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: 3 |
Silverman et al. | no | yes: 0 |
Pissara et al. | yes | yes: 12 |
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: 14 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 21 |
NetGPI | no | yes: 0, no: 21 |
Related structures:
AlphaFold database: A4H6L4
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 22 |
GO:0008289 | lipid binding | 2 | 22 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 59 | 63 | PF00656 | 0.426 |
DEG_APCC_KENBOX_2 | 101 | 105 | PF00400 | 0.347 |
DEG_SPOP_SBC_1 | 12 | 16 | PF00917 | 0.484 |
DOC_CKS1_1 | 28 | 33 | PF01111 | 0.463 |
DOC_USP7_MATH_1 | 56 | 60 | PF00917 | 0.452 |
DOC_USP7_MATH_1 | 8 | 12 | PF00917 | 0.673 |
DOC_WW_Pin1_4 | 150 | 155 | PF00397 | 0.365 |
DOC_WW_Pin1_4 | 27 | 32 | PF00397 | 0.409 |
LIG_14-3-3_CanoR_1 | 136 | 141 | PF00244 | 0.428 |
LIG_BRCT_BRCA1_1 | 317 | 321 | PF00533 | 0.328 |
LIG_BRCT_BRCA1_2 | 317 | 323 | PF00533 | 0.357 |
LIG_deltaCOP1_diTrp_1 | 288 | 296 | PF00928 | 0.446 |
LIG_FHA_1 | 109 | 115 | PF00498 | 0.203 |
LIG_FHA_1 | 211 | 217 | PF00498 | 0.310 |
LIG_FHA_1 | 248 | 254 | PF00498 | 0.333 |
LIG_FHA_1 | 300 | 306 | PF00498 | 0.529 |
LIG_FHA_2 | 108 | 114 | PF00498 | 0.344 |
LIG_FHA_2 | 235 | 241 | PF00498 | 0.298 |
LIG_LIR_Apic_2 | 286 | 292 | PF02991 | 0.416 |
LIG_LIR_Apic_2 | 68 | 74 | PF02991 | 0.462 |
LIG_LIR_Gen_1 | 113 | 123 | PF02991 | 0.300 |
LIG_LIR_Gen_1 | 175 | 185 | PF02991 | 0.343 |
LIG_LIR_Nem_3 | 113 | 118 | PF02991 | 0.300 |
LIG_LIR_Nem_3 | 125 | 130 | PF02991 | 0.398 |
LIG_LIR_Nem_3 | 133 | 138 | PF02991 | 0.362 |
LIG_LIR_Nem_3 | 175 | 180 | PF02991 | 0.347 |
LIG_LIR_Nem_3 | 53 | 57 | PF02991 | 0.325 |
LIG_NRBOX | 113 | 119 | PF00104 | 0.460 |
LIG_Pex14_1 | 317 | 321 | PF04695 | 0.328 |
LIG_Pex14_2 | 123 | 127 | PF04695 | 0.350 |
LIG_Pex14_2 | 272 | 276 | PF04695 | 0.493 |
LIG_PTB_Apo_2 | 157 | 164 | PF02174 | 0.345 |
LIG_SH2_CRK | 115 | 119 | PF00017 | 0.345 |
LIG_SH2_CRK | 28 | 32 | PF00017 | 0.422 |
LIG_SH2_CRK | 46 | 50 | PF00017 | 0.383 |
LIG_SH2_CRK | 71 | 75 | PF00017 | 0.466 |
LIG_SH2_NCK_1 | 71 | 75 | PF00017 | 0.552 |
LIG_SH2_STAP1 | 285 | 289 | PF00017 | 0.599 |
LIG_SH2_STAT3 | 235 | 238 | PF00017 | 0.324 |
LIG_SH2_STAT5 | 177 | 180 | PF00017 | 0.402 |
LIG_SH2_STAT5 | 205 | 208 | PF00017 | 0.369 |
LIG_SH2_STAT5 | 215 | 218 | PF00017 | 0.315 |
LIG_SH2_STAT5 | 235 | 238 | PF00017 | 0.298 |
LIG_SH2_STAT5 | 285 | 288 | PF00017 | 0.490 |
LIG_SH3_1 | 82 | 88 | PF00018 | 0.523 |
LIG_SH3_3 | 82 | 88 | PF00018 | 0.523 |
LIG_SUMO_SIM_par_1 | 136 | 141 | PF11976 | 0.407 |
LIG_WRC_WIRS_1 | 57 | 62 | PF05994 | 0.412 |
MOD_CDK_SPxK_1 | 27 | 33 | PF00069 | 0.308 |
MOD_CK1_1 | 11 | 17 | PF00069 | 0.683 |
MOD_CK1_1 | 141 | 147 | PF00069 | 0.404 |
MOD_CK1_1 | 20 | 26 | PF00069 | 0.511 |
MOD_CK1_1 | 210 | 216 | PF00069 | 0.351 |
MOD_CK2_1 | 107 | 113 | PF00069 | 0.460 |
MOD_GlcNHglycan | 10 | 13 | PF01048 | 0.745 |
MOD_GlcNHglycan | 140 | 143 | PF01048 | 0.404 |
MOD_GlcNHglycan | 224 | 227 | PF01048 | 0.491 |
MOD_GlcNHglycan | 34 | 37 | PF01048 | 0.431 |
MOD_GSK3_1 | 13 | 20 | PF00069 | 0.653 |
MOD_GSK3_1 | 180 | 187 | PF00069 | 0.392 |
MOD_GSK3_1 | 294 | 301 | PF00069 | 0.562 |
MOD_GSK3_1 | 4 | 11 | PF00069 | 0.717 |
MOD_GSK3_1 | 56 | 63 | PF00069 | 0.410 |
MOD_N-GLC_1 | 180 | 185 | PF02516 | 0.337 |
MOD_N-GLC_1 | 306 | 311 | PF02516 | 0.422 |
MOD_NEK2_1 | 118 | 123 | PF00069 | 0.324 |
MOD_NEK2_1 | 180 | 185 | PF00069 | 0.331 |
MOD_NEK2_1 | 252 | 257 | PF00069 | 0.326 |
MOD_PIKK_1 | 17 | 23 | PF00454 | 0.614 |
MOD_PIKK_1 | 184 | 190 | PF00454 | 0.203 |
MOD_PIKK_1 | 234 | 240 | PF00454 | 0.341 |
MOD_Plk_1 | 180 | 186 | PF00069 | 0.283 |
MOD_Plk_1 | 306 | 312 | PF00069 | 0.429 |
MOD_Plk_2-3 | 294 | 300 | PF00069 | 0.575 |
MOD_Plk_4 | 118 | 124 | PF00069 | 0.272 |
MOD_Plk_4 | 231 | 237 | PF00069 | 0.320 |
MOD_ProDKin_1 | 150 | 156 | PF00069 | 0.365 |
MOD_ProDKin_1 | 27 | 33 | PF00069 | 0.417 |
MOD_SUMO_for_1 | 305 | 308 | PF00179 | 0.517 |
MOD_SUMO_rev_2 | 76 | 85 | PF00179 | 0.506 |
TRG_DiLeu_BaEn_1 | 113 | 118 | PF01217 | 0.320 |
TRG_DiLeu_BaLyEn_6 | 153 | 158 | PF01217 | 0.203 |
TRG_ENDOCYTIC_2 | 115 | 118 | PF00928 | 0.345 |
TRG_ENDOCYTIC_2 | 177 | 180 | PF00928 | 0.396 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6J9 | Leptomonas seymouri | 36% | 88% |
A0A0N1I4D8 | Leptomonas seymouri | 71% | 96% |
A0A0S4INS4 | Bodo saltans | 39% | 100% |
A0A0S4KH88 | Bodo saltans | 35% | 82% |
A0A1X0NV84 | Trypanosomatidae | 51% | 100% |
A0A1X0P910 | Trypanosomatidae | 35% | 86% |
A0A3Q8IBA5 | Leishmania donovani | 79% | 100% |
A0A3Q8IJ21 | Leishmania donovani | 35% | 89% |
A0A3R7KCX0 | Trypanosoma rangeli | 36% | 89% |
A0A422MZR8 | Trypanosoma rangeli | 50% | 100% |
A4HUZ7 | Leishmania infantum | 79% | 78% |
A4I4Z0 | Leishmania infantum | 35% | 89% |
C9ZKK9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 88% |
D0A7F2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 44% | 100% |
E9AED5 | Leishmania major | 35% | 100% |
E9ALF1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 35% | 89% |
E9ANN2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 78% | 99% |
Q4QGZ1 | Leishmania major | 80% | 100% |
Q9JMD3 | Mus musculus | 33% | 100% |
Q9Y365 | Homo sapiens | 31% | 100% |
V5BC62 | Trypanosoma cruzi | 37% | 89% |
V5DT41 | Trypanosoma cruzi | 49% | 100% |