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: E9AIF6
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 110 | 112 | PF00675 | 0.629 |
CLV_NRD_NRD_1 | 129 | 131 | PF00675 | 0.719 |
CLV_NRD_NRD_1 | 167 | 169 | PF00675 | 0.620 |
CLV_NRD_NRD_1 | 184 | 186 | PF00675 | 0.570 |
CLV_NRD_NRD_1 | 57 | 59 | PF00675 | 0.622 |
CLV_NRD_NRD_1 | 71 | 73 | PF00675 | 0.576 |
CLV_NRD_NRD_1 | 82 | 84 | PF00675 | 0.526 |
CLV_PCSK_FUR_1 | 165 | 169 | PF00082 | 0.575 |
CLV_PCSK_FUR_1 | 80 | 84 | PF00082 | 0.575 |
CLV_PCSK_KEX2_1 | 110 | 112 | PF00082 | 0.634 |
CLV_PCSK_KEX2_1 | 127 | 129 | PF00082 | 0.729 |
CLV_PCSK_KEX2_1 | 167 | 169 | PF00082 | 0.636 |
CLV_PCSK_KEX2_1 | 184 | 186 | PF00082 | 0.602 |
CLV_PCSK_KEX2_1 | 252 | 254 | PF00082 | 0.688 |
CLV_PCSK_KEX2_1 | 262 | 264 | PF00082 | 0.592 |
CLV_PCSK_KEX2_1 | 71 | 73 | PF00082 | 0.612 |
CLV_PCSK_KEX2_1 | 82 | 84 | PF00082 | 0.526 |
CLV_PCSK_PC1ET2_1 | 127 | 129 | PF00082 | 0.729 |
CLV_PCSK_PC1ET2_1 | 252 | 254 | PF00082 | 0.688 |
CLV_PCSK_PC1ET2_1 | 262 | 264 | PF00082 | 0.592 |
CLV_PCSK_PC7_1 | 180 | 186 | PF00082 | 0.567 |
CLV_PCSK_SKI1_1 | 124 | 128 | PF00082 | 0.716 |
CLV_PCSK_SKI1_1 | 224 | 228 | PF00082 | 0.580 |
CLV_PCSK_SKI1_1 | 58 | 62 | PF00082 | 0.650 |
DOC_CKS1_1 | 103 | 108 | PF01111 | 0.545 |
DOC_CKS1_1 | 138 | 143 | PF01111 | 0.576 |
DOC_CKS1_1 | 21 | 26 | PF01111 | 0.636 |
DOC_CYCLIN_yClb1_LxF_4 | 8 | 14 | PF00134 | 0.494 |
DOC_MAPK_gen_1 | 4 | 13 | PF00069 | 0.598 |
DOC_PP4_FxxP_1 | 147 | 150 | PF00568 | 0.559 |
DOC_PP4_FxxP_1 | 7 | 10 | PF00568 | 0.623 |
DOC_USP7_MATH_1 | 196 | 200 | PF00917 | 0.620 |
DOC_USP7_MATH_1 | 2 | 6 | PF00917 | 0.669 |
DOC_USP7_MATH_1 | 208 | 212 | PF00917 | 0.574 |
DOC_USP7_UBL2_3 | 113 | 117 | PF12436 | 0.733 |
DOC_USP7_UBL2_3 | 127 | 131 | PF12436 | 0.712 |
DOC_USP7_UBL2_3 | 239 | 243 | PF12436 | 0.690 |
DOC_USP7_UBL2_3 | 248 | 252 | PF12436 | 0.626 |
DOC_USP7_UBL2_3 | 41 | 45 | PF12436 | 0.457 |
DOC_WW_Pin1_4 | 102 | 107 | PF00397 | 0.554 |
DOC_WW_Pin1_4 | 137 | 142 | PF00397 | 0.662 |
DOC_WW_Pin1_4 | 153 | 158 | PF00397 | 0.581 |
DOC_WW_Pin1_4 | 170 | 175 | PF00397 | 0.564 |
DOC_WW_Pin1_4 | 20 | 25 | PF00397 | 0.646 |
DOC_WW_Pin1_4 | 95 | 100 | PF00397 | 0.630 |
LIG_14-3-3_CanoR_1 | 122 | 127 | PF00244 | 0.623 |
LIG_14-3-3_CanoR_1 | 167 | 174 | PF00244 | 0.591 |
LIG_14-3-3_CanoR_1 | 184 | 191 | PF00244 | 0.590 |
LIG_14-3-3_CanoR_1 | 201 | 208 | PF00244 | 0.592 |
LIG_14-3-3_CanoR_1 | 237 | 243 | PF00244 | 0.561 |
LIG_14-3-3_CanoR_1 | 58 | 64 | PF00244 | 0.488 |
LIG_FHA_1 | 242 | 248 | PF00498 | 0.592 |
LIG_FHA_2 | 21 | 27 | PF00498 | 0.633 |
LIG_GBD_Chelix_1 | 47 | 55 | PF00786 | 0.416 |
LIG_LIR_Apic_2 | 5 | 10 | PF02991 | 0.625 |
LIG_MYND_1 | 92 | 96 | PF01753 | 0.562 |
LIG_MYND_1 | 99 | 103 | PF01753 | 0.540 |
LIG_SH2_STAT3 | 84 | 87 | PF00017 | 0.578 |
LIG_SH3_1 | 100 | 106 | PF00018 | 0.727 |
LIG_SH3_2 | 106 | 111 | PF14604 | 0.512 |
LIG_SH3_2 | 132 | 137 | PF14604 | 0.536 |
LIG_SH3_2 | 78 | 83 | PF14604 | 0.573 |
LIG_SH3_2 | 92 | 97 | PF14604 | 0.530 |
LIG_SH3_3 | 100 | 106 | PF00018 | 0.712 |
LIG_SH3_3 | 129 | 135 | PF00018 | 0.533 |
LIG_SH3_3 | 154 | 160 | PF00018 | 0.603 |
LIG_SH3_3 | 230 | 236 | PF00018 | 0.756 |
LIG_SH3_3 | 64 | 70 | PF00018 | 0.561 |
LIG_SH3_3 | 72 | 78 | PF00018 | 0.599 |
LIG_SH3_3 | 89 | 95 | PF00018 | 0.688 |
LIG_SUMO_SIM_par_1 | 15 | 23 | PF11976 | 0.659 |
LIG_TRAF2_1 | 23 | 26 | PF00917 | 0.629 |
LIG_WW_3 | 107 | 111 | PF00397 | 0.550 |
LIG_WW_3 | 94 | 98 | PF00397 | 0.581 |
MOD_CDK_SPK_2 | 102 | 107 | PF00069 | 0.528 |
MOD_CDK_SPK_2 | 153 | 158 | PF00069 | 0.555 |
MOD_CDK_SPK_2 | 95 | 100 | PF00069 | 0.568 |
MOD_CDK_SPxK_1 | 170 | 176 | PF00069 | 0.562 |
MOD_CDK_SPxxK_3 | 20 | 27 | PF00069 | 0.637 |
MOD_CK1_1 | 115 | 121 | PF00069 | 0.761 |
MOD_CK1_1 | 199 | 205 | PF00069 | 0.552 |
MOD_CK2_1 | 12 | 18 | PF00069 | 0.660 |
MOD_CK2_1 | 20 | 26 | PF00069 | 0.549 |
MOD_Cter_Amidation | 213 | 216 | PF01082 | 0.632 |
MOD_Cter_Amidation | 260 | 263 | PF01082 | 0.623 |
MOD_DYRK1A_RPxSP_1 | 137 | 141 | PF00069 | 0.549 |
MOD_DYRK1A_RPxSP_1 | 153 | 157 | PF00069 | 0.509 |
MOD_GlcNHglycan | 114 | 117 | PF01048 | 0.590 |
MOD_GlcNHglycan | 177 | 180 | PF01048 | 0.590 |
MOD_GlcNHglycan | 212 | 215 | PF01048 | 0.572 |
MOD_GSK3_1 | 159 | 166 | PF00069 | 0.623 |
MOD_GSK3_1 | 196 | 203 | PF00069 | 0.537 |
MOD_GSK3_1 | 237 | 244 | PF00069 | 0.509 |
MOD_NEK2_1 | 183 | 188 | PF00069 | 0.624 |
MOD_NEK2_1 | 247 | 252 | PF00069 | 0.668 |
MOD_NEK2_2 | 238 | 243 | PF00069 | 0.509 |
MOD_PIKK_1 | 160 | 166 | PF00454 | 0.591 |
MOD_PIKK_1 | 83 | 89 | PF00454 | 0.578 |
MOD_PK_1 | 145 | 151 | PF00069 | 0.559 |
MOD_PKA_1 | 167 | 173 | PF00069 | 0.650 |
MOD_PKA_1 | 71 | 77 | PF00069 | 0.562 |
MOD_PKA_2 | 167 | 173 | PF00069 | 0.644 |
MOD_PKA_2 | 175 | 181 | PF00069 | 0.643 |
MOD_PKA_2 | 183 | 189 | PF00069 | 0.560 |
MOD_PKA_2 | 200 | 206 | PF00069 | 0.585 |
MOD_PKA_2 | 208 | 214 | PF00069 | 0.564 |
MOD_PKA_2 | 71 | 77 | PF00069 | 0.588 |
MOD_PKB_1 | 120 | 128 | PF00069 | 0.543 |
MOD_PKB_1 | 165 | 173 | PF00069 | 0.567 |
MOD_PKB_1 | 235 | 243 | PF00069 | 0.512 |
MOD_Plk_4 | 228 | 234 | PF00069 | 0.691 |
MOD_ProDKin_1 | 102 | 108 | PF00069 | 0.552 |
MOD_ProDKin_1 | 137 | 143 | PF00069 | 0.662 |
MOD_ProDKin_1 | 153 | 159 | PF00069 | 0.580 |
MOD_ProDKin_1 | 170 | 176 | PF00069 | 0.567 |
MOD_ProDKin_1 | 20 | 26 | PF00069 | 0.640 |
MOD_ProDKin_1 | 95 | 101 | PF00069 | 0.630 |
MOD_SUMO_for_1 | 116 | 119 | PF00179 | 0.694 |
MOD_SUMO_rev_2 | 39 | 47 | PF00179 | 0.408 |
MOD_SUMO_rev_2 | 54 | 60 | PF00179 | 0.398 |
TRG_ER_diArg_1 | 109 | 111 | PF00400 | 0.656 |
TRG_ER_diArg_1 | 120 | 123 | PF00400 | 0.575 |
TRG_ER_diArg_1 | 165 | 168 | PF00400 | 0.667 |
TRG_ER_diArg_1 | 183 | 185 | PF00400 | 0.619 |
TRG_ER_diArg_1 | 234 | 237 | PF00400 | 0.541 |
TRG_ER_diArg_1 | 3 | 6 | PF00400 | 0.607 |
TRG_ER_diArg_1 | 70 | 72 | PF00400 | 0.725 |
TRG_ER_diArg_1 | 80 | 83 | PF00400 | 0.540 |
TRG_NLS_Bipartite_1 | 110 | 131 | PF00514 | 0.550 |
TRG_NLS_Bipartite_1 | 248 | 266 | PF00514 | 0.516 |
TRG_NLS_MonoCore_2 | 129 | 134 | PF00514 | 0.535 |
TRG_NLS_MonoExtC_3 | 126 | 131 | PF00514 | 0.721 |
TRG_NLS_MonoExtC_3 | 247 | 252 | PF00514 | 0.511 |
TRG_NLS_MonoExtN_4 | 124 | 131 | PF00514 | 0.717 |
TRG_NLS_MonoExtN_4 | 246 | 252 | PF00514 | 0.542 |
TRG_NLS_MonoExtN_4 | 259 | 266 | PF00514 | 0.507 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A3S7WW27 | Leishmania donovani | 53% | 97% |
A4HYU9 | Leishmania infantum | 53% | 97% |
E9AUP6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 51% | 97% |
Q4QCT9 | Leishmania major | 54% | 100% |