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: 7 |
NetGPI | no | yes: 0, no: 7 |
Related structures:
AlphaFold database: A0A3S7XB92
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 100 | 102 | PF00675 | 0.805 |
CLV_NRD_NRD_1 | 76 | 78 | PF00675 | 0.620 |
CLV_PCSK_KEX2_1 | 147 | 149 | PF00082 | 0.357 |
CLV_PCSK_KEX2_1 | 185 | 187 | PF00082 | 0.430 |
CLV_PCSK_KEX2_1 | 57 | 59 | PF00082 | 0.707 |
CLV_PCSK_KEX2_1 | 98 | 100 | PF00082 | 0.691 |
CLV_PCSK_PC1ET2_1 | 147 | 149 | PF00082 | 0.357 |
CLV_PCSK_PC1ET2_1 | 185 | 187 | PF00082 | 0.515 |
CLV_PCSK_PC1ET2_1 | 57 | 59 | PF00082 | 0.745 |
CLV_PCSK_PC1ET2_1 | 98 | 100 | PF00082 | 0.691 |
CLV_PCSK_SKI1_1 | 147 | 151 | PF00082 | 0.376 |
CLV_PCSK_SKI1_1 | 77 | 81 | PF00082 | 0.569 |
DEG_SPOP_SBC_1 | 109 | 113 | PF00917 | 0.723 |
DOC_USP7_MATH_1 | 109 | 113 | PF00917 | 0.669 |
DOC_USP7_MATH_1 | 121 | 125 | PF00917 | 0.477 |
DOC_USP7_MATH_1 | 79 | 83 | PF00917 | 0.581 |
DOC_USP7_UBL2_3 | 74 | 78 | PF12436 | 0.592 |
LIG_14-3-3_CanoR_1 | 173 | 178 | PF00244 | 0.501 |
LIG_BRCT_BRCA1_1 | 137 | 141 | PF00533 | 0.501 |
LIG_FHA_1 | 124 | 130 | PF00498 | 0.637 |
LIG_FHA_1 | 14 | 20 | PF00498 | 0.622 |
LIG_FHA_1 | 40 | 46 | PF00498 | 0.518 |
LIG_PDZ_Class_2 | 204 | 209 | PF00595 | 0.376 |
LIG_SUMO_SIM_anti_2 | 41 | 47 | PF11976 | 0.544 |
LIG_TRAF2_1 | 105 | 108 | PF00917 | 0.614 |
LIG_TRAF2_1 | 161 | 164 | PF00917 | 0.326 |
LIG_TRAF2_1 | 35 | 38 | PF00917 | 0.636 |
LIG_WRC_WIRS_1 | 1 | 6 | PF05994 | 0.600 |
MOD_CK1_1 | 111 | 117 | PF00069 | 0.700 |
MOD_CK1_1 | 124 | 130 | PF00069 | 0.629 |
MOD_CK1_1 | 84 | 90 | PF00069 | 0.702 |
MOD_CK2_1 | 102 | 108 | PF00069 | 0.606 |
MOD_CK2_1 | 177 | 183 | PF00069 | 0.397 |
MOD_CK2_1 | 190 | 196 | PF00069 | 0.333 |
MOD_CK2_1 | 62 | 68 | PF00069 | 0.630 |
MOD_Cter_Amidation | 202 | 205 | PF01082 | 0.376 |
MOD_GlcNHglycan | 122 | 126 | PF01048 | 0.689 |
MOD_GlcNHglycan | 83 | 86 | PF01048 | 0.711 |
MOD_GSK3_1 | 107 | 114 | PF00069 | 0.690 |
MOD_GSK3_1 | 117 | 124 | PF00069 | 0.510 |
MOD_GSK3_1 | 169 | 176 | PF00069 | 0.388 |
MOD_GSK3_1 | 99 | 106 | PF00069 | 0.768 |
MOD_LATS_1 | 171 | 177 | PF00433 | 0.501 |
MOD_NEK2_1 | 177 | 182 | PF00069 | 0.501 |
MOD_NEK2_1 | 197 | 202 | PF00069 | 0.171 |
MOD_PIKK_1 | 190 | 196 | PF00454 | 0.444 |
MOD_PIKK_1 | 62 | 68 | PF00454 | 0.643 |
MOD_PKA_1 | 99 | 105 | PF00069 | 0.729 |
MOD_PKA_2 | 115 | 121 | PF00069 | 0.584 |
MOD_PKA_2 | 99 | 105 | PF00069 | 0.741 |
MOD_Plk_2-3 | 103 | 109 | PF00069 | 0.592 |
MOD_SUMO_rev_2 | 139 | 149 | PF00179 | 0.426 |
MOD_SUMO_rev_2 | 180 | 187 | PF00179 | 0.501 |
TRG_DiLeu_BaLyEn_6 | 46 | 51 | PF01217 | 0.591 |
TRG_ER_diArg_1 | 99 | 101 | PF00400 | 0.809 |
TRG_NES_CRM1_1 | 38 | 52 | PF08389 | 0.590 |
TRG_NLS_MonoCore_2 | 97 | 102 | PF00514 | 0.727 |
TRG_NLS_MonoExtC_3 | 97 | 103 | PF00514 | 0.731 |
TRG_NLS_MonoExtN_4 | 97 | 102 | PF00514 | 0.736 |
TRG_Pf-PMV_PEXEL_1 | 49 | 53 | PF00026 | 0.543 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PDM8 | Leptomonas seymouri | 55% | 100% |
A0A1X0P3N2 | Trypanosomatidae | 37% | 100% |
A4HPL5 | Leishmania braziliensis | 74% | 100% |
A4ID49 | Leishmania infantum | 100% | 100% |
E9ATC7 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
Q4Q170 | Leishmania major | 89% | 100% |