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: E9AJH2
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
DEG_SPOP_SBC_1 | 118 | 122 | PF00917 | 0.304 |
DOC_USP7_MATH_1 | 2 | 6 | PF00917 | 0.520 |
DOC_WW_Pin1_4 | 59 | 64 | PF00397 | 0.535 |
LIG_14-3-3_CanoR_1 | 30 | 34 | PF00244 | 0.667 |
LIG_14-3-3_CanoR_1 | 64 | 69 | PF00244 | 0.443 |
LIG_14-3-3_CanoR_1 | 88 | 97 | PF00244 | 0.526 |
LIG_Clathr_ClatBox_1 | 96 | 100 | PF01394 | 0.556 |
LIG_FHA_1 | 138 | 144 | PF00498 | 0.392 |
LIG_FHA_1 | 202 | 208 | PF00498 | 0.435 |
LIG_FHA_1 | 4 | 10 | PF00498 | 0.438 |
LIG_FHA_2 | 20 | 26 | PF00498 | 0.396 |
LIG_GBD_Chelix_1 | 127 | 135 | PF00786 | 0.380 |
LIG_LIR_Gen_1 | 41 | 50 | PF02991 | 0.438 |
LIG_LIR_Nem_3 | 167 | 173 | PF02991 | 0.469 |
LIG_LIR_Nem_3 | 176 | 182 | PF02991 | 0.446 |
LIG_LIR_Nem_3 | 41 | 47 | PF02991 | 0.442 |
LIG_LIR_Nem_3 | 52 | 57 | PF02991 | 0.426 |
LIG_Pex14_2 | 164 | 168 | PF04695 | 0.459 |
LIG_Pex14_2 | 50 | 54 | PF04695 | 0.494 |
LIG_SH2_CRK | 179 | 183 | PF00017 | 0.342 |
LIG_SH2_GRB2like | 142 | 145 | PF00017 | 0.439 |
LIG_SH2_STAP1 | 175 | 179 | PF00017 | 0.343 |
LIG_SH2_STAT5 | 142 | 145 | PF00017 | 0.308 |
LIG_SH3_3 | 6 | 12 | PF00018 | 0.475 |
LIG_Sin3_3 | 170 | 177 | PF02671 | 0.228 |
LIG_TRAF2_1 | 33 | 36 | PF00917 | 0.353 |
MOD_CDK_SPK_2 | 59 | 64 | PF00069 | 0.276 |
MOD_CK1_1 | 114 | 120 | PF00069 | 0.443 |
MOD_CK1_1 | 90 | 96 | PF00069 | 0.533 |
MOD_CK2_1 | 19 | 25 | PF00069 | 0.397 |
MOD_CK2_1 | 29 | 35 | PF00069 | 0.511 |
MOD_GlcNHglycan | 116 | 119 | PF01048 | 0.322 |
MOD_GlcNHglycan | 31 | 34 | PF01048 | 0.603 |
MOD_GlcNHglycan | 82 | 85 | PF01048 | 0.545 |
MOD_GSK3_1 | 110 | 117 | PF00069 | 0.561 |
MOD_GSK3_1 | 87 | 94 | PF00069 | 0.526 |
MOD_N-GLC_1 | 111 | 116 | PF02516 | 0.575 |
MOD_N-GLC_1 | 64 | 69 | PF02516 | 0.507 |
MOD_NEK2_1 | 119 | 124 | PF00069 | 0.376 |
MOD_NEK2_1 | 164 | 169 | PF00069 | 0.393 |
MOD_NEK2_1 | 89 | 94 | PF00069 | 0.564 |
MOD_PIKK_1 | 121 | 127 | PF00454 | 0.439 |
MOD_PIKK_1 | 91 | 97 | PF00454 | 0.496 |
MOD_PK_1 | 64 | 70 | PF00069 | 0.369 |
MOD_PKA_2 | 29 | 35 | PF00069 | 0.662 |
MOD_PKA_2 | 87 | 93 | PF00069 | 0.524 |
MOD_Plk_1 | 111 | 117 | PF00069 | 0.530 |
MOD_Plk_1 | 175 | 181 | PF00069 | 0.349 |
MOD_Plk_1 | 64 | 70 | PF00069 | 0.502 |
MOD_Plk_2-3 | 19 | 25 | PF00069 | 0.397 |
MOD_Plk_4 | 137 | 143 | PF00069 | 0.409 |
MOD_ProDKin_1 | 59 | 65 | PF00069 | 0.550 |
TRG_DiLeu_BaEn_1 | 35 | 40 | PF01217 | 0.307 |
TRG_DiLeu_BaLyEn_6 | 151 | 156 | PF01217 | 0.394 |
TRG_DiLeu_BaLyEn_6 | 177 | 182 | PF01217 | 0.282 |
TRG_ENDOCYTIC_2 | 15 | 18 | PF00928 | 0.309 |
TRG_ENDOCYTIC_2 | 179 | 182 | PF00928 | 0.340 |
TRG_Pf-PMV_PEXEL_1 | 180 | 184 | PF00026 | 0.457 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IJ46 | Leptomonas seymouri | 48% | 100% |
A0A1X0NKM1 | Trypanosomatidae | 35% | 100% |
A0A422N6X4 | Trypanosoma rangeli | 30% | 100% |
A0A451EJE3 | Leishmania donovani | 86% | 100% |
A4H3A2 | Leishmania braziliensis | 77% | 100% |
A4HRK8 | Leishmania infantum | 86% | 100% |
C9ZIZ7 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 32% | 100% |
E9AC80 | Leishmania major | 86% | 100% |
V5BFA7 | Trypanosoma cruzi | 32% | 100% |