 0.433 |
DOC_PP2B_PxIxI_1 | 108 | 114 | PF00149 | 0.325 |
DOC_PP4_FxxP_1 | 19 | 22 | PF00568 | 0.627 |
DOC_PP4_FxxP_1 | 247 | 250 | PF00568 | 0.214 |
DOC_USP7_MATH_1 | 22 | 26 | PF00917 | 0.644 |
DOC_USP7_MATH_1 | 326 | 330 | PF00917 | 0.437 |
DOC_USP7_MATH_1 | 334 | 338 | PF00917 | 0.373 |
DOC_USP7_MATH_1 | 49 | 53 | PF00917 | 0.652 |
DOC_USP7_MATH_1 | 56 | 60 | PF00917 | 0.661 |
DOC_WW_Pin1_4 | 105 | 110 | PF00397 | 0.614 |
DOC_WW_Pin1_4 | 144 | 149 | PF00397 | 0.431 |
DOC_WW_Pin1_4 | 241 | 246 | PF00397 | 0.270 |
LIG_14-3-3_CanoR_1 | 219 | 227 | PF00244 | 0.356 |
LIG_Actin_WH2_2 | 120 | 137 | PF00022 | 0.491 |
LIG_BIR_III_4 | 302 | 306 | PF00653 | 0.214 |
LIG_Clathr_ClatBox_1 | 372 | 376 | PF01394 | 0.314 |
LIG_deltaCOP1_diTrp_1 | 351 | 359 | PF00928 | 0.337 |
LIG_FHA_1 | 118 | 124 | PF00498 | 0.336 |
LIG_FHA_1 | 140 | 146 | PF00498 | 0.517 |
LIG_FHA_1 | 190 | 196 | PF00498 | 0.285 |
LIG_FHA_1 | 215 | 221 | PF00498 | 0.429 |
LIG_FHA_1 | 270 | 276 | PF00498 | 0.289 |
LIG_FHA_2 | 141 | 147 | PF00498 | 0.451 |
LIG_FHA_2 | 207 | 213 | PF00498 | 0.435 |
LIG_FHA_2 | 263 | 269 | PF00498 | 0.316 |
LIG_FHA_2 | 320 | 326 | PF00498 | 0.397 |
LIG_FHA_2 | 384 | 390 | PF00498 | 0.324 |
LIG_FHA_2 | 91 | 97 | PF00498 | 0.612 |
LIG_HP1_1 | 371 | 375 | PF01393 | 0.321 |
LIG_IBAR_NPY_1 | 361 | 363 | PF08397 | 0.340 |
LIG_LIR_Apic_2 | 244 | 250 | PF02991 | 0.232 |
LIG_LIR_Apic_2 | 356 | 362 | PF02991 | 0.399 |
LIG_LIR_Gen_1 | 256 | 266 | PF02991 | 0.299 |
LIG_LIR_Gen_1 | 7 | 16 | PF02991 | 0.592 |
LIG_LIR_LC3C_4 | 120 | 125 | PF02991 | 0.325 |
LIG_LIR_LC3C_4 | 369 | 374 | PF02991 | 0.322 |
LIG_LIR_Nem_3 | 168 | 173 | PF02991 | 0.342 |
LIG_LIR_Nem_3 | 256 | 261 | PF02991 | 0.280 |
LIG_LIR_Nem_3 | 304 | 309 | PF02991 | 0.215 |
LIG_LIR_Nem_3 | 7 | 13 | PF02991 | 0.620 |
LIG_NRBOX | 111 | 117 | PF00104 | 0.360 |
LIG_Pex14_1 | 359 | 363 | PF04695 | 0.328 |
LIG_Pex14_2 | 10 | 14 | PF04695 | 0.595 |
LIG_SH2_GRB2like | 183 | 186 | PF00017 | 0.384 |
LIG_SH2_GRB2like | 363 | 366 | PF00017 | 0.337 |
LIG_SH2_STAP1 | 366 | 370 | PF00017 | 0.340 |
LIG_SH2_STAP1 | 84 | 88 | PF00017 | 0.634 |
LIG_SH2_STAT5 | 160 | 163 | PF00017 | 0.401 |
LIG_SH2_STAT5 | 348 | 351 | PF00017 | 0.392 |
LIG_SH2_STAT5 | 385 | 388 | PF00017 | 0.363 |
LIG_SH3_3 | 142 | 148 | PF00018 | 0.446 |
LIG_SH3_3 | 199 | 205 | PF00018 | 0.398 |
LIG_SUMO_SIM_anti_2 | 120 | 125 | PF11976 | 0.229 |
LIG_SUMO_SIM_par_1 | 369 | 377 | PF11976 | 0.322 |
LIG_TRAF2_1 | 92 | 95 | PF00917 | 0.586 |
LIG_TYR_ITIM | 124 | 129 | PF00017 | 0.462 |
MOD_CK1_1 | 144 | 150 | PF00069 | 0.435 |
MOD_CK1_1 | 47 | 53 | PF00069 | 0.727 |
MOD_CK1_1 | 73 | 79 | PF00069 | 0.636 |
MOD_CK2_1 | 140 | 146 | PF00069 | 0.555 |
MOD_CK2_1 | 319 | 325 | PF00069 | 0.367 |
MOD_CK2_1 | 90 | 96 | PF00069 | 0.601 |
MOD_GlcNHglycan | 288 | 291 | PF01048 | 0.454 |
MOD_GlcNHglycan | 29 | 32 | PF01048 | 0.485 |
MOD_GlcNHglycan | 355 | 358 | PF01048 | 0.504 |
MOD_GlcNHglycan | 376 | 379 | PF01048 | 0.543 |
MOD_GlcNHglycan | 47 | 50 | PF01048 | 0.464 |
MOD_GlcNHglycan | 52 | 55 | PF01048 | 0.472 |
MOD_GlcNHglycan | 72 | 75 | PF01048 | 0.362 |
MOD_GSK3_1 | 140 | 147 | PF00069 | 0.504 |
MOD_GSK3_1 | 181 | 188 | PF00069 | 0.353 |
MOD_GSK3_1 | 215 | 222 | PF00069 | 0.374 |
MOD_GSK3_1 | 383 | 390 | PF00069 | 0.408 |
MOD_GSK3_1 | 40 | 47 | PF00069 | 0.673 |
MOD_GSK3_1 | 5 | 12 | PF00069 | 0.790 |
MOD_N-GLC_1 | 268 | 273 | PF02516 | 0.510 |
MOD_N-GLC_1 | 364 | 369 | PF02516 | 0.546 |
MOD_NEK2_1 | 181 | 186 | PF00069 | 0.363 |
MOD_NEK2_1 | 220 | 225 | PF00069 | 0.304 |
MOD_NEK2_1 | 45 | 50 | PF00069 | 0.650 |
MOD_OFUCOSY | 186 | 191 | PF10250 | 0.531 |
MOD_PIKK_1 | 147 | 153 | PF00454 | 0.403 |
MOD_PKA_1 | 70 | 76 | PF00069 | 0.661 |
MOD_PKA_2 | 45 | 51 | PF00069 | 0.612 |
MOD_PKB_1 | 68 | 76 | PF00069 | 0.645 |
MOD_Plk_1 | 129 | 135 | PF00069 | 0.414 |
MOD_Plk_1 | 140 | 146 | PF00069 | 0.380 |
MOD_Plk_1 | 326 | 332 | PF00069 | 0.452 |
MOD_Plk_1 | 387 | 393 | PF00069 | 0.393 |
MOD_Plk_2-3 | 141 | 147 | PF00069 | 0.407 |
MOD_Plk_4 | 107 | 113 | PF00069 | 0.541 |
MOD_Plk_4 | 190 | 196 | PF00069 | 0.380 |
MOD_Plk_4 | 262 | 268 | PF00069 | 0.319 |
MOD_Plk_4 | 326 | 332 | PF00069 | 0.404 |
MOD_Plk_4 | 40 | 46 | PF00069 | 0.666 |
MOD_Plk_4 | 5 | 11 | PF00069 | 0.623 |
MOD_Plk_4 | 56 | 62 | PF00069 | 0.613 |
MOD_ProDKin_1 | 105 | 111 | PF00069 | 0.483 |
MOD_ProDKin_1 | 144 | 150 | PF00069 | 0.422 |
MOD_ProDKin_1 | 241 | 247 | PF00069 | 0.270 |
TRG_DiLeu_BaLyEn_6 | 271 | 276 | PF01217 | 0.275 |
TRG_ENDOCYTIC_2 | 126 | 129 | PF00928 | 0.386 |
TRG_ENDOCYTIC_2 | 16 | 19 | PF00928 | 0.625 |
TRG_ENDOCYTIC_2 | 236 | 239 | PF00928 | 0.274 |
TRG_ENDOCYTIC_2 | 309 | 312 | PF00928 | 0.248 |
TRG_ER_diArg_1 | 103 | 106 | PF00400 | 0.712 |
TRG_ER_diArg_1 | 133 | 136 | PF00400 | 0.397 |
TRG_ER_diArg_1 | 23 | 26 | PF00400 | 0.719 |
TRG_ER_diArg_1 | 234 | 236 | PF00400 | 0.264 |
TRG_ER_diArg_1 | 340 | 343 | PF00400 | 0.443 |
TRG_ER_diArg_1 | 67 | 70 | PF00400 | 0.649 |
TRG_ER_diArg_1 | 97 | 99 | PF00400 | 0.685 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PB04 | Leptomonas seymouri | 59% | 100% |
A0A1X0NR96 | Trypanosomatidae | 43% | 100% |
A0A3S7WZA9 | Leishmania donovani | 27% | 100% |
A4HLZ4 | Leishmania braziliensis | 38% | 100% |
A4HLZ6 | Leishmania braziliensis | 68% | 100% |
A4I1M7 | Leishmania infantum | 27% | 100% |
A4I9C6 | Leishmania infantum | 100% | 100% |
C9ZJ94 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
E9AXR1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
E9B4C6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 84% | 100% |
Q4Q3Q0 | Leishmania major | 86% | 100% |
Q4Q9R0 | Leishmania major | 28% | 100% |