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: 14 |
NetGPI | no | yes: 0, no: 14 |
Related structures:
AlphaFold database: A4HJM7
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_NRD_NRD_1 | 208 | 210 | PF00675 | 0.582 |
CLV_PCSK_FUR_1 | 222 | 226 | PF00082 | 0.310 |
CLV_PCSK_KEX2_1 | 208 | 210 | PF00082 | 0.512 |
CLV_PCSK_KEX2_1 | 224 | 226 | PF00082 | 0.428 |
CLV_PCSK_PC1ET2_1 | 224 | 226 | PF00082 | 0.428 |
CLV_PCSK_SKI1_1 | 209 | 213 | PF00082 | 0.515 |
CLV_PCSK_SKI1_1 | 46 | 50 | PF00082 | 0.416 |
CLV_PCSK_SKI1_1 | 99 | 103 | PF00082 | 0.479 |
DEG_Nend_UBRbox_2 | 1 | 3 | PF02207 | 0.550 |
DEG_SPOP_SBC_1 | 174 | 178 | PF00917 | 0.425 |
DOC_CKS1_1 | 14 | 19 | PF01111 | 0.597 |
DOC_MAPK_DCC_7 | 166 | 174 | PF00069 | 0.488 |
DOC_MAPK_gen_1 | 123 | 130 | PF00069 | 0.370 |
DOC_MAPK_gen_1 | 97 | 104 | PF00069 | 0.475 |
DOC_MAPK_MEF2A_6 | 123 | 130 | PF00069 | 0.370 |
DOC_MAPK_MEF2A_6 | 97 | 104 | PF00069 | 0.498 |
DOC_MAPK_NFAT4_5 | 97 | 105 | PF00069 | 0.499 |
DOC_USP7_MATH_1 | 114 | 118 | PF00917 | 0.580 |
DOC_USP7_UBL2_3 | 166 | 170 | PF12436 | 0.505 |
DOC_WW_Pin1_4 | 13 | 18 | PF00397 | 0.643 |
DOC_WW_Pin1_4 | 147 | 152 | PF00397 | 0.492 |
DOC_WW_Pin1_4 | 3 | 8 | PF00397 | 0.735 |
LIG_14-3-3_CanoR_1 | 233 | 238 | PF00244 | 0.456 |
LIG_14-3-3_CanoR_1 | 40 | 50 | PF00244 | 0.378 |
LIG_EH1_1 | 190 | 198 | PF00400 | 0.256 |
LIG_FHA_1 | 178 | 184 | PF00498 | 0.442 |
LIG_FHA_1 | 43 | 49 | PF00498 | 0.425 |
LIG_FHA_1 | 54 | 60 | PF00498 | 0.435 |
LIG_FHA_2 | 103 | 109 | PF00498 | 0.391 |
LIG_FHA_2 | 184 | 190 | PF00498 | 0.419 |
LIG_FHA_2 | 227 | 233 | PF00498 | 0.470 |
LIG_LIR_Apic_2 | 11 | 17 | PF02991 | 0.522 |
LIG_LIR_Gen_1 | 179 | 188 | PF02991 | 0.417 |
LIG_LIR_Gen_1 | 90 | 101 | PF02991 | 0.493 |
LIG_LIR_Nem_3 | 179 | 185 | PF02991 | 0.330 |
LIG_LIR_Nem_3 | 90 | 96 | PF02991 | 0.500 |
LIG_PCNA_yPIPBox_3 | 115 | 125 | PF02747 | 0.406 |
LIG_PDZ_Class_3 | 238 | 243 | PF00595 | 0.745 |
LIG_Pex14_1 | 181 | 185 | PF04695 | 0.386 |
LIG_SH2_CRK | 14 | 18 | PF00017 | 0.526 |
LIG_SH2_NCK_1 | 14 | 18 | PF00017 | 0.526 |
LIG_SH2_STAP1 | 191 | 195 | PF00017 | 0.424 |
LIG_SH2_STAT5 | 121 | 124 | PF00017 | 0.400 |
LIG_SH2_STAT5 | 14 | 17 | PF00017 | 0.527 |
LIG_SH3_1 | 14 | 20 | PF00018 | 0.522 |
LIG_SH3_3 | 14 | 20 | PF00018 | 0.617 |
LIG_SUMO_SIM_anti_2 | 28 | 34 | PF11976 | 0.309 |
LIG_SUMO_SIM_par_1 | 170 | 180 | PF11976 | 0.408 |
LIG_SUMO_SIM_par_1 | 44 | 53 | PF11976 | 0.431 |
LIG_SUMO_SIM_par_1 | 55 | 60 | PF11976 | 0.439 |
LIG_UBA3_1 | 196 | 204 | PF00899 | 0.501 |
LIG_WRC_WIRS_1 | 182 | 187 | PF05994 | 0.261 |
MOD_CDK_SPK_2 | 147 | 152 | PF00069 | 0.487 |
MOD_CK1_1 | 12 | 18 | PF00069 | 0.546 |
MOD_CK1_1 | 160 | 166 | PF00069 | 0.553 |
MOD_CK1_1 | 173 | 179 | PF00069 | 0.644 |
MOD_CK1_1 | 184 | 190 | PF00069 | 0.454 |
MOD_CK1_1 | 236 | 242 | PF00069 | 0.497 |
MOD_CK1_1 | 5 | 11 | PF00069 | 0.528 |
MOD_CK2_1 | 102 | 108 | PF00069 | 0.558 |
MOD_CK2_1 | 183 | 189 | PF00069 | 0.417 |
MOD_CK2_1 | 226 | 232 | PF00069 | 0.412 |
MOD_GlcNHglycan | 11 | 14 | PF01048 | 0.514 |
MOD_GlcNHglycan | 130 | 133 | PF01048 | 0.574 |
MOD_GlcNHglycan | 154 | 157 | PF01048 | 0.733 |
MOD_GlcNHglycan | 163 | 166 | PF01048 | 0.699 |
MOD_GlcNHglycan | 226 | 229 | PF01048 | 0.613 |
MOD_GSK3_1 | 135 | 142 | PF00069 | 0.598 |
MOD_GSK3_1 | 147 | 154 | PF00069 | 0.618 |
MOD_GSK3_1 | 157 | 164 | PF00069 | 0.547 |
MOD_GSK3_1 | 170 | 177 | PF00069 | 0.571 |
MOD_GSK3_1 | 183 | 190 | PF00069 | 0.408 |
MOD_GSK3_1 | 3 | 10 | PF00069 | 0.512 |
MOD_GSK3_1 | 42 | 49 | PF00069 | 0.417 |
MOD_GSK3_1 | 53 | 60 | PF00069 | 0.456 |
MOD_N-GLC_1 | 114 | 119 | PF02516 | 0.428 |
MOD_N-GLC_1 | 158 | 163 | PF02516 | 0.559 |
MOD_N-GLC_1 | 8 | 13 | PF02516 | 0.537 |
MOD_NEK2_1 | 102 | 107 | PF00069 | 0.503 |
MOD_NEK2_1 | 130 | 135 | PF00069 | 0.529 |
MOD_PIKK_1 | 15 | 21 | PF00454 | 0.651 |
MOD_PIKK_1 | 25 | 31 | PF00454 | 0.410 |
MOD_PIKK_1 | 57 | 63 | PF00454 | 0.359 |
MOD_PK_1 | 170 | 176 | PF00069 | 0.666 |
MOD_PKA_1 | 224 | 230 | PF00069 | 0.343 |
MOD_PKA_2 | 224 | 230 | PF00069 | 0.343 |
MOD_PKA_2 | 41 | 47 | PF00069 | 0.502 |
MOD_PKB_1 | 40 | 48 | PF00069 | 0.416 |
MOD_Plk_1 | 107 | 113 | PF00069 | 0.433 |
MOD_Plk_1 | 114 | 120 | PF00069 | 0.476 |
MOD_Plk_4 | 177 | 183 | PF00069 | 0.514 |
MOD_ProDKin_1 | 13 | 19 | PF00069 | 0.642 |
MOD_ProDKin_1 | 147 | 153 | PF00069 | 0.496 |
MOD_ProDKin_1 | 3 | 9 | PF00069 | 0.737 |
TRG_ER_diArg_1 | 40 | 43 | PF00400 | 0.533 |
TRG_Pf-PMV_PEXEL_1 | 46 | 51 | PF00026 | 0.452 |
TRG_Pf-PMV_PEXEL_1 | 71 | 76 | PF00026 | 0.587 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I8Q6 | Leptomonas seymouri | 38% | 100% |
A0A0N1ILD5 | Leptomonas seymouri | 27% | 86% |
A0A0N1PCW5 | Leptomonas seymouri | 29% | 100% |
A0A3Q8IF19 | Leishmania donovani | 41% | 100% |
A0A3S5H7Q5 | Leishmania donovani | 55% | 100% |
A4HJM8 | Leishmania braziliensis | 37% | 100% |
A4I749 | Leishmania infantum | 55% | 100% |
A4I750 | Leishmania infantum | 41% | 100% |
E9B242 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 27% | 100% |
E9B243 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 50% | 100% |
E9B244 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 38% | 100% |
Q4Q617 | Leishmania major | 41% | 100% |
Q4Q618 | Leishmania major | 51% | 70% |