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:0016020 | membrane | 2 | 10 |
GO:0110165 | cellular anatomical entity | 1 | 10 |
Related structures:
AlphaFold database: A4H8G9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 55 | 57 | PF00675 | 0.347 |
CLV_PCSK_KEX2_1 | 145 | 147 | PF00082 | 0.424 |
CLV_PCSK_PC1ET2_1 | 145 | 147 | PF00082 | 0.424 |
CLV_PCSK_SKI1_1 | 122 | 126 | PF00082 | 0.374 |
CLV_PCSK_SKI1_1 | 17 | 21 | PF00082 | 0.477 |
DEG_APCC_DBOX_1 | 154 | 162 | PF00400 | 0.334 |
DEG_Nend_Nbox_1 | 1 | 3 | PF02207 | 0.678 |
DEG_SCF_FBW7_1 | 94 | 101 | PF00400 | 0.501 |
DOC_MAPK_MEF2A_6 | 155 | 163 | PF00069 | 0.419 |
DOC_MAPK_MEF2A_6 | 4 | 13 | PF00069 | 0.664 |
DOC_USP7_MATH_1 | 185 | 189 | PF00917 | 0.327 |
DOC_USP7_MATH_1 | 25 | 29 | PF00917 | 0.651 |
DOC_WW_Pin1_4 | 144 | 149 | PF00397 | 0.472 |
DOC_WW_Pin1_4 | 94 | 99 | PF00397 | 0.479 |
LIG_14-3-3_CanoR_1 | 32 | 40 | PF00244 | 0.692 |
LIG_14-3-3_CanoR_1 | 86 | 91 | PF00244 | 0.490 |
LIG_BRCT_BRCA1_1 | 36 | 40 | PF00533 | 0.575 |
LIG_DLG_GKlike_1 | 86 | 94 | PF00625 | 0.490 |
LIG_FHA_1 | 232 | 238 | PF00498 | 0.314 |
LIG_FHA_1 | 8 | 14 | PF00498 | 0.649 |
LIG_FHA_1 | 99 | 105 | PF00498 | 0.425 |
LIG_FHA_2 | 114 | 120 | PF00498 | 0.515 |
LIG_FHA_2 | 145 | 151 | PF00498 | 0.441 |
LIG_FHA_2 | 228 | 234 | PF00498 | 0.390 |
LIG_FHA_2 | 76 | 82 | PF00498 | 0.592 |
LIG_LIR_Apic_2 | 42 | 47 | PF02991 | 0.696 |
LIG_LIR_Gen_1 | 160 | 171 | PF02991 | 0.307 |
LIG_LIR_Gen_1 | 223 | 231 | PF02991 | 0.337 |
LIG_LIR_Gen_1 | 78 | 88 | PF02991 | 0.573 |
LIG_LIR_Nem_3 | 109 | 114 | PF02991 | 0.496 |
LIG_LIR_Nem_3 | 160 | 166 | PF02991 | 0.420 |
LIG_LIR_Nem_3 | 193 | 198 | PF02991 | 0.351 |
LIG_LIR_Nem_3 | 78 | 83 | PF02991 | 0.595 |
LIG_PDZ_Class_2 | 253 | 258 | PF00595 | 0.419 |
LIG_Pex14_2 | 40 | 44 | PF04695 | 0.555 |
LIG_SH2_CRK | 195 | 199 | PF00017 | 0.327 |
LIG_SH2_STAP1 | 100 | 104 | PF00017 | 0.561 |
LIG_SH2_STAT5 | 100 | 103 | PF00017 | 0.479 |
LIG_SH2_STAT5 | 107 | 110 | PF00017 | 0.454 |
LIG_SH3_3 | 161 | 167 | PF00018 | 0.369 |
LIG_SH3_3 | 19 | 25 | PF00018 | 0.656 |
LIG_SH3_3 | 234 | 240 | PF00018 | 0.297 |
LIG_SUMO_SIM_anti_2 | 101 | 106 | PF11976 | 0.434 |
LIG_SUMO_SIM_anti_2 | 116 | 122 | PF11976 | 0.432 |
LIG_SUMO_SIM_par_1 | 251 | 257 | PF11976 | 0.195 |
LIG_TRFH_1 | 163 | 167 | PF08558 | 0.195 |
LIG_TYR_ITIM | 105 | 110 | PF00017 | 0.567 |
LIG_TYR_ITIM | 134 | 139 | PF00017 | 0.523 |
LIG_UBA3_1 | 124 | 133 | PF00899 | 0.485 |
LIG_UBA3_1 | 139 | 145 | PF00899 | 0.493 |
LIG_WRC_WIRS_1 | 228 | 233 | PF05994 | 0.226 |
MOD_CK1_1 | 200 | 206 | PF00069 | 0.451 |
MOD_CK1_1 | 27 | 33 | PF00069 | 0.691 |
MOD_CK1_1 | 35 | 41 | PF00069 | 0.657 |
MOD_CK2_1 | 113 | 119 | PF00069 | 0.508 |
MOD_CK2_1 | 144 | 150 | PF00069 | 0.535 |
MOD_CK2_1 | 227 | 233 | PF00069 | 0.359 |
MOD_CK2_1 | 86 | 92 | PF00069 | 0.501 |
MOD_GlcNHglycan | 200 | 203 | PF01048 | 0.658 |
MOD_GlcNHglycan | 27 | 30 | PF01048 | 0.531 |
MOD_GlcNHglycan | 37 | 40 | PF01048 | 0.439 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.372 |
MOD_GlcNHglycan | 41 | 44 | PF01048 | 0.389 |
MOD_GSK3_1 | 180 | 187 | PF00069 | 0.304 |
MOD_GSK3_1 | 196 | 203 | PF00069 | 0.424 |
MOD_GSK3_1 | 227 | 234 | PF00069 | 0.335 |
MOD_GSK3_1 | 23 | 30 | PF00069 | 0.699 |
MOD_GSK3_1 | 35 | 42 | PF00069 | 0.622 |
MOD_GSK3_1 | 94 | 101 | PF00069 | 0.493 |
MOD_LATS_1 | 84 | 90 | PF00433 | 0.495 |
MOD_N-GLC_1 | 33 | 38 | PF02516 | 0.379 |
MOD_NEK2_1 | 13 | 18 | PF00069 | 0.680 |
MOD_NEK2_1 | 170 | 175 | PF00069 | 0.346 |
MOD_NEK2_1 | 198 | 203 | PF00069 | 0.422 |
MOD_NEK2_1 | 231 | 236 | PF00069 | 0.404 |
MOD_NEK2_1 | 62 | 67 | PF00069 | 0.551 |
MOD_NEK2_2 | 227 | 232 | PF00069 | 0.343 |
MOD_PIKK_1 | 231 | 237 | PF00454 | 0.271 |
MOD_PKA_2 | 13 | 19 | PF00069 | 0.768 |
MOD_Plk_4 | 49 | 55 | PF00069 | 0.661 |
MOD_Plk_4 | 68 | 74 | PF00069 | 0.460 |
MOD_ProDKin_1 | 144 | 150 | PF00069 | 0.471 |
MOD_ProDKin_1 | 94 | 100 | PF00069 | 0.484 |
TRG_ENDOCYTIC_2 | 107 | 110 | PF00928 | 0.576 |
TRG_ENDOCYTIC_2 | 136 | 139 | PF00928 | 0.531 |
TRG_ENDOCYTIC_2 | 195 | 198 | PF00928 | 0.329 |
TRG_ENDOCYTIC_2 | 225 | 228 | PF00928 | 0.324 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I779 | Leptomonas seymouri | 55% | 100% |
A0A0S4JEF8 | Bodo saltans | 39% | 100% |
A0A1X0NHP7 | Trypanosomatidae | 46% | 100% |
A0A3S7WTT8 | Leishmania donovani | 85% | 100% |
A0A422N958 | Trypanosoma rangeli | 45% | 100% |
A4HWU3 | Leishmania infantum | 85% | 100% |
C9ZW39 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 41% | 100% |
E9AQK3 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |
Q4QEX5 | Leishmania major | 84% | 100% |
V5D515 | Trypanosoma cruzi | 42% | 100% |