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: E9ACF0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 208 | 210 | PF00675 | 0.528 |
CLV_NRD_NRD_1 | 236 | 238 | PF00675 | 0.574 |
CLV_NRD_NRD_1 | 92 | 94 | PF00675 | 0.625 |
CLV_PCSK_KEX2_1 | 158 | 160 | PF00082 | 0.348 |
CLV_PCSK_KEX2_1 | 208 | 210 | PF00082 | 0.490 |
CLV_PCSK_KEX2_1 | 236 | 238 | PF00082 | 0.580 |
CLV_PCSK_KEX2_1 | 34 | 36 | PF00082 | 0.600 |
CLV_PCSK_KEX2_1 | 94 | 96 | PF00082 | 0.617 |
CLV_PCSK_PC1ET2_1 | 158 | 160 | PF00082 | 0.348 |
CLV_PCSK_PC1ET2_1 | 34 | 36 | PF00082 | 0.660 |
CLV_PCSK_PC1ET2_1 | 94 | 96 | PF00082 | 0.617 |
CLV_PCSK_SKI1_1 | 208 | 212 | PF00082 | 0.475 |
DEG_APCC_DBOX_1 | 198 | 206 | PF00400 | 0.570 |
DEG_SPOP_SBC_1 | 67 | 71 | PF00917 | 0.654 |
DOC_MAPK_DCC_7 | 8 | 17 | PF00069 | 0.525 |
DOC_MAPK_gen_1 | 240 | 249 | PF00069 | 0.632 |
DOC_MAPK_gen_1 | 8 | 14 | PF00069 | 0.531 |
DOC_MAPK_MEF2A_6 | 8 | 17 | PF00069 | 0.502 |
DOC_PP1_SILK_1 | 84 | 89 | PF00149 | 0.515 |
DOC_PP4_FxxP_1 | 211 | 214 | PF00568 | 0.459 |
DOC_USP7_MATH_1 | 170 | 174 | PF00917 | 0.568 |
DOC_USP7_MATH_1 | 46 | 50 | PF00917 | 0.656 |
DOC_USP7_MATH_1 | 67 | 71 | PF00917 | 0.693 |
DOC_USP7_MATH_1 | 76 | 80 | PF00917 | 0.575 |
DOC_USP7_UBL2_3 | 154 | 158 | PF12436 | 0.589 |
DOC_WW_Pin1_4 | 190 | 195 | PF00397 | 0.502 |
DOC_WW_Pin1_4 | 238 | 243 | PF00397 | 0.599 |
DOC_WW_Pin1_4 | 258 | 263 | PF00397 | 0.687 |
DOC_WW_Pin1_4 | 72 | 77 | PF00397 | 0.768 |
LIG_14-3-3_CanoR_1 | 24 | 33 | PF00244 | 0.644 |
LIG_14-3-3_CanoR_1 | 95 | 102 | PF00244 | 0.674 |
LIG_BRCT_BRCA1_1 | 128 | 132 | PF00533 | 0.635 |
LIG_deltaCOP1_diTrp_1 | 203 | 211 | PF00928 | 0.495 |
LIG_deltaCOP1_diTrp_1 | 52 | 62 | PF00928 | 0.503 |
LIG_EH1_1 | 225 | 233 | PF00400 | 0.497 |
LIG_eIF4E_1 | 131 | 137 | PF01652 | 0.578 |
LIG_FHA_1 | 151 | 157 | PF00498 | 0.498 |
LIG_FHA_1 | 170 | 176 | PF00498 | 0.265 |
LIG_FHA_1 | 187 | 193 | PF00498 | 0.226 |
LIG_GBD_Chelix_1 | 252 | 260 | PF00786 | 0.489 |
LIG_LIR_Gen_1 | 133 | 142 | PF02991 | 0.452 |
LIG_LIR_Gen_1 | 16 | 21 | PF02991 | 0.467 |
LIG_LIR_Gen_1 | 203 | 211 | PF02991 | 0.416 |
LIG_LIR_Nem_3 | 128 | 134 | PF02991 | 0.490 |
LIG_LIR_Nem_3 | 16 | 20 | PF02991 | 0.467 |
LIG_LIR_Nem_3 | 203 | 207 | PF02991 | 0.398 |
LIG_LIR_Nem_3 | 241 | 247 | PF02991 | 0.607 |
LIG_LIR_Nem_3 | 52 | 58 | PF02991 | 0.626 |
LIG_MLH1_MIPbox_1 | 128 | 132 | PF16413 | 0.635 |
LIG_MYND_3 | 12 | 16 | PF01753 | 0.586 |
LIG_PDZ_Class_3 | 263 | 268 | PF00595 | 0.695 |
LIG_SH2_PTP2 | 167 | 170 | PF00017 | 0.552 |
LIG_SH2_STAP1 | 68 | 72 | PF00017 | 0.638 |
LIG_SH2_STAT5 | 131 | 134 | PF00017 | 0.480 |
LIG_SH2_STAT5 | 167 | 170 | PF00017 | 0.411 |
LIG_SUMO_SIM_par_1 | 179 | 184 | PF11976 | 0.497 |
LIG_SUMO_SIM_par_1 | 187 | 193 | PF11976 | 0.510 |
MOD_CDC14_SPxK_1 | 193 | 196 | PF00782 | 0.537 |
MOD_CDK_SPK_2 | 238 | 243 | PF00069 | 0.643 |
MOD_CDK_SPxK_1 | 190 | 196 | PF00069 | 0.515 |
MOD_CK1_1 | 119 | 125 | PF00069 | 0.628 |
MOD_CK1_1 | 184 | 190 | PF00069 | 0.514 |
MOD_CK1_1 | 258 | 264 | PF00069 | 0.647 |
MOD_CK1_1 | 71 | 77 | PF00069 | 0.763 |
MOD_CK2_1 | 46 | 52 | PF00069 | 0.725 |
MOD_CK2_1 | 95 | 101 | PF00069 | 0.726 |
MOD_GlcNHglycan | 109 | 112 | PF01048 | 0.628 |
MOD_GlcNHglycan | 48 | 51 | PF01048 | 0.701 |
MOD_GlcNHglycan | 76 | 79 | PF01048 | 0.751 |
MOD_GSK3_1 | 170 | 177 | PF00069 | 0.483 |
MOD_GSK3_1 | 186 | 193 | PF00069 | 0.266 |
MOD_GSK3_1 | 238 | 245 | PF00069 | 0.639 |
MOD_GSK3_1 | 254 | 261 | PF00069 | 0.631 |
MOD_GSK3_1 | 67 | 74 | PF00069 | 0.770 |
MOD_GSK3_1 | 82 | 89 | PF00069 | 0.514 |
MOD_NEK2_1 | 132 | 137 | PF00069 | 0.518 |
MOD_NEK2_1 | 256 | 261 | PF00069 | 0.618 |
MOD_PIKK_1 | 24 | 30 | PF00454 | 0.607 |
MOD_PKA_1 | 93 | 99 | PF00069 | 0.671 |
MOD_PKB_1 | 93 | 101 | PF00069 | 0.642 |
MOD_Plk_1 | 132 | 138 | PF00069 | 0.499 |
MOD_Plk_1 | 181 | 187 | PF00069 | 0.553 |
MOD_Plk_4 | 170 | 176 | PF00069 | 0.488 |
MOD_Plk_4 | 186 | 192 | PF00069 | 0.307 |
MOD_Plk_4 | 82 | 88 | PF00069 | 0.754 |
MOD_ProDKin_1 | 190 | 196 | PF00069 | 0.515 |
MOD_ProDKin_1 | 238 | 244 | PF00069 | 0.594 |
MOD_ProDKin_1 | 258 | 264 | PF00069 | 0.688 |
MOD_ProDKin_1 | 72 | 78 | PF00069 | 0.769 |
MOD_SUMO_for_1 | 42 | 45 | PF00179 | 0.733 |
TRG_DiLeu_BaEn_2 | 15 | 21 | PF01217 | 0.565 |
TRG_DiLeu_BaLyEn_6 | 10 | 15 | PF01217 | 0.550 |
TRG_ENDOCYTIC_2 | 131 | 134 | PF00928 | 0.480 |
TRG_ER_diArg_1 | 207 | 209 | PF00400 | 0.515 |
TRG_ER_diArg_1 | 29 | 32 | PF00400 | 0.546 |
TRG_ER_diArg_1 | 92 | 95 | PF00400 | 0.627 |
TRG_NLS_MonoExtC_3 | 92 | 97 | PF00514 | 0.722 |
TRG_NLS_MonoExtN_4 | 93 | 98 | PF00514 | 0.682 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1P9W5 | Leptomonas seymouri | 45% | 100% |
A0A1X0P8M5 | Trypanosomatidae | 29% | 100% |
A0A3R7KU56 | Trypanosoma rangeli | 29% | 100% |
A0A3S5H519 | Leishmania donovani | 89% | 100% |
A4H3H5 | Leishmania braziliensis | 74% | 100% |
E9AG22 | Leishmania infantum | 90% | 100% |
E9AJN8 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 100% |
V5ANT9 | Trypanosoma cruzi | 31% | 100% |