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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: A4H6N6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
DEG_SCF_FBW7_1 | 241 | 248 | PF00400 | 0.793 |
DEG_SPOP_SBC_1 | 134 | 138 | PF00917 | 0.609 |
DOC_PP2B_LxvP_1 | 190 | 193 | PF13499 | 0.490 |
DOC_PP4_FxxP_1 | 209 | 212 | PF00568 | 0.535 |
DOC_USP7_MATH_1 | 134 | 138 | PF00917 | 0.609 |
DOC_USP7_MATH_1 | 212 | 216 | PF00917 | 0.707 |
DOC_USP7_MATH_1 | 261 | 265 | PF00917 | 0.662 |
DOC_USP7_MATH_1 | 283 | 287 | PF00917 | 0.597 |
DOC_USP7_MATH_2 | 254 | 260 | PF00917 | 0.679 |
DOC_WW_Pin1_4 | 137 | 142 | PF00397 | 0.710 |
DOC_WW_Pin1_4 | 241 | 246 | PF00397 | 0.793 |
DOC_WW_Pin1_4 | 56 | 61 | PF00397 | 0.619 |
LIG_14-3-3_CanoR_1 | 189 | 193 | PF00244 | 0.749 |
LIG_14-3-3_CanoR_1 | 30 | 39 | PF00244 | 0.705 |
LIG_14-3-3_CanoR_1 | 48 | 58 | PF00244 | 0.479 |
LIG_Actin_WH2_2 | 176 | 191 | PF00022 | 0.722 |
LIG_Actin_WH2_2 | 303 | 321 | PF00022 | 0.625 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.516 |
LIG_BIR_III_2 | 227 | 231 | PF00653 | 0.521 |
LIG_BIR_III_4 | 216 | 220 | PF00653 | 0.542 |
LIG_BIR_III_4 | 7 | 11 | PF00653 | 0.437 |
LIG_BIR_III_4 | 78 | 82 | PF00653 | 0.573 |
LIG_BRCT_BRCA1_1 | 1 | 5 | PF00533 | 0.482 |
LIG_BRCT_BRCA1_1 | 166 | 170 | PF00533 | 0.645 |
LIG_Clathr_ClatBox_1 | 292 | 296 | PF01394 | 0.496 |
LIG_Clathr_ClatBox_1 | 3 | 7 | PF01394 | 0.464 |
LIG_FHA_1 | 104 | 110 | PF00498 | 0.489 |
LIG_FHA_1 | 311 | 317 | PF00498 | 0.457 |
LIG_FHA_1 | 33 | 39 | PF00498 | 0.452 |
LIG_FHA_1 | 53 | 59 | PF00498 | 0.478 |
LIG_FHA_1 | 80 | 86 | PF00498 | 0.568 |
LIG_FHA_2 | 171 | 177 | PF00498 | 0.612 |
LIG_GBD_Chelix_1 | 184 | 192 | PF00786 | 0.476 |
LIG_LIR_Apic_2 | 206 | 212 | PF02991 | 0.537 |
LIG_LIR_Apic_2 | 321 | 326 | PF02991 | 0.633 |
LIG_LIR_Gen_1 | 168 | 176 | PF02991 | 0.712 |
LIG_LIR_Gen_1 | 22 | 32 | PF02991 | 0.518 |
LIG_LIR_Nem_3 | 140 | 146 | PF02991 | 0.544 |
LIG_LIR_Nem_3 | 168 | 174 | PF02991 | 0.601 |
LIG_LIR_Nem_3 | 22 | 27 | PF02991 | 0.595 |
LIG_LIR_Nem_3 | 279 | 284 | PF02991 | 0.700 |
LIG_LYPXL_SIV_4 | 8 | 16 | PF13949 | 0.696 |
LIG_LYPXL_yS_3 | 143 | 146 | PF13949 | 0.484 |
LIG_PCNA_yPIPBox_3 | 67 | 75 | PF02747 | 0.490 |
LIG_PDZ_Class_2 | 322 | 327 | PF00595 | 0.640 |
LIG_SH2_CRK | 281 | 285 | PF00017 | 0.524 |
LIG_SH2_CRK | 323 | 327 | PF00017 | 0.641 |
LIG_SH2_NCK_1 | 281 | 285 | PF00017 | 0.782 |
LIG_SH2_SRC | 281 | 284 | PF00017 | 0.794 |
LIG_SH2_STAT5 | 323 | 326 | PF00017 | 0.516 |
LIG_SH2_STAT5 | 37 | 40 | PF00017 | 0.458 |
LIG_SH2_STAT5 | 92 | 95 | PF00017 | 0.619 |
LIG_SH3_3 | 138 | 144 | PF00018 | 0.715 |
LIG_SH3_3 | 243 | 249 | PF00018 | 0.606 |
LIG_SUMO_SIM_anti_2 | 157 | 162 | PF11976 | 0.586 |
LIG_SUMO_SIM_anti_2 | 311 | 319 | PF11976 | 0.627 |
LIG_SUMO_SIM_par_1 | 157 | 162 | PF11976 | 0.564 |
LIG_SUMO_SIM_par_1 | 197 | 204 | PF11976 | 0.527 |
LIG_WRC_WIRS_1 | 102 | 107 | PF05994 | 0.618 |
MOD_CK1_1 | 133 | 139 | PF00069 | 0.758 |
MOD_CK1_1 | 175 | 181 | PF00069 | 0.583 |
MOD_CK1_1 | 321 | 327 | PF00069 | 0.544 |
MOD_CK1_1 | 54 | 60 | PF00069 | 0.558 |
MOD_CK1_1 | 69 | 75 | PF00069 | 0.475 |
MOD_CK2_1 | 170 | 176 | PF00069 | 0.615 |
MOD_CK2_1 | 200 | 206 | PF00069 | 0.679 |
MOD_CK2_1 | 256 | 262 | PF00069 | 0.803 |
MOD_CK2_1 | 37 | 43 | PF00069 | 0.460 |
MOD_GlcNHglycan | 110 | 114 | PF01048 | 0.641 |
MOD_GlcNHglycan | 116 | 119 | PF01048 | 0.667 |
MOD_GlcNHglycan | 132 | 135 | PF01048 | 0.458 |
MOD_GlcNHglycan | 150 | 154 | PF01048 | 0.409 |
MOD_GlcNHglycan | 161 | 164 | PF01048 | 0.678 |
MOD_GlcNHglycan | 180 | 183 | PF01048 | 0.406 |
MOD_GlcNHglycan | 269 | 272 | PF01048 | 0.618 |
MOD_GlcNHglycan | 320 | 323 | PF01048 | 0.475 |
MOD_GSK3_1 | 130 | 137 | PF00069 | 0.676 |
MOD_GSK3_1 | 170 | 177 | PF00069 | 0.611 |
MOD_GSK3_1 | 188 | 195 | PF00069 | 0.648 |
MOD_GSK3_1 | 240 | 247 | PF00069 | 0.801 |
MOD_GSK3_1 | 283 | 290 | PF00069 | 0.502 |
MOD_GSK3_1 | 52 | 59 | PF00069 | 0.538 |
MOD_NEK2_1 | 109 | 114 | PF00069 | 0.544 |
MOD_NEK2_1 | 154 | 159 | PF00069 | 0.599 |
MOD_NEK2_1 | 164 | 169 | PF00069 | 0.548 |
MOD_NEK2_1 | 170 | 175 | PF00069 | 0.523 |
MOD_NEK2_1 | 188 | 193 | PF00069 | 0.487 |
MOD_NEK2_1 | 318 | 323 | PF00069 | 0.502 |
MOD_NEK2_1 | 32 | 37 | PF00069 | 0.535 |
MOD_NEK2_1 | 84 | 89 | PF00069 | 0.629 |
MOD_NEK2_1 | 93 | 98 | PF00069 | 0.601 |
MOD_PIKK_1 | 103 | 109 | PF00454 | 0.594 |
MOD_PKA_2 | 188 | 194 | PF00069 | 0.749 |
MOD_PKA_2 | 212 | 218 | PF00069 | 0.606 |
MOD_PKA_2 | 318 | 324 | PF00069 | 0.629 |
MOD_PKA_2 | 93 | 99 | PF00069 | 0.670 |
MOD_Plk_1 | 122 | 128 | PF00069 | 0.714 |
MOD_Plk_1 | 149 | 155 | PF00069 | 0.658 |
MOD_Plk_1 | 175 | 181 | PF00069 | 0.614 |
MOD_Plk_1 | 261 | 267 | PF00069 | 0.541 |
MOD_Plk_1 | 42 | 48 | PF00069 | 0.744 |
MOD_Plk_4 | 154 | 160 | PF00069 | 0.578 |
MOD_Plk_4 | 69 | 75 | PF00069 | 0.606 |
MOD_ProDKin_1 | 137 | 143 | PF00069 | 0.709 |
MOD_ProDKin_1 | 241 | 247 | PF00069 | 0.793 |
MOD_ProDKin_1 | 56 | 62 | PF00069 | 0.619 |
TRG_ENDOCYTIC_2 | 143 | 146 | PF00928 | 0.484 |
TRG_ENDOCYTIC_2 | 281 | 284 | PF00928 | 0.772 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1HZ79 | Leptomonas seymouri | 31% | 91% |
A0A3Q8I948 | Leishmania donovani | 62% | 97% |
A4HV20 | Leishmania infantum | 62% | 97% |
E8NHE2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 64% | 97% |
Q4QGW8 | Leishmania major | 63% | 100% |