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: E9APN5
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 110 | 112 | PF00675 | 0.700 |
CLV_NRD_NRD_1 | 161 | 163 | PF00675 | 0.467 |
CLV_PCSK_KEX2_1 | 109 | 111 | PF00082 | 0.714 |
CLV_PCSK_KEX2_1 | 161 | 163 | PF00082 | 0.467 |
CLV_PCSK_SKI1_1 | 161 | 165 | PF00082 | 0.533 |
CLV_PCSK_SKI1_1 | 176 | 180 | PF00082 | 0.573 |
CLV_Separin_Metazoa | 89 | 93 | PF03568 | 0.471 |
DEG_SPOP_SBC_1 | 72 | 76 | PF00917 | 0.655 |
DOC_PP2B_LxvP_1 | 136 | 139 | PF13499 | 0.644 |
DOC_USP7_MATH_1 | 117 | 121 | PF00917 | 0.730 |
DOC_USP7_MATH_1 | 63 | 67 | PF00917 | 0.678 |
DOC_USP7_MATH_1 | 72 | 76 | PF00917 | 0.626 |
DOC_WW_Pin1_4 | 121 | 126 | PF00397 | 0.601 |
LIG_14-3-3_CanoR_1 | 176 | 184 | PF00244 | 0.363 |
LIG_14-3-3_CanoR_1 | 47 | 52 | PF00244 | 0.443 |
LIG_14-3-3_CanoR_1 | 92 | 100 | PF00244 | 0.602 |
LIG_Actin_WH2_2 | 12 | 30 | PF00022 | 0.598 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.478 |
LIG_BIR_III_1 | 1 | 5 | PF00653 | 0.478 |
LIG_BIR_III_2 | 52 | 56 | PF00653 | 0.587 |
LIG_BIR_III_3 | 1 | 5 | PF00653 | 0.478 |
LIG_BRCT_BRCA1_1 | 133 | 137 | PF00533 | 0.576 |
LIG_FHA_1 | 177 | 183 | PF00498 | 0.522 |
LIG_FHA_1 | 74 | 80 | PF00498 | 0.725 |
LIG_FHA_2 | 80 | 86 | PF00498 | 0.510 |
LIG_LIR_Nem_3 | 158 | 163 | PF02991 | 0.525 |
LIG_SH2_CRK | 160 | 164 | PF00017 | 0.531 |
LIG_SH2_STAT5 | 144 | 147 | PF00017 | 0.600 |
LIG_SH3_3 | 135 | 141 | PF00018 | 0.710 |
LIG_SUMO_SIM_par_1 | 101 | 106 | PF11976 | 0.603 |
LIG_SUMO_SIM_par_1 | 62 | 68 | PF11976 | 0.609 |
MOD_CK1_1 | 131 | 137 | PF00069 | 0.713 |
MOD_CK1_1 | 33 | 39 | PF00069 | 0.439 |
MOD_CK1_1 | 71 | 77 | PF00069 | 0.736 |
MOD_CK1_1 | 84 | 90 | PF00069 | 0.568 |
MOD_CK2_1 | 74 | 80 | PF00069 | 0.684 |
MOD_GlcNHglycan | 105 | 108 | PF01048 | 0.598 |
MOD_GlcNHglycan | 150 | 153 | PF01048 | 0.487 |
MOD_GlcNHglycan | 24 | 27 | PF01048 | 0.605 |
MOD_GlcNHglycan | 70 | 73 | PF01048 | 0.655 |
MOD_GlcNHglycan | 76 | 79 | PF01048 | 0.696 |
MOD_GlcNHglycan | 95 | 98 | PF01048 | 0.478 |
MOD_GSK3_1 | 117 | 124 | PF00069 | 0.528 |
MOD_GSK3_1 | 143 | 150 | PF00069 | 0.579 |
MOD_GSK3_1 | 53 | 60 | PF00069 | 0.702 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.473 |
MOD_NEK2_1 | 32 | 37 | PF00069 | 0.542 |
MOD_NEK2_1 | 67 | 72 | PF00069 | 0.550 |
MOD_PIKK_1 | 117 | 123 | PF00454 | 0.816 |
MOD_PIKK_1 | 170 | 176 | PF00454 | 0.318 |
MOD_PIKK_1 | 65 | 71 | PF00454 | 0.559 |
MOD_PKB_1 | 45 | 53 | PF00069 | 0.433 |
MOD_Plk_2-3 | 81 | 87 | PF00069 | 0.504 |
MOD_ProDKin_1 | 121 | 127 | PF00069 | 0.600 |
TRG_ENDOCYTIC_2 | 160 | 163 | PF00928 | 0.527 |
TRG_ER_diArg_1 | 109 | 111 | PF00400 | 0.539 |
TRG_ER_diArg_1 | 160 | 162 | PF00400 | 0.485 |
TRG_ER_diArg_1 | 45 | 48 | PF00400 | 0.415 |
TRG_ER_FFAT_2 | 29 | 40 | PF00635 | 0.431 |
TRG_Pf-PMV_PEXEL_1 | 176 | 180 | PF00026 | 0.628 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PAD9 | Leptomonas seymouri | 46% | 100% |
A0A1X0NP94 | Trypanosomatidae | 28% | 85% |
A0A3Q8I9Q7 | Leishmania donovani | 81% | 100% |
A4H7K0 | Leishmania braziliensis | 71% | 100% |
A4HVY3 | Leishmania infantum | 81% | 100% |
Q4QFU4 | Leishmania major | 83% | 99% |