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: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: E9AZJ3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 311 | 315 | PF00656 | 0.620 |
CLV_C14_Caspase3-7 | 325 | 329 | PF00656 | 0.467 |
CLV_NRD_NRD_1 | 30 | 32 | PF00675 | 0.594 |
CLV_PCSK_KEX2_1 | 30 | 32 | PF00082 | 0.554 |
CLV_PCSK_KEX2_1 | 79 | 81 | PF00082 | 0.593 |
CLV_PCSK_PC1ET2_1 | 79 | 81 | PF00082 | 0.556 |
CLV_PCSK_PC7_1 | 26 | 32 | PF00082 | 0.567 |
CLV_PCSK_PC7_1 | 75 | 81 | PF00082 | 0.527 |
CLV_PCSK_SKI1_1 | 102 | 106 | PF00082 | 0.470 |
CLV_PCSK_SKI1_1 | 175 | 179 | PF00082 | 0.468 |
CLV_PCSK_SKI1_1 | 228 | 232 | PF00082 | 0.512 |
CLV_PCSK_SKI1_1 | 335 | 339 | PF00082 | 0.503 |
DEG_MDM2_SWIB_1 | 292 | 299 | PF02201 | 0.529 |
DOC_CYCLIN_yCln2_LP_2 | 128 | 134 | PF00134 | 0.460 |
DOC_MAPK_MEF2A_6 | 228 | 235 | PF00069 | 0.523 |
DOC_PP1_RVXF_1 | 165 | 171 | PF00149 | 0.522 |
DOC_PP2B_LxvP_1 | 128 | 131 | PF13499 | 0.428 |
DOC_PP2B_LxvP_1 | 242 | 245 | PF13499 | 0.478 |
DOC_USP7_MATH_1 | 24 | 28 | PF00917 | 0.532 |
DOC_USP7_MATH_1 | 245 | 249 | PF00917 | 0.587 |
DOC_USP7_MATH_1 | 316 | 320 | PF00917 | 0.606 |
DOC_WW_Pin1_4 | 216 | 221 | PF00397 | 0.426 |
DOC_WW_Pin1_4 | 271 | 276 | PF00397 | 0.498 |
DOC_WW_Pin1_4 | 278 | 283 | PF00397 | 0.519 |
DOC_WW_Pin1_4 | 35 | 40 | PF00397 | 0.560 |
LIG_14-3-3_CanoR_1 | 102 | 107 | PF00244 | 0.506 |
LIG_14-3-3_CanoR_1 | 114 | 121 | PF00244 | 0.431 |
LIG_Actin_WH2_2 | 11 | 28 | PF00022 | 0.528 |
LIG_APCC_ABBAyCdc20_2 | 335 | 341 | PF00400 | 0.421 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.751 |
LIG_BIR_III_4 | 160 | 164 | PF00653 | 0.340 |
LIG_FHA_1 | 125 | 131 | PF00498 | 0.490 |
LIG_FHA_1 | 194 | 200 | PF00498 | 0.538 |
LIG_FHA_1 | 249 | 255 | PF00498 | 0.506 |
LIG_FHA_1 | 266 | 272 | PF00498 | 0.197 |
LIG_FHA_1 | 278 | 284 | PF00498 | 0.441 |
LIG_FHA_1 | 286 | 292 | PF00498 | 0.241 |
LIG_FHA_1 | 329 | 335 | PF00498 | 0.540 |
LIG_FHA_1 | 36 | 42 | PF00498 | 0.489 |
LIG_FHA_2 | 106 | 112 | PF00498 | 0.482 |
LIG_LIR_Apic_2 | 35 | 40 | PF02991 | 0.515 |
LIG_LIR_Gen_1 | 148 | 159 | PF02991 | 0.530 |
LIG_LIR_Gen_1 | 293 | 304 | PF02991 | 0.546 |
LIG_LIR_Nem_3 | 148 | 154 | PF02991 | 0.533 |
LIG_LIR_Nem_3 | 293 | 299 | PF02991 | 0.524 |
LIG_PDZ_Class_1 | 337 | 342 | PF00595 | 0.566 |
LIG_Pex14_2 | 292 | 296 | PF04695 | 0.479 |
LIG_SH2_CRK | 125 | 129 | PF00017 | 0.363 |
LIG_SH2_SRC | 151 | 154 | PF00017 | 0.537 |
LIG_SH2_STAP1 | 151 | 155 | PF00017 | 0.427 |
LIG_SH2_STAP1 | 195 | 199 | PF00017 | 0.498 |
LIG_SH2_STAT3 | 195 | 198 | PF00017 | 0.503 |
LIG_SH2_STAT5 | 195 | 198 | PF00017 | 0.476 |
LIG_SH3_3 | 127 | 133 | PF00018 | 0.365 |
LIG_SH3_3 | 230 | 236 | PF00018 | 0.555 |
LIG_SH3_3 | 272 | 278 | PF00018 | 0.461 |
LIG_SH3_3 | 280 | 286 | PF00018 | 0.454 |
LIG_SH3_3 | 58 | 64 | PF00018 | 0.439 |
LIG_SUMO_SIM_par_1 | 102 | 108 | PF11976 | 0.392 |
LIG_TRAF2_1 | 315 | 318 | PF00917 | 0.522 |
LIG_TRAF2_1 | 32 | 35 | PF00917 | 0.319 |
LIG_TYR_ITSM | 147 | 154 | PF00017 | 0.490 |
LIG_WRC_WIRS_1 | 147 | 152 | PF05994 | 0.487 |
MOD_CDK_SPK_2 | 216 | 221 | PF00069 | 0.426 |
MOD_CK1_1 | 146 | 152 | PF00069 | 0.524 |
MOD_CK1_1 | 176 | 182 | PF00069 | 0.356 |
MOD_CK1_1 | 248 | 254 | PF00069 | 0.556 |
MOD_CK1_1 | 265 | 271 | PF00069 | 0.188 |
MOD_CK1_1 | 285 | 291 | PF00069 | 0.516 |
MOD_CK1_1 | 73 | 79 | PF00069 | 0.514 |
MOD_CK2_1 | 54 | 60 | PF00069 | 0.546 |
MOD_CMANNOS | 170 | 173 | PF00535 | 0.397 |
MOD_CMANNOS | 91 | 94 | PF00535 | 0.518 |
MOD_GlcNHglycan | 175 | 178 | PF01048 | 0.508 |
MOD_GlcNHglycan | 236 | 239 | PF01048 | 0.559 |
MOD_GlcNHglycan | 26 | 29 | PF01048 | 0.395 |
MOD_GlcNHglycan | 298 | 302 | PF01048 | 0.586 |
MOD_GlcNHglycan | 56 | 59 | PF01048 | 0.552 |
MOD_GlcNHglycan | 8 | 11 | PF01048 | 0.649 |
MOD_GlcNHglycan | 82 | 85 | PF01048 | 0.628 |
MOD_GSK3_1 | 222 | 229 | PF00069 | 0.433 |
MOD_GSK3_1 | 261 | 268 | PF00069 | 0.404 |
MOD_GSK3_1 | 278 | 285 | PF00069 | 0.513 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.707 |
MOD_NEK2_1 | 200 | 205 | PF00069 | 0.575 |
MOD_NEK2_1 | 210 | 215 | PF00069 | 0.325 |
MOD_NEK2_1 | 291 | 296 | PF00069 | 0.582 |
MOD_NEK2_1 | 53 | 58 | PF00069 | 0.543 |
MOD_NEK2_1 | 8 | 13 | PF00069 | 0.564 |
MOD_NEK2_2 | 70 | 75 | PF00069 | 0.453 |
MOD_PIKK_1 | 194 | 200 | PF00454 | 0.506 |
MOD_Plk_1 | 316 | 322 | PF00069 | 0.572 |
MOD_Plk_4 | 1 | 7 | PF00069 | 0.738 |
MOD_Plk_4 | 102 | 108 | PF00069 | 0.446 |
MOD_Plk_4 | 146 | 152 | PF00069 | 0.463 |
MOD_Plk_4 | 205 | 211 | PF00069 | 0.546 |
MOD_Plk_4 | 63 | 69 | PF00069 | 0.418 |
MOD_ProDKin_1 | 216 | 222 | PF00069 | 0.423 |
MOD_ProDKin_1 | 271 | 277 | PF00069 | 0.495 |
MOD_ProDKin_1 | 278 | 284 | PF00069 | 0.513 |
MOD_ProDKin_1 | 35 | 41 | PF00069 | 0.550 |
MOD_SUMO_rev_2 | 72 | 81 | PF00179 | 0.514 |
TRG_DiLeu_BaLyEn_6 | 250 | 255 | PF01217 | 0.522 |
TRG_ENDOCYTIC_2 | 125 | 128 | PF00928 | 0.367 |
TRG_ENDOCYTIC_2 | 151 | 154 | PF00928 | 0.537 |
TRG_ER_diArg_1 | 167 | 170 | PF00400 | 0.515 |
TRG_ER_diArg_1 | 29 | 31 | PF00400 | 0.545 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PEC4 | Leptomonas seymouri | 60% | 91% |
A0A1X0NW08 | Trypanosomatidae | 36% | 100% |
A0A3S7X175 | Leishmania donovani | 94% | 100% |
A0A422N6W1 | Trypanosoma rangeli | 34% | 100% |
A4HG73 | Leishmania braziliensis | 83% | 100% |
A4I3B6 | Leishmania infantum | 94% | 100% |
D0A7T5 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 34% | 90% |
Q4Q8N8 | Leishmania major | 92% | 100% |
V5BEI5 | Trypanosoma cruzi | 36% | 100% |