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: A4HJB9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 188 | 192 | PF00656 | 0.766 |
CLV_C14_Caspase3-7 | 294 | 298 | PF00656 | 0.426 |
CLV_C14_Caspase3-7 | 8 | 12 | PF00656 | 0.382 |
CLV_NRD_NRD_1 | 118 | 120 | PF00675 | 0.532 |
CLV_NRD_NRD_1 | 168 | 170 | PF00675 | 0.379 |
CLV_NRD_NRD_1 | 253 | 255 | PF00675 | 0.517 |
CLV_NRD_NRD_1 | 284 | 286 | PF00675 | 0.331 |
CLV_NRD_NRD_1 | 64 | 66 | PF00675 | 0.532 |
CLV_PCSK_KEX2_1 | 105 | 107 | PF00082 | 0.383 |
CLV_PCSK_KEX2_1 | 118 | 120 | PF00082 | 0.557 |
CLV_PCSK_KEX2_1 | 168 | 170 | PF00082 | 0.436 |
CLV_PCSK_KEX2_1 | 252 | 254 | PF00082 | 0.526 |
CLV_PCSK_KEX2_1 | 283 | 285 | PF00082 | 0.486 |
CLV_PCSK_KEX2_1 | 32 | 34 | PF00082 | 0.469 |
CLV_PCSK_KEX2_1 | 327 | 329 | PF00082 | 0.396 |
CLV_PCSK_KEX2_1 | 64 | 66 | PF00082 | 0.532 |
CLV_PCSK_PC1ET2_1 | 105 | 107 | PF00082 | 0.370 |
CLV_PCSK_PC1ET2_1 | 283 | 285 | PF00082 | 0.428 |
CLV_PCSK_PC1ET2_1 | 32 | 34 | PF00082 | 0.349 |
CLV_PCSK_PC1ET2_1 | 327 | 329 | PF00082 | 0.396 |
CLV_PCSK_PC7_1 | 279 | 285 | PF00082 | 0.430 |
CLV_PCSK_SKI1_1 | 284 | 288 | PF00082 | 0.410 |
CLV_PCSK_SKI1_1 | 65 | 69 | PF00082 | 0.531 |
DEG_APCC_DBOX_1 | 145 | 153 | PF00400 | 0.508 |
DEG_APCC_DBOX_1 | 271 | 279 | PF00400 | 0.376 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.489 |
DOC_CYCLIN_RxL_1 | 279 | 292 | PF00134 | 0.319 |
DOC_MAPK_gen_1 | 102 | 112 | PF00069 | 0.341 |
DOC_MAPK_gen_1 | 272 | 280 | PF00069 | 0.469 |
DOC_MAPK_gen_1 | 283 | 289 | PF00069 | 0.438 |
DOC_MAPK_gen_1 | 32 | 40 | PF00069 | 0.336 |
DOC_MAPK_MEF2A_6 | 105 | 114 | PF00069 | 0.390 |
DOC_MAPK_MEF2A_6 | 274 | 282 | PF00069 | 0.526 |
DOC_PP2B_LxvP_1 | 96 | 99 | PF13499 | 0.358 |
DOC_PP4_FxxP_1 | 135 | 138 | PF00568 | 0.520 |
DOC_USP7_MATH_1 | 12 | 16 | PF00917 | 0.570 |
DOC_USP7_MATH_1 | 138 | 142 | PF00917 | 0.441 |
DOC_USP7_MATH_1 | 213 | 217 | PF00917 | 0.731 |
DOC_USP7_MATH_1 | 23 | 27 | PF00917 | 0.430 |
DOC_USP7_MATH_1 | 260 | 264 | PF00917 | 0.460 |
LIG_14-3-3_CanoR_1 | 328 | 334 | PF00244 | 0.446 |
LIG_14-3-3_CanoR_1 | 33 | 39 | PF00244 | 0.455 |
LIG_Actin_WH2_2 | 109 | 126 | PF00022 | 0.426 |
LIG_Actin_WH2_2 | 89 | 104 | PF00022 | 0.362 |
LIG_APCC_ABBA_1 | 238 | 243 | PF00400 | 0.423 |
LIG_BIR_III_4 | 313 | 317 | PF00653 | 0.414 |
LIG_FHA_1 | 102 | 108 | PF00498 | 0.570 |
LIG_FHA_1 | 264 | 270 | PF00498 | 0.385 |
LIG_FHA_1 | 35 | 41 | PF00498 | 0.477 |
LIG_FHA_1 | 43 | 49 | PF00498 | 0.448 |
LIG_FHA_2 | 156 | 162 | PF00498 | 0.369 |
LIG_FHA_2 | 186 | 192 | PF00498 | 0.596 |
LIG_FHA_2 | 240 | 246 | PF00498 | 0.500 |
LIG_FHA_2 | 271 | 277 | PF00498 | 0.371 |
LIG_FHA_2 | 6 | 12 | PF00498 | 0.484 |
LIG_LIR_Nem_3 | 332 | 337 | PF02991 | 0.586 |
LIG_Pex14_2 | 131 | 135 | PF04695 | 0.509 |
LIG_SUMO_SIM_par_1 | 42 | 49 | PF11976 | 0.488 |
LIG_TRAF2_1 | 230 | 233 | PF00917 | 0.479 |
LIG_WRC_WIRS_1 | 13 | 18 | PF05994 | 0.629 |
MOD_CK1_1 | 263 | 269 | PF00069 | 0.385 |
MOD_CK1_1 | 42 | 48 | PF00069 | 0.502 |
MOD_CK1_1 | 58 | 64 | PF00069 | 0.376 |
MOD_CK2_1 | 155 | 161 | PF00069 | 0.523 |
MOD_CK2_1 | 205 | 211 | PF00069 | 0.774 |
MOD_CK2_1 | 239 | 245 | PF00069 | 0.415 |
MOD_CK2_1 | 270 | 276 | PF00069 | 0.377 |
MOD_GlcNHglycan | 207 | 210 | PF01048 | 0.741 |
MOD_GlcNHglycan | 254 | 257 | PF01048 | 0.388 |
MOD_GlcNHglycan | 262 | 265 | PF01048 | 0.366 |
MOD_GlcNHglycan | 34 | 37 | PF01048 | 0.451 |
MOD_GlcNHglycan | 58 | 61 | PF01048 | 0.593 |
MOD_GSK3_1 | 1 | 8 | PF00069 | 0.495 |
MOD_GSK3_1 | 185 | 192 | PF00069 | 0.601 |
MOD_GSK3_1 | 213 | 220 | PF00069 | 0.701 |
MOD_GSK3_1 | 248 | 255 | PF00069 | 0.463 |
MOD_N-GLC_1 | 194 | 199 | PF02516 | 0.566 |
MOD_NEK2_1 | 101 | 106 | PF00069 | 0.439 |
MOD_NEK2_1 | 34 | 39 | PF00069 | 0.474 |
MOD_NEK2_1 | 5 | 10 | PF00069 | 0.449 |
MOD_NEK2_1 | 76 | 81 | PF00069 | 0.591 |
MOD_NEK2_2 | 12 | 17 | PF00069 | 0.518 |
MOD_OFUCOSY | 326 | 331 | PF10250 | 0.404 |
MOD_PIKK_1 | 155 | 161 | PF00454 | 0.523 |
MOD_PIKK_1 | 263 | 269 | PF00454 | 0.482 |
MOD_PKA_1 | 252 | 258 | PF00069 | 0.545 |
MOD_PKA_1 | 32 | 38 | PF00069 | 0.338 |
MOD_PKA_1 | 327 | 333 | PF00069 | 0.380 |
MOD_PKA_2 | 252 | 258 | PF00069 | 0.451 |
MOD_PKA_2 | 32 | 38 | PF00069 | 0.574 |
MOD_PKA_2 | 327 | 333 | PF00069 | 0.404 |
MOD_Plk_1 | 270 | 276 | PF00069 | 0.408 |
MOD_Plk_1 | 42 | 48 | PF00069 | 0.426 |
MOD_SUMO_for_1 | 51 | 54 | PF00179 | 0.386 |
MOD_SUMO_rev_2 | 108 | 117 | PF00179 | 0.468 |
MOD_SUMO_rev_2 | 171 | 175 | PF00179 | 0.486 |
MOD_SUMO_rev_2 | 26 | 34 | PF00179 | 0.349 |
MOD_SUMO_rev_2 | 297 | 306 | PF00179 | 0.524 |
TRG_DiLeu_BaEn_4 | 270 | 276 | PF01217 | 0.377 |
TRG_ER_diArg_1 | 117 | 119 | PF00400 | 0.580 |
TRG_ER_diArg_1 | 168 | 170 | PF00400 | 0.370 |
TRG_ER_diArg_1 | 252 | 254 | PF00400 | 0.649 |
TRG_ER_diArg_1 | 272 | 275 | PF00400 | 0.413 |
TRG_ER_diArg_1 | 284 | 286 | PF00400 | 0.340 |
TRG_NES_CRM1_1 | 276 | 292 | PF08389 | 0.430 |
TRG_Pf-PMV_PEXEL_1 | 168 | 172 | PF00026 | 0.494 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HXL4 | Leptomonas seymouri | 38% | 100% |
A0A3S7X4F2 | Leishmania donovani | 73% | 100% |
A4I6R2 | Leishmania infantum | 74% | 100% |
C9ZWT4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 29% | 100% |
E9B1T4 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 74% | 100% |
Q4Q6C7 | Leishmania major | 73% | 100% |