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: 9 |
NetGPI | no | yes: 0, no: 9 |
Related structures:
AlphaFold database: A4HTC9
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 166 | 170 | PF00656 | 0.482 |
CLV_C14_Caspase3-7 | 93 | 97 | PF00656 | 0.589 |
CLV_NRD_NRD_1 | 85 | 87 | PF00675 | 0.645 |
CLV_PCSK_KEX2_1 | 29 | 31 | PF00082 | 0.553 |
CLV_PCSK_KEX2_1 | 316 | 318 | PF00082 | 0.411 |
CLV_PCSK_KEX2_1 | 85 | 87 | PF00082 | 0.655 |
CLV_PCSK_PC1ET2_1 | 29 | 31 | PF00082 | 0.426 |
CLV_PCSK_PC1ET2_1 | 316 | 318 | PF00082 | 0.502 |
CLV_PCSK_SKI1_1 | 196 | 200 | PF00082 | 0.467 |
CLV_PCSK_SKI1_1 | 269 | 273 | PF00082 | 0.488 |
CLV_PCSK_SKI1_1 | 313 | 317 | PF00082 | 0.536 |
DOC_CYCLIN_RxL_1 | 266 | 276 | PF00134 | 0.505 |
DOC_CYCLIN_yCln2_LP_2 | 46 | 52 | PF00134 | 0.463 |
DOC_PP2B_LxvP_1 | 10 | 13 | PF13499 | 0.592 |
DOC_PP2B_LxvP_1 | 56 | 59 | PF13499 | 0.431 |
DOC_PP4_FxxP_1 | 134 | 137 | PF00568 | 0.573 |
DOC_USP7_MATH_1 | 11 | 15 | PF00917 | 0.708 |
DOC_USP7_MATH_1 | 179 | 183 | PF00917 | 0.525 |
DOC_USP7_MATH_1 | 198 | 202 | PF00917 | 0.522 |
DOC_USP7_MATH_1 | 208 | 212 | PF00917 | 0.431 |
DOC_USP7_MATH_1 | 229 | 233 | PF00917 | 0.679 |
DOC_USP7_MATH_1 | 34 | 38 | PF00917 | 0.558 |
DOC_WW_Pin1_4 | 133 | 138 | PF00397 | 0.579 |
DOC_WW_Pin1_4 | 14 | 19 | PF00397 | 0.740 |
LIG_14-3-3_CanoR_1 | 206 | 215 | PF00244 | 0.544 |
LIG_14-3-3_CanoR_1 | 86 | 92 | PF00244 | 0.608 |
LIG_APCC_ABBA_1 | 290 | 295 | PF00400 | 0.378 |
LIG_BRCT_BRCA1_1 | 34 | 38 | PF00533 | 0.606 |
LIG_deltaCOP1_diTrp_1 | 244 | 251 | PF00928 | 0.446 |
LIG_FHA_1 | 189 | 195 | PF00498 | 0.553 |
LIG_FHA_1 | 295 | 301 | PF00498 | 0.496 |
LIG_FHA_1 | 98 | 104 | PF00498 | 0.385 |
LIG_FHA_2 | 197 | 203 | PF00498 | 0.439 |
LIG_FHA_2 | 304 | 310 | PF00498 | 0.593 |
LIG_FHA_2 | 91 | 97 | PF00498 | 0.606 |
LIG_LIR_Apic_2 | 132 | 137 | PF02991 | 0.294 |
LIG_LIR_Gen_1 | 117 | 127 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 117 | 122 | PF02991 | 0.451 |
LIG_NRBOX | 266 | 272 | PF00104 | 0.388 |
LIG_PCNA_PIPBox_1 | 161 | 170 | PF02747 | 0.458 |
LIG_PCNA_yPIPBox_3 | 61 | 75 | PF02747 | 0.512 |
LIG_SH2_SRC | 213 | 216 | PF00017 | 0.390 |
LIG_SH2_STAT5 | 213 | 216 | PF00017 | 0.491 |
LIG_SH3_3 | 171 | 177 | PF00018 | 0.536 |
LIG_WRC_WIRS_1 | 164 | 169 | PF05994 | 0.536 |
MOD_CDK_SPK_2 | 14 | 19 | PF00069 | 0.648 |
MOD_CK1_1 | 14 | 20 | PF00069 | 0.740 |
MOD_CK1_1 | 200 | 206 | PF00069 | 0.566 |
MOD_CK1_1 | 280 | 286 | PF00069 | 0.574 |
MOD_CK1_1 | 32 | 38 | PF00069 | 0.552 |
MOD_CK1_1 | 5 | 11 | PF00069 | 0.578 |
MOD_CK1_1 | 90 | 96 | PF00069 | 0.635 |
MOD_CK2_1 | 196 | 202 | PF00069 | 0.468 |
MOD_CK2_1 | 303 | 309 | PF00069 | 0.480 |
MOD_CK2_1 | 34 | 40 | PF00069 | 0.432 |
MOD_GlcNHglycan | 119 | 122 | PF01048 | 0.443 |
MOD_GlcNHglycan | 14 | 17 | PF01048 | 0.730 |
MOD_GlcNHglycan | 210 | 213 | PF01048 | 0.441 |
MOD_GlcNHglycan | 281 | 285 | PF01048 | 0.587 |
MOD_GlcNHglycan | 31 | 34 | PF01048 | 0.597 |
MOD_GlcNHglycan | 7 | 10 | PF01048 | 0.744 |
MOD_GSK3_1 | 117 | 124 | PF00069 | 0.422 |
MOD_GSK3_1 | 129 | 136 | PF00069 | 0.447 |
MOD_GSK3_1 | 196 | 203 | PF00069 | 0.569 |
MOD_GSK3_1 | 29 | 36 | PF00069 | 0.618 |
MOD_N-GLC_1 | 5 | 10 | PF02516 | 0.729 |
MOD_NEK2_1 | 2 | 7 | PF00069 | 0.554 |
MOD_PIKK_1 | 260 | 266 | PF00454 | 0.501 |
MOD_PKA_1 | 29 | 35 | PF00069 | 0.412 |
MOD_PKA_1 | 85 | 91 | PF00069 | 0.620 |
MOD_PKA_2 | 2 | 8 | PF00069 | 0.715 |
MOD_PKA_2 | 29 | 35 | PF00069 | 0.533 |
MOD_PKA_2 | 85 | 91 | PF00069 | 0.620 |
MOD_Plk_1 | 294 | 300 | PF00069 | 0.485 |
MOD_Plk_2-3 | 163 | 169 | PF00069 | 0.483 |
MOD_Plk_4 | 108 | 114 | PF00069 | 0.468 |
MOD_Plk_4 | 129 | 135 | PF00069 | 0.608 |
MOD_Plk_4 | 163 | 169 | PF00069 | 0.430 |
MOD_Plk_4 | 200 | 206 | PF00069 | 0.468 |
MOD_Plk_4 | 34 | 40 | PF00069 | 0.527 |
MOD_Plk_4 | 51 | 57 | PF00069 | 0.485 |
MOD_ProDKin_1 | 133 | 139 | PF00069 | 0.571 |
MOD_ProDKin_1 | 14 | 20 | PF00069 | 0.739 |
TRG_DiLeu_BaEn_1 | 310 | 315 | PF01217 | 0.432 |
TRG_DiLeu_BaEn_2 | 162 | 168 | PF01217 | 0.455 |
TRG_Pf-PMV_PEXEL_1 | 69 | 73 | PF00026 | 0.508 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PBF0 | Leptomonas seymouri | 50% | 71% |
A0A1X0NPV5 | Trypanosomatidae | 36% | 95% |
A0A3R7RGL1 | Trypanosoma rangeli | 36% | 100% |
A0A3S7WQ08 | Leishmania donovani | 99% | 100% |
E9AI29 | Leishmania braziliensis | 79% | 100% |
E9ALC2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 88% | 100% |
Q4QII3 | Leishmania major | 91% | 100% |
V5BYB8 | Trypanosoma cruzi | 36% | 100% |