| 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 | 
| Term | Name | Level | Count | 
|---|---|---|---|
| GO:0005739 | mitochondrion | 5 | 12 | 
| GO:0043226 | organelle | 2 | 12 | 
| GO:0043227 | membrane-bounded organelle | 3 | 12 | 
| GO:0043229 | intracellular organelle | 3 | 12 | 
| GO:0043231 | intracellular membrane-bounded organelle | 4 | 12 | 
| GO:0110165 | cellular anatomical entity | 1 | 12 | 
| GO:0005737 | cytoplasm | 2 | 1 | 
Related structures:
AlphaFold database: A4IB93
| Term | Name | Level | Count | 
|---|---|---|---|
| GO:0009987 | cellular process | 1 | 12 | 
| GO:0016043 | cellular component organization | 3 | 12 | 
| GO:0022607 | cellular component assembly | 4 | 12 | 
| GO:0043933 | protein-containing complex organization | 4 | 12 | 
| GO:0065003 | protein-containing complex assembly | 5 | 12 | 
| GO:0071840 | cellular component organization or biogenesis | 2 | 12 | 
| GO:0033615 | mitochondrial proton-transporting ATP synthase complex assembly | 8 | 1 | 
| GO:0043461 | proton-transporting ATP synthase complex assembly | 7 | 1 | 
| GO:0070071 | proton-transporting two-sector ATPase complex assembly | 6 | 1 | 
| Leishmania | From | To | Domain/Motif | Score | 
|---|---|---|---|---|
| CLV_NRD_NRD_1 | 16 | 18 | PF00675 | 0.320 | 
| CLV_PCSK_KEX2_1 | 13 | 15 | PF00082 | 0.433 | 
| CLV_PCSK_KEX2_1 | 172 | 174 | PF00082 | 0.300 | 
| CLV_PCSK_PC1ET2_1 | 13 | 15 | PF00082 | 0.433 | 
| CLV_PCSK_PC1ET2_1 | 172 | 174 | PF00082 | 0.297 | 
| CLV_PCSK_PC7_1 | 9 | 15 | PF00082 | 0.559 | 
| CLV_PCSK_SKI1_1 | 184 | 188 | PF00082 | 0.387 | 
| CLV_PCSK_SKI1_1 | 82 | 86 | PF00082 | 0.297 | 
| DEG_APCC_DBOX_1 | 16 | 24 | PF00400 | 0.308 | 
| DEG_MDM2_SWIB_1 | 48 | 56 | PF02201 | 0.313 | 
| DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.441 | 
| DEG_SCF_FBW7_2 | 96 | 103 | PF00400 | 0.351 | 
| DOC_CKS1_1 | 213 | 218 | PF01111 | 0.525 | 
| DOC_CYCLIN_RxL_1 | 124 | 135 | PF00134 | 0.357 | 
| DOC_MAPK_gen_1 | 125 | 132 | PF00069 | 0.300 | 
| DOC_PP4_FxxP_1 | 12 | 15 | PF00568 | 0.659 | 
| DOC_PP4_FxxP_1 | 74 | 77 | PF00568 | 0.297 | 
| DOC_WW_Pin1_4 | 212 | 217 | PF00397 | 0.530 | 
| DOC_WW_Pin1_4 | 30 | 35 | PF00397 | 0.301 | 
| DOC_WW_Pin1_4 | 68 | 73 | PF00397 | 0.402 | 
| DOC_WW_Pin1_4 | 96 | 101 | PF00397 | 0.351 | 
| LIG_14-3-3_CanoR_1 | 17 | 21 | PF00244 | 0.349 | 
| LIG_14-3-3_CanoR_1 | 54 | 64 | PF00244 | 0.308 | 
| LIG_APCC_ABBA_1 | 76 | 81 | PF00400 | 0.389 | 
| LIG_BIR_III_4 | 207 | 211 | PF00653 | 0.551 | 
| LIG_BRCT_BRCA1_1 | 70 | 74 | PF00533 | 0.389 | 
| LIG_deltaCOP1_diTrp_1 | 164 | 170 | PF00928 | 0.313 | 
| LIG_FHA_1 | 148 | 154 | PF00498 | 0.297 | 
| LIG_FHA_1 | 225 | 231 | PF00498 | 0.620 | 
| LIG_FHA_2 | 213 | 219 | PF00498 | 0.519 | 
| LIG_GBD_Chelix_1 | 220 | 228 | PF00786 | 0.599 | 
| LIG_LIR_Apic_2 | 71 | 77 | PF02991 | 0.335 | 
| LIG_LIR_Gen_1 | 138 | 149 | PF02991 | 0.256 | 
| LIG_LIR_Gen_1 | 178 | 186 | PF02991 | 0.491 | 
| LIG_LIR_Nem_3 | 138 | 144 | PF02991 | 0.435 | 
| LIG_LIR_Nem_3 | 158 | 162 | PF02991 | 0.317 | 
| LIG_LIR_Nem_3 | 178 | 182 | PF02991 | 0.297 | 
| LIG_LIR_Nem_3 | 207 | 212 | PF02991 | 0.518 | 
| LIG_LIR_Nem_3 | 58 | 64 | PF02991 | 0.319 | 
| LIG_LIR_Nem_3 | 71 | 76 | PF02991 | 0.269 | 
| LIG_MLH1_MIPbox_1 | 70 | 74 | PF16413 | 0.389 | 
| LIG_Pex14_1 | 166 | 170 | PF04695 | 0.313 | 
| LIG_Pex14_2 | 48 | 52 | PF04695 | 0.297 | 
| LIG_SH2_CRK | 157 | 161 | PF00017 | 0.313 | 
| LIG_SH2_STAP1 | 163 | 167 | PF00017 | 0.313 | 
| LIG_SH2_STAT5 | 11 | 14 | PF00017 | 0.672 | 
| LIG_SH2_STAT5 | 157 | 160 | PF00017 | 0.313 | 
| LIG_SH2_STAT5 | 73 | 76 | PF00017 | 0.297 | 
| LIG_TRFH_1 | 62 | 66 | PF08558 | 0.389 | 
| LIG_WRC_WIRS_1 | 167 | 172 | PF05994 | 0.389 | 
| MOD_CDK_SPK_2 | 30 | 35 | PF00069 | 0.176 | 
| MOD_CK2_1 | 16 | 22 | PF00069 | 0.313 | 
| MOD_CK2_1 | 24 | 30 | PF00069 | 0.313 | 
| MOD_Cter_Amidation | 15 | 18 | PF01082 | 0.297 | 
| MOD_NEK2_1 | 123 | 128 | PF00069 | 0.316 | 
| MOD_NEK2_1 | 2 | 7 | PF00069 | 0.536 | 
| MOD_NEK2_1 | 29 | 34 | PF00069 | 0.421 | 
| MOD_NEK2_2 | 24 | 29 | PF00069 | 0.433 | 
| MOD_PIKK_1 | 147 | 153 | PF00454 | 0.297 | 
| MOD_PKA_2 | 16 | 22 | PF00069 | 0.237 | 
| MOD_PKA_2 | 2 | 8 | PF00069 | 0.548 | 
| MOD_Plk_4 | 24 | 30 | PF00069 | 0.317 | 
| MOD_Plk_4 | 36 | 42 | PF00069 | 0.264 | 
| MOD_ProDKin_1 | 212 | 218 | PF00069 | 0.527 | 
| MOD_ProDKin_1 | 30 | 36 | PF00069 | 0.301 | 
| MOD_ProDKin_1 | 68 | 74 | PF00069 | 0.402 | 
| MOD_ProDKin_1 | 96 | 102 | PF00069 | 0.351 | 
| MOD_SUMO_for_1 | 136 | 139 | PF00179 | 0.433 | 
| MOD_SUMO_for_1 | 186 | 189 | PF00179 | 0.383 | 
| MOD_SUMO_rev_2 | 193 | 202 | PF00179 | 0.535 | 
| TRG_ENDOCYTIC_2 | 156 | 159 | PF00928 | 0.313 | 
| TRG_ENDOCYTIC_2 | 179 | 182 | PF00928 | 0.415 | 
| TRG_ENDOCYTIC_2 | 61 | 64 | PF00928 | 0.316 | 
| TRG_ENDOCYTIC_2 | 73 | 76 | PF00928 | 0.316 | 
| TRG_Pf-PMV_PEXEL_1 | 18 | 22 | PF00026 | 0.297 | 
| Protein | Taxonomy | Sequence identity | Coverage | 
|---|---|---|---|
| A0A0N0P324 | Leptomonas seymouri | 85% | 100% | 
| A0A0S4JHC0 | Bodo saltans | 70% | 99% | 
| A0A1X0P5W7 | Trypanosomatidae | 70% | 100% | 
| A0A3Q8IPF8 | Leishmania donovani | 100% | 100% | 
| A0A3R7RMJ9 | Trypanosoma rangeli | 68% | 98% | 
| A4HML6 | Leishmania braziliensis | 91% | 100% | 
| C9ZZL8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 71% | 95% | 
| E9AF17 | Leishmania major | 97% | 100% | 
| E9B673 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 97% | 100% | 
| V5B8Y3 | Trypanosoma cruzi | 68% | 98% |