This protein family is endemic to Kinetoplastids, might have emerged de novo and also expanded. . The family also contains Leishmaniid members lacking the signal peptide and only having an MTTPA- start sequence
| 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: 2, no: 9 |
| NetGPI | no | yes: 0, no: 11 |
| Term | Name | Level | Count |
|---|---|---|---|
| GO:0016020 | membrane | 2 | 10 |
| GO:0110165 | cellular anatomical entity | 1 | 10 |
Related structures:
AlphaFold database: A0A3S5H659
| Leishmania | From | To | Domain/Motif | Score |
|---|---|---|---|---|
| CLV_C14_Caspase3-7 | 134 | 138 | PF00656 | 0.693 |
| CLV_NRD_NRD_1 | 101 | 103 | PF00675 | 0.558 |
| CLV_NRD_NRD_1 | 110 | 112 | PF00675 | 0.528 |
| CLV_NRD_NRD_1 | 162 | 164 | PF00675 | 0.445 |
| CLV_NRD_NRD_1 | 69 | 71 | PF00675 | 0.446 |
| CLV_PCSK_FUR_1 | 99 | 103 | PF00082 | 0.515 |
| CLV_PCSK_KEX2_1 | 101 | 103 | PF00082 | 0.557 |
| CLV_PCSK_KEX2_1 | 110 | 112 | PF00082 | 0.527 |
| CLV_PCSK_KEX2_1 | 164 | 166 | PF00082 | 0.448 |
| CLV_PCSK_PC1ET2_1 | 164 | 166 | PF00082 | 0.437 |
| CLV_PCSK_SKI1_1 | 31 | 35 | PF00082 | 0.676 |
| CLV_PCSK_SKI1_1 | 70 | 74 | PF00082 | 0.419 |
| DEG_MDM2_SWIB_1 | 34 | 42 | PF02201 | 0.423 |
| DOC_CKS1_1 | 1 | 6 | PF01111 | 0.446 |
| DOC_MAPK_RevD_3 | 150 | 165 | PF00069 | 0.615 |
| DOC_USP7_MATH_1 | 119 | 123 | PF00917 | 0.732 |
| DOC_USP7_MATH_1 | 15 | 19 | PF00917 | 0.437 |
| DOC_USP7_UBL2_3 | 73 | 77 | PF12436 | 0.580 |
| LIG_14-3-3_CanoR_1 | 110 | 115 | PF00244 | 0.733 |
| LIG_14-3-3_CterR_2 | 163 | 167 | PF00244 | 0.672 |
| LIG_EVH1_2 | 29 | 33 | PF00568 | 0.434 |
| LIG_FHA_1 | 38 | 44 | PF00498 | 0.347 |
| LIG_FHA_2 | 138 | 144 | PF00498 | 0.672 |
| LIG_FHA_2 | 8 | 14 | PF00498 | 0.522 |
| LIG_FHA_2 | 95 | 101 | PF00498 | 0.642 |
| LIG_GBD_Chelix_1 | 50 | 58 | PF00786 | 0.256 |
| LIG_LIR_Gen_1 | 144 | 155 | PF02991 | 0.624 |
| LIG_LIR_Gen_1 | 18 | 29 | PF02991 | 0.460 |
| LIG_LIR_Nem_3 | 144 | 150 | PF02991 | 0.722 |
| LIG_LIR_Nem_3 | 18 | 24 | PF02991 | 0.472 |
| LIG_LIR_Nem_3 | 82 | 88 | PF02991 | 0.658 |
| LIG_Pex14_2 | 34 | 38 | PF04695 | 0.448 |
| LIG_PTB_Apo_2 | 80 | 87 | PF02174 | 0.600 |
| LIG_SH2_CRK | 21 | 25 | PF00017 | 0.421 |
| LIG_SH2_CRK | 39 | 43 | PF00017 | 0.235 |
| LIG_SH2_PTP2 | 147 | 150 | PF00017 | 0.638 |
| LIG_SH2_PTP2 | 53 | 56 | PF00017 | 0.451 |
| LIG_SH2_STAT3 | 66 | 69 | PF00017 | 0.648 |
| LIG_SH2_STAT5 | 147 | 150 | PF00017 | 0.638 |
| LIG_SH2_STAT5 | 39 | 42 | PF00017 | 0.396 |
| LIG_SH2_STAT5 | 53 | 56 | PF00017 | 0.296 |
| LIG_SH2_STAT5 | 80 | 83 | PF00017 | 0.722 |
| LIG_SH3_3 | 151 | 157 | PF00018 | 0.648 |
| LIG_SH3_3 | 9 | 15 | PF00018 | 0.473 |
| LIG_SUMO_SIM_anti_2 | 40 | 46 | PF11976 | 0.300 |
| LIG_TYR_ITIM | 19 | 24 | PF00017 | 0.395 |
| MOD_CK1_1 | 103 | 109 | PF00069 | 0.742 |
| MOD_CK1_1 | 136 | 142 | PF00069 | 0.743 |
| MOD_CK2_1 | 103 | 109 | PF00069 | 0.801 |
| MOD_CK2_1 | 119 | 125 | PF00069 | 0.637 |
| MOD_CK2_1 | 137 | 143 | PF00069 | 0.791 |
| MOD_CK2_1 | 7 | 13 | PF00069 | 0.426 |
| MOD_GlcNHglycan | 119 | 122 | PF01048 | 0.517 |
| MOD_GlcNHglycan | 133 | 136 | PF01048 | 0.469 |
| MOD_GSK3_1 | 100 | 107 | PF00069 | 0.755 |
| MOD_GSK3_1 | 109 | 116 | PF00069 | 0.719 |
| MOD_GSK3_1 | 131 | 138 | PF00069 | 0.722 |
| MOD_GSK3_1 | 90 | 97 | PF00069 | 0.697 |
| MOD_PIKK_1 | 94 | 100 | PF00454 | 0.754 |
| MOD_PKA_1 | 101 | 107 | PF00069 | 0.696 |
| MOD_PKA_1 | 110 | 116 | PF00069 | 0.684 |
| MOD_PKA_2 | 100 | 106 | PF00069 | 0.735 |
| MOD_PKA_2 | 109 | 115 | PF00069 | 0.744 |
| MOD_PKB_1 | 99 | 107 | PF00069 | 0.727 |
| MOD_Plk_4 | 110 | 116 | PF00069 | 0.646 |
| MOD_Plk_4 | 15 | 21 | PF00069 | 0.439 |
| MOD_Plk_4 | 29 | 35 | PF00069 | 0.370 |
| TRG_ENDOCYTIC_2 | 147 | 150 | PF00928 | 0.649 |
| TRG_ENDOCYTIC_2 | 21 | 24 | PF00928 | 0.553 |
| TRG_ENDOCYTIC_2 | 39 | 42 | PF00928 | 0.336 |
| TRG_ENDOCYTIC_2 | 53 | 56 | PF00928 | 0.415 |
| TRG_ER_diArg_1 | 162 | 165 | PF00400 | 0.667 |
| TRG_NLS_MonoExtC_3 | 69 | 74 | PF00514 | 0.639 |
| Protein | Taxonomy | Sequence identity | Coverage |
|---|---|---|---|
| A0A0N0P923 | Leptomonas seymouri | 43% | 79% |
| A0A3S7WQ87 | Leishmania donovani | 31% | 100% |
| A4H5C6 | Leishmania braziliensis | 39% | 100% |
| A4H5C7 | Leishmania braziliensis | 58% | 100% |
| A4HTK6 | Leishmania infantum | 31% | 100% |
| A4HTK7 | Leishmania infantum | 96% | 99% |
| E9AMD7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 36% | 93% |
| E9AMD8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 75% | 99% |
| Q4QIB1 | Leishmania major | 86% | 100% |
| Q4QIB2 | Leishmania major | 35% | 100% |