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: E9B764
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 170 | 174 | PF00656 | 0.511 |
CLV_NRD_NRD_1 | 165 | 167 | PF00675 | 0.354 |
CLV_PCSK_KEX2_1 | 27 | 29 | PF00082 | 0.459 |
CLV_PCSK_PC1ET2_1 | 27 | 29 | PF00082 | 0.407 |
CLV_PCSK_SKI1_1 | 105 | 109 | PF00082 | 0.481 |
CLV_PCSK_SKI1_1 | 15 | 19 | PF00082 | 0.436 |
CLV_PCSK_SKI1_1 | 167 | 171 | PF00082 | 0.610 |
CLV_PCSK_SKI1_1 | 209 | 213 | PF00082 | 0.524 |
CLV_PCSK_SKI1_1 | 224 | 228 | PF00082 | 0.460 |
CLV_PCSK_SKI1_1 | 28 | 32 | PF00082 | 0.371 |
DEG_APCC_KENBOX_2 | 43 | 47 | PF00400 | 0.364 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.643 |
DEG_SPOP_SBC_1 | 172 | 176 | PF00917 | 0.471 |
DEG_SPOP_SBC_1 | 202 | 206 | PF00917 | 0.282 |
DOC_CKS1_1 | 49 | 54 | PF01111 | 0.233 |
DOC_CYCLIN_RxL_1 | 12 | 19 | PF00134 | 0.479 |
DOC_CYCLIN_yCln2_LP_2 | 17 | 23 | PF00134 | 0.467 |
DOC_CYCLIN_yCln2_LP_2 | 75 | 78 | PF00134 | 0.478 |
DOC_MAPK_MEF2A_6 | 7 | 14 | PF00069 | 0.470 |
DOC_PP2B_LxvP_1 | 54 | 57 | PF13499 | 0.516 |
DOC_PP2B_LxvP_1 | 75 | 78 | PF13499 | 0.433 |
DOC_PP4_FxxP_1 | 165 | 168 | PF00568 | 0.464 |
DOC_PP4_FxxP_1 | 49 | 52 | PF00568 | 0.247 |
DOC_USP7_MATH_1 | 132 | 136 | PF00917 | 0.451 |
DOC_USP7_MATH_1 | 172 | 176 | PF00917 | 0.471 |
DOC_USP7_MATH_1 | 192 | 196 | PF00917 | 0.520 |
DOC_USP7_MATH_1 | 198 | 202 | PF00917 | 0.463 |
DOC_USP7_MATH_1 | 246 | 250 | PF00917 | 0.396 |
DOC_WW_Pin1_4 | 16 | 21 | PF00397 | 0.464 |
DOC_WW_Pin1_4 | 48 | 53 | PF00397 | 0.390 |
LIG_FHA_1 | 49 | 55 | PF00498 | 0.307 |
LIG_FHA_1 | 88 | 94 | PF00498 | 0.438 |
LIG_FHA_2 | 106 | 112 | PF00498 | 0.499 |
LIG_FHA_2 | 125 | 131 | PF00498 | 0.408 |
LIG_FHA_2 | 168 | 174 | PF00498 | 0.532 |
LIG_HCF-1_HBM_1 | 94 | 97 | PF13415 | 0.362 |
LIG_LIR_Apic_2 | 162 | 168 | PF02991 | 0.450 |
LIG_LIR_Gen_1 | 135 | 146 | PF02991 | 0.504 |
LIG_LIR_Nem_3 | 135 | 141 | PF02991 | 0.484 |
LIG_LIR_Nem_3 | 94 | 100 | PF02991 | 0.350 |
LIG_MYND_1 | 16 | 20 | PF01753 | 0.273 |
LIG_PDZ_Class_1 | 254 | 259 | PF00595 | 0.505 |
LIG_Pex14_1 | 161 | 165 | PF04695 | 0.396 |
LIG_RPA_C_Fungi | 191 | 203 | PF08784 | 0.337 |
LIG_SH2_SRC | 215 | 218 | PF00017 | 0.376 |
LIG_SH2_STAT5 | 101 | 104 | PF00017 | 0.336 |
LIG_SH2_STAT5 | 145 | 148 | PF00017 | 0.435 |
LIG_SH2_STAT5 | 159 | 162 | PF00017 | 0.336 |
LIG_SH2_STAT5 | 215 | 218 | PF00017 | 0.481 |
LIG_SH2_STAT5 | 234 | 237 | PF00017 | 0.362 |
LIG_SH2_STAT5 | 97 | 100 | PF00017 | 0.332 |
LIG_SH3_3 | 143 | 149 | PF00018 | 0.525 |
LIG_SH3_3 | 73 | 79 | PF00018 | 0.589 |
LIG_SUMO_SIM_anti_2 | 81 | 87 | PF11976 | 0.498 |
LIG_TRAF2_1 | 127 | 130 | PF00917 | 0.541 |
LIG_UBA3_1 | 82 | 87 | PF00899 | 0.526 |
MOD_CK1_1 | 201 | 207 | PF00069 | 0.524 |
MOD_CK1_1 | 249 | 255 | PF00069 | 0.459 |
MOD_CK1_1 | 34 | 40 | PF00069 | 0.393 |
MOD_CK2_1 | 105 | 111 | PF00069 | 0.388 |
MOD_CK2_1 | 124 | 130 | PF00069 | 0.423 |
MOD_GlcNHglycan | 114 | 117 | PF01048 | 0.415 |
MOD_GlcNHglycan | 175 | 178 | PF01048 | 0.520 |
MOD_GlcNHglycan | 2 | 5 | PF01048 | 0.616 |
MOD_GlcNHglycan | 200 | 203 | PF01048 | 0.545 |
MOD_GlcNHglycan | 256 | 259 | PF01048 | 0.489 |
MOD_GlcNHglycan | 33 | 36 | PF01048 | 0.587 |
MOD_GSK3_1 | 167 | 174 | PF00069 | 0.519 |
MOD_GSK3_1 | 198 | 205 | PF00069 | 0.406 |
MOD_NEK2_1 | 203 | 208 | PF00069 | 0.407 |
MOD_NEK2_1 | 211 | 216 | PF00069 | 0.412 |
MOD_NEK2_1 | 31 | 36 | PF00069 | 0.461 |
MOD_NEK2_2 | 100 | 105 | PF00069 | 0.426 |
MOD_PIKK_1 | 125 | 131 | PF00454 | 0.557 |
MOD_PIKK_1 | 252 | 258 | PF00454 | 0.329 |
MOD_PKA_2 | 123 | 129 | PF00069 | 0.507 |
MOD_Plk_1 | 249 | 255 | PF00069 | 0.558 |
MOD_Plk_4 | 211 | 217 | PF00069 | 0.519 |
MOD_ProDKin_1 | 16 | 22 | PF00069 | 0.462 |
MOD_ProDKin_1 | 48 | 54 | PF00069 | 0.384 |
TRG_DiLeu_BaLyEn_6 | 13 | 18 | PF01217 | 0.401 |
TRG_DiLeu_BaLyEn_6 | 49 | 54 | PF01217 | 0.449 |
TRG_ENDOCYTIC_2 | 101 | 104 | PF00928 | 0.345 |
TRG_ENDOCYTIC_2 | 236 | 239 | PF00928 | 0.400 |
TRG_Pf-PMV_PEXEL_1 | 209 | 213 | PF00026 | 0.411 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HXE1 | Leptomonas seymouri | 49% | 96% |
A0A1X0NWL1 | Trypanosomatidae | 27% | 92% |
A0A3S7XA73 | Leishmania donovani | 91% | 100% |
A0A422N815 | Trypanosoma rangeli | 21% | 97% |
A4HNJ9 | Leishmania braziliensis | 80% | 100% |
A4IC68 | Leishmania infantum | 91% | 100% |
E9AG11 | Leishmania major | 89% | 100% |
V5DS95 | Trypanosoma cruzi | 23% | 97% |