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: 9 |
NetGPI | no | yes: 0, no: 9 |
Related structures:
AlphaFold database: E9AXG2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 350 | 354 | PF00656 | 0.485 |
CLV_NRD_NRD_1 | 123 | 125 | PF00675 | 0.566 |
CLV_NRD_NRD_1 | 178 | 180 | PF00675 | 0.636 |
CLV_NRD_NRD_1 | 210 | 212 | PF00675 | 0.644 |
CLV_NRD_NRD_1 | 222 | 224 | PF00675 | 0.684 |
CLV_NRD_NRD_1 | 258 | 260 | PF00675 | 0.558 |
CLV_NRD_NRD_1 | 339 | 341 | PF00675 | 0.714 |
CLV_NRD_NRD_1 | 359 | 361 | PF00675 | 0.718 |
CLV_NRD_NRD_1 | 52 | 54 | PF00675 | 0.421 |
CLV_NRD_NRD_1 | 9 | 11 | PF00675 | 0.555 |
CLV_PCSK_KEX2_1 | 125 | 127 | PF00082 | 0.516 |
CLV_PCSK_KEX2_1 | 178 | 180 | PF00082 | 0.636 |
CLV_PCSK_KEX2_1 | 183 | 185 | PF00082 | 0.617 |
CLV_PCSK_KEX2_1 | 210 | 212 | PF00082 | 0.605 |
CLV_PCSK_KEX2_1 | 221 | 223 | PF00082 | 0.637 |
CLV_PCSK_KEX2_1 | 339 | 341 | PF00082 | 0.714 |
CLV_PCSK_KEX2_1 | 51 | 53 | PF00082 | 0.571 |
CLV_PCSK_KEX2_1 | 9 | 11 | PF00082 | 0.543 |
CLV_PCSK_PC1ET2_1 | 125 | 127 | PF00082 | 0.494 |
CLV_PCSK_PC1ET2_1 | 183 | 185 | PF00082 | 0.585 |
CLV_PCSK_PC1ET2_1 | 51 | 53 | PF00082 | 0.627 |
CLV_PCSK_PC7_1 | 179 | 185 | PF00082 | 0.637 |
CLV_PCSK_SKI1_1 | 10 | 14 | PF00082 | 0.571 |
CLV_PCSK_SKI1_1 | 102 | 106 | PF00082 | 0.706 |
CLV_PCSK_SKI1_1 | 126 | 130 | PF00082 | 0.524 |
CLV_PCSK_SKI1_1 | 178 | 182 | PF00082 | 0.606 |
CLV_PCSK_SKI1_1 | 222 | 226 | PF00082 | 0.660 |
CLV_PCSK_SKI1_1 | 339 | 343 | PF00082 | 0.585 |
CLV_PCSK_SKI1_1 | 36 | 40 | PF00082 | 0.502 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.591 |
DEG_SCF_FBW7_1 | 372 | 379 | PF00400 | 0.505 |
DOC_ANK_TNKS_1 | 156 | 163 | PF00023 | 0.436 |
DOC_CYCLIN_RxL_1 | 123 | 134 | PF00134 | 0.518 |
DOC_CYCLIN_RxL_1 | 206 | 218 | PF00134 | 0.613 |
DOC_MAPK_gen_1 | 124 | 131 | PF00069 | 0.489 |
DOC_MAPK_gen_1 | 51 | 59 | PF00069 | 0.519 |
DOC_USP7_MATH_1 | 243 | 247 | PF00917 | 0.580 |
DOC_USP7_MATH_1 | 296 | 300 | PF00917 | 0.719 |
DOC_USP7_MATH_1 | 303 | 307 | PF00917 | 0.742 |
DOC_USP7_MATH_1 | 371 | 375 | PF00917 | 0.636 |
DOC_USP7_MATH_1 | 77 | 81 | PF00917 | 0.617 |
DOC_USP7_UBL2_3 | 249 | 253 | PF12436 | 0.581 |
DOC_USP7_UBL2_3 | 357 | 361 | PF12436 | 0.693 |
DOC_WW_Pin1_4 | 132 | 137 | PF00397 | 0.575 |
DOC_WW_Pin1_4 | 267 | 272 | PF00397 | 0.735 |
DOC_WW_Pin1_4 | 309 | 314 | PF00397 | 0.610 |
DOC_WW_Pin1_4 | 372 | 377 | PF00397 | 0.544 |
LIG_14-3-3_CanoR_1 | 132 | 136 | PF00244 | 0.501 |
LIG_14-3-3_CanoR_1 | 178 | 187 | PF00244 | 0.677 |
LIG_14-3-3_CanoR_1 | 222 | 232 | PF00244 | 0.579 |
LIG_14-3-3_CanoR_1 | 259 | 269 | PF00244 | 0.624 |
LIG_BRCT_BRCA1_1 | 262 | 266 | PF00533 | 0.549 |
LIG_BRCT_BRCA1_1 | 337 | 341 | PF00533 | 0.676 |
LIG_FHA_1 | 141 | 147 | PF00498 | 0.438 |
LIG_FHA_1 | 86 | 92 | PF00498 | 0.581 |
LIG_FHA_1 | 96 | 102 | PF00498 | 0.708 |
LIG_FHA_2 | 200 | 206 | PF00498 | 0.523 |
LIG_FHA_2 | 225 | 231 | PF00498 | 0.511 |
LIG_FHA_2 | 313 | 319 | PF00498 | 0.648 |
LIG_GBD_Chelix_1 | 261 | 269 | PF00786 | 0.559 |
LIG_LIR_Gen_1 | 263 | 274 | PF02991 | 0.651 |
LIG_LIR_Nem_3 | 112 | 118 | PF02991 | 0.433 |
LIG_LIR_Nem_3 | 143 | 148 | PF02991 | 0.567 |
LIG_LIR_Nem_3 | 255 | 261 | PF02991 | 0.519 |
LIG_LIR_Nem_3 | 263 | 269 | PF02991 | 0.587 |
LIG_LIR_Nem_3 | 45 | 49 | PF02991 | 0.633 |
LIG_Pex14_1 | 7 | 11 | PF04695 | 0.654 |
LIG_Pex14_2 | 116 | 120 | PF04695 | 0.413 |
LIG_Pex14_2 | 341 | 345 | PF04695 | 0.473 |
LIG_SH2_CRK | 258 | 262 | PF00017 | 0.483 |
LIG_SH2_SRC | 195 | 198 | PF00017 | 0.598 |
LIG_SH2_STAT5 | 115 | 118 | PF00017 | 0.411 |
LIG_SH2_STAT5 | 127 | 130 | PF00017 | 0.477 |
LIG_SH2_STAT5 | 139 | 142 | PF00017 | 0.564 |
LIG_SH2_STAT5 | 145 | 148 | PF00017 | 0.494 |
LIG_SH2_STAT5 | 149 | 152 | PF00017 | 0.498 |
LIG_SH2_STAT5 | 195 | 198 | PF00017 | 0.623 |
LIG_SH2_STAT5 | 63 | 66 | PF00017 | 0.555 |
LIG_SH3_1 | 340 | 346 | PF00018 | 0.470 |
LIG_SH3_2 | 74 | 79 | PF14604 | 0.672 |
LIG_SH3_3 | 268 | 274 | PF00018 | 0.610 |
LIG_SH3_3 | 340 | 346 | PF00018 | 0.532 |
LIG_SH3_3 | 71 | 77 | PF00018 | 0.584 |
LIG_SUMO_SIM_par_1 | 127 | 135 | PF11976 | 0.558 |
LIG_SUMO_SIM_par_1 | 86 | 93 | PF11976 | 0.524 |
LIG_SxIP_EBH_1 | 39 | 53 | PF03271 | 0.608 |
LIG_TRAF2_1 | 119 | 122 | PF00917 | 0.469 |
LIG_TRAF2_1 | 254 | 257 | PF00917 | 0.540 |
LIG_TRFH_1 | 194 | 198 | PF08558 | 0.462 |
MOD_CDK_SPxK_1 | 372 | 378 | PF00069 | 0.552 |
MOD_CK1_1 | 106 | 112 | PF00069 | 0.471 |
MOD_CK1_1 | 239 | 245 | PF00069 | 0.617 |
MOD_CK1_1 | 276 | 282 | PF00069 | 0.595 |
MOD_CK1_1 | 312 | 318 | PF00069 | 0.517 |
MOD_CK1_1 | 325 | 331 | PF00069 | 0.656 |
MOD_CK1_1 | 97 | 103 | PF00069 | 0.662 |
MOD_CK2_1 | 116 | 122 | PF00069 | 0.466 |
MOD_CK2_1 | 199 | 205 | PF00069 | 0.525 |
MOD_CK2_1 | 251 | 257 | PF00069 | 0.607 |
MOD_CK2_1 | 261 | 267 | PF00069 | 0.677 |
MOD_CK2_1 | 269 | 275 | PF00069 | 0.733 |
MOD_CK2_1 | 325 | 331 | PF00069 | 0.610 |
MOD_CK2_1 | 87 | 93 | PF00069 | 0.604 |
MOD_GlcNHglycan | 152 | 156 | PF01048 | 0.509 |
MOD_GlcNHglycan | 243 | 246 | PF01048 | 0.716 |
MOD_GlcNHglycan | 306 | 309 | PF01048 | 0.810 |
MOD_GlcNHglycan | 353 | 356 | PF01048 | 0.664 |
MOD_GlcNHglycan | 66 | 71 | PF01048 | 0.680 |
MOD_GSK3_1 | 102 | 109 | PF00069 | 0.596 |
MOD_GSK3_1 | 183 | 190 | PF00069 | 0.582 |
MOD_GSK3_1 | 239 | 246 | PF00069 | 0.601 |
MOD_GSK3_1 | 269 | 276 | PF00069 | 0.524 |
MOD_GSK3_1 | 312 | 319 | PF00069 | 0.755 |
MOD_GSK3_1 | 325 | 332 | PF00069 | 0.743 |
MOD_GSK3_1 | 367 | 374 | PF00069 | 0.608 |
MOD_GSK3_1 | 83 | 90 | PF00069 | 0.577 |
MOD_GSK3_1 | 93 | 100 | PF00069 | 0.592 |
MOD_N-GLC_1 | 106 | 111 | PF02516 | 0.521 |
MOD_NEK2_1 | 130 | 135 | PF00069 | 0.555 |
MOD_NEK2_1 | 141 | 146 | PF00069 | 0.462 |
MOD_NEK2_1 | 224 | 229 | PF00069 | 0.522 |
MOD_NEK2_1 | 329 | 334 | PF00069 | 0.698 |
MOD_PKA_1 | 178 | 184 | PF00069 | 0.681 |
MOD_PKA_2 | 131 | 137 | PF00069 | 0.561 |
MOD_PKA_2 | 178 | 184 | PF00069 | 0.681 |
MOD_PKA_2 | 329 | 335 | PF00069 | 0.577 |
MOD_PKB_1 | 221 | 229 | PF00069 | 0.574 |
MOD_Plk_1 | 276 | 282 | PF00069 | 0.737 |
MOD_Plk_1 | 285 | 291 | PF00069 | 0.711 |
MOD_Plk_2-3 | 87 | 93 | PF00069 | 0.558 |
MOD_Plk_4 | 109 | 115 | PF00069 | 0.581 |
MOD_Plk_4 | 141 | 147 | PF00069 | 0.485 |
MOD_Plk_4 | 183 | 189 | PF00069 | 0.617 |
MOD_Plk_4 | 261 | 267 | PF00069 | 0.689 |
MOD_Plk_4 | 42 | 48 | PF00069 | 0.609 |
MOD_ProDKin_1 | 132 | 138 | PF00069 | 0.573 |
MOD_ProDKin_1 | 267 | 273 | PF00069 | 0.733 |
MOD_ProDKin_1 | 309 | 315 | PF00069 | 0.611 |
MOD_ProDKin_1 | 372 | 378 | PF00069 | 0.545 |
MOD_SUMO_rev_2 | 279 | 289 | PF00179 | 0.587 |
TRG_ENDOCYTIC_2 | 113 | 116 | PF00928 | 0.438 |
TRG_ENDOCYTIC_2 | 127 | 130 | PF00928 | 0.465 |
TRG_ENDOCYTIC_2 | 145 | 148 | PF00928 | 0.567 |
TRG_ENDOCYTIC_2 | 258 | 261 | PF00928 | 0.485 |
TRG_ER_diArg_1 | 124 | 127 | PF00400 | 0.587 |
TRG_ER_diArg_1 | 178 | 180 | PF00400 | 0.637 |
TRG_ER_diArg_1 | 209 | 211 | PF00400 | 0.651 |
TRG_ER_diArg_1 | 221 | 223 | PF00400 | 0.686 |
TRG_ER_diArg_1 | 339 | 341 | PF00400 | 0.713 |
TRG_ER_diArg_1 | 9 | 11 | PF00400 | 0.562 |
TRG_NLS_MonoExtC_3 | 50 | 56 | PF00514 | 0.638 |
TRG_NLS_MonoExtN_4 | 48 | 55 | PF00514 | 0.634 |
TRG_Pf-PMV_PEXEL_1 | 178 | 182 | PF00026 | 0.643 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1ILI8 | Leptomonas seymouri | 58% | 93% |
A0A1X0P4C2 | Trypanosomatidae | 29% | 100% |
A0A3S7WYY8 | Leishmania donovani | 86% | 100% |
A0A422MPP3 | Trypanosoma rangeli | 34% | 100% |
A4HE19 | Leishmania braziliensis | 66% | 100% |
A4I1C6 | Leishmania infantum | 86% | 100% |
Q4QA10 | Leishmania major | 78% | 100% |
V5BXG5 | Trypanosoma cruzi | 34% | 100% |