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: 6 |
NetGPI | no | yes: 0, no: 6 |
Related structures:
AlphaFold database: E9AIS4
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 100 | 102 | PF00675 | 0.585 |
CLV_NRD_NRD_1 | 59 | 61 | PF00675 | 0.391 |
CLV_NRD_NRD_1 | 96 | 98 | PF00675 | 0.619 |
CLV_PCSK_KEX2_1 | 58 | 60 | PF00082 | 0.405 |
CLV_PCSK_KEX2_1 | 96 | 98 | PF00082 | 0.626 |
CLV_PCSK_SKI1_1 | 17 | 21 | PF00082 | 0.633 |
CLV_PCSK_SKI1_1 | 170 | 174 | PF00082 | 0.618 |
CLV_PCSK_SKI1_1 | 205 | 209 | PF00082 | 0.600 |
DOC_USP7_MATH_1 | 141 | 145 | PF00917 | 0.574 |
DOC_USP7_MATH_1 | 147 | 151 | PF00917 | 0.577 |
DOC_USP7_MATH_1 | 39 | 43 | PF00917 | 0.529 |
DOC_USP7_MATH_1 | 48 | 52 | PF00917 | 0.706 |
DOC_USP7_MATH_1 | 80 | 84 | PF00917 | 0.556 |
DOC_WW_Pin1_4 | 19 | 24 | PF00397 | 0.566 |
LIG_14-3-3_CanoR_1 | 134 | 138 | PF00244 | 0.729 |
LIG_14-3-3_CanoR_1 | 17 | 23 | PF00244 | 0.632 |
LIG_14-3-3_CanoR_1 | 37 | 47 | PF00244 | 0.481 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.527 |
LIG_BIR_III_4 | 140 | 144 | PF00653 | 0.673 |
LIG_FHA_1 | 146 | 152 | PF00498 | 0.528 |
LIG_FHA_1 | 30 | 36 | PF00498 | 0.572 |
LIG_FHA_2 | 113 | 119 | PF00498 | 0.510 |
LIG_FHA_2 | 155 | 161 | PF00498 | 0.482 |
LIG_FHA_2 | 180 | 186 | PF00498 | 0.607 |
LIG_LIR_Nem_3 | 110 | 116 | PF02991 | 0.611 |
LIG_SH2_CRK | 113 | 117 | PF00017 | 0.651 |
LIG_SH2_STAT5 | 226 | 229 | PF00017 | 0.560 |
LIG_SH2_STAT5 | 240 | 243 | PF00017 | 0.541 |
LIG_SH3_3 | 100 | 106 | PF00018 | 0.585 |
LIG_WRC_WIRS_1 | 188 | 193 | PF05994 | 0.615 |
MOD_CK1_1 | 18 | 24 | PF00069 | 0.604 |
MOD_CK1_1 | 187 | 193 | PF00069 | 0.646 |
MOD_CK1_1 | 29 | 35 | PF00069 | 0.678 |
MOD_CK1_1 | 38 | 44 | PF00069 | 0.567 |
MOD_CK1_1 | 51 | 57 | PF00069 | 0.567 |
MOD_CK2_1 | 179 | 185 | PF00069 | 0.608 |
MOD_GlcNHglycan | 1 | 4 | PF01048 | 0.525 |
MOD_GlcNHglycan | 140 | 144 | PF01048 | 0.728 |
MOD_GlcNHglycan | 37 | 40 | PF01048 | 0.628 |
MOD_GSK3_1 | 141 | 148 | PF00069 | 0.572 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.701 |
MOD_GSK3_1 | 187 | 194 | PF00069 | 0.674 |
MOD_GSK3_1 | 26 | 33 | PF00069 | 0.491 |
MOD_GSK3_1 | 35 | 42 | PF00069 | 0.469 |
MOD_N-GLC_1 | 15 | 20 | PF02516 | 0.521 |
MOD_NEK2_1 | 132 | 137 | PF00069 | 0.728 |
MOD_NEK2_1 | 189 | 194 | PF00069 | 0.592 |
MOD_NEK2_2 | 147 | 152 | PF00069 | 0.513 |
MOD_PIKK_1 | 122 | 128 | PF00454 | 0.533 |
MOD_PKA_2 | 133 | 139 | PF00069 | 0.611 |
MOD_PKA_2 | 233 | 239 | PF00069 | 0.572 |
MOD_Plk_1 | 15 | 21 | PF00069 | 0.632 |
MOD_Plk_1 | 184 | 190 | PF00069 | 0.432 |
MOD_Plk_4 | 133 | 139 | PF00069 | 0.680 |
MOD_Plk_4 | 141 | 147 | PF00069 | 0.522 |
MOD_Plk_4 | 184 | 190 | PF00069 | 0.464 |
MOD_Plk_4 | 51 | 57 | PF00069 | 0.577 |
MOD_ProDKin_1 | 19 | 25 | PF00069 | 0.564 |
MOD_SUMO_for_1 | 119 | 122 | PF00179 | 0.465 |
TRG_ENDOCYTIC_2 | 113 | 116 | PF00928 | 0.519 |
TRG_ER_diArg_1 | 57 | 60 | PF00400 | 0.409 |
TRG_Pf-PMV_PEXEL_1 | 87 | 91 | PF00026 | 0.511 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1IJK2 | Leptomonas seymouri | 38% | 100% |
A0A3Q8ID42 | Leishmania donovani | 69% | 100% |
A4I362 | Leishmania infantum | 71% | 100% |
E9ACZ1 | Leishmania major | 72% | 100% |
E9AYR6 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 68% | 100% |