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: A4HI78
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 | 0.605 |
CLV_NRD_NRD_1 | 104 | 106 | PF00675 | 0.778 |
CLV_NRD_NRD_1 | 184 | 186 | PF00675 | 0.790 |
CLV_NRD_NRD_1 | 226 | 228 | PF00675 | 0.538 |
CLV_NRD_NRD_1 | 272 | 274 | PF00675 | 0.692 |
CLV_NRD_NRD_1 | 331 | 333 | PF00675 | 0.523 |
CLV_PCSK_KEX2_1 | 104 | 106 | PF00082 | 0.552 |
CLV_PCSK_KEX2_1 | 184 | 186 | PF00082 | 0.790 |
CLV_PCSK_KEX2_1 | 225 | 227 | PF00082 | 0.536 |
CLV_PCSK_KEX2_1 | 272 | 274 | PF00082 | 0.682 |
CLV_PCSK_KEX2_1 | 276 | 278 | PF00082 | 0.695 |
CLV_PCSK_KEX2_1 | 331 | 333 | PF00082 | 0.523 |
CLV_PCSK_PC1ET2_1 | 276 | 278 | PF00082 | 0.712 |
CLV_PCSK_PC7_1 | 272 | 278 | PF00082 | 0.784 |
CLV_TASPASE1 | 65 | 71 | PF01112 | 0.652 |
DEG_APCC_DBOX_1 | 261 | 269 | PF00400 | 0.575 |
DEG_APCC_DBOX_1 | 81 | 89 | PF00400 | 0.494 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.707 |
DEG_SPOP_SBC_1 | 194 | 198 | PF00917 | 0.556 |
DEG_SPOP_SBC_1 | 43 | 47 | PF00917 | 0.548 |
DOC_ANK_TNKS_1 | 207 | 214 | PF00023 | 0.507 |
DOC_CYCLIN_RxL_1 | 321 | 330 | PF00134 | 0.481 |
DOC_CYCLIN_yClb5_NLxxxL_5 | 50 | 57 | PF00134 | 0.484 |
DOC_CYCLIN_yCln2_LP_2 | 53 | 59 | PF00134 | 0.678 |
DOC_MAPK_gen_1 | 104 | 111 | PF00069 | 0.557 |
DOC_MAPK_gen_1 | 156 | 166 | PF00069 | 0.339 |
DOC_MAPK_MEF2A_6 | 104 | 111 | PF00069 | 0.557 |
DOC_MAPK_MEF2A_6 | 349 | 358 | PF00069 | 0.452 |
DOC_MAPK_NFAT4_5 | 104 | 112 | PF00069 | 0.558 |
DOC_PP1_RVXF_1 | 322 | 329 | PF00149 | 0.475 |
DOC_USP7_MATH_1 | 10 | 14 | PF00917 | 0.547 |
DOC_USP7_MATH_1 | 137 | 141 | PF00917 | 0.571 |
DOC_USP7_MATH_1 | 148 | 152 | PF00917 | 0.501 |
DOC_USP7_MATH_1 | 192 | 196 | PF00917 | 0.667 |
DOC_USP7_MATH_1 | 199 | 203 | PF00917 | 0.692 |
DOC_USP7_MATH_1 | 304 | 308 | PF00917 | 0.518 |
DOC_USP7_MATH_1 | 39 | 43 | PF00917 | 0.814 |
DOC_WW_Pin1_4 | 183 | 188 | PF00397 | 0.670 |
DOC_WW_Pin1_4 | 44 | 49 | PF00397 | 0.577 |
DOC_WW_Pin1_4 | 52 | 57 | PF00397 | 0.458 |
LIG_14-3-3_CanoR_1 | 146 | 155 | PF00244 | 0.586 |
LIG_14-3-3_CanoR_1 | 170 | 177 | PF00244 | 0.698 |
LIG_14-3-3_CanoR_1 | 227 | 233 | PF00244 | 0.474 |
LIG_BIR_III_2 | 301 | 305 | PF00653 | 0.543 |
LIG_BRCT_BRCA1_1 | 351 | 355 | PF00533 | 0.453 |
LIG_deltaCOP1_diTrp_1 | 71 | 74 | PF00928 | 0.535 |
LIG_FHA_1 | 104 | 110 | PF00498 | 0.521 |
LIG_FHA_1 | 125 | 131 | PF00498 | 0.640 |
LIG_FHA_1 | 233 | 239 | PF00498 | 0.492 |
LIG_FHA_1 | 265 | 271 | PF00498 | 0.591 |
LIG_FHA_1 | 88 | 94 | PF00498 | 0.309 |
LIG_FHA_1 | 9 | 15 | PF00498 | 0.656 |
LIG_FHA_2 | 27 | 33 | PF00498 | 0.498 |
LIG_LIR_Apic_2 | 3 | 8 | PF02991 | 0.504 |
LIG_LIR_Gen_1 | 212 | 222 | PF02991 | 0.485 |
LIG_LIR_Gen_1 | 352 | 363 | PF02991 | 0.504 |
LIG_LIR_Gen_1 | 58 | 66 | PF02991 | 0.602 |
LIG_LIR_Gen_1 | 90 | 99 | PF02991 | 0.384 |
LIG_LIR_Nem_3 | 150 | 155 | PF02991 | 0.579 |
LIG_LIR_Nem_3 | 16 | 21 | PF02991 | 0.387 |
LIG_LIR_Nem_3 | 212 | 217 | PF02991 | 0.422 |
LIG_LIR_Nem_3 | 352 | 358 | PF02991 | 0.494 |
LIG_LIR_Nem_3 | 58 | 62 | PF02991 | 0.505 |
LIG_LIR_Nem_3 | 71 | 77 | PF02991 | 0.445 |
LIG_LIR_Nem_3 | 90 | 95 | PF02991 | 0.458 |
LIG_Rb_LxCxE_1 | 16 | 35 | PF01857 | 0.430 |
LIG_SH2_CRK | 323 | 327 | PF00017 | 0.479 |
LIG_SH2_PTP2 | 214 | 217 | PF00017 | 0.591 |
LIG_SH2_SRC | 59 | 62 | PF00017 | 0.602 |
LIG_SH2_STAT3 | 258 | 261 | PF00017 | 0.334 |
LIG_SH2_STAT3 | 338 | 341 | PF00017 | 0.392 |
LIG_SH2_STAT5 | 21 | 24 | PF00017 | 0.475 |
LIG_SH2_STAT5 | 214 | 217 | PF00017 | 0.453 |
LIG_SH2_STAT5 | 258 | 261 | PF00017 | 0.397 |
LIG_SH2_STAT5 | 333 | 336 | PF00017 | 0.521 |
LIG_SH2_STAT5 | 59 | 62 | PF00017 | 0.602 |
LIG_SH3_3 | 1 | 7 | PF00018 | 0.528 |
LIG_SH3_3 | 152 | 158 | PF00018 | 0.481 |
LIG_SH3_3 | 73 | 79 | PF00018 | 0.388 |
LIG_SH3_3 | 90 | 96 | PF00018 | 0.307 |
LIG_SUMO_SIM_anti_2 | 343 | 349 | PF11976 | 0.472 |
LIG_SUMO_SIM_anti_2 | 58 | 64 | PF11976 | 0.606 |
LIG_TRAF2_1 | 129 | 132 | PF00917 | 0.706 |
LIG_TRAF2_1 | 311 | 314 | PF00917 | 0.425 |
LIG_TYR_ITIM | 57 | 62 | PF00017 | 0.506 |
MOD_CDC14_SPxK_1 | 47 | 50 | PF00782 | 0.535 |
MOD_CDK_SPxK_1 | 44 | 50 | PF00069 | 0.541 |
MOD_CK1_1 | 124 | 130 | PF00069 | 0.826 |
MOD_CK1_1 | 13 | 19 | PF00069 | 0.381 |
MOD_CK1_1 | 151 | 157 | PF00069 | 0.687 |
MOD_CK1_1 | 172 | 178 | PF00069 | 0.727 |
MOD_CK1_1 | 193 | 199 | PF00069 | 0.784 |
MOD_CK1_1 | 250 | 256 | PF00069 | 0.474 |
MOD_CK1_1 | 42 | 48 | PF00069 | 0.800 |
MOD_CK1_1 | 55 | 61 | PF00069 | 0.430 |
MOD_CK1_1 | 98 | 104 | PF00069 | 0.523 |
MOD_CK2_1 | 126 | 132 | PF00069 | 0.775 |
MOD_CK2_1 | 26 | 32 | PF00069 | 0.717 |
MOD_CK2_1 | 304 | 310 | PF00069 | 0.763 |
MOD_GlcNHglycan | 123 | 126 | PF01048 | 0.763 |
MOD_GlcNHglycan | 171 | 174 | PF01048 | 0.439 |
MOD_GlcNHglycan | 188 | 191 | PF01048 | 0.523 |
MOD_GlcNHglycan | 192 | 195 | PF01048 | 0.790 |
MOD_GlcNHglycan | 338 | 341 | PF01048 | 0.392 |
MOD_GlcNHglycan | 351 | 354 | PF01048 | 0.389 |
MOD_GlcNHglycan | 41 | 44 | PF01048 | 0.811 |
MOD_GlcNHglycan | 97 | 100 | PF01048 | 0.621 |
MOD_GSK3_1 | 147 | 154 | PF00069 | 0.563 |
MOD_GSK3_1 | 186 | 193 | PF00069 | 0.781 |
MOD_GSK3_1 | 194 | 201 | PF00069 | 0.790 |
MOD_GSK3_1 | 228 | 235 | PF00069 | 0.436 |
MOD_GSK3_1 | 304 | 311 | PF00069 | 0.503 |
MOD_GSK3_1 | 39 | 46 | PF00069 | 0.810 |
MOD_GSK3_1 | 6 | 13 | PF00069 | 0.623 |
MOD_NEK2_1 | 177 | 182 | PF00069 | 0.572 |
MOD_NEK2_2 | 26 | 31 | PF00069 | 0.597 |
MOD_PIKK_1 | 13 | 19 | PF00454 | 0.388 |
MOD_PKA_2 | 103 | 109 | PF00069 | 0.682 |
MOD_PKA_2 | 137 | 143 | PF00069 | 0.597 |
MOD_PKA_2 | 169 | 175 | PF00069 | 0.607 |
MOD_PKA_2 | 207 | 213 | PF00069 | 0.582 |
MOD_PKA_2 | 308 | 314 | PF00069 | 0.548 |
MOD_Plk_1 | 70 | 76 | PF00069 | 0.552 |
MOD_Plk_4 | 177 | 183 | PF00069 | 0.768 |
MOD_Plk_4 | 228 | 234 | PF00069 | 0.412 |
MOD_Plk_4 | 55 | 61 | PF00069 | 0.645 |
MOD_Plk_4 | 87 | 93 | PF00069 | 0.359 |
MOD_ProDKin_1 | 183 | 189 | PF00069 | 0.672 |
MOD_ProDKin_1 | 44 | 50 | PF00069 | 0.578 |
MOD_ProDKin_1 | 52 | 58 | PF00069 | 0.445 |
MOD_SUMO_rev_2 | 102 | 111 | PF00179 | 0.550 |
MOD_SUMO_rev_2 | 275 | 285 | PF00179 | 0.549 |
TRG_ENDOCYTIC_2 | 214 | 217 | PF00928 | 0.430 |
TRG_ENDOCYTIC_2 | 323 | 326 | PF00928 | 0.479 |
TRG_ENDOCYTIC_2 | 59 | 62 | PF00928 | 0.500 |
TRG_ER_diArg_1 | 224 | 227 | PF00400 | 0.523 |
TRG_ER_diArg_1 | 331 | 333 | PF00400 | 0.525 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8W0 | Leptomonas seymouri | 40% | 100% |
A0A3S7X392 | Leishmania donovani | 69% | 100% |
A4I5F7 | Leishmania infantum | 68% | 100% |
E9B0Q5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 70% | 100% |
Q4Q7H8 | Leishmania major | 69% | 100% |