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: 4 |
NetGPI | no | yes: 0, no: 4 |
Related structures:
AlphaFold database: A4IAU6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 133 | 135 | PF00675 | 0.699 |
CLV_NRD_NRD_1 | 146 | 148 | PF00675 | 0.681 |
CLV_PCSK_KEX2_1 | 133 | 135 | PF00082 | 0.699 |
CLV_PCSK_KEX2_1 | 146 | 148 | PF00082 | 0.687 |
CLV_PCSK_KEX2_1 | 166 | 168 | PF00082 | 0.679 |
CLV_PCSK_PC1ET2_1 | 166 | 168 | PF00082 | 0.731 |
CLV_PCSK_SKI1_1 | 161 | 165 | PF00082 | 0.633 |
CLV_PCSK_SKI1_1 | 88 | 92 | PF00082 | 0.291 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.662 |
DOC_CYCLIN_yCln2_LP_2 | 14 | 20 | PF00134 | 0.626 |
DOC_MAPK_gen_1 | 88 | 94 | PF00069 | 0.530 |
DOC_PP2B_LxvP_1 | 14 | 17 | PF13499 | 0.679 |
DOC_PP4_FxxP_1 | 107 | 110 | PF00568 | 0.509 |
DOC_USP7_MATH_1 | 188 | 192 | PF00917 | 0.452 |
DOC_USP7_MATH_2 | 50 | 56 | PF00917 | 0.636 |
DOC_WW_Pin1_4 | 190 | 195 | PF00397 | 0.533 |
DOC_WW_Pin1_4 | 20 | 25 | PF00397 | 0.692 |
DOC_WW_Pin1_4 | 61 | 66 | PF00397 | 0.656 |
LIG_14-3-3_CanoR_1 | 10 | 15 | PF00244 | 0.740 |
LIG_14-3-3_CanoR_1 | 190 | 194 | PF00244 | 0.447 |
LIG_Actin_WH2_2 | 93 | 111 | PF00022 | 0.272 |
LIG_FHA_1 | 103 | 109 | PF00498 | 0.345 |
LIG_FHA_1 | 176 | 182 | PF00498 | 0.459 |
LIG_FHA_1 | 49 | 55 | PF00498 | 0.687 |
LIG_FHA_2 | 175 | 181 | PF00498 | 0.436 |
LIG_LIR_Apic_2 | 105 | 110 | PF02991 | 0.506 |
LIG_LIR_Apic_2 | 132 | 138 | PF02991 | 0.466 |
LIG_SH2_CRK | 115 | 119 | PF00017 | 0.412 |
LIG_SH2_SRC | 135 | 138 | PF00017 | 0.469 |
LIG_SH2_STAP1 | 115 | 119 | PF00017 | 0.412 |
LIG_SH2_STAT5 | 106 | 109 | PF00017 | 0.664 |
LIG_SH2_STAT5 | 115 | 118 | PF00017 | 0.420 |
LIG_SH2_STAT5 | 135 | 138 | PF00017 | 0.521 |
LIG_SH3_3 | 191 | 197 | PF00018 | 0.527 |
LIG_SH3_3 | 44 | 50 | PF00018 | 0.643 |
LIG_SH3_3 | 64 | 70 | PF00018 | 0.678 |
LIG_SUMO_SIM_anti_2 | 74 | 81 | PF11976 | 0.607 |
LIG_TRFH_1 | 106 | 110 | PF08558 | 0.509 |
LIG_TYR_ITIM | 113 | 118 | PF00017 | 0.407 |
LIG_UBA3_1 | 80 | 89 | PF00899 | 0.564 |
LIG_WRC_WIRS_1 | 114 | 119 | PF05994 | 0.415 |
MOD_CDK_SPxxK_3 | 20 | 27 | PF00069 | 0.686 |
MOD_CK1_1 | 121 | 127 | PF00069 | 0.410 |
MOD_CK1_1 | 142 | 148 | PF00069 | 0.484 |
MOD_CK1_1 | 172 | 178 | PF00069 | 0.509 |
MOD_CK1_1 | 31 | 37 | PF00069 | 0.705 |
MOD_CK1_1 | 98 | 104 | PF00069 | 0.272 |
MOD_CK2_1 | 174 | 180 | PF00069 | 0.434 |
MOD_CK2_1 | 20 | 26 | PF00069 | 0.682 |
MOD_DYRK1A_RPxSP_1 | 190 | 194 | PF00069 | 0.447 |
MOD_GlcNHglycan | 10 | 13 | PF01048 | 0.550 |
MOD_GlcNHglycan | 120 | 123 | PF01048 | 0.576 |
MOD_GlcNHglycan | 148 | 151 | PF01048 | 0.718 |
MOD_GlcNHglycan | 155 | 158 | PF01048 | 0.706 |
MOD_GlcNHglycan | 33 | 36 | PF01048 | 0.593 |
MOD_GlcNHglycan | 37 | 40 | PF01048 | 0.579 |
MOD_GlcNHglycan | 54 | 57 | PF01048 | 0.479 |
MOD_GSK3_1 | 113 | 120 | PF00069 | 0.358 |
MOD_GSK3_1 | 121 | 128 | PF00069 | 0.399 |
MOD_GSK3_1 | 142 | 149 | PF00069 | 0.481 |
MOD_GSK3_1 | 153 | 160 | PF00069 | 0.417 |
MOD_GSK3_1 | 16 | 23 | PF00069 | 0.683 |
MOD_GSK3_1 | 172 | 179 | PF00069 | 0.471 |
MOD_GSK3_1 | 29 | 36 | PF00069 | 0.675 |
MOD_GSK3_1 | 48 | 55 | PF00069 | 0.600 |
MOD_GSK3_1 | 95 | 102 | PF00069 | 0.272 |
MOD_LATS_1 | 137 | 143 | PF00433 | 0.446 |
MOD_NEK2_1 | 117 | 122 | PF00069 | 0.326 |
MOD_NEK2_1 | 151 | 156 | PF00069 | 0.466 |
MOD_NEK2_1 | 29 | 34 | PF00069 | 0.711 |
MOD_NEK2_1 | 99 | 104 | PF00069 | 0.276 |
MOD_PIKK_1 | 108 | 114 | PF00454 | 0.415 |
MOD_PKA_1 | 146 | 152 | PF00069 | 0.526 |
MOD_PKA_2 | 108 | 114 | PF00069 | 0.394 |
MOD_PKA_2 | 146 | 152 | PF00069 | 0.526 |
MOD_PKA_2 | 183 | 189 | PF00069 | 0.556 |
MOD_Plk_4 | 10 | 16 | PF00069 | 0.754 |
MOD_Plk_4 | 102 | 108 | PF00069 | 0.320 |
MOD_Plk_4 | 113 | 119 | PF00069 | 0.322 |
MOD_Plk_4 | 121 | 127 | PF00069 | 0.394 |
MOD_Plk_4 | 95 | 101 | PF00069 | 0.320 |
MOD_ProDKin_1 | 190 | 196 | PF00069 | 0.532 |
MOD_ProDKin_1 | 20 | 26 | PF00069 | 0.692 |
MOD_ProDKin_1 | 61 | 67 | PF00069 | 0.655 |
TRG_DiLeu_BaEn_1 | 74 | 79 | PF01217 | 0.590 |
TRG_DiLeu_BaEn_2 | 86 | 92 | PF01217 | 0.602 |
TRG_DiLeu_BaLyEn_6 | 73 | 78 | PF01217 | 0.669 |
TRG_ENDOCYTIC_2 | 115 | 118 | PF00928 | 0.467 |
TRG_ER_diArg_1 | 133 | 135 | PF00400 | 0.455 |
TRG_ER_diArg_1 | 146 | 148 | PF00400 | 0.413 |
TRG_NES_CRM1_1 | 75 | 87 | PF08389 | 0.577 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7X8T7 | Leishmania donovani | 100% | 91% |
A4HM82 | Leishmania braziliensis | 47% | 100% |
E9AEM4 | Leishmania major | 79% | 100% |