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: 11 |
NetGPI | no | yes: 0, no: 11 |
Related structures:
AlphaFold database: Q4Q2Q0
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 10 | 12 | PF00675 | 0.742 |
CLV_NRD_NRD_1 | 154 | 156 | PF00675 | 0.660 |
CLV_NRD_NRD_1 | 215 | 217 | PF00675 | 0.594 |
CLV_NRD_NRD_1 | 218 | 220 | PF00675 | 0.588 |
CLV_NRD_NRD_1 | 37 | 39 | PF00675 | 0.540 |
CLV_NRD_NRD_1 | 52 | 54 | PF00675 | 0.560 |
CLV_PCSK_KEX2_1 | 10 | 12 | PF00082 | 0.742 |
CLV_PCSK_KEX2_1 | 152 | 154 | PF00082 | 0.676 |
CLV_PCSK_KEX2_1 | 266 | 268 | PF00082 | 0.533 |
CLV_PCSK_KEX2_1 | 36 | 38 | PF00082 | 0.533 |
CLV_PCSK_KEX2_1 | 52 | 54 | PF00082 | 0.553 |
CLV_PCSK_PC1ET2_1 | 152 | 154 | PF00082 | 0.689 |
CLV_PCSK_PC1ET2_1 | 266 | 268 | PF00082 | 0.533 |
CLV_PCSK_SKI1_1 | 42 | 46 | PF00082 | 0.654 |
DEG_SCF_FBW7_1 | 285 | 292 | PF00400 | 0.519 |
DOC_PP4_FxxP_1 | 66 | 69 | PF00568 | 0.683 |
DOC_USP7_MATH_1 | 116 | 120 | PF00917 | 0.670 |
DOC_USP7_MATH_1 | 227 | 231 | PF00917 | 0.556 |
DOC_WW_Pin1_4 | 285 | 290 | PF00397 | 0.743 |
LIG_14-3-3_CanoR_1 | 115 | 125 | PF00244 | 0.644 |
LIG_14-3-3_CanoR_1 | 281 | 286 | PF00244 | 0.728 |
LIG_BRCT_BRCA1_1 | 276 | 280 | PF00533 | 0.589 |
LIG_FHA_1 | 193 | 199 | PF00498 | 0.673 |
LIG_FHA_1 | 28 | 34 | PF00498 | 0.607 |
LIG_FHA_1 | 93 | 99 | PF00498 | 0.654 |
LIG_FHA_2 | 161 | 167 | PF00498 | 0.740 |
LIG_FHA_2 | 57 | 63 | PF00498 | 0.683 |
LIG_IBAR_NPY_1 | 274 | 276 | PF08397 | 0.566 |
LIG_LIR_Apic_2 | 199 | 205 | PF02991 | 0.571 |
LIG_LIR_Gen_1 | 95 | 105 | PF02991 | 0.653 |
LIG_LIR_Nem_3 | 21 | 27 | PF02991 | 0.513 |
LIG_LIR_Nem_3 | 250 | 255 | PF02991 | 0.485 |
LIG_LIR_Nem_3 | 75 | 81 | PF02991 | 0.644 |
LIG_SH2_CRK | 276 | 280 | PF00017 | 0.615 |
LIG_SH2_NCK_1 | 276 | 280 | PF00017 | 0.615 |
LIG_SH2_PTP2 | 202 | 205 | PF00017 | 0.569 |
LIG_SH2_STAP1 | 276 | 280 | PF00017 | 0.589 |
LIG_SH2_STAT3 | 235 | 238 | PF00017 | 0.658 |
LIG_SH2_STAT5 | 202 | 205 | PF00017 | 0.592 |
LIG_SH3_1 | 22 | 28 | PF00018 | 0.538 |
LIG_SH3_3 | 22 | 28 | PF00018 | 0.587 |
LIG_SH3_3 | 287 | 293 | PF00018 | 0.558 |
LIG_SUMO_SIM_par_1 | 256 | 261 | PF11976 | 0.580 |
LIG_TYR_ITSM | 74 | 81 | PF00017 | 0.727 |
LIG_UBA3_1 | 264 | 272 | PF00899 | 0.557 |
LIG_WW_3 | 288 | 292 | PF00397 | 0.677 |
MOD_CDK_SPxK_1 | 285 | 291 | PF00069 | 0.673 |
MOD_CK1_1 | 230 | 236 | PF00069 | 0.562 |
MOD_CK2_1 | 160 | 166 | PF00069 | 0.743 |
MOD_CK2_1 | 212 | 218 | PF00069 | 0.545 |
MOD_CK2_1 | 56 | 62 | PF00069 | 0.680 |
MOD_Cter_Amidation | 50 | 53 | PF01082 | 0.709 |
MOD_Cter_Amidation | 8 | 11 | PF01082 | 0.661 |
MOD_GlcNHglycan | 198 | 201 | PF01048 | 0.698 |
MOD_GSK3_1 | 117 | 124 | PF00069 | 0.630 |
MOD_GSK3_1 | 135 | 142 | PF00069 | 0.686 |
MOD_GSK3_1 | 192 | 199 | PF00069 | 0.652 |
MOD_GSK3_1 | 230 | 237 | PF00069 | 0.573 |
MOD_GSK3_1 | 27 | 34 | PF00069 | 0.557 |
MOD_GSK3_1 | 275 | 282 | PF00069 | 0.583 |
MOD_GSK3_1 | 285 | 292 | PF00069 | 0.726 |
MOD_GSK3_1 | 88 | 95 | PF00069 | 0.600 |
MOD_N-GLC_1 | 190 | 195 | PF02516 | 0.601 |
MOD_N-GLC_1 | 212 | 217 | PF02516 | 0.571 |
MOD_N-GLC_1 | 71 | 76 | PF02516 | 0.655 |
MOD_NEK2_1 | 1 | 6 | PF00069 | 0.659 |
MOD_NEK2_1 | 100 | 105 | PF00069 | 0.661 |
MOD_NEK2_1 | 13 | 18 | PF00069 | 0.509 |
MOD_NEK2_1 | 139 | 144 | PF00069 | 0.613 |
MOD_NEK2_1 | 190 | 195 | PF00069 | 0.617 |
MOD_NEK2_1 | 212 | 217 | PF00069 | 0.487 |
MOD_NEK2_1 | 234 | 239 | PF00069 | 0.526 |
MOD_NEK2_1 | 244 | 249 | PF00069 | 0.434 |
MOD_NEK2_1 | 280 | 285 | PF00069 | 0.723 |
MOD_NEK2_1 | 71 | 76 | PF00069 | 0.699 |
MOD_NEK2_2 | 275 | 280 | PF00069 | 0.591 |
MOD_PIKK_1 | 234 | 240 | PF00454 | 0.617 |
MOD_PKA_2 | 116 | 122 | PF00069 | 0.630 |
MOD_PKA_2 | 196 | 202 | PF00069 | 0.711 |
MOD_PKA_2 | 280 | 286 | PF00069 | 0.599 |
MOD_PKB_1 | 115 | 123 | PF00069 | 0.483 |
MOD_Plk_1 | 190 | 196 | PF00069 | 0.672 |
MOD_Plk_2-3 | 251 | 257 | PF00069 | 0.523 |
MOD_Plk_4 | 100 | 106 | PF00069 | 0.669 |
MOD_Plk_4 | 135 | 141 | PF00069 | 0.601 |
MOD_Plk_4 | 227 | 233 | PF00069 | 0.604 |
MOD_Plk_4 | 275 | 281 | PF00069 | 0.599 |
MOD_ProDKin_1 | 285 | 291 | PF00069 | 0.748 |
MOD_SUMO_rev_2 | 179 | 186 | PF00179 | 0.674 |
MOD_SUMO_rev_2 | 214 | 222 | PF00179 | 0.473 |
MOD_SUMO_rev_2 | 269 | 273 | PF00179 | 0.538 |
TRG_DiLeu_BaEn_2 | 38 | 44 | PF01217 | 0.674 |
TRG_DiLeu_BaLyEn_6 | 9 | 14 | PF01217 | 0.496 |
TRG_ENDOCYTIC_2 | 276 | 279 | PF00928 | 0.609 |
TRG_ENDOCYTIC_2 | 78 | 81 | PF00928 | 0.665 |
TRG_ER_diArg_1 | 10 | 12 | PF00400 | 0.741 |
TRG_ER_diArg_1 | 153 | 155 | PF00400 | 0.684 |
TRG_ER_diArg_1 | 35 | 38 | PF00400 | 0.525 |
TRG_Pf-PMV_PEXEL_1 | 188 | 192 | PF00026 | 0.586 |
TRG_Pf-PMV_PEXEL_1 | 42 | 47 | PF00026 | 0.682 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1PAU8 | Leptomonas seymouri | 59% | 100% |
A0A0S4IYA0 | Bodo saltans | 23% | 100% |
A0A1X0PA38 | Trypanosomatidae | 29% | 100% |
A0A3Q8ILA3 | Leishmania donovani | 90% | 96% |
A0A3R7KSA4 | Trypanosoma rangeli | 31% | 100% |
A4HB13 | Leishmania braziliensis | 74% | 100% |
A4IA70 | Leishmania infantum | 91% | 100% |
C9ZM36 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 27% | 100% |
E9B583 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 91% | 100% |
V5BV16 | Trypanosoma cruzi | 32% | 100% |