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: A0A3Q8IG02
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 189 | 191 | PF00675 | 0.538 |
CLV_NRD_NRD_1 | 219 | 221 | PF00675 | 0.460 |
CLV_NRD_NRD_1 | 48 | 50 | PF00675 | 0.439 |
CLV_PCSK_KEX2_1 | 189 | 191 | PF00082 | 0.539 |
CLV_PCSK_KEX2_1 | 47 | 49 | PF00082 | 0.470 |
CLV_PCSK_SKI1_1 | 100 | 104 | PF00082 | 0.680 |
CLV_PCSK_SKI1_1 | 163 | 167 | PF00082 | 0.602 |
CLV_PCSK_SKI1_1 | 281 | 285 | PF00082 | 0.698 |
DEG_Nend_UBRbox_1 | 1 | 4 | PF02207 | 0.426 |
DEG_SPOP_SBC_1 | 143 | 147 | PF00917 | 0.768 |
DOC_CKS1_1 | 87 | 92 | PF01111 | 0.787 |
DOC_CYCLIN_RxL_1 | 160 | 167 | PF00134 | 0.656 |
DOC_MAPK_gen_1 | 47 | 54 | PF00069 | 0.333 |
DOC_PP2B_LxvP_1 | 257 | 260 | PF13499 | 0.708 |
DOC_USP7_MATH_1 | 144 | 148 | PF00917 | 0.722 |
DOC_USP7_MATH_1 | 245 | 249 | PF00917 | 0.570 |
DOC_USP7_MATH_1 | 63 | 67 | PF00917 | 0.613 |
DOC_USP7_MATH_1 | 72 | 76 | PF00917 | 0.722 |
DOC_USP7_MATH_1 | 80 | 84 | PF00917 | 0.643 |
DOC_WW_Pin1_4 | 123 | 128 | PF00397 | 0.744 |
DOC_WW_Pin1_4 | 131 | 136 | PF00397 | 0.586 |
DOC_WW_Pin1_4 | 149 | 154 | PF00397 | 0.676 |
DOC_WW_Pin1_4 | 263 | 268 | PF00397 | 0.675 |
DOC_WW_Pin1_4 | 285 | 290 | PF00397 | 0.641 |
DOC_WW_Pin1_4 | 82 | 87 | PF00397 | 0.694 |
DOC_WW_Pin1_4 | 94 | 99 | PF00397 | 0.591 |
LIG_14-3-3_CanoR_1 | 189 | 197 | PF00244 | 0.539 |
LIG_FHA_1 | 217 | 223 | PF00498 | 0.560 |
LIG_FHA_1 | 263 | 269 | PF00498 | 0.689 |
LIG_FHA_1 | 27 | 33 | PF00498 | 0.521 |
LIG_LIR_Apic_2 | 250 | 256 | PF02991 | 0.593 |
LIG_LIR_Gen_1 | 180 | 191 | PF02991 | 0.596 |
LIG_LIR_Gen_1 | 35 | 44 | PF02991 | 0.428 |
LIG_LIR_Nem_3 | 180 | 186 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 35 | 40 | PF02991 | 0.423 |
LIG_MYND_1 | 127 | 131 | PF01753 | 0.779 |
LIG_PCNA_yPIPBox_3 | 163 | 177 | PF02747 | 0.573 |
LIG_PDZ_Class_2 | 289 | 294 | PF00595 | 0.681 |
LIG_PTB_Apo_2 | 176 | 183 | PF02174 | 0.566 |
LIG_PTB_Phospho_1 | 176 | 182 | PF10480 | 0.567 |
LIG_SH2_CRK | 253 | 257 | PF00017 | 0.620 |
LIG_SH2_GRB2like | 182 | 185 | PF00017 | 0.587 |
LIG_SH2_STAT3 | 182 | 185 | PF00017 | 0.587 |
LIG_SH2_STAT5 | 182 | 185 | PF00017 | 0.554 |
LIG_SH2_STAT5 | 3 | 6 | PF00017 | 0.420 |
LIG_SH2_STAT5 | 56 | 59 | PF00017 | 0.474 |
LIG_SH3_3 | 265 | 271 | PF00018 | 0.662 |
MOD_CDC14_SPxK_1 | 85 | 88 | PF00782 | 0.784 |
MOD_CDC14_SPxK_1 | 97 | 100 | PF00782 | 0.520 |
MOD_CDK_SPK_2 | 285 | 290 | PF00069 | 0.672 |
MOD_CDK_SPxK_1 | 263 | 269 | PF00069 | 0.680 |
MOD_CDK_SPxK_1 | 82 | 88 | PF00069 | 0.787 |
MOD_CDK_SPxK_1 | 94 | 100 | PF00069 | 0.525 |
MOD_CK1_1 | 125 | 131 | PF00069 | 0.689 |
MOD_CK1_1 | 134 | 140 | PF00069 | 0.647 |
MOD_CK1_1 | 262 | 268 | PF00069 | 0.659 |
MOD_CK2_1 | 196 | 202 | PF00069 | 0.469 |
MOD_CK2_1 | 58 | 64 | PF00069 | 0.590 |
MOD_CK2_1 | 76 | 82 | PF00069 | 0.473 |
MOD_GlcNHglycan | 191 | 194 | PF01048 | 0.522 |
MOD_GlcNHglycan | 198 | 201 | PF01048 | 0.489 |
MOD_GlcNHglycan | 213 | 217 | PF01048 | 0.494 |
MOD_GlcNHglycan | 249 | 252 | PF01048 | 0.553 |
MOD_GlcNHglycan | 253 | 256 | PF01048 | 0.592 |
MOD_GlcNHglycan | 276 | 279 | PF01048 | 0.743 |
MOD_GlcNHglycan | 59 | 63 | PF01048 | 0.551 |
MOD_GlcNHglycan | 64 | 68 | PF01048 | 0.585 |
MOD_GlcNHglycan | 74 | 77 | PF01048 | 0.654 |
MOD_GlcNHglycan | 78 | 81 | PF01048 | 0.524 |
MOD_GSK3_1 | 103 | 110 | PF00069 | 0.596 |
MOD_GSK3_1 | 145 | 152 | PF00069 | 0.692 |
MOD_GSK3_1 | 212 | 219 | PF00069 | 0.620 |
MOD_GSK3_1 | 247 | 254 | PF00069 | 0.533 |
MOD_GSK3_1 | 259 | 266 | PF00069 | 0.608 |
MOD_GSK3_1 | 72 | 79 | PF00069 | 0.643 |
MOD_GSK3_1 | 82 | 89 | PF00069 | 0.655 |
MOD_N-GLC_1 | 104 | 109 | PF02516 | 0.721 |
MOD_N-GLC_1 | 115 | 120 | PF02516 | 0.619 |
MOD_NEK2_1 | 103 | 108 | PF00069 | 0.709 |
MOD_NEK2_1 | 279 | 284 | PF00069 | 0.680 |
MOD_PKA_1 | 122 | 128 | PF00069 | 0.553 |
MOD_PKA_1 | 189 | 195 | PF00069 | 0.574 |
MOD_PKA_2 | 189 | 195 | PF00069 | 0.528 |
MOD_Plk_1 | 104 | 110 | PF00069 | 0.648 |
MOD_Plk_1 | 16 | 22 | PF00069 | 0.420 |
MOD_Plk_1 | 212 | 218 | PF00069 | 0.490 |
MOD_Plk_1 | 40 | 46 | PF00069 | 0.359 |
MOD_Plk_4 | 16 | 22 | PF00069 | 0.552 |
MOD_ProDKin_1 | 123 | 129 | PF00069 | 0.747 |
MOD_ProDKin_1 | 131 | 137 | PF00069 | 0.585 |
MOD_ProDKin_1 | 149 | 155 | PF00069 | 0.673 |
MOD_ProDKin_1 | 263 | 269 | PF00069 | 0.680 |
MOD_ProDKin_1 | 285 | 291 | PF00069 | 0.642 |
MOD_ProDKin_1 | 82 | 88 | PF00069 | 0.698 |
MOD_ProDKin_1 | 94 | 100 | PF00069 | 0.594 |
MOD_SUMO_for_1 | 177 | 180 | PF00179 | 0.460 |
MOD_SUMO_for_1 | 21 | 24 | PF00179 | 0.566 |
MOD_SUMO_for_1 | 38 | 41 | PF00179 | 0.284 |
MOD_SUMO_rev_2 | 238 | 245 | PF00179 | 0.522 |
TRG_AP2beta_CARGO_1 | 180 | 190 | PF09066 | 0.470 |
TRG_DiLeu_BaEn_4 | 13 | 19 | PF01217 | 0.545 |
TRG_ENDOCYTIC_2 | 3 | 6 | PF00928 | 0.450 |
TRG_ER_diArg_1 | 233 | 236 | PF00400 | 0.495 |
TRG_ER_diArg_1 | 47 | 49 | PF00400 | 0.496 |
TRG_Pf-PMV_PEXEL_1 | 163 | 167 | PF00026 | 0.641 |
TRG_Pf-PMV_PEXEL_1 | 220 | 224 | PF00026 | 0.488 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I2T5 | Leptomonas seymouri | 61% | 92% |
A0A1X0P1K4 | Trypanosomatidae | 40% | 100% |
A0A422NLQ1 | Trypanosoma rangeli | 40% | 100% |
A4HIK1 | Leishmania braziliensis | 80% | 100% |
A4I5U6 | Leishmania infantum | 100% | 100% |
C9ZR67 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 35% | 100% |
E9B141 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 95% | 100% |
Q4Q725 | Leishmania major | 92% | 100% |
V5BX71 | Trypanosoma cruzi | 42% | 100% |