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: A4HBA5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_PCSK_SKI1_1 | 104 | 108 | PF00082 | 0.511 |
CLV_PCSK_SKI1_1 | 21 | 25 | PF00082 | 0.375 |
CLV_PCSK_SKI1_1 | 62 | 66 | PF00082 | 0.558 |
CLV_PCSK_SKI1_1 | 93 | 97 | PF00082 | 0.575 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.468 |
DOC_CDC14_PxL_1 | 124 | 132 | PF14671 | 0.436 |
DOC_PP2B_LxvP_1 | 13 | 16 | PF13499 | 0.392 |
DOC_PP2B_LxvP_1 | 185 | 188 | PF13499 | 0.474 |
DOC_PP4_FxxP_1 | 152 | 155 | PF00568 | 0.465 |
DOC_USP7_MATH_1 | 188 | 192 | PF00917 | 0.480 |
DOC_USP7_MATH_1 | 263 | 267 | PF00917 | 0.431 |
DOC_WW_Pin1_4 | 136 | 141 | PF00397 | 0.694 |
DOC_WW_Pin1_4 | 144 | 149 | PF00397 | 0.695 |
DOC_WW_Pin1_4 | 4 | 9 | PF00397 | 0.594 |
LIG_14-3-3_CanoR_1 | 3 | 9 | PF00244 | 0.554 |
LIG_BRCT_BRCA1_1 | 155 | 159 | PF00533 | 0.537 |
LIG_BRCT_BRCA1_1 | 190 | 194 | PF00533 | 0.351 |
LIG_DCNL_PONY_1 | 1 | 4 | PF03556 | 0.459 |
LIG_DLG_GKlike_1 | 153 | 161 | PF00625 | 0.265 |
LIG_FHA_1 | 116 | 122 | PF00498 | 0.453 |
LIG_FHA_1 | 27 | 33 | PF00498 | 0.479 |
LIG_FHA_1 | 41 | 47 | PF00498 | 0.418 |
LIG_FHA_2 | 230 | 236 | PF00498 | 0.504 |
LIG_FHA_2 | 58 | 64 | PF00498 | 0.486 |
LIG_FHA_2 | 81 | 87 | PF00498 | 0.417 |
LIG_LIR_Apic_2 | 149 | 155 | PF02991 | 0.464 |
LIG_LIR_Gen_1 | 156 | 167 | PF02991 | 0.413 |
LIG_LIR_Gen_1 | 168 | 177 | PF02991 | 0.459 |
LIG_LIR_Nem_3 | 156 | 162 | PF02991 | 0.414 |
LIG_LIR_Nem_3 | 168 | 174 | PF02991 | 0.328 |
LIG_LIR_Nem_3 | 17 | 22 | PF02991 | 0.449 |
LIG_LIR_Nem_3 | 191 | 196 | PF02991 | 0.344 |
LIG_LIR_Nem_3 | 222 | 226 | PF02991 | 0.325 |
LIG_MLH1_MIPbox_1 | 190 | 194 | PF16413 | 0.464 |
LIG_NRBOX | 108 | 114 | PF00104 | 0.433 |
LIG_NRBOX | 206 | 212 | PF00104 | 0.412 |
LIG_PCNA_PIPBox_1 | 187 | 196 | PF02747 | 0.258 |
LIG_PTAP_UEV_1 | 124 | 129 | PF05743 | 0.430 |
LIG_RPA_C_Fungi | 111 | 123 | PF08784 | 0.367 |
LIG_SH2_SRC | 9 | 12 | PF00017 | 0.405 |
LIG_SH2_STAP1 | 9 | 13 | PF00017 | 0.388 |
LIG_SH2_STAT5 | 22 | 25 | PF00017 | 0.328 |
LIG_SH2_STAT5 | 80 | 83 | PF00017 | 0.631 |
LIG_SH3_3 | 122 | 128 | PF00018 | 0.655 |
LIG_SH3_3 | 252 | 258 | PF00018 | 0.538 |
LIG_SUMO_SIM_anti_2 | 29 | 36 | PF11976 | 0.432 |
LIG_TRAF2_1 | 166 | 169 | PF00917 | 0.432 |
LIG_TRAF2_1 | 8 | 11 | PF00917 | 0.574 |
MOD_CK1_1 | 108 | 114 | PF00069 | 0.482 |
MOD_CK1_1 | 139 | 145 | PF00069 | 0.608 |
MOD_CK1_1 | 26 | 32 | PF00069 | 0.490 |
MOD_CK2_1 | 108 | 114 | PF00069 | 0.421 |
MOD_CK2_1 | 11 | 17 | PF00069 | 0.526 |
MOD_CK2_1 | 229 | 235 | PF00069 | 0.471 |
MOD_CK2_1 | 4 | 10 | PF00069 | 0.731 |
MOD_CK2_1 | 57 | 63 | PF00069 | 0.453 |
MOD_CK2_1 | 80 | 86 | PF00069 | 0.426 |
MOD_CMANNOS | 181 | 184 | PF00535 | 0.330 |
MOD_GlcNHglycan | 125 | 128 | PF01048 | 0.581 |
MOD_GlcNHglycan | 245 | 250 | PF01048 | 0.482 |
MOD_GlcNHglycan | 265 | 268 | PF01048 | 0.395 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.682 |
MOD_GlcNHglycan | 74 | 77 | PF01048 | 0.548 |
MOD_GSK3_1 | 104 | 111 | PF00069 | 0.476 |
MOD_GSK3_1 | 153 | 160 | PF00069 | 0.533 |
MOD_GSK3_1 | 74 | 81 | PF00069 | 0.594 |
MOD_N-GLC_2 | 176 | 178 | PF02516 | 0.410 |
MOD_NEK2_1 | 105 | 110 | PF00069 | 0.467 |
MOD_NEK2_1 | 157 | 162 | PF00069 | 0.498 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.705 |
MOD_NEK2_1 | 210 | 215 | PF00069 | 0.536 |
MOD_NEK2_1 | 23 | 28 | PF00069 | 0.334 |
MOD_PIKK_1 | 80 | 86 | PF00454 | 0.693 |
MOD_PKA_2 | 115 | 121 | PF00069 | 0.514 |
MOD_PKA_2 | 2 | 8 | PF00069 | 0.590 |
MOD_Plk_1 | 188 | 194 | PF00069 | 0.512 |
MOD_Plk_1 | 9 | 15 | PF00069 | 0.388 |
MOD_Plk_1 | 97 | 103 | PF00069 | 0.400 |
MOD_Plk_2-3 | 11 | 17 | PF00069 | 0.323 |
MOD_Plk_4 | 108 | 114 | PF00069 | 0.364 |
MOD_Plk_4 | 153 | 159 | PF00069 | 0.375 |
MOD_Plk_4 | 97 | 103 | PF00069 | 0.386 |
MOD_ProDKin_1 | 136 | 142 | PF00069 | 0.695 |
MOD_ProDKin_1 | 144 | 150 | PF00069 | 0.681 |
MOD_ProDKin_1 | 4 | 10 | PF00069 | 0.592 |
MOD_SUMO_rev_2 | 58 | 67 | PF00179 | 0.543 |
MOD_SUMO_rev_2 | 86 | 95 | PF00179 | 0.562 |
TRG_DiLeu_BaEn_1 | 91 | 96 | PF01217 | 0.500 |
TRG_DiLeu_BaLyEn_6 | 252 | 257 | PF01217 | 0.430 |
TRG_DiLeu_BaLyEn_6 | 36 | 41 | PF01217 | 0.302 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PE51 | Leptomonas seymouri | 55% | 100% |
A0A0S4KKN8 | Bodo saltans | 28% | 96% |
A0A1X0ND66 | Trypanosomatidae | 32% | 100% |
A0A3Q8IEP6 | Leishmania donovani | 69% | 100% |
A0A422NSY2 | Trypanosoma rangeli | 35% | 100% |
A4IAF3 | Leishmania infantum | 69% | 100% |
C9ZLU1 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
E9B5H7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 69% | 100% |
Q4Q2F8 | Leishmania major | 66% | 100% |