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: Q4QAC0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 74 | 78 | PF00656 | 0.516 |
CLV_NRD_NRD_1 | 296 | 298 | PF00675 | 0.608 |
CLV_NRD_NRD_1 | 301 | 303 | PF00675 | 0.600 |
CLV_NRD_NRD_1 | 66 | 68 | PF00675 | 0.377 |
CLV_PCSK_KEX2_1 | 294 | 296 | PF00082 | 0.675 |
CLV_PCSK_KEX2_1 | 300 | 302 | PF00082 | 0.609 |
CLV_PCSK_PC1ET2_1 | 294 | 296 | PF00082 | 0.670 |
CLV_PCSK_PC7_1 | 296 | 302 | PF00082 | 0.577 |
CLV_PCSK_SKI1_1 | 204 | 208 | PF00082 | 0.601 |
CLV_PCSK_SKI1_1 | 67 | 71 | PF00082 | 0.393 |
DOC_CKS1_1 | 237 | 242 | PF01111 | 0.580 |
DOC_MAPK_DCC_7 | 281 | 290 | PF00069 | 0.666 |
DOC_MAPK_gen_1 | 281 | 290 | PF00069 | 0.666 |
DOC_MAPK_MEF2A_6 | 281 | 290 | PF00069 | 0.666 |
DOC_MAPK_MEF2A_6 | 93 | 102 | PF00069 | 0.338 |
DOC_PP2B_LxvP_1 | 102 | 105 | PF13499 | 0.357 |
DOC_PP2B_LxvP_1 | 288 | 291 | PF13499 | 0.678 |
DOC_USP7_MATH_1 | 153 | 157 | PF00917 | 0.516 |
DOC_USP7_MATH_1 | 169 | 173 | PF00917 | 0.357 |
DOC_USP7_MATH_1 | 202 | 206 | PF00917 | 0.623 |
DOC_USP7_MATH_1 | 250 | 254 | PF00917 | 0.689 |
DOC_WW_Pin1_4 | 14 | 19 | PF00397 | 0.608 |
DOC_WW_Pin1_4 | 177 | 182 | PF00397 | 0.481 |
DOC_WW_Pin1_4 | 225 | 230 | PF00397 | 0.791 |
DOC_WW_Pin1_4 | 236 | 241 | PF00397 | 0.511 |
DOC_WW_Pin1_4 | 270 | 275 | PF00397 | 0.762 |
LIG_14-3-3_CanoR_1 | 123 | 128 | PF00244 | 0.477 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.491 |
LIG_Clathr_ClatBox_1 | 127 | 131 | PF01394 | 0.393 |
LIG_eIF4E_1 | 86 | 92 | PF01652 | 0.306 |
LIG_FHA_1 | 25 | 31 | PF00498 | 0.481 |
LIG_Integrin_isoDGR_2 | 244 | 246 | PF01839 | 0.587 |
LIG_LIR_Apic_2 | 234 | 240 | PF02991 | 0.610 |
LIG_LIR_Gen_1 | 136 | 145 | PF02991 | 0.464 |
LIG_LIR_Gen_1 | 189 | 197 | PF02991 | 0.432 |
LIG_LIR_Gen_1 | 61 | 71 | PF02991 | 0.362 |
LIG_LIR_Nem_3 | 136 | 140 | PF02991 | 0.379 |
LIG_LIR_Nem_3 | 189 | 194 | PF02991 | 0.428 |
LIG_LIR_Nem_3 | 28 | 34 | PF02991 | 0.349 |
LIG_LIR_Nem_3 | 61 | 66 | PF02991 | 0.347 |
LIG_LIR_Nem_3 | 83 | 88 | PF02991 | 0.326 |
LIG_NRBOX | 161 | 167 | PF00104 | 0.559 |
LIG_PALB2_WD40_1 | 125 | 133 | PF16756 | 0.487 |
LIG_SH2_CRK | 146 | 150 | PF00017 | 0.477 |
LIG_SH2_CRK | 237 | 241 | PF00017 | 0.754 |
LIG_SH2_CRK | 32 | 36 | PF00017 | 0.493 |
LIG_SH2_NCK_1 | 237 | 241 | PF00017 | 0.543 |
LIG_SH2_STAP1 | 26 | 30 | PF00017 | 0.436 |
LIG_SH2_STAT3 | 110 | 113 | PF00017 | 0.376 |
LIG_SH2_STAT5 | 110 | 113 | PF00017 | 0.365 |
LIG_SH2_STAT5 | 26 | 29 | PF00017 | 0.433 |
LIG_SH2_STAT5 | 272 | 275 | PF00017 | 0.610 |
LIG_SH2_STAT5 | 86 | 89 | PF00017 | 0.313 |
LIG_SH3_3 | 15 | 21 | PF00018 | 0.627 |
LIG_SH3_3 | 226 | 232 | PF00018 | 0.790 |
LIG_SH3_3 | 95 | 101 | PF00018 | 0.350 |
LIG_TRAF2_1 | 303 | 306 | PF00917 | 0.537 |
LIG_TYR_ITIM | 30 | 35 | PF00017 | 0.485 |
MOD_CDK_SPK_2 | 14 | 19 | PF00069 | 0.564 |
MOD_CK1_1 | 225 | 231 | PF00069 | 0.721 |
MOD_CK1_1 | 59 | 65 | PF00069 | 0.467 |
MOD_CK2_1 | 155 | 161 | PF00069 | 0.444 |
MOD_Cter_Amidation | 298 | 301 | PF01082 | 0.620 |
MOD_GlcNHglycan | 146 | 149 | PF01048 | 0.425 |
MOD_GlcNHglycan | 157 | 160 | PF01048 | 0.371 |
MOD_GlcNHglycan | 177 | 180 | PF01048 | 0.490 |
MOD_GlcNHglycan | 22 | 25 | PF01048 | 0.353 |
MOD_GlcNHglycan | 233 | 236 | PF01048 | 0.708 |
MOD_GlcNHglycan | 252 | 255 | PF01048 | 0.666 |
MOD_GlcNHglycan | 5 | 8 | PF01048 | 0.500 |
MOD_GlcNHglycan | 58 | 61 | PF01048 | 0.405 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.495 |
MOD_GSK3_1 | 223 | 230 | PF00069 | 0.684 |
MOD_N-GLC_1 | 223 | 228 | PF02516 | 0.602 |
MOD_N-GLC_1 | 80 | 85 | PF02516 | 0.388 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.585 |
MOD_NEK2_1 | 108 | 113 | PF00069 | 0.503 |
MOD_NEK2_2 | 202 | 207 | PF00069 | 0.550 |
MOD_PIKK_1 | 257 | 263 | PF00454 | 0.742 |
MOD_Plk_1 | 108 | 114 | PF00069 | 0.469 |
MOD_Plk_1 | 169 | 175 | PF00069 | 0.505 |
MOD_Plk_1 | 223 | 229 | PF00069 | 0.607 |
MOD_Plk_1 | 80 | 86 | PF00069 | 0.438 |
MOD_Plk_4 | 123 | 129 | PF00069 | 0.503 |
MOD_Plk_4 | 202 | 208 | PF00069 | 0.602 |
MOD_ProDKin_1 | 14 | 20 | PF00069 | 0.602 |
MOD_ProDKin_1 | 177 | 183 | PF00069 | 0.474 |
MOD_ProDKin_1 | 225 | 231 | PF00069 | 0.788 |
MOD_ProDKin_1 | 236 | 242 | PF00069 | 0.514 |
MOD_ProDKin_1 | 270 | 276 | PF00069 | 0.761 |
TRG_DiLeu_BaEn_1 | 161 | 166 | PF01217 | 0.559 |
TRG_DiLeu_BaLyEn_6 | 103 | 108 | PF01217 | 0.404 |
TRG_DiLeu_BaLyEn_6 | 207 | 212 | PF01217 | 0.456 |
TRG_ENDOCYTIC_2 | 146 | 149 | PF00928 | 0.466 |
TRG_ENDOCYTIC_2 | 32 | 35 | PF00928 | 0.484 |
TRG_ER_diArg_1 | 295 | 297 | PF00400 | 0.588 |
TRG_ER_diArg_1 | 300 | 302 | PF00400 | 0.566 |
TRG_NES_CRM1_1 | 125 | 138 | PF08389 | 0.405 |
TRG_Pf-PMV_PEXEL_1 | 68 | 72 | PF00026 | 0.477 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I0R9 | Leptomonas seymouri | 64% | 100% |
A0A0S4IT31 | Bodo saltans | 27% | 100% |
A0A1X0NWE2 | Trypanosomatidae | 37% | 100% |
A0A3S7WYL9 | Leishmania donovani | 95% | 100% |
A4HDS1 | Leishmania braziliensis | 84% | 100% |
A4I119 | Leishmania infantum | 94% | 100% |
C9ZW91 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 37% | 100% |
E9AX56 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 92% | 100% |
V5AV25 | Trypanosoma cruzi | 38% | 100% |