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: E9AUV3
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 145 | 149 | PF00656 | 0.474 |
CLV_PCSK_KEX2_1 | 110 | 112 | PF00082 | 0.465 |
CLV_PCSK_KEX2_1 | 243 | 245 | PF00082 | 0.586 |
CLV_PCSK_PC1ET2_1 | 110 | 112 | PF00082 | 0.500 |
CLV_PCSK_PC1ET2_1 | 243 | 245 | PF00082 | 0.586 |
CLV_PCSK_SKI1_1 | 150 | 154 | PF00082 | 0.620 |
CLV_Separin_Metazoa | 55 | 59 | PF03568 | 0.606 |
DOC_MAPK_gen_1 | 95 | 104 | PF00069 | 0.479 |
DOC_MAPK_MEF2A_6 | 205 | 214 | PF00069 | 0.396 |
DOC_USP7_MATH_1 | 139 | 143 | PF00917 | 0.765 |
DOC_USP7_MATH_1 | 229 | 233 | PF00917 | 0.530 |
DOC_USP7_UBL2_3 | 93 | 97 | PF12436 | 0.482 |
DOC_WW_Pin1_4 | 64 | 69 | PF00397 | 0.557 |
DOC_WW_Pin1_4 | 9 | 14 | PF00397 | 0.647 |
LIG_14-3-3_CanoR_1 | 111 | 117 | PF00244 | 0.452 |
LIG_14-3-3_CanoR_1 | 16 | 24 | PF00244 | 0.615 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.529 |
LIG_FHA_1 | 52 | 58 | PF00498 | 0.541 |
LIG_FHA_1 | 70 | 76 | PF00498 | 0.670 |
LIG_FHA_2 | 158 | 164 | PF00498 | 0.739 |
LIG_FHA_2 | 25 | 31 | PF00498 | 0.516 |
LIG_Integrin_isoDGR_2 | 203 | 205 | PF01839 | 0.540 |
LIG_LIR_Nem_3 | 40 | 45 | PF02991 | 0.442 |
LIG_Pex14_2 | 108 | 112 | PF04695 | 0.397 |
LIG_RPA_C_Fungi | 232 | 244 | PF08784 | 0.578 |
LIG_SH2_CRK | 45 | 49 | PF00017 | 0.429 |
LIG_SH2_GRB2like | 219 | 222 | PF00017 | 0.477 |
LIG_SH2_NCK_1 | 45 | 49 | PF00017 | 0.429 |
LIG_SH2_PTP2 | 208 | 211 | PF00017 | 0.361 |
LIG_SH2_SRC | 208 | 211 | PF00017 | 0.493 |
LIG_SH2_SRC | 219 | 222 | PF00017 | 0.533 |
LIG_SH2_STAP1 | 219 | 223 | PF00017 | 0.530 |
LIG_SH2_STAT3 | 41 | 44 | PF00017 | 0.508 |
LIG_SH2_STAT5 | 208 | 211 | PF00017 | 0.361 |
LIG_SH2_STAT5 | 42 | 45 | PF00017 | 0.427 |
LIG_SH3_3 | 125 | 131 | PF00018 | 0.593 |
LIG_SH3_3 | 132 | 138 | PF00018 | 0.741 |
LIG_SH3_3 | 184 | 190 | PF00018 | 0.581 |
LIG_SH3_3 | 209 | 215 | PF00018 | 0.404 |
LIG_SH3_3 | 65 | 71 | PF00018 | 0.596 |
LIG_SUMO_SIM_anti_2 | 119 | 125 | PF11976 | 0.419 |
LIG_SUMO_SIM_anti_2 | 222 | 227 | PF11976 | 0.475 |
LIG_SUMO_SIM_par_1 | 210 | 218 | PF11976 | 0.398 |
LIG_TRAF2_1 | 215 | 218 | PF00917 | 0.476 |
MOD_CDK_SPxxK_3 | 9 | 16 | PF00069 | 0.684 |
MOD_CK1_1 | 12 | 18 | PF00069 | 0.562 |
MOD_CK1_1 | 142 | 148 | PF00069 | 0.622 |
MOD_CK1_1 | 154 | 160 | PF00069 | 0.691 |
MOD_CK1_1 | 2 | 8 | PF00069 | 0.594 |
MOD_CK2_1 | 229 | 235 | PF00069 | 0.478 |
MOD_GlcNHglycan | 144 | 147 | PF01048 | 0.769 |
MOD_GlcNHglycan | 153 | 156 | PF01048 | 0.723 |
MOD_GlcNHglycan | 175 | 178 | PF01048 | 0.474 |
MOD_GlcNHglycan | 184 | 187 | PF01048 | 0.615 |
MOD_GlcNHglycan | 4 | 7 | PF01048 | 0.631 |
MOD_GlcNHglycan | 76 | 80 | PF01048 | 0.613 |
MOD_GSK3_1 | 11 | 18 | PF00069 | 0.599 |
MOD_GSK3_1 | 112 | 119 | PF00069 | 0.426 |
MOD_GSK3_1 | 150 | 157 | PF00069 | 0.663 |
MOD_GSK3_1 | 20 | 27 | PF00069 | 0.591 |
MOD_GSK3_1 | 229 | 236 | PF00069 | 0.560 |
MOD_GSK3_1 | 47 | 54 | PF00069 | 0.521 |
MOD_N-GLC_1 | 112 | 117 | PF02516 | 0.440 |
MOD_N-GLC_1 | 139 | 144 | PF02516 | 0.785 |
MOD_N-GLC_1 | 20 | 25 | PF02516 | 0.602 |
MOD_NEK2_1 | 112 | 117 | PF00069 | 0.421 |
MOD_NEK2_1 | 166 | 171 | PF00069 | 0.279 |
MOD_NEK2_1 | 199 | 204 | PF00069 | 0.380 |
MOD_PK_1 | 58 | 64 | PF00069 | 0.603 |
MOD_PKA_2 | 15 | 21 | PF00069 | 0.475 |
MOD_PKA_2 | 157 | 163 | PF00069 | 0.533 |
MOD_Plk_1 | 112 | 118 | PF00069 | 0.426 |
MOD_Plk_1 | 179 | 185 | PF00069 | 0.410 |
MOD_Plk_1 | 20 | 26 | PF00069 | 0.637 |
MOD_Plk_1 | 58 | 64 | PF00069 | 0.472 |
MOD_Plk_4 | 229 | 235 | PF00069 | 0.554 |
MOD_ProDKin_1 | 64 | 70 | PF00069 | 0.563 |
MOD_ProDKin_1 | 9 | 15 | PF00069 | 0.645 |
TRG_DiLeu_BaLyEn_6 | 100 | 105 | PF01217 | 0.495 |
TRG_ENDOCYTIC_2 | 208 | 211 | PF00928 | 0.361 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I0J0 | Leptomonas seymouri | 74% | 82% |
A0A1X0NWJ0 | Trypanosomatidae | 53% | 90% |
A0A3Q8IKS5 | Leishmania donovani | 95% | 100% |
A0A422NTQ6 | Trypanosoma rangeli | 55% | 91% |
A4HZ01 | Leishmania infantum | 94% | 100% |
C9ZIM2 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 52% | 91% |
E9AIM0 | Leishmania braziliensis | 84% | 100% |
Q4QCN0 | Leishmania major | 95% | 100% |
V5B8D6 | Trypanosoma cruzi | 53% | 90% |