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: A0A3Q8IJF7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 164 | 168 | PF00656 | 0.623 |
CLV_C14_Caspase3-7 | 279 | 283 | PF00656 | 0.399 |
CLV_C14_Caspase3-7 | 90 | 94 | PF00656 | 0.408 |
CLV_MEL_PAP_1 | 274 | 280 | PF00089 | 0.490 |
CLV_NRD_NRD_1 | 218 | 220 | PF00675 | 0.295 |
CLV_NRD_NRD_1 | 236 | 238 | PF00675 | 0.140 |
CLV_NRD_NRD_1 | 276 | 278 | PF00675 | 0.419 |
CLV_PCSK_KEX2_1 | 218 | 220 | PF00082 | 0.305 |
CLV_PCSK_KEX2_1 | 236 | 238 | PF00082 | 0.305 |
CLV_PCSK_KEX2_1 | 276 | 278 | PF00082 | 0.419 |
CLV_PCSK_SKI1_1 | 10 | 14 | PF00082 | 0.414 |
CLV_PCSK_SKI1_1 | 259 | 263 | PF00082 | 0.309 |
DEG_COP1_1 | 309 | 321 | PF00400 | 0.511 |
DOC_USP7_MATH_1 | 238 | 242 | PF00917 | 0.524 |
DOC_USP7_MATH_1 | 326 | 330 | PF00917 | 0.504 |
DOC_USP7_MATH_1 | 91 | 95 | PF00917 | 0.423 |
DOC_USP7_UBL2_3 | 6 | 10 | PF12436 | 0.484 |
DOC_WW_Pin1_4 | 147 | 152 | PF00397 | 0.562 |
DOC_WW_Pin1_4 | 74 | 79 | PF00397 | 0.438 |
LIG_14-3-3_CanoR_1 | 213 | 217 | PF00244 | 0.454 |
LIG_14-3-3_CanoR_1 | 237 | 246 | PF00244 | 0.454 |
LIG_14-3-3_CanoR_1 | 276 | 286 | PF00244 | 0.502 |
LIG_14-3-3_CanoR_1 | 330 | 338 | PF00244 | 0.525 |
LIG_APCC_ABBA_1 | 189 | 194 | PF00400 | 0.377 |
LIG_APCC_ABBAyCdc20_2 | 219 | 225 | PF00400 | 0.454 |
LIG_FHA_1 | 333 | 339 | PF00498 | 0.488 |
LIG_FHA_2 | 164 | 170 | PF00498 | 0.611 |
LIG_FHA_2 | 298 | 304 | PF00498 | 0.469 |
LIG_FHA_2 | 318 | 324 | PF00498 | 0.467 |
LIG_FHA_2 | 88 | 94 | PF00498 | 0.564 |
LIG_Integrin_RGD_1 | 158 | 160 | PF01839 | 0.610 |
LIG_LIR_Gen_1 | 167 | 178 | PF02991 | 0.635 |
LIG_LIR_Gen_1 | 224 | 234 | PF02991 | 0.423 |
LIG_LIR_Gen_1 | 292 | 299 | PF02991 | 0.444 |
LIG_LIR_Nem_3 | 167 | 173 | PF02991 | 0.575 |
LIG_LIR_Nem_3 | 224 | 229 | PF02991 | 0.434 |
LIG_LIR_Nem_3 | 23 | 27 | PF02991 | 0.354 |
LIG_LIR_Nem_3 | 312 | 318 | PF02991 | 0.452 |
LIG_NRBOX | 66 | 72 | PF00104 | 0.440 |
LIG_PCNA_PIPBox_1 | 36 | 45 | PF02747 | 0.440 |
LIG_SH2_CRK | 226 | 230 | PF00017 | 0.432 |
LIG_SH2_STAT5 | 192 | 195 | PF00017 | 0.465 |
LIG_SH3_3 | 126 | 132 | PF00018 | 0.624 |
LIG_SH3_3 | 145 | 151 | PF00018 | 0.451 |
LIG_SH3_3 | 284 | 290 | PF00018 | 0.419 |
LIG_SH3_3 | 310 | 316 | PF00018 | 0.504 |
LIG_SH3_3 | 55 | 61 | PF00018 | 0.454 |
LIG_SH3_3 | 72 | 78 | PF00018 | 0.344 |
LIG_TRAF2_1 | 161 | 164 | PF00917 | 0.703 |
LIG_TRAF2_1 | 308 | 311 | PF00917 | 0.596 |
LIG_TRAF2_1 | 320 | 323 | PF00917 | 0.490 |
MOD_CK1_1 | 127 | 133 | PF00069 | 0.649 |
MOD_CK1_1 | 73 | 79 | PF00069 | 0.490 |
MOD_CK1_1 | 94 | 100 | PF00069 | 0.444 |
MOD_CK2_1 | 163 | 169 | PF00069 | 0.555 |
MOD_CK2_1 | 297 | 303 | PF00069 | 0.527 |
MOD_CK2_1 | 317 | 323 | PF00069 | 0.452 |
MOD_GlcNHglycan | 126 | 129 | PF01048 | 0.576 |
MOD_GlcNHglycan | 194 | 198 | PF01048 | 0.330 |
MOD_GlcNHglycan | 300 | 303 | PF01048 | 0.474 |
MOD_GlcNHglycan | 93 | 96 | PF01048 | 0.287 |
MOD_GSK3_1 | 142 | 149 | PF00069 | 0.608 |
MOD_GSK3_1 | 293 | 300 | PF00069 | 0.453 |
MOD_GSK3_1 | 332 | 339 | PF00069 | 0.558 |
MOD_GSK3_1 | 66 | 73 | PF00069 | 0.463 |
MOD_GSK3_1 | 87 | 94 | PF00069 | 0.520 |
MOD_NEK2_1 | 137 | 142 | PF00069 | 0.657 |
MOD_NEK2_1 | 212 | 217 | PF00069 | 0.454 |
MOD_NEK2_1 | 297 | 302 | PF00069 | 0.396 |
MOD_NEK2_1 | 5 | 10 | PF00069 | 0.428 |
MOD_NEK2_1 | 70 | 75 | PF00069 | 0.524 |
MOD_PIKK_1 | 27 | 33 | PF00454 | 0.423 |
MOD_PKA_1 | 276 | 282 | PF00069 | 0.426 |
MOD_PKA_2 | 212 | 218 | PF00069 | 0.454 |
MOD_PKA_2 | 276 | 282 | PF00069 | 0.509 |
MOD_Plk_2-3 | 163 | 169 | PF00069 | 0.759 |
MOD_Plk_4 | 212 | 218 | PF00069 | 0.513 |
MOD_Plk_4 | 66 | 72 | PF00069 | 0.451 |
MOD_Plk_4 | 94 | 100 | PF00069 | 0.452 |
MOD_ProDKin_1 | 147 | 153 | PF00069 | 0.563 |
MOD_ProDKin_1 | 74 | 80 | PF00069 | 0.438 |
TRG_DiLeu_BaLyEn_6 | 59 | 64 | PF01217 | 0.431 |
TRG_ENDOCYTIC_2 | 226 | 229 | PF00928 | 0.433 |
TRG_ER_diArg_1 | 217 | 219 | PF00400 | 0.507 |
TRG_ER_diArg_1 | 235 | 237 | PF00400 | 0.484 |
TRG_ER_diArg_1 | 275 | 277 | PF00400 | 0.411 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P8N5 | Leptomonas seymouri | 55% | 100% |
A0A0S4JM68 | Bodo saltans | 30% | 100% |
A0A422P3H1 | Trypanosoma rangeli | 36% | 100% |
A4HID1 | Leishmania braziliensis | 78% | 100% |
A4I5M4 | Leishmania infantum | 99% | 100% |
C9ZQZ6 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 33% | 100% |
E9B0W9 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
Q4Q797 | Leishmania major | 95% | 100% |
Q9W1V7 | Drosophila melanogaster | 25% | 75% |
V5BYU5 | Trypanosoma cruzi | 38% | 100% |