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: 9 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 1, no: 8 |
NetGPI | no | yes: 0, no: 9 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 155 | 157 | PF00675 | 0.499 |
CLV_NRD_NRD_1 | 184 | 186 | PF00675 | 0.582 |
CLV_NRD_NRD_1 | 197 | 199 | PF00675 | 0.560 |
CLV_NRD_NRD_1 | 2 | 4 | PF00675 | 0.579 |
CLV_NRD_NRD_1 | 57 | 59 | PF00675 | 0.432 |
CLV_NRD_NRD_1 | 9 | 11 | PF00675 | 0.580 |
CLV_PCSK_FUR_1 | 156 | 160 | PF00082 | 0.483 |
CLV_PCSK_KEX2_1 | 158 | 160 | PF00082 | 0.471 |
CLV_PCSK_KEX2_1 | 178 | 180 | PF00082 | 0.293 |
CLV_PCSK_KEX2_1 | 184 | 186 | PF00082 | 0.585 |
CLV_PCSK_KEX2_1 | 2 | 4 | PF00082 | 0.560 |
CLV_PCSK_KEX2_1 | 57 | 59 | PF00082 | 0.432 |
CLV_PCSK_KEX2_1 | 9 | 11 | PF00082 | 0.560 |
CLV_PCSK_PC1ET2_1 | 158 | 160 | PF00082 | 0.471 |
CLV_PCSK_PC1ET2_1 | 178 | 180 | PF00082 | 0.293 |
CLV_PCSK_SKI1_1 | 165 | 169 | PF00082 | 0.538 |
CLV_PCSK_SKI1_1 | 194 | 198 | PF00082 | 0.570 |
DEG_APCC_DBOX_1 | 57 | 65 | PF00400 | 0.431 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.584 |
DOC_CKS1_1 | 131 | 136 | PF01111 | 0.456 |
DOC_CYCLIN_RxL_1 | 159 | 171 | PF00134 | 0.385 |
DOC_MAPK_gen_1 | 57 | 64 | PF00069 | 0.425 |
DOC_USP7_MATH_1 | 17 | 21 | PF00917 | 0.700 |
DOC_USP7_MATH_1 | 173 | 177 | PF00917 | 0.555 |
DOC_USP7_MATH_1 | 210 | 214 | PF00917 | 0.753 |
DOC_USP7_MATH_1 | 34 | 38 | PF00917 | 0.649 |
DOC_WW_Pin1_4 | 130 | 135 | PF00397 | 0.447 |
DOC_WW_Pin1_4 | 206 | 211 | PF00397 | 0.575 |
DOC_WW_Pin1_4 | 68 | 73 | PF00397 | 0.409 |
LIG_14-3-3_CanoR_1 | 172 | 176 | PF00244 | 0.617 |
LIG_14-3-3_CanoR_1 | 44 | 52 | PF00244 | 0.526 |
LIG_Clathr_ClatBox_1 | 61 | 65 | PF01394 | 0.440 |
LIG_FHA_1 | 85 | 91 | PF00498 | 0.427 |
LIG_FHA_2 | 172 | 178 | PF00498 | 0.579 |
LIG_FHA_2 | 51 | 57 | PF00498 | 0.449 |
LIG_LIR_Nem_3 | 56 | 62 | PF02991 | 0.424 |
LIG_SUMO_SIM_anti_2 | 37 | 42 | PF11976 | 0.433 |
LIG_UBA3_1 | 131 | 136 | PF00899 | 0.531 |
LIG_UBA3_1 | 152 | 158 | PF00899 | 0.526 |
LIG_WW_3 | 245 | 249 | PF00397 | 0.795 |
MOD_CDK_SPxK_1 | 130 | 136 | PF00069 | 0.484 |
MOD_CK1_1 | 215 | 221 | PF00069 | 0.820 |
MOD_CK1_1 | 22 | 28 | PF00069 | 0.732 |
MOD_GlcNHglycan | 139 | 143 | PF01048 | 0.572 |
MOD_GlcNHglycan | 19 | 22 | PF01048 | 0.706 |
MOD_GlcNHglycan | 214 | 217 | PF01048 | 0.705 |
MOD_GlcNHglycan | 241 | 244 | PF01048 | 0.731 |
MOD_GlcNHglycan | 25 | 28 | PF01048 | 0.742 |
MOD_GlcNHglycan | 32 | 35 | PF01048 | 0.577 |
MOD_GlcNHglycan | 48 | 51 | PF01048 | 0.574 |
MOD_GSK3_1 | 143 | 150 | PF00069 | 0.599 |
MOD_GSK3_1 | 15 | 22 | PF00069 | 0.673 |
MOD_GSK3_1 | 206 | 213 | PF00069 | 0.774 |
MOD_GSK3_1 | 30 | 37 | PF00069 | 0.594 |
MOD_GSK3_1 | 46 | 53 | PF00069 | 0.555 |
MOD_NEK2_1 | 186 | 191 | PF00069 | 0.576 |
MOD_NEK2_1 | 30 | 35 | PF00069 | 0.645 |
MOD_PIKK_1 | 143 | 149 | PF00454 | 0.688 |
MOD_PKA_1 | 9 | 15 | PF00069 | 0.685 |
MOD_PKA_2 | 171 | 177 | PF00069 | 0.586 |
MOD_PKA_2 | 186 | 192 | PF00069 | 0.476 |
MOD_PKA_2 | 221 | 227 | PF00069 | 0.717 |
MOD_PKA_2 | 239 | 245 | PF00069 | 0.555 |
MOD_PKA_2 | 50 | 56 | PF00069 | 0.451 |
MOD_PKA_2 | 9 | 15 | PF00069 | 0.635 |
MOD_Plk_1 | 179 | 185 | PF00069 | 0.482 |
MOD_Plk_2-3 | 171 | 177 | PF00069 | 0.618 |
MOD_Plk_4 | 34 | 40 | PF00069 | 0.586 |
MOD_Plk_4 | 71 | 77 | PF00069 | 0.414 |
MOD_ProDKin_1 | 130 | 136 | PF00069 | 0.452 |
MOD_ProDKin_1 | 206 | 212 | PF00069 | 0.581 |
MOD_ProDKin_1 | 68 | 74 | PF00069 | 0.405 |
TRG_ER_diArg_1 | 1 | 3 | PF00400 | 0.587 |
TRG_ER_diArg_1 | 183 | 185 | PF00400 | 0.415 |
TRG_ER_diArg_1 | 57 | 59 | PF00400 | 0.432 |
TRG_ER_diArg_1 | 9 | 11 | PF00400 | 0.580 |
TRG_Pf-PMV_PEXEL_1 | 159 | 164 | PF00026 | 0.568 |
TRG_Pf-PMV_PEXEL_1 | 184 | 188 | PF00026 | 0.494 |
TRG_Pf-PMV_PEXEL_1 | 199 | 203 | PF00026 | 0.594 |
TRG_Pf-PMV_PEXEL_1 | 88 | 92 | PF00026 | 0.418 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P6N8 | Leptomonas seymouri | 77% | 100% |
A0A0S4JMA4 | Bodo saltans | 62% | 100% |
A0A3R7NZX6 | Trypanosoma rangeli | 80% | 100% |
A0A451EJ64 | Leishmania donovani | 94% | 100% |
A4H340 | Leishmania braziliensis | 75% | 100% |
A4HRC7 | Leishmania infantum | 93% | 100% |
C9ZXG9 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 62% | 100% |
E9AJ92 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 87% | 99% |