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: 7 |
NetGPI | no | yes: 0, no: 7 |
Related structures:
AlphaFold database: E9B1T4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 105 | 109 | PF00656 | 0.420 |
CLV_C14_Caspase3-7 | 184 | 188 | PF00656 | 0.479 |
CLV_C14_Caspase3-7 | 294 | 298 | PF00656 | 0.422 |
CLV_NRD_NRD_1 | 118 | 120 | PF00675 | 0.557 |
CLV_NRD_NRD_1 | 155 | 157 | PF00675 | 0.428 |
CLV_NRD_NRD_1 | 253 | 255 | PF00675 | 0.530 |
CLV_NRD_NRD_1 | 260 | 262 | PF00675 | 0.497 |
CLV_NRD_NRD_1 | 64 | 66 | PF00675 | 0.546 |
CLV_PCSK_FUR_1 | 62 | 66 | PF00082 | 0.447 |
CLV_PCSK_KEX2_1 | 118 | 120 | PF00082 | 0.581 |
CLV_PCSK_KEX2_1 | 155 | 157 | PF00082 | 0.461 |
CLV_PCSK_KEX2_1 | 167 | 169 | PF00082 | 0.449 |
CLV_PCSK_KEX2_1 | 252 | 254 | PF00082 | 0.536 |
CLV_PCSK_KEX2_1 | 283 | 285 | PF00082 | 0.485 |
CLV_PCSK_KEX2_1 | 64 | 66 | PF00082 | 0.546 |
CLV_PCSK_PC1ET2_1 | 167 | 169 | PF00082 | 0.418 |
CLV_PCSK_PC1ET2_1 | 283 | 285 | PF00082 | 0.427 |
CLV_PCSK_PC7_1 | 279 | 285 | PF00082 | 0.429 |
CLV_PCSK_SKI1_1 | 284 | 288 | PF00082 | 0.410 |
CLV_PCSK_SKI1_1 | 65 | 69 | PF00082 | 0.550 |
DEG_APCC_DBOX_1 | 145 | 153 | PF00400 | 0.502 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.519 |
DOC_MAPK_gen_1 | 232 | 240 | PF00069 | 0.455 |
DOC_MAPK_gen_1 | 283 | 289 | PF00069 | 0.437 |
DOC_MAPK_MEF2A_6 | 274 | 282 | PF00069 | 0.528 |
DOC_PP2B_LxvP_1 | 186 | 189 | PF13499 | 0.457 |
DOC_PP4_FxxP_1 | 135 | 138 | PF00568 | 0.516 |
DOC_USP7_MATH_1 | 12 | 16 | PF00917 | 0.589 |
DOC_USP7_MATH_1 | 138 | 142 | PF00917 | 0.431 |
DOC_USP7_MATH_1 | 213 | 217 | PF00917 | 0.733 |
DOC_USP7_MATH_1 | 23 | 27 | PF00917 | 0.432 |
DOC_USP7_UBL2_3 | 111 | 115 | PF12436 | 0.567 |
LIG_14-3-3_CanoR_1 | 100 | 110 | PF00244 | 0.495 |
LIG_14-3-3_CanoR_1 | 155 | 163 | PF00244 | 0.481 |
LIG_14-3-3_CanoR_1 | 328 | 334 | PF00244 | 0.437 |
LIG_14-3-3_CanoR_1 | 33 | 41 | PF00244 | 0.457 |
LIG_Actin_WH2_2 | 110 | 126 | PF00022 | 0.506 |
LIG_FHA_1 | 328 | 334 | PF00498 | 0.419 |
LIG_FHA_1 | 35 | 41 | PF00498 | 0.481 |
LIG_FHA_1 | 43 | 49 | PF00498 | 0.436 |
LIG_LIR_Nem_3 | 332 | 337 | PF02991 | 0.583 |
LIG_Pex14_2 | 131 | 135 | PF04695 | 0.510 |
LIG_SH2_GRB2like | 307 | 310 | PF00017 | 0.366 |
LIG_SH3_3 | 186 | 192 | PF00018 | 0.484 |
LIG_SUMO_SIM_par_1 | 43 | 49 | PF11976 | 0.470 |
LIG_WRC_WIRS_1 | 13 | 18 | PF05994 | 0.644 |
MOD_CK1_1 | 248 | 254 | PF00069 | 0.428 |
MOD_CK1_1 | 76 | 82 | PF00069 | 0.432 |
MOD_CK2_1 | 155 | 161 | PF00069 | 0.531 |
MOD_GlcNHglycan | 215 | 218 | PF01048 | 0.808 |
MOD_GlcNHglycan | 315 | 318 | PF01048 | 0.564 |
MOD_GlcNHglycan | 54 | 57 | PF01048 | 0.545 |
MOD_GlcNHglycan | 58 | 61 | PF01048 | 0.600 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.699 |
MOD_GSK3_1 | 248 | 255 | PF00069 | 0.476 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.705 |
MOD_N-GLC_1 | 194 | 199 | PF02516 | 0.569 |
MOD_NEK2_1 | 163 | 168 | PF00069 | 0.551 |
MOD_NEK2_1 | 34 | 39 | PF00069 | 0.480 |
MOD_NEK2_1 | 73 | 78 | PF00069 | 0.637 |
MOD_NEK2_2 | 12 | 17 | PF00069 | 0.536 |
MOD_OFUCOSY | 326 | 331 | PF10250 | 0.395 |
MOD_PIKK_1 | 155 | 161 | PF00454 | 0.531 |
MOD_PIKK_1 | 263 | 269 | PF00454 | 0.480 |
MOD_PKA_1 | 155 | 161 | PF00069 | 0.353 |
MOD_PKA_1 | 252 | 258 | PF00069 | 0.553 |
MOD_PKA_2 | 101 | 107 | PF00069 | 0.368 |
MOD_PKA_2 | 155 | 161 | PF00069 | 0.483 |
MOD_PKA_2 | 245 | 251 | PF00069 | 0.518 |
MOD_PKA_2 | 252 | 258 | PF00069 | 0.459 |
MOD_PKA_2 | 260 | 266 | PF00069 | 0.446 |
MOD_PKA_2 | 327 | 333 | PF00069 | 0.395 |
MOD_PKA_2 | 34 | 40 | PF00069 | 0.599 |
MOD_Plk_1 | 42 | 48 | PF00069 | 0.414 |
MOD_SUMO_rev_2 | 108 | 117 | PF00179 | 0.504 |
MOD_SUMO_rev_2 | 166 | 175 | PF00179 | 0.516 |
MOD_SUMO_rev_2 | 297 | 306 | PF00179 | 0.522 |
TRG_DiLeu_BaEn_1 | 176 | 181 | PF01217 | 0.352 |
TRG_DiLeu_BaLyEn_6 | 236 | 241 | PF01217 | 0.511 |
TRG_ER_diArg_1 | 117 | 119 | PF00400 | 0.607 |
TRG_ER_diArg_1 | 252 | 254 | PF00400 | 0.659 |
TRG_ER_diArg_1 | 62 | 65 | PF00400 | 0.447 |
TRG_ER_diArg_1 | 99 | 102 | PF00400 | 0.389 |
TRG_NES_CRM1_1 | 276 | 292 | PF08389 | 0.432 |
TRG_Pf-PMV_PEXEL_1 | 168 | 172 | PF00026 | 0.494 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HXL4 | Leptomonas seymouri | 39% | 100% |
A0A3S7X4F2 | Leishmania donovani | 86% | 100% |
A4HJB9 | Leishmania braziliensis | 74% | 100% |
A4I6R2 | Leishmania infantum | 86% | 100% |
C9ZWT4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
Q4Q6C7 | Leishmania major | 83% | 100% |