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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: E9B0Q5
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 3 |
GO:0016407 | acetyltransferase activity | 5 | 2 |
GO:0016740 | transferase activity | 2 | 3 |
GO:0016746 | acyltransferase activity | 3 | 2 |
GO:0016747 | acyltransferase activity, transferring groups other than amino-acyl groups | 4 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 251 | 255 | PF00656 | 0.517 |
CLV_C14_Caspase3-7 | 29 | 33 | PF00656 | 0.518 |
CLV_NRD_NRD_1 | 103 | 105 | PF00675 | 0.547 |
CLV_NRD_NRD_1 | 184 | 186 | PF00675 | 0.655 |
CLV_NRD_NRD_1 | 226 | 228 | PF00675 | 0.428 |
CLV_NRD_NRD_1 | 252 | 254 | PF00675 | 0.485 |
CLV_NRD_NRD_1 | 272 | 274 | PF00675 | 0.531 |
CLV_NRD_NRD_1 | 323 | 325 | PF00675 | 0.346 |
CLV_NRD_NRD_1 | 330 | 332 | PF00675 | 0.405 |
CLV_PCSK_KEX2_1 | 184 | 186 | PF00082 | 0.655 |
CLV_PCSK_KEX2_1 | 225 | 227 | PF00082 | 0.436 |
CLV_PCSK_KEX2_1 | 252 | 254 | PF00082 | 0.485 |
CLV_PCSK_KEX2_1 | 272 | 274 | PF00082 | 0.520 |
CLV_PCSK_KEX2_1 | 276 | 278 | PF00082 | 0.571 |
CLV_PCSK_KEX2_1 | 323 | 325 | PF00082 | 0.399 |
CLV_PCSK_KEX2_1 | 330 | 332 | PF00082 | 0.438 |
CLV_PCSK_PC1ET2_1 | 276 | 278 | PF00082 | 0.589 |
CLV_PCSK_PC7_1 | 272 | 278 | PF00082 | 0.627 |
CLV_PCSK_SKI1_1 | 273 | 277 | PF00082 | 0.605 |
CLV_TASPASE1 | 65 | 71 | PF01112 | 0.507 |
DEG_APCC_DBOX_1 | 261 | 269 | PF00400 | 0.427 |
DEG_APCC_DBOX_1 | 81 | 89 | PF00400 | 0.391 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.611 |
DOC_CYCLIN_RxL_1 | 320 | 329 | PF00134 | 0.376 |
DOC_CYCLIN_yCln2_LP_2 | 53 | 59 | PF00134 | 0.542 |
DOC_MAPK_gen_1 | 79 | 88 | PF00069 | 0.376 |
DOC_PP1_RVXF_1 | 321 | 328 | PF00149 | 0.367 |
DOC_PP2B_LxvP_1 | 53 | 56 | PF13499 | 0.551 |
DOC_USP7_MATH_1 | 10 | 14 | PF00917 | 0.496 |
DOC_USP7_MATH_1 | 137 | 141 | PF00917 | 0.523 |
DOC_USP7_MATH_1 | 39 | 43 | PF00917 | 0.675 |
DOC_USP7_MATH_1 | 78 | 82 | PF00917 | 0.444 |
DOC_WW_Pin1_4 | 172 | 177 | PF00397 | 0.685 |
DOC_WW_Pin1_4 | 183 | 188 | PF00397 | 0.568 |
DOC_WW_Pin1_4 | 198 | 203 | PF00397 | 0.484 |
DOC_WW_Pin1_4 | 43 | 48 | PF00397 | 0.538 |
LIG_14-3-3_CanoR_1 | 104 | 110 | PF00244 | 0.585 |
LIG_14-3-3_CanoR_1 | 170 | 176 | PF00244 | 0.680 |
LIG_14-3-3_CanoR_1 | 227 | 233 | PF00244 | 0.366 |
LIG_14-3-3_CanoR_1 | 264 | 269 | PF00244 | 0.258 |
LIG_14-3-3_CanoR_1 | 272 | 278 | PF00244 | 0.454 |
LIG_14-3-3_CanoR_1 | 282 | 286 | PF00244 | 0.468 |
LIG_deltaCOP1_diTrp_1 | 69 | 74 | PF00928 | 0.459 |
LIG_FHA_1 | 176 | 182 | PF00498 | 0.558 |
LIG_FHA_1 | 233 | 239 | PF00498 | 0.549 |
LIG_FHA_1 | 9 | 15 | PF00498 | 0.557 |
LIG_LIR_Gen_1 | 177 | 187 | PF02991 | 0.542 |
LIG_LIR_Gen_1 | 212 | 222 | PF02991 | 0.373 |
LIG_LIR_Gen_1 | 58 | 66 | PF02991 | 0.466 |
LIG_LIR_Nem_3 | 177 | 182 | PF02991 | 0.537 |
LIG_LIR_Nem_3 | 212 | 217 | PF02991 | 0.400 |
LIG_LIR_Nem_3 | 320 | 325 | PF02991 | 0.354 |
LIG_LIR_Nem_3 | 58 | 62 | PF02991 | 0.406 |
LIG_LIR_Nem_3 | 71 | 77 | PF02991 | 0.443 |
LIG_PDZ_Class_2 | 346 | 351 | PF00595 | 0.346 |
LIG_Rb_LxCxE_1 | 235 | 254 | PF01857 | 0.478 |
LIG_SH2_CRK | 179 | 183 | PF00017 | 0.544 |
LIG_SH2_CRK | 322 | 326 | PF00017 | 0.421 |
LIG_SH2_NCK_1 | 179 | 183 | PF00017 | 0.544 |
LIG_SH2_PTP2 | 214 | 217 | PF00017 | 0.436 |
LIG_SH2_SRC | 59 | 62 | PF00017 | 0.466 |
LIG_SH2_STAT5 | 21 | 24 | PF00017 | 0.439 |
LIG_SH2_STAT5 | 214 | 217 | PF00017 | 0.402 |
LIG_SH2_STAT5 | 258 | 261 | PF00017 | 0.330 |
LIG_SH2_STAT5 | 332 | 335 | PF00017 | 0.531 |
LIG_SH2_STAT5 | 59 | 62 | PF00017 | 0.466 |
LIG_SH3_3 | 216 | 222 | PF00018 | 0.474 |
LIG_SH3_3 | 288 | 294 | PF00018 | 0.487 |
LIG_SH3_3 | 41 | 47 | PF00018 | 0.516 |
LIG_SUMO_SIM_anti_2 | 342 | 348 | PF11976 | 0.344 |
LIG_SUMO_SIM_anti_2 | 58 | 64 | PF11976 | 0.470 |
LIG_TRAF2_1 | 129 | 132 | PF00917 | 0.599 |
LIG_TYR_ITIM | 57 | 62 | PF00017 | 0.408 |
MOD_CDK_SPxxK_3 | 43 | 50 | PF00069 | 0.495 |
MOD_CK1_1 | 121 | 127 | PF00069 | 0.654 |
MOD_CK1_1 | 148 | 154 | PF00069 | 0.564 |
MOD_CK1_1 | 172 | 178 | PF00069 | 0.699 |
MOD_CK1_1 | 180 | 186 | PF00069 | 0.582 |
MOD_CK1_1 | 193 | 199 | PF00069 | 0.626 |
MOD_CK1_1 | 42 | 48 | PF00069 | 0.663 |
MOD_CK2_1 | 126 | 132 | PF00069 | 0.674 |
MOD_CK2_1 | 303 | 309 | PF00069 | 0.745 |
MOD_GlcNHglycan | 122 | 126 | PF01048 | 0.656 |
MOD_GlcNHglycan | 128 | 131 | PF01048 | 0.583 |
MOD_GlcNHglycan | 147 | 150 | PF01048 | 0.558 |
MOD_GlcNHglycan | 153 | 156 | PF01048 | 0.515 |
MOD_GlcNHglycan | 171 | 174 | PF01048 | 0.406 |
MOD_GlcNHglycan | 188 | 191 | PF01048 | 0.500 |
MOD_GlcNHglycan | 192 | 195 | PF01048 | 0.641 |
MOD_GlcNHglycan | 41 | 44 | PF01048 | 0.675 |
MOD_GSK3_1 | 100 | 107 | PF00069 | 0.712 |
MOD_GSK3_1 | 109 | 116 | PF00069 | 0.593 |
MOD_GSK3_1 | 147 | 154 | PF00069 | 0.488 |
MOD_GSK3_1 | 186 | 193 | PF00069 | 0.709 |
MOD_GSK3_1 | 228 | 235 | PF00069 | 0.427 |
MOD_GSK3_1 | 264 | 271 | PF00069 | 0.515 |
MOD_GSK3_1 | 39 | 46 | PF00069 | 0.672 |
MOD_GSK3_1 | 6 | 13 | PF00069 | 0.574 |
MOD_NEK2_1 | 268 | 273 | PF00069 | 0.472 |
MOD_NEK2_2 | 16 | 21 | PF00069 | 0.449 |
MOD_NEK2_2 | 317 | 322 | PF00069 | 0.265 |
MOD_OFUCOSY | 147 | 152 | PF10250 | 0.573 |
MOD_PIKK_1 | 232 | 238 | PF00454 | 0.373 |
MOD_PKA_1 | 104 | 110 | PF00069 | 0.513 |
MOD_PKA_2 | 137 | 143 | PF00069 | 0.512 |
MOD_PKA_2 | 169 | 175 | PF00069 | 0.532 |
MOD_PKA_2 | 271 | 277 | PF00069 | 0.447 |
MOD_PKA_2 | 281 | 287 | PF00069 | 0.481 |
MOD_PKA_2 | 78 | 84 | PF00069 | 0.439 |
MOD_PKB_1 | 262 | 270 | PF00069 | 0.265 |
MOD_Plk_1 | 70 | 76 | PF00069 | 0.449 |
MOD_Plk_4 | 177 | 183 | PF00069 | 0.637 |
MOD_Plk_4 | 228 | 234 | PF00069 | 0.397 |
MOD_Plk_4 | 317 | 323 | PF00069 | 0.270 |
MOD_Plk_4 | 55 | 61 | PF00069 | 0.509 |
MOD_ProDKin_1 | 172 | 178 | PF00069 | 0.692 |
MOD_ProDKin_1 | 183 | 189 | PF00069 | 0.570 |
MOD_ProDKin_1 | 198 | 204 | PF00069 | 0.481 |
MOD_ProDKin_1 | 43 | 49 | PF00069 | 0.535 |
TRG_ENDOCYTIC_2 | 179 | 182 | PF00928 | 0.543 |
TRG_ENDOCYTIC_2 | 214 | 217 | PF00928 | 0.417 |
TRG_ENDOCYTIC_2 | 322 | 325 | PF00928 | 0.418 |
TRG_ENDOCYTIC_2 | 59 | 62 | PF00928 | 0.402 |
TRG_ER_diArg_1 | 224 | 227 | PF00400 | 0.419 |
TRG_ER_diArg_1 | 322 | 324 | PF00400 | 0.373 |
TRG_ER_diArg_1 | 330 | 332 | PF00400 | 0.407 |
TRG_NES_CRM1_1 | 52 | 65 | PF08389 | 0.476 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8W0 | Leptomonas seymouri | 44% | 100% |
A0A3S7X392 | Leishmania donovani | 86% | 100% |
A4HI78 | Leishmania braziliensis | 70% | 100% |
A4I5F7 | Leishmania infantum | 86% | 100% |
Q4Q7H8 | Leishmania major | 86% | 100% |