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: 8 |
NetGPI | no | yes: 0, no: 8 |
Related structures:
AlphaFold database: E9AYH8
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 145 | 149 | PF00656 | 0.508 |
CLV_C14_Caspase3-7 | 174 | 178 | PF00656 | 0.297 |
CLV_NRD_NRD_1 | 131 | 133 | PF00675 | 0.521 |
CLV_NRD_NRD_1 | 17 | 19 | PF00675 | 0.498 |
CLV_NRD_NRD_1 | 24 | 26 | PF00675 | 0.579 |
CLV_NRD_NRD_1 | 3 | 5 | PF00675 | 0.648 |
CLV_NRD_NRD_1 | 32 | 34 | PF00675 | 0.589 |
CLV_PCSK_KEX2_1 | 158 | 160 | PF00082 | 0.548 |
CLV_PCSK_KEX2_1 | 17 | 19 | PF00082 | 0.495 |
CLV_PCSK_KEX2_1 | 24 | 26 | PF00082 | 0.582 |
CLV_PCSK_KEX2_1 | 3 | 5 | PF00082 | 0.645 |
CLV_PCSK_KEX2_1 | 32 | 34 | PF00082 | 0.597 |
CLV_PCSK_PC1ET2_1 | 158 | 160 | PF00082 | 0.522 |
CLV_PCSK_SKI1_1 | 103 | 107 | PF00082 | 0.486 |
CLV_PCSK_SKI1_1 | 126 | 130 | PF00082 | 0.463 |
CLV_PCSK_SKI1_1 | 158 | 162 | PF00082 | 0.548 |
DOC_CKS1_1 | 48 | 53 | PF01111 | 0.671 |
DOC_MAPK_gen_1 | 103 | 113 | PF00069 | 0.612 |
DOC_MAPK_gen_1 | 115 | 122 | PF00069 | 0.446 |
DOC_MAPK_gen_1 | 161 | 170 | PF00069 | 0.490 |
DOC_MAPK_gen_1 | 179 | 187 | PF00069 | 0.614 |
DOC_MAPK_gen_1 | 32 | 38 | PF00069 | 0.616 |
DOC_MAPK_HePTP_8 | 160 | 172 | PF00069 | 0.494 |
DOC_MAPK_MEF2A_6 | 163 | 172 | PF00069 | 0.523 |
DOC_PP1_RVXF_1 | 181 | 188 | PF00149 | 0.309 |
DOC_USP7_MATH_1 | 65 | 69 | PF00917 | 0.800 |
DOC_USP7_UBL2_3 | 129 | 133 | PF12436 | 0.464 |
DOC_WW_Pin1_4 | 47 | 52 | PF00397 | 0.640 |
LIG_14-3-3_CanoR_1 | 115 | 121 | PF00244 | 0.492 |
LIG_14-3-3_CanoR_1 | 17 | 22 | PF00244 | 0.695 |
LIG_14-3-3_CanoR_1 | 200 | 205 | PF00244 | 0.531 |
LIG_14-3-3_CanoR_1 | 24 | 29 | PF00244 | 0.649 |
LIG_14-3-3_CanoR_1 | 32 | 37 | PF00244 | 0.546 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.707 |
LIG_CSL_BTD_1 | 8 | 11 | PF09270 | 0.628 |
LIG_FHA_2 | 172 | 178 | PF00498 | 0.372 |
LIG_FHA_2 | 65 | 71 | PF00498 | 0.729 |
LIG_LIR_Gen_1 | 125 | 131 | PF02991 | 0.419 |
LIG_LIR_Nem_3 | 125 | 130 | PF02991 | 0.455 |
LIG_LIR_Nem_3 | 169 | 175 | PF02991 | 0.571 |
LIG_LIR_Nem_3 | 50 | 56 | PF02991 | 0.613 |
LIG_PAM2_1 | 34 | 46 | PF00658 | 0.444 |
LIG_PDZ_Class_2 | 201 | 206 | PF00595 | 0.492 |
LIG_PTB_Apo_2 | 188 | 195 | PF02174 | 0.384 |
LIG_SH2_CRK | 192 | 196 | PF00017 | 0.455 |
LIG_SH2_STAT5 | 201 | 204 | PF00017 | 0.503 |
LIG_SH3_3 | 35 | 41 | PF00018 | 0.743 |
LIG_SH3_3 | 42 | 48 | PF00018 | 0.609 |
LIG_SH3_3 | 68 | 74 | PF00018 | 0.611 |
LIG_SUMO_SIM_par_1 | 97 | 102 | PF11976 | 0.602 |
LIG_WRC_WIRS_1 | 201 | 206 | PF05994 | 0.553 |
MOD_CK1_1 | 20 | 26 | PF00069 | 0.644 |
MOD_CK1_1 | 76 | 82 | PF00069 | 0.768 |
MOD_CK2_1 | 64 | 70 | PF00069 | 0.670 |
MOD_Cter_Amidation | 30 | 33 | PF01082 | 0.664 |
MOD_GlcNHglycan | 55 | 59 | PF01048 | 0.775 |
MOD_GSK3_1 | 16 | 23 | PF00069 | 0.615 |
MOD_GSK3_1 | 171 | 178 | PF00069 | 0.568 |
MOD_GSK3_1 | 190 | 197 | PF00069 | 0.518 |
MOD_N-GLC_1 | 190 | 195 | PF02516 | 0.389 |
MOD_NEK2_1 | 111 | 116 | PF00069 | 0.610 |
MOD_NEK2_1 | 168 | 173 | PF00069 | 0.408 |
MOD_PK_1 | 17 | 23 | PF00069 | 0.635 |
MOD_PKA_1 | 17 | 23 | PF00069 | 0.490 |
MOD_PKA_1 | 24 | 30 | PF00069 | 0.562 |
MOD_PKA_1 | 32 | 38 | PF00069 | 0.567 |
MOD_PKA_2 | 111 | 117 | PF00069 | 0.528 |
MOD_PKA_2 | 16 | 22 | PF00069 | 0.495 |
MOD_PKA_2 | 162 | 168 | PF00069 | 0.383 |
MOD_PKA_2 | 199 | 205 | PF00069 | 0.532 |
MOD_PKA_2 | 24 | 30 | PF00069 | 0.555 |
MOD_PKA_2 | 32 | 38 | PF00069 | 0.548 |
MOD_Plk_1 | 168 | 174 | PF00069 | 0.548 |
MOD_Plk_1 | 190 | 196 | PF00069 | 0.387 |
MOD_Plk_4 | 168 | 174 | PF00069 | 0.422 |
MOD_ProDKin_1 | 47 | 53 | PF00069 | 0.640 |
MOD_SUMO_for_1 | 105 | 108 | PF00179 | 0.443 |
MOD_SUMO_rev_2 | 155 | 160 | PF00179 | 0.497 |
TRG_ENDOCYTIC_2 | 201 | 204 | PF00928 | 0.571 |
TRG_ER_diArg_1 | 16 | 18 | PF00400 | 0.546 |
TRG_NLS_MonoExtC_3 | 131 | 137 | PF00514 | 0.440 |
TRG_NLS_MonoExtN_4 | 129 | 136 | PF00514 | 0.438 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A1X0P8F5 | Trypanosomatidae | 22% | 91% |
A0A1X0P8T2 | Trypanosomatidae | 23% | 91% |
A0A3Q8IPD3 | Leishmania donovani | 85% | 100% |
A4HF42 | Leishmania braziliensis | 67% | 100% |
A4I2C6 | Leishmania infantum | 85% | 100% |
C9ZX85 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 24% | 100% |
Q4Q8Z4 | Leishmania major | 81% | 100% |