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: 9 |
NetGPI | no | yes: 0, no: 9 |
Related structures:
AlphaFold database: Q4QIN0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 12 | 16 | PF00656 | 0.523 |
CLV_PCSK_KEX2_1 | 222 | 224 | PF00082 | 0.757 |
CLV_PCSK_PC1ET2_1 | 222 | 224 | PF00082 | 0.740 |
DEG_COP1_1 | 120 | 130 | PF00400 | 0.447 |
DEG_SCF_FBW7_1 | 146 | 153 | PF00400 | 0.615 |
DEG_SPOP_SBC_1 | 131 | 135 | PF00917 | 0.621 |
DOC_CKS1_1 | 147 | 152 | PF01111 | 0.695 |
DOC_CYCLIN_yCln2_LP_2 | 34 | 40 | PF00134 | 0.496 |
DOC_MAPK_JIP1_4 | 2 | 8 | PF00069 | 0.478 |
DOC_MAPK_MEF2A_6 | 2 | 10 | PF00069 | 0.357 |
DOC_PP1_RVXF_1 | 187 | 193 | PF00149 | 0.379 |
DOC_PP2B_LxvP_1 | 34 | 37 | PF13499 | 0.534 |
DOC_PP2B_LxvP_1 | 8 | 11 | PF13499 | 0.319 |
DOC_USP7_MATH_1 | 125 | 129 | PF00917 | 0.691 |
DOC_USP7_MATH_1 | 141 | 145 | PF00917 | 0.484 |
DOC_USP7_MATH_1 | 150 | 154 | PF00917 | 0.574 |
DOC_USP7_MATH_1 | 21 | 25 | PF00917 | 0.638 |
DOC_USP7_MATH_1 | 61 | 65 | PF00917 | 0.673 |
DOC_WW_Pin1_4 | 146 | 151 | PF00397 | 0.634 |
DOC_WW_Pin1_4 | 163 | 168 | PF00397 | 0.428 |
DOC_WW_Pin1_4 | 251 | 256 | PF00397 | 0.398 |
LIG_14-3-3_CanoR_1 | 187 | 193 | PF00244 | 0.471 |
LIG_Actin_WH2_2 | 1 | 16 | PF00022 | 0.331 |
LIG_FHA_1 | 242 | 248 | PF00498 | 0.470 |
LIG_FHA_1 | 31 | 37 | PF00498 | 0.459 |
LIG_FHA_1 | 42 | 48 | PF00498 | 0.379 |
LIG_FHA_1 | 74 | 80 | PF00498 | 0.728 |
LIG_FHA_1 | 88 | 94 | PF00498 | 0.392 |
LIG_FHA_2 | 147 | 153 | PF00498 | 0.608 |
LIG_FHA_2 | 181 | 187 | PF00498 | 0.511 |
LIG_LIR_Gen_1 | 174 | 181 | PF02991 | 0.391 |
LIG_LIR_Gen_1 | 191 | 196 | PF02991 | 0.372 |
LIG_LIR_Nem_3 | 174 | 179 | PF02991 | 0.394 |
LIG_LIR_Nem_3 | 191 | 195 | PF02991 | 0.362 |
LIG_Pex14_2 | 172 | 176 | PF04695 | 0.528 |
LIG_RPA_C_Fungi | 204 | 216 | PF08784 | 0.578 |
LIG_SH2_STAT5 | 110 | 113 | PF00017 | 0.498 |
LIG_SH3_3 | 124 | 130 | PF00018 | 0.606 |
LIG_SH3_3 | 144 | 150 | PF00018 | 0.719 |
LIG_SH3_3 | 33 | 39 | PF00018 | 0.434 |
LIG_SUMO_SIM_anti_2 | 246 | 252 | PF11976 | 0.416 |
LIG_SUMO_SIM_par_1 | 242 | 248 | PF11976 | 0.462 |
MOD_CK1_1 | 135 | 141 | PF00069 | 0.659 |
MOD_CK1_1 | 24 | 30 | PF00069 | 0.552 |
MOD_CK1_1 | 64 | 70 | PF00069 | 0.692 |
MOD_CK1_1 | 78 | 84 | PF00069 | 0.705 |
MOD_CK2_1 | 180 | 186 | PF00069 | 0.517 |
MOD_Cter_Amidation | 220 | 223 | PF01082 | 0.740 |
MOD_DYRK1A_RPxSP_1 | 165 | 169 | PF00069 | 0.471 |
MOD_GlcNHglycan | 104 | 107 | PF01048 | 0.460 |
MOD_GlcNHglycan | 127 | 130 | PF01048 | 0.691 |
MOD_GlcNHglycan | 134 | 137 | PF01048 | 0.670 |
MOD_GlcNHglycan | 173 | 176 | PF01048 | 0.454 |
MOD_GlcNHglycan | 213 | 216 | PF01048 | 0.551 |
MOD_GlcNHglycan | 23 | 26 | PF01048 | 0.644 |
MOD_GlcNHglycan | 235 | 239 | PF01048 | 0.605 |
MOD_GlcNHglycan | 27 | 30 | PF01048 | 0.592 |
MOD_GlcNHglycan | 47 | 50 | PF01048 | 0.452 |
MOD_GlcNHglycan | 59 | 62 | PF01048 | 0.597 |
MOD_GSK3_1 | 131 | 138 | PF00069 | 0.622 |
MOD_GSK3_1 | 141 | 148 | PF00069 | 0.554 |
MOD_GSK3_1 | 207 | 214 | PF00069 | 0.537 |
MOD_GSK3_1 | 21 | 28 | PF00069 | 0.633 |
MOD_GSK3_1 | 241 | 248 | PF00069 | 0.408 |
MOD_GSK3_1 | 41 | 48 | PF00069 | 0.385 |
MOD_GSK3_1 | 57 | 64 | PF00069 | 0.733 |
MOD_GSK3_1 | 75 | 82 | PF00069 | 0.652 |
MOD_N-GLC_1 | 207 | 212 | PF02516 | 0.677 |
MOD_N-GLC_1 | 64 | 69 | PF02516 | 0.491 |
MOD_NEK2_1 | 119 | 124 | PF00069 | 0.586 |
MOD_NEK2_1 | 190 | 195 | PF00069 | 0.477 |
MOD_NEK2_1 | 234 | 239 | PF00069 | 0.666 |
MOD_NEK2_1 | 45 | 50 | PF00069 | 0.358 |
MOD_PIKK_1 | 180 | 186 | PF00454 | 0.508 |
MOD_PKA_2 | 188 | 194 | PF00069 | 0.426 |
MOD_PKA_2 | 21 | 27 | PF00069 | 0.617 |
MOD_Plk_1 | 207 | 213 | PF00069 | 0.606 |
MOD_Plk_1 | 241 | 247 | PF00069 | 0.408 |
MOD_Plk_4 | 245 | 251 | PF00069 | 0.391 |
MOD_Plk_4 | 79 | 85 | PF00069 | 0.539 |
MOD_ProDKin_1 | 146 | 152 | PF00069 | 0.631 |
MOD_ProDKin_1 | 163 | 169 | PF00069 | 0.422 |
MOD_ProDKin_1 | 251 | 257 | PF00069 | 0.414 |
TRG_ER_diArg_1 | 187 | 190 | PF00400 | 0.472 |
TRG_Pf-PMV_PEXEL_1 | 222 | 226 | PF00026 | 0.649 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P403 | Leptomonas seymouri | 42% | 99% |
A0A1X0NPF9 | Trypanosomatidae | 25% | 100% |
A0A3R7K387 | Trypanosoma rangeli | 29% | 100% |
A0A3S5H5Y8 | Leishmania donovani | 83% | 100% |
A4H512 | Leishmania braziliensis | 66% | 100% |
A4HT86 | Leishmania infantum | 84% | 100% |
C9ZUN8 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
E9AL74 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 75% | 100% |