| 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: 6 |
| NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: Q4Q6U9
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_NRD_NRD_1 | 193 | 195 | PF00675 | 0.640 |
| CLV_NRD_NRD_1 | 59 | 61 | PF00675 | 0.509 |
| CLV_NRD_NRD_1 | 63 | 65 | PF00675 | 0.541 |
| CLV_PCSK_KEX2_1 | 193 | 195 | PF00082 | 0.640 |
| CLV_PCSK_KEX2_1 | 59 | 61 | PF00082 | 0.488 |
| CLV_PCSK_KEX2_1 | 63 | 65 | PF00082 | 0.515 |
| CLV_PCSK_PC7_1 | 189 | 195 | PF00082 | 0.610 |
| CLV_PCSK_PC7_1 | 59 | 65 | PF00082 | 0.511 |
| CLV_PCSK_SKI1_1 | 110 | 114 | PF00082 | 0.551 |
| CLV_PCSK_SKI1_1 | 59 | 63 | PF00082 | 0.522 |
| CLV_Separin_Metazoa | 56 | 60 | PF03568 | 0.503 |
| DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.515 |
| DOC_CYCLIN_RxL_1 | 105 | 114 | PF00134 | 0.560 |
| DOC_CYCLIN_yCln2_LP_2 | 62 | 68 | PF00134 | 0.640 |
| DOC_MAPK_gen_1 | 105 | 113 | PF00069 | 0.565 |
| DOC_MAPK_gen_1 | 59 | 68 | PF00069 | 0.553 |
| DOC_MAPK_MEF2A_6 | 105 | 113 | PF00069 | 0.565 |
| DOC_PP1_RVXF_1 | 62 | 69 | PF00149 | 0.600 |
| DOC_PP2B_LxvP_1 | 88 | 91 | PF13499 | 0.661 |
| DOC_PP4_FxxP_1 | 68 | 71 | PF00568 | 0.554 |
| DOC_USP7_MATH_1 | 142 | 146 | PF00917 | 0.729 |
| DOC_USP7_MATH_1 | 168 | 172 | PF00917 | 0.468 |
| DOC_USP7_MATH_1 | 20 | 24 | PF00917 | 0.427 |
| DOC_WW_Pin1_4 | 16 | 21 | PF00397 | 0.544 |
| DOC_WW_Pin1_4 | 31 | 36 | PF00397 | 0.352 |
| LIG_14-3-3_CanoR_1 | 25 | 29 | PF00244 | 0.626 |
| LIG_Actin_WH2_2 | 175 | 191 | PF00022 | 0.555 |
| LIG_APCC_ABBA_1 | 1 | 6 | PF00400 | 0.601 |
| LIG_APCC_ABBA_1 | 51 | 56 | PF00400 | 0.495 |
| LIG_FHA_1 | 153 | 159 | PF00498 | 0.674 |
| LIG_FHA_1 | 16 | 22 | PF00498 | 0.625 |
| LIG_LIR_Apic_2 | 31 | 35 | PF02991 | 0.544 |
| LIG_LIR_Gen_1 | 49 | 58 | PF02991 | 0.500 |
| LIG_LIR_Gen_1 | 6 | 16 | PF02991 | 0.493 |
| LIG_LIR_Nem_3 | 225 | 230 | PF02991 | 0.609 |
| LIG_LIR_Nem_3 | 49 | 54 | PF02991 | 0.506 |
| LIG_LIR_Nem_3 | 6 | 12 | PF02991 | 0.481 |
| LIG_NRBOX | 57 | 63 | PF00104 | 0.509 |
| LIG_PTB_Apo_2 | 173 | 180 | PF02174 | 0.624 |
| LIG_SH2_CRK | 100 | 104 | PF00017 | 0.605 |
| LIG_SH2_NCK_1 | 100 | 104 | PF00017 | 0.605 |
| LIG_SH2_NCK_1 | 32 | 36 | PF00017 | 0.530 |
| LIG_SH2_SRC | 45 | 48 | PF00017 | 0.573 |
| LIG_SH2_STAT5 | 197 | 200 | PF00017 | 0.574 |
| LIG_SH2_STAT5 | 45 | 48 | PF00017 | 0.601 |
| LIG_SH2_STAT5 | 89 | 92 | PF00017 | 0.587 |
| LIG_SH3_3 | 177 | 183 | PF00018 | 0.723 |
| LIG_TRAF2_1 | 8 | 11 | PF00917 | 0.514 |
| LIG_UBA3_1 | 106 | 110 | PF00899 | 0.563 |
| LIG_WRC_WIRS_1 | 21 | 26 | PF05994 | 0.557 |
| LIG_WW_3 | 102 | 106 | PF00397 | 0.619 |
| MOD_CK1_1 | 145 | 151 | PF00069 | 0.683 |
| MOD_CK1_1 | 23 | 29 | PF00069 | 0.634 |
| MOD_CK2_1 | 159 | 165 | PF00069 | 0.578 |
| MOD_CK2_1 | 41 | 47 | PF00069 | 0.473 |
| MOD_GlcNHglycan | 84 | 88 | PF01048 | 0.581 |
| MOD_GSK3_1 | 16 | 23 | PF00069 | 0.586 |
| MOD_GSK3_1 | 24 | 31 | PF00069 | 0.497 |
| MOD_N-GLC_1 | 145 | 150 | PF02516 | 0.682 |
| MOD_N-GLC_1 | 16 | 21 | PF02516 | 0.544 |
| MOD_N-GLC_2 | 50 | 52 | PF02516 | 0.374 |
| MOD_NEK2_1 | 111 | 116 | PF00069 | 0.566 |
| MOD_NEK2_1 | 24 | 29 | PF00069 | 0.549 |
| MOD_NEK2_1 | 83 | 88 | PF00069 | 0.771 |
| MOD_NEK2_2 | 20 | 25 | PF00069 | 0.547 |
| MOD_PKA_2 | 217 | 223 | PF00069 | 0.721 |
| MOD_PKA_2 | 24 | 30 | PF00069 | 0.625 |
| MOD_Plk_1 | 41 | 47 | PF00069 | 0.522 |
| MOD_Plk_1 | 83 | 89 | PF00069 | 0.656 |
| MOD_Plk_4 | 41 | 47 | PF00069 | 0.556 |
| MOD_Plk_4 | 69 | 75 | PF00069 | 0.515 |
| MOD_ProDKin_1 | 16 | 22 | PF00069 | 0.547 |
| MOD_ProDKin_1 | 31 | 37 | PF00069 | 0.348 |
| TRG_DiLeu_BaEn_1 | 225 | 230 | PF01217 | 0.656 |
| TRG_DiLeu_BaLyEn_6 | 102 | 107 | PF01217 | 0.605 |
| TRG_DiLeu_BaLyEn_6 | 124 | 129 | PF01217 | 0.565 |
| TRG_DiLeu_BaLyEn_6 | 57 | 62 | PF01217 | 0.476 |
| TRG_ENDOCYTIC_2 | 9 | 12 | PF00928 | 0.487 |
| TRG_ENDOCYTIC_2 | 99 | 102 | PF00928 | 0.647 |
| TRG_ER_diArg_1 | 58 | 60 | PF00400 | 0.490 |
| TRG_ER_diArg_1 | 62 | 64 | PF00400 | 0.529 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N1I2I1 | Leptomonas seymouri | 59% | 100% |
| A0A3Q8IJQ2 | Leishmania donovani | 90% | 100% |
| A4HIS8 | Leishmania braziliensis | 74% | 100% |
| A4I630 | Leishmania infantum | 91% | 100% |
| E9B1B5 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |