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: 14 |
NetGPI | no | yes: 0, no: 14 |
Related structures:
AlphaFold database: A4I749
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 199 | 201 | PF00675 | 0.414 |
CLV_NRD_NRD_1 | 25 | 27 | PF00675 | 0.394 |
CLV_NRD_NRD_1 | 53 | 55 | PF00675 | 0.478 |
CLV_PCSK_KEX2_1 | 140 | 142 | PF00082 | 0.700 |
CLV_PCSK_KEX2_1 | 150 | 152 | PF00082 | 0.582 |
CLV_PCSK_KEX2_1 | 199 | 201 | PF00082 | 0.417 |
CLV_PCSK_PC1ET2_1 | 140 | 142 | PF00082 | 0.700 |
CLV_PCSK_PC1ET2_1 | 150 | 152 | PF00082 | 0.582 |
CLV_PCSK_SKI1_1 | 145 | 149 | PF00082 | 0.587 |
CLV_PCSK_SKI1_1 | 200 | 204 | PF00082 | 0.504 |
CLV_PCSK_SKI1_1 | 226 | 230 | PF00082 | 0.547 |
CLV_PCSK_SKI1_1 | 39 | 43 | PF00082 | 0.435 |
CLV_PCSK_SKI1_1 | 92 | 96 | PF00082 | 0.433 |
DEG_APCC_DBOX_1 | 140 | 148 | PF00400 | 0.491 |
DOC_MAPK_gen_1 | 90 | 97 | PF00069 | 0.459 |
DOC_MAPK_MEF2A_6 | 90 | 97 | PF00069 | 0.459 |
DOC_MAPK_NFAT4_5 | 90 | 98 | PF00069 | 0.461 |
DOC_PP2B_PxIxI_1 | 20 | 26 | PF00149 | 0.412 |
DOC_USP7_MATH_1 | 129 | 133 | PF00917 | 0.618 |
DOC_USP7_MATH_1 | 136 | 140 | PF00917 | 0.500 |
DOC_USP7_MATH_1 | 159 | 163 | PF00917 | 0.766 |
DOC_USP7_MATH_1 | 164 | 168 | PF00917 | 0.617 |
DOC_WW_Pin1_4 | 75 | 80 | PF00397 | 0.368 |
LIG_14-3-3_CanoR_1 | 33 | 43 | PF00244 | 0.390 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.533 |
LIG_deltaCOP1_diTrp_1 | 216 | 225 | PF00928 | 0.342 |
LIG_FHA_1 | 169 | 175 | PF00498 | 0.420 |
LIG_FHA_1 | 36 | 42 | PF00498 | 0.427 |
LIG_FHA_2 | 175 | 181 | PF00498 | 0.458 |
LIG_FHA_2 | 225 | 231 | PF00498 | 0.491 |
LIG_FHA_2 | 96 | 102 | PF00498 | 0.391 |
LIG_LIR_Gen_1 | 83 | 94 | PF02991 | 0.490 |
LIG_LIR_Nem_3 | 60 | 66 | PF02991 | 0.413 |
LIG_LIR_Nem_3 | 72 | 77 | PF02991 | 0.490 |
LIG_LIR_Nem_3 | 83 | 89 | PF02991 | 0.482 |
LIG_Pex14_1 | 172 | 176 | PF04695 | 0.355 |
LIG_PTB_Apo_2 | 149 | 156 | PF02174 | 0.504 |
LIG_SH2_CRK | 63 | 67 | PF00017 | 0.449 |
LIG_SH2_CRK | 86 | 90 | PF00017 | 0.346 |
LIG_SH2_STAP1 | 182 | 186 | PF00017 | 0.426 |
LIG_SH3_4 | 6 | 13 | PF00018 | 0.570 |
LIG_SUMO_SIM_anti_2 | 183 | 188 | PF11976 | 0.446 |
LIG_SUMO_SIM_par_1 | 37 | 44 | PF11976 | 0.435 |
LIG_SUMO_SIM_par_1 | 48 | 53 | PF11976 | 0.443 |
LIG_TYR_ITIM | 61 | 66 | PF00017 | 0.532 |
LIG_UBA3_1 | 187 | 193 | PF00899 | 0.469 |
MOD_CK1_1 | 121 | 127 | PF00069 | 0.472 |
MOD_CK1_1 | 132 | 138 | PF00069 | 0.692 |
MOD_CK1_1 | 162 | 168 | PF00069 | 0.692 |
MOD_CK1_1 | 178 | 184 | PF00069 | 0.435 |
MOD_CK1_1 | 53 | 59 | PF00069 | 0.633 |
MOD_CK1_1 | 85 | 91 | PF00069 | 0.424 |
MOD_CK2_1 | 174 | 180 | PF00069 | 0.409 |
MOD_CK2_1 | 95 | 101 | PF00069 | 0.398 |
MOD_GlcNHglycan | 123 | 126 | PF01048 | 0.560 |
MOD_GlcNHglycan | 130 | 134 | PF01048 | 0.702 |
MOD_GlcNHglycan | 161 | 164 | PF01048 | 0.641 |
MOD_GSK3_1 | 102 | 109 | PF00069 | 0.543 |
MOD_GSK3_1 | 114 | 121 | PF00069 | 0.419 |
MOD_GSK3_1 | 132 | 139 | PF00069 | 0.576 |
MOD_GSK3_1 | 162 | 169 | PF00069 | 0.562 |
MOD_GSK3_1 | 174 | 181 | PF00069 | 0.401 |
MOD_GSK3_1 | 224 | 231 | PF00069 | 0.505 |
MOD_GSK3_1 | 35 | 42 | PF00069 | 0.410 |
MOD_N-GLC_1 | 15 | 20 | PF02516 | 0.755 |
MOD_NEK2_1 | 114 | 119 | PF00069 | 0.315 |
MOD_NEK2_1 | 154 | 159 | PF00069 | 0.646 |
MOD_NEK2_1 | 62 | 67 | PF00069 | 0.471 |
MOD_NEK2_1 | 95 | 100 | PF00069 | 0.484 |
MOD_PKA_2 | 34 | 40 | PF00069 | 0.494 |
MOD_PKA_2 | 53 | 59 | PF00069 | 0.357 |
MOD_PKB_1 | 33 | 41 | PF00069 | 0.401 |
MOD_Plk_1 | 100 | 106 | PF00069 | 0.400 |
MOD_Plk_1 | 129 | 135 | PF00069 | 0.582 |
MOD_Plk_1 | 165 | 171 | PF00069 | 0.408 |
MOD_Plk_4 | 118 | 124 | PF00069 | 0.441 |
MOD_ProDKin_1 | 75 | 81 | PF00069 | 0.366 |
MOD_SUMO_for_1 | 192 | 195 | PF00179 | 0.376 |
TRG_ENDOCYTIC_2 | 63 | 66 | PF00928 | 0.467 |
TRG_ENDOCYTIC_2 | 86 | 89 | PF00928 | 0.400 |
TRG_ER_diArg_1 | 33 | 36 | PF00400 | 0.538 |
TRG_NLS_MonoExtC_3 | 53 | 58 | PF00514 | 0.414 |
TRG_Pf-PMV_PEXEL_1 | 39 | 44 | PF00026 | 0.428 |
TRG_Pf-PMV_PEXEL_1 | 64 | 69 | PF00026 | 0.569 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I730 | Leptomonas seymouri | 25% | 100% |
A0A0N1I8Q6 | Leptomonas seymouri | 40% | 100% |
A0A0N1PCW5 | Leptomonas seymouri | 31% | 100% |
A0A3Q8IF19 | Leishmania donovani | 41% | 100% |
A0A3S5H7Q5 | Leishmania donovani | 99% | 99% |
A4HJM7 | Leishmania braziliensis | 55% | 100% |
A4HJM8 | Leishmania braziliensis | 36% | 100% |
A4I750 | Leishmania infantum | 41% | 100% |
E9B243 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 82% | 100% |
E9B244 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 37% | 100% |
Q4Q616 | Leishmania major | 23% | 100% |
Q4Q617 | Leishmania major | 40% | 100% |
Q4Q618 | Leishmania major | 85% | 100% |