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: 5 |
NetGPI | no | yes: 0, no: 5 |
Related structures:
AlphaFold database: E9AM27
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 74 | 78 | PF00656 | 0.610 |
CLV_NRD_NRD_1 | 184 | 186 | PF00675 | 0.627 |
CLV_NRD_NRD_1 | 62 | 64 | PF00675 | 0.663 |
CLV_NRD_NRD_1 | 66 | 68 | PF00675 | 0.728 |
CLV_PCSK_KEX2_1 | 184 | 186 | PF00082 | 0.751 |
CLV_PCSK_KEX2_1 | 62 | 64 | PF00082 | 0.663 |
CLV_PCSK_SKI1_1 | 226 | 230 | PF00082 | 0.612 |
DEG_Nend_UBRbox_3 | 1 | 3 | PF02207 | 0.690 |
DEG_SPOP_SBC_1 | 129 | 133 | PF00917 | 0.587 |
DEG_SPOP_SBC_1 | 217 | 221 | PF00917 | 0.626 |
DOC_CDC14_PxL_1 | 137 | 145 | PF14671 | 0.627 |
DOC_CDC14_PxL_1 | 30 | 38 | PF14671 | 0.653 |
DOC_CYCLIN_RxL_1 | 223 | 232 | PF00134 | 0.608 |
DOC_CYCLIN_yCln2_LP_2 | 111 | 117 | PF00134 | 0.617 |
DOC_PP2B_LxvP_1 | 111 | 114 | PF13499 | 0.623 |
DOC_USP7_MATH_1 | 167 | 171 | PF00917 | 0.677 |
DOC_USP7_MATH_1 | 18 | 22 | PF00917 | 0.633 |
DOC_USP7_MATH_1 | 212 | 216 | PF00917 | 0.637 |
DOC_USP7_MATH_1 | 217 | 221 | PF00917 | 0.589 |
DOC_WW_Pin1_4 | 199 | 204 | PF00397 | 0.625 |
DOC_WW_Pin1_4 | 22 | 27 | PF00397 | 0.495 |
LIG_BRCT_BRCA1_1 | 220 | 224 | PF00533 | 0.602 |
LIG_Clathr_ClatBox_1 | 116 | 120 | PF01394 | 0.637 |
LIG_eIF4E_1 | 145 | 151 | PF01652 | 0.610 |
LIG_EVH1_1 | 208 | 212 | PF00568 | 0.578 |
LIG_EVH1_2 | 34 | 38 | PF00568 | 0.780 |
LIG_FHA_1 | 177 | 183 | PF00498 | 0.656 |
LIG_FHA_1 | 220 | 226 | PF00498 | 0.620 |
LIG_FHA_1 | 67 | 73 | PF00498 | 0.552 |
LIG_FHA_1 | 92 | 98 | PF00498 | 0.695 |
LIG_GSK3_LRP6_1 | 199 | 204 | PF00069 | 0.515 |
LIG_LIR_Gen_1 | 15 | 22 | PF02991 | 0.609 |
LIG_LIR_Gen_1 | 202 | 213 | PF02991 | 0.578 |
LIG_LIR_Nem_3 | 15 | 20 | PF02991 | 0.612 |
LIG_LIR_Nem_3 | 202 | 208 | PF02991 | 0.583 |
LIG_LIR_Nem_3 | 32 | 36 | PF02991 | 0.654 |
LIG_LYPXL_yS_3 | 33 | 36 | PF13949 | 0.654 |
LIG_SH2_NCK_1 | 145 | 149 | PF00017 | 0.497 |
LIG_SH2_SRC | 155 | 158 | PF00017 | 0.565 |
LIG_SH2_STAT5 | 155 | 158 | PF00017 | 0.575 |
LIG_SH2_STAT5 | 163 | 166 | PF00017 | 0.495 |
LIG_SH3_3 | 161 | 167 | PF00018 | 0.597 |
LIG_SH3_3 | 188 | 194 | PF00018 | 0.793 |
LIG_SH3_3 | 197 | 203 | PF00018 | 0.686 |
LIG_SH3_3 | 206 | 212 | PF00018 | 0.749 |
LIG_SH3_3 | 28 | 34 | PF00018 | 0.623 |
LIG_SUMO_SIM_par_1 | 39 | 48 | PF11976 | 0.493 |
LIG_TYR_ITIM | 31 | 36 | PF00017 | 0.654 |
MOD_CK1_1 | 12 | 18 | PF00069 | 0.580 |
MOD_CK1_1 | 131 | 137 | PF00069 | 0.513 |
MOD_CK1_1 | 219 | 225 | PF00069 | 0.618 |
MOD_CK1_1 | 43 | 49 | PF00069 | 0.697 |
MOD_CK2_1 | 171 | 177 | PF00069 | 0.810 |
MOD_Cter_Amidation | 60 | 63 | PF01082 | 0.686 |
MOD_Cter_Amidation | 65 | 68 | PF01082 | 0.690 |
MOD_GlcNHglycan | 146 | 149 | PF01048 | 0.514 |
MOD_GlcNHglycan | 158 | 161 | PF01048 | 0.723 |
MOD_GlcNHglycan | 174 | 177 | PF01048 | 0.675 |
MOD_GlcNHglycan | 77 | 81 | PF01048 | 0.604 |
MOD_GSK3_1 | 167 | 174 | PF00069 | 0.750 |
MOD_GSK3_1 | 18 | 25 | PF00069 | 0.523 |
MOD_GSK3_1 | 212 | 219 | PF00069 | 0.599 |
MOD_GSK3_1 | 39 | 46 | PF00069 | 0.738 |
MOD_GSK3_1 | 6 | 13 | PF00069 | 0.598 |
MOD_GSK3_1 | 66 | 73 | PF00069 | 0.813 |
MOD_LATS_1 | 142 | 148 | PF00433 | 0.475 |
MOD_NEK2_1 | 10 | 15 | PF00069 | 0.478 |
MOD_NEK2_1 | 128 | 133 | PF00069 | 0.520 |
MOD_NEK2_1 | 218 | 223 | PF00069 | 0.613 |
MOD_PIKK_1 | 66 | 72 | PF00454 | 0.697 |
MOD_PKA_2 | 66 | 72 | PF00069 | 0.647 |
MOD_Plk_1 | 18 | 24 | PF00069 | 0.636 |
MOD_Plk_1 | 39 | 45 | PF00069 | 0.600 |
MOD_Plk_1 | 90 | 96 | PF00069 | 0.611 |
MOD_Plk_4 | 12 | 18 | PF00069 | 0.654 |
MOD_Plk_4 | 40 | 46 | PF00069 | 0.491 |
MOD_ProDKin_1 | 199 | 205 | PF00069 | 0.626 |
MOD_ProDKin_1 | 22 | 28 | PF00069 | 0.497 |
MOD_SUMO_for_1 | 88 | 91 | PF00179 | 0.566 |
TRG_DiLeu_BaEn_1 | 146 | 151 | PF01217 | 0.578 |
TRG_DiLeu_BaEn_2 | 123 | 129 | PF01217 | 0.510 |
TRG_DiLeu_BaEn_3 | 39 | 45 | PF01217 | 0.489 |
TRG_DiLeu_BaEn_4 | 90 | 96 | PF01217 | 0.523 |
TRG_DiLeu_BaLyEn_6 | 111 | 116 | PF01217 | 0.664 |
TRG_ENDOCYTIC_2 | 33 | 36 | PF00928 | 0.654 |
TRG_ER_diArg_1 | 183 | 185 | PF00400 | 0.641 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3Q8IR44 | Leishmania donovani | 87% | 100% |
A4HH53 | Leishmania braziliensis | 63% | 95% |
A4I4A4 | Leishmania infantum | 87% | 100% |
E9ADQ3 | Leishmania major | 82% | 97% |