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: 9 |
NetGPI | no | yes: 0, no: 9 |
Related structures:
AlphaFold database: E9AG11
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 170 | 174 | PF00656 | 0.492 |
CLV_NRD_NRD_1 | 165 | 167 | PF00675 | 0.352 |
CLV_PCSK_KEX2_1 | 27 | 29 | PF00082 | 0.462 |
CLV_PCSK_KEX2_1 | 87 | 89 | PF00082 | 0.468 |
CLV_PCSK_PC1ET2_1 | 27 | 29 | PF00082 | 0.410 |
CLV_PCSK_PC1ET2_1 | 87 | 89 | PF00082 | 0.468 |
CLV_PCSK_SKI1_1 | 105 | 109 | PF00082 | 0.481 |
CLV_PCSK_SKI1_1 | 144 | 148 | PF00082 | 0.516 |
CLV_PCSK_SKI1_1 | 15 | 19 | PF00082 | 0.444 |
CLV_PCSK_SKI1_1 | 167 | 171 | PF00082 | 0.584 |
CLV_PCSK_SKI1_1 | 196 | 200 | PF00082 | 0.606 |
CLV_PCSK_SKI1_1 | 209 | 213 | PF00082 | 0.536 |
CLV_PCSK_SKI1_1 | 224 | 228 | PF00082 | 0.465 |
CLV_PCSK_SKI1_1 | 28 | 32 | PF00082 | 0.387 |
DEG_APCC_KENBOX_2 | 43 | 47 | PF00400 | 0.379 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.670 |
DEG_SCF_TRCP1_1 | 123 | 128 | PF00400 | 0.477 |
DOC_CYCLIN_RxL_1 | 12 | 19 | PF00134 | 0.490 |
DOC_CYCLIN_RxL_1 | 24 | 34 | PF00134 | 0.461 |
DOC_CYCLIN_yCln2_LP_2 | 17 | 23 | PF00134 | 0.479 |
DOC_CYCLIN_yCln2_LP_2 | 75 | 78 | PF00134 | 0.474 |
DOC_MAPK_DCC_7 | 144 | 154 | PF00069 | 0.347 |
DOC_PP2B_LxvP_1 | 54 | 57 | PF13499 | 0.531 |
DOC_PP2B_LxvP_1 | 75 | 78 | PF13499 | 0.429 |
DOC_PP4_FxxP_1 | 165 | 168 | PF00568 | 0.455 |
DOC_USP7_MATH_1 | 13 | 17 | PF00917 | 0.603 |
DOC_USP7_MATH_1 | 192 | 196 | PF00917 | 0.531 |
DOC_USP7_MATH_1 | 198 | 202 | PF00917 | 0.472 |
DOC_WW_Pin1_4 | 16 | 21 | PF00397 | 0.477 |
DOC_WW_Pin1_4 | 48 | 53 | PF00397 | 0.402 |
LIG_FHA_1 | 37 | 43 | PF00498 | 0.449 |
LIG_FHA_1 | 49 | 55 | PF00498 | 0.319 |
LIG_FHA_1 | 88 | 94 | PF00498 | 0.448 |
LIG_FHA_2 | 106 | 112 | PF00498 | 0.500 |
LIG_FHA_2 | 168 | 174 | PF00498 | 0.511 |
LIG_HCF-1_HBM_1 | 94 | 97 | PF13415 | 0.363 |
LIG_LIR_Apic_2 | 162 | 168 | PF02991 | 0.449 |
LIG_LIR_Gen_1 | 135 | 146 | PF02991 | 0.504 |
LIG_LIR_Nem_3 | 135 | 141 | PF02991 | 0.488 |
LIG_LIR_Nem_3 | 94 | 100 | PF02991 | 0.349 |
LIG_PDZ_Class_1 | 254 | 259 | PF00595 | 0.492 |
LIG_Pex14_1 | 161 | 165 | PF04695 | 0.399 |
LIG_SH2_STAT5 | 101 | 104 | PF00017 | 0.330 |
LIG_SH2_STAT5 | 145 | 148 | PF00017 | 0.428 |
LIG_SH2_STAT5 | 159 | 162 | PF00017 | 0.340 |
LIG_SH2_STAT5 | 234 | 237 | PF00017 | 0.361 |
LIG_SH2_STAT5 | 97 | 100 | PF00017 | 0.328 |
LIG_SH3_3 | 143 | 149 | PF00018 | 0.522 |
LIG_SH3_3 | 4 | 10 | PF00018 | 0.440 |
LIG_SH3_3 | 73 | 79 | PF00018 | 0.583 |
LIG_SUMO_SIM_anti_2 | 81 | 87 | PF11976 | 0.504 |
LIG_SUMO_SIM_par_1 | 187 | 193 | PF11976 | 0.265 |
LIG_TRAF2_1 | 127 | 130 | PF00917 | 0.530 |
LIG_UBA3_1 | 82 | 87 | PF00899 | 0.532 |
MOD_CK1_1 | 16 | 22 | PF00069 | 0.513 |
MOD_CK1_1 | 201 | 207 | PF00069 | 0.533 |
MOD_CK1_1 | 218 | 224 | PF00069 | 0.457 |
MOD_CK1_1 | 252 | 258 | PF00069 | 0.543 |
MOD_CK1_1 | 34 | 40 | PF00069 | 0.408 |
MOD_CK2_1 | 105 | 111 | PF00069 | 0.388 |
MOD_GlcNHglycan | 123 | 126 | PF01048 | 0.541 |
MOD_GlcNHglycan | 173 | 176 | PF01048 | 0.515 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.642 |
MOD_GlcNHglycan | 200 | 203 | PF01048 | 0.554 |
MOD_GlcNHglycan | 33 | 36 | PF01048 | 0.613 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.434 |
MOD_GSK3_1 | 167 | 174 | PF00069 | 0.498 |
MOD_GSK3_1 | 192 | 199 | PF00069 | 0.514 |
MOD_GSK3_1 | 211 | 218 | PF00069 | 0.325 |
MOD_N-GLC_1 | 196 | 201 | PF02516 | 0.391 |
MOD_NEK2_1 | 121 | 126 | PF00069 | 0.466 |
MOD_NEK2_1 | 203 | 208 | PF00069 | 0.416 |
MOD_NEK2_1 | 211 | 216 | PF00069 | 0.425 |
MOD_NEK2_1 | 31 | 36 | PF00069 | 0.487 |
MOD_NEK2_2 | 100 | 105 | PF00069 | 0.420 |
MOD_PIKK_1 | 113 | 119 | PF00454 | 0.391 |
MOD_PIKK_1 | 125 | 131 | PF00454 | 0.559 |
MOD_PIKK_1 | 190 | 196 | PF00454 | 0.494 |
MOD_PKA_1 | 87 | 93 | PF00069 | 0.442 |
MOD_PKA_2 | 87 | 93 | PF00069 | 0.442 |
MOD_Plk_1 | 249 | 255 | PF00069 | 0.551 |
MOD_ProDKin_1 | 16 | 22 | PF00069 | 0.474 |
MOD_ProDKin_1 | 48 | 54 | PF00069 | 0.397 |
TRG_DiLeu_BaEn_1 | 81 | 86 | PF01217 | 0.398 |
TRG_DiLeu_BaLyEn_6 | 49 | 54 | PF01217 | 0.462 |
TRG_ENDOCYTIC_2 | 101 | 104 | PF00928 | 0.338 |
TRG_ENDOCYTIC_2 | 236 | 239 | PF00928 | 0.400 |
TRG_Pf-PMV_PEXEL_1 | 209 | 213 | PF00026 | 0.423 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HXE1 | Leptomonas seymouri | 48% | 96% |
A0A1X0NWL1 | Trypanosomatidae | 28% | 92% |
A0A3S7XA73 | Leishmania donovani | 92% | 100% |
A0A422N815 | Trypanosoma rangeli | 22% | 97% |
A4HNJ9 | Leishmania braziliensis | 80% | 100% |
A4IC68 | Leishmania infantum | 92% | 100% |
E9B764 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 100% |
V5DS95 | Trypanosoma cruzi | 23% | 97% |