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: 11 |
NetGPI | no | yes: 0, no: 11 |
Related structures:
AlphaFold database: A4HNP9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 21 | 23 | PF00675 | 0.544 |
CLV_NRD_NRD_1 | 6 | 8 | PF00675 | 0.552 |
CLV_NRD_NRD_1 | 99 | 101 | PF00675 | 0.495 |
CLV_PCSK_KEX2_1 | 142 | 144 | PF00082 | 0.548 |
CLV_PCSK_KEX2_1 | 164 | 166 | PF00082 | 0.533 |
CLV_PCSK_KEX2_1 | 21 | 23 | PF00082 | 0.468 |
CLV_PCSK_KEX2_1 | 62 | 64 | PF00082 | 0.338 |
CLV_PCSK_KEX2_1 | 99 | 101 | PF00082 | 0.452 |
CLV_PCSK_PC1ET2_1 | 142 | 144 | PF00082 | 0.287 |
CLV_PCSK_PC1ET2_1 | 164 | 166 | PF00082 | 0.539 |
CLV_PCSK_PC1ET2_1 | 62 | 64 | PF00082 | 0.338 |
CLV_PCSK_SKI1_1 | 164 | 168 | PF00082 | 0.444 |
CLV_PCSK_SKI1_1 | 35 | 39 | PF00082 | 0.566 |
CLV_PCSK_SKI1_1 | 62 | 66 | PF00082 | 0.466 |
CLV_PCSK_SKI1_1 | 99 | 103 | PF00082 | 0.299 |
CLV_Separin_Metazoa | 174 | 178 | PF03568 | 0.326 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.613 |
DOC_CDC14_PxL_1 | 78 | 86 | PF14671 | 0.469 |
DOC_CYCLIN_RxL_1 | 161 | 170 | PF00134 | 0.460 |
DOC_MAPK_gen_1 | 139 | 147 | PF00069 | 0.276 |
DOC_MAPK_gen_1 | 62 | 70 | PF00069 | 0.513 |
DOC_MAPK_MEF2A_6 | 62 | 70 | PF00069 | 0.538 |
DOC_MAPK_RevD_3 | 176 | 191 | PF00069 | 0.518 |
DOC_USP7_UBL2_3 | 36 | 40 | PF12436 | 0.535 |
DOC_WW_Pin1_4 | 121 | 126 | PF00397 | 0.345 |
DOC_WW_Pin1_4 | 154 | 159 | PF00397 | 0.484 |
LIG_14-3-3_CanoR_1 | 179 | 184 | PF00244 | 0.508 |
LIG_14-3-3_CanoR_1 | 7 | 11 | PF00244 | 0.550 |
LIG_14-3-3_CanoR_1 | 99 | 109 | PF00244 | 0.501 |
LIG_Actin_WH2_2 | 106 | 124 | PF00022 | 0.309 |
LIG_FHA_1 | 171 | 177 | PF00498 | 0.335 |
LIG_FHA_2 | 18 | 24 | PF00498 | 0.604 |
LIG_FHA_2 | 184 | 190 | PF00498 | 0.499 |
LIG_FHA_2 | 56 | 62 | PF00498 | 0.470 |
LIG_FHA_2 | 7 | 13 | PF00498 | 0.522 |
LIG_Integrin_isoDGR_2 | 92 | 94 | PF01839 | 0.558 |
LIG_LIR_Gen_1 | 111 | 121 | PF02991 | 0.486 |
LIG_LIR_Gen_1 | 131 | 140 | PF02991 | 0.190 |
LIG_LIR_Gen_1 | 157 | 167 | PF02991 | 0.418 |
LIG_LIR_Nem_3 | 111 | 117 | PF02991 | 0.491 |
LIG_LIR_Nem_3 | 131 | 135 | PF02991 | 0.190 |
LIG_LIR_Nem_3 | 157 | 162 | PF02991 | 0.399 |
LIG_LIR_Nem_3 | 46 | 52 | PF02991 | 0.486 |
LIG_NRBOX | 64 | 70 | PF00104 | 0.583 |
LIG_PCNA_PIPBox_1 | 42 | 51 | PF02747 | 0.563 |
LIG_PCNA_yPIPBox_3 | 35 | 49 | PF02747 | 0.483 |
LIG_REV1ctd_RIR_1 | 49 | 58 | PF16727 | 0.567 |
LIG_SH2_CRK | 180 | 184 | PF00017 | 0.486 |
LIG_SH3_3 | 67 | 73 | PF00018 | 0.510 |
LIG_SH3_3 | 79 | 85 | PF00018 | 0.354 |
LIG_TRAF2_1 | 58 | 61 | PF00917 | 0.441 |
LIG_TYR_ITIM | 178 | 183 | PF00017 | 0.307 |
LIG_UBA3_1 | 183 | 191 | PF00899 | 0.535 |
MOD_CK1_1 | 170 | 176 | PF00069 | 0.593 |
MOD_CK1_1 | 182 | 188 | PF00069 | 0.505 |
MOD_CK2_1 | 17 | 23 | PF00069 | 0.596 |
MOD_CK2_1 | 55 | 61 | PF00069 | 0.487 |
MOD_CK2_1 | 6 | 12 | PF00069 | 0.531 |
MOD_GlcNHglycan | 134 | 138 | PF01048 | 0.410 |
MOD_GSK3_1 | 117 | 124 | PF00069 | 0.330 |
MOD_GSK3_1 | 179 | 186 | PF00069 | 0.492 |
MOD_NEK2_1 | 109 | 114 | PF00069 | 0.494 |
MOD_NEK2_1 | 117 | 122 | PF00069 | 0.449 |
MOD_NEK2_1 | 183 | 188 | PF00069 | 0.433 |
MOD_NEK2_1 | 68 | 73 | PF00069 | 0.556 |
MOD_PIKK_1 | 167 | 173 | PF00454 | 0.370 |
MOD_PIKK_1 | 38 | 44 | PF00454 | 0.563 |
MOD_PKA_1 | 35 | 41 | PF00069 | 0.581 |
MOD_PKA_2 | 138 | 144 | PF00069 | 0.400 |
MOD_PKA_2 | 6 | 12 | PF00069 | 0.547 |
MOD_PKA_2 | 93 | 99 | PF00069 | 0.531 |
MOD_PKB_1 | 177 | 185 | PF00069 | 0.533 |
MOD_Plk_1 | 109 | 115 | PF00069 | 0.423 |
MOD_Plk_2-3 | 55 | 61 | PF00069 | 0.563 |
MOD_Plk_2-3 | 6 | 12 | PF00069 | 0.566 |
MOD_Plk_4 | 109 | 115 | PF00069 | 0.333 |
MOD_Plk_4 | 179 | 185 | PF00069 | 0.474 |
MOD_ProDKin_1 | 121 | 127 | PF00069 | 0.339 |
MOD_ProDKin_1 | 154 | 160 | PF00069 | 0.481 |
MOD_SUMO_rev_2 | 3 | 10 | PF00179 | 0.600 |
MOD_SUMO_rev_2 | 55 | 64 | PF00179 | 0.564 |
TRG_DiLeu_BaEn_1 | 61 | 66 | PF01217 | 0.520 |
TRG_DiLeu_BaEn_3 | 59 | 65 | PF01217 | 0.415 |
TRG_DiLeu_BaEn_4 | 26 | 32 | PF01217 | 0.508 |
TRG_DiLeu_BaLyEn_6 | 162 | 167 | PF01217 | 0.441 |
TRG_ENDOCYTIC_2 | 180 | 183 | PF00928 | 0.489 |
TRG_ER_diArg_1 | 176 | 179 | PF00400 | 0.544 |
TRG_ER_diArg_1 | 99 | 101 | PF00400 | 0.472 |
TRG_Pf-PMV_PEXEL_1 | 165 | 169 | PF00026 | 0.351 |
TRG_Pf-PMV_PEXEL_1 | 22 | 26 | PF00026 | 0.443 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I786 | Leptomonas seymouri | 81% | 100% |
A0A0S4JIF8 | Bodo saltans | 25% | 96% |
A0A1X0P8L2 | Trypanosomatidae | 44% | 100% |
A0A3S7XA94 | Leishmania donovani | 85% | 100% |
A0A422P2B0 | Trypanosoma rangeli | 40% | 99% |
A4ICU6 | Leishmania infantum | 85% | 100% |
D0A2K9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 45% | 99% |
E9ASF8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
Q4Q237 | Leishmania major | 85% | 100% |
V5BA10 | Trypanosoma cruzi | 49% | 100% |