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: E9AM49
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 125 | 129 | PF00656 | 0.577 |
CLV_C14_Caspase3-7 | 3 | 7 | PF00656 | 0.613 |
CLV_C14_Caspase3-7 | 66 | 70 | PF00656 | 0.529 |
CLV_NRD_NRD_1 | 158 | 160 | PF00675 | 0.677 |
CLV_NRD_NRD_1 | 186 | 188 | PF00675 | 0.704 |
CLV_NRD_NRD_1 | 285 | 287 | PF00675 | 0.635 |
CLV_NRD_NRD_1 | 330 | 332 | PF00675 | 0.476 |
CLV_NRD_NRD_1 | 77 | 79 | PF00675 | 0.466 |
CLV_PCSK_KEX2_1 | 157 | 159 | PF00082 | 0.609 |
CLV_PCSK_KEX2_1 | 186 | 188 | PF00082 | 0.704 |
CLV_PCSK_KEX2_1 | 77 | 79 | PF00082 | 0.466 |
CLV_PCSK_PC1ET2_1 | 157 | 159 | PF00082 | 0.593 |
CLV_PCSK_SKI1_1 | 19 | 23 | PF00082 | 0.578 |
CLV_PCSK_SKI1_1 | 258 | 262 | PF00082 | 0.245 |
CLV_PCSK_SKI1_1 | 281 | 285 | PF00082 | 0.547 |
DOC_MAPK_MEF2A_6 | 226 | 233 | PF00069 | 0.635 |
DOC_USP7_MATH_1 | 175 | 179 | PF00917 | 0.541 |
DOC_USP7_MATH_1 | 298 | 302 | PF00917 | 0.682 |
DOC_USP7_MATH_1 | 304 | 308 | PF00917 | 0.797 |
DOC_USP7_MATH_1 | 342 | 346 | PF00917 | 0.607 |
DOC_USP7_MATH_1 | 354 | 358 | PF00917 | 0.263 |
DOC_USP7_MATH_1 | 67 | 71 | PF00917 | 0.523 |
DOC_USP7_MATH_1 | 95 | 99 | PF00917 | 0.576 |
DOC_USP7_MATH_2 | 192 | 198 | PF00917 | 0.488 |
DOC_USP7_MATH_2 | 87 | 93 | PF00917 | 0.483 |
DOC_USP7_UBL2_3 | 274 | 278 | PF12436 | 0.629 |
DOC_WW_Pin1_4 | 30 | 35 | PF00397 | 0.432 |
LIG_14-3-3_CanoR_1 | 132 | 141 | PF00244 | 0.627 |
LIG_14-3-3_CanoR_1 | 265 | 271 | PF00244 | 0.557 |
LIG_14-3-3_CanoR_1 | 318 | 327 | PF00244 | 0.738 |
LIG_14-3-3_CanoR_1 | 360 | 368 | PF00244 | 0.245 |
LIG_14-3-3_CanoR_1 | 52 | 60 | PF00244 | 0.449 |
LIG_14-3-3_CanoR_1 | 9 | 16 | PF00244 | 0.549 |
LIG_Actin_WH2_2 | 33 | 48 | PF00022 | 0.503 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.673 |
LIG_FHA_1 | 24 | 30 | PF00498 | 0.548 |
LIG_FHA_1 | 319 | 325 | PF00498 | 0.466 |
LIG_FHA_2 | 117 | 123 | PF00498 | 0.469 |
LIG_FHA_2 | 259 | 265 | PF00498 | 0.300 |
LIG_FHA_2 | 271 | 277 | PF00498 | 0.620 |
LIG_LIR_Gen_1 | 118 | 129 | PF02991 | 0.586 |
LIG_LIR_Gen_1 | 164 | 173 | PF02991 | 0.632 |
LIG_LIR_Gen_1 | 36 | 47 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 118 | 124 | PF02991 | 0.686 |
LIG_LIR_Nem_3 | 143 | 148 | PF02991 | 0.616 |
LIG_LIR_Nem_3 | 164 | 169 | PF02991 | 0.537 |
LIG_LIR_Nem_3 | 36 | 42 | PF02991 | 0.466 |
LIG_SH2_NCK_1 | 208 | 212 | PF00017 | 0.598 |
LIG_SH2_STAP1 | 208 | 212 | PF00017 | 0.581 |
LIG_SH2_STAT5 | 198 | 201 | PF00017 | 0.552 |
LIG_SH3_2 | 313 | 318 | PF14604 | 0.681 |
LIG_SH3_3 | 136 | 142 | PF00018 | 0.629 |
LIG_SH3_3 | 185 | 191 | PF00018 | 0.761 |
LIG_SH3_3 | 196 | 202 | PF00018 | 0.579 |
LIG_SH3_3 | 224 | 230 | PF00018 | 0.569 |
LIG_SH3_3 | 310 | 316 | PF00018 | 0.686 |
LIG_SH3_3 | 350 | 356 | PF00018 | 0.310 |
LIG_SUMO_SIM_par_1 | 229 | 235 | PF11976 | 0.702 |
LIG_TRAF2_1 | 192 | 195 | PF00917 | 0.545 |
LIG_TRFH_1 | 198 | 202 | PF08558 | 0.604 |
LIG_WRC_WIRS_1 | 121 | 126 | PF05994 | 0.475 |
MOD_CK1_1 | 117 | 123 | PF00069 | 0.684 |
MOD_CK1_1 | 164 | 170 | PF00069 | 0.657 |
MOD_CK1_1 | 206 | 212 | PF00069 | 0.682 |
MOD_CK1_1 | 320 | 326 | PF00069 | 0.718 |
MOD_CK1_1 | 376 | 382 | PF00069 | 0.456 |
MOD_CK1_1 | 70 | 76 | PF00069 | 0.567 |
MOD_CK2_1 | 258 | 264 | PF00069 | 0.245 |
MOD_Cter_Amidation | 284 | 287 | PF01082 | 0.598 |
MOD_GlcNHglycan | 152 | 155 | PF01048 | 0.532 |
MOD_GlcNHglycan | 188 | 191 | PF01048 | 0.635 |
MOD_GlcNHglycan | 208 | 211 | PF01048 | 0.553 |
MOD_GlcNHglycan | 278 | 281 | PF01048 | 0.580 |
MOD_GlcNHglycan | 296 | 299 | PF01048 | 0.592 |
MOD_GlcNHglycan | 300 | 303 | PF01048 | 0.668 |
MOD_GlcNHglycan | 333 | 336 | PF01048 | 0.476 |
MOD_GlcNHglycan | 47 | 50 | PF01048 | 0.419 |
MOD_GlcNHglycan | 95 | 98 | PF01048 | 0.595 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.650 |
MOD_GSK3_1 | 116 | 123 | PF00069 | 0.569 |
MOD_GSK3_1 | 171 | 178 | PF00069 | 0.608 |
MOD_GSK3_1 | 266 | 273 | PF00069 | 0.612 |
MOD_GSK3_1 | 294 | 301 | PF00069 | 0.618 |
MOD_GSK3_1 | 89 | 96 | PF00069 | 0.614 |
MOD_N-GLC_1 | 115 | 120 | PF02516 | 0.548 |
MOD_N-GLC_1 | 181 | 186 | PF02516 | 0.682 |
MOD_N-GLC_1 | 206 | 211 | PF02516 | 0.461 |
MOD_NEK2_1 | 114 | 119 | PF00069 | 0.645 |
MOD_NEK2_1 | 131 | 136 | PF00069 | 0.460 |
MOD_NEK2_1 | 203 | 208 | PF00069 | 0.761 |
MOD_NEK2_1 | 23 | 28 | PF00069 | 0.485 |
MOD_NEK2_1 | 29 | 34 | PF00069 | 0.437 |
MOD_NEK2_1 | 373 | 378 | PF00069 | 0.368 |
MOD_NEK2_1 | 45 | 50 | PF00069 | 0.426 |
MOD_PIKK_1 | 181 | 187 | PF00454 | 0.709 |
MOD_PKA_1 | 186 | 192 | PF00069 | 0.685 |
MOD_PKA_1 | 331 | 337 | PF00069 | 0.459 |
MOD_PKA_2 | 131 | 137 | PF00069 | 0.623 |
MOD_PKA_2 | 186 | 192 | PF00069 | 0.685 |
MOD_PKA_2 | 29 | 35 | PF00069 | 0.471 |
MOD_PKA_2 | 317 | 323 | PF00069 | 0.762 |
MOD_PKA_2 | 45 | 51 | PF00069 | 0.428 |
MOD_Plk_1 | 194 | 200 | PF00069 | 0.484 |
MOD_Plk_4 | 140 | 146 | PF00069 | 0.497 |
MOD_Plk_4 | 194 | 200 | PF00069 | 0.488 |
MOD_Plk_4 | 320 | 326 | PF00069 | 0.451 |
MOD_ProDKin_1 | 30 | 36 | PF00069 | 0.432 |
MOD_SUMO_for_1 | 325 | 328 | PF00179 | 0.511 |
MOD_SUMO_rev_2 | 232 | 239 | PF00179 | 0.560 |
TRG_AP2beta_CARGO_1 | 36 | 46 | PF09066 | 0.435 |
TRG_DiLeu_BaEn_1 | 24 | 29 | PF01217 | 0.455 |
TRG_ENDOCYTIC_2 | 145 | 148 | PF00928 | 0.501 |
TRG_ER_diArg_1 | 186 | 188 | PF00400 | 0.704 |
TRG_NLS_MonoExtN_4 | 77 | 82 | PF00514 | 0.447 |
TRG_Pf-PMV_PEXEL_1 | 19 | 24 | PF00026 | 0.531 |
TRG_Pf-PMV_PEXEL_1 | 27 | 31 | PF00026 | 0.446 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IM20 | Leptomonas seymouri | 39% | 100% |
A0A3S7X263 | Leishmania donovani | 84% | 100% |
A4HH62 | Leishmania braziliensis | 64% | 98% |
A4I482 | Leishmania infantum | 84% | 100% |
E9ADN1 | Leishmania major | 77% | 100% |