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: 10 |
NetGPI | no | yes: 0, no: 10 |
Related structures:
AlphaFold database: Q4Q725
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 189 | 191 | PF00675 | 0.482 |
CLV_NRD_NRD_1 | 219 | 221 | PF00675 | 0.421 |
CLV_NRD_NRD_1 | 48 | 50 | PF00675 | 0.297 |
CLV_PCSK_KEX2_1 | 189 | 191 | PF00082 | 0.484 |
CLV_PCSK_KEX2_1 | 47 | 49 | PF00082 | 0.297 |
CLV_PCSK_SKI1_1 | 100 | 104 | PF00082 | 0.588 |
CLV_PCSK_SKI1_1 | 163 | 167 | PF00082 | 0.547 |
CLV_PCSK_SKI1_1 | 281 | 285 | PF00082 | 0.667 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.374 |
DEG_SPOP_SBC_1 | 144 | 148 | PF00917 | 0.730 |
DOC_CKS1_1 | 87 | 92 | PF01111 | 0.661 |
DOC_CYCLIN_RxL_1 | 160 | 167 | PF00134 | 0.612 |
DOC_PP2B_LxvP_1 | 257 | 260 | PF13499 | 0.640 |
DOC_USP7_MATH_1 | 144 | 148 | PF00917 | 0.668 |
DOC_USP7_MATH_1 | 260 | 264 | PF00917 | 0.702 |
DOC_USP7_MATH_1 | 63 | 67 | PF00917 | 0.481 |
DOC_USP7_MATH_1 | 72 | 76 | PF00917 | 0.608 |
DOC_WW_Pin1_4 | 123 | 128 | PF00397 | 0.678 |
DOC_WW_Pin1_4 | 131 | 136 | PF00397 | 0.626 |
DOC_WW_Pin1_4 | 149 | 154 | PF00397 | 0.620 |
DOC_WW_Pin1_4 | 263 | 268 | PF00397 | 0.647 |
DOC_WW_Pin1_4 | 285 | 290 | PF00397 | 0.659 |
DOC_WW_Pin1_4 | 82 | 87 | PF00397 | 0.637 |
LIG_14-3-3_CanoR_1 | 189 | 197 | PF00244 | 0.463 |
LIG_FHA_1 | 135 | 141 | PF00498 | 0.715 |
LIG_FHA_1 | 217 | 223 | PF00498 | 0.515 |
LIG_FHA_1 | 263 | 269 | PF00498 | 0.629 |
LIG_FHA_1 | 27 | 33 | PF00498 | 0.410 |
LIG_FHA_2 | 108 | 114 | PF00498 | 0.595 |
LIG_LIR_Apic_2 | 250 | 256 | PF02991 | 0.492 |
LIG_LIR_Gen_1 | 180 | 191 | PF02991 | 0.468 |
LIG_LIR_Gen_1 | 35 | 42 | PF02991 | 0.279 |
LIG_LIR_Nem_3 | 180 | 186 | PF02991 | 0.406 |
LIG_LIR_Nem_3 | 35 | 40 | PF02991 | 0.311 |
LIG_MYND_1 | 127 | 131 | PF01753 | 0.626 |
LIG_PCNA_yPIPBox_3 | 163 | 177 | PF02747 | 0.521 |
LIG_PDZ_Class_2 | 289 | 294 | PF00595 | 0.641 |
LIG_PTB_Apo_2 | 176 | 183 | PF02174 | 0.529 |
LIG_PTB_Phospho_1 | 176 | 182 | PF10480 | 0.530 |
LIG_SH2_CRK | 253 | 257 | PF00017 | 0.522 |
LIG_SH2_GRB2like | 182 | 185 | PF00017 | 0.462 |
LIG_SH2_STAT3 | 182 | 185 | PF00017 | 0.462 |
LIG_SH2_STAT5 | 182 | 185 | PF00017 | 0.518 |
LIG_SH2_STAT5 | 3 | 6 | PF00017 | 0.394 |
LIG_SH2_STAT5 | 56 | 59 | PF00017 | 0.466 |
MOD_CDC14_SPxK_1 | 85 | 88 | PF00782 | 0.650 |
MOD_CDK_SPK_2 | 285 | 290 | PF00069 | 0.635 |
MOD_CDK_SPxK_1 | 263 | 269 | PF00069 | 0.651 |
MOD_CDK_SPxK_1 | 82 | 88 | PF00069 | 0.658 |
MOD_CK1_1 | 134 | 140 | PF00069 | 0.590 |
MOD_CK1_1 | 262 | 268 | PF00069 | 0.639 |
MOD_CK2_1 | 196 | 202 | PF00069 | 0.418 |
MOD_CK2_1 | 58 | 64 | PF00069 | 0.509 |
MOD_GlcNHglycan | 117 | 120 | PF01048 | 0.575 |
MOD_GlcNHglycan | 191 | 194 | PF01048 | 0.493 |
MOD_GlcNHglycan | 198 | 201 | PF01048 | 0.469 |
MOD_GlcNHglycan | 213 | 217 | PF01048 | 0.476 |
MOD_GlcNHglycan | 253 | 256 | PF01048 | 0.593 |
MOD_GlcNHglycan | 262 | 265 | PF01048 | 0.628 |
MOD_GlcNHglycan | 276 | 279 | PF01048 | 0.598 |
MOD_GlcNHglycan | 59 | 63 | PF01048 | 0.547 |
MOD_GlcNHglycan | 69 | 72 | PF01048 | 0.655 |
MOD_GlcNHglycan | 74 | 77 | PF01048 | 0.615 |
MOD_GlcNHglycan | 96 | 100 | PF01048 | 0.619 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.594 |
MOD_GSK3_1 | 131 | 138 | PF00069 | 0.599 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.626 |
MOD_GSK3_1 | 212 | 219 | PF00069 | 0.428 |
MOD_GSK3_1 | 247 | 254 | PF00069 | 0.526 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.600 |
MOD_GSK3_1 | 63 | 70 | PF00069 | 0.496 |
MOD_GSK3_1 | 77 | 84 | PF00069 | 0.641 |
MOD_N-GLC_1 | 104 | 109 | PF02516 | 0.720 |
MOD_N-GLC_1 | 115 | 120 | PF02516 | 0.596 |
MOD_NEK2_1 | 103 | 108 | PF00069 | 0.684 |
MOD_NEK2_2 | 145 | 150 | PF00069 | 0.440 |
MOD_PKA_1 | 189 | 195 | PF00069 | 0.533 |
MOD_PKA_2 | 189 | 195 | PF00069 | 0.451 |
MOD_Plk_1 | 104 | 110 | PF00069 | 0.624 |
MOD_Plk_1 | 135 | 141 | PF00069 | 0.679 |
MOD_Plk_1 | 16 | 22 | PF00069 | 0.282 |
MOD_Plk_1 | 212 | 218 | PF00069 | 0.443 |
MOD_Plk_4 | 16 | 22 | PF00069 | 0.472 |
MOD_Plk_4 | 52 | 58 | PF00069 | 0.413 |
MOD_ProDKin_1 | 123 | 129 | PF00069 | 0.680 |
MOD_ProDKin_1 | 131 | 137 | PF00069 | 0.627 |
MOD_ProDKin_1 | 149 | 155 | PF00069 | 0.617 |
MOD_ProDKin_1 | 263 | 269 | PF00069 | 0.653 |
MOD_ProDKin_1 | 285 | 291 | PF00069 | 0.660 |
MOD_ProDKin_1 | 82 | 88 | PF00069 | 0.640 |
MOD_SUMO_for_1 | 177 | 180 | PF00179 | 0.401 |
MOD_SUMO_for_1 | 21 | 24 | PF00179 | 0.440 |
MOD_SUMO_for_1 | 38 | 41 | PF00179 | 0.184 |
MOD_SUMO_rev_2 | 238 | 245 | PF00179 | 0.436 |
TRG_AP2beta_CARGO_1 | 180 | 190 | PF09066 | 0.411 |
TRG_DiLeu_BaEn_4 | 13 | 19 | PF01217 | 0.410 |
TRG_ENDOCYTIC_2 | 3 | 6 | PF00928 | 0.426 |
TRG_ER_diArg_1 | 233 | 236 | PF00400 | 0.457 |
TRG_ER_diArg_1 | 47 | 49 | PF00400 | 0.325 |
TRG_Pf-PMV_PEXEL_1 | 163 | 167 | PF00026 | 0.600 |
TRG_Pf-PMV_PEXEL_1 | 220 | 224 | PF00026 | 0.428 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I2T5 | Leptomonas seymouri | 59% | 92% |
A0A1X0P1K4 | Trypanosomatidae | 39% | 100% |
A0A3Q8IG02 | Leishmania donovani | 92% | 100% |
A0A422NLQ1 | Trypanosoma rangeli | 39% | 100% |
A4HIK1 | Leishmania braziliensis | 80% | 100% |
A4I5U6 | Leishmania infantum | 91% | 100% |
C9ZR67 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
E9B141 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 93% | 100% |
V5BX71 | Trypanosoma cruzi | 44% | 100% |